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1. Scope 1.1 This Standard covers the following devices intended for connection to copper conductors only and for installation and use in hazardous locations: Class I, Groups A, B, C, and D; Class II, Group G, in coal or coke dust, and in gaseous mine

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1.1 This test method covers the determination of the ignition of a dust dispersed in air, within a closed vessel.1.2 This test method provides a measure of dust explosion pressure and rate of pressure rise. It does not provide a definitive determination of the flammability of a dust and has other severe limitations which are identified in Section 5. The preferred method for the design of safety equipment is Test Method E1226.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. For specific safety precautions see Section 7.1.4 The values stated in inch-pound units are to be regarded as the standard. The values in parentheses are for information only.

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5.1 This test method provides a procedure for performing laboratory tests to determine the minimum autoignition temperature (MAIT) of a dust cloud.5.2 The test data developed from this test method can be used to limit the temperature to which a dust cloud is exposed so as to prevent ignition of the cloud. Because of the short duration of the test, the data obtained are most applicable to industrial equipment where dust is present as a cloud for a short time. Because of the small scale of the test and the possible variation of the MAIT value with scale, the data obtained by this test method may not be directly applicable to all industrial conditions.5.3 The MAIT data can also be used in conjunction with minimum spark ignition data to evaluate the hazards of grinding and impact sparks in the presence of dust clouds (1 and 2).35.4 The test values obtained are specific to the sample tested, the method used, and the test equipment utilized. The test values are not to be considered intrinsic material constants, but may be used as a relative measure of the temperature at which a dust cloud self ignites.5.5 The test data are for cloud ignition. Dust in the form of a layer may ignite at significantly lower temperatures than the same dust in the form of a cloud (3). For liquid chemicals, see Test Method E659.1.1 This test method covers the minimum temperature at which a given dust cloud will autoignite when exposed to air heated in a furnace at local atmospheric pressure.1.2 Data obtained from this test method provide a relative measure of dust cloud autoignition temperatures.1.3 This test method should be used to measure and describe the properties of materials, products, or assemblies in response to heat and flame under controlled laboratory conditions and should not be used to describe or appraise the fire hazard or fire risk of materials, products, or assemblies under actual fire conditions. However, results of this test method may be used as elements of a fire risk assessment which takes into account all of the factors which are pertinent to an assessment of the fire hazard of a particular end use.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This specification covers requirements for wipe sampling materials that are used to collect settled dusts on surfaces for the subsequent determination of lead. The wipes shall be tested for conformance to background lead, lead recoverability, collection efficiency, ruggedness which shall be determined using butted vinyl-composite floor tiles as a test surface, moisture content, coefficient of variation in mass, linear dimensions such as mean area and mean length, and mean thickness requirements.1.1 This specification covers requirements for wipes that are used to collect settled dusts on surfaces for the subsequent determination of lead.1.2 For wipe materials used for the determination of beryllium in surface dust refer to Specification D7707. This is mentioned to insure that users of wipes recognize that there is some relationship between the analytical backgrounds found in wipes and the analyte of interest.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method provides a procedure for performing laboratory tests to evaluate relative deflagration parameters of dusts.5.2 Knowledge of the limiting oxygen (oxidant) concentration is needed for safe operation of some chemical processes. This information may be needed in order to start up, shut down or operate a process while avoiding the creation of flammable dust-gas atmospheres therein, or to pneumatically transport materials safely. NFPA 69 provides guidance for the practical use of LOC data, including the appropriate safety margin to use.5.3 Since the LOC as measured by this method may vary with the energy of the ignitor and the propagation criteria, the LOC should be considered a relative rather than absolute measurement.5.4 If too weak an ignition source is used, the measured LOC would be higher than the “true” value and would not be sufficiently conservative. This is an ignitability limit rather than a flammability limit, and the test could be described as “underdriven.” Ideally, the ignition energy is increased until the measured LOC is independent of ignition energy (that is, the “true” value). However, at some point the ignition energy may become too strong for the size of the test chamber, and the system becomes “overdriven.” When the ignitor flame becomes too large relative to the chamber volume, a test could appear to result in an explosion, while it is actually just dust burning in the ignitor flame with no real propagation beyond the ignitor (1-3).5 This LOC value would be overly conservative.5.5 The recommended ignition source for measuring the LOC of dusts in 20-L chambers is a 2500-J pyrotechnic ignitor.6 This ignitor contains 0.6 g of a powder mixture of 40 % zirconium, 30 % barium nitrate, and 30 % barium peroxide. Measuring the LOC at several ignition energies will provide information on the possible overdriving of the system to evaluate the effect of possible overdriving in a 20-L chamber, comparison tests may also be made in a larger chamber such as a 1-m3 chamber (1-3).5.6 The values obtained by this testing technique are specific to the sample tested (particularly the particle size distribution) and the method used and are not to be considered intrinsic material constants.NOTE 1: Much of the previously published LOC data (4). were obtained using a spark ignition source in a 1.2-L Hartmann chamber and may not be sufficiently conservative. The European method of LOC determination EN 14034–4 uses two 1000-J pyrotechnic igniters in the 20-L chamber.1.1 This test method is designed to determine the limiting oxygen concentration of a combustible dust dispersed in a mixture of air with an inert/nonflammable gas in a near-spherical closed vessel of 20 L or greater volume.1.2 Data obtained from this method provide a relative measure of the deflagration characteristics of dust clouds.1.3 This test method should be used to measure and describe the properties of materials in response to heat and flame under controlled laboratory conditions and should not be used to describe or appraise the fire hazard or fire risk of materials, products, or assemblies under actual fire conditions. However, results of this test may be used as elements of a fire risk assessment that takes into account all of the factors that are pertinent to an assessment of the fire hazard of a particular end use.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 8.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 This test method is useful for determining the amount of metallic zinc in zinc dust pigment, and also in dried films of both inorganic and organic zinc-rich coatings. Test Methods D521 is an appropriate method for analyzing zinc dust, but has shortcomings when applied to samples of cured coatings.1.1 This test method covers the determination by differential scanning calorimetry of the metallic zinc content of both zinc-dust pigment, and of dried films of zinc-rich coatings. This test method is applicable to both inorganic and organic zinc-rich coatings.1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This guide describes factors to be considered by an investigator designing a sampling program to compare the asbestos dust loadings in two environments and presents statistical methods for making the comparison. Each user is responsible for the design of an investigation and the interpretation of data collected when using dust data.5.2 This guide does not deal with situations where dusts of different compositions or from different surfaces are to be evaluated.5.3 This guide describes methods for interpreting the results of sampling and analysis performed in accordance with Test Methods D5755 and D6480. It may be appropriate to use the procedures in this guide with other dust collection and analysis methods, but it is the responsibility of the user to make this determination.5.4 The methods described in this guide are not intended to be used alone. They are intended to be used along with various evaluation methods that may include consideration of building use, activities within the building, air sampling, asbestos surveys (refer to Practice E2356), evaluation of building history and study of building ventilation systems.5.5 This guide describes methods for comparing environments and does not draw any conclusions relating asbestos surface loadings to the potential safety or habitability of buildings.5.6 This guide does not address risk assessments or the use of dust sampling in risk assessment. Health based risk assessments are beyond the scope of this guide.5.7 Warning—Asbestos fibers are acknowledged carcinogens. Breathing asbestos fibers can result in disease of the lungs including asbestosis, lung cancer, and mesothelioma. Precautions should be taken to avoid creating and breathing airborne asbestos particles when sampling and analyzing materials suspected of containing asbestos. Regulatory requirements addressing asbestos are defined by USEPA3,4 and OSHA.51.1 There are multiple purposes for determining the loading of asbestos in dust on surfaces. Each particular purpose may require unique sampling strategies, analytical methods, and procedures for data interpretation. Procedures are provided to facilitate application of available methods for determining asbestos surface loadings and/or asbestos loadings in surface dust for comparison between two environments. At present, this guide addresses one application of the ASTM surface dust methods. It is anticipated that additional areas will be added in the future. It is not intended that the discussion of one application should limit use of the methods in other areas.1.2 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 5.7.1.3 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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5.1 The primary purpose of this practice is to describe a procedure for collecting near real-time data on airborne particle concentration and size distribution in clean areas as indicated by single particle counting techniques. Implementation of some government and industry specifications requires acquisition of particle size and concentration data using an SPC.5.2 The processing requirements of many products manufactured in a clean room involves environmental cleanliness levels so low that a single particle counter with capability for detecting very small particles is required to characterize clean room air. Real-time information on concentration of airborne particles in size ranges from less than 0.1 μm to 5 μm and greater can be obtained only with an SPC. Definition of particles larger than approximately 0.05 μm may be carried out with direct measurement of light scattering from individual particles; other techniques may be required for smaller particles, such as preliminary growth by condensation before particle measurement.5.3 Particle size data are referenced to the particle system used to calibrate the SPC. Differences in detection, electronic and sample handling systems among the various SPCs may contribute to differences in particle characterization. Care must be exercised in attempting to compare data from particles that vary significantly in composition or shape from the calibration base material. Variations may also occur between instruments using similar particle sensing systems with different operating parameters. These effects should be recognized and minimized by using standard methods for SPC calibration and operation.5.4 In applying this practice, the fundamental assumption is made that the particles in the sample passing through the SPC are representative of the particles in the entire dust-controlled area being analyzed. Care is required that good sampling procedures are used and that no artifacts are produced at any point in the sample handling and analysis process; these precautions are necessary both in verification and in operation of the SPC.1.1 This practice covers the determination of the particle concentration, by number, and the size distribution of airborne particles in dust-controlled areas and clean rooms, for particles in the size range of approximately 0.01 to 5.0 μm. Particle concentrations not exceeding 3.5 × 106 particles/m 3 (100 000/ft3) are covered for all particles equal to and larger than the minimum size measured.1.2 This practice uses an airborne single particle counting device (SPC) whose operation is based on measuring the signal produced by an individual particle passing through the sensing zone. The signal must be directly or indirectly related to particle size.NOTE 1: The SPC type is not specified here. The SPC can be a conventional optical particle counter (OPC), an aerodynamic particle sizer, a condensation nucleus counter (CNC) operating in conjunction with a diffusion battery or differential mobility analyzer, or any other device capable of counting and sizing single particles in the size range of concern and of sampling in a cleanroom environment.1.3 Individuals performing tests in accordance with this practice shall be trained in use of the SPC and shall understand its operation.1.4 Since the concentration and the particle size distribution of airborne particles are subject to continuous variations, the choice of sampling probe configuration, locations, and sampling times will affect sampling results. Further, the differences in the physical measurement, electronic, and sample handling systems between the various SPCs and the differences in physical properties of the various particles being measured can contribute to variations in the test results. These differences should be recognized and minimized by using a standard method of primary calibration and by minimizing variability of sample acquisition procedures.1.5 Sample acquisition procedures and equipment may be selected for specific applications based on varying cleanroom class levels. Firm requirements for these selections are beyond the scope of this practice; however, sampling practices shall be stated that take into account potential spatial and statistical variations of suspended particles in clean rooms.NOTE 2: General references to cleanroom classifications follow Federal Standard 209E, latest revision. Where airborne particles are to be characterized in dust-controlled areas that do not meet these classifications, the latest revision of the pertinent specification for these areas shall be used.1.6 Units—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.1.7 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. For specific hazards statements, see Section 8.1.8 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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This test method covers the apparatuses required, sampling methods, standard procedures and calculations, and test reports for counting and sizing airborne microparticulate matter, the sampling areas for which are specifically those with contamination levels typical of cleanrooms and dust-controlled areas. The test method is based on the microscopical examination of particles impinged upon a membrane filter with the aid of a vacuum. Sampling may be done in a cleanroom, clean zone, or other controlle areas, or in a duct or pipe, wherein the number of sampling points is proportional to the floor area of the enclosure to be checked. The apparatus and facilities required are typical of a laboratory for the study of macroparticle contamination. The operator must have adequate basic training in microscopy and the techniques of particle sizing and counting.1.1 This test method covers counting and sizing airborne particulate matter 5 µm and larger (macroparticles). The sampling areas are specifically those with contamination levels typical of cleanrooms and dust-controlled areas.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 are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.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 Ultrasonic extraction using dilute nitric acid is a simpler and easier method for extracting lead from environmental samples than are traditional digestion methods that employ hot plate or microwave digestion with concentrated acids (3), (5), (7), (8). Hence, ultrasonic extraction may be used in lieu of the more rigorous strong acid/high temperature digestion methods (for example, see Ref (3) and Test Method E1613), provided that the performance is demonstrated using accepted criteria as delineated in Guide E1775.5.2 In contrast with hot plate or microwave digestion techniques, ultrasonic extraction is field-portable, which allows for on-site sample analysis.1.1 This practice covers an ultrasonic extraction procedure for the extraction of lead from environmental samples of interest in lead abatement and renovation (or related) work, for analytical purposes.1.2 Environmental matrices of concern include dry paint films, settled dusts, soils, and air particulates.1.3 Samples subjected to ultrasonic extraction are prepared for subsequent determination of lead by laboratory analytical methods.1.4 This practice includes, where applicable, descriptions of procedures for sample homogenization and weighing prior to ultrasonic extraction.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 This practice may be used to collect dust from carpeted or bare floor surfaces for gravimetric or chemical analysis. The collected sample is substantially unmodified by the sampling procedure.5.2 This practice provides for a reproducible dust removal rate from level loop and plush carpets, as well as bare floors. It has the ability to achieve relatively constant removal efficiency at different loadings of floor dust.5.3 This practice also provides for the efficient capture of semivolatile organic chemicals associated with the dust. The test system can be fitted with special canisters downstream of the cyclone for the capture of specific semivolatile organic chemicals that may volatilize from the dust particles during collection.5.4 This practice does not describe procedures for evaluation of the safety of floor surfaces or the potential human exposure to floor dust. It is the user's responsibility to evaluate the data collected by this practice and make such determinations in the light of other available information.5.5 This practice provides per-event dust chemical concentration and chemical loading. Advantages and trade-offs of different sampling approaches have been discussed (7).5.6 This practice uses a removable, cleanable dropout jar that facilitates per-event sampling. Other per-event vacuum attachments are commercially available. These are not directly comparable with composite sampling done using whole vacuum cleaner bags.1.1 This practice covers a procedure for the collection of a sample of dust from carpets and bare floors that can be analyzed for inorganic metals such as lead and organic compounds such as pesticides and other semi-volatile organic compounds (SVOCs).1.2 This practice is applicable to a variety of carpeted and bare floor surfaces. It has been tested for level loop and plush pile carpets and bare wood floors, specifically. This practice is not applicable to elevated, non-floor surfaces.1.3 This practice is not intended for the collection and evaluation of dust for the presence of asbestos fibers.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.5 This practice describes use of a sampling device, the High-Volume Small Surface Sampler (HVS3). Other event-based sampling devices that use commercially available vacuum attachments are not in scope. Composite sampling using whole vacuum cleaner bags is not in scope. Other approaches for floor or non-floor surface sampling (Practices D6966, D6661, D7144) are not within the scope.1.6 This practice only applies to the HVS3. Other dust sampling methods may or may not be directly comparable. Method evaluation for other dust sampling approaches is encouraged. This could be done by comparison with methods outlined in this standard practice for HVS3 or through independent evaluation using field spikes and certified reference materials.1.7 This practice provides information on dust loading, chemical dust concentration, and chemical dust loading. Information on the type of floor, the floor surface area sampled, and amount of dust collected is required (see Fig. 2). Cleaning the vacuum attachments in between sampling events is also required (see Section 13).1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.9 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The test is designed to quantify the amount of dust control material added to calcined coke. The dust control material is applied to calcined coke to help maintain a dust-free environment. It generally serves no other useful purpose. It adds mass to the coke and can have a negative effect on the quality of carbon and graphite artifacts made from the treated coke. For these reasons the coke customer wants to know the amount of dust control material on the coke and can specify a maximum level.1.1 This test method covers the determination of the amount of material applied to calcined coke to control dust associated with coke handling and transportation.1.2 This test method is limited to those materials that are soluble in a solvent that can be used in a Soxhlet extraction type of apparatus such as methylene chloride (dichloro-methane).NOTE 1: Methylene chloride is the most popular solvent for removing dust control oil at the time this procedure is being written. Toluene and methyl chloroform, however, have been used with equal results on all cokes tested which have included only those sprayed with aromatic or waxy materials.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see Section 7.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This practice is intended for the collection of settled dust samples for the subsequent measurement of beryllium and compounds. The practice is meant for use in the collection of settled dust samples that are of interest in clearance, hazard evaluation, risk assessment, and other purposes.5.2 This practice is intended solely for the collection of settled dust samples from hard, relatively smooth nonporous surfaces that may be compromised by water or other wetting agents and that are therefore not suitable for wet wipe sampling using Practice D6966 or micro-vacuum sampling using Practice D7144. Use of this practice for any purpose other than the intended purpose is discouraged due to the limited collection efficiency and high variability of dry wipe sampling as compared to wetted wipe or micro-vacuum sampling.35.3 This practice is less effective for collecting settled dust samples from surfaces with substantial texture such as rough concrete, brickwork, textured ceilings, and soft fibrous surfaces such as upholstery and carpeting. Micro-vacuum sampling using Practice D7144 may be more suitable for these surfaces.1.1 This practice covers the collection of settled dust containing beryllium and beryllium compounds on surfaces using the dry wipe sampling method, or both. These samples are collected in a manner that will permit subsequent extraction and determination of beryllium and compounds in the wipes using laboratory analysis techniques such as atomic spectrometry or fluorescence detection.1.2 This practice is limited in its scope to applications where wetted wipe sampling (using Practice D6966) or vacuum sampling (using Practice D7144) is not physically feasible (for example, if the surface to be wiped would be compromised by use of wetted wipes).1.3 This practice does not address the sampling design criteria (that is, sampling plan which includes the number and location of samples) that are used for clearance, hazard evaluation, risk assessment, and other purposes. To provide for valid conclusions, sufficient numbers of samples should be obtained as directed by a sampling plan. Additional guidance is provided in Guide D7659.1.4 This practice contains notes that are explanatory and are not part of the mandatory requirements of this practice.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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