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ASTM International, 06/01/2016
Publisher: ASTM
File Format: PDF
$34.00$69.00
Published:01/06/2016
Pages:12
File Size:1 file , 400 KB
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1.1 This test method covers a calorimetric measurement of the total absorbed dose delivered in a single pulse of electrons from an electron linear accelerator or a flash X-ray machine (FXR, e-beam mode) used as an ionizing source in radiation-effects testing. The test method is designed for use with pulses of electrons in the energy range from 10 to 50 MeV and is only valid for cases in which both the calorimeter and the test specimen to be irradiated are “thin” compared to the range of these electrons in the materials of which they are constructed.
1.2 The procedure described can be used in those cases in which (1) the dose delivered in a single pulse is 5 Gy(matl)2 [500 rd (matl)] or greater, or (2) multiple pulses of a lower dose can be delivered in a short time compared to the thermal time constant of the calorimeter. The units for the total absorbed dose delivered to a material require the specification of the material and the notation “matl” refers to the active material of the calorimeter. The minimum dose per pulse that can be acceptably monitored depends on the variables of the particular test, including pulse rate, pulse uniformity, and the thermal time constant of the calorimeter.
1.3 A determination of the total dose is made directly for the material of which the calorimeter block is made. The total dose in other materials can be calculated from this measured value by formulas presented in this test method. The need for such calculations and the choice of materials for which calculations are to be made shall be subject to agreement by the parties to the test.
1.4 The values stated in SI units are to be regarded as the standard. The values in parenthesis are provided for information only.
1.5 This standard does not purport to address the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
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