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4.1 Uses—This classification is intended for use by federal landholding agencies and DoD components in order to direct ECOP efforts. It is also intended for use by preparers and reviewers of environmental condition of property maps, explosives safety condition maps, and ECOP reports used to support CERFA uncontaminated parcel identifications and parcels suitable for transfer by lease or by deed. This classification should be used to facilitate standardized determinations of the environmental condition and explosives safety conditions of a federal landholding agency, FUDS, and DoD installation's real property. Such environmental condition of property and explosives safety condition determinations are necessary to assess the progress of ongoing environmental restoration, identify areas where further response may be required, identify areas where further evaluation is necessary, and to support FOSTs and FOSLs. An environmental condition of property map, and explosives safety condition map, if applicable, based upon the ECOP report prepared in accordance with Practice D6008, is prepared using this classification. The ECOP report may be used to determine the MILCON category (see Section 8 and Table X1.1 in Appendix X1).1.1 Purpose—The purpose of this classification is to define eight standard environmental condition of property area types for federally-owned real property with respect to the requirements of the Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) of 1980 Section 120(h), as amended by the Community Environmental Response Facilitation Act (CERFA) of 1992, and Section 331 of the National Defense Authorization Act for Fiscal Year 1997. As such, this classification is intended to permit a federal landholding agency to classify property into eight area types, in order to facilitate and support findings of suitability to transfer (FOSTs), findings of suitability to lease (FOSLs), and uncontaminated parcel determinations pursuant to the requirements of CERFA. Users of this classification should note that it does not address (except where noted explicitly) requirements for appropriate and timely regulatory consultation or concurrence, or both, during the identification and use of these environmental condition of property area types.1.1.1 Eight Recognized Standard Environmental Condition of Property Area Types—The goal of this classification is to permit federal landholding agencies to classify properties in order to support determinations of which properties are suitable and unsuitable for transfer by lease or by deed. The term “standard environmental condition of property area type” refers to one of the eight area types defined in this classification. An identification of an area type on an environmental condition of property map means that a federal landholding agency federally-owned has conducted sufficient studies to make a determination of the recognized environmental conditions of installation real property or has complied with the identification requirements of uncontaminated property under CERFA, or both, and has categorized the property into one of the following eight area types:1.1.1.1 Standard Environmental Condition of Property Area Type 1—An area or parcel of real property where no release, or disposal of hazardous substances or petroleum products or their derivatives has occurred (including no migration of these substances from adjoining properties).1.1.1.2 Standard Environmental Condition of Property Area Type 2—An area or parcel of real property where only the release or disposal of petroleum products or their derivatives has occurred.1.1.1.3 Standard Environmental Condition of Property Area Type 3—An area or parcel of real property where release, disposal, or migration, or some combination thereof, of hazardous substances has occurred, but at concentrations that do not require a removal or remedial action.1.1.1.4 Standard Environmental Condition of Property Area Type 4—An area or parcel of real property where release, disposal, or migration, or some combination thereof, of hazardous substances has occurred, and all remedial actions necessary to protect human health and the environment have been taken.1.1.1.5 Standard Environmental Condition of Property Area Type 5—An area or parcel of real property where release, disposal, or migration, or some combination thereof, of hazardous substances has occurred and removal or remedial actions, or both, are under way, but all required actions have not yet been taken.1.1.1.6 Standard Environmental Condition of Property Area Type 6—An area or parcel of real property where release, disposal, or migration, or some combination thereof, of hazardous substances has occurred, but required response actions have not yet been initiated.1.1.1.7 Standard Environmental Condition of Property Area Type 7—An area or parcel of real property that is unevaluated or requires additional evaluation.1.1.1.8 Standard Environmental Condition of Property Area Type 8—An area or parcel of real property where the release, disposal, or migration, or some combination thereof of hazardous substances or emerging contaminants of environmental concern has likely occurred, but response actions either (1) have not yet been determined, or (2) are being managed under the auspices of an ARAR, such as a federal or state health advisory, or other federal regulatory program such as the Toxic Substances Control Act (TSCA).1.1.2 CERCLA Section 120(h) Requirements—This classification of environmental condition of property area types is consistent with CERCLA § 120(h) requirements relating to the transfer of contaminated federal real property (42 USC 9601 et seq.). Areas classified as Area Types 1 through 4, as defined in this classification, are suitable, with respect to CERCLA § 120(h) requirements, for deed transfer to a non-federal recipient.1.1.3 CERFA Requirements—This classification of environmental condition of property area types can be used in conjunction with the reporting requirements of CERFA, which amended CERCLA (Public Law 102-426, 106 Statute 2174). As defined in this classification, areas classified as Type 1 areas are eligible for reporting as “uncontaminated property” under the provisions of CERFA. At federal installations listed on the national priorities list, Environmental Protection Agency (EPA) concurrence must be obtained for a parcel to be considered uncontaminated and therefore transferable under CERCLA § 120(h)(4). EPA has stated as a matter of policy that there may be instances in which it would be appropriate to concur with the military service that certain parcels can be identified as uncontaminated under CERCLA § 120(h)(4), although some limited quantity of hazardous substances or petroleum products have been stored, released, or disposed of on the parcel. If the information available indicates that the storage, release, or disposal was associated with activities that would not be expected to pose a threat to human health or the environment (for example, housing areas, petroleum-stained pavement areas, and areas having undergone routine application of pesticides), such parcels should be eligible for expeditious reuse.1.1.4 Petroleum Products—Petroleum products and their derivatives are included within the scope of this classification. Under existing agency-specific and US EPA policy, areas on which petroleum products and their derivatives have been released or disposed of may not be suitable for deed transfer until a response action has been completed.1.2 Objectives—The objectives guiding the development of this classification are as follows: (1) to synthesize and put in writing a standard classification of environmental condition of property area types; (2) to facilitate the development of high-quality, standardized environmental condition of property maps that can be used to support FOSTs and FOSLs; (3) to facilitate the development of a standard practice for conducting environmental baseline surveys; and (4) to facilitate the development of a standard guide for preparing environmental baseline survey reports.1.3 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 for the chemical analysis of metals and alloys are primarily intended as referee methods to test such materials for compliance with compositional specifications, particularly those under the jurisdiction of ASTM Committee A04 on Iron Castings. It is assumed that all who use these test methods will be trained analysts capable of performing common laboratory procedures skillfully and safely. It is expected that work will be performed in a properly equipped laboratory under appropriate quality control practices such as those described in Guide E882.1.1 These test methods cover the chemical analysis of pig iron, gray cast iron (including alloy and austenitic), white cast iron, malleable cast iron, and ductile (nodular) iron having chemical compositions within the following limits:Element Composition Range, % Aluminum 0.003 to  0.50Antimony 0.005 to  0.03Arsenic 0.02  to  0.10Bismuth 0.001 to  0.03Boron 0.001 to  0.10Cadmium 0.001 to 0.005Carbon 1.25  to  4.50Cerium 0.005 to  0.05Chromium 0.01  to 30.00Cobalt 0.01  to  4.50Copper 0.03  to  7.50Lead 0.001 to  0.15Magnesium 0.002 to  0.10Manganese 0.06  to  2.50Molybdenum 0.01  to  5.00Nickel 0.01  to 36.00Phosphorus 0.01  to  0.90Selenium 0.001 to  0.06Silicon 0.10 to 6.0   Sulfur 0.005 to  0.25Tellurium 0.001 to  0.35Tin 0.001 to  0.35Titanium 0.001 to  0.20Tungsten 0.001 to  0.20Vanadium 0.005 to  0.50Zinc 0.005 to  0.201.2 The test methods in this standard are contained in the sections indicated below:  Sections Carbon, Graphitic, by the Direct Combustion Infrared Absorption Method (1 % to 3 %) 108–115Carbon, Total by the Combustion Gravimetric Method (1.25 % to 4.50 %)—Discontinued 2012  97–107Cerium and Lanthanum by the Direct Current Plasma Atomic Emission Spectrometry Method (Ce: 0.003 % to 0.5 %; La: 0.001 % to 0.30 %) 237–245Chromium by the Atomic Absorption Method (0.006 % to 1.00 %) 208–217Chromium by the Peroxydisulfate Oxidation—Titration Method (0.05 % to 30.0 %) 218–226Chromium by the Peroxydisulfate-Oxidation Titrimetric Method (0.05 % to 30.0 %)—Discontinued 1980 144–151Cobalt by the Ion-Exchange—Potentiometric Titration Method (2.0 % to 4.5 %)  53–60Cobalt by the Nitroso-R-Salt Spectrophotometric Method (0.01 % to 4.50 %)  61–70Copper by the Neocuproine Spectrophotometric Method (0.03 % to 7.5 %) 116–125Copper by the Sulfide Precipitation-Electrodeposition Gravimetric Method (0.03 % to 7.5 %)  81–88Lead by the Ion-Exchange—Atomic Absorption Spectrometry Method (0.001 % to 0.15 %) 126–135Magnesium by the Atomic Absorption Spectrometry Method (0.002 % to 0.10 %)  71–80Manganese by the Periodate Spectrophotometric Method (0.10 % to 2.00 %)   9–18Manganese by the Peroxydisulfate-Arsenite Titrimetric Method (0.10 % to 3.5 %) 152–159Molybdenum by the Ion Exchange–8-Hydroxyquinoline Gravimetric Method 257–264Molybdenum by the Thiocyanate Spectrophotometric Method (0.01 % to 1.5 %) 196–207Nickel by the Dimethylglyoxime Gravimetric Method (0.1 % to 36.00 %) 168–175Nickel by the Ion Exchange-Atomic Absorption Spectrometry Method (0.005 % to 1.00 %) 176–185Phosphorus by the Alkalimetric Method (0.02 % to 0.90 %) 160–167Phosphorus by the Molybdenum Blue Spectrophotometric Method (0.02 % to 0.90 %)  19–30Silicon by the Gravimetric Method (0.1 % to 6.0 %)  46–52Sulfur by the Gravimetric Method—Discontinued 1988  30–36Sulfur by the Combustion-Iodate Titration Method (0.005 % to 0.25 %)—Discontinued 2012  37–45Sulfur by the Chromatographic Gravimetric Method—Discontinued 1980 136–143Tin by the Solvent Extraction-Atomic Absorption Spectrometry Method (0.002 % to 0.10 %)  186–195Tin by the Sulfide Precipitation-Iodometric Titration Method (0.01 % to 0.35 %)   89–96Titanium by the Diantipyrylmethane Spectrophotometric Method (0.006 % to 0.35 %)  246–256Vanadium by the Atomic Absorption Spectrometry Method (0.006 % to 0.15 %)  227–2361.3 Procedures for the determination of carbon and sulfur not included in these test methods can be found in Test Methods E1019.1.4 Some of the composition ranges given in 1.1 are too broad to be covered by a single method and therefore this standard contains multiple methods for some elements. The user must select the proper method by matching the information given in the and Interference sections of each method with the composition of the alloy to be analyzed.1.5 The values stated in SI units are to be regarded as 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. Specific hazards statements are given in Section 6 and in special “Warning” paragraphs throughout these Methods.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 A knowledge of the hydrocarbon composition of process streams and petroleum products boiling within the range of 160 °C to 343 °C (320 °F to 650 °F) is useful in following the effect of changes in process variables, diagnosing the source of plant upsets, and in evaluating the effect of changes in composition on product performance properties.5.2 A test method to determine total cycloparafins and low level aromatic content is necessary to meet specifications for aviation turbine fuel containing synthesized hydrocarbons.1.1 This test method covers an analytical scheme using the mass spectrometer to determine the hydrocarbon types present in conventional and synthesized hydrocarbons that have a boiling range of 160 °C to 343 °C (320 °F to 650 °F), 5 % to 95 % by volume  as determined by Test Method D86. Samples with average carbon number value of paraffins between C12 and C16 and containing paraffins from C10 and C18 can be analyzed. Eleven hydrocarbon types are determined. These include: paraffins, noncondensed cycloparaffins, condensed dicycloparaffins, condensed tricycloparaffins, alkylbenzenes, indans or tetralins, or both, CnH 2n-10 (indenes, etc.), naphthalenes, CnH2n-14  (acenaphthenes, etc.), CnH 2n-16 (acenaphthylenes, etc.), and tricyclic aromatics.NOTE 1: This test method was developed on Consolidated Electrodynamics Corporation Type 103 Mass Spectrometers. Operating parameters for users with a Quadrupole Mass Spectrometer are provided.1.2 This test method is intended for use with full boiling range products that contain no significant olefin content.Biodiesel (FAME components) could interfere with the separation of the sample and the characteristic mass fragments of FAME compounds are not defined in the procedure.Hydrocarbons containing tertiary carbon fragments, sometimes found in synthetic aviation fuels, will interfere with the characteristic mass fragments of paraffins and result in a false, elevated cycloparaffin content.NOTE 2: “No significant olefin content” for this method means <2.0 % by volume by Test Method D1319.1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For a specific warning statement, see 11.1.1.5 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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3.1 The compression resistance perpendicular to the faces, the resistance to the extrusion during compression, and the ability to recover after release of the load are indicative of a joint filler's ability to continuously fill a concrete expansion joint and thereby prevent damage that might otherwise occur during thermal expansion. The asphalt content is a measure of the fiber-type joint filler's durability and life expectancy. In the case of cork-type fillers, the resistance to water absorption and resistance to boiling hydrochloric acid are relative measures of durability and life expectancy.NOTE 2: The quality of the results produced by this standard are dependent on the competence of the personnel performing the procedure and the capability, calibration, and maintenance of the equipment used. Agencies that meet the criteria of Specification D3666 are generally considered capable of competent and objective testing, sampling, inspection, etc. Users of this standard are cautioned that compliance with Specification D3666 alone does not completely ensure reliable results. Reliable results depend on many factors; following the suggestions of Specification D3666 or some similar acceptable guideline provides a means of evaluating and controlling some of those factors.1.1 These test methods cover the physical properties associated with preformed expansion joint fillers. The test methods include:  Property SectionExpansion in Boiling Water 7.1Recovery and Compression 7.2Extrusion 7.3Boiling in Hydrochloric Acid 7.4Asphalt Content 7.5Water Absorption 7.6Density 7.7NOTE 1: Specific test methods are applicable only to certain types of joint fillers, as stated herein.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 The text of this standard references notes and footnotes which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered as requirements of the 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 specification covers throw-away, flat panel-type filter units for use in air conditioning, heating, and ventilating systems. This specification also includes panel-type filters with pleated media. The filters are furnished in two types as follows: type I - throw-away frames and media, and type II - permanent frames with replaceable media. The filters are furnished in three grades as follows: grade A - standard dust-holding capacity, grade B - high dust-holding capacity, and grade C - high resistance. The adhesive oil, filter initial resistance, filter average arrestance, and filter dust holding capacity conform to the requirements specified.1.1 This specification covers throw-away, flat panel-type filter units for use in air conditioning, heating, and ventilating systems. This specification also includes panel-type filters with pleated media.1.2 The values stated in inch-pound units are to be regarded as the standard.

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4.1 Dangerous goods (hazardous materials) regulations require performance tests to be conducted on packaging or IBC designs before being authorized for use. The regulations do not include standardized procedures for conducting performance tests and, because of this, may result in a non-uniform approach and differences in test results between testing facilities.4.2 The purpose of this standard is to provide guidance and to establish a set of common practices for conducting hydrostatic pressure tests on IBC designs subjected to UN certification testing.4.3 Intermediate bulk container designs are required to be tested in a sequence. This guide focuses on conducting the hydrostatic pressure test, which is preceded in the test sequence by the leakproofness test. The fittings and adaptors applied to the container for the hydrostatic pressure test may also be used for the leakproofness test.1.1 This guide is intended to provide a standardized method and a set of basic instructions for performing hydrostatic pressure testing on Intermediate Bulk Containers (IBCs) designs as required by the United States Department of Transportation Title 49 Code of Federal Regulations (CFR) and the United Nations Recommendations on the Transport of Dangerous Goods (UN).1.2 This guide focuses on composite and rigid plastic IBCs and is suitable for testing IBCs of any design or material type.1.3 This guide provides information to help clarify various terms used as part of the United Nations (UN) certification process that may assist in determining the applicable test.1.4 This guide provides the suggested minimum information that should be documented when conducting pressure testing.1.5 This guide provides information for recommended equipment and fittings for conducting pressure tests.1.6 This guide is based on the current information contained in 49 CFR 178.814.1.7 When testing packaging designs intended for hazardous materials (dangerous goods), the user of this guide shall be trained in accordance with 49 CFR 172.700 and other applicable hazardous materials regulations such as the International Civil Aviation Organization (ICAO) Technical Instructions for the Safe Transport of Dangerous Goods by Air, the International Maritime Dangerous Goods Code (IMDG Code), and carrier rules such as the International Air Transport Association (IATA) Dangerous Goods Regulations.1.8 Units—”The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this guide.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.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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This specification covers the standard requirements for flat-rolled nonoriented fully processed electrical steel intended primarily for commercial power frequency applications in magnetic devices. These electrical steels are low-carbon, silicon iron, or silicon-aluminum-iron alloys that may be made by basic-oxygen, electric-furnace, or other steelmaking practice. Desirable core-loss and permeability characteristics are developed during mill processing, so additional heat treatment is usually not required. The grades contained in this specification have thicknesses of 0.014 in. (0. 36 mm), 0.0185 in. (0.47 mm) and 0.0250 in. (0.64 mm). For a given thickness there are from 7 to 9 types based on the maximum value of core loss measured at 60 Hz and 15 kG (1.5 T) using the Epstein test method. Test methods to determine the required magnetic and mechanical properties are specified. Other typical magnetic and physical properties are listed for reference.1.1 This specification covers the detailed requirements to which flat-rolled nonoriented fully processed electrical steel shall conform.1.2 This steel is produced to specified maximum core-loss values and is intended primarily for commercial power frequency (50 Hz and 60 Hz) applications in magnetic devices. Desirable core-loss and permeability characteristics are developed during mill processing, so additional heat treatment by the user is usually not necessary.1.3 These nonoriented fully processed electrical steels are low-carbon, silicon-iron, or silicon-aluminum-iron alloys containing up to about 3.5 % silicon and a small amount of aluminum.1.4 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to customary (cgs-emu and inch-pound) units which are provided for information only and are not considered 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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1.1 This specification covers the detailed requirements to which flat-rolled nonoriented fully processed electrical steel shall conform.1.2 This steel is produced to specified maximum core-loss values and is intended primarily for commercial power frequency (50 and 60 Hz) applications in magnetic devices. Desirable core loss and permeability characteristics are developed during mill processing, so further heat treatment by the purchaser is not usually necessary.1.3 These nonoriented fully processed electrical steels are low-carbon, silicon-iron or silicon-aluminum-iron alloys containing up to about 3.5% silicon and a small amount of aluminum.Note 1-This specification is the metric companion of Specification A677.

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5.1 A knowledge of the hydrocarbon composition of process streams and petroleum products boiling within the range 205 °C to 540 °C (400 °F to 1000 °F) is useful in following the effect of changes in process variables, diagnosing the source of plant upsets, and in evaluating the effect of changes in composition on product performance properties. This method, when used together with Test Method D2786, provides a detailed analysis of the hydrocarbon composition of such materials.1.1 This test method2 covers the determination by high ionizing voltage, low resolution mass spectrometry of 18 aromatic hydrocarbon types and 3 aromatic thiophenotypes in straight run aromatic petroleum fractions boiling within the range from 205 °C to 540 °C (400 °F to 1000 °F) (corrected to atmospheric pressure). Samples must be nonolefinic, must contain not more than 1 % by mass of total sulfur, and must contain not more than 5 % nonaromatic hydrocarbons. Composition data are in volume percent.NOTE 1: Although names are given to 15 of the compound types determined, the presence of other compound types of the same empirical formulae is not excluded. All other compound types in the sample, unidentified by name or empirical formula, are lumped into six groups in accordance with their respective homologous series.1.2 The values stated in acceptable SI units are to be regarded as the standard. The values given in parentheses are provided for information purposes 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 and health practices and determine the applicability of regulatory limitations prior to use.

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This specification covers the standard requirements for semi-processed cold-rolled magnetic lamination quality steels. These steels shall be made by the basic-oxygen or electric-furnace method and shall be processed by hot rolling, pickling, cold rolling, annealing, and temper rolling. Magnetic lamination steels shall have low-carbon contents and may have manganese, phosphorus, silicon, and aluminum additions to enhance punchability and to improve magnetic characteristics by increasing the electrical resistivity. There are no fixed chemical requirements for these steels only the requirement to meet the specified magnetic properties. These steels must be heat treated by the user to develop the specified magnetic properties. This specification covered steels with thicknesses of 0.0185 in. ( 0.47 mm), 0.022 in. (0.56 mm), 0.025 in. (0.64 mm), 0.028 in. (0.71 mm) and 0.031 in. (0.79 mm). For a given thickness there are three or more core loss types distinguished by maximum allowable core loss after a specified quality development anneal. Magnetic testing shall be done after the specified quality development anneal and shall use the Epstein test method. Magnetic testing shall be done at a test frequency of 60 Hz and a maximum flux density of 15 kG (1.5 T). Test methods to determine the magnetic and mechanical properties are listed. Other typical magnetic and physical properties are listed for reference. 1.1 This specification covers cold-rolled carbon sheet steel used for magnetic applications. These products, commonly called “cold-rolled magnetic lamination steel” (CRML) are usually intended for applications in which the stamped laminations or assembled core structures for electrical equipment are annealed to develop the desired core loss and permeability characteristics. 1.2 This steel is produced to maximum specific core-loss values and is intended primarily for commercial power frequency (50- and 60-Hz) applications in magnetic devices. Specific core-loss and permeability characteristics in conformance with this specification are developed through heat treatment by the user. 1.3 Non-guaranteed core-loss types, usually made to controlled chemical compositions, are available but are not covered by this specification. 1.4 Higher quality core-loss types are low carbon, silicon-iron, or silicon-aluminum-iron alloys containing up to about 2.5 % silicon and less than 1 % aluminum. These steels are usually given a critical reduction on a temper-mill to yield specified magnetic properties after a suitable lamination anneal. These products, typically called semiprocessed magnetic lamination steel, are classified by the ASTM Code Letter D in accordance with Practice A664. 1.5 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to customary (cgs-emu and inch-pound) units which are provided for information only and are not considered 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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1.1 This test method covers determination of the susceptibility of Types III and IV polyethylene plastics (as defined in the table on Classification of Polyethylene Plastics Molding and Extrusion Materials According to Type, in Specification D1248) to thermal stress-cracking.Note 1--It has also been found useful in testing specimens from fabricated items such as pipe or conduit.1.2 The values stated in SI units are to be regarded as the standard, except in cases where materials, products, or equipment are available only in inch-pound units. The values in parentheses are given 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 and health practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Note 7.Note 2--There is no similar or equivalent ISO standard.

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5.1 The determination of the total volume percent of saturates, olefins, and aromatics in petroleum fractions is important in characterizing the quality of petroleum fractions as gasoline blending components and as feeds to catalytic reforming processes. This information is also important in characterizing petroleum fractions and products from catalytic reforming and from thermal and catalytic cracking as blending components for motor and aviation fuels. This information is also important as a measure of the quality of fuels, such as specified in Specification D1655.1.1 This test method covers the determination of hydrocarbon types of total aromatics, total olefins, and total saturates in petroleum fractions that distill below 315 °C. Samples containing dark-colored components that interfere in reading the chromatographic bands cannot be analyzed.NOTE 1: For the determination of olefins below 0.3 % by volume, other test methods are available, such as Test Method D2710.1.2 This test method is intended for use with full boiling range products. Cooperative data have established that the precision statement does not apply to narrow boiling petroleum fractions near the 315 °C limit. Such samples are not eluted properly, and results are erratic.1.3 This test method is also applicable to automotive spark-ignition engine fuels which are gasolines with and without blended oxygenates, such as alcohols and ethers (for example MTBE, ethanol) and where gasoline is the primary component by volume in the blend.1.4 The applicability of this test method to products derived from fossil fuels other than petroleum, such as coal, shale, or tar sands, has not been determined, and the precision statement may or may not apply to such products.1.5 This test method has two precision statements depicted in Table 3 and Table 4.1.5.1 Table 3 is applicable to fuels that do not contain oxygenated blending components over the test method concentration working ranges from 5 % to 99 % by volume aromatics, 1 % to 55 % by volume olefins, and 1 % to 95 % by volume saturates in petroleum fractions and with a final boiling point of <315 °C. It may or may not apply to automotive gasolines containing lead antiknock mixtures.1.5.2 Table 4 precision was derived from an ILS containing only blended oxygenated (for example, MTBE, ethanol) and non-oxygenated automotive spark-ignition engine fuels (gasolines) and is applicable only in the test method concentration working range of 13 % to 40 % by volume aromatics, 4 % to 33 % by volume olefins, and 45 % to 68 % by volume saturates.1.5.3 Non-oxygenated automotive spark-ignition engine fuels (gasolines) outside the inclusive valid test result reporting concentration ranges of Table 4 may use the precision in Table 3 and its applicable concentration ranges.1.6 The oxygenated blending components, methanol, ethanol, methyl-tert-butylether (MTBE), tert-amylmethylether (TAME), and ethyl-tert-butylether (ETBE), do not interfere with the determination of hydrocarbon types at concentrations normally found in commercial blends. These oxygenated components are not detected since they elute with the alcohol desorbent. Other oxygenated compounds shall be individually verified. When samples containing oxygenated blending components are analyzed, correct the results to a total-sample basis.1.7 This test method includes a relative bias section based on Practice D6708 accuracy assessment between Test Method D1319 and Test Method D5769 for total aromatics in spark-ignition engine fuels as a possible Test Method D1319 alternative to Test Method D5769 for U.S. EPA spark-ignition engine fuel regulations reporting. The Practice D6708 derived correlation equation is only applicable for fuels in the total aromatic concentration range from 3.3 % to 34.4 % by volume as measured by Test Method D1319 and the distillation temperature T95, at which 95 % of the sample has evaporated, ranges from 149.1 °C to 196.6 °C (300.3 °F to 385.8 °F) when tested according to Test Method D86.1.7.1 The applicable Test Method D5769 range for total aromatics is 3.7 % to 29.4 % by volume as reported by Test Method D5769 and the distillation temperature T95 values, at which 95 % of the sample has evaporated, when tested according to Test Method D86 is from 149.1 °C to 196.6 °C (300.3 °F to 385.8 °F).1.7.2 Regulations may change over time and the user is advised to verify current regulatory requirements.1.8 WARNING—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use caution when handling mercury and mercury-containing products. See the applicable product Safety Data Sheet (SDS) for additional information. The potential exists that selling mercury or mercury-containing products, or both, is prohibited by local or national law. Users must determine legality of sales in their location.1.9 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.1.10 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 warning statements, see Section 7, 8.1, and 10.5.1.11 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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A knowledge of spark-ignition engine fuel composition is useful for regulatory compliance, process control, and quality assurance.The quantitative determination of olefins and other hydrocarbon types in spark-ignition engine fuels is required to comply with government regulations.This test method is not applicable to M85 and E85 fuels, which contain 85 % methanol and ethanol, respectively.1.1 This test method provides for the quantitative determination of oxygenates, paraffins, olefins, naphthenes, and aromatics in low-olefin spark-ignition engine fuels by multidimensional gas chromatography. Each hydrocarbon type can be reported either by carbon number (see ) or as a total through C10, except for olefins, which can only be reported through C9. Higher boiling hydrocarbons cannot be reported by type and are reported as a composite group. The lower limit of detection for a single hydrocarbon component or carbon number type is 0.05 mass %.Note 1—There can be an overlap between the C9 and C10 aromatics; however, the total is accurate. Isopropyl benzene is resolved from the C8 aromatics and is included with the other C9 aromatics. Naphthalene is determined with the C11+ components.1.2 This test method is applicable for total olefins in the range from 0.05 to 13 mass %. The test method can quantitatively determine olefins in samples where the olefin concentration does not exceed 0.6 % C4 or 4.0 % C5 or 4.5 % of the combined C4 and C5. Although the precision for benzene was determined in the range from 0.3 to 1.0 mass %, this test method can be used to determine benzene concentrations up to 5.0 mass %.1.3 This test method is not intended to determine individual hydrocarbon components except for those hydrocarbon types for which there is only one component within a carbon number. Individually determined hydrocarbons are benzene, toluene, cyclopentane, propane, propylene, and cyclopentene.1.4 Precision data has only been obtained on samples containing MTBE. Application of this test method to determine other oxygenates shall be verified in the user's laboratory. Methanol cannot be determined and shall be quantitated by an appropriate oxygenate method such as Test Method D 4815 or D 5599. Methanol is fully resolved and does not interfere with the determination of other components or groups.1.5 Although specifically written for spark-ignition engine fuels containing oxygenates, this test method can also be applied to other hydrocarbon streams having similar boiling ranges, such as naphthas and reformates.1.6 The values stated in SI units are to be regarded as the 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 and health practices and determine the applicability of regulatory limitations prior to use.

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4.1 This practice supports test methods designed to evaluate the performance of fluid-filter media, for example, Practice F796 wherein particle size distributions are addressed and at the same time this practice provides a means to compare size measurements obtained from several different types of instruments.4.2 The factor for converting one kind of diameter scale to another is only valid for the specific test particles studied.1.1 This practice provides a procedure for comparing the sizes of nonspherical particles in a test sample determined with different types of automatic particle counters, which operate on different measuring principles.1.2 A scale factor is obtained by which, in the examination of a given powder, the size scale of one instrument may be multiplied to agree with the size scale of another.1.3 The practice considers rigid particles, free of fibers, of the kind used in studies of filtration, such as: commercially available test standards of quartz or alumina, or fly ash, or some powdered chemical reagent, such as iron oxide or calcium sulfate.1.4 Three kinds of automatic particle counters are considered:1.4.1 Image analyzers, which view stationary particles under the microscope and, in this practice, measure the longest end-to-end distance of an individual particle.1.4.2 Optical counters, which measure the area of a shadow cast by a particle as it passes by a window; and1.4.3 Electrical resistance counters, which measure the volume of a particle as it passes through an orifice in an electrically conductive liquid.1.5 This practice also considers the use of instruments that provide sedimentation analyses, which is to say provide measures of the particle mass distribution as a function of Stokes diameter. The practice provides a way to convert mass distribution into number distribution so that the meaning of Stokes diameter can be related to the diameter measured by the instruments in 1.4.1.6 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 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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1.1 This specification covers preformed expansion joint filler having relatively little extrusion and substantial recovery after release from compression.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.NOTE 1: Attention is called to Specifications D1752 and D994/D994M.1.3 The text of this standard references notes and footnotes which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered as requirements of the 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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