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ISO/ASTM 51649-2005 在300 keV 和25 MeV 能量之間輻射加工用電子束設(shè)備中劑量測定的實施規(guī)程

作者:百檢網(wǎng) 時間:2021-07-15

標(biāo)準(zhǔn)號:ISO/ASTM 51649-2005
中文標(biāo)準(zhǔn)名稱:在300 keV 和25 MeV 能量之間輻射加工用電子束設(shè)備中劑量測定的實施規(guī)程
英文標(biāo)準(zhǔn)名稱:Practice for dosimetry in an electron beam facility for radiation processing at energies between 300 keV and 25 MeV
標(biāo)準(zhǔn)類型:F80
發(fā)布日期:1999/12/31 12:00:00
實施日期:1999/12/31 12:00:00
中國標(biāo)準(zhǔn)分類號:F80
國際標(biāo)準(zhǔn)分類號:17.240
適用范圍:1 This practice covers dosimetric procedures to be fol-lowed in Installation Qualification, Operational Qualification and Performance Qualifications (IQ, OQ, PQ), and routine processing at electron beam facilities to ensure that the product has been treated with an acceptable range of absorbed doses. Other procedures related to IQ, OQ, PQ, and routine product processing that may influence absorbed dose in the product are also discussed. Note 1—For guidance in the selection and calibration of dosimeters, see ISO/ASTM Guide 51261. For further guidance in the use of specific dosimetry systems, and interpretation of the measured absorbed dose in the product, also see ISO/ASTM Practices 51275, 51276, 51431, 51607, 51631, 51650, and 51956. For use with electron energies above 5 MeV, see Practice E 1026, and ISO/ASTM Practices 51205, 51401, 51538, and 51540 for discussions of specific large volume dosimeters. For discussion of radiation dosimetry for pulsed radiation, see ICRU Report 34. 2 The electron beam energy range covered in this practice is between 300 keV and 25 MeV, although there are some discussions for other energies. 3 Dosimetry is only one component of a total quality assurance program for an irradiation facility. Other measures besides dosimetry may be required for specific applications such as medical device sterilization and food preservation. 4 Other specific ISO and ASTM standards exist for the irradiation of food and the radiation sterilization of health care products. For food irradiation, see ISO/ASTM Practice 51431. For the radiation sterilization of health care products, see ISO 11137. In those areas covered by ISO 11137, that standard takes precedence. 5 This standard does not purport to address all of the safety concerns, if any, associated with, its use. It is the responsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory requirements prior to use.

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