5.1 An accurate measure of the total absorbed dose is necessary to ensure the validity of the data taken, to enable comparison to be made of data taken at different facilities, and to verify that components or circuits are tested to the radiation specification applied to the system for which they are to be used.5.2 The primary value of a calorimetric method for measuring dose is that the results are absolute. They are based only on physical properties of materials, that is, the specific heat of the calorimeter-block material and the Seebeck EMF of the thermocouple used or the temperature coefficient of resistance (α) of the thermistor used, all of which can be established with non-radiation measurements.5.3 The method permits repeated measurements to be made without requiring entry into the radiation cell between measurements.1.1 This test method covers a calorimetric measurement of the total absorbed dose delivered by a single pulse of electrons from an electron linear accelerator or a flash X-ray machine (FXR, e-beam mode). 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 using Eq 3 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 all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method is useful for the analysis of total uranium in water following wet-ashing, as required, due to impurities or suspended materials in the water.1.1 This test method covers the determination of total uranium, by mass concentration, in water within the calibrated range of the instrument, 0.1 μg/L or greater. Samples with uranium mass concentrations above the laser phosphorimeter dynamic range are diluted to bring the concentration to a measurable level.1.2 This test method was used successfully with reagent water. It is the user’s responsibility to ensure the validity of this test method for waters of untested matrices.1.3 The values stated in SI units are to be regarded as the standard.1.4 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 appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method is a standard procedure for determining the resistance to water penetration during rapid cyclic pulses of dynamic air pressure differences. The air-pressure differences acting across a building envelope vary greatly. These factors should be fully considered prior to specifying the test pressure difference to be used.5.2 The median test pressure used in this test method is defined as the specified test pressure supplied by the user and related to the maximum positive building design pressure. This test method departs from the format of other ASTM water penetration resistance test methods based on a maximum test pressure related to a maximum positive building design pressure.5.3 As the specified or median test pressure is increased, the maximum test pressure in this procedure is also increased to 1.5 times the specification median test pressure. This higher maximum test pressure may not be representative of actual building service conditions. For this reason the maximum recommended median test pressure is 480 Pa (10 psf), which corresponds to a maximum test pressure of 720 Pa (15 psf).5.4 The pulsed pressure of this test method may act to pump water past dry seals and breather systems of units incorporating these features, thereby making the test method more severe than a static pressure test method. On the other hand, the low pressure portions of the pressure cycles of this test method may allow weep systems and drainage dams to dissipate water from units incorporating these features, thereby making the test method less severe than a static pressure test method.NOTE 1: In applying the results of tests by this test method, note that the performance of a wall or its components, or both, may be a function of proper installation and adjustment. In service, the performance will also depend on the rigidity of supporting construction and on the resistance of components to deterioration by various causes, (vibration, thermal expansion and contraction, and so forth). It is difficult to accurately simulate the actual complex wetting conditions that can be encountered in service, with large wind-blown water drops, increasing water drop impact pressures with increasing wind velocity and lateral or upward moving air and water. Some designs are more sensitive than others to this upward moving water.NOTE 2: This test does not identify unobservable liquid water which may penetrate into the test specimen.1.1 This test method covers the determination of the resistance of exterior windows, skylights, and doors to water penetration when water is applied to the outdoor face and exposed edges simultaneously with a rapid pulsed air pressure at the outdoor face higher than the pressure at the indoor face.1.2 This test method is applicable to windows, skylights, or doors alone. Those interested in testing curtain walls to rapid pulsed air pressure differences should use AAMA 501.1-94.1.3 This test method addresses water penetration through a manufactured assembly. Water that penetrates the assembly, but does not result in a failure as defined herein, may have adverse effects on the performance of contained materials such as sealants and insulating or laminated glass. This test method does not address these issues.1.4 The proper use of this test method requires a knowledge of the principles of pressure measurement.1.5 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.1.6 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 appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This guide is intended to illustrate the fabrication of ultrasonic reference blocks that are representative of the production material to be examined. Care in material selection and fabrication can result in the manufacture of reference blocks that are ultrasonically similar to the production material thus eliminating the reference block as an examination variable.1.1 This guide covers general procedures for the material selection and fabrication of reference blocks made of metal or metal alloys and intended to be used for the examination of the same or similar production materials by pulsed longitudinal ultrasonic waves applied perpendicular to the beam entry surface. Primary emphasis is on solid materials but some of the techniques described may be used for midwall examination of pipes and tubes of heavy wall thickness. Near-surface resolution in any material depends upon the characteristics of the instrument and search unit employed.1.2 This guide covers the fabrication of reference blocks for use with either the immersion or the contact method of ultrasonic examination.1.3 Reference blocks fabricated in accordance with this guide can be used to determine proper ultrasonic system operation. Area-amplitude and distance-amplitude curves can also be determined with these reference blocks.1.4 This guide does not specify reference reflector sizes or product rejection limits. It does describe typical industry fabrication practices and commonly applied tolerances where they lend clarity to the guide. In all cases of conflict between this guide and customer specifications, the customer specification shall prevail.1.5 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.1.6 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 to determine the applicability of regulatory limitations prior to use.

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5.1 Hydrogen content represents a fundamental quality of a petroleum distillate that has been correlated with many of the performance characteristics of that product. Combustion properties of gas turbine fuels are related primarily to hydrogen content. As hydrogen content of these fuels decreases, soot deposits, exhaust smoke, and thermal radiation increase. Soot deposits and thermal radiation can increase to the point that combustor liner burnout will occur. Hydrogen content is a procurement requirement of the following military fuels: JP-5 specified in MIL-DTL-5624, JP-8 specified in MIL-DTL-83133, and Naval Distillate Fuel specified in MIL-DTL-16884.5.2 This test method provides a simple and precise alternative to existing test methods (D3701, D4808, and D5291) for determining the hydrogen content of petroleum distillate products.1.1 This test method covers the determination of the hydrogen content of middle distillate petroleum products using a low-resolution pulsed nuclear magnetic resonance (NMR) spectrometer. The boiling range of distillates covered by the test method is 150 °C to 390 °C. While this test method may be applicable to middle distillates outside this boiling range, in such cases the precision statements may not apply. The test method is generally based on Test Methods D3701 and D4808, with a major difference being the use of a pulsed NMR spectrometer instead of a continuous wave NMR spectrometer.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.2.1 The preferred units are mass %.1.3 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 appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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1.1 This practice² describes an ultrasonic examination procedure for detecting discontinuities in material using instruments that transmit and receive pulsed longitudinal ultrasonic waves introduced into the material to be examined while immersed in or impinged upon by a liquid coupling agent. This practice applies to any material that can conduct sound waves of an appropriate frequency, and can be immersed in a liquid coupling agent for inspection, or can be subject to inspection by the use of a column or stream of the couplant between the search unit and the material being examined.Note 1—Practice E 1001 is a complementary document that extends Practice E 214 by describing more detailed procedures.1.2 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 appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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4.1 Flash X-ray facilities provide intense bremsstrahlung radiation environments, usually in a single sub-microsecond pulse, which often fluctuates in amplitude, shape, and spectrum from shot to shot. Therefore, appropriate dosimetry must be fielded on every exposure to characterize the environment, see ICRU Report 34. These intense bremsstrahlung sources have a variety of applications which include the following:4.1.1 Studies of the effects of X-rays and gamma rays on materials.4.1.2 Studies of the effects of radiation on electronic devices such as transistors, diodes, and capacitors.4.1.3 Computer code validation studies.4.2 This guide is written to assist the experimenter in selecting the needed dosimetry systems for use at pulsed X-ray facilities. This guide also provides a brief summary of the information on how to use each of the dosimetry systems. Other guides (see Section 2) provide more detailed information on selected dosimetry systems in radiation environments and should be consulted after an initial decision is made on the appropriate dosimetry system to use. There are many key parameters which describe a flash X-ray source, such as dose, dose rate, spectrum, pulse width, etc., such that typically no single dosimetry system can measure all the parameters simultaneously. However, it is frequently the case that not all key parameters must be measured in a given experiment.1.1 This guide provides assistance in selecting and using dosimetry systems in flash X-ray experiments. Both dose and dose-rate techniques are described.1.2 Operating characteristics of flash X-ray sources are given, with emphasis on the spectrum of the photon output.1.3 Assistance is provided to relate the measured dose to the response of a device under test (DUT). The device is assumed to be a semiconductor electronic part or system.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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