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4.1 Water-insoluble materials present in a solvent expected to be completely water miscible may interfere with many uses of the solvent. This test method provides a measure of the miscibility of water-soluble solvents with a polar medium-water. It also provides a qualitative indication of the presence or absence of water-immiscible contaminants.4.2 The results of this test method may be used in assessing compliance with a specification. Prior to agreeing to this test method as the basis of a specification requirement, it may be desirable that the interpretation of what constitutes cloudiness or turbidity be agreed upon between the supplier and the purchaser.1.1 This test method covers the determination of the miscibility of water-soluble solvents with water. While written specifically for testing acetone, isopropyl alcohol (isopropanol), and methyl alcohol (methanol), the method is suitable for testing most water-soluble solvents.1.2 This test method serves to detect water-immiscible contaminants qualitatively; the level of detection of these impurities varies widely with both the type of solvent and the type of impurity.1.3 The level of detection of water-insoluble materials depends upon the solvent tested and the type of impurity or impurities present, that is paraffin, olefin, aromatic, high molecular weight alcohol, or ketone, etc. There is, therefore, no specific level of impurity detected by this procedure.NOTE 1: This test method is normally performed at ambient, but other temperatures may be used as specified by the consumer and supplier.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.5 For specific hazard information and guidance, consult the supplier’s Safety Data Sheet for materials listed in this test method.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 test method is suitable for determining the quantity of hydrogen peroxide, organic hydroperoxides, and organic peroxides as total active oxygen in various hydrocarbon streams for both quality control and quality assurance of the product.1.1 This test method covers the determination of trace peroxides in various hydrocarbon streams. A list of typical hydrocarbon streams can be found in Appendix X2.1.2 This test method is applicable to the determination of peroxides in petroleum liquids including, but not limited to, 1,3-butadiene, styrene, methylcyclohexane, and alpha olefins in the range of 0.1 mg/kg to 100 mg/kg active oxygen. The limit of detection (LOD) is 0.03 mg/kg for active oxygen and the limit of quantitation (LOQ) is 0.11 mg/kg active oxygen. The upper limit has been determined by the calibration range.NOTE 1: LOD and LOQ were calculated using data obtained during development of the method.1.3 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.1.4 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.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. For specific hazard statements, see Section 9.1.6 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 Sources of particulate and water-soluble gaseous fluorides in the atmosphere include the fertilizers, aluminum reduction plants, phosphate processors, steel mills, coal burning operations, brick and tile manufacturers, and various less significant sources (5). Gaseous fluorides can cause adverse effects when ingested or inhaled by animals or humans, or absorbed by plants. The procedures documented in this test method provide a means of determining of particulate and water soluble gaseous fluoride in atmospheres.5.2 This test method provides a means of separation and collection of particulate and water soluble gaseous fluoride and provides samples that are convenient to analyze.1.1 This test method provides a procedure for separation and collection of particulate and water-soluble gaseous fluorides from the atmosphere on a chemically treated filter and in an impinger. The sampling rate may vary from 30  L/min (1.0 ft3/min) to 15 L/min (0.5 ft3/min) for longer sampling periods depending on the atmospheric fluoride concentration. This test method is not intended to be applied to gaseous fluorine compounds that are not water-soluble.1.2 There are several limitations of the test method:1.2.1 Although the acid-treated, medium retentive, prefilter has been shown to allow passage of HF, it restricts passage of particulate matter only as small as about 1 μm. Thus, smaller particulate matter may pass through the filter and be collected in or pass through the impingers.1.2.2 The maximum sample volume to be taken using this test method prior to changing the acid-treated prefilter is recommended as 12 m3. This recommendation is made to minimize any effects due to particulate matter build-up.1.3 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.1.4 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. For specific precautionary statements, see 7.4.3.1.5 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 It is expected that this practice will be suitable to identify and quantify contaminants found in systems, system materials, and components used in systems requiring a high level of cleanliness, such as components for oxygen service. Nonmetallic piece parts such as seals and valve seats can be tested as received. Warning—If parts being tested are to be subsequently installed in an oxygen-enriched system, residual extraction solvent remaining in the part due to inadequate drying may increase the susceptibility of the system to ignition. The extraction solvent shall be thoroughly removed from the parts prior to service.5.2 Processing materials such as gloves and wipers, or samples thereof, to be used in the cleaning operation can be evaluated prior to use to ensure that the proposed cleaning solvent does not extract contaminants that may be deposited as residues on the surface to be cleaned.NOTE 1: Test methods that do not require Soxhlet equipment, such as Test Methods E1560 and E1731, may be suitable alternatives for evaluation of processing materials. Test Method G144 with Practice G136 may be suitable for use when the material to be tested is not degraded by sonication. However, results from this test method cannot be directly compared to results from other test methods. Soxhlet extraction may be more aggressive than other extraction methods.5.3 Wipers or other cleaning supplies can be tested before and after use to determine the amount of contaminant removed from a surface. The type of contaminant removed from the surface may also be determined by qualitative analysis of the extracted NVR using analytical methods such as Fourier Transform Infrared (FTIR). This procedure can be used to obtain samples for NVR analysis using contaminated control coupons that were subjected to the cleaning process as controls to validate cleaning operations.5.4 The selection of the solvent requires some knowledge of the contaminant (see Practice G93 for recommendations). If a nonvolatile residue (NVR) analysis is to be performed on the molecular contaminant, the boiling point of the solvent shall be significantly lower than that of the contaminant. For other analytical methods, the tester must know the accuracy of the analytical methods, and the solvent shall be chosen so as not to interfere with the selected analytical method. To identify the composition of the NVR, analytical methods such as infrared spectroscopy or gas chromatography/mass spectroscopy have been used satisfactorily.1.1 This practice describes a procedure for the determination of residual contamination in materials to be used within or in contact with hardware requiring a high level of cleanliness, such as components for oxygen service, by Soxhlet extraction.1.2 This practice may be used for extracting nonvolatile and semivolatile residues from solids such as new and used gloves, new and used wipers, contaminated test specimens or control coupons, small piece parts (metallic or nonmetallic), etc. When used with proposed consumable cleaning materials (wipers, gloves, etc.), this practice may be used to determine the potential of the proposed solvent to extract contaminants (plasticizers, residual detergents, brighteners, etc.) from the cleaning material and deposit them on the surface being cleaned.1.3 This practice is not suitable for the evaluation of particulate contamination.1.4 The values stated in SI units are standard.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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4.1 In general, with materials of this type, softening does not take place at a definite temperature. As the temperature rises, these materials gradually and imperceptibly change from brittle solids to soft, viscous liquids. For this reason, the determination of the softening point must be made by a fixed, arbitrary, and closely defined methods if the results are to be comparable.1.1 This test method covers the determination of the softening point of certain alkali-soluble resins having uniform plastic flow characteristics as the melting point is approached.1.2 The resin manufacturer should specify whether or not this test method may be used for his product(s).1.3 This test method is not suitable for styrene-maleic anhydride resins.NOTE 1: For testing rosin and other resins, see Test Method E28. For testing asphalts, tars, and pitches, see Test Method D2398.1.4 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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