prEN IEC 62387
(Main)Radiation protection instrumentation - Dosimetry systems with integrating passive detectors for individual, workplace and environmental monitoring of photon and beta radiation
Radiation protection instrumentation - Dosimetry systems with integrating passive detectors for individual, workplace and environmental monitoring of photon and beta radiation
This document applies to all kinds of passive dosimetry systems that are used for measuring: - the personal dose equivalent Hp(10) (for individual whole body monitoring), - the personal dose equivalent Hp(3) (for individual eye lens monitoring), - the personal dose equivalent Hp(0,07) (for whole body skin and local skin for extremity monitoring), - the ambient dose equivalent H*(10) (for workplace and environmental monitoring), - the directional dose equivalent H'(3) (for workplace and environmental monitoring), or - the directional dose equivalent H'(0,07) (for workplace and environmental monitoring).
Strahlenschutz-Messgeräte - Dosimetriesysteme mit integrierenden passiven Detektoren zur Personen-, Arbeitsplatz- und Umgebungsüberwachung auf Photonen- und Betastrahlung
Instrumentation pour la radioprotection - Systèmes dosimétriques avec détecteurs intégrés passifs pour le contrôle radiologique individuel, du lieu de travail et de l'environnement des rayonnements photoniques et bêta
IEC 62387:2020 est disponible sous forme de IEC 62387:2020 RLV qui contient la Norme internationale et sa version Redline, illustrant les modifications du contenu technique depuis l'édition précédente. L'IEC 62387:2020 s’applique à toutes sortes de systèmes dosimétriques passifs utilisés pour la mesure de: - l’équivalent de dose individuel Hp(10) (pour le contrôle radiologique individuel du corps entier), - l’équivalent de dose individuel Hp(3) (pour le contrôle radiologique individuel des cristallins), - l’équivalent de dose individuel Hp(0,07) (pour le contrôle radiologique individuel de la peau du corps entier et de la peau locale et des extrémités), - l’équivalent de dose ambiant H*(10) (pour le contrôle radiologique du lieu de travail et de l'environnement), - l’équivalent de dose directionnel H'(3) (pour le contrôle radiologique du lieu de travail et de l'environnement), ou - l’équivalent de dose directionnel H’(0,07) (pour le contrôle radiologique du lieu de travail et de l'environnement). Le présent document s’applique aux systèmes dosimétriques qui mesurent les rayonnements photoniques et/ou bêta externes dans la plage de dose comprise entre 0,01 mSv et 10 Sv et dans les plages d’énergie données dans le Tableau 1. Toutes les valeurs d’énergie données sont des valeurs moyennes par rapport à la fluence. Les systèmes dosimétriques utilisent habituellement des dispositifs électroniques pour l’évaluation des données et sont donc souvent commandés par ordinateur.
Instrumenti za zaščito pred sevanjem - Sistemi za dozimetrijo z integriranimi pasivnimi detektorji za posamezno, delovno in okoljsko spremljanje fotonskega in beta sevanja
General Information
RELATIONS
Standards Content (sample)
SLOVENSKI STANDARD
oSIST prEN IEC 62387:2022
01-julij-2022
Instrumenti za zaščito pred sevanjem - Sistemi za dozimetrijo z integriranimi
pasivnimi detektorji za posamezno, delovno in okoljsko spremljanje fotonskega in
beta sevanja
Radiation protection instrumentation - Dosimetry systems with integrating passive
detectors for individual, workplace and environmental monitoring of photon and beta
radiationStrahlenschutz-Messgeräte - Dosimetriesysteme mit integrierenden passiven Detektoren
zur Personen-, Arbeitsplatz- und Umgebungsüberwachung auf Photonen- undBetastrahlung
Instrumentation pour la radioprotection - Systèmes dosimétriques avec détecteurs
intégrés passifs pour le contrôle radiologique individuel, du lieu de travail et de
l'environnement des rayonnements photoniques et bêtaTa slovenski standard je istoveten z: prEN IEC 62387
ICS:
13.280 Varstvo pred sevanjem Radiation protection
oSIST prEN IEC 62387:2022 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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oSIST prEN IEC 62387:2022
EUROPEAN STANDARD DRAFT
prEN IEC 62387
NORME EUROPÉENNE
EUROPÄISCHE NORM
May 2022
ICS 13.280 Will supersede EN 62387:2016 and all of its
amendments and corrigenda (if any)
English Version
Radiation protection instrumentation - Dosimetry systems with
integrating passive detectors for individual, workplace and
environmental monitoring of photon and beta radiation
(IEC 62387:2020)
Instrumentation pour la radioprotection - Systèmes Strahlenschutz-Messgeräte - Dosimetriesysteme mit
dosimétriques avec détecteurs intégrés passifs pour le integrierenden passiven Detektoren zur Personen-,
contrôle radiologique individuel, du lieu de travail et de Arbeitsplatz- und Umgebungsüberwachung auf Photonen-
l'environnement des rayonnements photoniques et bêta und Betastrahlung(IEC 62387:2020) (IEC 62387:2020)
This draft European Standard is submitted to CENELEC members for enquiry.
Deadline for CENELEC: 2022-08-05.
The text of this draft consists of the text of IEC 62387:2020.
If this draft becomes a European Standard, CENELEC members are bound to comply with the CEN/CENELEC Internal Regulations which
stipulate the conditions for giving this European Standard the status of a national standard without any alteration.
This draft European Standard was established by CENELEC in three official versions (English, French, German).
A version in any other language made by translation under the responsibility of a CENELEC member into its own language and notified to
the CEN-CENELEC Management Centre has the same status as the official versions.CENELEC members are the national electrotechnical committees of Austria, Belgium, Bulgaria, Croatia, Cyprus, the Czech Republic,
Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, the
Netherlands, Norway, Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland,
Turkey and the United Kingdom.Recipients of this draft are invited to submit, with their comments, notification of any relevant patent rights of which they are aware and to
provide supporting documentation.Warning : This document is not a European Standard. It is distributed for review and comments. It is subject to change without notice and
shall not be referred to as a European Standard.European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung
CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2022 CENELEC All rights of exploitation in any form and by any means reserved worldwide for CENELEC Members.
Project: 75396 Ref. No. prEN IEC 62387 E---------------------- Page: 3 ----------------------
oSIST prEN IEC 62387:2022
prEN IEC 62387:2022 (E)
European foreword
This document (prEN IEC 62387:2022) consists of the text of IEC 62387:2020 prepared by IEC/SC 45B
“Radiation protection instrumentation” of IEC/TC 45 "Nuclear instrumentation".This document is currently submitted to the Enquiry.
The following dates are proposed:
• latest date by which the existence of this document (doa) dor + 6 months
has to be announced at national level
• latest date by which this document has to be (dop) dor + 12 months
implemented at national level by publication of an
identical national standard or by endorsement
• latest date by which the national standards (dow) dor + 36 months
conflicting with this document have to be withdrawn (to be confirmed or
modified when voting)
This document will supersede EN 62387:2016 and all of its amendments and corrigenda (if any).
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prEN IEC 62387:2022 (E)
Annex ZA
(normative)
Normative references to international publications
with their corresponding European publications
The following documents are referred to in the text in such a way that some or all of their content constitutes
requirements of this document. For dated references, only the edition cited applies. For undated references,
the latest edition of the referenced document (including any amendments) applies.
NOTE 1 Where an International Publication has been modified by common modifications, indicated by (mod), the
relevant EN/HD applies.NOTE 2 Up-to-date information on the latest versions of the European Standards listed in this annex is available here:
www.cenelec.eu.Publication Year Title EN/HD Year
IEC 61000-4-2 - Electromagnetic compatibility (EMC) - Part 4- EN 61000-4-2 -
2: Testing and measurement techniques -
Electrostatic discharge immunity test
IEC 61000-4-3 - Electromagnetic compatibility (EMC) - Part 4- EN IEC 61000-4-3 -
3 : Testing and measurement techniques -
Radiated, radio-frequency, electromagnetic
field immunity test
IEC 61000-4-4 - Electromagnetic compatibility (EMC) - Part 4- EN 61000-4-4 -
4: Testing and measurement techniques -
Electrical fast transient/burst immunity test
IEC 61000-4-5 - Electromagnetic compatibility (EMC) - Part 4- EN 61000-4-5 -
5: Testing and measurement techniques -
Surge immunity test
IEC 61000-4-6 - Electromagnetic compatibility (EMC) - Part 4- EN 61000-4-6 -
6: Testing and measurement techniques -
Immunity to conducted disturbances, induced
by radio-frequency fields
IEC 61000-4-8 - Electromagnetic compatibility (EMC) - Part 4- EN 61000-4-8 -
8: Testing and measurement techniques -
Power frequency magnetic field immunity
test
IEC 61000-4-11 - Electromagnetic compatibility (EMC) - Part 4- EN IEC 61000-4-11 -
11: Testing and measurement techniques -Voltage dips, short interruptions and voltage
variations immunity tests for equipment with
input current up to 16 A per phase
IEC 61000-6-2 - Electromagnetic compatibility (EMC) - Part 6- EN IEC 61000-6-2 -
2: Generic standards - Immunity standard for
industrial environments
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oSIST prEN IEC 62387:2022
prEN IEC 62387:2022 (E)
ISO 4037 series Radiological protection - X and gamma EN ISO 4037 series
reference radiation for calibrating
dosemeters and doserate meters and for
determining their response as a function of
photon energy
ISO 4037-3 2019 Radiological protection - X and gamma EN ISO 4037-3 2021
reference radiation for calibrating
dosemeters and doserate meters and for
determining their response as a function of
photon energy - Part 3: Calibration of area
and personal dosemeters and the
measurement of their response as a function
of energy and angle of incidence
ISO 6980 series Nuclear energy - Reference beta-particle - -
radiation
ISO 6980-3 - Nuclear energy - Reference beta-particle - -
radiation - Part 3: Calibration of area and
personal dosemeters and the determination
of their response as a function of beta
radiation energy and angle of incidence
ISO 8529 series Reference neutron radiations – Part 1: - -
Characteristics and methods of production
ISO/IEC Guide 98-3 2008 Uncertainty of measurement - Part 3: Guide - -
to the expression of uncertainty in
measurement (GUM:1995)
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oSIST prEN IEC 62387:2022
IEC 62387
Edition 2.0 2020-01
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
colour
inside
Radiation protection instrumentation – Dosimetry systems with integrating
passive detectors for individual, workplace and environmental monitoring of
photon and beta radiation
Instrumentation pour la radioprotection – Systèmes dosimétriques avec
détecteurs intégrés passifs pour le contrôle radiologique individuel, du lieu
de travail et de l'environnement des rayonnements photoniques et bêta
INTERNATIONAL
ELECTROTECHNICAL
COMMISSION
COMMISSION
ELECTROTECHNIQUE
INTERNATIONALE
ICS 13.280 ISBN 978-2-8322-7696-9
Warning! Make sure that you obtained this publication from an authorized distributor.
Attention! Veuillez vous assurer que vous avez obtenu cette publication via un distributeur agréé.
® Registered trademark of the International Electrotechnical CommissionMarque déposée de la Commission Electrotechnique Internationale
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oSIST prEN IEC 62387:2022
– 2 – IEC 62387:2020 © IEC 2020
CONTENTS
FOREWORD ........................................................................................................................... 7
INTRODUCTION ..................................................................................................................... 9
1 Scope ............................................................................................................................ 10
2 Normative references .................................................................................................... 11
3 Terms and definitions .................................................................................................... 12
4 Units and symbols ......................................................................................................... 22
5 General test procedures ................................................................................................ 22
5.1 Basic test procedures ........................................................................................... 22
5.1.1 Instructions for use ........................................................................................ 22
5.1.2 Nature of tests ............................................................................................... 22
5.1.3 Reference conditions and standard test conditions ........................................ 22
5.1.4 Production of reference radiation ................................................................... 22
5.1.5 Choice of phantom for the purpose of testing ................................................. 23
5.1.6 Position of dosemeter for the purpose of testing ............................................ 23
5.2 Test procedures to be considered for every test .................................................... 23
5.2.1 Number of dosemeters used for each test ...................................................... 23
5.2.2 Consideration of the uncertainty of the conventional quantity value ............... 23
5.2.3 Consideration of non-linearity ........................................................................ 23
5.2.4 Consideration of natural background radiation ............................................... 23
5.2.5 Consideration of several detectors or signals in a dosemeter ......................... 23
5.2.6 Performing the tests efficiently ....................................................................... 24
6 Performance requirements: summary ............................................................................ 24
7 Capability of a dosimetry system ................................................................................... 25
7.1 General ................................................................................................................. 25
7.2 Measuring range and type of radiation .................................................................. 25
7.3 Rated ranges of the influence quantities ............................................................... 25
7.4 Maximum rated measurement time t ............................................................... 25
max7.5 Reusability ............................................................................................................ 26
7.6 Model function ...................................................................................................... 26
7.7 Example for the capabilities of a dosimetry system ............................................... 26
8 Requirements for the design of the dosimetry system .................................................... 27
8.1 General ................................................................................................................. 27
8.2 Indication of the dose value (dosimetry system) .................................................... 27
8.3 Assignment of the dose value to the dosemeter (dosimetry system) ...................... 27
8.4 Information given on the devices (reader and dosemeter) ..................................... 27
8.5 Retention and removal of radioactive contamination (dosemeter) .......................... 28
8.6 Algorithm to evaluate the indicated value (dosimetry system)................................ 28
8.7 Use of dosemeters in mixed radiation fields (dosimetry system) ............................ 28
9 Instruction manual ......................................................................................................... 28
9.1 General ................................................................................................................. 28
9.2 Specification of the technical data ......................................................................... 28
10 Software, data and interfaces of the dosimetry system .................................................. 29
10.1 General ................................................................................................................. 29
10.2 Design and structure of the software ..................................................................... 30
10.2.1 Requirements ................................................................................................ 30
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10.2.2 Method of test................................................................................................ 30
10.3 Identification of the software ................................................................................. 30
10.3.1 Requirements ................................................................................................ 30
10.3.2 Method of test................................................................................................ 31
10.4 Authenticity of the software and the presentation of results ................................... 31
10.4.1 Requirements ................................................................................................ 31
10.4.2 Method of test................................................................................................ 31
10.5 Alarm and stop of system operation under abnormal operating conditions ............. 31
10.5.1 Requirements ................................................................................................ 31
10.5.2 Method of test................................................................................................ 32
10.6 Control of input data by the dosimetry system ....................................................... 32
10.6.1 Requirements ................................................................................................ 32
10.6.2 Method of test................................................................................................ 32
10.7 Storage of data ..................................................................................................... 32
10.7.1 Requirements ................................................................................................ 32
10.7.2 Method of test................................................................................................ 33
10.8 Transmission of data ............................................................................................. 33
10.8.1 Requirements ................................................................................................ 33
10.8.2 Method of test................................................................................................ 34
10.9 Hardware interfaces and software interfaces ......................................................... 34
10.9.1 Requirements ................................................................................................ 34
10.9.2 Method of test................................................................................................ 34
10.10 Documentation for the software test ...................................................................... 34
10.10.1 Requirements ................................................................................................ 34
10.10.2 Method of test................................................................................................ 35
11 Radiation performance requirements and tests (dosimetry system) ................................ 35
11.1 General ................................................................................................................. 35
11.2 Coefficient of variation .......................................................................................... 36
11.3 Non-linearity ......................................................................................................... 36
11.3.1 Requirements ................................................................................................ 36
11.3.2 Method of test................................................................................................ 36
11.3.3 Interpretation of results .................................................................................. 36
11.4 Overload characteristics, after-effects, and reusability .......................................... 37
11.4.1 Requirements ................................................................................................ 37
11.4.2 Method of test................................................................................................ 38
11.4.3 Interpretation of the results ............................................................................ 38
11.5 Radiation energy and angle of incidence for H (10) or H*(10) dosemeters ............ 39
11.5.1 Photon radiation ............................................................................................ 39
11.5.2 Beta radiation ................................................................................................ 41
11.6 Radiation energy and angle of incidence for H (3) or H'(3) dosemeters ................ 41
11.6.1 Photon radiation ............................................................................................ 41
11.6.2 Beta radiation ................................................................................................ 43
11.7 Radiation energy and angle of incidence for H (0,07) or H'(0,07) dosemeters ...... 44
11.7.1 Photon radiation ............................................................................................ 44
11.7.2 Beta radiation ................................................................................................ 46
11.8 Over indication due to radiation incident from the side of an H (10), H (3) or
p pH (0,07) dosemeter .............................................................................................. 47
11.8.1 Requirements ................................................................................................ 47
11.8.2 Method of test................................................................................................ 47
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11.8.3 Interpretation of the results ............................................................................ 48
11.9 Indication of the presence of beta dose for H (0,07) whole body dosemeters ....... 48
12 Response to mixed irradiations (dosimetry system) ....................................................... 48
12.1 Requirements ....................................................................................................... 48
12.2 Method of test ....................................................................................................... 49
12.2.1 General ......................................................................................................... 49
12.2.2 Preparation of the test ................................................................................... 49
12.2.3 Practical test ................................................................................................. 49
12.3 Interpretation of the results ................................................................................... 50
13 Environmental performance requirements and tests ....................................................... 50
13.1 General ................................................................................................................. 50
13.1.1 General requirement ...................................................................................... 50
13.1.2 General method of test .................................................................................. 50
13.2 Ambient temperature and relative humidity (dosemeter) ........................................ 51
13.2.1 General ......................................................................................................... 51
13.2.2 Requirements ................................................................................................ 51
13.2.3 Method of test................................................................................................ 51
13.2.4 Interpretation of the results ............................................................................ 51
13.3 Light exposure (dosemeter) .................................................................................. 52
13.3.1 General ......................................................................................................... 52
13.3.2 Requirements ................................................................................................ 52
13.3.3 Method of test................................................................................................ 52
13.3.4 Interpretation of the results ............................................................................ 52
13.4 Dose build-up, fading and self-irradiation (dosemeter) .......................................... 52
13.4.1 General ......................................................................................................... 52
13.4.2 Requirements ................................................................................................ 53
13.4.3 Method of test................................................................................................ 53
13.4.4 Interpretation of the results ............................................................................ 53
13.5 Sealing (dosemeter) .............................................................................................. 53
13.6 Reader stability (reader) ....................................................................................... 53
13.6.1 General ......................................................................................................... 53
13.6.2 Requirements ................................................................................................ 54
13.6.3 Method of test................................................................................................ 54
13.6.4 Interpretation of the results ............................................................................ 54
13.7 Ambient temperature (reader) ............................................................................... 54
13.7.1 General ......................................................................................................... 54
13.7.2 Requirements ................................................................................................ 54
13.7.3 Method of test................................................................................................ 54
13.7.4 Interpretation of the results ............................................................................ 55
13.8 Light exposure (reader) ......................................................................................... 55
13.8.1 General ......................................................................................................... 55
13.8.2 Requirements ................................................................................................ 55
13.8.3 Method of test................................................................................................ 55
13.8.4 Interpretation of the results ............................................................................ 56
13.9 Primary power supply (reader) .............................................................................. 56
13.9.1 General ......................................................................................................... 56
13.9.2 Requirements ................................................................................................ 56
13.9.3 Method of test................................................................................................ 56
13.9.4 Interpretation of the results ............................................................................ 57
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14 Electromagnetic performance requirements and tests (dosimetry system) ..................... 57
14.1 General ................................................................................................................. 57
14.2 Requirements ....................................................................................................... 57
14.3 Method of test ....................................................................................................... 58
14.4 Interpretation of the results ................................................................................... 58
15 Mechanical performance requirements and tests ........................................................... 58
15.1 General requirement ............................................................................................. 58
15.2 Drop (dosemeter) .................................................................................................. 59
15.2.1 Requirements ................................................................................................ 59
15.2.2 Method of test................................................................................................ 59
15.2.3 Interpretation of the results ............................................................................ 59
16 Documentation .............................................................................................................. 60
16.1 Type test report .................................................................................................... 60
16.2 Certificate issued by the laboratory performing the type test ................................. 60
Annex A (normative) Confidence limits ................................................................................. 73
A.1 General ................................................................................................................. 73
A.2 Confidence interval for the mean, x ..................................................................... 73
A.3 Confidence interval for a combined quantity .......................................................... 74
Annex B (informative) Causal connection between readout signals, indicated value
and measured value ............................................................................................................. 76
Annex C (informative) Overview of the necessary actions that have to be performed
for a type test according to this document ............................................................................. 77
Annex D (informative) Uncertainty of dosimetry systems ...................................................... 78
Annex E (informative) Conversion coefficients h (0,07;source;α), h' (0,07;source;α),
pD Dh (3;source;α), and h' (3;source;α) from personal absorbed dose in 0,07 mm depth,
pD DD (0,07), to the corresponding dose equivalent quantities for radiation qualities
defined in ISO 6980-1 .......................
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