Decommissioning of medical cyclotron

This document provides information and guidelines on the decommissioning of a medical cyclotron facility, with a focus on activated or contaminated parts. Useful information and guidelines are given on decommissioning strategy and plan, safety assessment, and various decommissioning activities. This document also provides the guideline on the estimation of activation level using Monte Carlo simulation and the methodology for the measurement of activated radionuclides in the main structure, system components, and shielding walls, ceilings and floors during operation and decommissioning. Financial provisions and radioactive waste management aspects are also included. This document can be used by organizations responsible for operation and decommissioning of a medical cyclotron facility. In addition, it is expected that organizations that design a medical cyclotron or manage radioactive waste generated by cyclotron can utilize or refer to this document in whole or in part.

Démantèlement des cyclotrons médicaux

General Information

Status
Published
Publication Date
15-Oct-2025
Current Stage
6060 - International Standard published
Start Date
16-Oct-2025
Due Date
12-Jul-2025
Completion Date
16-Oct-2025
Ref Project
Standard
ISO 8939:2025 - Decommissioning of medical cyclotron Released:10/16/2025
English language
18 pages
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Standards Content (Sample)


International
Standard
ISO 8939
First edition
Decommissioning of medical
2025-10
cyclotron
Démantèlement des cyclotrons médicaux
Reference number
© ISO 2025
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting on
the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address below
or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Decommissioning planning for a medical cyclotron facility . 3
4.1 General .3
4.2 Responsibilities .3
4.3 Decommissioning strategy .4
4.4 Decommissioning plan .4
4.5 Project management . .5
4.6 Decommissioning activities .5
4.7 Safety assessment .5
4.7.1 Identification of relevant safety criteria .6
4.7.2 Risk assessment .6
4.8 Quality assurance programme.6
4.9 Radiation protection programme .7
4.10 Financial resources .8
4.11 Final radiological survey .8
4.12 Final decommissioning report .8
5 Activation evaluation . 8
5.1 General .8
5.2 Activation level estimation method .9
5.2.1 Monte Carlo computer simulation .10
5.2.2 Measurement of activation . .11
5.3 Nuclides of concern .11
6 Management of radioactive waste .12
6.1 General . 12
6.2 Minimization of waste . 13
6.3 Categorization and characterization of waste . 13
6.4 Discharge control of liquid or airborne radioactive effluents. 13
6.5 Onsite handling and processing of waste . 13
6.6 Onsite storage of waste.14
6.7 Shipment of waste .14
Annex A (informative) Measurement method for determining thermal neutron fluence rate on
concrete surface .15
Annex B (informative) Measurement method for determining specific activity using a
scintillation survey meter. 16
Bibliography . 17

iii
Foreword
This document was prepared by Technical Committee ISO/TC 85, Nuclear energy, nuclear technologies, and
radiological protection, Subcommittee SC 5, Nuclear installations, processes and technologies.
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out through
ISO technical committees. Each member body interested in a subject for which a technical committee
has been established has the right to be represented on that committee. International organizations,
governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely
with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are described
in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the different types
of ISO documents should be noted. This document was drafted in accordance with the editorial rules of the
ISO/IEC Directives, Part 2 (see www.iso.org/directives).
ISO draws attention to the possibility that the implementation of this document may involve the use of (a)
patent(s). ISO takes no position concerning the evidence, validity or applicability of any claimed patent
rights in respect thereof. As of the date of publication of this document, ISO had not received notice of (a)
patent(s) which may be required to implement this document. However, implementers are cautioned that
this may not represent the latest information, which may be obtained from the patent database available at
www.iso.org/patents. ISO shall not be held responsible for identifying any or all such patent rights.
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and expressions
related to conformity assessment, as well as information about ISO's adherence to the World Trade
Organization (WTO) principles in the Technical Barriers to Trade (TBT), see www.iso.org/iso/foreword.html.
This document was prepared by Technical Committee ISO/TC 85, Nuclear energy, nuclear technologies, and
radiological protection, Subcommittee SC 5, Nuclear installations, processes and technologies.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www.iso.org/members.html.

iv
Introduction
Many types of accelerators have been installed and operated in the last several decades primarily for nuclear
research and radioisotope production worldwide.
A cyclotron is a type of particle accelerator invented by Ernest O. Lawrence in 1934 in which charged
particles are accelerated outwards from the centre along a spiral path. Cyclotrons have been the best
sources of high–energy beams for nuclear physics experiments for the last several decades. Additionally,
cyclotrons can be used in particle therapy to treat various types of cancers. Ion beams from cyclotrons can
be used to penetrate the body and eliminate tumours by radiation treatment, such as in proton therapy.
Cyclotron beams can be used to bombard other atoms to produce various radioisotopes for diagnostic
imaging in positron emission tomography (PET), single photon emission computed tomography (SPECT)
and therapeutic applications in brachytherapy and alpha particle therapy. According to IAEA NW-T-2.9, it is
estimated to be over 1500 cyclotron facilities worldwide as of 2025.
Some cyclotron facilities have been dismantled and decommissioned because they have reached the end of
design life or because of ageing, accidents or other reasons like the changes in the purpose of use, location,
etc. Even though any standardized technical or administrative procedures for decommissioning of medical
cyclotron facilities have not been established yet, however, a safe decommissioning process is needed.
Therefore, it is necessary to analyse the major considerations such as activation and radioactive waste
management during the decommissioning of various kinds of cyclotron facilities.
Decommissioning actions typically involve different radiation protection strategies, such as radiological
surveys and monitoring; decontamination; dismantling and removal of structures, systems and components
and management of the radioactive waste generated during decommissioning. These actions are carried
out to achieve a progressive and systematic reduction in radiological hazards during decommissioning and
are conducted on a basis of planning and assessment to ensure the safety and protection of the workers, the
public and the environment and to ensure that the facility meets the planned decommissioning end state.
It is necessary to clarify the dismantling procedures at each stage from installation to decommissioning
of a medical cyclotron and to take measures to minimize decommissioning costs. This document aims to
develop proper decommissioning procedures and methods for medical cyclotron facilities, that accelerate
11 13 15 18
protons or deuterons for PET radiotracers ( C, N, O, F) by
— development of procedural guidelines for the decommissioning of a medical cyclotron facility,
— establishment of activation evaluation techniques for the end of operation of each cyclotron type, and
— consideration of the management of radioactive waste during the decommissioning of a medical cyclotron
facility.
v
International Standard ISO 8939:2025(en)
Decommissioning of medical cyclotron
1 Scope
This document provides information and guidelines on the decommissioning of a medical
...

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