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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 flat-rolled, nonoriented semiprocessed 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, and are classified according to core-loss. Unlike the fully processed electrical steels covered by ASTM A 677, the electrical steels in this specification require heat treatment by the user to develop the specified magnetic properties. The steels covered by this specification have a thickness of either 0.0185 in. (0.47 mm) or 0.025 in. (0.64 mm). For each thickness there are four core loss types. The core loss shall be determined following the use of a quality evaluation anneal listed in the specification. The core loss is determined using the Epstein test method at a test frequency of 60 Hz and a maximum flux density of 15 kG (1.5 T). Test methods to determine other required physical and mechanical properties are listed. Other typical magnetic and physical properties are listed for reference.1.1 This specification covers the detailed requirements to which flat-rolled, nonoriented semiprocessed 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 through heat treatment by the user.1.3 These nonoriented, semiprocessed electrical steels are low carbon, silicon-iron or silicon-aluminum-iron alloys containing up to about 2.5 % silicon and less than 1 % 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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5.1 The determination of WPPO composition is useful in optimization of process variables, diagnosing unit performance, and in evaluating the effect of changes in waste plastic composition on WPPO performance properties.5.1.1 Aromatics and olefin hydrocarbon type analysis, including sub-classes, may be useful for evaluating suitability of WPPO as a feedstock for further processing.1.1 This test method covers a standard procedure for the determination of hydrocarbon types (saturates, olefins, styrenes, aromatics and polyaromatics) of waste plastic process oil (WPPO) from chemical or thermal processes using gas chromatography and vacuum ultraviolet absorption spectroscopy detection (GC-VUV).1.1.1 This test method is applicable for plastic recycling and circular schemes including wide range density material from polyethylene and polypropylene.1.1.2 The test method is applicable to waste plastic process oil having a final boiling point of 545 °C or lower at atmospheric pressure as measured by this test or Test Method D2887. This test method is limited to samples having a boiling range greater than 36 °C, and having a vapor pressure sufficiently low to permit sampling at ambient temperature.1.1.3 WPPOs with initial boiling points less than nC5 (36 °C) and final boiling point less than nC15 (271 °C) may be analyzed by Test Method D8369.1.1.4 Appendix X3 is applicable to waste plastic process oils that are predominantly hydrocarbons in the boiling range of pentane, nC5 (36 °C) to tetrahexacontane, nC64 (629 °C).1.2 Concentrations of group type totals are determined by percent mass or percent volume. The applicable working ranges are as follows:Total Aromatics %Mass 1 to 50Monoaromatics %Mass 1 to 50Diaromatics %Mass 1 to 15Tri-plus aromatics %Mass 0.5 to 5PAH %Mass 0.5 to 15Saturates %Mass 5 to 99Olefins %Mass 1 to 80Conjugated diolefins %Mass 0.2 to 5Styrenes %Mass 0.2 to 5The final precision concentration ranges will be defined by a future ILS.1.2.1 Saturates totals are the result of the summation of normal paraffins, isoparaffins, and naphthenes.1.2.2 Aromatics are the summation of monoaromatic and polyaromatic group types. Polyaromatic totals are the result of the summation of diaromatic and tri-plus aromatic group types.1.2.3 Olefin totals are the result of the sum of mono-olefins, conjugated diolefins, non-conjugated diolefins, and cyclic olefins.1.2.4 Styrenes totals are the sum of styrene and alkylated styrenes. Styrenes are classified separately, neither as aromatic nor olefin.1.3 Waste plastic process oil containing mixed plastic types such as polyethylene terephthalate PET and polyvinyl chloride or other material may yield compounds including hetero-compounds that are not speciated by this test method.1.4 Individual components are typically not baseline separated by the procedure described in this test method. The coelutions are resolved at the detector using VUV absorbance spectra and deconvolution algorithms.1.5 This test method may apply to other process oils from sources such as tires and bio-mass boiling between pentane (36 °C) and tetratetracontane (545 °C), but has not been extensively tested for such applications.1.6 Units—The values stated in SI units are to be regarded as standard. No other units of measurement, other than the boiling point of normal paraffins (°F) in Table 2 and Table X.3.1, are included in this standard.1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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Information Technology - Multimedia Framework (MPEG-21) - Part 6: Rights Data Dictionary AMENDMENT 1: Digital Item Identifier Relationship Types

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ASTM D2252-18 Standard Specification for Fineness of Types of Alpaca Active 发布日期 :  1970-01-01 实施日期 : 

4.1 This specification for fineness is intended as a guide for production, preparation, and marketing (Note 1) by comparing the average fiber diameter of a measured specimen with the fineness specifications for the various types listed in Table 1. The standard deviation which expresses measured variability of a specimen may be compared with the average shown in Table X2.1.NOTE 1: Test Method D2130 does not include any values for the precision to be expected in the testing of alpaca fibers. In an interlaboratory test in which six laboratories each made one test on each of six type samples, HTB-CB, HAXB-CB, HAAB-CB, HAB-CB, HLPB-CL, and HSKB-CL, the coefficient of variation of the average fiber diameters between laboratories, including test variation, was 3.2, 4.7, 3.8, 4.5, 2.2, and 0.93 % for the respective alpaca types.AbstractThis specification is applicable in the classification of alpaca into types according to fineness. Five types of alpaca have been classified according to its average diameter limit, namely Type T Extra, Type T, Type X, Type AA, Type A, Type SK, and Type LP.1.1 This specification is applicable in the classification of alpaca into types according to fineness.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 A knowledge of the hydrocarbon composition of the middle distillates, including the biodiesel blends 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. The total aromatics content and polycyclic aromatics content are also important to evaluate the quality of diesel fuels/biodiesel blends. It requires an appropriate analytical method to make such determinations for diesel fuel/biodiesel blends production process and quality control.5.2 This test method provides a comprehensive analytical strategy for the determination of the total aromatics contents, polycyclic aromatics contents and the detail hydrocarbon composition of diesel fuel/biodiesel blends to ensure compliance with certain specifications or regulations.5.3 Test Method D2425 is applicable to the determination of the detailed hydrocarbon composition in middle distillates, however, the pre-separation procedure of elution chromatography is time-consuming and not eco-friendly. By combining with the separation procedures described in Test Method D8144, the dual column GC-MS system proposed in this method can determine the total aromatic hydrocarbon contents, polycyclic aromatic hydrocarbon contents and detailed hydrocarbon composition of diesel fuel/biodiesel blends simultaneously. The content of FAME in biodiesel blends can also be determined by GC. It is demonstrated to be time-saving and eco-friendly for the quality control of diesel fuel and biodiesel blends.1.1 This test method covers an analytical scheme using the gas chromatography/mass spectrometry (GC-MS) to determine the hydrocarbon types present in middle distillates 170 °C to 365 °C boiling range, 5 % to 95 % by volume as determined by Test Method D86, including biodiesel blends with up to 20 % by volume of fatty acid methyl ester (FAME). The detailed hydrocarbon composition, total aromatic hydrocarbon and polycyclic aromatic hydrocarbon contents can be determined. The hydrocarbon types include: paraffins, noncondensed cycloparaffins, condensed dicycloparaffins, condensed tricycloparaffins, alkylbenzenes, indans or tetralins, or both, CnH2n-10 (indenes, etc.), naphthalenes, CnH2n-14 (acenaphthenes, etc.), CnH2n-16 (acenaphthylenes, etc.), and tricyclic aromatics. The content of FAME in biodiesel blends can also be determined by GC.1.2 The values stated in acceptable SI units are to be regarded as the standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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1.1 This specification covers the detailed requirements to which flat-rolled thin-gauge nonoriented fully processed electrical steel shall conform. Nominal thicknesses included in this specification are 0.10 mm (0.004 in.) to 0.30 mm (0.012 in.).1.1.1 Refer to Specification A677 for properties of flat-rolled nonoriented fully processed electrical steel in nominal thicknesses of 0.36 mm (0.014 in.) to 0.64 mm (0.025 in.).1.1.2 Refer to Specification A876 for properties of flat-rolled grain-oriented fully processed electrical steel.1.1.3 Thin-gauge nonoriented electrical steels with a high silicon content (typically 61/2 %) manufactured using silicon vapor-deposition or similar processes are not included in this specification.1.2 The steel covered in this specification is produced to specified maximum core loss values and is intended primarily for use in rotating electrical machinery and other electromagnetic devices operating at moderate to elevated frequencies (100 Hz and greater). Desirable core loss and permeability characteristics are developed during mill processing; however, lamination manufacturing processes may adversely affect these mill-produced properties. Additional stress-relief heat treatment by the user may therefore be helpful in remediating these properties in the manufactured laminations. Stress-relief annealing is discussed further in Appendix X2.1.3 These thin-gauge nonoriented fully processed electrical steels are low-carbon, silicon-iron, or silicon-aluminum-iron alloys typically containing 2.5 to 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.1.4.1 There are selected values presented in two units, both of which are in acceptable SI units. These are differentiated by the word “or,” as in “g/cm3, or, (kg/m3).”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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1.1 This document represents research methodology and the tables represent charted data from subjects. Some terminology is specific to the research. The data represent the first body measurements ever taken of women aged 55 and older and is not a standard of average current apparel industry practices as represented in all other sizing standards.1.2 These tables list body measurements of adult women age 55 and over. The body measurements tables can be used as a baseline in designing apparel for adult women in this age group, taking into account such factors as fabric type, desired ease of body movement, styling, and fit.1.3 Measurement tables correspond to the figure types and numerical size designations in the PS 42-70 database. Until body measurements of all adult women are updated, companies will have to analyze the older customer's differences by body measurements and proportions instead of hang tag numbers, and adapt them to currently marketed sizes and figure types. Companies especially affected are those who are today using smaller numbered hang tag designations, who offer mainly S, M, and L sizes, or who have adjusted their charts from the PS 42-70 database to reflect the specific body measurements of their 1990's customer.1.4 The values stated in either acceptable SI units or inch-pound units shall be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system must be used independently of the other, without combining values.

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1.1 This document represents research methodology and the tables represent charted data from subjects. Some terminology is specific to the research. The data represent the first body measurements ever taken of women aged 55 and older and is not a standard of average current apparel industry practices as represented in all other sizing standards.1.2 These tables list body measurements of adult women age 55 and over. The body measurements tables can be used as a baseline in designing apparel for adult women in this age group, taking into account such factors as fabric type, desired ease of body movement, styling, and fit.1.3 Measurement tables correspond to the figure types and numerical size designations in the PS 42-70 database. Until body measurements of all adult women are updated, companies will have to analyze the older customer's differences by body measurements and proportions instead of hang tag numbers, and adapt them to currently marketed sizes and figure types. Companies especially affected are those who are today using smaller numbered hang tag designations, who offer mainly S, M, and L sizes, or who have adjusted their charts from the PS 42-70 database to reflect the specific body measurements of their 1990's customer.1.4 The values stated in either acceptable SI units or inch-pound units shall be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system must be used independently of the other, without combining values.

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5.1 Accurate quantitative information on aromatic hydrocarbon types can be useful in determining the effects of petroleum processes on production of various finished fuels. This information can also be useful for indicating the quality of fuels and for assessing the relative combustion properties of finished fuels.1.1 This test method covers a high performance liquid chromatographic test method for the determination of mono-aromatic and di-aromatic hydrocarbon contents in aviation kerosenes and petroleum distillates boiling in the range from 50 °C to 300 °C, such as Jet A or Jet A-1 fuels. The total aromatic content is calculated from the sum of the individual aromatic hydrocarbon-types.NOTE 1: Samples with a final boiling point greater than 300 °C that contain tri-aromatic and higher polycyclic aromatic compounds are not determined by this test method and should be analyzed by Test Method D6591 or other suitable equivalent test methods.1.2 This test method is applicable to distillates containing from 0.8 % to 44.0 % by mass mono-aromatic hydrocarbons, 0.23 % to 6.20 % by mass di-aromatic hydrocarbons, and 0.7 % to 50 % by mass total aromatics. Although this method generates results in m/m, results may also be quoted in v/v.1.3 The precision of this test method has been established for kerosene boiling range distillates containing from 0.40 % to 44.0 % by mass mono-aromatic hydrocarbons, 0.02 % to 6.20 % by mass di-aromatic hydrocarbons, and 0.40 % to 50.0 % by mass total aromatics. If results are quoted in volume, the precision is 0.3 % to 41.4 % by volume mono-aromatics, 0.01 % to 5.00 % by volume di-aromatics, and 0.30 % to 46.3 % by volume total aromatics. As calculated by IP 367-1.1.4 Compounds containing sulfur, nitrogen, and oxygen are possible interferents. Mono-alkenes do not interfere, but conjugated di- and poly-alkenes, if present, are possible interferents.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 Knowledge of the olefinic, aromatic, and benzene content is very important in quality specifications of petroleum products, such as spark ignition fuels (gasoline) and hydrocarbon solvents. Fast and accurate determination of hydrocarbon types and benzene of petroleum distillates and products is also important in optimization of process units.5.2 This test method provides a fast standard procedure for determination of hydrocarbon types and benzene in light oxygenate-free petroleum distillates and products.1.1 This test method covers and provides for the quantitative determination of total saturates, total olefins, total aromatics and benzene in light petroleum distillates having a final boiling point below 215 °C by multidimensional gas chromatography. Each hydrocarbon grouping as well as benzene can be reported in both volume and mass percent.1.2 This test method is applicable to light petroleum distillates such as oxygenate-free motor gasoline or spark ignition fuels, naphthas and hydrocarbon solvents over the content ranges from 1 % (V/V) to 70 % (V/V) total olefins, 1 % (V/V) to 80 % (V/V) total aromatics and 0.2 % to 10 % (V/V) benzene. This test method may apply to concentrations outside these ranges, but the precision has not been determined. Interlaboratory testing for precision used full range blending streams, such as FCC, reformates and spark ignition fuel or blended motor gasolines.1.3 This test method is not intended to determine oxygenated components. Light petroleum distillate products such as motor gasoline may contain oxygenates. Oxygenates such as methyl tert-butyl ether (MTBE), tert-amyl methyl ether (TAME), ethyl tert-butyl ether (ETBE), ethanol and methanol etc. will coelute with specific hydrocarbon groups. If there is any suspicion the sample contains oxygenates, the absence of oxygenates should be confirmed by other standard test methods such as Test Methods D4815, D5599, or D6839 before using this test method.1.4 This test method is not applicable for the determination of individual hydrocarbon components with the exception of benzene. Test Method D6733 may be used to determine a large number of individual hydrocarbons to complement this test method.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 A knowledge of the hydrocarbon composition of process streams and petroleum products boiling within the range of 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.5.2 This test method, when used together with Test Method D3239, provides a detailed analysis of the hydrocarbon composition of such materials.1.1 This test method2 covers the determination by high ionizing voltage mass spectrometry of seven saturated hydrocarbon types and one aromatic type in saturate petroleum fractions having average carbon numbers 16 through 32. The saturate types include alkanes (0-rings), single-ring naphthenes, and five fused naphthene types with 2, 3, 4, 5, and 6 rings. The nonsaturate type is monoaromatic. Noncondensed naphthenes are analyzed as single rings. Samples must be nonolefinic and must contain less than 5 volume % monoaromatic. Composition data are in volume percent.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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5.1 A knowledge of the hydrocarbon composition of gasoline process streams, blending stocks and finished motor fuels is useful in following the effect of changes in plant operating conditions, diagnosing process upsets, blending finished products and in evaluating the relationship between composition and performance properties.1.1 This test method covers the determination by mass spectrometry of the total paraffins, monocycloparaffins, dicycloparaffins, alkylbenzenes, indans or tetralins or both, and naphthalenes in gasoline having an olefin content of less than 3 % by volume and a 95 % distillation point of less than 210 °C (411 °F) as determined in accordance with Test Method D86. Olefins are determined by Test Method D1319, or by Test Method D875.1.2 It has not been determined whether this test method is applicable to gasoline containing oxygenated compounds (for example, alcohols and ethers).1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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