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3.1 This test method defines a procedure for testing components being considered for installation into a high-purity gas distribution system. Application of this test method is expected to yield comparable data among components tested for purposes of qualification for this installation.1.1 This test method covers a procedure for testing components for oxygen contribution to ultra-high purity gas distribution systems at ambient temperature. In addition, this test method allows testing of the component at elevated ambient temperatures as high as 70°C.1.2 This test method applies to in-line components containing electronics grade materials such as those used in a semiconductor gas distribution system.1.3 Limitations: 1.3.1 This test method is limited by the sensitivity of current instrumentation, as well as the response time of the instrumentation. This test method is not intended to be used for test components larger than 12.7-mm (1/2-in.) outside diameter nominal size. This test method could be applied to larger components; however, the stated volumetric flow rate may not provide adequate mixing to ensure a representative sample. Higher flow rates may improve the mixing but excessively dilute the sample.1.3.2 This test method is written with the assumption that the operator understands the use of the apparatus at a level equivalent to six months of experience.1.4 The values stated in SI units are to be regarded as the standard. The inch-pound units given in parentheses are 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. Specific hazard statements are given in Section 5.1.6 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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3.1 The purpose of this test method is to define a procedure for testing components being considered for installation into a high-purity gas distribution system. Application of this test method is expected to yield comparable data among components tested for the purposes of qualification for this installation.1.1 This test method covers testing components for total moisture contribution to a gas distribution system at ambient temperature. In addition, the test method allows testing at elevated ambient temperatures as high as 70°C and of the component moisture capacity and recovery.1.2 This test method applies to in-line components containing electronics grade materials such as those used in semiconductor gas distribution systems.1.3 Limitations: 1.3.1 This test method is limited by the sensitivity of current instrumentation, as well as by the response time of the instrumentation. This test method is not intended to be used for test components larger than 12.7-mm (1/2-in.) outside diameter nominal size. This test method could be applied to larger components; however, the stated volumetric flow rate may not provide adequate mixing to ensure a representative sample. Higher flow rates may improve the mixing but excessively dilute the sample.1.3.2 This test method is written with the assumption that the operator understands the use of the apparatus at a level equivalent to six months of experience.1.4 The values stated in SI units are to be regarded as the standard. The inch-pound units given in parentheses are 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. Specific hazard statements are given in Section 5.1.6 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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3.1 The purpose of this test method is to define a procedure for testing components being considered for installation into a high-purity gas distribution system. Application of this test method is expected to yield comparable data among components tested for purposes of qualification for this installation.1.1 This test method covers the testing of components for total hydrocarbons (THC) contribution to a gas distribution system at ambient temperature. In addition, this test method allows testing of the component at elevated ambient temperatures as high as 70°C.1.2 This test method applies to in-line components containing electronics grade materials in the gaseous form, such as those used in semiconductor gas distribution systems.1.3 Limitations: 1.3.1 This test method is limited by the sensitivity of current instrumentation, as well as by the response time of the instrumentation. This test method is not intended to be used for components larger than 12.7-mm (1/2-in.) outside diameter nominal size. This test method could be applied to larger components; however, the stated volumetric flow rate may not provide adequate mixing to ensure a representative sample. Higher flow rates may improve the mixing but excessively dilute the sample.1.3.2 Different instrumental methods (such as flame ionization detector (FID), mass spectrometer (MS)) will yield total hydrocarbon (THC) levels that are not comparable due to different sensitivities to different molecular species. Hydrocarbon contaminants of high-purity gas distribution systems can be subdivided into two general categories: (1) noncondensable hydrocarbons (4), that are present due to difficulty of removal and relative atmospheric abundance, and (2) condensable hydrocarbons, that are often left behind on component surfaces as residues. Condensable hydrocarbons include pump oils, degreasing agents, and polishing compound vehicles.1.3.3 Because of the tremendous disparity of hydrocarbon species, it is suggested that direct comparisons be made only among data gathered using the same detection method.1.3.4 This test method is intended for use by operators who understand the use of the apparatus at a level equivalent to six months of experience.1.4 The values stated in SI units are to be regarded as the standard. The inch-pound units given in parentheses are 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. Specific hazard statements are given in Section 5.1.6 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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1.1 This specification covers crosslinked polyethylene (PEX) pipe that is outside diameter controlled in metric pipe sizes (DN 16 to 1000) and inch pipe sizes (NPS 3 to 54), and pressure rated (see Appendix X1) using the MRS rating system. This Specification is intended for PEX pipe made by various processes, as long as the PEX pipe made by that process meets all the requirements of this Specification. Included are requirements and test methods for material, workmanship, UV protection, dimensions, hydrostatic sustained pressure, stabilizer functionality, bent-pipe hydrostatic pressure, chemical resistance, minimum operating temperature, degree of crosslinking, squeeze-off, and hydrostatic burst pressure. Requirements for pipe markings are also given. The pipe covered by this specification is intended for natural gas distribution.1.2 This specification also includes requirements for qualifying joints made using polyethylene electrofusion fittings (such as Specification F3373) and PEX pipe. Fittings to be used with PEX pipe manufactured to this specification are in Specification F2829/F2829M. Installation considerations are in X3.2.NOTE 1: NPS fittings should not be used for DN sized pipe, and DN sized fittings should not be used for NPS pipe.1.3 The text of this specification references notes, footnotes, and appendixes, which provide explanatory material. These notes and footnotes (excluding those in tables and figures) should not be considered as requirements of the specification.1.4 Units—The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.1.4.1 For consistency with ISO 9080, MRS values are only in MPa and degrees Centigrade for conversion to the pipe material designation code (for example PEX pipe with an MRS of 8 MPa is called a PEX 80.1.5 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 It is important to recognize that the results obtained by this test method or any other method for particle size determination utilizing different physical principles may disagree. The results are strongly influenced by physical principles employed by each method of particle size analysis. The results of any particle sizing method should be used only in a relative sense and should not be regarded as absolute when comparing results obtained by other methods. Particularly for fine materials (that is, average particle size < 20 μm), significant differences are often observed for laser light scattering instruments of different manufacturers. These differences include lasers of different wavelengths, detector configuration, and the algorithms used to convert scattering to particle size distribution. Therefore, comparison of results from different instruments may be misleading.35.2 Light scattering theories (Fraunhofer Diffraction4 and Mie Scattering5) that are used for determination of particle size have been available for many years. Several manufacturers of testing equipment now have units based on these principles. Although each type of testing equipment utilizes the same basic principles for light scattering as a function of particle size, different assumptions pertinent to application of the theory and different models for converting light measurements to particle size, may lead to different results for each instrument. Furthermore, any particles which are outside the size measurement range of the instrument will be ignored, causing an increase in the reported percentages within the detectable range. A particle size distribution which ends abruptly at the detection limit of the instrument may indicate that particles outside the range are present. Therefore, use of this test method cannot guarantee directly comparable results from different types of instruments.5.3 This test method can be used to determine particle size distributions of catalysts, supports, and catalytic raw materials for specifications, manufacturing control, and research and development work.5.4 For fine materials (that is, average particle size < 20 μm), it is critical that Mie Scattering Theory be applied. This involves entering an “optical model” consisting of the “real” and “imaginary” refractive indices of the solid at the wavelength of the laser. The “imaginary” refractive index is also referred to as the “absorbance,” as it has a value of zero for transparent materials such as glass beads. For common materials and naturally occurring minerals (for example, kaolin), these values are known and published, and usually included in the manufacturer’s instrument manual (for example, as an appendix). For example, kaolinite measured at 589.3 nm has a “real” refractive index of 1.55. The absorbance (imaginary component) for minerals and metal oxides is normally taken as 0.001, 0.01 or 0.1. Many of the published values were measured at 589.3 nm (sodium light) but often values at other wavelengths are also given. Extrapolation, interpolation, or estimation to the wavelength of the laser being used can therefore be made.61.1 This test method covers the determination of the particle size distribution of catalyst, catalyst carrier, and catalytic raw material particles and is one of several found valuable for the measurement of particle size. The range of average particle sizes investigated was from 1 to 300 μm equivalent spherical diameter. The technique is capable of measuring particles above and below this range. The angle and intensity of laser light scattered by the particles are selectively measured to permit calculation of a volume distribution using light-scattering techniques.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 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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5.1 The determination of the boiling range distribution of gasoline by gas chromatographic simulated distillation provides an insight into the composition of the components from which the gasoline has been blended. Knowledge of the boiling range distribution of gasoline blending components is useful for the control of refinery processes and for the blending of finished gasoline.5.2 The determination of the boiling range distribution of light hydrocarbon mixtures by gas chromatographic simulated distillation has better precision than the conventional distillation by Test Method D86. Additionally, this test method provides more accurate and detailed information about the composition of the light ends. The distillation data produced by this test method are similar to that which would be obtained from a cryogenic, true boiling point (15 theoretical plates) distillation.1.1 This test method covers the determination of the boiling range distribution of gasoline and liquid gasoline blending components. It is applicable to petroleum products and fractions with a final boiling point of 280 °C (536 °F) or lower, as measured by this test method.1.2 This test method is designed to measure the entire boiling range of gasoline and gasoline components with either high or low vapor pressure and is commonly referred to as Simulated Distillation (SimDis) by gas chromatographers.1.3 This test method has been validated for gasoline containing ethanol. Gasolines containing other oxygenates are not specifically excluded, but they were not used in the development of this test method.1.4 This test method can estimate the concentration of n-pentane and lighter saturated hydrocarbons in gasoline.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.5.1 Results in degrees Fahrenheit can be obtained by simply substituting Fahrenheit boiling points in the calculation of the boiling point-retention time correlation.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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