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4.1 This test method was developed for the determination of nitrogen trichloride in samples of carbon tetrachloride liquid taken from the compressor suction chiller bottoms of chlorine production plants and other places in the plants that may collect and concentrate nitrogen trichloride to levels that could explode. The test method was then modified to measure the lower levels of nitrogen trichloride observed in product liquid chlorine. This test method is sensitive enough to measure the levels of nitrogen trichloride observed in the normal production of liquid chlorine.4.2 This test method for nitrogen trichloride will require the dilution (100:1) of highly concentrated in-process samples to bring them within the working range of the analysis.1.1 This test method uses high performance liquid chromatography (HPLC) to determine nitrogen trichloride levels in liquid chlorine at the 0.1 to 600 μg/g (ppm) range. Solvent samples from chlorine production facilities containing very high concentrations of nitrogen trichloride may be analyzed by dilution with methanol.1.2 Review the current safety data sheet (SDS) for detailed information concerning toxicity, first aid procedures, and safety precautions.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 and health practices and determine the applicability of regulatory limitations prior to use. Specific hazard statements are given in Section 8.

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4.1 This test method was developed for the determination of bromine chloride in liquid chlorine. Bromide is a common contaminant in all salt sources that are used in the production of chlorine. This bromide content of the salt is converted into bromine chloride in the liquid chlorine product. This test method is sensitive enough to measure the levels of bromine chloride observed in normal production chlorine.1.1 This test method uses high performance liquid chromatography (HPLC) to determine bromine chloride levels in liquid chlorine at the 10 to 1400 μg/g (ppm) range.1.2 Review the current safety data sheet (SDS) for detailed information concerning toxicity, first aid procedures, and safety precautions.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 and health practices and determine the applicability of regulatory limitations prior to use. Specific hazard statements are given in Section 8.

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5.1 Specification D1655 provides a maximum permissible concentration (5.7 mg/L) of MDA in aviation turbine fuel. This test method will allow the quantification of MDA in aviation turbine fuels. The MDA additive is used for fuel thermal stability control and to reduce fuel degradation caused by the presence of trace metals (copper in particular) in aviation fuels.1.1 This test method covers the determination of the metal deactivator additive (MDA) content of aviation turbine fuels. The specific MDA determined and used to develop this test method is N,N′-disalicylidene-1,2-propanediamine. Other MDAs have not been tested by this test method.1.1.1 This test method specifically covers the determination of uncomplexed MDA content in aviation turbine fuel. MDA is a chelator of divalent metal ions, and the MDA-metal ion complexed species content of aviation turbine fuel will not be accounted for by this test method.1.2 This test method is divided into two procedures: (1) Procedure A uses a semi-portable capillary-liquid chromatography system (Capillary-HPLC) that may be used in the field or laboratory; (2) Procedure B uses a standard laboratory version of liquid chromatography (Conventional-HPLC). Procedures A and B have separate precisions.1.3 The test method has an interim repeatability determined in accordance with Practice D6300. Based on the mean values of the samples used in the interim repeatability study, Procedure A is applicable in the range of 0.50 mg/mL to 10.0 mg/mL; the range for Procedure B is 0.60 mg/mL to 9.6 mg/mL. Higher concentrations can be determined by dilution, but the precision of the test method has not been determined.1.3.1 An extended interlaboratory study (ILS) will be conducted in the future to determine the full repeatability and reproducibility and the final applicable concentration ranges.1.3.2 The test method applies to MDA in petroleum-based aviation fuels and Synthetic Aviation Fuels (SAF). However, for the interim precision, a petroleum-based aviation fuel was used. Future ILS will include petroleum-based and SAFs. The test method is applicable to aviation fuels conforming to Specification D1655.1.4 Appendix X2 indicates other additives that have been verified to not interfere with the analysis of this test method.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 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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4.1 This test method provides for the qualitative and quantitative determination of denatonium benzoate in engine coolant in milligrams per litre to low percent range and requires approximately 1 mL per test, with results available in less than 10 min. Denatonium benzoate is a compound composed of a quaternary ammonium cation, denatonium and an inert anion, benzoate. In solution the denatonium benzoate exists in equilibrium between the denatonium benzoate compound, the denatonium cation and benzoate anion. By slightly adjusting the pH of the solution to be more acidic (≈ pH 4.6) the equilibrium will be shifted to the direction of forming more denatonium and benzoate ions in the solution.1.1 This test method covers the chemical analysis of engine coolant for denatonium benzoate (DNB) by high-performance liquid chromatography (HPLC). DNB is added to potentially render engine coolant unpalatable to animals and humans. This analytical method was designed for the analysis of DNB and is not valid for any other bittering agents such as denatonium saccharide.1.2 This test method is applicable to both new and used coolants.1.3 Coelution of other ions may cause interferences in the detection of the denatonium cation. In the case of unfamiliar formulations, identification verification should be performed by either or both fortification and dilution of the sample matrix with denatonium ion.1.4 The values stated in SI units are to be regarded as standard. The values 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.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 The average sulfur chain length is an important parameter in determining the behavior of the silane in a rubber mixture.1.1 This test method covers the characterization of silanes, or of admixtures of silane and carbon black (see 10.4), of the type bis-(triethoxysilylpropyl)sulfane by high performance liquid chromatography.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 Furanic compounds are generated by the degradation of cellulosic materials used in the solid insulation systems of electrical equipment.5.2 Furanic compounds which are oil soluble to an appreciable degree will migrate into the insulating liquid.5.3 High concentrations or unusual increases in the concentrations of furanic compounds in oil may indicate cellulose degradation from aging or incipient fault conditions. Testing for furanic compounds may be used to complement dissolved gas in oil analysis as performed in accordance with Test Method D3612.1.1 This test method covers the determination in electrical insulating liquids of products of the degradation of cellulosic materials such as paper, pressboard, and cotton materials typically found as insulating materials in electrical equipment. These degradation products are substituted furan derivatives, commonly referred to as furanic compounds or furans. This test method allows either liquid/liquid or solid phase extraction (SPE) of the furanic compounds from the sample matrix followed by analysis for specific furanic compounds by HPLC or direct injection for analysis of specific furanic compounds by HPLC.1.2 The individual furanic compounds that may be identified and quantified include the following:5-hydroxymethyl-2-furaldehydefurfuryl alcohol2-furaldehyde2-acetylfuran5-methyl-2-furaldehyde1.3 The direct injection method generally has a higher limit of detection, especially for furfuryl alcohol. Greater interference for furfuryl alcohol may be expected when using the direct injection method as opposed to extraction methods.1.4 This test method has been used to successfully test for furanic compounds in mineral insulating oil, silicone fluid, high fire point electrical insulating oils of mineral origin, askarels, and perchloroethylene-based dielectric fluids.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 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 The composition of a lubricating oil has a large effect on the characteristicsand uses of the oil. The determination of saturates, aromatics, and polars is a key analysis of this composition. The characterization of the composition of lubricating oils is important in determining their interchangeability for use in blending etcetera.1.1 This test method covers the determination of total aromatics and total saturats in additive-free lube basestocks using high performance liquid chromatography (HPLC) with refractive index (RI) detection. This test method is applicable to samples containing total saturates in the concentration range of 74.9 % to 100.0 % by mass and aromatics in the concentration range of 0.0 % to 25.1 % by mass. The precision is expressed in terms of the total saturates.1.1.1 Polar comounds, if present, are combined with the total aromatics. Precision was determined for basestocks with polars content <1.0 % by mass.1.2 This test method includes a relative bias section for total saturates in basestocks based n a Practice D6708 accuracy assessment between Test Method D7419 and Test Method D2007. The derived correlation equation is only applicable for basestocks in the total saturates concentration range from 75.0 % to 100.0 % by mass as measured by Test Method D7419.1.2.1 The applicable range for total saturates by Test Method D2007D2007.1.3 The vlues 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 responibility 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 accordnce 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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