INTERNATIONAL ATOMIC ENERGY AGENCY AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION |
DISTANCE LEARNING MATERIALS
RADIATION PROTECTION
Module 2.1
Prepared by Safety and Radiation Science
Australian Nuclear Science and Technology Organisation
With the assistance of consultants in Australia and the United Kingdom, and IAEA experts from Korea, Mongolia, New Zealand, the Philippines and Thailand
Use of this material, acknowledging the IAEA and ANSTO as the source, is permitted for non-profit training
Acknowledgements
This material has been prepared by an extensive team of international experts from the fields of radiation protection, medicine and education. It is not possible to mention by name all those who have had an input to; the initial planning; writing modules and workbooks; preparing and marking final assignments; proof-reading and editing; using the material and providing valuable feedback; organizing and hosting review meetings; and general administrative support.
The support of ANSTO management in providing the resource and encouragement is gratefully acknowledged.
The enthusiastic support of IAEA Technical Officers has been vital to the success of this project.
PART 2
RADIATION PROTECTION
MODULE 2.1
PRINCIPLES OF RADIATION PROTECTION
CONTENTS
OVERVIEW
Module 1.6 explained how ionizing radiation may affect the body. The major objective of radiation protection is to control exposures to radiation so that deterministic effects are avoided and chances of stochastic effects are minimized. In this module you will learn how radiation protection principles can be applied in order to achieve this objective while still allowing the beneficial uses of ionizing radiation.
TIME ALLOCATION
It is estimated that you will need to spend five to seven hours to complete this module before commencing the final assignment. This time estimate is for guidance only. Do not worry if you need more time to understand the module.
MATERIALS
You will need your workbook and writing materials to take notes and answer the questions in this module.
NOW YOU ARE READY TO START WORK
1.INTRODUCTION TO RADIATION PROTECTION
All human beings are exposed to ionizing radiation from natural and artificial sources. Exposure to natural radiation arises from both cosmic and terrestrial sources, as well as from natural radioactivity in our food and drink. Throughout history, man has been exposed to natural radiation, and it is impossible to decide whether this radiation has been harmful or beneficial to the human species. In contrast, artificial radiation sources have only been introduced in the last 100 years and although many benefits have been gained from their use (e.g. medical, industrial and agricultural uses), it has been realized that exposure to these sources can be harmful to us. For this reason, a system of radiation protection has been developed to protect people from unnecessary or excessive exposure to ionizing radiation. As the effects of ionizing radiation are better understood, this system is updated to ensure the best possible protection for both radiation workers and for members of the general public.
2.RADIATION PROTECTION AND RISK
For the purpose of this learning material, it is important to clearly define the term radiation protection. In simple terms, radiation protection is defined as the science and practice of limiting harm to human beings from radiation. As we are only concerned with the effects of ionizing radiation, all references used in this module refer to ionizing radiation only.
In every activity of our daily lives humans are exposed to hazards. For example, every time you cross the road there is a possibility that you may be hit by a car, and each time a person smokes a cigarette there is an increased chance of that person contracting lung cancer. Although we are all aware of the possible consequences, people still cross roads and still smoke cigarettes. This apparent disregard for our own safety may be because we have some appreciation of the probability and size of the consequence of each action; that is, we have an idea of the risk of crossing the road or smoking a cigarette. This also applies in the field of radiation protection; in all radiological activities it is important to have some idea of the risk associated with the use of ionizing radiation. In simple terms, risk is defined as a combination of the probability that a harmful consequence may occur and the size of that consequence.
The information used to estimate the risk of ionizing radiation is derived from detailed accident investigations and long-term epidemiological studies of populations exposed to radiation, such as the survivors of the atomic bombing of Hiroshima and Nagasaki in Japan in 1945. Two main organizations (the United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) and the Advisory Committee on the Biological Effects of Ionizing Radiation (BEIR)) are responsible for collecting and summarizing the relevant data, and for producing detailed reports on their findings. These reports are then collated to establish risk estimates on which a system of radiological protection can be based. The organization responsible for making recommendations based on these risk estimates is known as the International Commission on Radiation Protection (ICRP) and Figure 1 illustrates the responsibilities and relationship of these different committees.
Figure 1
The Relationship Between UNSCEAR, BEIR and the ICRP
3.INTRODUCTION TO THE ICRP
3.1History Of The ICRP
The International Commission on Radiological Protection (ICRP) was established in 1928. At that time, people were concerned with the hazards associated with X-rays and radium and the ICRP was primarily responsible for protecting workers exposed to these sources. In 1950 the ICRP’s responsibilities were extended to deal with the new problems arising from the introduction of nuclear reactors and the organization was subsequently restructured. Since then, the interests of the ICRP have broadened to take account of the increasing uses of ionizing radiation and of practices that involve the generation of radiation and radioactive materials. Nowadays the ICRP considers radiation protection issues which affect members of the public as well as people who work with sources of ionizing radiation.
3.2The Role Of The ICRP
The ICRP is a non-governmental scientific organization which is responsible for making recommendations and providing guidance on the fundamental principles of radiation protection. It brings together expertise from outside the ICRP as well as from its own committees to produce reports on the latest radiation protection methods and advances. The ICRP intends these reports to be of help to regulatory and advisory agencies at national, regional and international levels. Because of the differing conditions in various countries, the ICRP does not intend to provide legal texts. Instead, the recommendations of the ICRP are designed to be incorporated into the regulations of each country as required. In this way, the ICRP intends to provide an internationally consistent but flexible framework for a universal system of radiation protection.
3.3Recommendations Of The ICRP
The ICRP produces regular publications concerning radiation protection issues. In addition to reports on specific radiation protection issues such as radiation protection in medicine, dentistry and mining, more general documents are also produced. These documents are known as Recommendations of the ICRP and they cover issues which are important to all aspects of radiation protection. The first Recommendations of the ICRP appeared as Publication 1 in 1959 and many other publications have been produced since then. Each publication represents an increase in knowledge of the risk associated with radiation exposure. The Recommendations are reviewed annually, and amendments and clarifications are issued as required. Figure 2 shows the sequence and dates of the Recommendations of the ICRP along with their publication numbers.
Figure 2
The Sequence of The Recommendations of The ICRP
The most recent publication was produced in 1990 and is commonly known as ICRP 60. The Recommendations of this document are discussed later in Section 8.
4.BASIC SAFETY STANDARDS
In 1990, the Inter-Agency Committee on Radiation Safety (IACRS) was established to further promote consistency in the practical application of radiation protection. This committee consisted of a group of international organizations with a common interest in radiation protection. As a result, a detailed document (called the International Basic Safety Standards for Protection against Ionizing Radiation and for the Safety of Radiation Sources) was prepared. This document, commonly known as the Basic Safety Standards (BSS), is intended to serve as a practical guide for the design and implementation of an effective radiation protection program. It contains standards which are primarily based on the principles of radiation protection recommended by the ICRP. It also takes into account nuclear safety principles as recommended by the International Nuclear Safety Advisory Group (INSAG), a group which has been producing Nuclear Safety Standards (NUSS) specifically for nuclear installations since 1985. Many of the principles recommended by INSAG are relevant to other radiation sources and installations. Figure 3 illustrates the development of the Basic Safety Standards.
Figure 3
The Development of the Basic Safety Standards
Like the ICRP recommendations, the Basic Safety Standards are intended for guidance only and not as legal text. The standards are designed such that they may be incorporated into the legislation of individual countries as required to form a practical basis for the specific radiation protection needs of that country.
SELF CHECK 1
Now see how much you have understood by answering the following questions in your workbook:
Match the terms radiation protection, risk, and ICRP with the following descriptions:
a) The organization which makes recommendations and provides guidance on the fundamental principles of radiation protection.
b) The probability of harm or damage.
c) The science and practice of limiting harm to human beings from radiation.
On which evidence are risk estimates based?
How often does the ICRP review its recommendations?
Which ICRP Publication contains the most recent Recommendations of the ICRP?
What is the function of the Basic Safety Standards?
Now check your answers with the model answers in your workbook.
5.PRACTICES AND INTERVENTIONS
Human activities which increase the overall exposure to radiation are called practices. Practices may either introduce a new facility or procedure (e.g. a new nuclear medicine procedure, a new chest X-ray screening procedure or new mineral sands processing plant) or change an existing one in such a way that more radiation is produced or more radioactive waste is released to the environment (e.g. increasing the capacity of an existing nuclear power plant or changing a chemical process such that an increase in volatile radioactive materials released to the air is observed).
Interventions are any human activities that are intended to reduce the existing radiation exposure, or the possibility of exposure. These apply to both chronic exposure situations such as radon in buildings, and emrgency situations.
6.EXPOSURES
6.1Introduction To Exposures
Exposure is defined as the actual process of a human being exposed to radiation or radioactive materials. Exposure to ionizing radiation will lead to a radiation dose and the amount of dose received depends on many factors. You will learn more about this in Module 2.5 Personal Dosimetry.
Exposure can be either external (i.e. exposure from a source outside the body) or internal (i.e. exposure from a source inside the body).
6.2Potential Exposures
The idea of potential exposure was introduced to cover the possibility, but not certainty, of exposure. For example, transport accidents are possible, but not certain to occur. In the routine use of radioactive materials, accidents can always happen but they rarely occur. A radiation protection system must try to control the probability and the size of the potential exposure.
6.3Types Of Exposure
The ICRP refers to three types of exposure:
Occupational exposure is the exposure of a person in the workplace and mainly as a result of the work they perform. It can be controlled at three levels; at the source (e.g. shielding); in the environment (e.g. ventilation); and at the level of the worker (e.g. work practices, protective clothing).
Medical exposure is the exposure of a person as part of a medical diagnosis or treatment. The exposure is controlled at the same three levels as for occupational exposure but is included as part of the diagnosis or treatment plan, not as part of a radiation protection system.
Public exposure is the exposure of a person by means other than occupational or medical exposure. The controls should be applied at the source. They should only be applied to the environment or to the individuals if source controls are not effective, as, for example, in a serious accident such as Chernobyl.
6.4Levels Of Exposure
In order to compare the amount (or level) of exposure from different sources, we need to be able to quantify exposure. For the purpose of this module, we use the level of dose received from each source (in units of millisieverts) to provide a comparison. The units and definitions of dose will be further discussed in Module 2.5 Personal Dosimetry.
Figure 4 compares the average levels of occupational and medical exposures with the average radiation levels from natural sources.
* From UNSCEAR Publication 1993
Figure 4
Comparison of Levels of Exposure
7.DOSE LIMITS AND DOSE CONSTRAINTS
7.1Dose Limits
Dose limits are defined as the level of dose (i.e. the amount of radiation received or absorbed) which must not be exceeded under normal controlled conditions. Occupational dose limits were originally introduced in 1934 to avoid directly observable non-malignant effects such as changes to the skin. By 1950, it was recognized that cancer, particularly leukaemia, was one of the risks of exposure to ionizing radiation. Consequently, the set dose limits were intended to reduce the incidence of cancer and hereditary effects, and to prevent deterministic effects. Over the years, these limits have been expressed in a variety of ways; so comparisons are not easy. In broad terms, however, the annual occupational exposure of the whole body was reduced by a factor of about three between 1934 and 1950, and by a further factor of three, to the equivalent of 50 millisieverts per year, in 1958. Since then, new information on the risk of radiation-induced cancers has become available and occupational exposures were reduced by a further factor of 2.5 in 1990 to the present limit.
Limits on public exposure were first introduced by the ICRP in 1959. Since then, these limits have been reduced in line with occupational dose limits to the current limit of 1 millisievert per year. Dose limits recommended by ICRP Publication 60 are discussed in Section 8.3 of this module.
7.2Dose Constraints
People may be exposed to radiation from several different sources or from a source which may increase with time (e.g. a radioactive store or waste repository). In this case it is necessary to restrict the exposure from each source to ensure that regulatory dose limits are not exceeded. A dose constraint is the upper restriction on dose that may be received from a single source, and these constraints are particularly applicable to public exposure. Statutory authorities control potential doses to the local population by applying suitable dose constraints. For example, a member of the public may live close to a radiotherapy practice and a nuclear power plant. The statutory authority will decide that the radiotherapy practice can only give rise to a certain percentage of the 1 millisievert public dose limit, and the nuclear power plant may give rise to another part of the 1 millisievert. This concept of dividing the dose amongst the sources of ionizing radiation is referred to as applying dose constraints.
SELF-CHECK 2
Now see how much you have understood by answering the following questions in your workbook:
Match the terms practices, interventions and potential exposure with the following descriptions:
a) Human activities which decrease the overall exposure to ionizing radiation.
b) The possibility of exposure to ionizing radiation.
c) Human activities which increase the overall exposure to ionizing radiation.
Give two examples of practices and two examples of interventions.
What are the three types of exposure referred to by the ICRP and when do they apply?
Define the terms dose limit and dose constraint.
Compare the terms dose limit and dose constraint by giving examples of how they are used.
Using the information in Section 6.4, compare:
a) the average annual exposure of workers in the nuclear industry with the average annual exposure from natural background radiation;
b) the maximum annual exposure of members of the public from non-natural sources with the average annual exposure from natural background radiation; and
c) the average annual medical exposure from diagnostic procedures with the average annual exposure from natural background radiation.
Now check your answers with the model answers in your workbook.
8.THE SYSTEM OF RADIATION PROTECTION
The system of radiation protection recommended by the ICRP in Publication 60 is based on three major principles. These principles are known as justification, optimization, and dose limitation. The ICRP recommends that these three general principles are applied in the control of new and current practices. Figure 5 illustrates the relationship between the radiation protection system and the three principles. Each principle is discussed further in Sections 8.1, 8.2 and 8.3.
Benefit > Risk ALARA Numerical Dose Limits
Figure 5
The Three Major Principles of Radiation Protection
It is important to remember that none of the principles should be used on their own. An effective radiological protection system should use the three principles to ensure that all radiation doses are kept as low as possible.
8.1Justification of a Practice
In terms of radiation protection, decisions concerning the adoption of new practices or the continuation of existing practices must take into consideration the risks of radiation effects as a result of that practice. A practice which involves exposures or potential exposures should only be adopted if it is likely to produce sufficient benefit to the individual or to society to outweigh the detriment or harm to health it may cause. For example, a mass screening program for the detection of breast cancer must be shown to have sufficient benefit by detecting the cancer early to outweigh the additional risk associated with the increased radiation doses. Figure 7 illustrates the principle of justification of a practice.
Figure 6
The Principle of Justification of a Practice
8.2The Optimization of Protection
Individual doses, the number of people exposed and the likelihood and magnitude of potential exposures should all be kept as low as reasonably achievable, economic and social factors being taken into account. This is known as the ALARA principle. It means that radiation sources and installations should be provided with the best practical protection and safety measures possible, with all social and economic factors being considered. Protection and safety should be optimized. For example, before additional shielding is added to a nuclear installation, it should be shown that individual doses and the number of people exposed will be decreased sufficiently to justify the potential doses to the people installing the shielding and the cost. It is important to remember the principle of ALARA as shown in Figure 7.
Figure 7
The Principle of ALARA
8.3Individual Dose Limits
The ICRP recommends that the exposure of individuals should be subject to dose limits. The occupational dose limits are aimed at ensuring that no individual is exposed to unacceptable risks as well as preventing any deterministic effects and minimising the chance of stochastic effects. Figure 8 shows the principle of occupational dose limitation as adopted by the ICRP.
Figure 8
The Principle of Occupational Dose Limitation
For members of the public, the ICRP recommends a dose limit which is approximately the same as the average dose from natural sources, excluding radon, at sea level.
Occupational dose limits and public dose limits apply to exposures resulting from practices, and exclude medical exposures and natural background.The annual occupational dose limit for effective dose is 20 mSv with a further provision that it should not exceed 50 mSv in any single year. The annual public dose limit is 1 mSv, but in special circumstances a higher public dose could be allowed as long as the average over five years does not exceed 1 mSv per year.
The term effective dose applies to a dose to the whole body. There are additional dose limits for the lens of the eye and the skin, 150 mSv and 500 mSv respectively, which provide protection against deterministic effects, such as cataracts in the lens of the eye, erythema (skin burns) and desquamation (shedding of layers of skin). The effective dose limit provides sufficient protection against stochastic effects in these organs. The 500 mSv skin dose limit is averaged over any one square centimetre, regardless of the area exposed.
The current dose limits recommended in ICRP Publication 60 are summarized in Table 1. Doses are given in millisieverts (mSv) but do not worry about the terms and units. These will be explained in Module 2.5, Personal Dosimetry.
Table 1
Dose Limits Recommended in ICRP Publication 60
Occupational Dose Limit | Public Dose Limit | |
Effective dose | 20 mSv per year, averaged over defined periods of 5 years | 1 mSv per year |
Annual equivalent dose in: | ||
the lens of the eye | 150 mSv | 15 mSv |
the skin | 500 mSv | 50 mSv |
the hands and feet | 500 mSv | No recommendation |
8.3.1The Occupational Exposure Of Pregnant Women
It is considered by the ICRP that, if the recommended system of protection is in place, then there is no need to have special occupational dose limits for women who may become pregnant. However the foetus should be treated like a member of the public and it may be necessary to adapt the woman’s working conditions if she becomes pregnant to ensure that this occurs. In particular, the type of work the woman does should not carry a significant probability of high accidental exposure or intake of radionuclides.
The ICRP recommends that once pregnancy has been declared, the equivalent dose to the surface of the woman’s abdomen should be limited to 2 mSv and the intake of radionuclides should be limited to about one twentieth of the intake limit of other radiation workers. You will learn about restricting the amount of radionuclides entering the body in Module 2.3 Protection from Internal Hazards.
SELF-CHECK 3
Now see how much you have understood by answering the following questions in your workbook:
What are the three basic principles of radiation protection upon which a system of radiation protection should be based?
How may a practice be justified?
What is the ALARA principle?
What are the three criteria for setting dose limits?
What types of exposure are not included in the occupational and public dose limits?
What is the annual effective dose limit for the following people?
a) A person who works with radioactive materials.
b) A person who lives next to a nuclear power plant but who does not work there.
Now check your answers with the model answers in your workbook.
RESEARCH ASSIGNMENT
RESEARCH ASSIGNMENT
With the help of your supervisor, find out what the dose limits are for your country. Write your answers in the space provided in your workbook.
9.IMPLEMENTING A SYSTEM OF RADIATION PROTECTION
The most important principle of radiation protection is to keep all doses as low as possible while still allowing the beneficial use of ionizing radiation. The recommendations of the ICRP can be applied at several levels in order to control the hazards from radiation. These levels are as follows:
Regulatory.
Management.
Operational.
9.1Regulatory Requirements
The formulation and implementation of regulations and legislation varies from country to country. Regulations provide a link between the ICRP recommendations and their implementation in the workplace. The country’s regulators (an agency or government department) should be responsible for assessing whether a practice is justified, and for prohibiting it if there is no justification. The regulations should set a satisfactory standard of protection which can be applied to all justified practices.
9.2Management Requirements
It is not possible for workers to implement satisfactory standards of safety without the support and direct involvement of management. Hence, a formal management structure should be introduced to deal specifically with the issues of radiation protection. One of main responsibilities of this management is to encourage a good attitude to safety and a recognition that safety is a personal responsibility. In addition, the management should optimize protection by defining responsibilities clearly and providing clear and simple operating instructions. It should also take potential exposures into account and provide a system for safety analysis to identify possible causes of accidents and limit the probability and effect of such accidents.
9.3Operational Requirements
In addition to regulatory and management requirements, control is necessary at the operational level to ensure safe practices in the workplace. These practical considerations should include such aspects as –
safe storage of radioactive materials;
safe transport of radioactive materials;
use of time, distance and shielding to reduce radiation fields;
use of containment to limit the spread of radioactive materials into workplaces and the public environment;
adequate maintenance of plant and equipment to reduce the probability of failure; and
safe management of radioactive wastes.
The operational requirements listed above will be covered in detail in later modules. In addition there is a requirement on individual workers that they accept responsibility for their own safety. They must use all protective equipment supplied and work according to safety procedures.
SELF-CHECK 4
Now see how much you have understood by answering the following questions in your workbook:
What are the three levels at which radiation protection principles can be applied?
What is the purpose of regulations?
Name two responsibilities of the management structure.
Name three practical requirements at the operational level.
Now check your answers with the model answers in your workbook.
KEY POINTS
Radiation protection is defined as the science and practice of limiting harm to human beings from radiation.
Risk is defined as a combination of the probability that a harmful consequence may occur and the size of that consequence.
The risk from ionizing radiation is determined by the study of populations exposed to high doses.
UNSCEAR and BEIR publish information on the risk of radiation-induced cancer in humans.
The ICRP prepares reports on specialised areas of radiation protection and produces general recommendations for the establishment of radiation protection systems.
The Basic Safety Standards are practical working documents for the establishment of a radiation safety system.
Human activities which increase the overall exposure to radiation are called practices.
Human activities which decrease the overall exposure are called interventions.
Exposure is defined as the actual process of a human being exposed to radiation or radioactive materials.
Potential exposure is used to describe the possibility, but not certainty, of exposure.
Occupational exposure is the exposure of a person in the workplace and mainly as a result of the work they perform.
Medical exposure is the exposure of a person as part of a medical diagnosis or treatment.
Public exposure is the exposure of a person by means other than occupational or medical exposure.
Natural background exposure is the exposure from natural sources.
Dose limits are defined as the level of dose which must not be exceeded under normal controlled conditions.
Dose constraints are a means of controlling doses from several sources.
The three basic principles of radiation protection are justification, optimization and dose limitation.
For justification of a practice, the benefits must be shown to outweigh the risks.
Optimization of protection requires individual doses, the number of people exposed and the likelihood and magnitude of potential exposures to be kept as low as reasonably achievable, economic and social factors being taken into account. This is known as the ALARA principle.
Dose limits are necessary to ensure that no individual is exposed to unacceptable risks. They are set such that deterministic effects are prevented and the chance of stochastic effects is minimized.
It is considered by the ICRP that the foetus of a pregnant woman should be treated as if it were a member of the public.
The ICRP recommends that once pregnancy has been declared, the equivalent dose to the surface of the woman’s abdomen should be limited to 2 mSv and the intake of radionuclides should be limited to about one twentieth of the intake limit of other radiation workers.
The principles of radiation protection should be implemented at three levels: regulatory, management and operational.
FINAL ASSIGNMENT
This assignment is to be completed under test conditions, so spend some time now studying this module. Then contact your supervisor to arrange a suitable time to complete this assignment.
GLOSSARY OF TERMS
ALARA | As low as reasonably achievable. |
BSS | Basic Safety Standards. The practical guide for the design and implementation of an effective radiation protection system. |
Constraint | Restriction on the exposure to ionizing radiation. |
Dose | A measure of the radiation received or absorbed by a human being. |
Dose constraint | Restriction on the dose received as a result of ionizing radiation. |
Dose limit | The value of dose that may not be exceeded under normal operational conditions. |
Exposure | The process of a human being exposed to radiation or radioactive materials. |
ICRP | International Commission on Radiological Protection. The organization which makes recommendations and provides guidance on the fundamental principles of radiation protection. |
Intervention | A human activity which decreases the overall exposure to ionizing radiation. |
Justification | The benefits of a practice are greater than the risks of that practice. |
Medical exposure | The exposure of a person to ionizing radiation as a result of a medical diagnosis or treatment. |
Occupational exposure | The exposure of a person to ionizing radiation in the workplace as a result of their work. |
Optimization | Individual doses, the number of people exposed and the likelihood and magnitude of potential exposures should all be kept as low as reasonably achievable, economic and social factors being taken into account. |
Potential exposure | Radiation exposure that is not expected to occur but which could arise from events such as equipment failures or operator errors. |
Practice | A human activity which increases the overall exposure to ionizing radiation. |
Public exposure | Public exposure applies to the exposure of a person to ionizing radiation other than from occupational or medical exposure. |
Radiation Protection | The science and practice of limiting harm to human beings from radiation. |
Risk | The combination of the probability that a harmful consequence may occur and the size of that consequence. |
INTERNATIONAL ATOMIC ENERGY AGENCY AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION |
DISTANCE LEARNING MATERIALS
RADIATION PROTECTION
Module 2.2
Prepared by Safety and Radiation Science
Australian Nuclear Science and Technology Organisation
With the assistance of consultants in Australia and the United Kingdom, and IAEA experts from Korea, Mongolia, New Zealand, the Philippines and Thailand
Use of this material, acknowledging the IAEA and ANSTO as the source, is permitted for non-profit training
Acknowledgements
This material has been prepared by an extensive team of international experts from the fields of radiation protection, medicine and education. It is not possible to mention by name all those who have had an input to; the initial planning; writing modules and workbooks; preparing and marking final assignments; proof-reading and editing; using the material and providing valuable feedback; organizing and hosting review meetings; and general administrative support.
The support of ANSTO management in providing the resource and encouragement is gratefully acknowledged.
The enthusiastic support of IAEA Technical Officers has been vital to the success of this project.
PART 2
RADIATION PROTECTION
MODULE 2.2
PROTECTION FROM EXTERNAL RADIATION HAZARDS
CONTENTS
OVERVIEW
In this module, you will learn about the three main methods of protection against external radiation hazards – those of time, distance and shielding. You will also learn how to apply these methods for protection against the common types of radiation emitted by sealed sources and by radiation apparatus.
TIME ALLOCATION
It is estimated that you will need to spend eight to ten hours to complete this module before commencing the final assignment. The estimated time is for your guidance only. Do not worry if you need more time to understand the module.
MATERIALS
You will need to have writing materials to take notes and answer questions and assignments in the module. A scientific calculator would assist with the calculations.
NOW YOU ARE READY TO START WORK
10.EXTERNAL RADIATION HAZARDS
10.1Introduction
External radiation is radiation from a source outside the body. An external radiation hazard exists when ionizing radiation from a source outside the body has the potential to cause harm. This is different from an internal radiation hazard which exists when there is a potential for exposure from radioactive materials entering the body (see Module 2.3 Protection from Internal Hazards). We use different methods to control the external and internal radiation hazards.
10.2The Effect of Radiation Type on External Radiation Hazard
Alpha and beta particles, gamma rays, x-rays and neutrons are all types of ionizing radiation (see Module 1.4 Interaction of Radiation With Matter). However, not all of these are external radiation hazards. The degree to which each is an external radiation hazard is discussed below.
Alpha particles have only a very short range in air (a few centimetres), and are not considered an external radiation hazard since they cannot penetrate the outer layers of the skin.
Beta particles are more penetrating than alpha particles, with the penetrating power of beta particles being dependent on their energy. Energetic beta particles can travel several metres in air and can also penetrate the outer layers of the skin to a few millimetres (e.g. 1 MeV beta particles close to the skin can penetrate approximately 5 mm). If a solution containing a beta emitting radionuclide is spilled onto the skin, even a small drop may give a large dose to the skin tissue. The only other organ of importance in the case of external beta irradiation of the eye – beta particles are not considered to be an external radiation hazard to any other body organs. Bremsstrahlung radiation arising from high energy beta interactions with high atomic number materials will lead to the production of x-rays which are a greater external radiation hazard than the original beta particles.
X- and gammarays are forms of short wavelength electromagnetic radiation which will penetrate all organs of the body and are a significant external radiation hazard. The energy of the x-ray and gamma photons is an important factor in determining the magnitude of the external radiation hazard.
Neutrons are also highly penetrating. They give energy to the body as they are scattered in body tissues. Neutrons are an important external radiation hazard which require careful control.
Table 1 summarises the relative hazard of the different types of radiation from sources outside the human body.
Table 2
Relative External Radiation Hazards
Radiation Type
Relative External Radiation Hazard
Alpha Particles
None
Beta Particles
Slight
Gamma Rays
Severe
X-Rays
Severe
Neutrons
Severe
10.3Sources of External Radiation Hazards
External radiation hazards can be produced in two ways. One way is from equipment or devices, that when operated, produce ionizing radiation. The second way is from radioactive materials.
X-ray generators are a common ionizing radiation emitting device. When they are turned on, x-rays are produced and the device represents an external radiation hazard. However, when turned off, the production of x-rays is stopped and the external radiation hazard is eliminated.
In contrast, beta particles, X- and gamma rays emitted from radioactive materials represent a continuous external radiation hazard. Radioactive materials cannot be turned off but they can be placed in containers or surrounded in a shielding material that will reduce the external radiation hazard to an acceptable level.
SELF-CHECK 1
Now see how much you have understood by answering the following questions in your workbook:
What is the difference between an external and internal radiation hazard?
Why are alpha particles not considered to be an external radiation hazard?
For which organs can beta particles be an external radiation hazard?
Which types of radiation can penetrate the body?
What is the major difference between X-ray generators and radioactive materials as external radiation hazards?
Now check your answers with the model answers in the your workbook.
11.CONTROLLING THE EXTERNAL RADIATION HAZARD
11.1Basic Techniques
There are three basic methods for controlling external radiation hazards. These are:
Time.
Distance.
Shielding.
Application of these methods can reduce the dose received as a result of exposure to external ionizing radiation. Each method is discussed in detail in the following sections.
11.1.1Time
Controlling time is an important method for reducing the exposure to ionizing radiation. By reducing the time spent working with or being exposed to radioactive materials, the dose received can be minimized. In simple terms, the radiation dose received by a person working in an area with a certain dose rate is dependent on the time spent in that area.
This relationship is given by Equation 1:
D = R x T[1]
where D = Dose received
R = Dose rate
T = Time of exposure
Hence, if the time of exposure to a fixed dose rate source is decreased, then the overall dose received is also decreased. This is illustrated by Example 1.
Example 1
Question
An occupationally exposed person usually spends 3 hours working on a process which has an accompanying dose rate of 5 Sv h-1 (i.e. 5 microsieverts per hour). The process is improved such that the process time is reduced to 1.5 hours. What is the difference in dose received by the worker?
Answer
Using Equation 1:
Before the change in process, the total dose received was:
D = 5 Sv h-1 x 3 h = 15 Sv
After the change in process, the total dose received is:
D = 5 Sv h-1 x 1.5 h = 7.5 Sv
Hence, the difference in dose received is:
15 Sv - 7.5 Sv = 7.5 Sv
It can also be seen from Example 1 that, for a fixed dose rate:
If you halve the exposure time, the dose received is halved.
Conversely:
If you double the exposure time, the dose received is doubled.
It is important to remember these rules both for your own protection and for the protection of other radiation workers.
The relationship in Equation 1 can also be used to ensure that dose limits and constraints are not exceeded in the workplace. Controlling the hourly dose rates of occupational workers, ensures that annual limits or constraints are not exceeded. This is illustrated in Example 2.
Example 2
Question
If a radiation worker spends 40 hours per week, 50 weeks per year working with sources of radiation and the annual dose constraint is 10 mSv, what is the maximum hourly dose rate allowed?
Answer
Maximum dose allowable = 10 000 Sv
Time of Exposure = 40 x 50 = 2 000 hours
From Equation 1:
10 000 Sv = R x 2 000 h
Hence
R = 10 000 Sv = 5 Sv h-1
2 000 h
The maximum dose rate allowed is therefore 5 Sv h-1. To ensure that workers do not exceed the annual dose constraint, their exposure should be controlled to an average of 5 Sv h-1.
The concept of time is also useful in planning work that may lead to external radiation exposure. Often it may be useful to practice a technique without an actual radiation source being present. This should help to reduce the exposure time and hence the total dose received.
11.1.2Distance
Controlling distance is another useful method of external radiation control. In simple terms, the greater the distance from a source of penetrating radiation, the less the overall exposure.
The relationship between the dose rate from a point source (a source which is small in size) and the distance from the source is given by Equation 2:
R = k[2]
d2
where R = Dose rate
d = Distance from the source
k = A constant value for a particular radioactive source.
The relationship in Equation 2 is known as the inverse square law and you will gain practical experience of this law in Practical Activity 1 of this module.
Equation 2 can be rewritten to form Equation 3:
R d2 = k[3]
As k is a constant value for a particular source, if the source is not changed then we can write Equation 4:
R1 d12 = R2 d22[4]
where R1 = Dose rate at distance d1 from the point source
R2 = Dose rate at distance d2 from the point source
In practice, we can assume that physically small sources are, in effect, point sources provided that the distance from the source is at least ten times the largest dimension of the source.
In radiation protection, distance is often used to reduce exposure to ionizing radiation, e.g. by restricting access close to sources or by using long handling tools (e.g. tongs).
If we know the dose rate at a particular distance from the source, then it is possible to calculate the distance at which dose rates are considered acceptable. This concept is illustrated in Example 3.
Example 3
Question
The dose rate at 2 m from a gamma source is 125 Sv h-1. At what distance will it give an acceptable dose rate of 5 Sv h-1?
Answer
Using Equation 4 and substituting the values gives:
125 x 22 = 5 x d22
Rearranging this equation gives:
d22 = 500 = 100
5
d2 = 100 m = 10 m
Hence, by increasing the distance from the source from 2 m to 10 m, we can reduce the dose rate considerably.
A useful way of remembering the distance principle is:
When the distance from a radiation source is doubled, the dose rate is reduced to a quarter of its original value.
Again, it is important to remember this rule in order to reduce exposure to yourself and your colleagues.
PRACTICAL ACTIVITY 1
Gamma Radiation and the Inverse Square Law
In this practical activity, you will measure the dose rate at various distances from a gamma source in order to investigate the inverse square law. Details of the procedure to follow are given in your workbook. You should contact your supervisor to arrange a suitable time to do the practical.
11.1.3Shielding
Example 3 above gives a good illustration of how distance may be used to reduce the dose rates and hence overall dose received. However, in many situations it is not possible to work with a source if it is more than a metre away from you. A more practical method for reducing exposure in workplace situations is to shield the source. By using this method, dose rates may be reduced whilst still allowing work to be performed.
The amount and type of shielding material required depend on the following factors:
The type and energy of radiation.
The activity of the source (or intensity of radiation from a generator).
The acceptable dose rate outside the shielding.
In Section 1.2 you learnt about the penetrating power of different types of radiation. This is summarized in Figure 1.
Figure 9
The Penetrating Properties of Ionizing Radiation
Alpha particles have a short range in air (a few centimetres) and are easily absorbed so they do not require shielding.
Low energy beta particles such as those from tritium (maximum energy 0.019 MeV) are also easily absorbed and do not require shielding.
However, higher energy beta particles such as those from phosphorus-32 (maximum energy 1.7 MeV) are more penetrating and interact with shielding materials to produce bremsstrahlung radiation. Beta shields constructed of a low atomic number material (e.g. perspex) will reduce the intensity of beta particles and minimize the production of bremsstrahlung radiation. It may, however, still be necessary to use additional shielding to protect the worker from the bremsstrahlung. In which case, perspex surrounded by lead is recommended.
It is important not to underestimate the hazard of unshielded beta sources as they are capable of imparting large doses (especially to the hands and fingers) if they are handled directly. This is particularly important for people handling vials or syringes containing beta emitters in solution. For example, a small volume of solution containing a high level of activity of phosphorus-32 may give dose rates at the surface of thin-walled plastic tubes in excess of 1 mSv min-1.
X- and gamma rays are much more penetrating than either alpha or beta particles. Shielding with materials of a high atomic number (e.g. concrete, lead or iron) is necessary to attenuate the radiation and reduce the dose rate to acceptable levels. The amount of attenuation is dependent on the shielding material, its thickness and the energy of the incident photons.
Shielding for neutrons is more complex due to the wide range of energies and the different reactions that may occur. The process of shielding neutrons involves firstly the slowing of energetic neutrons by elastic scattering, and then their capture. For these two actions to occur, a suitable shielding material should incorporate a combination of material with a high hydrogen content (e.g. water, paraffin wax, polythene, concrete) to slow down the neutrons plus boron to absorb them. Borated paraffin wax is the name given to a mixture of paraffin wax and boron which may be used as a small area shield. The capture reaction with boron-10 is written as follows:
10 B (n,) 7 Li
This means that the boron-10 nucleus absorbs a neutron, emits an alpha particle and becomes a lithium-7 nucleus. The alpha particle is easily absorbed in the surrounding material. The reaction also produces a gamma ray with an energy of 0.48 MeV which may require additional shielding. Other neutron capture reactions can produce high energy gamma radiation. An example of such a reaction is neutron absorption by iron-58. This is written as follows:
58 Fe (n, ) 59 Fe
This reaction produces a gamma ray with a high energy of 7.6 MeV. Hence, iron is not a good shield in a nuclear reactor environment.
Table 2 shows shielding materials which are recommended for different types of radiation. The methods used for estimating the thickness of shielding required for beta particles, x- and gamma rays will be discussed in Section 3 of this module.
Table 3
Recommended Shielding Material
Radiation Type
Recommended Shielding Material
Alpha Particles
None
Low Energy Beta Particles
None
High Energy Beta Particles
Perspex surrounded by lead
X- and Gamma Rays
Concrete, lead, iron
Neutrons
Concrete, water, polythene, borated paraffin wax
Note that the choice of shielding material is often related to cost, space and convenience. Lead is not easy to work with, is poisonous and, in large sheets, can sag without good support. On the other hand, concrete is cheaper and easier to handle but large thicknesses may be required for effective shielding.
SELF-CHECK 2
Now see how much you have understood by answering the following questions in your workbook:
What are the three basic methods that can be used to control the external radiation hazard?
An occupationally exposed person usually spends 15 hours working on a process which has an accompanying dose rate of 5 Sv h-1 (i.e. 5 microsieverts per hour). The process is improved such that the process time is reduced to 7.5 hours. What is the difference in dose received by the worker?
If an occupationally exposed worker spends 20 hours per week working with radioactive materials and the maximum acceptable external dose for that person is 200 Sv per week, what is the maximum hourly dose rate allowable?
The dose rate at 1m from a certain gamma source is 900 Sv h-1. At what distance will the dose rate be 25 Sv h-1?
What factors are important when considering the amount and type of shielding materials required for external radiation?
Give a suitable shielding material for each of the following radiations:
Alpha particles.
Low energy beta particles (e.g. tritium).
High energy beta particles (e.g. phosphorus-32).
X-rays and gamma rays.
Neutrons.
Now check your answers with the model answers in the your workbook.
11.2Administrative Controls
An administrative control is a method of administration which prevents or minimizes exposure to the external radiation hazard. Administrative controls include the following procedures:
Classification of areas.
Display of clear signs for each classified area.
Radiological protection training for workers and managers.
Workprocedures which incorporate the use of time, distance and shielding.
Local rules (e.g. restriction of access to certain areas) and conditions of work (e.g. requirement to wear an alarming dosimeter).
Maintenance of source inventories for each area.
Radiation safetyauditing system which includes safety assessment of work procedures, plant and equipment.
Use of investigation levels for personal dose monitoring and workplace monitoring results.
The controls of time, distance and shielding have already been discussed in Section 2.1. The classification of areas, the international radiation warning symbol and the use of investigation levels will be discussed in the next three sections. The other methods of administrative controls will be discussed in the relevant modules of Parts 4 and 5 of this distance learning material.
11.2.1Classification of areas
Work areas can be classified according to the level of the external radiation hazard. (They may also be classified according to the level of the internal hazard. This will be discussed in Module 2.3 Protection from Internal Hazards.) A classification system in which areas may be classified as controlled or supervised is recommended in the Basic Safety Standards.
A controlled area is one where specific protection measures and safety provisions are or could be required to control normal exposures and to prevent or limit potential exposures.
A supervised area is where occupational exposure conditions are kept under review but no specific protection measures are required.
An unclassified area is where no protection methods are required and the occupational exposures do not need to be kept under review.
Generally, the classification of areas varies in accordance with the particular needs of the workplace and is usually based on operational experience and judgement. One way of classifying areas is with respect to the potential annual dose to workers. Table 3 shows an example of how potential annual doses can be used in the classification of areas.
Table 4
Example of Area Classification with Respect to Annual Dose
Area Classification | Potential Annual Dose (mSv) |
Controlled | Greater than 6 |
Supervised | 1 to 6 |
Unclassified | Less than 1 |
In practice, areas are usually classified according to the measured dose rate at the boundary of the area. Dose rate values are determined by considering the potential dose which is acceptable as an annual dose together with the amount of time spent by workers in the classified area (occupancy time). The occupancy time is often written as a fraction of the total work time and is known as the occupancy factor. For example an occupancy factor of 0.2 means that a worker spends one fifth (or 20%) of their working time in a particular area. This corresponds to 400 working hours during one year (assuming a standard working year of 50 weeks, 40 hours per week). Table 4 shows how areas could be classified according to dose rate if an occupancy factor of 0.2 is assumed.
Table 5
Example of Area Classification with Respect to Annual Dose Rate
Area Classification | Average Dose Rate* Sv h-1 |
Controlled | greater than 15 |
Supervised | 2.5 to 15 |
Unclassified | less than 2.5 |
* Assuming an occupancy factor of 0.2
The dose rate values given in Table 4 have been calculated by dividing the annual dose (in microsieverts) given in Table 3 by 400 hours.
Note that the values given above are an example only and the dose rate approach to area classification must be used very carefully, taking into account the individual workplace conditions. It is very difficult to assess an average dose rate, and information about the length of time the dose rate stays at or above the defined levels along with the risk of potential exposure should be considered. However, this method, if applied carefully, does provide adequate control of the external radiation hazard.
Once areas have been classified in a workplace, these areas should be clearly marked with visual signs to ensure that workers and visitors are aware of the classification in that area and what the classification means . In addition, the boundaries to each area should be clearly defined.
It should also be noted that when working in classified areas with high dose rates, additional administrative controls may need to be applied. For example, local rules may include a written system of work which limits the time spent in the area on a particular type of work.
11.2.2The radiation warning symbol
As human senses cannot detect ionizing radiation, it is important to use warning signs wherever an external radiation hazard is present. Warning signs should be placed on the source itself as well as in the vicinity of the source and at barriers/boundaries to the area where the source is stored. The international symbol for ionizing radiation is the trefoil as shown in Figure 2.
Figure 10
The Radiation Warning Symbol
This symbol can be used to warn of radiological hazards in areas or on sources themselves. The trefoil is internationally accepted as black on a yellow background. However, these colours may vary in some countries.
11.2.3Investigation levels
As part of an effective radiation protection program, routine monitoring of the workplace and personnel should be performed. The results of these measurements should be reviewed regularly and any irregularities or differences from normal measurement values should be noted. In addition, investigation levels should be set such that for any measured value at or above a certain level, an investigation into the cause takes place. For example, a routine area survey indicates an unusually high dose rate of 50 Sv h-1 at the surface of a working facility. The usual dose rate is less than 5 Sv h-1 and the investigation level is set at 10 Sv h-1. In this case, an investigation into the cause of the high dose rate should be performed. This investigation should include such things as an examination of work practices, equipment and/or plant to identify the cause. Once the reason for the high dose rate has been established, preventative measures should be taken to ensure that the potential exposure of workers remains as low as reasonably achievable at all times. In this way, the exposure to external radiation hazards can be controlled on a routine basis.
In practice, investigation levels are usually defined during the planning of a radiation protection program. They should however be reviewed at regular intervals to ensure compliance with relevant dose limits and constraints and to ensure that exposures are kept as low as reasonably achievable.
11.3Physical Controls
Although administrative controls provide a basis for a radiation protection program, these controls rely on familiarity with written procedures. If a new worker is not aware of these procedures, or these procedures are not followed correctly for any other reason, then the potential exists for accidental exposure to ionizing radiation. In order to ensure that the chance of accidental exposure is as low as possible, physical controls are employed in the workplace. These controls are essentially physical barriers which incorporate a range of radiation protection techniques. The following list gives some useful examples of physical controls:
The use of engineering interlocks which restrict or prevent access to hazardous area.
The incorporation of fixed shielding into the design of plant and equipment.
The use of remote manipulators to eliminate direct handling and provide increased source – operator distance.
The use of preset timers in the case of radiography equipment to control exposure times.
SELF CHECK 3
Draw the international radiation warning sign, indicating its colour and background colour.
Give two examples of administrative controls (other than time, distance and local shielding) which can be used for the protection from external radiation hazards.
Define the following terms:
Controlled area.
Supervised area.
Unclassified area.
Once an area has been classified, what should be done to ensure that workers and visitors are aware of the classification in that particular area?
a) What does an occupancy factor of 0.5 mean?
b) Suggest average dose rates which could be used to classify areas where the occupancy factor is 0.5.
a) Define the term investigation level.
b) Why should investigation levels be used in radiation protection?
Give two examples of physical controls which can be used for the protection from external radiation hazards.
Now check your answers with the model answers your workbook.
12.SHIELDING CALCULATIONS
The information in this section will enable you to make estimations of the thickness of shielding required for beta particles, x- and gamma rays. This material is intended to be an introduction to shielding. Further information for shielding in industrial and medical facilities (e.g dose rates from x-ray generators) is given in the industry specific modules in Part 4 of this distance learning course. Neutron shielding calculations are complex and beyond the scope of this course.
12.1Shielding of Beta Particles
The thickness of material required to effectively shield beta particles can be determined from the maximum range of the beta particles in the shielding material. This can be estimated for water, polyethylene and perspex (with an assumed density of 1 g cm-3) using the general rule that the distance travelled in centimetres equals the maximum beta energy in MeV divided by 2. This relationship is shown in Equation 5:
d = E[5]
2
where d = Distance travelled (in cm)
E = Maximum energy of the beta particles (in MeV)
!
This rule only applies for absorbing material with an approximate density of 1 g cm-3.This method of shielding beta particles is illustrated in Example 4.
Example 4
Question
Yttrium-90 has a maximum beta particle energy of 2.3 MeV. What thickness of perspex shielding would you need to effectively shield this source?
Answer
E = 2.3 MeV
From Equation 5 above:
d = 2.3 = 1.15 cm
2
As the distance travelled is equal to the shield thickness needed to absorb all the beta particles, then 1.15 cm of perspex would be needed as an effective shield for the beta radiation.
Although Example 4 provides a reliable estimate for the shielding of beta particles, it is important to remember that when beta particles interact with matter scattered x-rays, known as bremsstrahlung radiation, are produced. Therefore, shielding of beta particles involves not only the shielding of the particles themselves, but also involves the minimization of bremsstrahlung radiation. The fraction of beta particle energy converted to bremsstrahlung x-rays is given by Equation 6:
F = 3.3 x 10-4 ZE[6]
where F = Fraction of beta particle energy converted into x-rays
Z = Atomic number of the absorber/shielding material
E = Maximum energy of beta particles (in MeV)
Equation 6 indicates that the lower the atomic number of the shielding material, the lower the amount of bremsstrahlung x-rays produced. Since many shielding materials are made out of compounds (e.g. perspex) rather than elements (e.g. lead), the value of Z is really an effective atomic number rather than a true atomic number. Perspex, polythene and water are all assumed to have an effective atomic number of 6 or 7 for radiation protection purposes. These materials are all suitable shielding for beta particles but some bremsstrahlung radiation will still be produced. This is illustrated in Example 5.
Example 5
Question
What fraction of the beta particle energy from a yttrium-90 source (maximum beta energy of 2.3 MeV) is converted to x-rays in a perspex shield with an effective atomic number of 7?
Answer
E = 2.3 MeV
Z = 7
From Equation 6:
F = 3.3 x10-4 x 7 x 2.3
F = 5 x 10-3
F = 0.5%
For low activity sources, this quantity of bremsstrahlung x-rays produced will not be significant. However, at activity levels in the order of megabecquerels (MBq), the bremsstrahlung radiation from a source such as yttrium-90 will require additional shielding. This is usually in the form of a higher atomic number absorber (e.g. lead). Hence, the most effective and commonly used shielding for energetic beta particles is perspex (to shield the betas) surrounded by lead (to shield the bremsstrahlung x-rays).
12.2Shielding of X- and Gamma Rays
12.2.1The attenuation of x- and gamma rays
When x- and gamma rays pass through material they are not totally absorbed by that material. Instead they are attenuated (i.e. reduced in intensity). X- and gamma rays are attenuated exponentially when they pass through material. This attenuation can be represented mathematically by Equation 7:
Rx = Ro e-x[7]
where Rx = Dose rate after passing through a shield of thickness x
Ro = Dose rate without shielding
x = Shield thickness
= A constant known as the linear absorption coefficient of the shielding material
The linear absorption coefficient depends on the type of shielding material used and also on the energy of the incident X- or gamma ray. It is usually given in units of cm-1 (i.e. the absorption per centimetre of shielding).
Although Equation 7 can be used to give a value for the amount of shielding material required, in practice simpler methods are used. These methods use experimentally determined shielding quantities known as Half Value Layers and Tenth Value Layers.
12.2.2Half value and tenth value layers
The half-value layer (HVL) (also known as the half-value thickness), for a particular shielding material, is the thickness of a shielding material required to reduce the intensity of radiation to half its original value.
Equation 7 is similar to the radioactive decay equation (A = A0e-T) and is used in a simpler form for shielding calculations using half value layers, in the same way that the radioactive decay equation is used in a simpler form using radiological half-lives. The simpler form of Equation 7 is given by Equation 8:
Rx = R0 8
2n
where n = the thickness of the shielding in terms of the number of HVLs
Rx = Dose rate after passing through a shield of thickness x
Ro = Dose rate when unshielded
The actual thickness (x) of the shielding can be written in terms of Half Value Layers (HVL’s) as shown in Equation 9:
x = nHVL9
The relationship between the linear absorption coefficient () and the half value layer (HVL) is represented by Equation 10:
HVL = 0.69310
Another useful shielding value is known as the tenth value layer (TVL). This is defined as the thickness of a shielding material required to reduce the intensity of radiation to a tenth of its original value. Equation 11 can be used with tenth value layers:
Rx = R0 11
10n
where n = the thickness of the shielding in terms of the number of TVLs
Rx = Dose rate after passing through a shield of thickness x
Ro = Dose rate when unshielded
In this case, the actual thickness (x) of the shielding can be written in terms of Tenth Value Layers (TVL’s) as shown in Equation 9:
x = nTVL12
The relationship between the linear absorption coefficient () and the tenth value layer (TVL) is represented by Equation 13.
TVL = 2.30313
Some typical values for HVL and TVL are shown in Table 5. Table 5 gives the energies of the photons and the HVLs and TVLs for concrete and lead. Notice that the values of HVL and TVL increase with increasing X- or gamma ray energy. This means that a thicker shield is required for a cobalt-60 source than for a caesium-137 source. Note also that the HVL or TVL is larger for concrete than for lead. This means that concrete shielding will need to be thicker than lead shielding.
Table 6
HVL and TVL Values for Several X- and Gamma Ray Sources
Source | Gamma Ray Energy | HVL (cm) | TVL (cm) | ||
(MeV) | Concrete | Lead | Concrete | Lead | |
226Ra | 0.047 to 2.4 | 6.9 | 1.66 | 23.4 | 5.5 |
60Co | 1.17, 1.33 | 6.2 | 1.20 | 20.6 | 4.0 |
137Cs | 0.66 | 4.8 | 0.65 | 15.7 | 2.1 |
192Ir | 0.13 to 1.06 | 4.3 | 0.60 | 14.7 | 2.0 |
50 kVp x-rays | 0.43 | 1.50 | |||
100 kVp x-rays | 1.6 | 5.3 | |||
Note: Values taken from NCRP Report No. 49 1976
The X-ray sources are described in terms of the maximum (or peak) voltage (in kilovolts) applied to the tube. This is written as kVp. There will only be a very few x-rays at the energy corresponding to peak voltage and so the average x-ray energy will much less.
The values in Table 5 can be used to estimate the thickness of shielding required in order to reduce x- or gamma radiation dose rates to workers. Example 6 illustrates how half value layers may be used in practice.
Example 6
Question
The dose rate near a cobalt-60 source is measured at 160 Sv h-1. What thickness of lead is needed to reduce this dose rate to 10 Sv h-1?
Answer
This question can be answered using either HVLs or TVLs. In this example half value layers will be used. Using the HVL of lead for cobalt-60 from Table 5 we have the following data:
HVL = 1.20 cm
Rx = 10 Sv h-1
R0 = 160 Sv h-1
Using equation 8
10 = 160
2n
2n = 160
10
2n = 16
Since
16 = 2 x 2 x 2 x 2 = 24
n = 4
Four HVLs of lead are required.
Hence, the thickness of lead needed is 4 x 1.2 = 4.8 cm.
Note that 2n may not work out to be a number which is easy to process to obtain n. In which case you will need to use logarithms in the same way as in Module 1.3 Ionizing Radiation and Radioactive Decay.
For the above example
2n = 16
Using logarithms
nlog2 = log 16
(Note that common logs or natural logs can be used.)
n = log 16
log 2
n = 1.204
0.3010
n = 4
Example 7 shows a similar calculation for tenth value layers.
Example 7
Question
The dose rate near a small caesium-137 source is measured at 40 Sv h-1. What thickness of concrete is needed to reduce this dose rate to 10 Sv h-1?
Answer
This question can be answered using either HVLs or TVLs. In this example tenth value layers will be used. Using the TVL of concrete for caesium-137 from Table 5 we have the following data:
TVL = 15.7 cm
Rx = 10 Sv h-1
R0 = 40 Sv h-1
Using equation 8
10 = 40
10n
10n = 40
10
10n = 4
Using logarithms
nlog10 = log 4
n = log 4 = 0.6021
log 10 1
n = 20.6021
Hence, the thickness of concrete needed is 0.6021 x 15.7 = 9.5 cm.
Remember that it is often more practical to use shielding to reduce exposure rather than using distance. Example 8 shows a direct comparison between the two protection methods of distance and shielding.
Example 8
Question
For a caesium-137 source with a dose rate of 390 Sv h-1 at 1 m, what would be the amount of lead shielding needed to reduce the dose rate to 25 Sv h-1.
What distance would achieve this lower dose rate, if no shielding was available?
Answer
a) For shielding:
From Table 5, the lead HVL of lead for caesium-137 is
HVL = 0.65 cm
Rx = 25 Sv h-1
R0 = 390 Sv h-1
Using equation 8
25 = 390
2n
2n = 390
25
2n = 15.6
Using logarithms
nlog2 = log 15.6
n = log 15.6
log 2
n = 1.193
0.3010
n = 3.96
Alternatively, since shielding calculations are used to provide estimates of shielding requirements, 15.6 is approximately equal to 16.
Therefore,
2n = 16
n = 4
Approximately 4 HVLs are required.
Therefore the thickness of lead needed is 4 x 0.65 = 2.6 cm.
b) For distance:
Using Equation 4 from Section 2.1.2 and substituting the values:
R1 = 390 Sv h-1
R2 = 25 Sv h-1
r1 = 1 m
390 x (12 ) = 25 x r22
Then
r2 = (15.6) = 3.95 m (approximately 4 m)
Hence, shielding at one metre with 2.6 cm of lead achieves the same reduced dose rate as moving four metres away from the source. The latter option is not practical if work has to be performed on equipment near the source. So, in practice the most efficient way of reducing exposure is to shield the source.
It is important to note that the calculations shown in this section deal with the theory of shielding x-and gamma rays. In practice, others factors relating to the energy and geometry of the beam and type of shielding material will affect the amount of radiation transmitted. In fact, these factors can result in an underestimate the amount of shielding required and hence higher dose rates than expected. To overcome this problem, numerical multiplication factors known as build-up factors have been calculated for various energies, geometrys and shielding materials. The theory and application of these factors is beyond the scope of this course but you should be aware that, although the above equations give an approximate estimation of the shielding required, practical considerations may mean that you could underestimate the necessary amount of shielding. Hence, it is always a good idea to measure the dose rates after the shielding is in place to ensure that the required dose rate reduction has been achieved.
To ensure that dose rates are reduced in accordance with your estimates, you should always measure the dose rates after the shielding is in place.
If the measured dose rates are greater than expected then more shielding may be necessary.
PRACTICAL ACTIVITY 2
Measurement of Half Value Layers
In this practical assignment you will measure the effect of different thicknesses of various shielding materials on gamma dose rates. You will then be able to estimate half value layers for the shielding materials you have used. You should contact your supervisor to arrange a suitable time to do the practical.
SELF-CHECK 4
Phosphorus-32 has a maximum beta energy of 1.71 MeV. What thickness of perspex shielding would you need to effectively shield this source?
a) What are the two important factors which control the amount of bremsstrahlung produced in a shielding material?
b) What fraction of the beta particle energy from a phosphorus-32 source (maximum beta energy of 1.71 MeV) is converted to x-rays in a perspex shield with an effective atomic number of 7?
Define the following terms:
a) Half Value Layer (HVL).
b) Tenth Value Layer (TVL)
a) A cobalt-60 source gives a dose rate of 400 Sv h-1 at 1 m. At what distance from the source must a barrier be placed if the dose rate at the barrier must not exceed 25 Sv h-1?
b) Using the values for HVL in Table 5, calculate the thicknesses of the following materials which would give the same protection at the original distance of 1 m from the source:
i) Lead.
ii) Concrete.
Now check your answers with the model answers your workbook.
13.CALCULATING GAMMA RAY DOSE RATES FOR DIFFERENT RADIONUCLIDES
13.1Introduction
In many situations in radiation protection (e.g. when designing new plant or increasing the amount of radioactive materials kept in a store), it is useful to estimate what the dose rate would be at a particular distance from a radioactive source. For this reason, values known as specific gamma dose rate constants have been calculated and are available in radiation protection reference material.
13.2Calculating Dose Rates Using The Specific Gamma Dose Rate Constant
The specific gamma dose rate constant (or specific gamma ray constant) is denoted by the Greek symbol (the Greek upper case letter for ‘G’). This value is constant for a particular gamma-emitting radionuclide and is defined as the unshielded dose rate (in Sv h-1) at 1 metre per gigabecquerel (GBq) of activity. Some examples of for different radionuclides are shown in Table 6.
Table 7
Specific Gamma Dose Rate Constants for Some Common Radionuclides
Radionuclide | (Sv h-1 at 1 metre per GBq) |
60Co | 370 |
99mTc | 33 |
131I | 77 |
137Cs | 103 |
192Ir | 160 |
Note: Values for are taken from Health Physics and Radiological
Heath Handbook, 1992
Example 9 shows how the value of may be used to calculate theoretical dose rates for a particular radionuclide.
Example 9
Question
What would the dose rate be at 1 m from a technetium-99m source with an activity of 100 MBq?
Answer
From Table 6:
for Tc-99m is 33 Sv h-1 per GBq at 1 metre.
That is, the dose rate at 1m from 1 GBq of Tc-99m is 33 Sv h-1.
We have only 100 MBq of activity:
100 MBq = 0.1 GBq
So for 100 MBq of Tc-99m, we multiply by 0.1:
33 x 0.1 = 3.3 Sv h-1
Hence, the dose rate at 1 m from 100 MBq of Tc-99m would be 3.3 Sv h-1.
In addition, the gamma ray dose constant for any radionuclide can be used in conjunction with Equation 4 in Section 2.1.2 to calculate dose rates at different distances. This calculation is shown in Example 10.
Example 10
Question
What is the dose rate at 0.5 m from an iridium-192 source with an activity of 250 MBq?
Answer
From Table 6:
for Ir-192 is 160 Sv h-1.
That is, the dose rate at 1 m from 1 GBq of Ir-192 is 160 Sv h-1.
We have only 250 MBq of activity:
250 MBq = 0.25 GBq
So for 250 MBq of Ir-192, we multiply by 0.25:
160 x 0.25 = 40 Sv h-1 at a distance of 1 m
Using Equation 4:
R1 = 40 Sv h-1
r1 = 1 m
r2 = 0.5 m
40 x 12 = R2 x 0.52
Rearranging this equation gives:
R2 = 40 = 160 Sv h-1
0.25
Hence, the dose rate at 0.5 metre for 250 MBq of Ir-192 is 160 Sv h-1.
SELF-CHECK 5
Define the term specific gamma dose rate constant.
What are the units of the specific gamma dose rate constant ()?
What is the dose rate at 1 m from an iodine-131 source of activity 260 MBq?
What is the dose rate at 5 m from a caesium-137 source of activity 10 GBq?
Now check your answers with the model answers in your workbook.
KEY POINTS
An external radiation hazard is described as a hazard from a radioactive source outside the body.
An internal radiation hazard exists when there is a potential for exposure from radioactive materials entering the body.
Beta particles, x-rays, gamma rays and neutrons are all external radiation hazards.
X-ray generators only present an external radiation hazard when they are turned on.
Radioactive materials represent a continuous radiation hazard.
External radiation hazards are controlled by applying three basic methods; those of time, distance and shielding.
The radiation dose received by a person working in an area and exposed to a certain dose rate depends on the time spent in the area.
If you halve the exposure time, the dose received is halved. Conversely, if you double the exposure time, the dose received is also doubled.
The greater the distance from a source of penetrating radiation, the less the overall exposure.
When the distance from a radiation source is doubled, the dose rate is reduced to a quarter of its original value.
Shielding a source allows dose rates to be reduced whilst still allowing work to be performed.
The amount and type of shielding material depends on the type and energy of radiation, the activity of the source (or intensity of radiation from a machine) and the acceptable dose rate outside the shielding.
Alpha and low energy beta particles do not represent an external radiation hazard and therefore do not require shielding.
Perspex surrounded by lead (to stop bremsstrahlung) is recommended for shielding high energy beta particles.
Concrete, lead or iron are recommended for shielding x-and gamma rays.
Concrete, water , polythene or borated paraffin wax are recommended for shielding neutrons.
Administrative controls can be used in the workplace to minimize exposure to ionizing radiation.
Example of administrative controls include: classification of areas, warning signs, training, work procedures, local rules, source inventories, radiation safety auditing systems and investigation levels.
Work areas may be classified into controlled, supervised and unclassified areas according to the level of external radiation hazard.
A controlled area is one where specific protection measures and safety provisions are or could be required to control normal exposures and to prevent or limit potential exposures.
A supervised area is where occupational exposure conditions are kept under review but no specific protection measures are required.
An unclassified area is where no protection methods are required and the occupational exposures do not need to be kept under review.
Occupancy time is the amount of time a worker spends in a particular classified area.
The occupancy factor is the fraction of work time spent in a particular classified area. It is often written as a percentage.
The internationally accepted symbol for ionizing radiation is a black trefoil on a yellow background.
Investigation levels are set levels of a measured value. For any measured value above this level, an investigation into the cause should take place.
Physical controls are essentially physical barriers which ensure that the chance of accidental exposure is as low as possible.
Example of physical controls are interlocks, fixed shielding, remote manipulators and preset timers.
The thickness of material required to effectively shield beta particles can be determined from the maximum range of the beta particles in the shielding material.
When x-and gamma rays pass through a matter they are attenuated exponentially.
The half-value layer (HVL) is the thickness of a material required to reduce the intensity of x- or gamma radiation to a half of its original value.
The tenth-value layer (TVL) is the thickness of a material required to reduce the intensity of x- or gamma radiation to a tenth of its original value.
Half value and tenth value layers can be used to estimate the thickness of material necessary to shield a particular source of ionizing radiation.
Due to certain practical considerations, you should always measure the dose rates after the estimated thickness of shielding is in place to ensure that the required dose rate reduction has been achieved.
The specific gamma dose rate constant () is constant for a particular gamma-emitting radionuclide and is defined as the dose rate in Sv h-1 at 1 metre per gigabecquerel (GBq) of activity.
FINAL ASSIGNMENT
This assignment is to be completed under test conditions, so spend some time now studying this module. Then contact your supervisor to arrange a suitable time to complete the assignment.
GLOSSARY OF TERMS
Build-up factors | Numerical multiplication factors which can be used to accurately calculate required shielding thicknesses. They take into consideration the energy and geometry of the radiation beam as well as the type of shielding material. |
Controlled area | An area where specific protection measures and safety provisions are or could be required to control normal exposures and to prevent or limit potential exposures. |
External radiation hazard | Ionizing radiation from a radioactive source outside the body with the potential to cause harm. |
Half value layer (HVL) | The thickness of shielding required to reduce the intensity of radiation to half its original value. |
Internal radiation hazard | The hazard which exists when there is the potential for a source of ionizing radiation to enter the body and cause harm. |
Investigation level | A set level of a measured quantity (e.g. dose rate, personal dosimetry results) at or above which the cause of the high result should be investigated. |
Occupancy factor | The fraction of total work time spent in a particular work area. |
Occupancy time | The time that workers spend in a particular work area. |
Specific gamma dose rate constant | A constant for a gamma-emitting radionuclide which is defined as the dose rate (in Sv h-1) at 1 metre per gigabecquerel (GBq) of activity. |
Supervised area | An area where occupational exposure conditions are kept under review but no specific protection measures are required. |
Tenth value layer (TVL) | The thickness of shielding required to reduce the intensity of radiation to a tenth of its original value. |
Unclassified area | An area where no protection methods are required and the occupational exposures do not need to be kept under review. |
INTERNATIONAL ATOMIC ENERGY AGENCY AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION |
DISTANCE LEARNING MATERIALS
RADIATION PROTECTION
Module 2.3
Prepared by Safety and Radiation Science
Australian Nuclear Science and Technology Organisation
With the assistance of consultants in Australia and the United Kingdom, and IAEA experts from Korea, Mongolia, New Zealand, the Philippines and Thailand
Use of this material, acknowledging the IAEA and ANSTO as the source, is permitted for non-profit training
Acknowledgements
This material has been prepared by an extensive team of international experts from the fields of radiation protection, medicine and education. It is not possible to mention by name all those who have had an input to; the initial planning; writing modules and workbooks; preparing and marking final assignments; proof-reading and editing; using the material and providing valuable feedback; organizing and hosting review meetings; and general administrative support.
The support of ANSTO management in providing the resource and encouragement is gratefully acknowledged.
The enthusiastic support of IAEA Technical Officers has been vital to the success of this project.
PART 2
RADIATION PROTECTION
MODULE 2.3
PROTECTION FROM INTERNAL RADIATION HAZARDS
CONTENTS
OVERVIEW
In this module you will learn how radioactive material can enter the body and how doses to body tissue can be assessed. Most importantly, you will learn control methods which are used to reduce the chances of radioactive material entering the body.
TIME ALLOCATION
It is estimated that you will need to spend eight to ten hours to complete this module before commencing the final assignment. This time estimate is for guidance only. Do not worry if you need more time to understand the module.
MATERIALS
You will need your workbook and writing materials to take notes and answer the questions in this module. A scientific calculator would assist with the calculations.
NOW YOU ARE READY TO START WORK
14.INTERNAL RADIATION HAZARDS
14.1Introduction
You have learned about external radiation hazards in Module 2.2 Protection from External Radiation Hazards. Remember that an external radiation hazard is due to potentially harmful ionizing radiation from a radioactive source outside the body. An internal radiation hazard exists when there is a possibility of harm due to radioactive material entering the body. Hence, an external radiation hazard could also be an internal radiation hazard if there is a possibility of the radioactive material entering the body. The radiation protection methods for each type of hazard are different and this module covers the protection from internal radiation hazards only. Figure 1 illustrates external and internal radiation hazards.
Figure 11
External and Internal Radiation Hazards
14.2Unsealed Sources and Radioactive Contamination
Sources of radioactive materials can be divided into two types – sealed and unsealed sources. A sealed source is defined as radioactive material that is either sealed in a capsule or is in a solid form whereby none of its radioactive material can be lost under normal use. Conversely, an unsealed source is radioactive material that is not sealed or is in a form whereby some of the radioactive material could be lost under normal use (e.g. a powder, a liquid or a gas). When radioactive material is sealed, it may present an external radiation hazard to the people working nearby. However, when it is unsealed, it can presentan internal radiation hazard as there is a chance that this material may enter the body. In addition, unsealed sources may also be an external radiation hazard, although usually to a lesser extent than sealed sources.
Radioactive material when released inadvertently or when present in any location where it is not wanted (including in or on the body) is defined as contamination. If sources are incorrectly handled or involved in an accident, some of the radioactive material may be dispersed to the surrounding area and result in the radioactive contamination of equipment, benches, floors and/or personnel. This contamination can either become securely fixed to a particular surface (fixed contamination), or it can be free to move (removable contamination). The presence of removable contamination, either as surface contamination or airborne contamination, poses an internal radiation hazard as this radioactive material may enter the body and cause internal doses to body tissue.
It is important to remember that quite small quantities of contamination which represent an insignificant external radiation hazard may pose an appreciable internal hazard. There are two main reasons for this:
Once radioactive material enters the body it will continue to irradiate the tissues and organs of the body until either the radioactive material has decayed or until the material is excreted. You cannot walk away from the hazard or shield it, unlike an external radiation source.
Once radioactive material enters the body it is in contact with body tissue. This is particularly hazardous for alpha emitting radionuclides such as americium-241 or plutonium-239. These emitted alpha particles have a very small range in tissue (in the order of micrometres) and deposit all their energy in a very small volume. Hence, the damage to the tissue is so great that the body cells are unlikely to be repaired.
As an example consider the potential doses from plutonium-239. The external dose rate from 200 Bq of plutonium-239 is negligible. However, if the same quantity of plutonium-239 were inhaled, this could lead to a committed effective dose of approximately 100 mSv (five times the annual effective dose limit recommended by ICRP Publication 60).
In general, only unsealed sources of radioactive materials are considered to pose an internal hazard but it should be noted that, if a sealed source is accidentally or deliberately breached, then it would also represent an internal hazard.
14.3Practices Which Use Unsealed Sources
The use of unsealed sources in industry, science and medicine is common. In industry and science, the use of radioactive tracer sources is well established and research experiments use unsealed sources as a common practice. The most widespread use of unsealed sources is in nuclear medicine where the chemical composition of radioactive material and its carrier is carefully chosen so that they will go to a specific organ in the body. The ability to detect the radiation from these sources makes them a useful diagnostic tool. An example of this is the use of technetium-99m combined with various carriers for scans of the brain, liver, lungs, spleen and bone marrow. In a similar way, iodine-131 can be used in therapy to kill malignant thyroid cells. Sources which are used for medical purposes (i.e. diagnostic and therapeutic purposes) are known as radiopharmaceuticals.
SELF-CHECK 1
Define the following terms:
Sealed source.
Unsealed source.
Contamination.
What is the difference between removable and fixed contamination?
Why does the presence of removable contamination present an internal hazard?
Why may small quantities of contamination represent a significant internal hazard?
Which type of source (sealed or unsealed) is generally considered to pose an internal radiation hazard?
Now check your answers with the model answers in the your workbook.
14.4The Effect of Radiation Type on Internal Radiation Hazards
An important consideration in the protection from internal radiation hazards is the type of radiation emitted by the radioactive contamination. The degree to which each type of radiation represents an internal radiation hazard is dependent on the range of each type of radiation in body tissue.
As already mentioned in Module 2.2 Protection from External Hazards, alpha particles pose no external radiation hazard due to their poor penetrating ability. However, alpha radiation from radioactive material inside the body can damage body organs due to both the close proximity of the contamination to the organs or tissues and the short range of alpha particles in the body. Hence internal alpha contamination deposits large amounts of energy over a very small volume of body tissue and this could result in damage to the organ or tissue surrounding the source.
Internal beta contamination may also pose a localized radiation hazard but to a lesser extent than alpha contamination. In general, beta particles have a higher range than alpha particles in the body and hence their energy is transferred over a larger volume of tissue. This in turn lessens the overall effect of the source on the surrounding organs and tissue.
Gamma emitting contamination represents less of an internal radiation hazard than either alpha or beta contamination. This is due to the high penetrating ability and long range of this type of radiation in tissue.
Due to the nature of x-ray and neutron production, it would be rare to encounter internal x-ray or neutron contamination.
Table 1 summarizes the effect of radiation type on external and internal radiation hazards.
Table 8
The Effect Of Radiation Type On External And Internal Radiation Hazards
Type of Contamination
External Hazard
Internal Hazard
Alpha
None
Severe
Beta
Moderate
Moderate
Gamma
Severe
Slight
From Table 1 you can see that unsealed radioactive materials which emit alpha radiation are the most severe internal radiation hazard. There must be very strict control over the use of unsealed alpha sources. You will learn about methods of control later in this module.
14.5How Radioactive Material Enters the Body
Contamination can exist in the form of a liquid, a gas or a powder (or dust) and this radioactive material can enter the body in several ways. The four routes of entry are:
inhalation of airborne contamination;
ingestion through the mouth;
absorption through the skin; and
entry through an open wound.
Figure 2 represents the four routes by which radioactive material can enter the body.
Figure 12
Routes of Entry for Radioactive Material
When contamination is inhaled, a certain fraction will pass from the lungs into the bloodstream, another fraction will be exhaled and a third component will be swallowed when it is cleared from the lungs. The relative size of these fractions depends on the chemical and physical form of the contamination and the physiology of the person involved. Similarly, when contamination is ingested, the amount passing through the wall of the digestive tract and into body fluids depends on the nature of the contamination and the physiological conditions at the time of ingestion.
Some radioactive materials, such as tritiated water or radionuclides dissolved in organic solvents, are easily absorbed through the skin and can enter the body transport system. In addition, contamination may also enter the bloodstream directly through an open wound. Entry could be through a wound received whilst working with radioactive materials (e.g. a needlestick injury) or through a healing wound which may become contaminated during unsealed radioactive work.
SELF-CHECK 2
a) Which type of radiation poses the most severe internal radiation hazard?
b) Why is this so?
a) Which types of radiation pose the least severe internal radiation hazard?
b) Why is this so?
State the four principle routes of entry of radioactive material into the body.
Now check your answers with the model answers in your workbook.
15.MEASUREMENT OF INTERNAL RADIATION HAZARDS
When radioactive material enters the human body it may deliver radiation doses to various body organs and tissues. In radiation protection, it is important to be able to assess the level of the hazard associated with an intake of radioactive material. This is much harder to do accurately for the internal radiation hazard than for the external radiation hazard. The effect of radiation on individual organs in the body is hard to determine because people have very different anatomical (size and shape), physiological (body processes such as respiration) and metabolic (changes such as rate of food digestion) characteristics. In this section you will learn how assumptions are made in order to assess the level of internal radiation hazards.
15.1ICRP Reference Man and IAEA Reference Asian Man
There is a wide variation in the anatomical, physiological and metabolic characteristics of human beings. For the purposes of radiation protection, ICRP Publication 23 defined Reference Man to describe the characteristics of a human being. Reference Man was chosen to represent an average person over a wide range of human characteristics and is intended for use as a model for calculations and comparisons of the internal effects of ionizing radiation. The data is currently being updated using studies of European and North American populations. Appendix A gives some characteristics of Reference Man.
However, Reference Man is not a good representation of an Asian population and therefore equivalent data for Reference Asian Man have been produced by the International Atomic Energy Agency (IAEA).
15.2Biological and Effective Half-Lives
Whenever an intake of radioactive material occurs, it is important to have some idea of how long the material will remain in the body in order to assess the hazard. As already discussed in Module 1.3 Ionizing Radiation and Radioactive Decay, radioactive materials decay exponentially with time. However, other bodily processes (e.g. urination and defecation) also act to remove these materials from our body and the rate at which the body excretes radioactive material is also approximately exponential. In order to calculate the effective rate at which radioactive materials decay or are removed from the body, we need to combine both the rate of radioactive decay and also the rate of excretion. In radiation protection the term effective decay constant (eff) is used to describe the rate of decay and removal of radioactive materials from the body. A mathematical definition of this term is given in Equation 1.
eff= r + b[1]
where eff = effective decay constant
r = radioactive decay constant
b = biological decay constant
Equation 1 can be related to effective, biological and radioactive half-lives (and hence time) by remembering that the radioactive decay constant can be written as:
r = ln 2
Tr
where r = radioactive decay constant
Tr = half-life of the radioactive material
ln 2 = loge 2 = 0.693
As both the effective decay constant and biological decay constant can be written in a similar way, Equation 1 can be rewritten as Equation 2:
1 = 1 + 1[2]
Teff Tr Tb
where Teff = effective half-life of a radionuclide in the body (i.e. the effective time taken for the activity of a radionuclide in the body to be reduced to half its original value by the combination of radioactive decay and biological excretion).
Tr = radioactive half-life of a radionuclide in the body (i.e. the time taken for the activity of a radionuclide in the body to be reduced to half its original value by radioactive decay).
Tb = biological half-life of a radionuclide in the body (i.e. the time taken for the activity of a radionuclide in the body to be reduced to half its original value by biological excretion).
Hence, if the values for Tr and Tb are known, then it is possible to calculate Teff from Equation 2.
The radioactive half-life is a physical constant which depends only on the radionuclide. The biological half-life (and hence the effective half-life) is dependent on the chemical and physical nature of the radioactive contamination and on the anatomical, physiological and metabolic nature of the person. If the radioactive material is chemically similar to other elements in the body, it can change places with them. For example, strontium has similar chemical properties to calcium, so strontium-90 can replace calcium in bones. The physical form of the contaminant is important as it determines the characteristics of the material, such as solubility, which affect how the material is absorbed into the body.
Example 1 illustrates how Equation 2 is used to calculate the effective half-life of radioactive contamination in the body.
EXAMPLE 1
Question
Calculate the effective half-life for cobalt-60 in body tissue if the radioactive half-life is 1.9 x 103 days and the biological half-life is 10 days.
Answer
Using Equation 2:
1 = 1 + 1
Teff 1.9 x 10310
Hence:
Teff = 9.95 days (approximately 10 days)
!
Remember when using Equation 2 that you must invert your answer to the right hand side of the equation in order to obtain the value of Teff.
It can be seen from Example 1 that if the biological and radioactive half-lives differ greatly, then it is the smaller number that determines the effective value.
Table 2 gives some examples of radioactive, biological and effective half-lives for different radionuclides.
Table 9
Radioactive, Biological and Effective Half-Lives For Some Radionuclides
Radionuclide
Critical Organ
Tr
(days)
Tb
(days)
Teff
(days)
60Co
Total body
1.9 x 103
10
10
90Sr
Total body
1.1 x 104
1.1 x 104
5.5 x 103
137Cs
Total body
1.1 x 104
70
70
Values taken from Medical Effects of Ionizing Radiation, Mettler and Moseley, 1985
SELF-CHECK 3
Now see how much you have understood by answering the following questions in your workbook:
Define the following terms:
Effective half-life.
Biological half-life.
Radioactive half-life.
Which factors determine the biological half-life (and hence the effective half-life) of a particular radionuclide?
Calculate the effective half-life for tritiated water in body tissue if the radioactive half-life is 4.5 x 103 days and the biological half-life is 12 days.
Now check your answers with the model answers in your workbook.
15.3Dose Coefficients
The level of the internal radiation hazard depends on the size of the dose that occurs after radioactive contamination has entered the body. Dose coefficients for Reference Man have been determined using Reference Man data and models of the human body which describe how the body works. Dose coefficients (h) are measured in Sv Bq-1 and give the dose to the whole body (committed effective dose) resulting from an intake of radioactive material.
The committed effective dose per becquerel of intake for a particular nuclide is dependent on the method of intake. The values for h for ingestion and inhalation for different radionuclides have been determined for occupationally exposed workers and are listed in ICRP Publication 68 and in Table II-III of the IAEA Basic Safety Standards.
Values of h for members of the public which take into account different age groups, have also been published in the IAEA Basic Safety Standards (Tables II-VI and II-VII) and in ICRP Publications 71 and 72.
Note that, as yet, no dose coefficients exist for Reference Asian Man. Hence dose coefficients for Reference Man are used both in the IAEA Basic Safety Standards and throughout this module.
15.4Annual Limit On Intake
The internal radiation hazard can be assessed by comparing the amount of radioactive material that could be taken into the body with the amount which would result in a dose equal to the relevant annual limit (currently, this dose limit for occupationally exposed workers is 20 mSv). This gives us a quantity known as the Annual Limit on Intake (ALI).
Mathematically, the ALI (in becquerels) for a particular radionuclide is calculated using Equation 4:
ALI = L[4]
h
where L = the relevant annual effective dose limit.
h = the committed effective dose per becquerel of intake (in units of Sv Bq-1).
An example of how to calculate ALIs for occupationally exposed personnel is given in Example 2.
EXAMPLE 2
Question
Calculate the ALI for inhalation for an occupationally exposed worker who is using unsealed phosphorus-32 where the dose coefficient h (inhalation) is 2.9 x 10-9 Sv Bq-1.
Answer
The relevant dose limit for an occupationally exposed worker is 20 mSv, i.e. 0.02 Sv.
Using Equation 4:
ALI (inhalation) = 0.02 = 6.9 x 106 Bq
2.9 x 10-9
Hence, an intake by inhalation of 6.9 x 106 Bq of phosphorus-32 is equivalent to one ALI and, hence, is also equivalent to an annual committed effective dose of 20 mSv.
Some examples of ALIs for occupationally exposed workers are given in Table 3.
Table 10
Annual Limits on Intake For Radiation Workers For Selected Radionuclides
Radionuclide
ALI for Inhalation*
(Bq)
ALI for Ingestion
(Bq)
32P
6.9 x 106
8.3 x 106
60Co
1.2 x 106
5.9 x 106
90Sr
2.6 x 105
7.1 x 105
99mTc
6.9 x 108
9.1 x 108
131I
1.8 x 106
9.1 x 105
137Cs
3.0 x 106
1.5 x 106
* These values are based on values recommended in the IAEA Basic Safety Standards with the slowest possible absorption from the lungs.
The dose received by a person following an intake of radioactive material may be quoted in terms of a fraction of an ALI or in units of millisieverts. Example 3 illustrates this concept.
EXAMPLE 3
Question
A radiation worker accidentally ingests 1.48 x 106 Bq of cobalt-60. Estimate the dose received by the worker (using the Reference Man model);
a) in terms of ALI.
b) in millisieverts.
Answer
Using Table 3:
5.9 x 106 Bq = 1 ALI for ingestion
So:
Number of ALIs ingested = 1.48 x 106 = 0.25 ALI
5.9 x 106
As 1 ALI is equivalent to a committed effective dose of 20 mSv, then 0.25 ALI is equivalent to a committed effective dose of 5 mSv.
Therefore, the dose received can be quoted in terms of:
a) 0.25 ALI or
b) 5 mSv.
SELF-CHECK 4
Now see how much you have understood by answering the following questions in your workbook:
In which documents can the dose coefficients be found for occupationally exposed workers?
Define the term annual limit on intake (ALI).
Calculate the ALI for an occupationally exposed worker for ingestion of americium-241 where the dose coefficient for ingestion is 2 x 10-7 Sv Bq-1.
A radiation worker accidentally ingests 2.25 x 106 Bq of caesium-137. Estimate the committed effective dose received by the worker (using the Reference Man model);
a) in terms of ALI.
b) in millisieverts.
Now check your answers with the model answers in your workbook.
16.CONTAMINATION LIMITS IN THE WORKPLACE
The internal radiation hazard in the workplace is assessed by measuring levels of surface and airborne contamination and comparing these measured values to potential doses. This comparison is done for surface contamination by using a quantity known as the Derived Limit (DL) for surface contamination and for airborne contamination using a quantity called the Derived Air Concentration (DAC).
16.1Derived Limits for Surface Contamination
Derived Limits (DLs) can be used to assess and control the hazard from surface contamination in the workplace. They are quoted in terms of becquerels per square centimetre (Bq cm-2) for ease of comparison with measured levels, and are often used to classify work areas (as discussed in Section 4.2.1 of this module).
The method of determining Derived Limits (DLs) is quite complex but essentially they are calculated by considering the highest potential dose that could result from the skin contamination, inhalation or ingestion of a particular radionuclide, and relating this value to the relevant ICRP dose limit. Although Derived Limits are not internationally defined, they are usually based on one times the total dose limit. For example, in Australia, exposure to one Derived Limit (DL) for 2000 hours (8 hours a day, 5 days a week, 50 weeks per year) is deemed to result in a committed effective dose of 20 mSv (i.e. one times the ICRP dose limit for an occupationally exposed worker). However, in other countries, exposure to one Derived Limit (DL) for 2000 hours could be taken to mean a fraction or multiple of the ICRP dose limit. Hence, when referring to Derived Limits is important that you know the definition of a Derived Limit for that particular country or state.
When referring to Derived Limits (DLs), it is important that you know the correct definition of that limit for the particular country or state you are in.
The potential dose that a particular radionuclide can deliver to a human when taken into the body depends on the amount of harm that the radionuclide can cause. This is known as the radiotoxicity of a particular radionuclide and it is dependent on:
the type of radiation emitted by the radionuclide;
its effective half life; and
the radiosensitivity of the body organs it is likely to target.
To simplify the use of Derived Limits (DLs) in radiation protection, radionuclides with similar radiotoxicity are grouped together. Appendix B gives the radionuclide groupings and corresponding Derived Limits for surfaces in classified areas as recommended by the National Health and Medical Research Council of Australia. An example of a radionuclide in each group is given in Table 4.
Table 11
Radiotoxicity and Derived Limits for Surface Contamination
Group
Radiotoxicity
Example
Derived Limit*
(Bq cm-2)
1
Very High
Am-241
0.1
2
High
U-238
1
3
Higher Medium
Sr-90
10
4
Lower Medium
I-131
100
5
Low
Tc-99m
1000
* Based on an annual dose limit of 20mSv as recommended by ICRP 60.
Note that Group 1 and Group 2 radionuclides are alpha emitters and are classed as highly radiotoxic due to the severe effects of an intake. Hence, the DL values for this group are much lower than any other group.
Example 4 shows how it is possible to compare and assess the hazard from surface contamination by using Derived Limits (DLs) as a guide.
EXAMPLE 4
Question
On a routine survey of an iodine-131 laboratory, you find a removable surface contamination level of approximately 50 Bq cm-2. What is this level in terms of DLs and what is the annual committed effective dose which could result from the exposure to this surface contamination level?
Answer
From Table 4, the DL for iodine-131 (I-131) is quoted as 100 Bq cm-2 by the National Health and Medical Research Council of Australia.
Hence, the measured level is equivalent to (50 100) 0.5 DL’s.
According to the Australian definition of a Derived Limit, exposure to 1 DL for 2000 hours (8 hours per day, five days a week, 50 weeks a year) would result in a committed effective dose of 20 mSv.
Hence, we can say that exposure to 0.5 DL’s for 2000 hours would result in a committed effective dose of (0.5 x 20 mSv) 10 mSv.
Obviously, this surface contamination will decay away with time but, in accordance with the ALARA principle, levels of this magnitude should be reduced as far as possible. However, this example shows how, by quoting surface contamination levels in terms of Derived Limits, we can assess the level of internal hazard.
Note that for comparison purposes, surface contamination measurements are usually averaged over certain areas. For example, skin contamination is averaged over 100 cm2 (except for the hand where the whole hand is averaged). For walls, floors and ceilings, the contamination is averaged over 1000 cm2. The usual area for other surfaces is 300 cm2.
16.2Derived Air Concentration
Derived Air Concentrations (DACs) are used in the workplace to compare measured airborne contamination levels with levels which could result in an intake of one ALI.
The Reference Man model is used which gives a breathing rate of 2 400m3 per year (i.e. a nominal breathing rate of 1.2m3 per hour for an 8 hour day, 5 days per week and 50 weeks per year).
The mathematical definition for DAC is given in Equation 5:
DAC = ALI (inhalation) [5]
2 400
An example of how to calculate DACs for work areas is shown in Example 5.
EXAMPLE 5
Question
Using the annual limits on intake given in Table 3, calculate the Derived Air Concentration (DAC) for phosphorus-32.
Answer
From Table 3:
ALI (inhalation) = 6.9 x 106 Bq
Using Equation 5:
DAC = 6.9 x 106 = 2.875 x 103 Bq m-3
2400
Hence the DAC for phosphorus-32 is 2.875 x 103 Bq m-3
Example 6 shows how the internal hazard can be assessed by comparing measured airborne activity with Derived Air Concentrations (DACs) and hence recommended dose limits.
EXAMPLE 6
Question
The airborne contamination in a laboratory which deals solely with iodine-131 is measured as 75 Bq m-3. What is this airborne contamination level in terms of Derived Air Concentrations (DACs) and what is the annual committed effective dose associated with this airborne contamination level?
Answer
From Table 3:
ALI (inhalation) = 1.8 x 106 Bq
Using Equation 5:
DAC = 1.8 x 106 = 7.5 x 102 Bq m-3= 750 Bq m-3
2400
The airborne contamination in the laboratory is measured as 75 Bq m-3.
Hence, the airborne contamination in terms of Derived Air Concentrations is:
75 = 0.1 DAC
750
Remembering that 1 DAC is the concentration of a radionuclide which would result in inhaling 1 ALI in a year, then 0.1 DAC would result in inhaling 0.1 ALIs in a year. Also remembering that an intake of 1 ALI would result in an intake of 20 mSv. Then an intake of 0.1 DACs would result in a committed effective dose of (0.1 x 20) 2mSv.
Hence, by using DAC levels as a guide, it is possible to compare and assess the internal radiation hazard from airborne contamination for particular work areas. In addition, DAC levels may be used to classify work areas in terms of their internal radiation hazard. This concept will be further discussed in Section 4.2.1 of this module.
SELF-CHECK 5
Now see how much you have understood by answering the following questions in your workbook:
What are the three main uses of Derived Limits in the workplace?
a) Which type of radionuclides are the most radiotoxic?
Why is this so?
On a routine survey of a sulphur-35 (S-35) production facility, you find a removable surface contamination level of approximately 250 Bq cm-2. a) What is this surface contamination level in terms of Derived Limits?
b) What is the annual committed effective dose which could result from the exposure to this surface contamination level?
Define the term Derived Air Concentration (DAC).
Using the Annual Limits on Intake given in Table 3, calculate the Derived Air Concentration for:
a) cobalt-60.
b) technetium-99m.
The airborne contamination in a laboratory which deals solely with phosphorus-32 is measured as 5.8 x 102 Bq m-3.
What is this airborne contamination level in terms of Derived Air Concentrations?
What is the annual committed effective dose associated with this airborne contamination level?
Now check your answers with the model answers in your workbook.
17.CONTROLLING INTERNAL RADIATION HAZARDS
There are three basic techniques to consider when controlling the internal radiation hazard in a particular area:
Minimization of the amount of activity being handled;
Administrative controls; and
Physical controls to contain the activity.
17.1Minimization of Radioactive Materials
In all processes involving the handling of radionuclides, the amount of activity should be reduced as far as possible. This is in accordance with the ALARA principle. In addition to reducing the hazards due to contamination, minimization of the activity also reduces the external dose rates to workers.
As an example, consider the situation in which radioactive material is being used in a tracer experiment. The minimum amount of activity used will depend on the minimum amount that can be detected by the measuring equipment and the amount of activity that may be lost before reaching the measuring equipment. Example 7 shows how to work out the minimum activity to use.
EXAMPLE 7
Question
An experiment is being conducted using phosphorus-32 (P-32) to see what fraction of phosphorus in the soil is taken up into the leaves of a certain plant. Mathematical modelling predicts that 10% of P-32 will be taken up. For statistical accuracy 1 kBq is the minimum activity to be detected by the measuring equipment. Previous experiments have indicated an error factor of 2. What minimum activity of phosphorus-32 would you recommend?
Answer
Minimum activity to be detected = 1 kBq
Predicted take up factor = 10%
Therefore:
Initial activity = 10 x 1 kBq = 10 kBq
To allow for an error of 2:
Minimum activity recommended = 2 x 10 kBq = 20 kBq
17.2Administrative Controls
An administrative control is a method of administration which prevents or minimizes exposure to radiation hazards. Administrative controls for internal radiation hazards are very similar to those for external radiation hazards, although the emphasis must be on preventing radioactive material from entering the body. The following list gives some useful examples of administrative controls:
Classification of areas.
Display of clear signs for each classified area.
Radiological protection training for workers and managers.
Work procedures which incorporate the use of physical controls.
Local rules, (e.g. restriction of access to certain areas) and conditions of work, (e.g. requirement to wear protective clothing and respiratory protection).
Maintenance of source inventories for each area.
Radiation safety auditing system which includes safety assessment of workplace plant and equipment.
Use of investigation levels for personal dose monitoring and workplace monitoring results.
The classification of areas and local rules which have particular relevance to the internal radiation hazard will be discussed in the next two sections. Other methods of administrative control will be discussed in the relevant modules of Parts 3 and 4 of this distance learning material.
17.2.1Classification of work areas
Work areas can be classified according to the level of the internal radiation hazard. A classification system in which areas may be classified as controlled or supervised is recommended in the IAEA Basic Safety Standards. The definitions given here are the same as those given in Module 2.2 Protection from External Radiation Hazards.
A controlled area is one where specific protection measures and safety provisions are or could be required to control normal exposures and to prevent or limit potential exposures.
A supervised area is where occupational exposure conditions are kept under review but no specific protection measures are required.
An unclassified area is where no protection methods are required and the occupational exposures do not need to be kept under review.
Generally, the classification of areas varies in accordance with the particular needs of the workplace and is usually based on operational experience and judgement. If the major radiological hazard is due to external radiation then the classification system suggested in Module 2.2 Protection from External Radiation Hazards may provide sufficient control of the internal radiation hazard as well. If however the external radiation hazard is small compared with the internal radiation hazard, it is useful to classify areas according to the potential for airborne and surface contamination. The area classifications are determined by considering what radionuclides are being used, how they are being used and the maximum activity used at any one time. Table 5 illustrates one example of how the DL and DAC values can be used to classify areas which have an occupancy factor of 1 (i.e. a 100% occupancy of the classified area). Of course, in practice the levels should be set locally depending on the conditions in the working areas and on the occupancy factor.
Table 12
Area Classification In Terms of Surface and Airborne Contamination Levels
Classification Type | Surface Contamination Levels | Airborne Contamination Levels |
Controlled | Greater than 0.3 DL | Greater than 0.3 DAC |
Supervised | 0.05 to 0.3 DL | 0.05 to 0.3 DAC |
Unclassified | Less than 0.05 DL | Less than 0.05 DAC |
17.2.2Local Rules
Local rules are used in the workplace to control contamination levels and reduce the chance of radioactive material being taken into the body. The following list gives some examples of subjects which should be covered in local working procedures:
Prohibition of eating, drinking, smoking or applying cosmetics in classified areas.
Maintenance of good housekeeping procedures.
Use of protective clothing and respiratory protection.
Regular area and personnel contamination monitoring.
Controlling access to classified areas.
Procedures for entering and leaving classified areas.
Maintenance of source inventories.
17.3Physical Controls
Although administrative controls provide a basis for a radiation protection program, these controls rely on familiarity with written procedures. If a new worker is not aware of these procedures, or these procedures are not followed correctly for any other reason, then the potential exists for accidental exposure to internal radiation hazards. In order to ensure that the chance of accidental exposure is as low as possible, physical controls are employed in the workplace to prevent the spread of radioactive materials. The following list gives some useful examples of physical controls:
Splash trays.
Barriers.
Fume cupboards.
Glove boxes.
Shielded cells.
Interlocks.
17.3.1Containment Systems
Containment systems consist of physical structures, (which may be as simple as a splash tray or as complex as a system of sealed containers with associated ventilation), which contain the radioactive materials and prevent the spread of contamination. The choice of equipment for the effective containment of radioactivity depends on the quantity of activity and the physical form of the radioactive material. As physical form may change during various processes (e.g. by boiling a liquid to produce the vapour), it is important to be aware of all operations being performed in a particular area when designing suitable containment systems.
Most containment systems for unsealed sources have at least two levels of containment. Figure 3 shows four levels of containment suitable for handling radioactive liquids in a laboratory.
Figure 13
Four Levels of Containment For Handling Radioactive Liquids
Greater levels of containment are needed to control airborne contamination hazards such as vapour and dust. Gloveboxes (i.e. boxes with fitted gloves) and shielded cells with remote manipulators are types of containment which allow handling of radioactive materials without any contamination coming into contact with the body. Gloveboxes such as that shown in Figure 4 should only be used for handling alpha or beta emitters as they are usually made of perspex and have little or no shielding to protect against the external hazard.
Figure 14
Schematic Drawing of a Glove Box
For high dose rate gamma emitters with airborne or surface contamination hazards, a shielded cell such as that shown in Figure 5 can be used. This is a cell with a thick lead glass shielding window and ‘master-slave’ manipulators for indirect handling of unsealed radionuclides.
Figure 15
Work Being Conducted in a Shielded Cell
The ventilation systems for glove boxes and cells usually involve inlet and exhaust filters. The atmosphere inside is kept at a lower pressure than that outside so that should a leak develop, air will flow into the enclosure and prevent contamination from escaping.
A lower level of containment is provided by a fume cupboard (as shown in Figure 6) where the material is handled through an opening in the front. Air is drawn from the laboratory through the front opening and into the fume cupboard. This is then expelled through exhaust outlets and may be filtered before entering the environment. The controls for services such as electricity and ventilation are positioned outside the fume cupboard to reduce the number of times the airflow through the front opening is disturbed. It is important that fume cupboards are used correctly to ensure that contamination is being controlled. This means that equipment in the fume cupboard should be minimized (no unnecessary storage), the area around the front of the fume cupboard should be kept free of obstruction, air flow at the face of the fume cupboard should be monitored and the opening at the front of the fume cupboard should be kept to a minimum.
Figure 16
A Fume Cupboard
17.3.2Control of Radioactive Waste
Good containment of radioactive waste materials is an important aspect of contamination control and is often overlooked. You will learn about safe methods of storing and handling radioactive waste in Module 3.4, Safe Handling of Radioactive Waste.
17.3.3Laboratory Design
Design features of a laboratory in which unsealed radioactive materials are used may also be considered as physical controls. It is important that surfaces which may become contaminated (bench tops, floors, walls etc.) are easy to clean, and that there are no absorbent surfaces or cracks which could trap contamination. If you work in a radioisotope laboratory, or are involved in designing suitable laboratories, you will learn more about this in Module 4.3 Safety in Radioisotope Laboratories.
SELF-CHECK 6
Now see how much you have understood by answering the following questions in your workbook:
What are the three basic principles for the control of internal radiation hazards?
Give three examples of administrative controls for the protection of individuals against the internal contamination hazard.
Give three examples of local rules which help control the internal radiation hazard.
Describe what is meant by a containment system and give four examples of containment in a laboratory.
Now check your answers with the model answers in your workbook.
KEY POINTS
An internal radiation hazard exists when there is a possibility of harm due to ionizing radiation from a radioactive source entering the body.
Unsealed radioactive material in an undesirable location is known as contamination.
A sealed source is defined as radioactive material that is permanently sealed in a capsule or is in a solid form which cannot conceivably lose any of its material.
An unsealed source is defined as radioactive material that is not sealed or is in a form whereby it could lose some of its material (e.g. a liquid or gas).
Removable contamination is surface or airborne contamination which can move freely. Fixed contamination is attached to a particular surface.
Quite small quantities of contamination which represent an insignificant external radiation hazard may pose an appreciable internal hazard.
In general, only unsealed sources of radioactive materials are considered to pose an internal hazard but, if a sealed source is accidentally or deliberately breached, then it would also represent an internal hazard.
Alpha radiation represents the most severe internal radiation hazard due its relatively high energy and short range in organs and tissue.
Unsealed radioactive materials can enter the body through inhalation, ingestion, absorption through the skin and through a wound.
The length of time a radionuclide stays in the body depends on the chemical and physical form of the contamination and the physiology of the person involved.
The ICRP recommends Reference Man as a model for internal radiation hazard calculations.
The term effective decay constant (eff) is used to describe the rate of decay and removal of radioactive materials from the body.
The effective half-life (Teff) of a radioactive material in the body is the time taken for the radioactive material in the body to be reduced to half its original value by the processes of radioactive decay and biological excretion.
The radioactive half-life (Tr) of a material is the time taken for the radioactive material to be reduced to half its original value by radioactive decay.
The biological half-life (Tb) of a radioactive material in the body is the time taken for the radioactive material in the body to be reduced to half its original value by biological excretion.
Dose conversion coefficients are used to calculate the amount of activity taken into the body to a committed effective dose.
The annual limit on intake (ALI) is defined as the intake of a particular radionuclide by inhalation, ingestion or absorption through the skin or wound such that would result in an annual committed effective dose equal to the relevant dose limit.
Derived Limits (DL) are limits of surface contamination such that DACs, ALIs and skin dose limits are not exceeded.
The Derived Air Concentration (DAC) is defined as the concentration of a particular radionuclide that would result in an occupationally exposed person inhaling one ALI in a year.
Areas may be classified in terms of the internal radiation hazard (DACs and DLs).
The internal hazard can be controlled by minimization of radioactive materials, administrative controls and physical controls.
Local rules are necessary in areas where unsealed radioactive material is used.
Containment systems are physical structures which are designed to prevent the spread of radioactive contamination.
FINAL ASSIGNMENT
This assignment is to be completed under test conditions, so spend some time now studying this module. Then contact your supervisor to arrange a suitable time to complete the assignment.
APPENDIX A
SOME CHARACTERISTICS OF REFERENCE MAN
Some Organs of Reference Man (Adult Male)
Organ
Mass (kg)
% of Total Body
Total Body
70
100
Skeleton
10
14
Muscle
28
40
Fat
13.3
19
Blood
5.5
7.9
Gastrointestinal Tract
2.2
3.1
Thyroid Gland
0.02
0.029
Water Balance
Intake Method
Litres/day
Excretion
Litres/day
Foods
0.70
Urine
1.40
Fluid
1.95
Sweat
0.65
Oxidation of Food
0.35
Insensible*
0.85
Total
3.00
Faeces
0.10
*In exhaled air, and as a result of diffusion through the skin and a very low sweat rate
Air Inhalation Volumes
Air inhaled during 8 hour working day
9.6 m3
Air inhaled during 16 hours not at work
13.2 m3
APPENDIX B
SURFACE CONTAMINATION LIMITS
0.1 Bq cm-2 | 1 Bq cm-2 | 10 Bq cm-2 | 1000 Bq cm-2 | ||||
Th-230 | Sm-147 | Sr-90 | Na-22 | Ag-110m | H-3 | Br-77 | Ce-139 |
Th-232 | Sm-153 | Ra-223 | P-32 | Cd-109 | C-14 | Rb-81 | Ce-141 |
Pa-231 | Pb-210 | Ra-224 | Co-56 | In-113m | Na-24 | Sr-85 | Nd-147 |
U-232 | Po-210 | Co-60 | Sb-124 | S-35 | Sr-87m | Gd-153 | |
Pu-238 | Ra-226 | Cu-64 | I-125 | Cl-36 | Y-87 | Tb-160 | |
Pu-239 | Th-227 | Cu-67 | I-131 | Ca-45 | Y-88 | Eb-169 | |
Am-241 | Th-228 | Zn-65 | Cs-134 | Ca-47 | Mo-99 | Tm-170 | |
Cm-244 | U-234 | Ga-68 | Cs-137 | Sc-46 | Tc-99m | Yb-169 | |
U-235 | Se-75 | La-140 | Sc-47 | Tc-99 | Lu-177 | ||
U-236 | Rb-86 | Pm-147 | Cr-51 | Ru-103 | Hf-181 | ||
U-238 | Sr-89 | Eu-152 | Mn-54 | Ag-111 | W-185 | ||
Y-90 | Eu-154 | Fe-55 | In-111 | Re-186 | |||
Ru-106 | Bi-210 | Fe-59 | Sn-113 | Ir-192 | |||
Co-57 | Sb-125 | Au-198 | |||||
Co-58 | I-123 | Hg-197 | |||||
Ni-63 | Cs-129 | Hg-203 | |||||
Ga-67 | Cs-131 | Tl-201 | |||||
Ge-68 | Ba-133 | Tl-204 |
Taken from Recommended limits on radioactive Contamination on Surfaces in Laboratories (1995), Radiation Health Series No. 38, Australian National Health and Medical Research Council.
GLOSSARY OF TERMS
Annual limit on intake (ALI) | The amount of radioactivity, measured in becquerels, which if taken into the body by Reference Man would result in a committed effective dose equal to the relevant dose limit. |
Biological half-life | The time taken for the activity of a radionuclide in the body to be reduced to half its original value by biological excretion. |
Containment Systems | Physical structures which prevent the spread of radioactive material. |
Contamination | Uncontained radioactive material present in a location where it is not wanted. |
Controlled area | An area where specific protection measures and safety provisions are or could be required to control normal exposures and to prevent or limit potential exposures. |
Derived Air Concentration (DAC) | The concentration of a radionuclide (in becquerels per metre cubed) in the air which would result in a worker in the area receiving one ALI in a working year.. |
Derived limit for surface contamination (DL) | Limit which controls the amount of surface contamination in order to keep doses below the relevant dose limits. |
Dose Coefficient | Coefficient used to determine the committed effective dose per unit intake of radioactive material for adults (Sv Bq-1) calculated over 50 years following the intake. |
Effective half-life | The time taken for the activity of a radionuclide in the body to be reduced to half its original value by the combination of radioactive decay and biological excretion. |
External radiation hazard | Ionizing radiation from a radioactive source outside the body with the potential to cause harm. |
Fixed contamination | Contamination fixed to a surface. |
IAEA | International Atomic Energy Agency. |
ICRP | International Commission on Radiological Protection. The organization which makes recommendations and provides guidance on the fundamental principles of radiation protection. |
Internal radiation hazard | The hazard which exists when there is the potential for a source of ionizing radiation to enter the body and cause harm. |
Radioactive half-life | The time taken for the activity of a radionuclide to reduce to half its original value by radioactive decay. |
Radiotoxicity | The measure of the amount of harm which may be caused if the radionuclide is taken into the body. |
Reference Asian Man | A reference man model developed by the International Atomic Energy Agency specifically for Asian populations. |
Reference Man | A model developed by the ICRP for dose calculations following the intake of radionuclides. The model describes average characteristics of a human being. |
Removable contamination | Radioactive contamination which is not fixed to a surface. |
Sealed source | Radioactive material sealed in such a way that none can escape under normal working conditions. |
Supervised area | An area where occupational exposure conditions are kept under review but no specific protection measures are required. |
Unclassified area | An area where no protection methods are required and the occupational exposures do not need to be kept under review. |
Unsealed source | Radioactive material which is not sealed and may lose some of its contents under normal working conditions. |
INTERNATIONAL ATOMIC ENERGY AGENCY AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION |
DISTANCE LEARNING MATERIALS
RADIATION PROTECTION
Module 2.4
Prepared by Safety and Radiation Science
Australian Nuclear Science and Technology Organisation
With the assistance of consultants in Australia and the United Kingdom, and IAEA experts from Korea, Mongolia, New Zealand, the Philippines and Thailand
Use of this material, acknowledging the IAEA and ANSTO as the source, is permitted for non-profit training
Acknowledgements
This material has been prepared by an extensive team of international experts from the fields of radiation protection, medicine and education. It is not possible to mention by name all those who have had an input to; the initial planning; writing modules and workbooks; preparing and marking final assignments; proof-reading and editing; using the material and providing valuable feedback; organizing and hosting review meetings; and general administrative support.
The support of ANSTO management in providing the resource and encouragement is gratefully acknowledged.
The enthusiastic support of IAEA Technical Officers has been vital to the success of this project.
PART 2
RADIATION PROTECTION
MODULE 2.4
USE OF RADIATION MONITORING INSTRUMENTS
CONTENTS
OVERVIEW
An important part of a radiation protection program is the monitoring of areas where radiation hazards may exist. Levels of the radiation hazard can be assessed by performing dose rate surveys (for the external hazard) and contamination surveys (for the internal hazard). In this module you will learn how to select appropriate instruments for measuring radiation hazards and how to use them effectively. You will also learn how to perform radiological surveys safely for dose rates and contamination, and how to report the results in a meaningful way.
Before proceeding with this module, you may wish to revise Module 1.5 Methods of Radiation Detection.
TIME ALLOCATION
It is estimated that you will need to spend ten to twelve hours to complete this module. This time estimate is only for guidance only. Do not worry if you need to spend more time to understand this module.
MATERIALS
MATERIALS
You will need writing materials to take notes and answer questions. Access to a scientific calculator is also desirable.
NOW YOU ARE READY TO START WORK
Radiation detectors are the part of the instrument which interacts with incoming radiation and converts the energy into something (usually light or electric charge) which can be measured. By studying Module 1.5 Methods of Radiation Detection, you have gained basic knowledge about how the following types of detector work:
Gas-filled detectors (ionization chambers, proportional counters, GM counters);
Solid state conductivity detectors; and
Scintillation detectors.
Radiation measuring instruments must be able to detect and quantify external exposure from radiation sources outside the body and detect and quantify contamination which may enter the body and cause internal exposure. Hence, there are two types of measuring instrument which are used in the workplace:
Dose rate meters (for the external hazard); and
Contamination monitors (for the internal hazard).
As you may remember from Module 1.5 Methods of Radiation Detection, other instruments (known as spectrometers) can be used for spectroscopy purposes (i.e. to separate out energies and hence identify radionuclides). As the operation of these instruments is more complex, they are not covered in this module.
Dose rate meters contain a detector capable of detecting penetrating radiation and some beta particles. Two typical dose rate meters are shown in Figure 1.
Geiger-Müller Tube
Dose Rate Meter
Ion Chamber
Dose Rate Meter
Figure 17
Two Typical Dose Rate Meters
Most dose rate meters can measure both gamma and x-ray dose rates, and those with thin end windows can also measure beta dose rates. As you should remember from Module 2.2 Protection from External Radiation Hazards, alpha particles cannot penetrate the skin and therefore do not present an external radiation hazard. Hence, dose rate monitoring for these particles is unnecessary. Neutrons are more difficult to monitor because they do not cause ionization directly. It is therefore usual to measure neutron dose rates with specially designed neutron monitors (as discussed in Module 1.5 Methods of Radiation Detection). As monitoring for neutron radiation is less common for routine surveys, the use of these specialised neutron monitoring instruments is not discussed in this module.
Dose rate meters usually give a direct reading of dose rate in units of microsieverts per hour (Sv h1) (see Figure 2).
Figure 18
Monitoring for Dose Rate
The most popular unit on older dose rate meters is mrem h-1 and the easiest way to convert from mrem h-1 to Sv h-1 is to remember that:
1 mrem h-1 = 10 Sv h-1
For example, if a dose rate monitor showed a dose rate of 0.75 mrem h-1,this is equivalent to 7.5 Sv h-1 (i.e. 0.75 x 10 Sv h-1).
Some specialised dose rate meters used for dosimetry or environmental monitoring may give readings in units of micrograys per hour (Gy h-1). Although for these specialist uses it may be necessary to use factors which depend on the radiation energy and the material being exposed, for most safety related measurements of dose rate from gamma or x-ray sources, it is usual to assume grays (Gy) and sieverts (Sv) are the same.
For most safety related measurements of dose rate from gamma or x-ray sources:
1 mGy = 1 mSv
A brief overview of these units is given in Reference Material R1. They will also be discussed more fully in Module 2.5 Personal Dosimetry.
Note that the detectors in dose rate meters are actually measuring the effect of ionizing radiation on the detecting material. However, in radiation protection, we are more concerned with the effect of the radiation on a person. In fact, if you remember from Module 2.1 Principles of Radiation Protection, dose limits are given in terms of effective dose per year (a quantity, explained in Module 2.5, used to describe the dose received by a person). So, in order to estimate the effective dose due to a particular source, we would need to know the effect in all the tissues and organs of the body. Of course, this is very difficult to assess and impossible to measure. To overcome this, dose rate meters are set to measure an operational quantity known as the ambient dose equivalent rate. The relationship between effective dose and ambient dose equivalent is quite complicated and is based on many assumptions, so we will not go into too much detail in this module. However, it is sufficient to say that the measurement of ambient dose equivalent is set such that it gives a reasonable approximation of effective dose.
Dose rate meters measure the operational quantity of ambient dose equivalent rate. For most applications, this measurement gives a good approximation of the effective dose rate to our bodies.
So, when we are measuring the ambient dose equivalent rate with our dose rate meters, we are actually getting a good approximation of the effective dose rate to our bodies. For correctness, however, the term ‘dose’ is used throughout this module to mean ambient dose equivalent (where ambient dose equivalent is the operational quantity measured by area monitoring instruments).
One way of determining the total dose from a dose rate meter is by multiplying the exposure time by the measured dose rate (as discussed in Module 2.2 Protection from External Radiation Hazards). However, some dose rate meters are able to sum (or integrate) the dose received over a given time and give a read out in dose units (Sv) rather than dose rate units. These instruments are known as integrating or electronic dosimeters and they are particularly useful for monitoring personal dose rather than for area monitoring. Integrating dosimeters are very light and portable as they usually contain a small G-M tube or a silicon PIN photodiode detector. A typical integrating dosimeter is shown in Figure 3.
Figure 19
A Typical Integrating Dosimeter
An integrating dose rate meter should also be used to monitor the external hazard from some x-ray generators. This is because the dose rate may be changing rapidly with time and many typical dose rate meters are unable to provide an accurate response to such radiation fields.
Two types of contamination monitors are used in the workplace:
Surface contamination monitors (for measuring contamination on surfaces); and
Airborne contamination monitors (for measuring contamination in the air.)
Which ever type of monitor you are using, it is important to remember that no contamination monitor can measure all of the contamination present either on a surface or in air (i.e. no instrument is 100% efficient). Each instrument will have different efficiencies (ranging from 0% to approximately 30%) for different radionuclides and an important result of this is that some monitors will not detect some radionuclides.
No radiation monitoring instrument is 100% efficient and some contamination monitors will not detect some radionuclides.
Surface contamination monitors must be able to detect the presence of low levels of radioactive material on surfaces. This is particularly important if the radionuclide is an alpha emitter, because even low concentrations may be able to enter the body and cause a significant internal dose.
Surface contamination monitor usually consist of a monitor connected to a detector (or probe) which is capable of measuring the different types of radiation. A typical surface contamination monitor and two different types of probes are shown in Figure 4.
Figure 20
A Typical Surface Contamination Monitor and Two Probes
The radiation detected by a surface contamination monitor will be from the contamination present in the area under the probe. This is the total contamination in that area and is made up of both the fixed contamination and the removable contamination. Although the presence of any contamination in an area is not desirable, the amount of removable contamination is the most important to know as this is the radioactive material that could get into a persons body and lead to internal exposure.
The fixed contamination is only a radiological problem if it becomes removable or the dose rate from it is significant. Section 5 of this module tells you how to determine the levels of fixed and removable surface contamination.
Most surface contamination monitors give a reading in counts per second (cps) or counts per minute (cpm). However, it is more important to know what the surface contamination levels are in terms of activity per unit area (i.e. in units of becquerels per square centimetre (Bq cm-2) or becquerels per square metre (Bq m-2)) as this will enable you to compare your measured contamination levels with the limits given in national and international regulations. So, if your monitor measures in cps or cpm, you will need to convert these values to Bq cm-2 or Bq m-2 (see Section 5 of this module).
Figure 5 shows the units used for measuring surface contamination.
Figure 21
Monitoring for Surface Contamination
Note that some surface contamination monitors display the reading directly in becquerels per square centimetre (Bq cm-2). However, when using this type of instrument, you must make sure that it is suitable for the radionuclide being measured (i.e that it has been calibrated for that radionuclide - see Section 1.3 of this module), otherwise the amount of contamination indicated on the monitor may be incorrect.
When using a surface contamination monitor which displays the reading in Bq cm-2, you must make sure that the instrument has been calibrated for the radionuclide being measured.
Airborne contamination monitors must be able to detect and quantify radioactive contamination in air as this contamination has the potential to cause harm to humans. Airborne contamination can be considered as both an internal and an external hazard due to the fact that not only can airborne contamination be breathed in (internal hazard), but also, submersion in a cloud of some radioactive gases can lead to a significant external dose (external hazard).
Monitoring for airborne contamination is more complex than monitoring for surface contamination as airborne contamination can exist in three forms, either as:
particulates (i.e. consist of particles such as dust or smoke);
gases (i.e. consist of gaseous radionuclides); or
vapours (i.e. consist of small droplets of liquid radionuclides, or the gaseous form of a radionuclide which is usually a solid or liquid at room temperature).
For each type of airborne contamination, the monitoring process is slightly different. However, in general, airborne contamination monitoring involves two stages. Firstly, the air is either filtered or collected by using a pump known as an air sampler. Then the count rate from the filter paper or air sample is measured using a radiation detector. Although some air sampling equipment incorporates both the air sampler and the radiation detector (e.g. real time airborne contamination monitors), it is more usual to sample the air for a set period of time and then measure the count rate from the filter paper or air sample. This count rate can then be converted into units of Bq m-3 for comparison with national and international regulations. Section 6 of this module details the methods of monitoring for each type of airborne contamination and also shows how the units may be converted. Figure 6 shows the units used for measuring airborne contamination.
Figure 22
Monitoring for Airborne Contamination
Note that real time airborne contamination monitors give continuous readings of the airborne concentration in Bq cm-3 or Bq m-3. However, they must be calibrated for the radionuclide being measured otherwise the readings will be incorrect. Real time airborne contamination monitors can be particularly useful in areas where the levels of airborne contamination could present a problem as they can be set to alarm if air sampling results exceed pre-set values.
SELF-CHECK 1
Now see how much you have understood by answering the following questions in your workbook:
a)Which part of a radiation monitoring instrument interacts with the incoming ionizing radiation?
b)Name two types of detector which can detect ionizing radiation.
What are the two types of instruments used for measuring ionizing radiation?
Fill in the gaps with a suitable word or phrase:
Dose rate meters usually give a direct reading in units of _________ ___ _____ (_____ ___). They actually measure dose in terms of the _________ __________ ____ rate which is an operational quantity used to estimate the effective dose received by humans.
A dose rate monitor shows a dose rate of 2.5 mrem h-1. What is this dose rate in Sv h-1?
Name the two types of contamination monitors used in the workplace.
Fill in the gaps with a suitable word or phrase.
Surface contamination monitors usually show readings in _______ ___ ________ (___) or counts per minute (cpm). In order to compare these levels with national and international regulations, these readings need to be converted to units of _________ per _______ squared (__ ___). Some surface contamination monitors give direct readings of surface contamination but when using this instrument you must make sure that the monitor is calibrated for the radionuclide being measured otherwise _________________________________________________________.
7.a)What are the three types of airborne contamination?
b)What units is airborne contamination measured in?
Now check your answers with the model answers in your workbook.
All radiation protection survey instruments must be calibrated against calibration sources representative of the sources the instrument will be used to measure. This ensures that the instruments are capable of responding within acceptable levels of accuracy. To ensure the national and international uniformity of response, these calibration sources must be traceable to a primary or secondary standard, and these standards are usually held at a national or international standards laboratory. The primary standards used for the calibration of radiation protection monitoring equipment include exposure, dose rate, emission rate and activity. Secondary standards are calibrated against primary standards and it is a requirement that national standards laboratories compare their standards against each other at regular intervals to ensure international uniformity.
Dose rate meter calibration is performed by determining the instrument response in a specific radiation field delivering a known dose rate at a particular set distance from the source. The instrument controls are then either adjusted to read the desired dose rate or a calibration factor is determined and included in a calibration report. As dose rate meters generally have different ranges (e.g. Sv, mSv, or Sv h-1, mSv h-1), response determination should be performed on all ranges.
A simplified diagram of dose meter calibration facility is shown in Figure 7.
Figure 23
A Typical Dose Rate Meter Calibration Facility
For instruments designed to measure surface contamination, there are a number of ways of calibrating the instruments. The most common way is to determine the detector reading per unit surface activity. Calibration factors will then be given to enable you to relate the detector reading to the actual the surface contamination in Bq cm-2.
Instruments which give direct readings of airborne contamination levels in Bq m-3 are calibrated by determining the detector reading per unit volume of airborne activity. The instrument controls are then adjusted to read the desired airborne activity level.
It is important to remember that dose rate meters and contamination monitors are calibrated against specific sources (each with specific types and energies of radiation). Although many dose rate meters are energy compensated for gamma radiation, and should have a relatively flat response over a wide range of gamma energies, in practice, the monitor may not be suitable to monitor gamma sources with energies different to the calibration source. In addition, if the sources in the workplace are beta or x-ray emitters and the monitor was calibrated against a source with a single gamma energy, the monitor may not be suitable. It is therefore important to ensure that the calibration is valid for the radionuclides being monitored.
When monitoring in the workplace, a wide range of radionuclides may be present. You should therefore ensure that the monitoring equipment you use is calibrated for the sourcesbeing measured.
Sometimes it is impossible to find a monitor which has been calibrated for all the radionuclides you wish to measure. In this case, when a mixture of radionuclides is present in a particular area, it is common to assume the contamination being measured is due to the radionuclide for which the instrument has the lowest response. You will then overestimate the total contamination level, but you will be operating safely. If the overestimated contamination is at a level that might represent a problem, then the actual radionuclide can be identified by estimating its’ energy by alpha, beta or gamma spectroscopy.
Calibration of instruments should be performed both before initial use as well as regularly during use. The requirements for calibration frequency vary according to local regulations but usually one calibration per year is recommended for each instrument.
Details of the instrument calibration should be included in a calibration report. This report should detail:
any relevant calibration factors;
the performance of the instrument over specific energy ranges;
the conditions under which the instrument was calibrated;
the response to the conditions for which it was designed; and
the response to all radiations and conditions for which it may be used in the field.
When performing radiological surveys, it is important to know what is the lowest dose rate or contamination detectable by the equipment. Background radiation will always be detected by radiation detectors and this makes it very difficult to distinguish between natural background levels and other small amounts of radioactivity.
For laboratory counting equipment, an accurate lower limit of detection (LLD) can be calculated from the standard deviation (see Module 1.2 Basic Mathematics) of the background counts measured by the equipment. For dose rate and contamination monitors this is not really possible and a more simple method is commonly used. This simple method assumes that, because of the fluctuation in background and instrument reading, you can only be confident the monitor is detecting radiation in addition to background if the monitor reading is twice the background value. (The background value should be measured in an area where there is no man-made radiation present. This is not always possible and the background will be elevated.) If the reading is not equal to or greater than twice the background, you do not know if there is any radioactivity present, all you can quote is that the value possibly present is less than the LLD.
For dose rate and contamination monitors, you can only be confident the monitor is detecting radiation in addition to background if the monitor reading is at least twice the background value.
The natural background dose rate level in most areas is not usually a radiological problem, so the dose rates measured are normally quoted directly from instruments. However, when trying to measure contamination levels, the ambient background dose rate will produce a background reading on most contamination monitors and the actual contamination level is found by subtracting the background from the measured value (see Equation 1).
L = R – BG[1]
whereL = the actual contamination level
R = the reading on the contamination monitor
BG = the background reading
The LLD is an important factor you should take into account when monitoring low levels of contamination. In some cases, contamination monitors cannot measure down to very low levels and to be able to quantify your results, you need to know what the lowest level of detection is. Basically, the LLD (in cps or cpm) for a contamination monitor is twice background minus the normal background value. This is because anything less than twice background cannot be considered valid, but the normal background value is attributed to ‘natural’ background levels rather than to the contamination being measured. Hence the LLD of the monitor is the difference between these two values. Obviously, twice background minus background equals background and hence the LLD (in cps or cpm) can be taken as the background level. To convert this value to a meaningful reading in Bq cm-2, we need to divide the background reading by the monitor’s calibration factor as shown in Equation 2.
LLD = 2BG – BG = BG[2]
CF CF
whereLLD = the lower limit of detection in Bq cm-2
BG = the background reading in cps
CF = the monitor’s calibration factor in cps per Bq cm-2
An example of an LLD calculation is shown in Example 1.
EXAMPLE 1
Question
A contamination monitor has a background reading of 5 cps and the maximum reading seen on the monitor while monitoring a bench surface was 7cps. The calibration factor for the monitor and radionuclide used in the area is 2 cps = 1 Bq cm-2. What is the lower limit of detection (LLD) of this monitor and how would we quote this reading?
Answer
The LLD can be calculated from Equation 2 as follows
LLD = BG = 5 = 2.5 Bq cm-2.
CF 2
Hence, the LLD for this monitor is 2.5 Bq cm-2.
From Equation 1:
L = 7 – 5 = 2 cps
As this contamination level is not equal to or greater than 2 times the background, we can therefore only quote that the contamination level less than the LLD i.e. the contamination level is less than 2.5 Bq cm-2.
Note that, if the LLD of a monitoring system is below the level you are trying to measure (e.g. some regulations quote acceptable surface contamination levels of less than 1 Bq cm-2), then this monitoring system is unsuitable for performing the measurement.
SELF-CHECK 2
Now see how much you have understood by answering the following questions in your workbook:
Why is it important to calibrate radiation monitoring instruments?
Where must the calibration of instruments be traceable to?
How are dose rate meters calibrated?
What is the most common way of calibrating surface contamination monitors?
Why is it important to remember that dose rate and contamination monitors are calibrated against specific sources?
a)If contamination is found in an area containing a mixture of radionuclides, which radionuclide should you use to perform your calculations?
b)Why is this so?
In simple terms, how can you be sure that a reading on a dose rate or contamination monitor is a correct reading?
A contamination monitor has a background reading of 10 cps and the maximum reading seen on the monitor while monitoring a bench surface was 14cps. The calibration factor for the monitor and radionuclide used in the area is 4 cps = 1 Bq cm-2. What is the lower limit of detection (LLD) of this monitor and how would we quote this reading?
Now check your answers with the model answers in your workbook.
The ideal radiation monitoring instrument should be capable of monitoring all forms of ionizing radiation and should be portable, easy to use and directly indicate ambient dose equivalent rate or contamination levels. In practice, it is not possible to design a single instrument to fulfil all of these requirements and hence, when performing a radiological survey, the instrument that best suits the needs of the job should be selected.
Monitor Considerations
When selecting a suitable monitoring device for a specific radiological survey, the following items should be considered:
The type of survey you wish to perform (e.g. dose rate or contamination survey).
The type of radiation you wish to detect (e.g. alpha, beta, gamma, x-ray or neutron radiation).
The energy of the radiation you wish to detect (e.g. keV or MeV).
The required sensitivity of the detection instrument (e.g. Sv h-1, mSv h-1 or Sv h-1, the maximum number of cps or Bq cm-2).
Once these items have been considered, the selection of monitoring device can be narrowed down.
Type of survey
The type of instrumentation used to carry out a survey depends on the type of survey required. When performing a detailed radiological survey, monitoring usually includes dose rate, surface and airborne contamination monitoring. However, you may wish to measure only one of these things and it is important to know the type of survey required in order to select the correct instrumentation.
Remember that dose rates in the workplace are usually measured in units of Sv h-1 or mSv h-1. Surface contamination levels are measured in counts per second (cps) (which may be converted to Bq cm-2), and airborne contamination levels are usually measured in Bq m-3.
Type of radiation
As we have already seen in Module 1.5 Methods of Radiation Detection, different types of detector are sensitive to different types of radiation. Therefore it is important to know which radiation you are looking for whenever a survey is performed.
When monitoring dose rates, remember that alpha radiation does not penetrate the dead layer of skin and therefore alpha external dose rates are not monitored. In fact, dose rate meters are designed to monitor beta, gamma, x-ray and neutron radiations.
Dose rate meters can be designed to respond to one or more types of radiation but they may have different sensitivities to each type of radiation. In mixed radiation fields, the type of radiation therefore needs to be identified if multiplying factors are to be used to determine the dose rate accurately. Typically thin end window G-M tubes or ion chambers (see Figure 8) will measure photon and beta dose rates. To tell the difference between these, a thin metal plate can be used to attenuate the beta particles.
Front View Rear View
Figure 24
A Typical Ion Chamber Dose Rate Monitoring Instrument
Some neutron monitors also respond to gamma radiation and the neutron dose rate will then appear higher than it really is. To overcome this the gamma response of the monitor and the gamma dose rate in the area should be known. The neutron indication (which is really due to gamma radiation) can then be subtracted. The gamma response can be determined at the routine calibration.
Contamination monitors may also respond to different types of radiation. To help identify the radionuclides present and determine their significance, the type and quantity of each type of radiation needs to be determined. This can be achieved by electronic discrimination of the probe signal or by using filters to attenuate one or more of the types of radiation. The monitors that include discrimination are usually the most convenient to use.
You may find it useful to consider the following general points when you determine a suitable contamination probe:
Zinc sulphide scintillation probes and proportional counters can be used with alpha and beta discrimination.
Beta probes usually also respond to photon radiation, and a relatively low gamma background could lead to an overestimation of the beta contamination.
Alpha probes and phosphors do not usually respond to photon radiation.
G-M tubes respond to alpha, beta and photon radiation and cannot directly discriminate between them.
You will need to balance the advantages of the type of measurement you make with the disadvantages. For example, if you wanted to monitor low levels of a particular radionuclide which emits alpha, beta and gamma radiations (such as natural uranium or thorium in equilibrium), as the alpha particles are likely to be attenuated, you could monitor the beta radiation. However, if the gamma dose rate is high, the beta response could be a gross overestimate, so you will need to either monitor the alpha levels or use an absorber to distinguish the beta from the gamma reading. A monitor calibrated in terms of gamma emissions from the source might also be used, but you may find the sensitivity is poor compared to the alpha or beta response.
Energy of radiation
The energy response of instruments measuring x-ray or gamma ray dose rates is important as dose rate survey meters are often calibrated using a particular source such as caesium-137 which has an effective photon energy of 0.66 MeV. If the instrument is then used to measure radiation of different photon energy, it may overestimate or underestimate the dose rate. In general, although the energy responses of the different types of GM detectors may be different, most instruments are now compensated to give a uniform response to x- and gamma radiation in the range 0.1 to 3 MeV. Energy compensation of G-M detectors is usually achieved by surrounding most of the detector with a metal filter to selectively attenuate the lower energy radiations.
For contamination monitors the detection method and design of the detector determines the type and energy of the radiation that can be measured. The specified response to the radionuclide of interest must therefore be checked. Tritiated water and tritium (hydrogen-3) compounds are very difficult to monitor directly, so smears are commonly taken. These smears are then monitored in a liquid organic scintillation counter.
Sensitivity of the instrument
The selection of dose rate meter depends on the sensitivity required. For example, a simple ion chamber will measure a wide range of energies of beta, x- or gamma radiations but to monitor very low dose rates (tenths of microsieverts per hour), much larger chambers are required which are not as portable.
Dose rate units are usually displayed in Sv h-1 or mSv h-1, Gy h-1 or mGy h-1 and the range in dose rate depends on the application (see Table 1).
Table 13
The Range of Different Types of Monitoring
Type of Monitoring
Range
Occupational
0.1 Sv h-1 to a few mSv h-1
Environmental
nSv h-1 to hundreds of Sv h-1
Emergency
Sv h-1 to a few Sv h-1
Note that for emergency monitoring, the range required varies from Sv h-1 to a few Sv h-1. For this type of monitoring, a special instrument known as a teletector is required. This instrument incorporates a number of different range G-M tubes positioned at the end of an extending telescopic handle to maximise source to person distance (see Figure 9).
Figure 25
A Teletector
For contamination monitors, their sensitivity depends on the design of the detector. The display range is usually in counts per second (cps) or directly in Bq cm-2. The range of a contamination monitor can typically be from zero to either a few hundred to a few thousand cps, (or the equivalent in the other units). It is important that the maximum range you chose allows you to monitor the levels of contamination which might reasonably be expected in a particular area. Otherwise, some instruments may indicate a full scale reading but you will not be able to tell the actual levels. For radionuclide facilities, a maximum range of 5000 cps would be reasonable while in a counting laboratory a few hundred cps would be more appropriate.
As even low amounts of loose alpha contamination can present an internal radiation hazard, suitable alpha contamination monitors must be able to detect low levels of alpha contamination.
Once the requirements listed in 2.1.1 to 2.1.4 above have been determined, the choice of instrument type is narrowed down. Some of the more commonly used monitoring instruments are shown in Figure 10.
123 456
Dose Rate MetersContamination Monitors
Figure 26
Some Commonly Used Radiation Protection Instruments
Table 2 below shows the suitability of these detector types and others for dose rate and surface contamination surveys.
Table 14
The Suitability of Detector Types for Dose Rate and Surface Contamination Surveys
| x, 10 - 50 keV | x, > 50 keV | | | x, | |
Ion chamber with thin end window | | | | | | |
Energy compensated G-M | | | | | | |
Thin end window G-M | O | O | O | O | + | |
Air-filled proportional counter | | | | | | |
Organic or noble gas-filled proportional counter | O | | | | + | O |
Zinc sulphide scintillator | O | | | | + | |
Sodium iodide scintillator | | | | | | |
Liquid organic scintillators* | | | | | | |
SELF-CHECK 3
SELF-CHECK 3
Now see how much you have understood by answering the following question in your workbook:
What four aspects of a radiation survey must be considered before choosing an appropriate monitoring device?
A thin end window G-M tube can be used to monitor beta and gamma contamination. How can we distinguish between these two types of contamination?
As the Radiation Safety Officer of a university, you are told that high dose rates are suspected in one of the research laboratories. This particular laboratory uses only phosphorous-32 (a pure beta emitter). Which type of monitoring instrument would be the most appropriate for performing a dose rate survey in this area?
You are responsible for performing random monitoring surveys in an area which deals with alpha emitters. Which type of instrument would you use to directly monitor for alpha contamination?
Now check your answers with the model answers in your workbook.
Once the type of monitoring device has been narrowed down, there are a number of other design considerations which should be taken into account. These are as follows:
The ease of use of the instrument (e.g. portability, design, simple display).
The suitability of the detector for the environment in which measurements are to be taken (e.g. effects of temperature and humidity, and whether it is intrinsically safe for hazardous atmospheres).
The location of the detector within the instrument (i.e. whether the detector is positioned in the body of the instrument or whether it is a separate probe on a cable).
The physical size of the detector for effectively measuring dose rates in narrow beams.
The response time for short exposures or high radiation fields.
The directional response of monitor.
The resistance to foldback in high radiation fields (for G-M detectors).
The presence of a speaker to help identify changing levels.
An illuminated scale for night work.
Radiation instruments should be portable, have ergonomically designed displays/switches/buttons and be easy to decontaminate. It should be easy to replace and check the batteries and read the display.
Neutron detectors usually incorporate a significant quantity of a hydrogenous material (like polyethylene) to thermalise the neutrons and this results in a heavy instrument that is not so portable. With the present generation of neutron monitors their weight is a disadvantage that has to be accepted.
The application and environment that the instrument is subjected to are also important factors in selection. The effect of exposure to humidity, temperature and radiofrequency (RF) signals should be considered as these may affect the operation of the instrument.
Particular care must be taken in hazardous areas. If there is a possibility of explosive gases in the area, as in the chemical or oil and gas industries, intrinsically safe monitors may need to be used. Although intrinsically safe dose rate meters are available, at this time there are no intrinsically safe contamination monitors.
In some situations you may need to take a contamination or dose rate measurement in an area where normal access is difficult but which may be occupied in some other situation. It is therefore helpful in this situation if the probe is on a cable rather than in the body of the detector so you can reach into the area and still read the monitor display. This is common when monitoring the inside of vessels where contamination may be present or measuring dose rates in and around equipment where only hand access is possible.
To obtain an accurate dose rate measurement, the whole of the useful volume of the detector should be irradiated. If this is not the case, the reading will be an underestimate. If narrow radiation beams are to be monitored, a detector with a small cross section should be used. In this case, the detector is usually on a cable rather than in the body of the monitor so you can locate the detector accurately at the position of the narrow beam.
Where the radiation field is changing or is only present for a short period you will need to use a monitor with a fast response to be able to detect the radiation. The disadvantage of a fast response is that the reading may fluctuate significantly and an accurate reading is difficult to obtain. Manufacturers try to provide monitors which compromise between a fast response and a stable reading.
With some short exposures the response time of the monitor cannot be quick enough to measure dose rate. In this case a total dose reading from an integrating dose meter over a number of exposures can be an alternative method. From the total dose recorded, either the dose per exposure or the dose rate can be calculated by dividing the total dose measured by the number of exposures or the total time of all the exposures.
The speed of response of a monitor should increase with increasing dose rate. You do not want to be waiting for a monitor to respond while you are in a high radiation field.
With contamination monitors it is easy to see that they will be more sensitive to radiation falling on the detector window. With dose rate meters the manufacturers try to ensure the detector is sensitive to radiation arriving from any direction. However in practice this is very difficult to achieve and they may provide a polar response graph which indicates the sensitivity for radiation from different angles. Usually the monitor is most sensitive to radiation approaching from the front of the detector.
As you may remember from Module 1.5 Methods of Radiation Detection, G-M tubes can saturate in high dose rate fields and can then stop indicating the presence of radiation (this is known as fold-back). You should therefore ensure that the monitor you use is protected from fold-back to ensure that the monitor continues to indicate a high value.
Speakers on both dose rate and contamination monitors are useful to quickly identify areas of high dose rate or contamination. They are also helpful where you are using a probe on a cable and are watching where you are monitoring and do not want to keep looking at the instrument display.
There may be occasions where measurements need to be taken outside at night or where visibility is poor. A self-illuminating scale is a great help in this situation. However, you should be careful as the light might significantly reduce the battery life of the monitor and spare batteries might be needed.
When purchasing monitoring equipment, two other aspects should be considered:
1.The cost of the instrument (e.g. initial purchase price and maintenance costs).
2.The availability of batteries and spare parts.
The initial purchase cost and the costs of routine maintenance and calibration must be considered when choosing a suitable instrument. The vulnerability of a dose rate meter could determine the selection based on detector replacement alone. Dose rate instruments usually incorporate the detector and display into one unit and occasionally this is completely sealed into a moulded case which makes repair very difficult.
In the past some monitors used batteries which were only available from the manufacturer and were expensive. You should ensure the batteries are of a type commonly available. You should also check the time it would take to have the monitor repaired by the manufacturer or supplier. If spare parts are available, it is advisable for you to hold some in case the monitor needs minor repairs.
SELF-CHECK 4
SELF-CHECK 4
Now see how much you have understood by answering the following question in your workbook:
Give three examples of design considerations which should be taken into account when selecting a monitoring instrument.
As a radiation safety officer at a radiopharmaceutical production facility, you are asked to assess the gamma dose rates in a small hand access area where maintenance work needs to be carried out. You have a choice of an ion chamber instrument or a thin end window G-M probe (see Figure 10). Which instrument would be most suitable for measuring the dose rates in this area?
A small radioactive materials storage facility has been constructed in a laboratory. A suitable amount of lead shielding has been added but you have found that there is a short path (i.e. a narrow radiation beam) coming from the area where two lead sheets join. What is the most important design consideration of a detector which could be used to accurately measure this dose rate?
You work in the x-ray department of a hospital. The dose rates in this area change rapidly with time and many typical dose rate meters are unable to provide an accurate response to such radiation fields. How could you estimate the average dose rate in this particular environment?
What are the two other aspects of monitoring instruments which need to be considered when purchasing equipment?
Now check your answers with the model answers in your workbook.
There are a number of items to be addressed before a radiological survey can begin. These are as follows:
Prepare radiological survey diagrams and forms for the area to be surveyed.
Refer to any previous surveys to estimate the dose rates and contamination levels expected in the area.
Perform appropriate pre-use response checks to ensure that the instrument is working correctly.
Before a radiological survey can begin, a diagram of the area to be surveyed should be drawn. An example of a radiological survey diagram for a laboratory is shown in Figure 11.
Figure 27
Radiological Survey Diagram of a Laboratory
As shown in Figure 11, the locations where measurements are taken should be numbered. These numbered areas can then be used as reference locations for future surveys of the same area and for detecting trends in measured values. They can also be easily referred to on a radiological survey form as shown in Figure 12. Note that dose rate measurements should be taken at contact distance and at 1 m to give an indication of the overall dose rates to people working in this area. Contamination levels can be determined directly or by taking a smear of the area (see Section 5).
Other than providing a record of the radiological survey measurements, the survey form (Figure 12) also has space for the signatures and comments of the technician (i.e. the person performing the survey) and/or the radiation safety officer (RSO) (i.e. the person responsible for the radiological safety of the area). The area supervisor (i.e. the person generally responsible for the area) should also sign the form to ensure that the comments are noted and that appropriate actions are being taken.
Figure 28
Radiological Survey Form
Referring to previous surveys can give an idea of the dose rates and contamination levels expected in the area. From these surveys, it may also be possible to decide whether time limitation or protective clothing is necessary.
Before using any monitoring instrument it is necessary to ensure that it is operating correctly. Hence, the following checks should be performed prior to use:
Visual check.
Battery check.
Calibration check.
Light sensitivity check.
Source check.
The frequency of these checks depends on how often the equipment is used. However, the minimum recommended frequency is once per day of operation. Note that if you have any doubts about the operation of a particular detector, it is better to use a different instrument and have the faulty one repaired as soon as possible.
The first check to be performed is a visual check of the instrument to ensure that it is not damaged in any way. Visual checks should include an inspection of the outer casing of the instrument and also the probe. If damage is visible (e.g a visible hole in the thin end window), the instrument should be repaired and recalibrated before use.
The first thing to check after an instrument is switched on is the battery. For an instrument with an analogue display, the movement of a needle to a preset place on the dial usually indicates that the battery is in a good condition. With electronic displays, the battery checks are automatically performed when the instrument is switched on and periodically whilst being used. With this type of display, a low battery indicator is usually a feature of the instrument. You should be aware of such design features which should be described in detail in the instrument manual.
If this check indicates that the battery is low, then the battery should be replaced before using the instrument. In general, the instrument does not need to be recalibrated after a battery change unless it fails other operational checks.
Before use, it is important to confirm that an instrument has been calibrated and that it is within its calibration dates. This information is usually given in the instrument manual or on a calibration certificate. The requirements for the frequency of calibration vary according to local regulations but usually one calibration per year is recommended for each instrument. If an instrument is not within its calibration dates or it has been repaired for any reason, it should be recalibrated before it is used again.
Scintillation detectors operate by detecting bursts of light resulting from incident radiation interacting with the detector. These detectors are sensitive to light and will give incorrect results if the thin window is punctured with a hole orthe construction is no longer light tight. You can check this by holding the detector up to bright light and observing the response. If the detector is sensitive to light, the response displayed will be very large and the instrument will need to be repaired and recalibrated. With some end window G-M detectors, strong sunlight can cause a current to flow across the tube and a signal to be recorded on the display. This is usually when the metallic coating on the window peals off.
Instrument performance may change depending on the environment and frequency of use. For this reason, pre-use radioactive source checks should be used to detect and monitor any changes in performance quality. For contamination probes, check sources giving greater than 100 cps with a surface area equal or larger than the probe size should be used for these checks. A small source can also be used if it is placed in the same position relative to the probe face each time the check is carried out. If alpha, beta and gamma contamination is to be monitored, then three independent sources are required.
To check dose rate instruments, the check source used should be of a similar energy and radiation type to that being monitored during surveys. In addition, the radioactive source should give a dose rate of the order of 10 Sv h-1 at 2 to 3 cm from the source.
The actual count rate or dose rate recorded by the instrument should be compared to the count rate or dose rate expected from the source. This should be performed in a low background area and the background recorded and subtracted from instrument values. If the two values (instrument and source) differ by more than 30% then the instrument should not be used. Instead it should be repaired and recalibrated.
SELF-CHECK 5
SELF-CHECK 5
Now see how much you have understood by answering the following question in your workbook:
What are the three items which need to be addressed before a radiation survey can begin?
Why is it important to perform pre-use response checks?
How often should pre-use response checks be performed?
Complete the following table with the names of the five pre-use instrumentation checks and what should be done if the instrument fails the test:
Instrument Check | What should be done if the instrument fails the test? |
V______ Check | |
B______ Check | |
C_________ Check | |
L____ S_______ Check | |
S______ Check |
Why can it be useful to refer to previous surveys of the area?
Now check your answers with the model answers in your workbook.
Dose rate surveys are carried out for a variety of reasons. They may be performed to estimate personal doses or show compliance with relevant dose limits. In addition, monitoring can be performed to define radiological areas, detect departures from normal operations and guide operational decisions. Whatever the reason for monitoring, there are five main steps to remember when performing a dose rate survey. These are as follows:
Select a suitable instrument.
Perform pre-use response checks.
Perform survey taking relevant safety precautions.
Write a survey report.
Compare the measured values with those accepted by local rules and/or national or international regulations and make recommendations where necessary.
The first two steps have already been covered in Sections 2 and 3. This section deals with performing the dose rate survey, writing the final survey report and comparing the measured values and making recommendations.
When performing a dose rate survey, firstly you will need to select a suitable dose rate meter. This selection was discussed in detail in Section 2 of this module and typical equipment used for routine dose rate monitoring was shown in Figure 10.
If surface or airborne contamination is present, you may also need personal protective equipment (such as protective coats, overshoes or suitable respiratory protection) as discussed in Section 5 of this module.
A number of safety precautions should be considered whilst performing dose rate surveys. Many of these have been covered in previous modules and are summarized as follows:
Minimize the exposure time in each surveyed area.
Maximize the distance from sources of radiation.
Shield the sources of radiation where possible.
Monitor the radiation dose of workers performing the survey.
If the dose rate meter is not self ranging, you should select the highest range equal to the dose rate you expect. If you are not familiar with the expected dose rates in the area, check the dose rate while moving towards the measurement position.
If the meter has an audible signal, it can be used as an early indication of increasing dose rates. If the meter reading increases significantly or goes full scale, you should move to an area of lower dose rate and consider the consequences of these measurements.
One of the consequences might be that the dose rate has exceeded a value at which access to the area should be restricted. If so, then the measurement of the maximum dose rate will not be needed. In this case, you should restrict access to this area by using physical barriers and warning signs.
If it is necessary to measure the maximum dose rate in the area, it may be advisable to use a teletector (as shown in Figure 9) so that the technician (i.e. person doing the survey) can extend the probe and keep away from the area of high dose rate.
If the technician is working in potentially high dose rate areas, it is advisable for them to wear an integrating dose meter to measure the cumulative dose. An electronic device that incorporates a pre-set dose alarm would be the best choice.
Note that it can be difficult to detect the presence of beams of gamma radiation with an energy compensated G-M dose rate meter (as shown in Figure 10) due to the small size of the detector. It may be easier to use an ion chamber (see Figure 10) to identify the presence of radiation and then use a thin end window G-M probe attached by a cable to a dose rate meter to localize the beam and carry out the dose rate measurements.
Notes should be taken throughout the survey of the instruments used and the measured dose rates. On completion of the survey, a detailed survey report should be produced. This report should include:
a diagram of the area including numbered reference locations (see Figure 11); and
a radiological survey form indicating the location and magnitude of the dose rates, the instruments used and any remedial action which needs to be taken (see Figure 12).
Obviously, if high dose rates are measured during a survey, appropriate action should be taken immediately to restrict access to the area. Wherever slightly elevated dose rates are noted, the measured values should be compared with local rules and/or national and international regulations and consideration should be given to reducing the dose rate in accordance with the ALARA principle. To ensure that recommended actions are noted and followed up, recommendations should be detailed on the radiological surveyform (see Figure 12).
SELF-CHECK 6
SELF-CHECK 6
Now see how much you have understood by answering the following question in your workbook:
What are the five main steps to remember when performing a dose rate survey?
What safety precautions should be considered whilst performing dose rate surveys?
You are monitoring radiation dose rates in an area and the dose rate increases from normal background levels (1 Sv h-1) to 15 Sv h-1 as you approach a small radioactive materials store. Local rules indicate that dose rates in this area should be restricted to less than 7.5 Sv h-1. What should you do in this situation?
What is the correct procedure for measuring beams of gamma radiation?
What information should be included in a dose rate survey report?
Now check your answers with the model answers in your workbook.
PRACTICAL ACTIVITY 1
Performing a Dose Rate Survey
In this practical activity, you will perform a dose rate survey of an area. Practical notes are given in your workbook. You should arrange a suitable time with your supervisor to perform this practical activity.
The total contamination on a surface is a mixture of fixed and removable contamination and this total contamination level can be assessed by using direct surface monitoring techniques (i.e. directly placing the probe as close as possible to the surface without actually touching it). Although this type of monitoring gives a measure of the total contamination, it will not differentiate between the fixed and removable contamination.
The level of removable contamination can be assessed by indirect surface monitoring (i.e. by taking a smear of an area and monitoring the level of contamination on the smear). This is explained in detail in Section 5.2 of this module. Indirect surface monitoring techniques are also useful in areas of high background dose rates, as such dose rates can affect the assessment of surface contamination levels. By taking a smear in these areas and then measuring the smear in a low background area, an assessment of the contamination level can be made.
Note that if there is a lot of surface contamination in an area, there may also be a significant external dose rate. Hence, if high contamination levels are detected when using a beta or gamma probe, then the dose rate should also be measured.
The main steps for performing a direct surface contamination monitoring survey are the same as for a dose rate survey. These are as follows:
Select a suitable instrument.
Perform pre-use checks.
Perform survey taking relevant safety precautions.
Write a survey report.
Compare the measured values with those accepted by local rules and/or national or international regulations and make recommendations where necessary.
The first two steps have already been covered in Sections 2 and 3. This section deals with performing the dose rate survey, writing the final survey report and comparing the measured values and making recommendations.
Appropriate portable instrumentation for direct surface monitoring usually consists of a probe and a battery operated contamination monitor as shown in Figure 10.
For alpha or beta contamination, the probe can be a zinc sulphide scintillation detector or a G-M detector with an end window thin enough to allow alpha particles to penetrate. Remember that for the detection of alpha contamination, the probe must be kept close to the surface (less than 1 cm) due to the short range of alpha particles in air.
For gamma contamination, the probe can be a G-M detector, an organic or noble gas-filled proportional counter, or a sodium iodide scintillation detector.
When monitoring for surface contamination, gloves, overshoes, protective coats and safety glasses should be worn. If there is the possibility of airborne contamination, suitable respiratory protection should also be considered.
Remember that in areas where contamination exists, it is possible that you could become contaminated yourself. It is therefore important that you adhere to safe work practices during the survey to minimize the chance of becoming contaminated. You should also make sure that you monitor yourself (including your body, hands, feet and hair) after the survey but before leaving the contamination area. This will ensure that if you are contaminated, the contamination can be removed as soon as possible. It will also ensure that there is no spread of contamination outside the contamination area.
Remember to monitor yourself after performing a contamination survey to ensure that you have not become contaminated.
If you have become contaminated, certain decontamination techniques can be used to remove the contamination (e.g. washing the contaminated area). Details of these decontamination techniques can be found in Module 3.5 Emergency Response.
Note that if appreciable dose rates are associated with the survey, you should also consider minimizing the exposure time, maximizing the distance and shielding the contamination where possible. The radiation dose of the workers performing the survey should also be monitored.
When performing direct surface monitoring, the probe should be moved slowly over the surface of the area in a systematic way. Be careful not to make contact between the probe and surface as the probe may become damaged or contaminated. An easy way to cover a large area is to map out the area with imaginary grid lines (squares), record this on the survey sheet and monitor each imaginary square in turn. This method is illustrated in Figure 13.
Start | Finish | ||
| | | |
| | | |
| | | |
Move probe in direction of arrow
Figure 29
Method of Performing Direct Surface Monitoring
You should record the highest reading obtained from each square for inclusion in your monitoring report. Whilst monitoring, sufficient time should be allowed for the probe to respond to changes in count rate.
Remember that surface contamination can be found in three dimensions. Hence when performing this type of survey, you should not only monitor bench tops but also the fronts of benches, fume cupboards and sinks. You should pay particular attention to items which could have been touched with contaminated hands (e.g. sink taps and door handles).
Remember to monitor for surface contamination in three dimensions and pay particular attention to items which could have been touched with contaminated hands.
For monitors which indicate in counts per second (cps), the readings from a direct monitoring detector can be converted to a surface activity value by considering the efficiency of the counter and the area over which the sample was taken. This relationship is given in Equation 3.
T = C x 100 x 13
Ec A
where T = Total contamination level in Bq cm-2
C = Net count rate in cps (i.e. count rate corrected for background)
Ec = Percentage efficiency of counting system
A = Area of probe in cm2
Equation 4 may then be used to calculate surface contamination levels from direct monitoring results (as shown in Example 2).
EXAMPLE 2
Question
A sodium iodide scintillation detector is used to measure the count rate from a surface contaminated with gamma contamination. The average count is measured at 160 counts per second (cps) and the background count rate is measured at 10 counts per second. If the area of the probe is 20 cm2 and the efficiency of the counter is quoted as 5% for the radionuclide being detected, what is the total surface contamination level in Bq cm-2?
Answer
C = 160 cps – 10 cps = 150 cps
A = 20 cm2
Ec = 5%
Using Equation 3 and substituting:
T = 150 x 100 x 1 = 150 Bq cm-2
5 20
Hence, the total surface contamination level is 150 Bq cm-2.
Note that some calibration facilities provide a calibration factor for how many cps equal 1 Bq cm-2 for the probe and radionuclide being measured. In this case, the net count rate is simply divided by this factor to obtain a total surface contamination reading (see Equation 4).
T = C4
F
where T = Total contamination level of a particular radionuclide in Bq cm-2
C = Net count rate in cps (i.e. count rate corrected for background)
F = Calibration factor in cps per Bq cm-2
Example 3 shows how this equation may be used.
EXAMPLE 3
Question
A sodium iodide scintillation probe is used to measure the count rate from a surface contaminated with iodine-131. The average gamma count is measured at 450 counts per second (cps) and the background count rate is measured at 15 counts per second. If a calibration factor of 15 cps = 1 Bq cm-2 is quoted for iodine-131 and for that particular probe, what is the total surface contamination level in Bq cm-2?
Answer
C = 450 cps – 15 cps = 435 cps
F = 15 cps per Bq cm-2
Using Equation 4 and substituting:
T = 435 = 29 Bq cm-2
15
Hence, the total surface contamination level is 29 Bq cm-2.
Sometimes contamination levels are quoted in becquerels per metre squared (Bq m-2). In this case, you should remember that 1 Bq cm-2 is equal to 104 Bq m-2.
1 Bq cm-2 = 104 Bq m-2
Notes should be taken throughout the survey of the instruments used and the measured total contamination levels. On completion of the survey, a detailed survey report should be produced. This report is similar to the dose rate survey report and should include:
a diagram of the area including numbered reference locations (see Figure 11);
a radiological survey form indicating the location and magnitude of the contamination levels, the instruments used and any remedial action which needs to be taken (see Figure 12).
As the most concern is with removable contamination levels (as this type of contamination could enter the body), limits are not usually set on total contamination levels from direct probe monitoring. It is more usual to set limits on the removable component of the surface contamination (see Section 5.2.6). If, however, the fixed contamination is likely to become loose, or there is an appreciable dose rate associated with the fixed contamination, the levels should be reduced in accordance with the ALARA principle.
Indirect (smear or swab) surface monitoring can be used to:
measure the amount of removable contamination on a surface;
detect the amount of removable contamination in high background areas;
detect lower levels of contamination than with direct monitoring; and
detect radionuclides with energies too low to be detected by direct monitoring.
The main steps to be taken when performing an indirect surface contamination survey are similar to that for direct probe monitoring (see Section 5.1).
To perform indirect surface monitoring, you will need some non-abrasive filter paper. The filter paper (e.g. glass fibre or hardened ashless paper) should not be less than 5.5 cm diameter and should be moistened with distilled water before use.
You will also need a system of counting the activity on the filter paper. The counting system will depend on the type of radiation to be measured but may include either a G-M tube, a proportional counter or a scintillation detector situated in a low background area.
The safety considerations for indirect surface monitoring are similar to those for direct surface monitoring (see Section 5.1.2).
The moistened filter paper should be held between the thumb and first two fingers and wiped over an area of approximately 100 cm2 (10 cm x 10 cm). As an alternative, forceps can also be used to hold the inside of a folded filter paper while the surface is being wiped. The paper should be moved across the surface in a similar way to the direct monitoring probe movements shown in Figure 13. The paper should then be taken to an area of low background for measurement.
If the efficiency of the monitoring instrument and the area over which the sample was taken are known, then they can be used to count the smear paper and calculate the removable contamination level (as shown in Equation 5).
R = C x 100 x 15
Ec A
where R = Removable contamination level in Bq cm-2
C = Net count rate in cps (i.e count rate corrected for background)
Ec = Percentage efficiency of counting system
A = Area smeared in cm2
This removable contamination can then be used to estimate the total contamination by incorporating another factor to take into account the efficiency of the smear technique (see Equation 6):
T = R x 100 = C x 100 x 1 x 1006
Er Ec A Er
where T = Total surface contamination level in Bq cm-2
C = Net count rate in cps (i.e count rate corrected for background)
Ec = Percentage efficiency of counting system
A = Area smeared in cm2
Er= Percentage of contamination removed from surface by smear paper
The value of Er is difficult to determine for smear papers but it is assumed to be 10%.
An example of how to calculate the loose surface contamination levels from indirect monitoring results is shown in Example 4.
EXAMPLE 4
Question
The average count rate for gamma radiation from a smear test of a laboratory workplace is measured at 85 counts per second (cps). A background count rate was measured at 10 cps. If the area smeared is 100 cm2 and the efficiency of the counter is quoted as 7%, what are the removable and total surface contamination levels in Bq cm-2? (Assume that the percentage of contamination removed from surface by smear paper is 10%.)
Answer
C = 85 cps – 10 cps = 75 cps
A = 100 cm2
Ec = 7%
Er= 10%
Using Equation 5 and substituting:
R= 75 x 100 x 1 = 10.7 Bq cm-2
7 100
Using Equation 6 and substituting:
T= 75 x 100 x 1 x 100 = 107 Bq cm-2
7 100 10
Hence, the removable surface contamination level is 10.7 Bq cm-2 and the total contamination level is 107 Bq cm-2.
If the removable contamination on the smear is measured by a probe which has been assigned a suitable calibration factor for the radionuclide being measured, then the removable surface contamination level can be determined as shown in Example 3 (Section 5.1.3).
Again, you should remember that contamination levels are sometimes quoted in becquerels per metre squared (Bq m-2) and that 1 Bq cm-2 is equal to 104 Bq m-2.
Notes should be taken throughout the survey of the instruments used and the measured removable contamination levels. On completion of the survey, a detailed survey report should be produced. This report should include:
a diagram of the area including numbered reference locations (see Figure 11);
a radiological survey form indicating the location and magnitude of the contamination levels, the instruments used and any remedial action which needs to be taken (see Figure 12).
If removable contamination is detected during a survey, appropriate action should be taken immediately to restrict access to the area and/or remove the contamination. In general, even low levels of removable contamination are considered unacceptable as they may enter the body and cause harm. Hence, it is usual to ensure that removable contamination levels are kept as low as possible at all times.
In order to assess the hazard from removable contamination, the measured values should be compared with local rules and/or national and international regulations. Although limits may be given in terms of maximum Bq cm-2 levels, in practice, contamination levels for removable contamination are often quoted as fractions or multiples of the Derived Limit (DL) for surface contamination for a particular radionuclide (see Module 2.3 Protection from Internal Radiation Hazards). As these Derived Limits are set such that dose limits are not exceeded, by quoting contamination levels in DL’s, you can gain some appreciation of the possible committed effective dose associated with these contamination levels (see Example 5). (Committed doses are doses received from the intake of radioactive material and will be explained in Module 2.5.)
EXAMPLE 5
Question
The DL for phosphorous-32 (P-32) is quoted as 100 Bq cm-2 by the Australian National Health and Medical Research Council. On a routine survey of a phosphorous-32 laboratory, you find a surface contamination level of approximately 25 Bq cm-2. What is the annual committed effective dose which could result from the exposure to this surface contamination level?
Answer
Exposure to 1 DL for 2000 hours (8 hours per day, five days a week, 50 weeks a year) would result in a committed effective dose of 20 mSv (according to the Australian definition of a Derived Limit).
We have (25 100) = 0.25 DL’s.
Hence, we can say that exposure to 0.25 DL’s for 2000 hours would result in a committed effective dose of (0.25 x 20 mSv) = 5 mSv.
Obviously, surface contamination levels of this magnitude should be reduced in accordance with the ALARA principle. However, this example shows how, by quoting surface contamination levels in terms of Derived Limits, we can assess the level of internal hazard.
It is important to note that Derived Limits are not internationally defined and may differ between countries and states. They are usually based on dose and intake limits set by the ICRP but, in some cases, they are set in terms of a fraction of the dose and intake limit instead of the total limit. Hence, when referring to Derived Limits, it is important that you know the definition of that limit for the country or state in which you are measuring the surface contamination. This will then enable you to correctly assess the dose associated with the measured contamination level.
When referring to Derived Limits, it is important that you know the correct definition of that limit as this will enable you to correctly assess the dose associated with the measured contamination level.
SELF-CHECK 7
SELF-CHECK 7
Now see how much you have understood by answering the following questions in your workbook:
Fill in the gaps with a suitable word or phrase:
The total contamination on a surface is made up of _______ and ___________ contamination. The total contamination level can be measured by directly placing a probe as close as possible to the surface being monitored. This is known as ________ surface monitoring. The level of removable contamination can be assessed by taking a _______ of an area and monitoring the contamination which is picked up. This is known as _________ surface monitoring.
What kind of protective clothing should be worn in surface contaminated areas?
Why should you monitor yourself after performing a contamination survey?
When performing a direct surface monitoring survey, why should you be careful to ensure that the probe does not touch the surface?
A zinc sulphide scintillation detector is used to measure the count rate directly from a surface contaminated with beta contamination. The average count is measured at 300 counts per second (cps) and the background count rate is measured at 10 counts per second. If the area of the probe is 20 cm2 and the efficiency of the counter is quoted as 10% for the radionuclide being detected, what is the total surface contamination level in Bq cm-2?
Briefly describe the method of performing a smear test.
a)You are monitoring a laboratory for surface contamination. You perform a smear test and find that the average count rate from the smear is 100 counts per second (cps) of gamma contamination. A background count rate was measured at 10 cps. If the area smeared is 100 cm2 and the efficiency of the counter is quoted as 5%, what are the removable and total surface contamination levels in Bq cm-2? (Assume that the percentage of contamination removed from surface by smear paper is 10%.)
b) A gamma spectroscopy measurement of the smear shows the contamination to be gallium-67. The DL for gallium-67 (Ga-67) is quoted as 1000 Bq cm-2 by the Australian National Health and Medical Research Council. What is the annual committed effective dose resulting from the exposure to this surface contamination level?
Now check your answers with the model answers in your workbook.
PRACTICAL ACTIVITY 2
Performing a Surface Contamination Survey
In this practical activity, you will perform a surface contamination survey of an area. Practical notes are given in your workbook. You should arrange a suitable time with your supervisor to perform this practical activity.
Airborne contamination levels should be measured wherever airborne contamination may occur. This type of survey usually involves sampling the air and measuring either the count rate from the filtration material or the air sample itself. However, as airborne contamination can exist in three forms (particulates, gases or as vapours), three slightly different methods are used.
When monitoring for particulates, air is drawn through a filter paper by a pump at a certain flow rate for a certain period of time. After the appropriate monitoring time, the filter paper is counted in a low background area and the airborne contamination concentration can then be calculated.
When monitoring for particulate airborne contamination you will need:
an air sampling instrument incorporating a pump and flow rate meter;
a suitable type of filter paper;
a timing device; and
a detector capable of measuring the count rate from the filter paper.
Typical air sampling instruments usually consist of a mains or battery operated pump (which draws air through a filter paper) and a calibrated flow meter to measure the air flow rate (see Figure 14).
Figure 30
An Air Sampler for Particulate Airborne Contamination
Glass fibre filters are usually used for particulate airborne contamination monitoring. These filters are specially designed to allow air through and trap particulates. They can also be designed to collect particles of a particular range of sizes.
The general filter papers used in the laboratory are unlikely to be suitable for air monitoring. Check before you use filters for air sampling that they are suitable. The supplier should have this information.
The choice of detector for measuring the count rate from the filter paper will depend on the type of contamination being monitored for. For alpha or beta contamination, the probe can be a zinc sulphide scintillation detector or a G-M detector with an end window thin enough to allow alpha particles to penetrate. For gamma contamination, the probe can be a G-M detector, an organic or noble gas-filled proportional counter, or a sodium iodide scintillation detector.
When monitoring for airborne contamination, gloves, overshoes, protective coats and safety glasses should be worn. Consideration should also be given to suitable respiratory protection if elevated airborne contamination levels are likely to exist.
Again, you should remember to monitor yourself after the survey has been completed as you may have become contaminated from either surface or airborne contamination.
The method of sampling for particulate airborne contamination is quite simple. Essentially, air is drawn through a filter paper by a pump. This filter paper collects the particulate contamination and after a certain time, the filter paper is counted. By knowing the air flow rate, the sampling time and the efficiency of the counting system, the airborne contamination concentration can then be calculated (see Section 6.1.4).
There are, however, a number of practical considerations to remember when performing particulate airborne contamination monitoring and these are as follows:
In general, a flow rate of 30 – 60 litres per minute and at least 30 minutes sampling time is recommended to give a representative sample. However you may need to sample for longer depending on the airborne concentration level you wish to measure and the efficiency of your counting system.
If the flow rates differ between the starting and finishing times, the average of the starting and finishing flow rates may be used for your calculations.
Air samples should be taken as close as possible to the breathing zone of the worker without impeding the work so that it is representative of air that is breathed in.
Care needs to be taken in dirty areas to ensure the sampler does not draw loose dust or contaminated material onto the filter from loose material on surfaces near the sampler.
In an enclosed area where the build up of radon-222 gas may occur from natural sources, the radon progeny may cause the filter paper count to be higher than expected (especially if it is counted shortly after sampling). Hence, the filter papers should be counted twice, once soon after sampling and again several hours later to obtain a count after the decay of radon progeny.
Care must be taken not to transfer removable contamination from gloves or surfaces to filter papers when loading or unloading air samplers. In addition, the papers should be transferred to the counter in bags, envelopes or Petrie dishes to prevent contamination from any other sources.
Air sample filter holders and retainers should be cleaned using tissues and monitored for contamination prior to re-use.
The airborne activity is calculated from the count rate on the filter paper using Equation 7:
A = C x 100 x 17
Ec V
where A = Airborne activity in Bq m-3
C = Net count rate in cps (i.e count rate corrected for background)
Ec = Percentage efficiency of counting system
V = Volume of air sampled in m3
Note that many air flow rate measurements are given in units of litres per minute (L min-1). For conversion, one litre per minute is equal to 10-3 cubic metres per minute as shown below:
1 L min-1 = 10-3 m3 min-1
Hence, to convert from L min-1to m3 min-1you need to multiply the L min-1by 10-3 to obtain the volume sampling rate in m3 min-1. To obtain the total volume of air sampled (in m3) you will then need to multiply this value by the total sampling time (see Equation 8).
V = F x 10-3 x t[8]
whereV = Volume sampled (in m3)
F = Flow rate (in L min-1)
t = Total sampling time (in mins)
An example of this conversion is given in Example 6.
EXAMPLE 6
Question
A filter paper shows a count rate of 40 cps after air was drawn through it for 30 minutes at a flow rate of 40 L min-1. The background level was measured as 10 cps. If the efficiency of the detector is quoted as 10%, what is the particulate airborne contamination level?
Answer
C = 40 cps - 10 cps = 30 cps
Ec = 10%
F = 40 L min-1
t = 30 mins
Using Equation 8
V = F x 10-3 x t = 40 x 10-3 x 30 = 1.2 m3
Using Equation 7
A = 30 x 100 x 1 = 250 Bq m-3
10 1.2
Hence the airborne contamination level is 250 Bq m-3
Notes should be taken of the instruments used and the measured airborne contamination levels. On completion of the survey, a detailed survey report should be produced. This report should include:
a diagram of the area showing the location where air sampling was carried out (see Figure 11); and
an airborne contamination survey form indicating the location and magnitude of the airborne contamination levels, the instruments used and any remedial action which needs to be taken (see Figure 15).
Figure 31
Airborne Contamination Survey Form
If appreciable airborne contamination is detected during a survey, appropriate action should be taken immediately to restrict access to the area. In general, even low levels of airborne contamination are considered unacceptable as they may enter the body and cause harm. Hence, it is usual to ensure that airborne contamination levels are kept as low as possible at all times.
In order to assess the hazard from airborne contamination, the measured values should be compared with local rules and/or national and international regulations. Although limits may be given in terms of maximum Bq m-3 levels, in practice, activity levels for airborne contamination are often quoted as fractions or multiples of the Derived Air Concentration (DAC) for a particular radionuclide (see Module 2.3 Protection from Internal Radiation Hazards). Like Derived Levels for surface contamination, DAC values are used in the workplace to assess the internal radiation hazard by relating measured airborne levels to dose limits (see Example 7).
EXAMPLE 7
Question
The DAC for phosphorous-32 (P-32) is calculated as 2.875 x 103 Bq m-3 from ICRP recommendations (see Module 2.3 Protection from Internal Radiation Hazards). On a routine survey of a phosphorous-32 laboratory, you find airborne contamination levels of approximately 150 Bq m-3. What is the annual committed effective dose which could result from the exposure to this airborne contamination levels?
Answer
Exposure to 1 DAC for 2000 hours (8 hours per day, five days a week, 50 weeks a year) would result in a worker inhaling one ALI in a year. From the definition of an ALI, this intake would result in a committed effective dose of 20 mSv.
We have (150 2.875 x 103) = 0.05 DAC’s.
Hence, we can say that exposure to 0.05 DAC’s for 2000 hours would result in a committed effective dose of (0.05 x 20 mSv) = 1 mSv.
The method of sampling for gases involves using a pump to draw air through a high efficiency filter into a chamber. The chamber can either then be sealed and taken for measurement or the air sample can be continuously monitored.
When monitoring for gaseous airborne contamination you will need:
an air collection chamber;
a pump;
a suitable type of filter paper; and
a detector capable of measuring the count rate from the air sample.
For continuous monitoring you will also need:
An air flow rate meter; and
a timing device.
The safety considerations for gaseous airborne contamination monitoring are similar to those for particulate airborne contamination (see Section 6.1.2).
A pump is used to draw air through a high efficiency filter into a chamber. The filter stops the particulates and only the gaseous contamination enters the chamber. The air in the chamber can then either be counted as the sample flows through the chamber (continuous monitoring) or it can be sealed and then counted in a low background area (grab sampling).
Care should be taken if vapours such as iodine or tritiated water are present in the air as the filter may not stop these vapours. If such vapours are present, they are likely to enter the chamber and condense, thereby causing the chamber to become contaminated. Hence, if there is a possibility of vapours being present, you must ensure that the filter will prevent the vapours from passing into the chamber. The best way to do this is to ask the filter supplier if the vapours will be stopped.
If vapours are likely to be present with the gaseous airborne contamination you must ensure that the filter can also stop the vapours from entering the chamber.
The airborne activity is calculated using the count rate from the air sample. A calculation similar to that shown in Example 6 in Section 6.1.4 can be performed to give the gaseous airborne contamination level.
A detailed survey report should be produced for gaseous airborne contamination surveys. This report should include:
a diagram of the area showing the location where air sampling was carried out (see Figure 11); and
a detailed airborne contamination survey form indicating the location and magnitude of the airborne contamination levels, the instruments used and any remedial action which needs to be taken (see Figure 15).
The airborne activity levels should be compared with local rules and/or national or international regulations to ensure that you are operating safely. The method of comparison is similar to that for particulate airborne contamination given in Section 6.1.6.
Two types of vapours are commonly monitored in nuclear facilities – tritium (hydrogen-3) and radioiodines (commonly iodine-131). The methods of monitoring vary but essentially both methods involve trapping the vaporous radionuclide from the air using a suitable trapping material, and then measuring the level of contamination on the trapping material. Suitable trapping materials include activated charcoal for radioiodines and distilled water for tritium.
The equipment needed for monitoring radioiodines is similar to that used for particulate airborne contamination monitoring except that an additional activated charcoal filter is necessary. So, when monitoring for radioiodines you will need:
an air sampling instrument incorporating a pump and flow rate meter;
a suitable particulate pre-filter to remove particulates from the air;
an activated charcoal filter to trap the radioiodines;
a timing device; and
a detector capable of measuring the count rate from the charcoal filter.
Suitable equipment for radioiodine monitoring is shown in Figure 16.
Figure 32
Equipment for Monitoring for Radioiodines
When monitoring for tritium, a bubbler technique is employed. This involves drawing air through a glass jar filled with distilled water (which acts as a trap) at a known flow rate. When monitoring for tritium you will need:
a pump;
an air flow rate meter;
a glass jar filled with distilled water to trap the tritium;
a timing device; and
a liquid organic scintillation detector to measure the count rate from the tritium contamination.
Suitable equipment for tritium monitoring is shown in Figure 17.
Figure 33
Bubbler Sampler for Tritium Monitoring
The safety considerations for monitoring for vapours are similar to those for particulate airborne contamination (see Section 6.1.2).
The method for radioiodine monitoring is similar to that for particulate airborne contamination monitoring (see Section 6.1.3). However, a particulate filter should be placed in front of the activated charcoal filter to ensure that the particulates are trapped before the air enters the charcoal filter.
Remember that the charcoal filter should be measured twice, once soon after sampling and once a few hours later to account for radon decay progeny.
For tritium monitoring, the air is drawn through a bottle containing distilled water at a sampling rate of approximately 10 L min-1. At the end of the sampling period, a sample of the water is taken and measured in a liquid scintillation counter.
Note that when you are trying a trapping system for the first time you should confirm it is trapping all the vapour in the air. This can be done by having two or three traps connected after each other in series. When the material in each trap is sampled individually, you will be able to see how many traps were needed to collect the vapour. One feature that will determine how many traps are needed is the air flow rate. If this increases significantly you will need more traps.
For both radioiodine and tritium monitoring, the airborne activity is calculated using the count rate from the trapping material. A calculation similar to that shown in Example 6 in Section 6.1.4 can be performed to give the airborne contamination level.
A detailed survey report should be produced for gaseous airborne contamination surveys. This report should include:
a diagram of the area showing the location where air sampling was carried out (see Figure 11); and
a detailed airborne contamination survey form indicating the location and magnitude of the airborne contamination levels, the instruments used and any remedial action which needs to be taken (see Figure 15).
The airborne activity levels should be compared with local rules and/or national or international regulations to ensure that you are operating safely. The method of comparison is similar to that for particulate airborne contamination given in Section 6.1.6.
SELF-CHECK 8
SELF-CHECK 8
Now see how much you have understood by answering the following questions in your workbook:
Fill in the gaps with a suitable word or phrase.
When monitoring for particulate airborne contamination, the particulates are trapped by a ______ ______ filter paper.
When monitoring for gaseous airborne contamination, the air if filtered and then _________ in an air chamber. The air in the chamber can then either be counted as the sample flows through the chamber (__________ monitoring) or it can be sealed and then counted in a low background area (_____ sampling).
An _________ ________ filter is used for monitoring radioiodines. To ensure that the particulates are trapped before reaching the main filter, a particulate filter should be placed __ ______ __ the main filter.
Tritium can be trapped in _________ ______. A sample of the trapping material can them be taken and measured in a ________ __________ counter.
Air samples should be taken close to the breathing zone of a worker. Why is this so?
Filter papers should be counted twice, once immediately after sampling and again several hours later. Why is this so?
a) Iodine-131 (I-131) is used in a laboratory where part of a chemical process may cause airborne contamination. An air sampler is run in the laboratory for one hour with an air flow rate of 30 L min-1. The activated charcoal filter is counted on a counter with 5% efficiency and a sample count of 45 24 counts was obtained in a count time of 300 seconds. The background level was measured at 24 counts in 300 seconds. Assuming no contribution from radon progeny, calculate the airborne activity of I-131 in Bq m-3.
b) The DAC for iodine-131 is calculated as 7.5 x 102 Bq m-3 from ICRP recommendations (see Module 2.3 Protection from Internal Radiation Hazards). What is the annual committed effective dose which could result from the exposure to the airborne contamination levels calculated in a) above?
Now check your answers with the model answers in your workbook.
KEY POINTS
KEY POINTS
Radiation detectors detect ionizing radiation.
Radiation monitoring instruments consist of a radiation detector and associated electronics to detect and quantify levels of radiation and contamination.
Two types of measuring instruments are used in the workplace dose rate meters and contamination monitors.
Dose rate meters detect penetrating and some beta radiation. They usually give a direct reading of dose rate in microsieverts per hour (Sv h-1).
Dose rate meters actually measure an operational quantity known as ambient dose equivalent rate. This quantity gives a good approximation to the effective dose rate received by humans.
Some dose rate meters are able to sum the dose received over a given time. These are known as electronic dosimeters and are used for personal dosimetry and in areas where dose rates change rapidly.
Two types of contamination monitors are used in the workplace – surface contamination monitors and airborne contamination monitors.
No contamination monitor is 100% efficient. Each monitor has different efficiencies for different radionuclides.
Surface contamination monitors measure the contamination on a surface. They usually consist of a monitor connected to a detector. Surface contamination monitors usually read in units of counts per second or Bq cm-2.
Airborne contamination monitors measure the contamination in the air. Their measurements can be converted to units of Bq m-3.
There are three types of airborne contamination: particulates, gases and vapours. The methods of monitoring are slightly different for each type.
All radiation protection survey instruments must be calibrated against calibration sources representative of the sources the instrument will be used to measure. This ensures that the instruments are capable of responding within acceptable levels of accuracy.
To ensure the national and international uniformity of response, calibration sources must be traceable to a primary or secondary standard, and these standards are usually held at national or international standards laboratory.
Dose rate and contamination monitoring instruments are calibrated by exposing the instrument to a known quantity and either adjusting the instrument controls to read the desired reading or assigning a calibration factor to the instrument.
Dose rate and contamination monitoring instruments are calibrated against specific sources with specific types and energies of radiation. Therefore they do not respond uniformly to all sources of ionizing radiation or contamination.
In general, you cannot be sure that a monitor is detecting radiation unless the monitor is reading at least two times background.
When selecting appropriate instrumentation, you should consider the type of survey you wish to perform, the type and energy of radiation you wish to detect and the required sensitivity of the instrument.
Design considerations which should be considered include: the ease of use of the instrument; the suitability of the detector for the environment in which measurements are to be taken; the location of the detector within the instrument; the physical size of the detector for effectively measuring dose rates in narrow beams; the response time for short exposures or high radiation fields; the directional response of monitor; the resistance to foldback in high radiation fields (for G-M detectors); the presence of a speaker to help identify changing levels and an illuminated scale for night work.
Other considerations include: the cost of the instrument and the availability of batteries and spare parts.
When planning a radiological survey you should draw up survey diagrams and forms for the area, refer to any previous surveys and perform instrument pre-use response checks.
Pre-use response checks include: a visual check; a battery check; a calibration check; a light sensitivity check and a source check.
When performing any type of radiological survey, you should think about the safety precautions you may need to take.
When performing dose rate surveys, be aware of possible radiation beams and the limitations of some instruments to detect them.
In direct surface monitoring the total contamination under the probe is monitored.
In direct surface monitoring, the removable contamination is monitored.
Remember to monitor yourself after contamination surveys to ensure that you are not contaminated.
Surface contamination levels can be converted to surface activity in units of Bq cm-2.
Surface contamination levels should be compared with local rules and/or national and international regulations.
Removable surface contamination levels are often quoted in terms of Derived Limits (DL’s).
Air samplers should be run as close as possible to the breathing zone of workers when measuring airborne contamination.
When monitoring for particulate airborne contamination, the air is filtered using a glass fibre filter. The contamination on the filter is measured and this can then be converted to units of Bq m-3.
When monitoring for gaseous airborne contamination, the air is filtered using a high efficiency filter. The air is then collected in a chamber and sampled continuously or taken away and counted in a low background area.
When monitoring for radioiodines, an activated filter is used to trap the radioisotopes.
A bubbler technique is used for monitoring for tritium.
Filters should be monitored twice once soon after counting and again a few hours later to account for radon-222 decay.
FINAL ASSIGNMENT
FINAL ASSIGNMENT
This assignment is to be completed under test conditions, so spend some time now studying this module. Then contact your supervisor to arrange a suitable time to complete the assignment.
GLOSSARY OF TERMS
Airborne contamination | Radioactive contamination in the air measured in becquerels per metre cubed. |
Ambient dose equivalent | The operational quantity of dose measured by dose rate meters. This measurement is a good approximation to effective dose. |
Annual limit on intake (ALI) | The amount of radioactivity, measured in becquerels, which if taken into the body of a Reference man would result in a committed effective dose equal to the relevant dose limit |
Calibration | The process of determining the absolute values corresponding to the graduations on an arbitrary scale of an instrument. |
Calibration factors | Factors which can be used to relate a measured value to a true activity, dose rate or contamination level. |
Contamination monitor | An instrument which can be used to measure contamination levels. |
Derived air concentration (DAC) | The concentration of a radionuclide (in becquerels per metre cubed) in the air which would result in a worker in the area receiving one ALI in a working year. |
Derived limit for surface contamination (DL) | Limit which controls the amount of surface contamination in order to keep doses below the relevant dose limits. |
Direct surface monitoring | The process of measuring the total contamination on a surface by monitoring the surface directly with a probe. |
Dose rate meter | An instrument used to measure dose rates from a radiation source. |
Fixed contamination | Radioactive contamination fixed to a surface. |
Indirect surface monitoring | The process of taking a smear from a surface to assess the level of removable contamination. |
Grab sampling | The process of collecting a sample of gas in a chamber and measuring the sample for airborne contamination in a low background area. |
Removable contamination | Radioactive contamination which is not fixed to a surface. |
Lower limit of detection | The lowest dose rate or contamination level detectable by an instrument. |
Primary standard | An absolute standard of measurement used for calibrating radiation monitoring instruments. |
Probe | A radiation detector. |
Radiation detector | The part of a radiation monitoring instrument which detects ionizing radiation. |
Radiation instrument | An instrument which incorporates a radiation detector and associated electronics to measure the amount of incident ionizing radiation. |
Secondary standard | A standard of measurement which is directly traceable to a primary standard and which can be used for calibrating radiation monitoring instruments. |
Surface contamination | Radioactive contamination on a surface measured in becquerels per centimetre (or metre) squared. |
INTERNATIONAL ATOMIC ENERGY AGENCY AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION |
DISTANCE LEARNING MATERIALS
RADIATION PROTECTION
Module 2.5
Prepared by Safety and Radiation Science
Australian Nuclear Science and Technology Organisation
With the assistance of consultants in Australia and the United Kingdom, and IAEA experts from Korea, Mongolia, New Zealand, the Philippines and Thailand
Use of this material, acknowledging the IAEA and ANSTO as the source, is permitted for non-profit training
Acknowledgements
This material has been prepared by an extensive team of international experts from the fields of radiation protection, medicine and education. It is not possible to mention by name all those who have had an input to; the initial planning; writing modules and workbooks; preparing and marking final assignments; proof-reading and editing; using the material and providing valuable feedback; organizing and hosting review meetings; and general administrative support.
The support of ANSTO management in providing the resource and encouragement is gratefully acknowledged.
The enthusiastic support of IAEA Technical Officers has been vital to the success of this project.
PART 2
RADIATION PROTECTION
MODULE 2.5
PERSONAL DOSIMETRY
CONTENTS
OVERVIEW
Personnel working with ionizing radiation may be exposed to sources both inside and outside their bodies. You will also learn in this module how personal doses from internal and external radiations may be assessed, and the problems associated with making accurate dose assessments. You should then realize the importance of controlling the levels of radiation to prevent or limit the exposure.
TIME ALLOCATION
It is estimated that you will need to spend eight to ten hours to complete this module before commencing the assignment. This estimated time is for your guidance only. Do not worry if you need more time to understand the module.
MATERIALS
NOW YOU ARE READY TO START WORK
18.RADIATION AND DOSE MEASUREMENTS
In radiation protection we need to be able to determine the potential hazard from radiation. To do this we need to measure the quantities which describe the radiation field (known as radiometric quantities) and we also need to measure the effects produced by the radiation dose (known as dosimetric quantities). To ensure consistency between these quantities, a special organization known as the International Commission on Radiation Units and Measurements (ICRU) is responsible for recommending the appropriate definitions and conversion factors for use in radiation protection.
18.1Radiometric Quantities
Radiometric quantities describe the radiation field (in terms of particles or rays) and the quantity of ionization produced by the radiation.
18.1.1Energy
The SI unit of energy is the joule. However, as this is a very large unit, it is not convenient for use in radiation protection. Instead, the energy of ionizing radiation is measured in terms of electronvolts(eV), where one electronvolt is the amount of energy gained by an electron when it is accelerated through a potential difference of one volt. In terms of joules:
1 eV = 1.6 x 10-19 J
The electronvolt is a very small unit of energy, even in atomic terms, so in practice the energy of radiation is usually given in kiloelectronvolts (keV) or megaelectronvolts (MeV).
18.1.2Fluence (
A radiation field consisting of any type of radiation can be described in terms of the fluence, which is the number of particles (or photons) passing through unit area. It is measured in particles per square metre (m-2) and has the symbolFluence rate is the number of particles passing through unit area in unit time. It is usually measured in m-2 s-1.
18.1.3Exposure (X)
Historically, x-rays and gamma rays were quantified by the amount of ionization they produced in air (i.e. the exposure). The special unit of exposure (symbol X) was originally called the roentgen (R), named after the discoverer of x-rays, Wilhelm Roentgen. The SI unit of exposure is the coulomb per kilogram (C kg-1) and this is related to the roentgen as follows:
1 R = 2.58 x 10-4 C kg-1 of air
The roentgen is no longer used in radiation protection but there are many instruments which give readings in roentgen (R) or roentgen per hour (R h-1). ICRU Reports 39, 43 and 47 provide coefficients to convert data for exposure in roentgen to the SI units of dose provided that the energy of the x- or gamma ray is known.
18.1.4Kerma (K)
The idea of kerma (K) was originally introduced by the ICRU in 1962 to take into account the problem of measuring exposure. The term kerma actually refers to the kinetic energy released per unit mass of absorber and is basically a measure of the kinetic energy of charged particles produced in an absorbing medium by uncharged radiations (i.e. photons and neutrons). When the absorbing medium is air, the term air kerma is used.
The unit of kerma is the joule per kilogram and it is given the special name gray (Gy):
1 Gy = 1 J kg-1
For x- and gamma-ray energies up to 1 MeV, the interactions which take place between the radiation and the particles of air are nearly the same for both exposure measurement and air kerma measurement. At x- and gamma ray energies above 1 MeV interactions occur which lead to different measurements of air kerma compared with exposure. For example, cobalt-60 has two gamma radiations with energies 1.173 MeV and 1.333 MeV and the measurement of air kerma produced by these radiations will be about 0.3% higher than if only exposure is considered.
18.1.5Summary of radiometric quantities
Table 1 summarizes the radiometric quantities.
Table 15
Summary of Radiometric Quantities
Quantity | Symbol | SI Unit | SI Unit Name | Conversion |
Energy | Joule J | electronvolt (eV) | 1 eV = 1.6 x 10-19 J | |
Fluence | | Particles per square metre m-2 | ||
Exposure | X | Coulomb per kilogram C kg-1 | 1 R= 2.58 x 10-4 C kg-1 | |
Kerma | K | Joule per kilogram J kg-1 | gray (Gy) | 1 Gy = 1 J kg-1 |
18.2Dosimetric Quantities
The term dose is a very general term which applies to the amount of energy deposited when radiation passes through a material. It is often used very loosely and, depending on the context, may actually mean absorbed dose, equivalent dose, effective dose or even exposure or kerma. The following sections explain the basic dosimetric quantities used in radiation protection.
18.2.1Absorbed dose (D)
Absorbed dose is a measure of the energy deposited in any medium by any type of radiation. It is given the symbol D and DT R means the absorbed dose in tissue or organ T delivered by radiation type R. For example, DLung means the absorbed dose to the lung from alpha radiation.
The SI unit of absorbed dose, like that of kerma, is the joule per kilogram (J kg-1) and is given the name of gray (Gy). However, when we are talking about absorbed dose, it is very important to specify the type of material in which the energy is being deposited, for example 1.3 mGy absorbed dose to water.
The original unit of absorbed dose was the radiation absorbed dose(rad) and one gray is equal to 100 rad.
1 Gy = 100 rad
or 1 mrad = 10 Gy
In radiation protection, we often need to convert between old (non-SI) and new (SI) units for dose and dose rates. Example 1 shows how this conversion is performed for absorbed dose. (Note that you may need to refer to Reference Material R1 for unit prefix information.)
EXAMPLE 1
Question
Convert the following absorbed doses and dose rates between old and new units:
a)0.4 mrad to Gy.
b)7.5 Gy h-1 to rad h-1.
Answer
a) 1 mrad = 10 Gy
So 0.4 mrad = 0.4 x 10 Gy = 4 Gy
Hence 0.4 mrad is equal to 4 Gy or 4 x 10-6 Gy
b) 1 Gy h-1 = 100 rad h-1
or 1 Gy h-1 = 0.1 mrad h-1
So 7.5 Gy h-1 = 7.5 x 0.1 mrad h-1 = 7.5 x 10-4 rad h-1 = 0.75 mrad h-1
Hence 7.5 Gy h-1 is equal to 0.75 mrad h-1 or 7.5 x 10-4 rad h-1
18.2.2Equivalent Dose (H)
Absorbed dose tells us how much energy is deposited in an absorbing material but it does not tell us how much damage may be done to tissue, nor does it indicate the level of the potential hazard. For example, the level of damage produced by an absorbed dose to tissue of 0.5 Gy would be very much greater if the energy were deposited by alpha radiation or by neutrons than it would be if the energy were deposited by gamma radiation. Hence, a quantity known as equivalent dose is used as a measure of the biological effect of a particular type of radiation on organs or tissues. It is calculated by multiplying the absorbed dose to an organ or tissue (measured in gray) by a dimensionless factor called the radiation weighting factor (wR). Radiation weighting factors as recommended in ICRP 60 are given in Table 2.
Table 16
Radiation Weighting Factors
Type and Energy Range | Radiation Weighting Factor (wR) |
Alpha particles, all energies | 20 |
Beta particles, all energies | 1 |
Gamma and x-rays, all energies | 1 |
Neutrons: | |
<10 keV | 5 |
10 keV to 100 keV | 10 |
> 100 keV to 2 MeV | 20 |
> 2 MeV to 20 MeV | 10 |
> 20 MeV | 5 |
Equivalent dose (symbol H) is defined as shown in Equation 1 for a particular type of radiation interacting with a particular organ or tissue:
[1]
where is the equivalent dose to an organ or tissue T delivered by radiation type R
is the absorbed dose to an organ or tissue T delivered by radiation type R
is the radiation weighing factor for radiation type R
The SI unit for equivalent dose is also the joule per kilogram but it is given the special name of sievert (Sv) to distinguish it from absorbed dose.
1 Sv = 1 J kg-1
Example 2 shows how the equivalent dose may be determined from absorbed dose.
EXAMPLE 2
Question
a) Convert the following absorbed doses in a particular organ or tissue to equivalent doses:
2 mGy from alpha particles.
2 mGy from beta particles.
2 mGy from gamma radiation.
b) Which of these would be the most damaging to organs or tissue?
Answer
i) D T = 2 mGy
From Table 2
w = 20
From Equation 1
H T = D T x w = 2 x 20 = 40 mSv
Hence the equivalent dose in a particular organ or tissue due to an absorbed dose from alpha particles of 2 mGy is 40 mSv.
ii) D T = 2 mGy
From Table 2
w = 1
From Equation 1
H T = D T x w = 2 x 1 = 2 mSv
Hence the equivalent dose in a particular organ or tissue due to an absorbed dose from beta particles of 2 mGy is 2 mSv.
iii) D T = 2 mGy
From Table 2
w = 1
From Equation 1
H T = D T x w = 2 x 1 = 2 mSv
Hence the equivalent dose in a particular organ or tissue due to an absorbed dose from gamma rays of 2 mGy is 2 mSv.
From a) above, alpha particles would impart the greatest dose so they would do the most damage to the particular organ or tissue.
If an organ is irradiated by more than one type of radiation, it is necessary to sum the equivalent doses to account for the different types of radiation. Equation 2 shows how the total dose to a particular organ from a variety of types of radiation may be determined:
where is the total equivalent dose to an organ or tissue T delivered by all radiation types
indicates the sum for each radiation type R
is the absorbed dose to an organ or tissue T delivered by radiation type R
is the radiation weighing factor for radiation type R
Example 3 shows how the equivalent dose to a particular organ or tissue for different types of radiation can be determined.
EXAMPLE 3
Question
What is the equivalent dose to a particular organ or tissue from 2 mGy from alpha particles, 2 mGy from beta particles and 2 mGy from gamma radiation?
Answer
From Example 2 above we know that:
D T x w = 40 mSv
D T x w = 2 mSv
D T x w = 2 mSv
From Equation 2:
= D T x w + D T x w + D T x w = 40 + 2 + 2 = 44 mSv
Hence the equivalent dose to a particular organ or tissue from 2 mGy from alpha particles, 2 mGy from beta particles and 2 mGy from gamma radiation is 44 mSv.
Note that the original unit of equivalent dose was the rem where one sievert is equal to 100 rem.
1 Sv = 100 rem
or 1 mrem = 10 Sv
Example 4 shows how we can convert between these old and new units:
EXAMPLE 4
Question
Convert the following equivalent doses and dose rates between old and new units:
a)0.25 mrem to Sv
b) 0.3 mSv h-1 to rem h-1
Answer
a) 1 mrem = 10 Sv.
So 0.25 mrem = 0.25 x 10 Sv = 2.5 Sv
Hence 0.25 mrem is equal to 2.5 Sv or 2.5 x 10-6 Sv
b) 1 mSv h-1 = 100 mrem h-1
So 0.3 mSv h-1 = 0.3 x 100 mrem h-1 = 30 mrem h-1 = 0.03 rem h-1
Hence 0.3 mSv h-1 is equal to 30 mrem h-1 or 0.03 rem h-1
18.2.3Effective Dose (E)
Some tissues and body organs are more sensitive to radiation than others and an equivalent dose in one organ may be more hazardous than the same equivalent dose in another organ. The ICRP recommends tissue weighting factors (wT) which are applied to specific body organs. These dimensionless factors take into consideration the different radiosensitivities of the different organs and tissues. Table 3 lists the tissue weighting factors as recommended in ICRP 60.
Table 17
Tissue Weighting Factors
Tissue | Tissue Weighting Factor (wT) |
Gonads | 0.20 |
Bone marrow (red) | 0.12 |
Colon | 0.12 |
Lung | 0.12 |
Stomach | 0.12 |
Bladder | 0.05 |
Breast | 0.05 |
Liver | 0.05 |
Oesophagus | 0.05 |
Thyroid | 0.05 |
Skin | 0.01 |
Bone Surface | 0.01 |
Remainder | 0.05 |
The effective dose (symbol E) to an organ or tissue is found by multiplying the equivalent dose by the appropriate tissue weighting factor as shown in Equation 3:
[3]
where is the effective dose to an organ or tissue type T
is the equivalent dose to an organ or tissue type T
is the tissue weighing factor for an organ or tissue type T
As the tissue weighting factors are dimensionless, the units for effective dose are the same as the units for equivalent dose (i.e. Sv or rem). The same conversion factors between the old units (rem) and new SI units (Sv) also apply.
Example 5 shows how effective dose may be determined for an equivalent dose to the different organs of the body.
EXAMPLE 2
Question
a) Calculate the effective dose resulting from 5 mSv equivalent dose to the following organs and tissues:
to the skin.
to the thyroid.
to the lung.
to the gonads.
b) For which organ or tissue does this equivalent dose represent the biggest hazard?
Answer
i) H skin = 5 mSv
From Table 3
w skin = 0.01
From Equation 3
E skin = H skin x w skin = 5 x 0.01 = 0.05 mSv
Hence the effective dose to the skin due to an equivalent dose of 5 mSv is 0.05 mSv.
ii) H thyroid = 5 mSv
From Table 3
w thyroid = 0.05
From Equation 3
E thyroid = H thyroid x w thyroid = 5 x 0.05 = 0.25 mSv
Hence the effective dose to the thyroid due to an equivalent dose of 5 mSv is 0.25 mSv.
iii)H lung = 5 mSv
From Table 3
w lung = 0.12
From Equation 3
E lung = H lung x w lung = 5 x 0.12 = 0.6 mSv
Hence the effective dose to the lung due to an equivalent dose of 5 mSv is 0.6 mSv.
iv)H gonads = 5 mSv
From Table 3
w gonads = 0.20
From Equation 3
E gonads = H gonads x w gonads = 5 x 0.20 = 1 mSv
Hence the effective dose to the gonads due to an equivalent dose of 5 mSv is 1 mSv.
From a) above, the biggest hazard would be to the gonads as they would receive the largest effective dose.
The total effective dose for all exposed organs is the sum of the tissue equivalent doses multiplied by the appropriate tissue weighting factor for those organs and tissues (see Equation 4):
[4]
where E is the total effective dose to all exposed organs and tissues
indicates the sum for each organ or tissue type T
is the equivalent dose to an organ or tissue T
is the tissue weighing factor for an organ or tissue type T
Note that the effective dose to the whole body is generally the most useful quantity in radiation protection. This is because, in most work environments, the whole body effective dose is more likely to approach dose limits than individual organ or tissue doses are. Assuming uniform irradiation to the whole body, the total effective dose can be calculated either by summing the effective doses to each individual organ or tissue, or more simply we can just assume a tissue weighting factor of 1 for the whole body (see Example 5).
EXAMPLE 5
Question
What is the effective dose for the whole body being irradiated uniformly with an equivalent dose of 5 mSv?
Answer
From Equation 4
= (5 x w gonads) + (5 x w bone marrow (red)) + (5 x w colon) + (5 x w lung) + (5 x w stomach) + (5 x w bladder) + (5 x w breast) + (5 x w liver) + (5 x w oesophagus) + (5 x w thyroid) + (5 x w skin) + (5 x w bone surface) + (5 x w remainder)
= 5 x (0.2 + 0.12 + 0.12 +0.12 + 0.12 + +0.05 + 0.05 + 0.05 + 0.05 + 0.05 + 0.01 + 0.01 + 0.05)
= 5 x 1 = 5 mSv
Alternatively, from Equation 3:
= 5 x 1 = 5 mSv
Hence the effective dose for the whole body being irradiated uniformly with an equivalent dose of 5 mSv is 5 mSv.
1.2.4Committed Dose
The quantities discussed so far have come from radiation sources outside the human body. However, as you have learnt in Module 2.3 Protection from Internal Radiation Hazards, if an intake of radioactive material occurs, it will continue to irradiate the body until either the radioactivity has decayed away or the body has excreted the substance. You will also remember that once the radioactive material is inside the body, it may be distributed throughout the body or it may concentrate in particular organs. We therefore also need to be able to indicate doses which arise from intakes of radioactive materials and these doses are known as committed doses.
Committed dose is defined as the dose accumulated by the body over 50 years following the intake (except in the case of intakes by children where it is defined as the dose accumulated until the age of 70). Committed dose can be committed absorbed dose, committed equivalent dose or committed effective dose. It is given the symbols D(50), H(50), or E(50) where 50 represents the number of years over which the dose is being calculated.
1.2.5Summary of dosimetric quantities
Figure 1 and Table summarize the dosimetric quantities and their units.
Figure 34
A Summary of Dosimetric Quantities
(With acknowledgments to Lt. Cdr J Kelly, RN and An Introduction to Radiation Protection, Alan Martin and Samuel Harbison)
Table 18
Summary of Dosimetric Quantities and Their Units
Quantity | Symbol | SI Unit | SI Unit Name | Conversion |
Absorbed Dose | D | Joule per kilogram J kg-1 | gray (Gy) | 1 Gy = 100 rad |
Equivalent Dose | H | Joule per kilogram J kg-1 | sievert (Sv) | 1 Sv = 100 rem |
Effective Dose | E | Joule per kilogram J kg-1 | sievert (Sv) | 1 Sv = 100 rem |
SELF-CHECK 1
Classify the following into radiometric and dosimetric quantities:
FluenceEffective dose Energy Committed dose
ExposureAbsorbed doseKermaEquivalent dose
Radiometric Quantities
Dosimetric Quantities
2.Convert the following doses and dose rates into the appropriate SI units:
a) 2 rad
30 mrad h-1
200 mrem
4 rem h-1
3.Convert the following doses and dose rates into the appropriate old units:
100 Gy
5 mGy h-1
2.5 mSv
20 Sv h-1
Fill in the gaps with an appropriate word or phrase:
______ is the quantity used to describe the amount of ionization in air caused by x-rays or gamma radiation.
The quantity __________ dose takes into consideration the type of incident radiation but not the radiosensitivity of organs and tissues. It is measured in SI units of _____.
_________ dose is the quantity which takes into consideration the different radiosensitivities of organs and tissues. It is measured in SI units of _________.
The quantity ________ dose describes the amount of energy deposited in a particular medium but does not take into account the type of radiation. The SI units of this quantity are _________.
_________ dose is the term used to denote a dose arising from an intake of radioactive material.
a) Convert the following absorbed doses in tissue to equivalent doses:
5 mGy from gamma radiation
5 mGy from slow neutrons (energy of 20 keV)
5 mGy from fast neutrons (energy of 1.5 MeV).
b) Which of these would be the most damaging to organs or tissue?
If the thyroid receives an equivalent dose of 14 mSv and the lung receives an equivalent dose of 100 mSv what is the effective whole body dose?
Now check your answers with the model answers in your workbook.
19.OPERATIONAL QUANTITIES
As it is impossible to directly measure the amount of energy deposited by each type of radiation in each body organ, the quantities of equivalent and effective dose are not measurable in practice. To overcome this difficulty, ICRU Report 47 recommends the following operational dose quantities for area monitoring:
Ambient dose equivalent
Directional dose equivalent
and for individual monitoring, it recommends:
Personal dose equivalent
The ICRU definitions for these operational quantities are explained in Sections 2.1 and 2.2. These definitions are actually quite complex so do not worry if you do not understand them fully. The most important thing to remember is that these quantities are intended to give a reasonable approximation to equivalent and effective doses avoiding both underestimation and excessive overestimation.
Operational quantities are intended to give reasonable approximations to equivalent and effective doses.
19.1For Area Monitoring
For modelling purposes, the ICRU quantities refer to a 30cm diameter, tissue-equivalent sphere (known as the ICRU sphere) which represents the human body. In practice, the operational quantities do not require the presence of this sphere but merely refer to the dose (in sieverts (Sv)) that would exist in the sphere if it were placed in the radiation field.
19.1.1Ambient dose equivalent
Ambient dose equivalent (symbol H*(d)) at a point in a radiation field is defined as the dose equivalent that would be produced by the corresponding field in the ICRU sphere at a depth d mm. This quantity is mostly used to assess doses from strongly penetrating radiation where the recommended depth is 10 mm.
In practical terms, most radiation monitoring instruments are calibrated in terms of this quantity (as recommended by the ICRP). The reading on these monitors then gives a reasonable approximation to the effective dose.
19.1.2Directional dose equivalent
Directional dose equivalent (symbol H’(d)) at a point in a radiation field is defined as the dose equivalent that would be produced by the corresponding field in the ICRU sphere at a depth d mm in a specified direction. This quantity is suitable for area monitoring of fields containing weakly penetrating radiation where the depth is taken as 0.07 mm (for skin) and 3 mm (for the eye).
In practical terms, a radiation monitoring instrument calibrated for this quantity gives us an indication of the equivalent dose in superficial tissue.
19.2For Individual Monitoring
We have already discussed the use of radiation monitoring instruments in Module 2.4. In this module we are more concerned with methods used to monitor the radiation dose to people. This type of monitoring is often known as personal dosimetry and for this type of monitoring, a different operational quantity known as personal dose equivalent is defined.
19.2.1Personal dose equivalent
Personal dose equivalent (symbol Hp(d)) is defined as the dose equivalent in soft tissue below a specified point on the body at a depth d mm. Depending on the type of incident radiation, the depth can be taken as 0.07 mm for skin or 3 mm for the eye for weakly penetrating radiation, and as 10 mm for the whole body exposed to strongly penetrating radiation (see Figure 2).
Figure 35
Defined Depths for Measurement of Personal Dose Equivalent
In practice, measurements of Hp (10) and Hp (0.07) are achieved by placing a detector at the body surface covered with an appropriate thickness of tissue-equivalent material. This method of monitoring will be further explained in Section 4.2.
19.3Operational Dose Limits
As you have already learnt in Module 2.1 Principles of Radiation Protection, occupational dose limits as defined in ICRP 60 are given in terms of equivalent and effective doses. In practice, we know that these quantities are not actually measurable. However, as measured operational quantities can be taken as reasonable approximations to equivalent and effective doses, we can also apply these occupational dose limits to measurable operational quantities as well as theoretical quantities (see Table 5).
Table 19
Dose Limits as Recommended in ICRP 60
Theoretical Quantity | Operational Quantity | Annual Occupational Dose Limit |
Effective dose | Personal dose equivalent to whole body Hp (10) | 20 mSv per year (averaged over defined periods of 5 years) |
Equivalent dose in: | Personal dose equivalent in: | |
the lens of the eye | the lens of the eye Hp (3) | 150 mSv |
the skin | the skin Hp (0.07) | 500 mSv |
SELF-CHECK 2
Why are operational quantities necessary?
Fill in the gaps with a suitable word or phrase:
___________ _____ __________ (symbol _____) is the operational quantity used to define doses to individuals.
___________ _____ __________ (symbol _____) is the operational quantity used to calibrate most radiation monitoring instruments. This quantity gives a reasonable approximation to effective dose.
___________ _____ __________ (symbol _____) is the operational quantity used in area monitoring to give a reading of dose to superficial tissue.
For operational quantities, what penetration depths are used for:
strongly penetrating radiation?
weakly penetrating radiation to skin?
weakly penetrating radiation to the eye?
Now check your answers with the model answers in your workbook.
20.INTRODUCTION TO PERSONAL DOSIMETRY
The IAEA Basic Safety Standards (BSS) recommend that workers in controlled areas should be individually monitored where it is appropriate, adequate and feasible. Where it is not, the exposure of a worker should be assessed on the results obtained from area (workplace) monitoring, and from the location and duration of exposure of the worker. Workplace monitoring has already been discussed in detail in Module 2.4, Use of Radiation Monitoring Instruments. In the following sections of this module, you will learn how doses to individual people are determined. In these sections, the term personal dosimetry is used to describe the measurement of dose to individuals.
Note that personal dosimetry can be divided into two categories:
external dosimetry (i.e. the measurement of dose due to sources outside the body); and
internal dosimetry (i.e. measurement of dose due to sources inside the body).
External dosimetry methods are discussed in Section 4 of this module and internal dosimetry methods are covered in Section 5.
21.METHODS OF EXTERNAL DOSIMETRY
Two methods are used for external dosimetry and these are active and passive monitoring.
21.1Active Monitoring
Active monitoring involves the use of an instrument or device which will react to radiation received by the wearer and give an immediate reading of the whole body personal dose equivalent (Hp(10)). Dosimeters of this type are commonly electronic (electronic dosimeters) and consist of a G-M or semiconductor detector (to detect x-rays and gamma radiation) with associated electronic circuitry, display and battery (see Figure 3).
Figure 36
Example of an Electronic Dosimeter
Electronic dosimeters are relatively inexpensive and are usually quite rugged. They also have the advantage of being easily reset, meaning that they can be reused at different times by different individuals.
Some sophisticated instruments give the dose rate at the time of reading as well as the total accumulated dose. These instruments are very useful for monitoring external exposure in areas where dose rates are high or unknown. Other electronic dosimeters can also display the dose information in real time and then store it so that the information can be transferred to a dose record system at a later date. These are useful for recording doses in local areas and for comparison with passive dosimeter results.
A quartz fibre electroscope (QFE) is another example of an active dosimeter. Although this type of dosimeter is gradually being replaced electronic dosimeters, you may still see some in the workplace. QFE’s consists of a small ionization chamber in which incident radiation affects the overall charge. This change in charge then deflects the quartz fibre on a calibrated display in the eyepiece lens (see Figure 4).
The major disadvantage of this type of dosimeter is that they are easily damaged if dropped or roughly handled. They still have the advantage, however, of being easily reset and so can be worn by different workers.
Calibrated Scale
in Eyepiece
Figure 37
A Quartz Fibre Electroscope
Other active dosimeters exist for neutron dosimetry such as superheated drop (bubble) detectors. Bubble detectors contain microscopic liquid drops suspended in a gel-like material. Incoming neutrons transfer enough energy to the liquid drops to make them suddenly boil and change into a bubble. These bubbles are visible to the eye and can be counted (see Figure 5).
Figure 38
Bubble Detectors Before (left) and After (right) Neutron Exposure
The actual neutron dose is proportional to the density of bubbles, and these remain fixed in the material until the dosimeter is reset. Once again, these dosimeters are quite fragile and should not be roughly handled.
Active dosimeters are usually small enough to be worn clipped to the clothing on the chest of the wearer (see Figure 6). They are also sometimes worn at the waist or on the collar. In many workplace situations, active dosimeters are worn in addition to passive dosimeters to provide both an immediate estimate of dose as well as more accurate dose information.
Figure 39
Correct Positioning of Active Dosimeters
SELF-CHECK 3
What do the Basic Safety Standards recommend for monitoring of radiation workers?
If individual monitoring is not feasible, how should doses to individuals be assessed?
Fill in the gaps with an appropriate word or phrase:
___________ dosimetry is the measurement of dose due to sources inside the body.
___________ monitoring provides an immediate reading of the accumulated dose.
___________ dosimetry is the measurement of dose due to sources outside the body.
___________ monitoring does not give immediate readings of accumulated dose. Instead, the dosimeter has to be worn for a period of time and then processed.
Name two types of active dosimeters.
Now check your answers with the model answers in your workbook.
21.2Passive Monitoring
Passive monitoring involves the storage of dose information in such a way that the monitor has to be removed from the wearer and processed to obtain individual dose results. This means that these monitors do not give immediate readings of dose or dose rate, but instead they retain dose information until the relevant signal is read at the end of the wearing period.
One advantage of passive dosimeters is that they can record dose information in a stable form which will not be lost easily. Another advantage is that the personal dose equivalent values of Hp(10) (whole body), Hp(0.07) (skin) and Hp(3) (eyes) can be measured with passive dosimeters whereas with active dosimeters, only Hp(10) is usually measured.
Some examples of passive dosimeters are as follows:
film dosimeters for personal dosimetry;
thermoluminescent dosimeters (TLDs) for personal and environmental dosimetry; and
nuclear emulsion or track etch dosimeters for neutron dosimetry.
21.2.1Film dosimeters
Film dosimeters (commonly known as film badges) consist of a piece of photographic film in a holder. The holder is fitted with a range of filters which allows us to distinguish between beta, x-ray, gamma and thermal neutron radiations and also allows determination of the personal dose equivalent for Hp(10), Hp(0.07) and Hp(3) (see Figure 7).
Figure 40
A Standard Film Badge
By determining the degree of blackening (optical density) on the developed film and comparing it with calibrated films that have been exposed to known doses, it is possible to ascertain both the total dose received by the wearer and also the contribution to total dose by each type of radiation. The various filters used in film badges to ascertain whole body Hp(10), skin Hp(0.07) and eye Hp(3) doses are shown in Table 5.
Table 20
Application of the Standard Film Badge Filters
Filter | Material | Application |
1 | Open Window | For admission of beta particles and very soft x-rays |
2 | Plastic (50 mg cm-2) | For quantitative determination of and x-ray dose and energy |
3 | Plastic (300 mg cm-2) | For quantitative determination of and x-ray dose and energy |
4 | Dural (0.040”) | For quantitative determination of and x-ray dose and energy |
6 | Sn + Pb (0.028” 0.012”) | For quantitative determination of and x-ray dose and energy |
5 | Cd + Pb (0.028” 0.012”) | For detection of slow neutrons by the gamma rays emitted subsequent to their capture by cadmium |
7 | Lead (0.012”) | Edge shielding to prevent overlap of film blackening due to angled incident radiation |
8 | Indium (0.4 g) | For monitoring after large accidental neutron radiation exposure |
Film badges are particularly useful for measuring doses to individuals as information on both the type and energy of the radiation received can often be determined. Also, the presence of surface contamination on the holder can be ascertained by an irregular darkening of the film. Another advantage of this type of dosimeter is that the films can be kept as a permanent record of an individual’s dose. This means that they can be reassessed at a later date if necessary.
Undesirable features of the film badge are their adverse effects to light and heat. They also require dark room facilities (with associated development chemicals) and significant manual handling during assessment. Another major disadvantage is that the films cannot be reused and, although they are cheap, they are in limited supply.
21.2.2Thermoluminescent dosimeters (TLDs)
The ability of thermoluminescent (TL) materials to detect ionizing radiation has already been discussed in Module 1.5 Methods of Radiation Detection. If you remember from this module, the electrons in thermoluminescent materials are raised to forbidden bands when energy from incident radiation is absorbed. These electrons are then trapped at these higher levels until the material undergoes a specific heating pattern and the energy is released as light. This light can then be converted into an electrical signal which can be related to the amount of incident radiation.
Various thermoluminescent materials are commercially available depending on the application. Lithium based thermoluminescent dosimeters (TLDs) are preferable for personal dosimetry because of their tissue-equivalence. Calcium based TLDs are more useful for environmental monitoring due to their high sensitivity. The most common types of TL materials are as follows:
lithium fluoride doped with manganese (LiF:Mn) for personal dosimetry;
lithium borate doped with manganese (Li2B4O7:Mn) for high dose range dosimetry;
calcium fluoride doped with dyprosium (CaF2:Dy) for environmental monitoring; and
calcium sulphate doped with dyprosium (CaSO4:Dy) also for environmental monitoring.
Thermoluminescent materials are available in many different forms (e.g. powder, hot pressed chips, pellets, impregnated teflon disks). A usual TLD consists of a card containing the TL material and a holder with filters of various thicknesses and materials (usually copper and plastics) to measure the values of deep dose, skin dose and eye dose. An example of a LiF:Mn TLD badge is shown in Figure 8.
Figure 41
An Example of a LiF:Mn TLD Badge
The read-out instrument (reader) for TLDs consists of a method to heat the TLD material, a device to convert the light output to an electrical pulse and other associated electronics. The heating process can consist of an electrically heated tray or probe, a hot gas or a radiofrequency radiation heater. In order to reduce non-ionizing radiation induced TL effects, the dosimeters are heated in an inert gas during read-out.
When the TL material is heated by a specific heat pattern, a light signal is produced. This light signal is amplified and converted to an electrical signal using a photomultiplier (PM) tube (see Module 1.5 Methods of Radiation detection). The PM tube output is seen as a series of pulses which are fed to a data handling system. The resulting read-out consists of a graph of light emitted against time of heating. This is commonly known as a glow curve. Glow curves are characteristic of the TL material, the heating profile and the readout temperature. Figure 9 shows a typical glow curve of a LiF:Mn TLD after irradiation to 1 Sv.
Figure 42
Typical Glow Curve of LiF:Mn after Irradiation to 1 Sv
By using parameters determined by calibration TLDs, it is then possible to determine the actual dose received by the wearer and in some cases, the type and energy of the radiation can also be determined.
One advantage of TLDs is their small size (only milligram quantities of TL material is needed). This means that they are particularly useful as extremity dosimeters when some parts of the body are more exposed than others (see Figure 10). Another advantage of TLDs is their ability to be reused.
Figure 43
Wrist, Head and Finger TLDs
The main disadvantage of TLDs is that dose information is usually only given once during heating and cannot be repeated by subsequent heating. They are also subject to fading (i.e. the loss of dose information due to temperature or light effects). Post-irradiation heating as part of the read-out cycle can reduce the thermal fading and storing the TLDs in a light-tight container can reduce the light effects. However, fading of the image can limit the assessment period and lengthy storage prior to read-out is not recommended for TLD materials.
21.2.3Passive dosimeters for neutron monitoring
Neutron dosimetry is very difficult to undertake due to the complex interaction mechanisms neutrons have with tissue (see Module 1.4 Interaction of Radiation with Matter) and due to the range of radiation weighting factors over all neutron energies. Therefore, to ensure that the dosimeter is measuring correctly, it is important that neutron dosimeters are calibrated in the energy range of the neutrons to be monitored.
One option for neutron dosimetry is the use of TLDs as they can be used to measure neutron radiation of all energies. However, it is important to know the expected energies as the actual response varies greatly over the thermal to 20 MeV energy range.
Other dosimeters for neutron monitoring include nuclear emulsions painted on photographic films (nuclear emulsion dosimeters). These dosimeters record the tracks made by recoil protons that are formed when incident neutrons interact with the base of the emulsion. These tracks can be visibly seen when the film is developed (see Figure 11). By counting the number of tracks under a microscope, the neutron dose can then be determined.
Figure 44
A Nuclear Emulsion Dosimeter and Processed Film
The disadvantages of nuclear emulsion dosimeters are their poor response in the range below 700 keV and their tendency to fade due to their sensitivity to light and heat.
A more common type of neutron dosimeter is the solid state neutron track dosimeter (SSTND). These dosimeters are comprised of a plastic material (such as polyallyl diglycol carbonate (PADC)) held in a polypropylene holder. If suitable filters are used, this type of dosimeter can detect both thermal and fast neutrons with a reasonably uniform energy response.
The basic principle of SSTNDs is that when the detector is in the holder, incident neutrons interact with the holder and its various filters to produce protons. These protons then directly damage the surface of the detector and when the detector is processed, the tracks are etched as visible pits (see Figure 12). By counting these pits under a microscope, the dose can be determined.
Figure 45
A Neutron Track Dosimeter and Processed PADC Insert
The main advantage of SSNTDs is that they do not have serious fading problems and can therefore be worn for 3 months or longer.
21.3Energy Response And Angular Response
When determining personal dose from both active and passive dosimeters, it is important to consider the response of the dosimeter to a wide range of energies and angles. As you have already learnt in the previous sections, some dosimeters have limitations on their energy response and you should be aware of these before you attempt to use them to measure doses.
In both film and TLD badges, the response of the dosimeter to different energies is determined by the use of filters. In many cases, TLD materials such as LiF are chosen for personal dosimetry due to their ability to respond in a similar way to tissue for a large range of radiation energies. However the angular (directional) response of TLDs to radiation is dependent on the type and thickness of the TL material and the filters in the dosimeter holder and if high Z materials are used, the TLD will have a poor angular response to photons.
SELF-CHECK 4
Now see how much you have understood by answering the following questions in your workbook.
Give two advantages of passive dosimeters over active dosimeters.
Why are filters used in passive dosimeters?
How is dose determined using film dosimeters?
How is dose determined using thermoluminescent dosimeters?
Why are lithium based TLDs often used for personal dosimetry?
Why are calcium based TLDs often used for environmental dosimetry?
Fill in the following table:
Film Dosimeters
Thermoluminescent Dosimeters
Advantages
Disadvantages
Advantages
Disadvantages
1.
1.
1.
1.
2.
2.
2.
2.
3.
3.
Name two types of dosimeters used to measure neutron doses.
Now check your answers with the model answers in your workbook.
22.METHODS OF INTERNAL DOSIMETRY
Following an intake of radioactive material into the body (or to confirm no intakes have occurred), an assessment of internal dose is required. The three types of measurement performed to achieve the assessment of internal dose are as follows:
in-vivo counting;
bio-assay; and
air sampling.
22.1In-vivo Counting
In-vivo counting is the term used to describe the detection of radiation emanating from within the body using detectors situated in contact or as close as possible to the body surfaces. This technique is sometimes known as whole body or part bodycounting.
Whole body counters consist of an array of semiconductor or crystal detectors which are used to detect the x-ray and gamma spectra from internal contaminants. These detectors are operated with the individual seated or lying in a shielded location to reduce background radiation (see Figure 13).
Figure 46
Whole Body Counting
From the monitoring results, a measurement of radioactivity content (in Bq) of each radionuclide in the body can be achieved. From these results, it is possible to determine whether an intake has occurred and what the magnitude of this intake is.
For part body counting, a small detector arrangement is placed as close as possible to the organ of interest. The most common organs assessed are the lung (to measure actinide activity) and the thyroid counting (to measure radioactive iodine content). Figure 14 shows the measurement of radioiodine uptake in the thyroid gland.
Figure 47
Part Body Counting of the Thyroid Gland
The important factors that influence the detection efficiency are the geometry of the counting arrangement (location of the individual to the detector) and the physical characteristics of the individual being counted.
In order to achieve suitable lower limits of detection, routine counting times may be several minutes (up to 40 minutes) depending on the comfort and convenience of persons to be counted. Calibration for the radionuclides of interest is achieved using phantoms doped with known amounts of radioactivity.
It is possible to calibrate some in-vivo counters so that the bremsstrahlung x-rays from energetic pure beta emitters such as P-32 can also be assessed.
22.2Bio-assay
Bio-assay sampling is the taking of biological samples from the human body and analyzing the samples for radioactivity in order to perform an internal dose assessment. The most common examples are tritium in urine analysis, and plutonium and uranium in urine and faeces analysis. Liquid scintillation and alpha spectrometry are two analytical techniques employed. Other types of sampling which are complex and not very accurate are chromosome aberrations in blood samples for high exposures (above 50 mSv) and analysis of nose blow samples for airborne intakes. These latter two are used in accident dosimetry.
22.3Air Sampling
Where airborne levels of radioactivity present an internal hazard, such as alpha emitters, the levels in the work environment can be assessed. Using occupancy times for individuals or groups of workers, individual dose assessment may be achieved from routine air sampling results (see Module 2.4 Use of Radiation Monitoring Instruments). More accurate dosimetry can be achieved by the use of personal air samplers (PAS) (see Figure 15).
Figure 48
Worker Wearing a Personal Air Sampler
Personal Air Samplers consist of a battery powered pump which draws air through a small filter. The air intake unit is worn as close as possible to the nose and mouth to simulate the individual’s actual intake. At the end of the working period, the filter is assessed for contaminants and the activity concentrations (in Bq m-3) are calculated using the known flow rates (see Module 2.4 Use of Radiation Monitoring Instruments). Note that the filter papers will need to be counted twice to account for radon decay progeny.
PASs are usually used for assessment of alpha particles in the workplace. They can be used together with In-vivo counting to improve the overall accuracy of the dosimetry assessment. Other passive devices (such as track etch detectors) are available to assess the exposure to airborne contamination such as radon progeny.
22.4Calculations of Committed Dose Equivalent
Calculations of committed dose equivalent from the internal measurement techniques described in Sections 5.1, 5.2 and 5.3 can be performed using the models described by ICRP Report 54. These models describe the behaviour of radionuclides in the body for the purposes of measuring activity in the body, or that excreted from the body. By using these models, the values for the intake of radioactivity can be assessed and dose conversion factors (as detailed in the IAEA Basic Safety Standards) can be applied to calculate committed dose equivalents.
23.PERSONAL MONITORING PROGRAMS AND RECORD KEEPING
To achieve effective exposure control in radiation protection, a personal monitoring program is recommended. This may include several (or just one) of the dosimetry assessments described in this module. The requirements of the workplace will determine the actual size of this program. In addition to the regulatory and recommended requirements for dosimetry, there may be a need for reassurance monitoring (i.e. both radiation workers and non-radiation workers may want their doses monitored to reassure themselves that they are low).
The IAEA Basic Safety Standards recommend that exposure records be maintained for persons occupationally exposed to radiation. This includes all assessments performed by the dosimetry service. As the dosimetry service may be contracted from another organization, only copies of the records may be kept at the workplace.
Dosimetry records can be analyzed for compliance with dose limits and local dose constraints. They can also be used to monitor trends in individual and collective doses. Radiation workers should have access to their own records at all times, and dose summaries for individuals are usually provided for radiation workers when they transfer from one place of employment to another.
SELF CHECK 5
Now see how much you have understood by answering the following questions in your workbook:
Fill in the gaps with a suitable word or phrase:
________ sampling involves taking biological samples from the body (e.g. urine and faeces) and analyzing the samples for radioactive content.
________ counting involves the detection of radiation being emitted from the body by use of detectors situated as close as possible to the body surfaces.
_________ ________ __________ are used to assess the amount of radioactive material taken into the body by the inhalation pathway.
What are the main uses of dosimetry records?
Why may some non-radiation workers want to be monitored for dose?
Now check your answers with the model answers in your workbook.
KEY POINTS
Fluence, exposure and kerma are primary physical quantities known as radiometric quantities.
Dosimetric quantities are absorbed dose, equivalent dose and effective dose.
Fluence () is the number of particles or photons passing through a unit area.
Exposure (X) is the amount of ionization produced by photons in air.
Kerma (K) is a measure of the amount of kinetic energy of charged particles produced in an absorbing medium by uncharged radiations.
Absorbed dose (D) is a measure of the energy deposited in any medium by any type of radiation. The old unit of absorbed dose is the rad. The SI unit is the gray. 1 Gy = 100 rad.
Equivalent dose (H) is a measure of the biological effect of a particular type of radiation on an organ or tissue. The old unit of equivalent dose is the rem. The SI unit is the sievert. 1 Sv = 100 rem.
Effective dose (E) is a measure of a particular type of radiation on a particular organ or tissue. The old unit of effective dose is the rem. The SI unit is the sievert. 1 Sv = 100 rem.
Operational quantities are defined by the ICRU to provide reasonable approximations to equivalent and effective doses.
Ambient dose equivalent H*(d) is the operational quantity used to calibrate most radiation monitoring instruments. The reading gives a good approximation to effective dose.
Directional dose equivalent H’(d) is the operational quantity used to calibrate radiation monitoring instruments where an estimate of the equivalent dose in superficial tissue is required.
Personal dose equivalent Hp(d) is the operational quantity used to assess the dose to an individual.
For operational quantities, d is taken as 0.07 mm (skin), 3 mm (eye) and 10mm (whole body).
Personal dosimetry is the term used to describe the measurement of dose to individuals.
External dosimetry is the measurement of dose due to sources outside the body.
Internal dosimetry is the measurement of dose due to sources inside the body.
External dosimetry can be performed using active or passive techniques.
Active monitors give a direct reading of external dose.
Examples of active monitors are electronic dosimeters, QFEs and neutron bubble dosimeters.
Passive monitors need to be processed in some way before an external dose reading can be obtained.
Passive techniques include film, thermoluminescent and nuclear emulsion and track etch dosimetry.
Film dosimeters consist of a piece of photographic film in a holder. Filters are used to distinguish between the types and energies of the incident radiation.
The advantages of film dosimeters are that they can be used to provide information on the type and energy of incident radiation, they can be kept as a permanent record of individual dose and are cheap.
The disadvantages of film dosimeters is that they are subject to light and heat effects, they require dark room facilities and significant manual handling and they cannot be reused.
Thermoluminescent dosimeters (TLDs) consist of a material which, when heated, emit light in proportion to the amount of incident ionizing radiation.
The advantages of TLDs are their small size and their ability to be reused.
The disadvantages of TLDs are that information can only be read once and they are subject to fading.
Nuclear emulsion and solid state neutron track dosimeters are used for neutron dosimetry.
Nuclear emulsion dosimeters show tracks when processed. Solid state neutron track detectors show pits.
When using external monitoring dosimeters you should be aware their energy and angular response.
Internal dosimetry can be achieved using in-vivo counting, bio-assay and personal air sampling.
In-vivo counting is the detection of radiation emanating from within the body using detectors situated in contact or as close as possible to the body surfaces
Bio-assay sampling is the taking of biological samples from the human body and analyzing the samples for radioactivity.
Personal air samplers can be used to assess activity intake from airborne contamination.
Dose records can be used to analyze compliance with dose limits and dose constraints, and to monitor trends in individual and collective dose.
FINAL ASSIGNMENT
This assignment is to be completed under test conditions, so spend some time now studying this module. Then contact your supervisor to arrange a suitable time to complete the assignment.
GLOSSARY OF TERMS
Absorbed dose (D) | A measure of the energy deposited in any medium by any type of radiation. Measured in gray. |
Active monitoring | Real-time monitoring of dose. |
Air Kerma | A measure of the kinetic energy of charged particles produced in air by uncharged radiations. |
Ambient dose equivalent H*(d) | The operational quantity used to calibrate most radiation monitoring instruments for a reasonable approximation to effective dose. |
Bioassay sampling | The taking of biological samples from the human body and analyzing the samples for radioactivity. |
Committed dose | The dose to an organ (absorbed or equivalent dose) or whole body (effective dose) resulting from an intake of radioactive material, calculated over 50 years for adults (70 years for children). |
Directional dose equivalent H’(d) | The operational quantity used to calibrate radiation monitoring instruments for a reasonable approximation to equivalent dose to superficial tissue. |
Dosimetric quantity | A quantity used to measure the effects produced by a radiation field. |
Effective dose (E) | A measure of the effect of radiation on the whole body. It is calculated by multiplying the equivalent dose to an organ or tissue by the tissue weighting factor (wT). Measured in sieverts. |
Equivalent dose (H) | A measure of the effect of a particular type of radiation on a specific organ or tissue. It is calculated by multiplying the absorbed dose to an organ or tissue by the radiation weighting factor (wR). Measured in sieverts. |
Exposure (X) | The amount of ionization produced in air by photons. |
Fluence () | The number of particles (or photons) passing through unit area. |
In-vivo counting | The detection of radiation emanating from within the body using detectors situated in contact or as close as possible to the body surfaces. |
Kerma (K) | A measure of the kinetic energy of charged particles produced in an absorbing medium by uncharged radiations. |
Passive monitoring | Monitoring of dose by dosimeters which need to be processed after a certain wearing period. |
Personal dose equivalent Hp(d) | The operational quantity used for assessment of equivalent and effective doses. |
Radiation weighting factor (wR) | A dimensionless factor used to take into consideration the different effects of different types of radiation on organs and tissues. |
Radiometric quantity | A quantity used to describe the radiation field. |
Tissue weighting factor (wT) | A factor which considers the differences in probability of cancer and its seriousness for different organs and tissues. |