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定价: 124元 / 折扣价: 106 加购物车

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5.1 Accurate determination of the gravity of petroleum and its products is necessary for the conversion of measured volumes to volumes at the standard temperature of 60 °F (15.56 °C).5.2 This procedure is most suitable for determining the API gravity of low viscosity transparent liquids. This test method can also be used for viscous liquids by allowing sufficient time for the hydrometer to reach temperature equilibrium, and for opaque liquids by employing a suitable meniscus correction. Additionally for both transparent and opaque fluids the readings shall be corrected for the thermal glass expansion effect before correcting to the reference temperature.5.3 When used in connection with bulk oil measurements, volume correction errors are minimized by observing the hydrometer reading at a temperature as close to reference temperature as feasible.5.4 Gravity is a factor governing the quality of crude oils. However, the gravity of a petroleum product is an uncertain indication of its quality. Correlated with other properties, gravity can be used to give approximate hydrocarbon composition and heat of combustion.5.5 Gravity is an important quality indicator for automotive, aviation and marine fuels, where it affects storage, handling and combustion.1.1 This test method covers the determination by means of a glass hydrometer in conjunction with a series of calculations of the API gravity of crude petroleum and petroleum products normally handled as liquids and having a Reid vapor pressure (Test Method D323) of 14.696 psi (101.325 kPa) or less. Values are determined at existing temperatures and corrected to values at 60 °F (15.56 °C), or converted to values at 60 °F, by means of Adjunct to D1250 Standard Guide for the Use of the Joint API and ASTM Adjunct for Temperature and Pressure Volume Correction Factors for Generalized Crude Oils, Refined Products, and Lubricating Oils (API MPMS Chapter 11.1). These tables are not applicable to nonhydrocarbons or essentially pure hydrocarbons such as the aromatics.1.2 The initial values obtained are uncorrected hydrometer readings and not density measurements. Values are measured on a hydrometer at either the reference temperature or at another convenient temperature, and readings are corrected for the meniscus effect, the thermal glass expansion effect, alternate calibration temperature effects and to the reference temperature by means of the petroleum measurement tables; values obtained at other than the reference temperature being hydrometer readings and not density measurements.1.3 The initial hydrometer readings determined shall be recorded before performing any calculations. Then the calculations required in Section 9 shall be performed and documented before using the final result in a subsequent calculation procedure (measurement ticket calculation, meter factor calculation, or base prover volume determination).1.4 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.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statement, see 8.5.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The density or relative density of light hydrocarbons and liquefied petroleum gases is used in custody transfer quantity calculations or to satisfy transportation, storage, and regulatory requirements.1.1 This test method covers the determination of the density or relative density of light hydrocarbons including liquefied petroleum gases (LPG) having Reid vapor pressures exceeding 101.325 kPa (14.696 psi).1.2 The prescribed apparatus should not be used for materials having vapor pressures higher than 1.4 MPa (200 psi) at the test temperature. This pressure limit is dictated by the type of equipment. Higher pressures can apply to other equipment designs.1.3 The initial pressure hydrometer readings obtained are uncorrected hydrometer readings and not density measurements. Readings are measured on a hydrometer at either the reference temperature or at another convenient temperature, and readings are corrected for the meniscus effect, the thermal glass expansion effect, alternate calibration temperature effects and to the reference temperature by means of calculations and Adjunct to D1250 Guide for Petroleum Measurement Tables (API MPMS Chapter 11.1) or API MPMS Chapter 11.2.4 (GPA TP-27), as applicable.1.4 Values determined as density or relative density can be converted to equivalent values in the other units or alternative reference temperatures by means of Interconversion Procedures API MPMS Chapter 11.5, or Adjunct to D1250 Guide for Petroleum Measurement Tables (API MPMS Chapter 11.1) or API MPMS Chapter 11.2.4 (GPA TP-27), as applicable.1.5 The calculations required in Section 11 shall be applied to the initial pressure hydrometer reading with observations and results reported as required by Section 11 prior to use in a subsequent calculation procedure (measurement ticket calculation, meter factor calculation, or base prover volume determination).1.6 Annex A1 contains a procedure for verifying or certifying the equipment for this test method.1.7 The values in SI units are to be regarded as the standard. US Customary values shown in adjacent parentheses are for information only and may not be exactly equivalent. Both SI and customary units have been rounded so that they may not be exactly equivalent.1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.9 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

定价: 590元 / 折扣价: 502 加购物车

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5.1 Accurate determination of the density, relative density (specific gravity), or API gravity of petroleum and its products is necessary for the conversion of measured volumes to volumes or masses, or both, at the standard reference temperatures of 15 °C or 60 °F during custody transfer.5.2 This procedure is most suitable for determining the density, relative density (specific gravity), or API gravity of low viscosity transparent liquids. This procedure can also be used for viscous liquids by allowing sufficient time for the hydrometer to reach temperature equilibrium, and for opaque liquids by employing a suitable meniscus correction. Additionally for both transparent and opaque fluids the readings shall be corrected for the thermal glass expansion effect and alternative calibration temperature effects before correcting to the reference temperature.5.3 When used in connection with bulk oil measurements, volume correction errors are minimized by observing the hydrometer reading at a temperature close to that of the bulk oil temperature.5.4 Density, relative density, or API gravity is a factor governing the quality and pricing of crude petroleum. However, this property of petroleum is an uncertain indication of its quality unless correlated with other properties.5.5 Density is an important quality indicator for automotive, aviation and marine fuels, where it affects storage, handling and combustion.1.1 This test method covers the laboratory determination using a glass hydrometer in conjunction with a series of calculations, of the density, relative density, or API gravity of crude petroleum, petroleum products, or mixtures of petroleum and nonpetroleum products normally handled as liquids, and having a Reid vapor pressure of 101.325 kPa (14.696 psi) or less. Values are determined at existing temperatures and corrected to 15 °C or 60 °F by means of a series of calculations and international standard tables.1.2 The initial hydrometer readings obtained are uncorrected hydrometer readings and not density measurements. Readings are measured on a hydrometer at either the reference temperature or at another convenient temperature, and readings are corrected for the meniscus effect, the thermal glass expansion effect, alternative calibration temperature effects and to the reference temperature by means of the Petroleum Measurement Tables; values obtained at other than the reference temperature being hydrometer readings and not density measurements.1.3 Readings determined as density, relative density, or API gravity can be converted to equivalent values in the other units or alternative reference temperatures by means of Interconversion Procedures (API MPMS Chapter 11.5), or Adjunct to D1250 Guide for Petroleum Measurement Tables (API MPMS Chapter 11.1), or both, or tables, as applicable.1.4 The initial hydrometer readings determined in the laboratory shall be recorded before performing any calculations. The calculations required in Section 10 shall be applied to the initial hydrometer reading with observations and results reported as required by Section 11 prior to use in a subsequent calculation procedure (ticket calculation, meter factor calculation, or base prover volume determination).1.5 Annex A1 contains a procedure for verifying or certifying the equipment for this test method.1.6 The values stated in SI units are to be regarded as standard.1.6.1 Exception—The values given in parentheses are provided for information only.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.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.

定价: 590元 / 折扣价: 502 加购物车

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5.1 Particle-size distribution (gradation) is a descriptive term referring to the proportions by dry mass of a soil distributed over specified particle-size ranges. The gradation curve generated using this method yields the distribution of silt and clay size fractions present in the soil based on size definitions, not mineralogy or Atterberg limit classification.5.2 Unless the sedimentation sample is representative of the entire sample, the sedimentation results must be combined with a sieve analysis to obtain the complete particle size distribution.5.3 The clay size fraction is material finer than 2 µm. The clay size fraction is used in combination with the Plasticity Index (Test Methods D4318) to compute the activity, which provides an indication of the mineralogy of the clay fraction.5.4 The gradation of the silt and clay size fractions is an important factor in determining the susceptibility of fine-grained soils to frost action.5.5 The gradation of a soil is an indicator of engineering properties such as hydraulic conductivity, compressibility, and shear strength. However, soil behavior for engineering and other purposes is dependent upon many factors, such as effective stress, mineral type, structure, plasticity, and geological origin, and cannot be based solely upon gradation.5.6 Some types of soil require special treatment in order to correctly determine the particle sizes. For example, chemical cementing agents can bond clay particles together and should be treated in an effort to remove the cementing agents when possible. Hydrogen peroxide and moderate heat can digest organics. Hydrochloric acid can remove carbonates by washing and Dithionite-Citrate-Bicarbonate extraction can be used to remove iron oxides. Leaching with test water can be used to reduce salt concentration. All of these treatments, however, add significant time and effort when performing the sedimentation test and are allowable but outside the scope of this test method.5.7 The size limits of the sedimentation test are from about 100 µm to about 0.1 µm. The length of time required to obtain a stable initial reading on the hydrometer controls the upper range of results, and the test duration controls the lower range.5.8 The shape and density of the grains are important to the results. Stokes’ Law is assumed to be valid for spherical particles even though fine silt- and clay-sized particles are more likely to be plate-shaped and have greater mineral densities than larger particles.5.9 High plasticity clays develop structured water layers on their surfaces. According to Zhang and Lu3 this near surface water can be as dense as 1.4 g/L. This high-density structured water causes an error in this test method and shifts the particle size distribution curve upwards. Correction for the structured water is beyond the scope of this standard but values of percent passing above 100 % are possible and should not be excluded from the report.NOTE 5: The quality of the result produced by this standard is dependent on the competence of the personnel performing it, and the suitability of the equipment and facilities used. Agencies that meet the criteria of Practice D3740 are generally considered capable of competent and objective testing/sampling/inspection/etc. Users of this standard are cautioned that compliance with Practice D3740 does not in itself assure reliable results. Reliable results depend on many factors; Practice D3740 provides a means of evaluating some of those factors.1.1 This test method covers the quantitative determination of the distribution of particle sizes of the fine-grained portion of soils. The sedimentation by hydrometer method is used to determine the particle-size distribution (gradation) of the material that is finer than the No. 200 (75-µm) sieve and larger than about 0.2-µm. The test is performed on material passing the No. 10 (2.0-mm) or finer sieve and the results are presented as the mass percent finer of this fraction versus the log of the particle diameter.1.2 This method can be used to evaluate the fine-grained fraction of a soil with a wide range of particle sizes by combining the sedimentation results with results from a sieve analysis using D6913 to obtain the complete gradation curve. The method can also be used when there are no coarse-grained particles or when the gradation of the coarse-grained material is not required or not needed.NOTE 1: The significant digits recorded in this test method preclude obtaining the grain size distribution of materials that do not contain a significant amount of fines. For example, clean sands will not yield detectable amounts of silt and clay sized particles, and therefore should not be tested with this method. The minimum amount of fines in the sedimentation specimen is 15 g.1.3 When combining the results of the sedimentation and sieve tests, the procedure for obtaining the material for the sedimentation analysis and calculations for combining the results will be provided by the more general test method, such as Test Methods D6913 (Note 2).NOTE 2: Subcommittee D18.03 is currently developing a new test method “Test Method for Particle-Size Analysis of Soils Combining the Sieve and Sedimentation Techniques.”1.4 The terms “soil” and “material” are used interchangeably throughout the standard.1.5 The sedimentation analysis is based on the concept that larger particles will fall through a fluid faster than smaller particles. Stokes’ Law gives a governing equation used to determine the terminal velocity of a spherical particle falling through a stationary liquid. The terminal velocity is proportional to the square of the particle diameter. Therefore, particles are sorted by size in both time and position when settling in a container of liquid.1.5.1 Stokes’ Law has several assumptions which are: the particles are spherical and smooth; there is no interference between the particles; there is no difference between the current in the middle of the container and the sides; flow is laminar; and the particles have the same density. These assumptions are applied to soil particles of various shapes and sizes.1.6 A hydrometer is used to measure the fluid density and determine the quantity of particles in suspension at a specific time and position. The density of the soil-water suspension depends upon the concentration and specific gravity of the soil particles and the amount of dispersant added. Each hydrometer measurement at an elapsed time is used to calculate the percentage of particles finer than the diameter given by Stokes’ Law. The series of readings provide the distribution of material mass as a function of particle size.1.7 This test method does not cover procurement of the sample or processing of the sample prior to obtaining the reduced sample in any detail. It is assumed that the sample is obtained using appropriate methods and is representative of site materials or conditions. It is also assumed that the sample has been processed such that the reduced sample accurately reflects the particle-size distribution (gradation) of this finer fraction of the material.1.8 Material Processing—Material is tested in the moist or as-received state unless the material is received in an air-dried state. The moist preparation method shall be used to obtain a sedimentation test specimen from the reduced sample. Air-dried preparation is only allowed when the material is received in the air-dried state. The method to be used may be specified by the requesting authority; however, the moist preparation method shall be used for referee testing.1.9 This test method is not applicable for the following soils:1.9.1 Soils containing fibrous peat.1.9.2 Soils containing less than approximately 5 % of fine-grained material (Note 1).1.9.3 Soils containing extraneous matter, such as organic solvents, oil, asphalt, wood fragments, or similar items (Note 3).NOTE 3: If extraneous matter, such as wood, can be easily removed by hand, it is permissible to do so. However, there may be cases where the extraneous matter is being evaluated as part of the material and it should not be removed from the material.1.9.4 Materials that contain cementitious components, such as cement, fly ash, lime, or other stabilization admixtures.1.10 This test method may not produce consistent test results within and between laboratories for the following soils. To test these soils, this test method must be adapted and these adaptations documented.1.10.1 Soils that flocculate during sedimentation. Such materials may need to be treated to reduce salinity or alter the pH of the suspension.1.10.2 Friable soils in which processing changes the gradation of the soil. Typical examples of these soils are some residual soils, most weathered shales, decomposed granites, and some weakly cemented soils.1.10.3 Soils that will not readily disperse, such as glauconitic clays or some dried plastic clays.1.11 Samples that are not soils, but are made up of particles may be tested using this method. The applicable sections above should be used in applying this standard.1.12 Units—The values stated in SI units are to be regarded as standard. Except the sieve designations, they are identified using the “alternative” system in accordance with Practice E11, such as 3-in. and No. 200, instead of the “standard” designation of 75-mm and 75-µm, respectively. Reporting of test results in units other than SI shall not be regarded as non-conformance with this test method. The use of balances or scales recording pounds of mass (lbm) shall not be regarded as nonconformance with this standard.1.13 All observed and calculated values shall conform to the guidelines for significant digits and rounding established in Practice D6026, unless superseded by this test method.1.13.1 The procedures used to specify how data are collected/recorded and calculated in the standard are regarded as the industry standard. In addition, they are representative of the significant digits that generally should be retained. The procedures used do not consider material variation, purpose for obtaining the data, special purpose studies, or any considerations for the user’s objectives; and it is common practice to increase or reduce significant digits of reported data to be commensurate with these considerations. It is beyond the scope of this test method to consider significant digits used in analysis methods for engineering or other data.1.14 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.1.15 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.

定价: 843元 / 折扣价: 717 加购物车

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1.1 This test method covers the determination of the particle-size distribution in the sub-sieve size range of the common extender pigments such as aluminum silicate (kaolin clay), magnesium silicate (talc), calcium carbonate (calcite or dolomite or precipitated calcium carbonate), and mica pigments, and may also be extended to the denser prime pigments such as the white titanium pigments (rutile or anatase) and similar mineral pigments when and if such information is of concern. Particle-size distribution has significance in the evaluation of rheological and pigmentary properties of pigments in paint and also may sometimes be used to characterize the identity or grade of pigments. 1.2 Sedimentation methods having as their basis Stoke's law have found general acceptance for this purpose. Results are expressed in terms of equivalent spherical diameter (e.s.d.), the diameter of a sphere having the same specific gravity as the particle in question and which settles at the same rate. Most mineral pigment particles are more-or-less asymmetrical, but despite differences in the relationship between equivalent spherical diameter and actual dimensions, the results of a sedimentation particle-size analysis can be correlated readily with many pigment properties. 1.3 Procedures limited to gravitational sedimentation are relatively inaccurate for pigment particles smaller than about 1 [mu]m e.s.d., and centrifugal procedures may be required for the much finer ranges. Nevertheless, the data obtained above the 1 [mu]m limitation provide useful information. This method is particularly applicable to pigments if a major fraction of the particles fall in the range from about 15 to 1.5 [mu]m, but have a total particle-size range of at least two decades. 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.

定价: 0元 / 折扣价: 0

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5.1 Dispersive clays are those which normally deflocculate when exposed to water of low-salt concentration, the opposite of aggregated clays that would remain flocculated in the same soil-water system (3, 4, 7). Generally, dispersive clays are highly erosive, possibly subject to high shrink-swell potential, may have lower shear strength, and have lower permeability rates than aggregated clays.5.2 When the percent dispersion equals 100, it indicates a completely dispersive clay-size fraction. When the percent dispersion equals 0, it indicates completely nondispersive clay-size fraction.5.3 Available data (1) indicates that the test method has about 85 % reliance in predicting dispersive performance (85 % of dispersive clays show more than 35 % dispersion).5.4 Since this test method may not identify all dispersive clays, design decisions based solely on this test method may not be conservative. It is often run in conjunction with the crumb test (D6572) (4, 7), the pinhole test (D4647/D4647M), or the analysis of the pore water extract (D4542) (4, 7), or combination thereof, to identify possible dispersive clay behavior.NOTE 1: The quality of the result produced by this standard is dependent on the competence of the personal performing it, and the suitability of the equipment and facilities used. Agencies that meet the criteria of Practice D3740 are generally considered capable of competent and objective testing/sampling/inspection/etc. Users of this standard are cautioned that compliance with Practice D3740 does not in itself assure reliable results. Reliable results depends on many factors; Practice D3740 provides a means of evaluating some of those factors.1.1 This test method provides an indication of the natural dispersive characteristics of clay soils by comparing the amount of particles finer than 2-μm as determined by this method compared to the amount of particles finer than 2-μm as determined by Test Method D7928 (1).2 In order to do this comparison, two similar specimens must be obtained from the sample.1.2 This test method follows the procedure given in Test Method D7928 with the exception that the soil slurry is not mechanically dispersed and no dispersing agent is added.1.3 This test method is applicable only to soils where the position of the plasticity index versus liquid limit plots (Test Methods D4318) falls on or above the “A” line (Practice D2487) and more than 12 % of the soil fraction is finer than 2-μm as determined in accordance with Test Method D7928 (2).1.4 Since this test method may not identify all dispersive clay soils, other tests such as, pinhole dispersion (Test Methods D4647/D4647M), crumb (Test Methods D6572) (3-5) and the analysis of pore water extraction (Test Methods D4542) (4-7) may be performed individually or used together to help verify dispersion.1.5 Units—The values stated in SI units are to be regarded as the standard. Reporting of test results in units other than SI shall not be regarded as nonconformance with this test method.1.6 All observed and calculated values shall conform to the guidelines for significant digits and rounding established in Practice D6026.1.6.1 The procedures used to specify how data are collected/recorded or calculated, in this standard are regarded as the industry standard. In addition, they are representative of the significant digits that generally should be retained. The procedures used do not consider material variation, purpose for obtaining the data, special purpose studies, or any considerations for the user's objectives; and it is common practice to increase or reduce significant digits of reported data to be commensurate with these considerations. It is beyond the scope of this standard to consider significant digits used in analysis methods for engineering design.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.

定价: 590元 / 折扣价: 502 加购物车

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4.1 The relative density of an engine coolant may be used to determine the approximate percent glycol, freezing point, and boiling point, provided the glycol type is known.4.2 The relative density of an engine coolant concentrate can be used as a production control test.4.3 ASTM specifications normally state the temperatures for relative density of fluids; 25 °C, 20 °C, and 15.6 °C are commonly used temperatures.1.1 This test method covers the determination of the relative density of glycols, glycerin, heat transfer fluids, engine coolant concentrates, and aqueous engine coolants.1.2 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.1.3 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.

定价: 515元 / 折扣价: 438 加购物车

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5.1 Accurate determination of the density, specific gravity, or API gravity of cutback asphalts is necessary for the conversion of measured volumes to volumes at the standard temperature of 15 °C or 60 °F.5.2 Similarly, accurate determination is necessary for converting volumes to mass as required in other ASTM tests on cutback asphalts.5.3 Values corrected to 15 °C and 60 °F will be different because the two temperatures are not equal.1.1 This test method covers the laboratory determination, using a glass hydrometer, of the density, specific gravity, or API gravity of cutback asphalts as defined in Specifications D2026, D2027, and D2028 (Note 1). Values are measured on a hydrometer at convenient temperatures, readings of density, specific gravity, and API gravity being reduced to 15 °C or 60 °F by means of international standard tables. By means of these same tables, values determined in one of the three systems of measurement are convertible to equivalent values in either system so that measurements may be made in the units of local convenience.NOTE 1: This test method is applicable to cutback asphalts and in general follows, but provides more explicit routines than, the procedure outlined in Test Method D1298.1.2 Units—The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in nonconformance with the 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. Specific precautionary statements are given in Section 7.1.4 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.

定价: 515元 / 折扣价: 438 加购物车

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