RADIONUCLIDE

AND
RADIATION PROTECTION
DATA HANDBOOK 2002

D. Delacroix*
J. P. Guerre**
P. Leblanc**
C. Hickman

* Commissariat à l’Energie Atomique, CEA/DAM - Ile de France, France

**Commissariat à l’Energie Atomique, CEA/Saclay, France

ISBN 1 870965 87 6
RADIATION PROTECTION DOSIMETRY Vol. 98 No 1, 2002
Published by Nuclear Technology Publishing
 RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK
2nd Edition (2002)

All rights reserved. No part of this book may be reproduced, stored in a retrieval system or
transmitted in any form or by any means, electronic, electrostatic, magnetic, mechanical, photo-
copying, recording or otherwise, without permission in writing from the publishers.

British Library Cataloguing in Publication Data

A catalogue record of this book is available at the British Library

ISBN 1 870965 87 6
COPYRIGHT  2002 Nuclear Technology Publishing
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Radiation Protection Dosimetry
Vol. 98, No. 1, pp. 5–6 (2002)
Nuclear Technology Publishing

RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK

2nd Edition (2002)

Contents
Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

SCOPE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

CLASSIFICATION OF RADIONUCLIDES . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

PHYSICAL CHARACTERISTICS OF RADIONUCLIDES . . . . . . . . . . . . . . . . . . . . . 10

RADIOLOGICAL CONTROL . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

External exposure risks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

Internal exposure risks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Dose limits for workers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

EXTERNAL EXPOSURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

Assumptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Distant (point source) external exposure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Exposures to a uniformly contaminated surface . . . . . . . . . . . . . . . . . . . . . . . . . 12
External contact exposure (receptacles) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12

SHIELDING OF BETA AND GAMMA EMITTERS . . . . . . . . . . . . . . . . . . . . . . . 12

CONTAMINATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12

Contact exposure due to external skin contamination. . . . . . . . . . . . . . . . . . . . . . . 12

Decay products . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Decay of heavy elements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Derived surface contamination limits (DSCL) . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Determination of removable and fixed contamination values . . . . . . . . . . . . . . . . . . . 14
Contamination control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Detection probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14

5
CONTENTS (continued)

INTERNAL EXPOSURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14

Committed effective dose per unit intake . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14

Annual Limits on Intake (ALI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
The ‘highest dose organ’. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

MAXIMUM RECOMMENDED ACTIVITIES. . . . . . . . . . . . . . . . . . . . . . . . . . . 15

Calculation models . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Dependence of maximum recommended activities on equipment and working areas . . . . . . . . 15
Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

DESCRIPTION OF DATA SHEETS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

GLOSSARY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

TABLE OF RADIONUCLIDES LISTED . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

DATA SHEETS (144) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

APPENDIX – HEAVY ELEMENT DECAY . . . . . . . . . . . . . . . . . . . . . . . . . . . 165

is abstracted or indexed in RADIATION PROTECTION

ABSTRACTS, Chemical Abstracts, CURRENT CONTENTS, Energy Information Abstracts (Cambridge),
EXCERPTA MEDICA (EMBASE), Health and Safety Science Abstracts (Cambridge), INIS ATOMINDEX
(hard copy and CD ROM), INSPEC, Nuclear Energy (Czech Republic), QUEST and Referativmaja Zhurnal.

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Radiation Protection Dosimetry
Vol. 98, No. 1, p. 7 (2002)
Nuclear Technology Publishing

Preface
RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK (2002)

This handbook is an updated and expanded (2nd edition) version of the handbook with the same title published
in 1998. That handbook was in turn based on an earlier French laboratory guidebook A Guide on Radionuclides
and Radioprotection by D. Delacroix, J.P. Guerre, and P. Leblanc, published in 1994 (1). The earlier publication
was very much oriented towards guidance on the handling of radionuclides used in medicine. The present handbook
is much more broadly based in its outlook and application and incorporates updated information to take account
of the most recent ICRP and IAEA recommendations (1–4). The radionuclides listed in the earlier publication were
supplemented by commonly used radionuclides in the nuclear industry and in other areas. Moreover, the main
purpose of this handbook (and its 1998 predecessor) is the provision of data sheets and the models or sources
used to assemble the data, rather than as a radiation protection guide for laboratory users.
This practical handbook of data for handling radioactive materials is intended for radiation protection specialists
as well as all others who use or transport radionuclides. Its publication should satisfy a major need for all health
physics departments and is intended to assist in informing and training personnel in radiation protection. It consists
of an explanatory text followed by specific radiation data sheets for selected radionuclides. Because of the dispari-
ties in the approaches adopted by different countries, it is essential that users also refer to the relevant national
regulations with which they must comply.
The present handbook includes 36 additional radionuclides than the previous edition, giving a total of 144
nuclides. Additional data are included covering dose rates above uniformly contaminated surfaces (infinite plane
source). Some corrections to data in the previous edition have been incorporated. The list of nuclides is not
exhaustive but those included have been selected on the basis of being most commonly used, taking into account
the requirements of users in industry, medicine and research. Finally, account is taken of the need to consider
decay chain products for several heavy elements. To this end, an appendix is provided giving the decay products
and their activities as a function of time (age), together with decay charts for four of the more complex chains.

Directeur Central de la Sécurité

Commissariat à l’Energie Atomique, France

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Radiation Protection Dosimetry
Vol. 98, No. 1, pp. 9–18 (2002)
Nuclear Technology Publishing

RADIONUCLIDE AND RADIATION PROTECTION DATA

HANDBOOK 2nd Edition (2002)
D. Delacroix*, J. P. Guerre**, P. Leblanc** and C. Hickman
*Commissariat à l’Energie Atomique, CEA/DAM - Ile de France, France
**Commissariat à l’Energie Atomique, CEA/SACLAY, France

Abstract — This handbook is a reference source of radionuclide and radiation protection information. Its purpose is to provide
users of radionuclides in medicine, research and industry with consolidated and appropriate information and data to handle and
transport radioactive substances safely. It is mainly intended for users in low and intermediate activity laboratories. Individual
data sheets are provided for a wide range of commonly used radionuclides (144 in total). These radionuclides are classified into
five different groups as a function of risk level, represented by colours red, orange, yellow, green and blue, in descending order
of risk.

INTRODUCTION in the form of data sheets in an easy to use format for

In recent years the need for a compilation of essential
data for commonly used radionuclides, for both practice
and training, has become increasingly apparent.
This handbook contains individual data sheets for a
range of radionuclides and is mainly intended for users
of unsealed radioactive sources in low and intermediate
activity laboratories, industrial applications and trans-
port.
Individual data sheets corresponding to the different
radionuclides give the physical characteristics, reference
transport activities, exemption levels, contamination
derived limits and appropriate detection probes, dose
rates from skin contamination, half and tenth value
shielding thicknesses, external exposure data, dose coef-
ficients for ingestion and inhalation, derived 20 mSv
ALI values, and the highest dose organ. The maximum
activities recommended to be handled on benches, under
fume hoods and in glove boxes are also given. However,
this information is most appropriate in laboratories
handling low and intermediate levels of radioactive
materials. In order to facilitate the user’s understanding,
pictorial illustrations have been employed and data is
presented in tabular form.
It should be noted that the data provided, although
drawn from appropriate recent international recommen-
dations, should in no way be taken to supersede existing
local or national regulations. The data may, of course,
be used to review existing local regulations which may
have become out of date.
The text preceding the data sheets provides the back-
ground, derivation and substantiation for the data given,
enabling users to satisfy any quality assurance arrange-
ments that may be in place.
SCOPE
This handbook provides the most up to date internal
and external dosimetry information and control criteria
144 of the most commonly used radionuclides in medi-
cine, research and industry. It is designed as a ready
reference source of information, gathering together in
one place, in the form of individual data sheets, the most
up to date isotopic and radiation protection data. The
information includes:
䉬 half-life and specific activity,
䉬 main emissions,
䉬 IAEA Basic Safety Standards exemption levels,
䉬 IAEA A1 and A2 transport values,
䉬 external exposure data for a range of geometries,
䉬 surface contamination data, detection and limits,
䉬 shielding information,
䉬 ICRP dose per unit intake data by ingestion and
inhalation,
䉬 20 mSv ALI values and the highest organ dose, and,
䉬 maximum recommended activities in Controlled and
Supervised Areas.
Most of the data provided are relevant to all users.
However, the section and data dealing with maximum
recommended activities are only appropriate to low and
intermediate activity laboratories. These laboratories are
frequently limited to two to three orders of magnitude
higher than the exemption limits by local or national
regulations.
CLASSIFICATION OF RADIONUCLIDES
Radionuclides have been divided in this handbook
into five ‘risk groups’. The classification used is based
on the BSS ‘quantity’ exemption limit values. Exemp-
tion limit values have been chosen for this purpose
because they reflect both internal and external exposure
risks. Each group is associated with a colour (red,
orange, yellow, green and blue successively represent
decreasing levels of risk). The data sheets have been
appropriately coloured providing the reader with a rapid
visual means of appreciating the risk associated with

9
 D. DELACROIX, J. P. GUERRE, P. LEBLANC and C. HICKMAN
particular radionuclides. The five risk groups have been The nature of the main radiation (5)
defined as follows:
␣, ␤, e⫺, X, ␥ radiation and neutron emissions are
Group 1: exemption limit ⱕ 104 Bq (red) given, together with the corresponding energies
Group 2: exemption limit = 105 Bq (orange) expressed in keV, and corresponding percentage emis-
Group 3: exemption limit = 106 Bq (yellow) sions. A maximum of the three most characteristic emis-
Group 4: exemption limit = 107 Bq (green) sions is given for each type of radiation, the criterion
Group 5: exemption limit ⱖ 108 Bq (blue) adopted being the relevance of the emissions from the
radiation protection standpoint. However, in order to
In the rare cases for which exemption levels have not remedy the restrictive effects of this approach (some
been defined (e.g. 11C, a nuclide sometimes used for radionuclides exhibit multiple emissions, e.g. 140La and
medical imaging) a group has been assigned by analogy 152
Eu), the relative percentage emissions not taken into
with other radionuclides of the same type. consideration are nevertheless given.
Attention is drawn to the fact that radioactive sub-
stances are also chemical substances, the handling of
which may involve hazards of non-radiological origin. RADIOLOGICAL CONTROL
Moreover, radioactive substances are often intimately
mixed with chemical products having an aggressive External exposure risks
action on the human body (toxic, mutagenic and car-
cinogenic effects). Chemical hazards should therefore The following modes of exposure are considered.
never be neglected.
Contact
PHYSICAL CHARACTERISTICS OF When handling radioactive materials, the operator
RADIONUCLIDES may touch the receptacle (e.g. beaker, pipette, syringe)
containing the radioactive substance or materials con-
The following characteristics are considered in
taminated with this substance. The radioactive substance
these sheets.
can also become deposited on the skin.
Half-lives expressed in the most appropriate units
(hours, days, years).
Distant source
Specific activities expressed as Bq.g⫺1.
All parts of the operator’s body generally remain dis-
Exemption levels tant from the radioactive substances being handled, even
though certain parts of the body such as the hands and
Exempt activity concentrations (Bq.g⫺1) and exempt forearms occasionally approach these substances during
activities (Bq) are defined in the IAEA Basic Safety handling operations with or without manipulators.
Standards (2) and in the L159 Euratom Directive (3).
These limits can be used by regulatory authorities to
define criteria for exemption against formal registration Immersion in a cloud
of the premises and may also be used to develop clear-
This type of relatively infrequent hazard is encoun-
ance levels for materials leaving the premises. The
tered when handling gaseous radioactive sources. The
exemption levels also apply in the transport regulations.
corresponding risks must be taken into consideration,
The correct use of these limits by users is of utmost
for example, in laboratories using cyclotrons to manu-
importance. Users should refer to the above men-
facture short half-life radionuclides (e.g. 18F, 11C, 123I).
tioned references.

Internal exposure risks

A1 and A2 reference transport activities
A1 and A2 are the maximum activities (expressed in
TBq) that can be transported by A type packages. A1
corresponds to radioactive matter in ‘special form’ and
A2 to the other cases.
In the data sheets, the values correspond to values in
the 1996 edition of The IAEA publication Regulations
for the Safe Transport of Radioactive Materials (4), with
which the international modal transport authorities
(RID, ADR, IMO, ICAO, etc.) are harmonised. Users
seeking further details are referred to the referenced
texts.
The risks arise from three different possible paths into
the human body:
䉬 Inhalation after the dispersion of gases, vapours or
aerosols in the environment;
䉬 Ingestion by contaminated hands or objects through
contact with the mouth;
䉬 Transfer through the skin with or without an associa-
ted wound following contamination of parts of the
body (which have not been sufficiently rapidly
decontaminated) or following simple contact with
highly penetrating radionuclides (e.g. tritium in

10
 RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK 2nd Edition (2002)
tritiated water) or chemically aggressive substances
(acidic solutions, solvents, etc.).
(2,6)
Dose limits for workers
The occupational exposure of any worker should not
exceed the following limits, but may also be subject to
more restrictive limits in appropriate local or national
regulations.
䉬 an effective dose of 100 mSv over a period of five
consecutive years (i.e. 20 mSv per year) averaged
over this period;
䉬 an effective dose of 50 mSv in any single year;
䉬 an equivalent dose to the lens of the eye of 150 mSv
in a year;
䉬 an equivalent dose to the extremities (hands and feet)
or the skin of 500 mSv in a year.
It is noted that the IAEA (2) states that
Compliance with the foregoing requirements for
application of the dose limits on effective dose
shall be determined by one of the following
methods:
(a) by comparing the total effective dose with the
relevant limit, where the total effective dose ET is
calculated according to the following formula:
ET = Hp(d) + ⌺je(g)j,ingestion.Ij,ingestion
+ ⌺je(g)j,inhalation.Ij,inhalation,
where Hp(d) is the personal dose equivalent from
exposure to penetrating radiation during the year.
Note that e(g)j,ingestion and e(g)j,inhalation are the com-
mitted effective dose per unit intake by ingestion
and inhalation for radionuclide j by the group of
age g, and Ij,ingestion and Ij,inhalation are the intakes via
ingestion or inhalation for radionuclide j during the
same period.
(b) by satisfying the following conditions:
Hp(d)/DL + ⌺j(Ij,ingestion/Ij,ingestion,L)
+ ⌺j(Ij,inhalation/Ij,inhalation,L) ⱕ 1
where DL is the relevant dose limit on effective
dose, and Ij,ingestion,L and Ij,inhalation,L. are the annual
limits on intake (ALI) via ingestion or inhalation
of radionuclide j.
(c) by any other approved method.
Note that the symbols used in the quote are consistent
with those used in this handbook but not the original
IAEA document. The above quantities are briefly
explained in Schedule II of Reference 2.
11
EXTERNAL EXPOSURE
Assumptions
X ray, ␥, ␤, e⫺ and neutron emissions lead to external
exposures depending on the nature and energies of the
corresponding radiation as well as the packaging and
geometry of the source. Depending on the particular
case being studied, superficial exposures (or skin
exposures) defined at a depth of 7 mg.cm⫺2 or deep
body exposures (7) are taken into consideration.
Various handling postures and situations commonly
encountered in laboratories are considered. Calculations
have been performed for unique values of source or sol-
ution activity; in this way a direct comparison between
the values obtained under different circumstances can
be made. A nominal activity of 1 MBq has been adopted
for external exposures, exposures resulting from con-
tacts with receptacles and exposures to distant sources.
A nominal value of 1 kBq has been adopted for the case
of skin contamination due to droplets and 1 kBq.cm⫺2
for uniform skin contamination. Exposures due to
an infinite and uniformly contaminated surface at
1 MBq.cm−2 are also considered. Data are provided for
distances of 10 cm and 1 m from the contaminated sur-
face for beta and photon radiation for the skin and deep
tissue. The quantity adopted for all geometries for tabu-
lated data is dose equivalent, expressed in mSv.h⫺1
(millisievert per hour).
The handling postures adopted in this handbook for
some operations with radionuclides in the form of un-
sealed sources may not actually represent what is done
in practice (e.g. use of a syringe or beaker). However,
the user, by analogy, can transform the values indicated
into those corresponding to other receptacles of similar
dimensions, on the basis that the situations shown are
reasonably typical.
The following codes have been used for the calcu-
lations:
䉬 Microshield Version 4.10 has been used for ␥ and
X ray calculations (Grove Engineering, 15215 Shady
Grove Road, Rockville, USA, 1996)
䉬 Varskin mod 2 for ␤ radiation and Varskin mod 2
modified for monoenergetic electrons (J.S. Durham,
Pacific Northwest Laboratory, PO Box 999, Rich-
land, Washington 99352, USA).
Distant (point source) external exposure
The cases of a point source at a distance of 30 cm
(average length of forearm) in air and a ‘penicillin’ type
vial at a distance of 1 m in air (8) are considered success-
ively. In the latter case, the source is represented by a
cylinder with a density of 1 g.cm⫺3, 2.3 cm in diameter
and 2.5 cm high enclosed in a 1.5 mm thick glass
(density 2.7 g.cm⫺3) envelope.
In the case of a point source at 30 cm, the deep or
whole-body dose equivalent due to X and ␥ ray compo-
 D. DELACROIX, J. P. GUERRE, P. LEBLANC and C. HICKMAN
nents is distinguished from the superficial or skin dose
equivalent due to ␤ and e⫺ components. This is done
in order to draw the operator’s attention to the fact that
the superficial dose equivalent can be considerably
reduced by interposing a screen with a thickness
equivalent to the maximum range of the ␤ and e⫺
components.
A deep dose equivalent is given for a vial at 1 m (this
corresponds to the distance between the operator and
the bench or table).
Exposures to a uniformly contaminated surface
Exposures due to a uniformly contaminated source
(floors) are considered. The contributions due to beta
radiation and photons are considered separately for dis-
tances of 10 cm and 1 m from an infinitely and uni-
formly contaminated surface. This separation enables
users to make appropriate decisions as to what measure-
ment equipment should be used. Pure beta emitters
generally cannot be detected with gamma detectors.
Dose rates at 10 cm and 1 m are often similar because
the increased distance is compensated by the
increased solid angle. Data is quoted for the dose
equivalent at depths representing the skin and deep
tissue respectively.
External contact exposure (receptacles)
The cases of a 50 cm3 beaker containing 20 cm3 of
solution and a 5 cm3 syringe containing 2.5 cm3 of sol-
ution are considered. The beaker is represented by a cyl-
inder with a density of 1 g.cm⫺3, 4 cm in diameter,
1.6 cm high enclosed in a 2 mm thick glass (density
2.7 g.cm⫺3) envelope.
The syringe is represented by a cylinder with a den-
sity of 1 g.cm⫺3, 1.2 cm in diameter, 2.2 cm high
enclosed in a 1 mm thick plastic (density 1 g.cm⫺3)
envelope.
In both cases dose equivalents have been calculated
under 7 mg.cm⫺2 at the level of the solution (an arrow
indicates the position taken into consideration) (8).
The position indicated corresponds to the maximum
dose equivalent to which an operator can be exposed
when manipulating these receptacles. Attention is drawn
to the fact that these drawings, for pedagogical reasons,
show the operator’s hands and fingers as far away from
the source as possible.
The dose equivalents depicted take both ␤ and ␥
components into consideration. It should, however, be
noted that in the case of a beaker (2 mm thick glass), ␤
components (other than those emitted by radionuclides
such as 42K, 90Y and 144Pr) can be neglected. In the case
of a syringe (1 mm thick plastic), the ␤ contribution can
be highly significant (e.g. 24 mSv.h⫺1 for 1 MBq 32P).
Note that good agreement is observed between the
values quoted here and those found in the literature (9–12).
␤ ray absorption in shielding gives rise to bremsstrah-
12
lung (X rays). With high activity sources bremsstrah-
lung radiation can make a significant contribution to
dose. Attention is drawn to this in the data sheets. It is
for this reason that ’Brem. Rad.’ is indicated on data
sheets corresponding to pure ␤ emitters (14C, 35S, 33P,
36
Cl and 45Ca) for which the calculated dose rates
behind shielding are very low or even zero. These radio-
nuclides are very much used in laboratories.
SHIELDING OF BETA AND GAMMA EMITTERS
The range of betas and electrons and the attenuation
of X and ␥ rays in shielding materials depends on the
energies of the incident radiation and the nature of the
shielding material.
Total absorption thicknesses have been determined
for ␤ and e⫺ radiation in glass and plastic (13); these
materials are those most commonly used for this pur-
pose. In the case of ␥ and X rays, the first half-value and
tenth-value thicknesses of lead and steel (attenuating the
incident radiation by a factor of 2 and 10 respectively)
are given.
Attention is drawn to the fact that some radionuclides
simultaneously emit significant low and high energy
components for which first half-value and tenth-value
thicknesses may be considerably less than second half-
value and tenth-value thicknesses. 123I is an example but
the data provided here do not cover this situation.
CONTAMINATION
Contact exposure due to external skin
contamination
Two situations have been considered to illustrate
body contamination. Firstly, exposure due to an exten-
sive uniformly spread out contamination of the
skin (9,14,15) is considered and secondly, the projection of
a 0.05 cm3 droplet of a radioactive substance. The drop-
let is represented by a cylinder with a density of
1 g.cm⫺3, a cross sectional area of 1 cm2 and a height
of 0.5 mm (8).
Dose equivalent values have been calculated for an
average 70 ␮m basal layer depth. At this depth the main
component of the dose resulting from superficial con-
tamination of the skin is due to ␤ rays and electrons
from the radionuclide; the ␥ contribution to the dose is
generally just a few per cent. Comparison between the
values due to a uniform (infinitely thin) deposit and
those due to a droplet highlights the effects of ␤ attenu-
ation in tissue. It is assumed here that penetration of the
contamination in the skin can be neglected.
Decay products
Decaying radionuclides are generally treated as
follows:
 RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK 2nd Edition (2002)
䉬 radionuclides (parent–progeny) couples are assumed
to be in equilibrium;
䉬 calculations are performed for a nominal activity of
the parent nuclide (e.g. 1 kBq.cm⫺2 for uniform
skin contamination);
䉬 parent–progeny radionuclide decay schemes are
normally covered in a single sheet, but when physi-
cal separation of the constituents is possible (e.g. by
elution), progeny products are treated in individual
sheets. The 99Mo–99mTc couple is an example of this.
The reader will find both 99Mo–99mTc and 99mTc
sheets.
Decay of heavy elements
In the case of heavy element decay chains (e.g. lead,
radium, uranium, plutonium and americium), where the
parent and progeny are not necessarily in equilibrium
(e.g. after chemical separation or extraction of an
element) the respective activities of each of the progeny
in the chain will depend upon the age of the sample. It
is not possible to cover all situations likely to be
encountered but the Appendix to this handbook includes
selected major heavy element decay chains and the
activities of respective progeny in the chain are given
as a fraction of the parent activity as a function of time
(age since separation) for 0.1 day, 1 day, 10 days, 100
days, 1 year, 10 years and 100 years. The parent radio-
nuclides for which this information is provided are
marked ‘!!’ in the main data sheets, including an indi-
cation of the first and last elements within the chains.
A similar approach can be adopted if data on natural
uranium or re-constituted ‘natural’ uranium are required
by taking into account the isotopic composition.
The data in the Appendix are derived using RadDecay
version 1.13 (16).
Derived surface contamination limits
The derived surface contamination limit (DSCL) is a
non- regulatory quantity enabling exposure risks due to
removable and/or fixed surface contamination to be
quantified. Exposure to the DSCL leads to a dose which
does not exceed the maximum annual occupational
exposure limit (corresponding to 2000 working hours).
A model is used to determine the DSCL values corre-
sponding to the different radionuclides dealt with (17).
This model takes different modes of exposure and trans-
fer parameters into consideration. These data are given
for completeness and the values do not supersede limits
imposed by regulations, which are invariably much
lower.
Occupational exposures may result from:
䉬 transfer of surface contamination to the atmosphere
leading to internal exposure through inhalation
䉬 transfer of surface contamination to the organism
through ingestion
13
䉬 transfer of surface contamination to the skin leading
to external extremity exposures
䉬 whole-body exposure due to surface contamination.
The DSCL is defined by the following equation:
1/DSCL = 1/Asatm + 1/Asingestion
+ 1/Asskin + 1/Assurf
where Asj is the activity per unit surface area of the
contaminated zone leading to annual limits due to each
of the four modes of exposure (considered separately).
Limits of 20 mSv.y⫺1 and 500 mSv.y⫺1 are considered
for whole body external exposure and skin exposure,
respectively. The most restrictive ALIinhalation and
ALIingestion values calculated for 20 mSv.y⫺1 are used in
the following derivations of surface activity for limiting
internal contamination.
Calculation of Asatm
Asatm is the value of the activity per unit surface area
of the contaminated zone which leads to an ALIinhalation
dose with an atmospheric re-suspension factor, Tatm, of
10-4 m⫺1 and an annual occupational exposure of 2000 h
with a respiratory volume rate, R, of 1.2 m3.h⫺1.
Asatm (Bq.cm⫺2) is given by the following equation:
Asatm = ALIinhalation/(Tatm × 2000 R × 104)
Calculation of Asingestion
Asingestion is the value of the activity per unit surface
area of the contaminated zone which leads to an
ALIingestion dose with an organ transfer factor, Tingestion,
of 1 cm2.h⫺1 and an annual occupational exposure of
2000 h. This component may simulate, for example, the
risk due to a chronic exposure at a working post.
Asingestion (Bq.cm⫺2) is given by the following
equation:
Asingestion = ALIingestion/(2000 Tingestion)
Calculation of Asskin
Asskin is the value of the activity per unit surface area
of the contaminated zone leading to an annual skin dose
of 500 mSv for an occupational exposure of 2000 h and
a skin transfer factor, Tskin of 0.1. It is assumed that
contamination is eliminated on a daily basis when the
user washes on leaving the working zone. Neither radio-
active decay nor the renewal of skin cells (which con-
tribute towards eliminating radioactivity) are taken
into account.
Asskin (Bq.cm⫺2) is given by the following equation:
Asskin = 500/(Tskin × 2000 × Dp)
where Dp (mSv.h⫺1) is a conversion coefficient giving
 D. DELACROIX, J. P. GUERRE, P. LEBLANC and C. HICKMAN
the dose rate in tissue beneath 7 mg.cm⫺2 for a skin
contamination of 1 Bq.cm⫺2(14,15).
Calculation of Assurf
Assurf (Bq.cm⫺2) is the value of the activity per unit
surface area of the contaminated zone leading to an
effective dose equivalent of 20 mSv for an occupation
exposure of 2000 h.
Assurf (Bq.cm⫺2) is given by the following equation:
Assurf = 20/(2000 Dfloor)
where Dfloor (mSv.h⫺1) is a conversion coefficient giving
the effective dose equivalent 1 m above a floor infinitely
and uniformly contaminated at 1 Bq.cm⫺2(14).
Alpha emitters
The DSCL value corresponding to most radionuclides
lies between 1 Bq.cm⫺2 and 105 Bq.cm⫺2, and, in gen-
eral, is of the order of 100 Bq.cm⫺2. In the case of alpha
emitters, the model can lead to very restrictive values;
a lower limit of 0.04 Bq.cm⫺2 has been imposed for
alpha emitters.
Determination of removable and fixed
contamination values
DSCL values enable derived limits to be determined
for removable (or non-fixed) and fixed contamination.
The above limits enable the potential risk to users from
surface contamination to be assessed together with the
most appropriate means for decontamination.
In the case of removable contamination, the derived
limit is defined as being equivalent to 1/10th of the
DSCL value of the radionuclide considered (this allows
possible occupational exposures of other origins to be
taken into consideration).
In the case of fixed contamination, the derived level
is defined as the value corresponding to a whole-body
exposure from a uniformly contaminated floor equival-
ent to 1/10th of the annual exposure limits of 20 mSv.
The DSCL value for fixed contamination always
exceeds the value for removable contamination. For
some radionuclides such as ‘pure’ beta or alpha emit-
ters, the ratio of the two values can be highly significant
(radiation from the floor being negligible). In this hand-
book, the DSCL value for fixed contamination is set at a
maximum of 100 times the derived limit for removable
contamination (e.g. see 14C on page 24). Regulations do
not usually include specific limits for fixed contami-
nation since its effect is taken into account in external
radiation levels.
Contamination control
The level of removable contamination of working
zones and materials must be kept as low as reasonably
14
practicable by appropriate maintenance and cleaning
operations. When accidental contamination (even of
very low level) occurs, decontamination must be carried
out as quickly as possible.
Detection probes
Surface contamination due to many of the radio-
nuclides covered in these sheets can be detected with
soft ␤, ␤, ␣, X ray or ␥ probes.
Preferences given to particular types of probe or
instrument are indicated for each type of radiation. A
single + means that such a type of probe or instrument
can possibly be used, double ++ means that this type of
probe or instrument is recommended, whilst the absence
of a + sign means that that type of probe or instrument
is not suitable. Absence of a + sign in any box means
that direct measurement is inappropriate and a wipe test,
in association with a suitable detection system, such as
liquid scintillation methods, would be appropriate. This
applies only to tritium in this handbook but the same
technique can be applied with advantage to low levels
of contamination of other radionuclides, especially those
with low penetration emissions.
INTERNAL EXPOSURE
Committed effective dose per unit intake
Internal exposures resulting from ingestion and
inhalation are evaluated with the dose coefficients,
e(g)ingestion and e(g)inhalation, expressed in Sv.Bq⫺1, and
identically given by the ICRP (18), the IAEA Basic
Safety Standards (2) and the L159 Euratom Directive (3).
Listed values take the age of exposed individuals into
account (⬎1 year, 1–2 years, 2–7 years, 7–12 years, 12–
17 years and ⬎17 years) as well as their status (public
or occupational exposure). In this handbook only occu-
pational exposures are considered.
The committed effective dose per unit intake via
ingestion is given for different gut transfer factor, f1,
values. This factor quantifies the proportion of intake
transferred to body fluids in the gut and depends on the
chemical form of the radionuclide.
The committed effective dose per unit intake via inha-
lation is given for three default lung absorption types
(fast, moderate, slow). These coefficients depend on the
chemical form and particle size of the aerosol. It is
recalled that particle size is quantified by aerodynamic
median activity diameter (AMAD) parameters. Inha-
lation coefficients are given for 1 and 5 ␮m AMAD
values. Indication of the different forms for each nuclide
that correspond to different gut transfer factors and lung
absorption types are given in the data sheets. In some
cases, for example phosphorus and sulphur, where the
nuclide may form part of the anion, the gut transfer
factor or lung absorption types may be predominantly
 RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK 2nd Edition (2002)
determined by the associated cation. These are indicated
in the data sheets.
Annual Limits on Intake (ALI)
Annual Limits on Intake by ingestion and inhalation
(Iingestion,L and Iinhalation,L) are given in order to assist
users who are not familiar with the dose per unit intake
coefficients discussed above. Iingestion,L and Iinhalation,L are
calculated using the following relationship (19):
IL = DL/e(g)
where DL is the average annual limit of 20 mSv. IL
values can be considered to be ALI values.
ALIingestion and ALIinhalation values are given in the
data sheets for an average annual 20 mSv limit and the
most restrictive e(g) values, respectively. They are cal-
culated values (19), not values given by ICRP, and users
should be aware of this. The references should be con-
sulted, where appropriate, for further information.
The ‘highest dose organ’
Various metabolic and dosimetric models have
enabled retention and excretion functions after intake
by inhalation by Reference Man to be established (19–21).
These models have also enabled committed whole-body
and organ doses to be determined. Some organs prefer-
entially concentrate particular radionuclides. Therefore,
the data sheets indicate which is the ‘highest dose
organ’ (e.g. the thyroid in the case of iodine nuclides).
The ‘highest dose organ’ depends on physicochemical
form and whether intake results from ingestion or inha-
lation. Only inhalation (for an AMAD of 1 ␮m) is con-
sidered in this handbook. It should also be noted that
these functions depend on the clearance time from the
pulmonary region to the remainder of the body (F, M,
S). Therefore, the ‘highest dose organ’ may also depend
on the elimination class. 90Sr is an example; depending
on whether F or S classes are considered either bone
surface or lungs can be considered as being the ‘highest
dose organ’. However, for some chemical forms the
associated anion or cation may be more important in
this context.
General
Internal exposure values are determined using various
established metabolic and dosimetric models and
hypotheses, which are subject to review by ICRP.
Interpretation of the results of these analyses should be
done by specialists.
MAXIMUM RECOMMENDED ACTIVITIES
Operators or competent radiation protection personnel
often require order-of-magnitude estimates on the
maximum activities that can be handled with available
15
equipment (chemical benches, fume hoods, glove
boxes) or in given working areas (controlled or super-
vised areas). Whilst the purpose of this handbook is to
provide data rather than advice on practices, it is felt
appropriate to include information on ‘maximum
recommended activities’.
The data provided are appropriate to low and inter-
mediate level laboratories and not to high level labora-
tories, where extensive professional radiation protection
expertise will be available.
Calculation models
The maximum activity (Ao) corresponding to a parti-
cular nuclide and handling situation is characterised by
the potential risk associated with handling specific
nuclides. External exposure due to ␥ and ␤ radiation
components and the re-suspension of the nuclide in the
atmosphere are taken into consideration.
Ao (Bq) is determined from the following relation-
ship:
1/Ao = 1/Abeta + 1/Agamma + 1/Avolatile
where Abeta (Bq) and Agamma (Bq) represent the
maximum activities determined for a point source at a
distance of 30 cm in air. These activities are calculated
for the following dose rate limits:
250 ␮Sv.h⫺1 under 7 mg.cm⫺2 for beta components,
10 ␮Sv.h⫺1 for gamma components.
Avolatile (Bq) is related to potential atmospheric con-
tamination risks directly dependent on the volatility of
the radioactive product.
In free air, Avolatile is given by the expression:
Avolatile = 10⫺2 ALIinhalation/k,
where k is the volatility factor.
It should be noted that the maximum recommended
activities given in these sheets have been determined
using the most restrictive ALIinhalation values described
above; k values, related to the volatility of the product,
are defined as follows:
䉬 k = 1: gases, substances with high saturation vapour
pressures of about 1 bar at 20°C, substances pen-
etrating the skin, particles smaller than 5 ␮m.
䉬 k = 0.1: substances with saturation vapour pressures
of about 0.1 bar at 20°C, particles larger than 5 ␮m.
䉬 k = 0.01: low volatility substances with saturation
vapour pressures of about 0.01 bar at 20°C (e.g.
water).
䉬 k = 0.001: non-volatile substances with saturation
vapour pressures less than 0.01 bar at 20°C.
Dependence of maximum recommended activities
on equipment and working areas
The following additional rules are used to determine
 D. DELACROIX, J. P. GUERRE, P. LEBLANC and C. HICKMAN
the recommended limits for benches, fume cupboards
and glove boxes:
䉬 It is forbidden to manipulate highly volatile sub-
stances (k ⬎ 0.01) or radionuclides with ALIinhalation
values lower than 1000 Bq on chemical benches
because even a low level contamination could lead
to a significant ALIinhalation fraction that would be dif-
ficult to detect.
䉬 Manipulating substances under a fume hood is con-
sidered to increase protection by a factor of 10 in
comparison with an open bench.
䉬 Manipulating substances in a glove box is considered
to increase protection by a factor of 100 in compari-
son with fume hoods.
䉬 Maximum recommended levels of activity in super-
vised areas are nominally 3/10 of those in controlled
zones (this approximately represents the respective
exposure limits defined for these areas). However,
the installation of glove boxes in supervised zones
is generally deprecated; the level of protection
afforded by a glove box is considered incompatible
with the definition of such zones. It should be noted
that the factor of 3/10 may be masked by rounding
the data to one significant figure; rounding in any
other way may imply an unjustified degree of accu-
racy in the models used for deriving the rec-
ommended levels of activity.
Limitations
Area control
The values indicated in these sheets apply mainly to
the supervised and controlled areas of low and inter-
mediate activity laboratories. Maximum recommended
activities have further been limited to:
Group 1 (red) 0.5 GBq
Group 2 (orange) 5 GBq
Group 3 (yellow) 5 GBq
Group 4 (green) 5 GBq
Group 5 (blue) 50 GBq
These limits have been imposed because such labora-
tories are not generally equipped with either a means
for continuously monitoring the working environment,
or for rejecting gases at a sufficient height to ensure that
no recycling takes place.
It should be noted that values calculated in com-
pliance with these rules are guide values and are only
indicative since other non-quantifiable parameters such
as working methods and human factors must also be
taken into account. Nevertheless, it has been observed
that when practices are performed in accordance with
these simple rules, only very low levels of atmospheric
contamination and exposure occur.
The maximum recommended levels for elemental trit-
16
ium (3H), tritiated water and 37Ar have been deliberately
reduced because of the difficulty of detecting the corre-
sponding surface or atmospheric contamination. This
factor can be modified in particular situations,
depending on survey and control frequencies. In the
case of iodine isotopes (123I, 125I, 131I), the existence of
particularly unstable states (with the possibility of I2
release) has been considered. The corresponding limi-
tations are consequently much more stringent.
Radiation control
Handled or stored activity values must comply with
external exposure limits in situations where the external
radiation hazard may be more restrictive than the
internal radiation hazard. Attention is drawn to this fact
in the data sheets by the remark ‘Subject to external
exposure requirements which may be more restrictive’.
Stored activities may exceed maximum recommended
activities by a factor of 10, subject to any limits imposed
by local or national regulations.
In particular cases, listed values may be varied in
local regulations, based upon assessments by pro-
fessional radiation protection specialists.
DESCRIPTION OF DATA SHEETS
General
Individual data sheets provide data in five main areas,
namely basic radionuclide date, external exposure, con-
tamination, internal exposure and maximum rec-
ommended activities in laboratory situations. These are
divided into physical characteristics, (half life, specific
activity and decay scheme, A1 and A2 reference trans-
port activities, exemption levels, data for external
exposure for five different geometries, external and
internal exposure limits, appropriate contamination
detection probes and half-value and tenth-value shield-
ing thicknesses. The maximum activities that can be
handled on benches, under fume hoods or in glove
boxes are also given. The ‘highest dose organ’ is indi-
cated, even where this is the whole body. As described
earlier the data sheets are coloured red, orange, yellow,
green or blue, indicating, in descending order of risk,
the level of risk posed by the particular radionuclide.
GLOSSARY
Activity
The number of nuclear transformations occurring in
a given amount of radionuclide per unit time. The SI
unit of activity is the reciprocal second, s⫺1, with the
special name becquerel (Bq).
 RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK 2nd Edition (2002)
Annual limit of intake where DT,R is the absorbed dose delivered by radiation
type R averaged over a tissue or organ T and WR is the
The intake by inhalation or ingestion of a given radio-
radiation weighting factor for type R radiation. When
nuclide in a year by the Reference Man which would the radiation field is composed of different radiation
result in a committed dose equal to the relevant dose types, the equivalent dose is HT = ⌺RWR DT,R.
limit.

Bremsstrahlung
X rays produced by deceleration of ␤ particles in
materials.
Committed equivalent dose
Following an intake to the body of a radioactive
material, the time integral of the equivalent dose rate is
called the committed equivalent dose. If the integration
time following the intake is not specified, it is implied
that the value is 50 years for adults.
Effective dose
The quantity E, defined as a summation of the tissue
equivalent doses, each multiplied by the appropriate
tissue weighting factor (E = ⌺TWT HT where HT is the
equivalent dose in tissue T and WT is the tissue weight-
ing factor for tissue T). From the definition of equivalent
dose it follows that E = ⌺TWT ⌺RWR DT,R.
Radioactive half-life
Time required for a radioactive substance to lose 50%
of its activity by radioactive decay.

Equivalent dose Half-value and tenth-value thickness (or layer)

The equivalent dose, HT,R is defined as The thickness of material necessary to reduce the
intensity of X or gamma radiation by a factor of 2 and
HT,R = WR DT,R 10, respectively.

REFERENCES
1. Delacroix, D., Guerre, J. P. and Leblanc, P. Radionuclides and Radioprotection. (French Atomic Energy Commission),
(June 1994).
2. IAEA. International Basic Safety Standards for Protection against Ionising Radiation and for the Safety of Radiation Sources.
Safety Series No. 115, (Vienna: IAEA) (1996).
3. EURATOM DIRECTIVE; L159, 13 May 1996.
4. IAEA. Regulations for the Safe Transport of Radioactive Material. 1996 Edition. Safety Standards Series No.
ST1/Requirements (Vienna: IAEA) (1996).
5. Lagoutine, F., Coursol, N. and Legrand, J. Tables des Radionucléides. CEA-ORIS, 4 vol, (1983–1987).
6. ICRP. 1990 Recommendations of the International Commission on Radiological Protection. Publication 60, (Oxford:
Pergamon) (1990).
7. ICRP. Data for Use in Radioprotection against External Radiation. Publication 51 (Oxford: Pergamon) (1987).
8. Delacroix, D., Chazot, C. and Guerre, J. P. Calcul des Débits de Dose ␤ et ␥ en Fonction de la Géométrie de la Source.
CE. Report DSCE/SRI-A/93-362, (April 1993).
9. Takaku, Y. and Kida, T. Radiation Dose to the Skin and Bone of Fingers from Handling Radioisotopes in a Syringe. Health
Phys 22, 295–297 (1971).
10. Henson, P. W. Radiation Dose to the Skin in Contact with Unshielded Syringes Containing Radioactive Substances. Br. J.
Radiol. 46, 972–977 (1973).
11. Perotin, J. P. and Goubert, J. Evaluation des Risques d’Irradiation des Mains dans un Laboratoire de Contrôle Radiopharma-
ceutique. D. CEA-Saclay. Report SPR/SRI (1979).
12. Schmidt, W., Nowotny, R., Kletter, P. and Frisschauf, H. Radiation Exposure due to 99mTc and 131I Manipulated in Syringes.
J. Nucl. Med. 4, 389–391 (1979).
13. Moreau, A. La Radioprotection dans les Laboratoires de Faible et Moyenne Radioactivité. CEA-Saclay. Report SPR/SRI,
1981.
14. Kocher, D. C. and Eckerman, K. F. Electron Dose Rate Conversion Factors for External Exposure of the Skin from Uniformly
Deposited Activity on the Body Surface. Health Phys. 53(2) 135–141 (1987).
15. Piechowski, J., Menoux, B., Chaptinel, Y. and Durand, F. Dosimétrie et Thérapeutique des Contaminations Cutanés. CEA
Report 5441 (1988).
16. RadDecay Version 1.13. Grove Enginering (Rockville, Maryland, USA) (1996).
17. Delacroix, D., Guerre, J. P. and Leblanc, P. Détermination des limites de contamination surfacique pour les principaux
radionucléides. CEA-Saclay. Report DSCE/SRI, January 1992.

17
 D. DELACROIX, J. P. GUERRE, P. LEBLANC and C. HICKMAN
18. ICRP. Dose Coefficients for Intakes of Radionuclides by Workers. Publication 68 (Oxford: Pergamon) (1994).
19. ICRP. Individual Monitoring for Internal Exposure of Workers, Replacement of ICRP Publication 54. Publication 78 (Oxford:
Pergamon) (1997).
20. ICRP. Limits for Intakes of Radionuclides by Workers. Publication 30 (Parts 1–4 and Supplements) (Oxford: Pergamon)
1979–1988).
21. ICRP. Individual Monitoring for Intakes of Radionuclides by Workers: Design and Interpretation. Publication 78 (Oxford:
Pergamon) (1998).

18
 RADIONUCLIDE AND RADIATION PROTECTION DATA (2002)

Radiation Protection Dosimetry

Vol. 98, No. 1, pp. 19–20 (2002)
Nuclear Technology Publishing

TABLE OF RADIONUCLIDES LISTED

Nuclide Symbol Page Arsenic - 73 (73As33) 66

Arsenic - 74 (74As33) 67
Tritium (3H1) 21 Arsenic - 76 (76As33) 68
Beryllium - 7 (7Be4) 22 Arsenic - 77 (77As33) 69
Carbon - 11 (11C6) 23 Selenium - 75 (75Se34) 70
Carbon - 14 (14C6) 24 Bromine - 77 (77Br35) 71
Nitrogen - 13 (13N7) 25 Bromine - 82 (82Br35) 72
Oxygen - 15 (15O8) 26 Krypton - 81 (81Kr36) 73
Fluorine - 18 (18F9) 27 Krypton - 83m (83mKr36) 74
Sodium - 22 (22Na11) 28 Krypton - 85 (85Kr36) 75
Sodium - 24 (24Na11) 29 Krypton - 85m (85mKr36) 76
Aluminium - 26 (26Al13) 30 Rubidium - 86 (86Rb37) 77
Silicon - 31 (31Si14) 31 Strontium - 85 (85Sr38) 78
Phosphorus - 32 (32P15) 32 Strontium - 89 (89Sr38) 79
Phosphorus - 33 (33P15) 33 Strontium - 90 / Yttrium - 90 (90Sr38 / 90Y39) 80
Sulphur - 35 (35S16) 34 Yttrium - 90 (90Y39) 81
Chlorine - 36 (36Cl17) 35 Yttrium - 91 (91Y39) 82
Argon - 37 (37Ar18) 36 Zirconium - 95 / Niobium - 95 (95Zr40 / 95Nb41) 83
Argon - 41 (41Ar18) 37 Molybdenum - 99 / Technetium - 99m (99Mo42 / 99mTc43) 84
Potassium - 40 (40K19) 38 Technetium - 99m (99mTc43) 85
Potassium - 42 (42K19) 39 Technetium - 99 (99Tc43) 86
Potassium - 43 (43K19) 40 Ruthenium - 103 / Rhodium - 103m (103Ru44 / 103mRh45) 87
Calcium - 45 (45Ca20) 41 Ruthenium - 106 / Rhodium - 106 (106Ru44 / 106Rh45) 88
Calcium - 47 / Scandium - 47 (47Ca20 / 47Sc21) 42 Palladium - 103 / Rhodium - 103m (103Pd46 / 103mRh45) 89
Scandium - 46 (46Sc21) 43 Silver - 110m (110mAg47) 90
Scandium - 47 (47Sc21) 44 Silver - 111 (111Ag47) 91
Vanadium - 48 (48V23) 45 Cadmium - 109 (109Cd48) 92
Chromium - 51 (51Cr24) 46 Indium - 111 (111In49) 93
Manganese - 52m (52mMn25) 47 Indium - 113m (113mIn49) 94
Manganese - 52 (52Mn25) 48 Indium - 115m (115mIn49) 95
Manganese - 54 (54Mn25) 49 Tin - 125 (125Sn50) 96
Manganese - 56 (56Mn25) 50 Antimony - 122 (122Sb51) 97
Iron - 52 (52Fe26) 51 Antimony - 124 (124Sb51) 98
Iron - 55 (55Fe26) 52 Antimony - 125 / Tellurium - 125m (125Sb51 / 125mTe52) 99
Iron - 59 (59Fe26) 53 Antimony - 126 (126Sb51) 100
Cobalt - 56 (56Co27) 54 Tellurium - 123m (123mTe52) 101
Cobalt - 57 (57Co27) 55 Tellurium - 125m (125mTe52) 102
Cobalt - 58 (58Co27) 56 Tellurium - 132 / Iodine - 132 (132Te52/132I53) 103
Cobalt - 60 (60Co27) 57 Iodine - 123 (123I53) 104
Nickel - 63 (63Ni28) 58 Iodine - 124 (124I53) 105
Nickel - 65 (65Ni28) 59 Iodine - 125 (125I53) 106
Copper - 64 (64Cu29) 60 Iodine - 129 (129I53) 107
Copper - 67 (67Cu29) 61 Iodine - 131 (131I53) 108
Zinc - 65 (65Zn30) 62 Iodine - 132 (132I53) 109
Gallium - 66 (66Ga31) 63 Iodine - 133 (133I53) 110
Gallium - 67 (67Ga31) 64 Xenon - 133 (133Xe54) 111
Gallium - 68 (68Ga31) 65 Caesium - 131 (131Cs55) 112

19
 D. DELACROIX, J. P. GUERRE, P. LEBLANC and C. HICKMAN
Caesium - 134 (134Cs55) 113 Thallium - 201 (201Tl81) 139
Caesium - 137 / Barium - 137m (137Cs55 / 137mBa56) 114 Thallium - 204 (204Tl81) 140
Barium - 133 (133Ba56) 115 Lead - 210 (210Pb82) 141
Barium - 140 / Lanthanum - 140 (140Ba56 / 140La57) 116 Lead - 214 (214Pb82) 142
Lanthanum - 140 (140La57) 117 Bismuth - 207 (207Bi83) 143
Cerium - 139 (139Ce58) 118 Bismuth - 210 (210Bi83) 144
Cerium - 141 (141Ce58) 119 Bismuth - 214 (214Bi83) 145
Cerium - 143 (143Ce58) 120 Polonium - 210 (210Po84) 146
Praseodymium - 143 (143Pr59) 121 Radium - 226 (226Ra88) 147
Praseodymium - 144 (144Pr59) 122 Thorium - 231 (231Th90) 148
Promethium - 147 (147Pm61) 123 Thorium - 234 (234Th90) 149
Samarium - 153 (153Sm62) 124 Protactinium - 234 (234Pa91) 150
Europium - 152 (152Eu63) 125 Protactinium - 234m (234mPa91) 151
Europium - 154 (154Eu63) 126 Uranium - 233 (233U92) 152
Europium - 155 (155Eu63) 127 Uranium - 234 (234U92) 153
Europium - 156 (156Eu63) 128 Uranium - 235 (235U92) 154
Erbium - 169 (169Er68) 129 Uranium - 238 (238U92) 155
Thulium - 170 (170Tm69) 130 Neptunium - 239 (239Np93) 156
Thulium - 171 (171Tm69) 131 Plutonium - 238 (238Pu94) 157
Ytterbium - 169 (169Yb70) 132 Plutonium - 239 (239Pu94) 158
Rhenium - 186 (186Re75) 133 Plutonium - 240 (240Pu94) 159
Rhenium - 188 (188Re75) 134 Plutonium - 241 (241Pu94) 160
Iridium - 192 (192Ir77) 135 Americium - 241 (241Am95) 161
Gold - 198 (198Au79) 136 Americium - 243 (243Am95) 162
Mercury - 197 (197Hg80) 137 Curium - 244 (244Cm96) 163
Mercury - 203 (203Hg80) 138 Californium - 252 (252Cf98) 164

20
 !

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 RADIONUCLIDE AND RADIATION PROTECTION DATA (2002)
Radiation Protection Dosimetry
Vol. 98, No. 1, pp. 165–168 (2002)
Nuclear Technology Publishing

APPENDIX – HEAVY ELEMENT DECAY

Pb-210 decay Pb-210 to Po-210 (see pages 13 and 141)

Nuclide Half-life 0.1 day 1 day 10 days 100 days 1 year 10 years 100 years

Pb-210 2.22E+1 yr 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00

Bi-210 5.01E+0 d 1.37E-02 1.29E-01 7.48E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Po-210 1.38E+2 d 3.44E-06 3.30E-04 2.52E-02 3.69E-01 8.43E-01 1.02E+00 1.02E+00

Ra-226 decay Ra-226 to Po-210 (see pages 13 and 147)

Nuclide Half-life 0.1 day 1 day 10 days 100 days 1 year 10 years 100 years

Ra-226 1.60E+3 yr 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00

Rn-222 3.82E+0 d 1.80E-03 1.65E-01 8.40E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Po-218 3.05E+0 min 1.74E-02 1.65E-01 8.40E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Pb-214 2.68E+1 min 1.27E-02 1.61E-01 8.30E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Bi-214 1.99E+1 min 9.46E-03 1.58E-01 8.30E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Po-214 1.64E-4 sec 9.46E-03 1.58E-01 8.30E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Pb-210 2.22E+1 yr 2.70E-08 6.60E-06 4.55E-04 8.01E-03 3.01E-02 2.66E-01 9.73E-01
Bi-210 5.01E+0 d 8.90E-11 2.84E-07 1.69E-04 7.40E-03 2.95E-02 2.66E-01 9.73E-01
Po-210 1.38E+2 d 8.40E-15 3.44E-10 2.40E-06 1.41E-03 1.57E-02 2.53E-01 9.73E-01

U-235 decay U-235 to Po-211 (see pages 13 and 154)

Nuclide Half-life 0.1 day 1 day 10 days 100 days 1 year 10 years 100 years

U-235 7.04E+8 yr 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00

Th-231 2.55E+1 hr 6.31E-02 4.78E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Pa-231 3.28E+4 yr 1.84E-10 1.53E-08 4.90E-07 5.70E-06 2.10E-05 2.11E-04 2.11E-03
Ac-227 2.18E+1 yr ⬍E-10 ⬍E-10 1.90E-10 2.44E-08 3.30E-07 3.03E-05 1.48E-03
Fr-223 2.18E+1 min ⬍E-10 ⬍E-10 ⬍E-10 3.36E-10 4.55E-09 4.18E-07 2.04E-05
Ra-223 1.14E+1 d ⬍E-10 ⬍E-10 ⬍E-10 2.42E-10 4.17E-09 4.15E-07 2.04E-05
Rn-219 3.96E+0 sec ⬍E-10 ⬍E-10 ⬍E-10 2.42E-10 4.17E-09 4.15E-07 2.04E-05
Po-215 1.78E-3 sec ⬍E-10 ⬍E-10 ⬍E-10 2.42E-10 4.17E-09 4.15E-07 2.04E-05
Pb-211 3.61E+1 min ⬍E-10 ⬍E-10 ⬍E-10 2.42E-10 4.17E-09 4.15E-07 2.04E-05
Bi-211 2.13E+0 min ⬍E-10 ⬍E-10 ⬍E-10 2.42E-10 4.17E-09 4.15E-07 2.04E-05
Tl-207 4.77E+0 min ⬍E-10 ⬍E-10 ⬍E-10 2.42E-10 4.15E-09 4.14E-07 2.03E-08

Po-211 5.16E-1 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.13E-09 5.6E-08

Th-227 1.87E+1 d ⬍E-10 ⬍E-10 ⬍E-10 1.44E-08 2.81E-07 2.95E-05 1.45E-03

Ra-223 1.14E+1 d ⬍E-10 ⬍E-10 ⬍E-10 9.76E-09 2.55E-07 2.93E-05 1.45E-03
Rn-219 3.96E+0 sec ⬍E-10 ⬍E-10 ⬍E-10 9.76E-09 2.55E-07 2.93E-05 1.45E-03
Po-215 1.78E-3 sec ⬍E-10 ⬍E-10 ⬍E-10 9.76E-09 2.55E-07 2.93E-05 1.45E-03
Pb-211 3.61E+1 min ⬍E-10 ⬍E-10 ⬍E-10 9.75E-09 2.55E-07 2.93E-05 1.45E-03
Bi-211 2.13E+0 min ⬍E-10 ⬍E-10 ⬍E-10 9.75E-09 2.55E-07 2.93E-05 1.45E-03
Tl-207 4.77E+0 min ⬍E-10 ⬍E-10 ⬍E-10 9.72E-09 2.55E-07 2.92E-05 1.45E-03

Po-211 5.16E-1 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 6.97E-10 7.99E-08 3.97E-06

165
 D. DELACROIX, J. P. GUERRE, P. LEBLANC and C. HICKMAN
U-238 decay U-238 to Po-210 (see pages 13 and 155)

Nuclide Half-life 0.1 day 1 day 10 days 100 days 1 year 10 years 100 years

U-238 4.47E+9 yr 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00

Th-234 2.41E+1 d 2.87E-03 2.83E-02 2.50E-01 9.44E-01 1.00E+00 1.00E+00 1.00E+00
Pa-234m 1.17E+0 min 2.83E-03 2.83E-02 2.50E-01 9.44E-01 1.00E+00 1.00E+00 1.00E+00
Pa-234 6.70E+0 hr 5.14E-07 2.87E-05 3.86E-04 1.50E-03 1.60E-03 1.60E-03 1.60E-03
U-234 2.44E+5 yr ⬍E-10 ⬍E-10 ⬍E-10 8.30E-10 4.10E-09 4.49E-08 4.3E-07
Th-230 7.7E+4 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 2.0E-10
Ra-226 1.60E+3 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Rn-222 3.82E+0 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Po-218 3.05E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-214 2.68E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Bi-214 1.99E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Po-214 1.64E-4 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-210 2.23E+1 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Bi-210 5.0E+0 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Po-210 1.38E+2 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

U-234 2.44E+5 yr ⬍E-10 1.01E-08 1.01E-18 5.21E-07 2.56E-06 2.80E-05 2.83E-04

Th-230 7.7E+4 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.25E-09 1.27E-07
Ra-226 1.60E+3 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 2.27E-10
Rn-222 3.82E+0 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.81E-09
Po-218 3.05E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.81E-09
Pb-214 2.68E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.81E-09
Bi-214 1.99E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.81E-09
Po-214 1.64E-4 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.81E-09
Pb-210 2.23E+1 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 8.44E-10
Bi-210 5.01E+0 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 8.44E-10
Po-210 1.38E+2 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 8.28E-10

Pu-241 decay Pu-241 to Pb-209 (see pages 13 and 160)

Nuclide Half-life 0.1 day 1 day 10 days 100 days 1 year 10 years 100 years

Pu-241 1.44E+1 yr 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00

Am-241 4.32E+2 yr 4.39E-07 4.39E-06 4.39E-05 4.48E-04 1.64E-03 2.04E-02 3.58E+00
Np-237 2.14E+6 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 2.69E-10 3.58E-08 9.85E-05
Pa-233 2.70E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 2.17E-10 3.51E-08 9.85E-05
U-233 1.59E+5 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.85E-08
Th-229 7.34E+3 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Ra-225 1.48E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Ac-225 1.00E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Fr-221 4.8E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
At-217 3.23E-2 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Bi-213 4.56E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Tl-209 2.20 E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-209 3.24E+0 hr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Po-213 4.20E-6 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-209 3.25E+0 hr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

U-237 6.75E+6 2.50E-07 2.39E-06 1.57E-05 2.48E-05 2.46E-05 2.45E-05 2.45E-05

Np-237 2.14E+6 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 2.00E-08
Pa-233 2.70E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 2.00E-08
U-233 1.59E+5 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Th-229 7.34E+3 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Ra-225 1.48E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Continued

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 RADIONUCLIDE AND RADIATION PROTECTION DATA (2002)
Pu-241 decay (Continued)

Ac-225 1.00E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Fr-221 4.8E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
At-217 3.23E-2 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Bi-213 4.56E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Tl-209 2.20 E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-209 3.24E+0 hr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Po-213 4.20E-6 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-209 3.25E+0 hr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Am-243 decay Am-243 to Po-211 (see pages 13 and 162)

Nuclide Half-life 0.1 day 1 day 10 days 100 days 1 year 10 years 100 years

Am-243 7.38E+3 yr 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00 1.00E+00

Np-239 2.35E+0 d 2.90E-02 2.55E-01 9.47E-01 1.00E+00 1.00E+00 1.00E+00 1.00E+00
Pu-239 2.41E+4 yr 1.14E-10 1.05E-08 5.33E-07 7.60E-06 2.84E-05 2.87E-04 2.88E-03
U-235 7.04E+8 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.42E-10
Th-231 2.55E+1 hr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 1.42E-10
Pa-231 3.28E+4 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Ac-227 2.18E+1 yr ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Fr-223 2.18E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Ra-223 1.14E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Rn-219 3.96E+0 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Po-215 1.78E-3 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-211 3.61E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Bi-211 2.13E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Tl-207 4.77E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Po-211 5.16E-1 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Th-227 1.87E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Ra-223 1.14E+1 d ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Rn-219 3.96E+0 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Po-215 1.78E-3 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Pb-211 3.61E+1 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Bi-211 2.13E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10
Tl-207 4.77E+0 min ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Po-211 5.16E-1 sec ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10 ⬍E-10

Note:
The above tables for U-235, U-238, Pu-241 and Am-243 should be read in conjunction with the corresponding decay chains
shown overleaf. These chains clearly show the branching in the decay chains, clarifying the lines apparently repeated in the tables.

REFERENCE

1. RadDecay for Windows Version 1.13. Grove Engineering (Maryland) 1996.

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