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3.1 This classification establishes a series of definite viscosity levels so that lubricant suppliers, lubricant users, and equipment designers will have a uniform and common basis for designating, specifying, or selecting the viscosity of industrial fluid lubricants.3.2 This classification is used to eliminate unjustified intermediate viscosities, thereby reducing the total number of viscosity grades used in the lubrication of industrial equipment.3.3 This system provides a suitable number of viscosity grades, a uniform reference temperature, a uniform viscosity tolerance, and a nomenclature system for identifying the viscosity characteristics of each grade.3.4 This system implies no evaluation of lubricant quality and applies to no property of a fluid other than its viscosity at the reference temperature. It does not apply to those lubricants used primarily with automotive equipment and identified with an SAE number.AbstractThis classification is applicable to all petroleum-base fluid lubricants and to those nonpetroleum materials which may be readily blended to produce fluid lubricants of a desired viscosity, that is, lubricants for bearings, gears, compressor cylinders, hydraulic fluids, etc. This classification is used to eliminate unjustified intermediate viscosities, thereby reducing the total number of viscosity grades used in the lubrication of industrial equipment. The lubricants shall be classified according to viscosity grades: ISO VG 2; ISO VG 3; ISO VG 5; ISO VG 7; ISO VG 10; ISO VG 15; ISO VG 22; ISO VG 32; ISO VG 46; ISO VG 68; ISO VG 100; ISO VG 150; ISO VG 220; ISO VG 320; ISO VG 460; ISO VG 680; ISO VG 1000; ISO VG 1500; ISO VG 2200; and ISO VG 3200.1.1 This classification is applicable to all petroleum-base fluid lubricants and to those nonpetroleum materials which may be readily blended to produce fluid lubricants of a desired viscosity, that is, lubricants for bearings, gears, compressor cylinders, hydraulic fluids, etc.1.2 This classification is applicable to fluids ranging in kinematic viscosity from 2 cSt to 3200 cSt (mm2/s) as measured at a reference temperature of 40 °C. In the category of petroleum-base fluids, this covers the range from kerosene to heavy cylinder oils.1.3 Fluids of either lesser or greater viscosity than the range described in 1.2 are, at present, seldom used as industrial lubricants. Should industrial practices change, then this system, based on a mathematical series of numbers, may be extended to retain its orderly progression.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 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 standard describes how to evaluate the relative sensitivity of materials and components to dynamic pressure impacts by various gaseous fluid media (can include gas mixtures).4.2 Changes or variations in test specimen configurations, thickness, preparation, and cleanliness can cause a significant change in their impact ignition sensitivity/reaction. For material tests, the test specimen configuration shall be specified on the test report.4.3 Changes or variation in the test system configuration from that specified herein may cause a significant change in the severity produced by a dynamic pressure surge of the gaseous media.4.4 A reaction is indicated by an abrupt increase in test specimen temperature, by obvious changes in odor, color, or material appearance, or a combination thereof, as observed during post-test examinations. Odor alone is not considered positive evidence that a reaction has occurred. When an increase in test specimen temperature is observed, a test specimen reaction must be confirmed by visual inspection. To aid with visual inspection, magnification less than 10× can be used.4.5 When testing components, the test article must be disassembled and the nonmetallic materials examined for evidence of ignition after completion of the specified pressure surge cycles.4.6 Ignition or precursors to ignition for any test sample shall be considered a failure and are indicated by burning, material loss, scorching, or melting of a test material detected through direct visual means. Ignition is often indicated by consumption of the non-metallic material under test, whether as an individual material or within a component. Partial ignition can also occur, as shown in Fig. 3a, b, and c, and shall also be considered an ignition (failure) for the purpose of this test standard.FIG. 3 a Untested PCTFE (10X Magnification) (Polychlorotrifluoroethylene) Sample.FIG. 3 b Untested Nylon (PA, polyamide) Valve Seat (10X magnification) (continued)FIG. 3 c Untested Pin-Index Sealing Washer (10X magnification) (continued)NOTE 1: For the purpose of this standard, test samples that visually appear in these conditions, or similar, are considered to be representative of ignition.FIG. 3 Photographs Representing Partial Reactions Including Scorching, Discoloration, Melting and Material Loss or Material Consumption. For the purpose of this standard, test samples that visually appear in these conditions, or similar, are considered to be representative of ignition.NOTE 2: A representative (exemplar) material or component may be requested by the test laboratory personnel for visual comparison with the post-test condition of the test samples.4.7 For material testing, the prescribed procedure is conducted on multiple samples until a statistically significant number of ignitions or no-ignitions, or both, are achieved at various test pressures. The data is then analyzed by a procedure that calculates the median failure pressure (i.e., the 50 % reaction pressure) or the functional form of the ignition probability versus pressure by logistic regression analysis. Materials tested in a similar configuration can be ranked against each other by either of these two criteria. The initial test gas temperature may be varied as required depending on the requirements of the test.4.8 For component testing, a specified number of pressure surge cycles are conducted at a defined test pressure, usually specified by a particular industry test standard. Usually, this pressure is 1.2 times the maximum allowable working pressure of the component. The initial test gas temperature may be varied depending on the requirements of the test; however, most commonly the initial test gas temperature is 60 ± 3 °C.1.1 This test method describes a method to determine the relative sensitivity of nonmetallic materials (including plastics, elastomers, coatings, etc.) and components (including valves, regulators flexible hoses, etc.) to dynamic pressure impacts by gases such as oxygen, air, or blends of gases containing oxygen.1.2 This test method describes the test apparatus and test procedures employed in the evaluation of materials and components for use in gases under dynamic pressure operating conditions up to gauge pressures of 69 MPa and at elevated temperatures.1.3 This test method is primarily a test method for ranking of materials and qualifying components for use in gaseous oxygen. The material test method is not necessarily valid for determination of the sensitivity of the materials in an “as-used” configuration since the material sensitivity can be altered because of changes in material configuration, usage, and service conditions/interactions. However, the component testing method outlined herein can be valid for determination of the sensitivity of components under service conditions. The current provisions of this method were based on the testing of components having an inlet diameter (ID bore) less than or equal to 14 mm (see Note 1).1.4 A 5 mm Gaseous Fluid Impact Sensitivity (GFIS) test system and a 14 mm GFIS test system are described in this standard. The 5 mm GFIS system is utilized for materials and components that are directly attached to a high-pressure source and have minimal volume between the material/component and the pressure source. The 14 mm GFIS system is utilized for materials and components that are attached to a high pressure source through a manifold or other higher volume or larger sized connection. Other sizes than these may be utilized but no attempt has been made to characterize the thermal profiles of other volumes and geometries (see Note 1).NOTE 1: The energy delivered by this test method is dependent on the gas volume being rapidly compressed at the inlet to the test specimen or test article. Therefore the geometry of the upstream volume (diameter and length) is crucial to the test and crucial to the application of the results to actual service conditions. It is therefore recommended that caution be exercised in applying the results of this testing to rapid pressurization of volumes larger than those standardized by this test method. This energy delivered by this standard is based on the rapid compression of the volume in either a 5 mm ID by 1000 mm long impact tube or a 14 mm ID by 750 mm long impact tube. These two upstream volumes are specified in this standard based on historic application within the industry.1.5 This test method can be utilized to provide batch-to-batch comparison screening of materials when the data is analyzed according to the methods described herein. Acceptability of any material by this test method may be based on its 50 % reaction pressure or its probability of ignition based on a logistic regression analysis of the data (described herein).1.6 Many ASTM, CGA, and ISO test standards require ignition testing of materials and components by gaseous fluid impact, also referred to as adiabatic compression testing. This test method provides the test system requirements consistent with the requirements of these other various standards. The pass/fail acceptance criteria may be provided within other standards and users should refer to those standards. Pass/fail guidance is provided in this standard such as that noted in section 4.6. This test method is designed to ensure that consistent gaseous fluid impact tests are conducted in different laboratories.1.7 The criteria used for the acceptance, retest, and rejection, or any combination thereof of materials and components for any given application shall be determined by the user and are not fixed by this method. However, it is recommended that at a minimum the 95 % confidence interval be established for all test results since ignition by this method is inherently probabilistic and should be treated by appropriate statistical methods.1.8 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.9 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 precautions see Section 7.1.10 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 provides laboratory procedures for rating the relative bioresistance of metalworking fluid formulations, for determining the need for microbicide addition prior to or during fluid use in metalworking systems and for evaluating microbicide performance. General considerations for microbicide selection are provided in Practice E2169.5.2 The factors affecting challenge population numbers, taxonomic diversity, physiological state, inoculation frequency and biodeterioration effects in recirculating metalworking fluid systems are varied and only partially understood. Consequently, the results of tests completed in accordance with this practice should be used only to compare the relative performance of products or microbicide treatments included in a test series. Results should not be construed as predicting actual field performance.1.1 This practice addresses the evaluation of the relative inherent bioresistance of water-miscible metalworking fluids, the bioresistance attributable to augmentation with antimicrobial pesticides or both. It replaces Methods D3946 and E686.1.2 In this practice relative bioresistance is determined by challenging metalworking fluids with a biological inoculum that may either be characterized (comprised of one or more known biological cultures) or uncharacterized (comprised of biologically contaminated metalworking fluid or one or more unidentified isolates from deteriorated metalworking fluid). Challenged fluid bioresistance is defined in terms of resistance to biomass increase, viable cell recovery increase, chemical property change, physical property change or some combination thereof.1.3 This practice is applicable to antimicrobial agents that are incorporated into either the metalworking fluid concentrate or end-use dilution. It is also applicable to metalworking fluids that are formulated using non-microbicidal, inherently bioresistant components.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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5.1 This is a performance-based method, and modifications are allowed to improve performance.5.1.1 Due to the rapid development of newer instrumentation and column chemistries, changes to the analysis described in this standard are allowed as long as better or equivalent performance data result. Any modifications shall be documented and performance data generated. The user of the data generated by this standard shall be made aware of these changes and given the performance data demonstrating better or equivalent performance.5.2 Organophosphate pesticides affect the nervous system by disrupting the enzyme that regulates acetylcholine, a neurotransmitter. They were developed during the early 19th century, but their effects on insects, which were similar to their effects on humans, were discovered in 1932. Some are poisonous and were used as chemical weapon agents. Organophosphate pesticides are usually not persistent in the environment.7,85.3 This test method is for the analysis of selected organophosphorous based pesticide degradation products.5.4 This method has been investigated for use with various soils.1.1 This procedure covers the determination of Diisopropyl Methylphosphonate (DIMP), Ethyl Methylphosphonic Acid (EMPA), Isopropyl Methylphosphonic Acid (IMPA), Methylphosphonic Acid (MPA), and Pinacolyl Methylphosphonic Acid (PMPA), referred to collectively as organophosphonates (OPs) in this test method, in soil. This method is based upon solvent extraction of a soil by pressurized fluid extraction (PFE). The extract is filtered and analyzed by liquid chromatography/tandem mass spectrometry (LC/MS/MS). OPs are qualitatively and quantitatively determined by this method.1.2 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 The method detection limit2 (MDL), electrospray ionization (ESI) mode, and reporting range3 for the OPs are listed in Table 1.1.4 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 test method covers the gravimetric measurement4 of metal removal fluid aerosol concentrations in workplace atmospheres.5.2 This test method provides total particulate matter concentrations for comparison with historical exposure databases collected with the same technology.5.3 This test method provides an extension to current non-standardized methods by adding an extractable mass concentration which reduces interferences from nonmetal removal fluid aerosols.5.4 This test method does not address differences between metal removal fluid types, but it does include extraction with a broad spectrum of solvent polarity to adequately remove many of the current fluid formulations from insoluble background aerosol.55.5 This test method does not identify or quantify any specific putative toxins in the workplace that can be related to metal removal fluid aerosols or vapors.5.6 This test method does not address the loss of semivolatile compounds from the filter during or after collection.1.1 This test method covers a procedure for the determination of both total collected particulate matter and extractable mass metalworking fluid aerosol concentrations in the range of 0.07 to 5 mg/m3 in workplace atmospheres.1.2 This test method describes a standardized means of collecting worker exposure information that can be compared to existing exposure databases, using a test method that is also more specific to metal removal fluids.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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This guide defines purity standards for carbon dioxide to ensure the suitability of liquefied carbon dioxide gas for use in supercritical fluid extraction (SFE) and supercritical fluid chromatography (SFC) applications. This guide defines quantitation, labeling, and statistical standards for impurities in carbon dioxide that are necessary for successful SFE or SFC laboratory work, and it suggests methods of analysis for quantifying these impurities. These contaminants are those components that either cause detector signals that interfere with those of the target analytes or physically impede the SFE or SFC experiment. Also, this guide is provided for use by specialty gas suppliers who manufacture carbon dioxide specifically for SFE or SFC applications. SFE or SFC CO2 products offered with a claim of adherence to this guide will meet certain absolute purity and contaminant detectability requirements matched to the needs of current SFE or SFC techniques.1.1 This guide defines purity standards for carbon dioxide to ensure the suitability of liquefied carbon dioxide gas for use in SFE and SFC applications (see Guide E1449 for definitions of terms). This guide defines quantitation, labeling, and statistical standards for impurities in carbon dioxide that are necessary for successful SFE or SFC laboratory work, and it suggests methods of analysis for quantifying these impurities.1.2 This guide is provided for use by specialty gas suppliers who manufacture carbon dioxide specifically for SFE or SFC applications. SFE or SFC carbon dioxide (CO2) products offered with a claim of adherence to this guide will meet certain absolute purity and contaminant detectability requirements matched to the needs of current SFE or SFC techniques. The use of this guide allows different SFE or SFC CO2 product offerings to be compared on an equal purity basis.1.3 This guide considers contaminants to be those components that either cause detector signals that interfere with those of the target analytes or physically impede the SFE or SFC experiment.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 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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AS 1322-1987 Shipbuilding - Recommended fluid velocities in ships' pipes 被代替 发布日期 :  1970-01-01 实施日期 : 

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5.1 Fluid analysis is one of the pillars in determining fluid and equipment conditions. The results of fluid analysis are used for planning corrective maintenance activities, if required.5.2 The objective of a proper fluid sampling process is to obtain a representative fluid sample from critical location(s) that can provide information on both the equipment and the condition of the lubricant or hydraulic fluid.5.3 The additional objective is to reduce the probability of outside contamination of the system and the fluid sample during the sampling process.5.4 The intent of this guide is to help users in obtaining representative and repeatable fluid samples in a safe manner while preventing system and fluid sample contamination.1.1 This guide is applicable for collecting representative fluid samples for the effective condition monitoring of steam and gas turbine lubrication and generator cooling gas sealing systems in the power generation industry. In addition, this guide is also applicable for collecting representative samples from power generation auxiliary equipment including hydraulic systems.1.2 The fluid may be used for lubrication of turbine-generator bearings and gears, for sealing generator cooling gas as well as a hydraulic fluid for the control system. The fluid is typically supplied by dedicated pumps to different points in the system from a common or separate reservoirs. Some large steam turbine lubrication systems may also have a separate high pressure pump to allow generation of a hydrostatic fluid film for the most heavily loaded bearings prior to rotation. For some components, the lubricating fluid may be provided in the form of splashing formed by the system components moving through fluid surfaces at atmospheric pressure.1.3 Turbine lubrication and hydraulic systems are primarily lubricated with petroleum based fluids but occasionally also use synthetic fluids.1.4 For large lubrication and hydraulic turbine systems, it may be beneficial to extract multiple samples from different locations for determining the condition of a specific component.1.5 The values stated in SI units are regarded as standard.1.5.1 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 The aromatic hydrocarbon content of motor diesel fuels is a factor that can affect their cetane number and exhaust emissions.5.2 The United States Environmental Protection Agency (USEPA) regulates the aromatic content of diesel fuels. California Air Resources Board (CARB) regulations place limits on the total aromatics content and polynuclear aromatic hydrocarbon content of motor diesel fuel, thus requiring an appropriate analytical determination to ensure compliance with the regulations. Producers of diesel fuels will require similar determinations for process and quality control. This test method can be used to make such determinations.5.3 This test method is applicable to materials in the boiling range of motor diesel fuels and is unaffected by fuel coloration. Test Method D1319, which has been mandated by the USEPA for the determination of aromatics in motor diesel fuel, excludes materials with final boiling points greater than 315 °C (600 °F) from its scope. Test Method D2425 is applicable to the determination of both total aromatics and polynuclear aromatic hydrocarbons in diesel fuel, but is much more costly and time consuming to perform.5.4 Results obtained by this test method have been shown to be statistically more precise than those obtained from Test Method D1319 for typical diesel fuels, and this test method has a shorter analysis time.3 Results from this test method for total polynuclear aromatic hydrocarbons are also expected to be at least as precise as those of Test Method D2425.1.1 This test method covers the determination of the total amounts of monoaromatic and polynuclear aromatic hydrocarbon compounds in motor diesel fuels and blend stocks by supercritical fluid chromatography (SFC). The range of aromatics concentration to which this test method is applicable is from 1 % to 75 % by mass. The range of polynuclear aromatic hydrocarbon concentrations to which this test method is applicable is from 0.5 % to 50 % by mass.1.2 This test method includes relative bias for Test Method D5186 versus Test Method D1319 and Test Method D6591 versus Test Method D5186 for diesel fuels. The applicable ranges of the correlation ranges are presented in the Relative Bias section. The correlations are applicable only in the stated ranges and only to diesel fuels.1.3 This test method and correlations were developed for diesel samples not containing biodiesel; the presence of biodiesel will interfere with the results. The correlation equations are only applicable between these concentration ranges and to diesel fuels that do not contain biodiesel.1.4 The values stated in SI units are to be regarded as standard. The values stated in inch-pound units 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 Effective antifouling coatings are essential for the retention of speed and reduction of operating costs of ships. This test method is designed as a screening test to evaluate antifouling coating systems under conditions of hydrodynamic stress caused by water flow alternated with static exposure to a fouling environment. A dynamic test is necessary because of the increasing availability of AF coatings that are designed to ablate in service to expose a fresh antifouling surface. Because no ship is underway continually, a static exposure phase is included to give fouling microorganisms the opportunity to attach under static conditions. After an initial 30-day static exposure, alternated 30-day dynamic and static exposures are recommended as a standard cycle. The initial static exposure is selected to represent vessels coming out of drydock and sitting pierside while work is being completed. This gives the paint time to lose any remaining solvents, complete curing, absorb water, and, in general, stabilize to the in-water environment.5.2 This test method is intended to provide a comparison with a control antifouling coating of known performance in protecting underwater portions of ships’ hulls. This test method gives an indication of the performance and anticipated service life of antifouling coatings for use on seagoing vessels. However, the degree of correlation between this test method and service performance has not been determined.1.1 This test method covers the determination of antifouling performance and reduction of thickness of marine antifouling (AF) coatings by erosion or ablation (see Section 3) under specified conditions of hydrodynamic shear stress in seawater alternated with static exposure in seawater. An antifouling coating system of known performance is included to serve as a control in antifouling studies.1.2 The values stated in SI units are to be regarded as the standard. The values 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. For a specific hazards statement, see Section 8.1.4 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 This is a performance-based method, and modifications are allowed to improve performance.5.1.1 Due to the rapid development of newer instrumentation and column chemistries, changes to the analysis described in this test method are allowed as long as better or equivalent performance data result. Any modifications shall be documented and performance data generated. The user of the data generated by this test method shall be made aware of these changes and given the performance data demonstrating better or equivalent performance.5.2 The first reported synthesis of BPA was by the reaction of phenol with acetone by Zincke.7 BPA has become an important high-volume industrial chemical used in the manufacture of polycarbonate plastic 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.85.3 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 and will biodegrade. BPA has been reported to have adverse effects in aquatic organisms and may be released into environmental waters directly at trace levels through landfill leachate and sewage treatment plant effluents. This method has been investigated for use with soil, sludge, and biosolids.5.4 The land application of biosolids has raised concerns over the fate of BPA in the environment, and a standard method is needed to monitor concentrations. This method has been investigated for use with various soils.1.1 This procedure covers the determination of Bisphenol A (BPA) in soil, sludge, and biosolids. This test method is based upon solvent extraction of a soil matrix by pressurized fluid extraction (PFE). The extract is filtered and analyzed by liquid chromatography/tandem mass spectrometry (LC/MS/MS). BPA is qualitatively and quantitatively determined by this test method.1.2 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 The method detection limit (MDL),2 electrospray ionization (ESI) mode, and reporting range3 for BPA are listed in Table 1.1.4 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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This guide deals primarily with the terms and relationships used in supercritical fluid chromatography, including techniques, apparatuses, and reagents.1.1 This guide deals primarily with the terms and relationships used in supercritical fluid chromatography.1.2 Since many of the basic terms and definitions also apply to gas chromatography and liquid chromatography, this guide is using, whenever possible, symbols identical to Practices E355 and E682.1.3 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 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 Evaluations by both test methods differentiate between fluids having low, medium, and high levels of extreme-pressure properties. The user should establish any correlation between results by either method and service performance.NOTE 3: Relative ratings by both test methods on the fluids covered in Table X2.1 and Table X2.2 are in good general agreement with four-ball weld-point relative ratings obtained on these same fluids, covered in Test Method D2783.1.1 These test methods cover two procedures for making a preliminary evaluation of the load-carrying properties of fluid lubricants by means of the Falex Pin and Vee Block Test Machine.NOTE 1: Additional information can be found in Appendix X1 regarding coefficient of friction, load gauge conversions, and load gauge calibration curve.1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI 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, 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 This practice is intended as a solution to the difficulty of obtaining reproducible test results from heterogeneous samples.5.2 This practice works best with multilayered liquids, but can also be applied to samples with solid particles that are sufficiently small in size to be suspended in an emulsion.5.3 The emulsified/suspended sample can be used for all bulk property testing such as microwave digestion/inductively coupled argon plasma (ICAP), ion chromatography, heat of combustion, ash content, water, nonvolatile residue, and pH. It may be prudent to retain a portion of the sample in its original, multiphase form for some types of analyses.1.1 This practice covers the generation of a uniform mixture or emulsion from multiphase samples which are primarily liquid in order to facilitate sample preparation, transfer, and analysis.1.2 This practice is designed to keep a multiphase fluid sample in an emulsified/suspended state long enough to take a single, composite sample that is representative of the sample as a whole. The sample may reform multiple layers after standing.1.3 The emulsion/suspension generated by following this practice can be used only for analytical procedures designed for the total sample and procedures not significantly affected by the emulsifier or the presence of an emulsion/suspension.1.4 This practice assumes that a representative sample of not more than 1 L has been obtained.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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