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4.1 High-purity ethylene is required as a feedstock for some manufacturing processes, and the presence of trace amounts of carbon dioxide and some hydrocarbons can have deleterious effects. This method is suitable for setting specifications, for use as an internal quality control tool and for use in development or research work.1.1 This test method covers the determination of carbon dioxide, methane, ethane, acetylene, and other hydrocarbons in high-purity ethylene. Hydrogen, nitrogen, oxygen, and carbon monoxide are determined in accordance with Test Method D2504. The percent ethylene is obtained by subtracting the sum of the percentages of the hydrocarbon and nonhydrocarbon impurities from 100. The method is applicable over the range of impurities from 1 to 500 parts per million volume (ppmV).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. For some specific hazard statements, see Section 6.1.3 The values stated in SI units are to be regarded as the standard. The values in parentheses are for information only.

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5.1 The determination of WPPO composition is useful in optimization of process variables, diagnosing unit performance, and in evaluating the effect of changes in waste plastic composition on WPPO performance properties.5.1.1 Aromatics and olefin hydrocarbon type analysis, including sub-classes, may be useful for evaluating suitability of WPPO as a feedstock for further processing.1.1 This test method covers a standard procedure for the determination of hydrocarbon types (saturates, olefins, styrenes, aromatics and polyaromatics) of waste plastic process oil (WPPO) from chemical or thermal processes using gas chromatography and vacuum ultraviolet absorption spectroscopy detection (GC-VUV).1.1.1 This test method is applicable for plastic recycling and circular schemes including wide range density material from polyethylene and polypropylene.1.1.2 The test method is applicable to waste plastic process oil having a final boiling point of 545 °C or lower at atmospheric pressure as measured by this test or Test Method D2887. This test method is limited to samples having a boiling range greater than 36 °C, and having a vapor pressure sufficiently low to permit sampling at ambient temperature.1.1.3 WPPOs with initial boiling points less than nC5 (36 °C) and final boiling point less than nC15 (271 °C) may be analyzed by Test Method D8369.1.1.4 Appendix X3 is applicable to waste plastic process oils that are predominantly hydrocarbons in the boiling range of pentane, nC5 (36 °C) to tetrahexacontane, nC64 (629 °C).1.2 Concentrations of group type totals are determined by percent mass or percent volume. The applicable working ranges are as follows:Total Aromatics %Mass 1 to 50Monoaromatics %Mass 1 to 50Diaromatics %Mass 1 to 15Tri-plus aromatics %Mass 0.5 to 5PAH %Mass 0.5 to 15Saturates %Mass 5 to 99Olefins %Mass 1 to 80Conjugated diolefins %Mass 0.2 to 5Styrenes %Mass 0.2 to 5The final precision concentration ranges will be defined by a future ILS.1.2.1 Saturates totals are the result of the summation of normal paraffins, isoparaffins, and naphthenes.1.2.2 Aromatics are the summation of monoaromatic and polyaromatic group types. Polyaromatic totals are the result of the summation of diaromatic and tri-plus aromatic group types.1.2.3 Olefin totals are the result of the sum of mono-olefins, conjugated diolefins, non-conjugated diolefins, and cyclic olefins.1.2.4 Styrenes totals are the sum of styrene and alkylated styrenes. Styrenes are classified separately, neither as aromatic nor olefin.1.3 Waste plastic process oil containing mixed plastic types such as polyethylene terephthalate PET and polyvinyl chloride or other material may yield compounds including hetero-compounds that are not speciated by this test method.1.4 Individual components are typically not baseline separated by the procedure described in this test method. The coelutions are resolved at the detector using VUV absorbance spectra and deconvolution algorithms.1.5 This test method may apply to other process oils from sources such as tires and bio-mass boiling between pentane (36 °C) and tetratetracontane (545 °C), but has not been extensively tested for such applications.1.6 Units—The values stated in SI units are to be regarded as standard. No other units of measurement, other than the boiling point of normal paraffins (°F) in Table 2 and Table X.3.1, are included in this standard.1.7 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.1.8 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 Nonylphenol,4 octylphenol, and bisphenol A have been shown to have toxic effects in aquatic organisms. The source of nonylphenol and octylphenol is prominently from the use of common commercial surfactants. The most widely used surfactant is NPEO which has an average ethoxylate chain of 9 mol of ethoxylate. The ethoxylate chain is readily biodegraded to form NP1EO and NP2EO, nonylphenol carboxylate (NPEC) and, under anaerobic conditions, nonylphenol. Nonylphenol will also biodegrade, but may be released into environmental waters directly at trace levels. This test method has been investigated for use with surface water and waste treatment effluent samples and is applicable to these matrices. It has not been investigated for use with salt water or solid sample matrices.5.2 The first reported synthesis of BPA was by the reaction of phenol with acetone by Zincke.5 BPA has become an important high volume industrial chemical used in the manufacture of polycarbonate plastics and epoxy resins. Polycarbonate plastic and resins are used in numerous products including electrical and electronic equipment, automobiles, sports and safety equipment, reusable food and drink containers, electrical laminates for printed circuit boards, composites, paints, adhesives, dental sealants, protective coatings, and many other products.6 The environmental source of BPA is predominantly from the decomposition of polycarbonate plastics and resins. BPA is not classified as bio-accumulative by the U.S. Environmental Protection Agency (EPA) and will biodegrade. BPA may be released into the environment waters directly at trace levels through landfill leachate and sewage treatment plant effluents.1.1 This test method covers determination of nonylphenol (NP), nonylphenol ethoxylate (NP1EO), nonylphenol diethoxylate (NP2EO), octylphenol (OP), and bisphenol A (BPA) that are partitioned into organic solvent, separated using gas chromatography and detected with mass selective detection. These compounds or isomer mixtures are qualitatively and quantitatively determined by this test method. This test method adheres to selected ion monitoring mass spectrometry but full scan mass spectrometry has also been shown to work well under these conditions. Either analysis may be used.1.2 The method detection limit (MDL) and reporting limit (RL) for NP, NP1EO, NP2EO, OP, and BPA are listed in Table 1.(A) MDL determined following the Code of Federal Regulations, 40 CFR Part 136, Appendix B.(B) Lowest point of the reporting range is calculated from the LV1 concentration calibration standard in Table 4.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this 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 Manufacturers of carpet need to monitor emissions of VOCs to assess the environmental impact of their products indoors. These results are also used to demonstrate compliance with VOC emission limits for individual VOCs.5.2 These data are also used to understand which VOCs are emitted from a product or material and to measure the magnitude of those emissions.5.3 Emission data may be used to compare different lots of carpet of the same materials of construction, or carpets composed of different materials of construction, in order to develop products with lower emissions and lower potential environmental impact.5.4 This test method should be used in conjunction with practices/guidelines for emissions testing such as Guide D5116, Practice D7143, Practice D7706, ISO 16000-9, and ISO 16000-10. These detail how to select and prepare samples and how and when to carry out emissions tests such that the concentration and profile of vapors in the exhaust air of the emission chamber/cell are representative of the product under test. This test method covers the sampling and analysis of volatile organic compounds in the exhaust gas from the chamber/cell using thermal desorption—compatible sorbent tubes and will provide the necessary analytical consistency to ensure that reproducible data is obtained for the analysis of identical vapor samples by different laboratories.1.1 This test method describes an analytical procedure for identifying and quantifying the masses of individual volatile organic compounds (individual VOCs or IVOCs) that are emitted into a flow of air from carpet specimens and collected on sorbent sampling tubes during emissions testing.1.2 This test method will be used in conjunction with a standard practice for sampling and preparing carpet specimens for emissions testing. If a specific chamber practice is not available for the carpet specimens, this test method should be used in conjunction with approved standard practices for emissions testing and sample preparation.1.3 When used in conjunction with standard practices for carpet specimen preparation and collection of vapor-phase emissions , this test method will provide a standardized means of determining the levels of IVOC in the exhaust stream of the emissions test chamber/cell. If this test method is used with a reliable practice for emissions testing, these IVOC levels can be used to determine the emission rate from a unit quantity (usually surface area) of the sample material under test.1.4 VOCs in the exhaust stream of an emissions test device are collected on thermal desorption tubes packed with a specific combination of sorbents using active (pumped) sampling. (See Practice D6196 for a more general description of vapor collection using pumped sampling onto sorbent tubes.) The samples are analyzed by thermal desorption (TD) with gas chromatography and mass spectrometry detection (GC/MS) and/or flame ionization detection (FID) depending upon the requirements of the specific materials emissions testing/certification protocol.1.5 This test method can be used for the measurement of most GC-compatible organic vapors ranging from the approximate volatility from n-hexane to n-hexadecane (that is, compounds with vapor pressures ranging from 16 kPa to 4 × 10-4 kPa at 25°C). Properties other than a compound’s vapor pressure such as affinity for the sorbent may need to be taken into account. Compounds with vapor pressures outside this range may or may not be quantifiable by this test method. However, qualitative data concerning the identity of a compound(s), outside the stated volatility range for quantitation, may still be useful to the user. This test method can be applied to analytes over a wide concentration range—typically 1 μg/m3 to 1 mg/m3 concentration of vapor in the exhaust air from the emission cell or chamber.1.6 This test method is not capable of quantifying all compounds which are emitted from carpets. See the appropriate test practices/methods for determining other compounds that are not amenable to analysis by gas chromatography (that is, Test Method D5197 for the determination of aldehydes).1.7 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.8 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.1.9 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 These test methods were developed to measure the types and amounts of aromatics in mineral spirits to determine compliance with air pollution regulations that restrict the aromatic content of solvents. They have been demonstrated to be workable and to produce accurate results. However, due to the sensitivity of the tests to operating variables, some laboratories having limited experience with gas chromatographic analyses of hydrocarbons may experience difficulty in performing the tests.1.1 These test methods cover the determination of ethylbenzene and total eight-carbon (C8) and heavier aromatics in the concentration range from 0.1 to 30 % in mineral spirits having a distillation range from 149 to 210 °C (300 to 410 °F) as determined by Test Method D86. The procedures permit the identification and calculation of concentrations of aromatic components to 0.1 volume %.1.2 It is recognized by analytical chemists that a single column gas chromatography analysis of an unknown sample is risky. In such cases, multiple and different analytical techniques must be used for absolutely positive identification, for example, several different gas chromatography columns, gas chromatography/mass spectrometer, or gas chromatography/infrared, etc. In these test methods the material is known and is clearly defined.1.3 Oxygenated compounds, if present, may interfere and cause erroneous results. Such oxygenated compounds are not normally present in mineral spirits.1.4 Three test methods are covered as follows:1.4.1 Test Method A, measurement of ethylbenzene content, C8 plus higher aromatics (except ethylbenzene), and total aromatics by means of a single packed column gas chromatographic analysis.1.4.2 Test Method B, measurement of ethylbenzene content by means of a rapid packed column gas chromatographic analysis.1.4.3 Test Method C, measurement of ethylbenzene content, C8 plus higher aromatics (except ethylbenzene) and total aromatics by means of a capillary column gas chromatographic analysis.1.5 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.6 For purposes of determining conformance of an observed or a calculated value using this test method to relevant specifications, test result(s) shall be rounded off “to the nearest unit” in the last right-hand digit used in expressing the specification limit, in accordance with the rounding-off method of Practice E29.1.7 For hazard information and guidance, see the supplier’s Material Safety Data Sheet.1.8 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.1.9 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 Vinyl chloride-containing polymers are widely used to package a variety of materials, including foods.5.2 Vinyl chloride monomer has been shown to be a human carcinogen. Threshold toxicity value has not been established.5.3 Plastic manufacturers, food packagers, government agencies, etc. have a need to know the residual vinyl chloride monomer content of vinyl chloride-containing polymers.1.1 This test method is suitable for determining the residual vinyl chloride monomer (RVM) content of homopolymer and copolymers of vinyl chloride down to a concentration of ∼5 µg/kg (ppb).1.2 This test method is applicable to any polymer form, such as resin, compound, film, bottle wall, etc. that can be dissolved in a suitable solvent.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. Specific hazard statements are given in Section 9 and Note 10.NOTE 1: This standard is equivalent to ISO 6401.1.4 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 Low operating temperature fuel cells such as PEMFCs require high purity hydrogen for optimal performance and longevity. Organic halides and formaldehyde can react with catalyst in PEMs and non-methane hydrocarbons degrade PEM stack performance.1.1 The gas chromatography/mass spectrometry (GC/MS) procedure described in this test method is used to determine concentrations of total organic halides and total non-methane hydrocarbons (TNMHC) in hydrogen by measurement of individual target halocarbons (Table 1) and hydrocarbons (including formaldehyde, Table 1 and Table 2), respectively.1.2 Mention of trade names in this test method does not constitute endorsement or recommendation for use. Other manufacturers’ equipment or equipment models can be used.1.3 Units—The values stated in SI units are to be regarded as 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 practice is useful in identifying the major organic constituents in wastewater for support of effective in-plant or pollution control programs. Currently, the most practical means for tentatively identifying and measuring a range of volatile organic compounds is gas-liquid chromatography. Positive identification requires supplemental testing (for example, multiple columns, speciality detectors, spectroscopy, or a combination of these techniques).1.1 This practice covers general guidance applicable to certain test methods for the qualitative and quantitative determination of specific organic compounds, or classes of compounds, in water by direct aqueous injection gas chromatography (1, 2, 3, 4).21.2 Volatile organic compounds at aqueous concentrations greater than about 1 mg/L can generally be determined by direct aqueous injection gas chromatography.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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