5.1 Knowledge of the water content is important in lubrication, as large amounts of water can cause corrosion fatigue in steel bearings, and the complete absence of water can cause metal scuffing.5.2 High water content has an accelerating effect on oxidation of lubricants, and can also contribute to foaming, especially at high altitude or temperature, or both.1.1 This test method covers a procedure for estimating the equilibrium solubility of water and its vapor in hydrocarbon and aliphatic ester lubricants, at temperatures between 277 K and 373 K. The test method is limited to liquids of low to moderate polarity and hydrogen bonding, with predicted solubilities not over 1000 ppm by weight in hydrocarbons, or 30 000 ppm by weight in oxygenated compounds, at 298 K.1.2 Specifically excluded are olefins, nitriles, nitro compounds, and alcohols.1.3 This test method is recommended only for liquids not containing widely different chemical species. This excludes blends of esters with hydrocarbons, and lubricants containing detergents, dispersants, rust preventives, or load carrying additives.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 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 The significance and use of each test method will depend on the system in use and the purpose of the test method listed under Section 6. Use the most recent editions of the test methods.1.1 This guide covers information without specific limits, for selecting standard test methods for testing hydrocarbon-based quench oils for quality and aging.1.2 The values stated in SI units are to be regarded as standard.1.2.1 Exception—The units given in parentheses are for information only.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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p>The significance and use of the individual test methods are to be found in the individual methods referenced. For significance specifically applicable to electrical insulation materials, refer to Test Methods D 176.1.1 These test methods cover a compendium of tests that apply to mineral waxes of petroleum origin in general, but more specifically to the so-called microcrystalline types used as either electrical insulation or moisture-proofing mediums, or both, for treating, impregnating, coating, and filling electrical apparatus. These test methods are also applicable to other waxes of natural or synthetic origin, provided that their characteristics are similar to those of the so-called microcrystalline waxes. Note 1—There is no equivalent ISO or IEC standard. 1.2 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to inch-pound units that are provided for information only and are not considered 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific precautions, see Section 5.

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5.1 The boiling range distribution of light and medium petroleum distillate fractions provides an insight into the composition of feed stocks and products related to petroleum refining processes. This gas chromatographic determination of boiling range can be used to replace conventional distillation methods for control of refining operations. This test method can be used for product specification testing with the mutual agreement of interested parties.5.2 This test method extends the scope of Test Method D2887 (538 °C) boiling range determination by gas chromatography to include sulfur boiling range distribution in the petroleum distillate fractions. Knowledge of the amount of sulfur and its distribution in hydrocarbons is economically important in determining product value and in determining how best to process or refine intermediate products. Sulfur compounds are known to affect numerous properties of petroleum and petrochemical products. The corrosion of metals and poisoning of catalysts is of particular concern. In addition, the content of sulfur in various refined products may be subject to governmental regulations. Test Methods, such as, D2622, D3120, D5504 and D5623, are available to determine total sulfur content or content of individual sulfur compounds in petroleum and petroleum products. Test Methods, such as, D86, D1160, D2887, D3710, and D2892, are also available to determine the hydrocarbon boiling ranges of such samples. The gas chromatographic determination of the sulfur boiling range assists in process development, in treatment and control of refining operations and is useful for assessing product quality. This determination produces detailed information about the sulfur distribution in a sample that cannot be obtained by either total sulfur analysis or analysis of sulfur in discreet distillation cuts.5.2.1 The hydrocarbon boiling range distributions obtained by Test Method D2887 are theoretically equivalent to those obtained by true boiling point (TBP) distillation (see Test Method D2892). They are not equivalent to results from low efficiency distillation such as those obtained with Test Method D86 or D1160.1.1 This test method covers the determination of the boiling range distribution of petroleum products. The test method is applicable to petroleum products and fractions having a final boiling point of 538 °C (1000 °F) or lower at atmospheric pressure as measured by this test method. This test method is limited to samples having a boiling range greater than 55 °C (100 °F), and having a vapor pressure sufficiently low to permit sampling at ambient temperature.1.1.1 The applicable sulfur concentration range will vary to some extent depending on the boiling point distribution of the sample and the instrumentation used; however, in most cases, the test method is applicable to samples containing levels of sulfur above 10 mg/kg.1.2 This test method requires the use of both FID and SCD for detection. The hydrocarbon simulated distillation data obtained from the FID signal should be performed according to Test Method D2887 Procedure B.1.3 The test method is not applicable for analysis of petroleum distillates containing low molecular weight components (for example, naphthas, reformates, gasolines, crude oils). Materials containing heterogeneous components (for example, alcohols, ethers, acids, or esters) or residue are not to be analyzed by this test method. See Test Methods D3710, D7096, D5307, D7169, or D7500.1.4 This test method does not purport to identify all sulfur species in a sample. The detector response to sulfur is equimolar for all sulfur compounds within the scope (1.1) of this test method. Thus, unidentified sulfur compounds are determined with equal precision to that of identified substances. Total sulfur content is determined from the total area of the sulfur detector.1.4.1 This test method uses the principles of simulated distillation methodology.1.5 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.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 useful for characterization and rapid quantification of PAH mixtures including petroleum oils, fuels, creosotes, and industrial organic mixtures, either waterborne or obtained from tanks.5.2 The unknown PAH mixture is first characterized by its fluorescence emission and synchronous scanning spectra. Then a suitable site-specific calibration standard with similar spectral characteristics is selected as described in Annex A1. This calibration standard may also be well-characterized by other independent methods such as gas chromatography (GC), GC-mass spectrometry (GC-MS), or high performance liquid chromatography (HPLC). Some suggested independent analytical methods are included in References (1-7)4 and Test Method D4657. Other analytical methods can be substituted by an experienced analyst depending on the intended data quality objectives. Peak maxima intensities of appropriate fluorescence emission spectra are then used to set up suitable calibration curves as a function of concentration. Further discussion of fluorescence techniques as applied to the characterization and quantification of PAHs and petroleum oils can be found in References (8-18).5.3 For the purpose of the present test method polynuclear aromatic hydrocarbons are defined to include substituted polycyclic aromatic hydrocarbons with functional groups such as carboxyl acid, hydroxy, carbonyl and amino groups, and heterocycles giving similar fluorescence responses to PAHs of similar molecular weight ranges. If PAHs in the more classic definition, that is, unsubstituted PAHs, are desired, chemical reactions, extractions, or chromatographic procedures may be required to eliminate these other components. Fortunately, for the most commonly expected PAH mixtures, such substituted PAHs and heterocycles are not major components of the mixtures and do not cause serious errors.1.1 This test method covers a means for quantifying or characterizing total polycyclic aromatic hydrocarbons (PAHs) by fluorescence spectroscopy (Fl) for waterborne samples. The characterization step is for the purpose of finding an appropriate calibration standard with similar emission and synchronous fluorescence spectra.1.2 This test method is applicable to PAHs resulting from petroleum oils, fuel oils, creosotes, or industrial organic mixtures. Samples can be weathered or unweathered, but either the same material or appropriately characterized site-specific PAH or petroleum oil calibration standards with similar fluorescence spectra should be chosen. The degree of spectral similarity needed will depend on the desired level of quantification and on the required data quality objectives.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 Accurate quantitative compositional information on hydrocarbon types can be useful in determining the effects of processes in the production of various finished fuels. Producers may require additional determinations such as n-paraffins, i-paraffins, naphthenes, and aromatics for process optimization. This information also may be useful for indicating the quality of fuels and for assessing the relative combustion properties of finished fuels. This test method can be used to make such determinations.1.1 This test method covers the quantitative determination of total n-paraffins, total i-paraffins, total naphthenes (cycloparaffins), total one ring (1R) and total two ring plus (2R+) aromatic hydrocarbons in hydrocarbon liquids having a boiling point between 36 °C and 343 °C by GCxGC (flow modulated comprehensive two-dimensional gas chromatography). The method has been applied to aviation turbine fuels and is applicable to other low olefinic fuels in the stated boiling point range.1.2 This test method has an interim precision. An expanded full interlaboratory study is to be completed in <5 years. The test method working concentration ranges in mass percent for which the interim precision has been determined are as follows:Hydrocarbon Type Lower limit(mass percent) Upper limit(mass percent)Total i-paraffins 22.0 24.3Total n-paraffins 19.0 21.9Total naphthenes (cycloparaffins) 34.3 36.7Total one ring aromatics 18.7 21.8Total two ring plus aromatics 0.5 1.91.3 This test method is applicable to other group type concentration ranges, to other hydrocarbon types such as selected individual components, for example, benzene, toluene, or n-paraffins by carbon number, or to other hydrocarbon streams; however, precision has not been determined at this time. A future ILS will include a variety of sample types and extend the reporting.1.4 This test method is not intended to determine unsaturated hydrocarbons, such as olefins, content which may interfere with the cycloparaffins; this test method is applicable to samples with < 1% by mass total olefins as determined by D1319.1.5 This test method is not intended to determine FAME (fatty acid methyl esters). For such applications, Test Method D7797, IP 585, or equivalent test methods are available.1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.7 This standard test method does not mandate or describe a specific software package for data processing and display. Any commercially available GCxGC software used for data processing and display shall meet the requirements for the calculation of the results. Appendix X1 provides some guidelines.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 The heat of combustion is a measure of the energy available from a fuel. A knowledge of this value is essential when considering the thermal efficiency of equipment for producing either power or heat.5.2 The heat of combustion as determined by this test method is designated as one of the chemical and physical requirements of both commercial and military turbine fuels and aviation gasolines.5.3 The mass heat of combustion, the heat of combustion per unit mass of fuel, is a critical property of fuels intended for use in weight-limited craft such as airplanes, surface effect vehicles, and hydrofoils. The range of such craft between refueling is a direct function of the heat of combustion and density of the fuel.1.1 This test method covers the determination of the heat of combustion of liquid hydrocarbon fuels ranging in volatility from that of light distillates to that of residual fuels.1.2 Under normal conditions, this test method is directly applicable to such fuels as gasolines, kerosines, Nos. 1 and 2 fuel oil, Nos. 1-D and 2-D diesel fuel and Nos. 0-GT, 1-GT, and 2-GT gas turbine fuels.1.3 This test method is not as repeatable and not as reproducible as Test Method D4809.1.4 The values stated in SI units are to be regarded as standard. The values 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. For specific hazard statements, see Sections 7 and 9 and A1.10 and Annex A3.1.6 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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