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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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ASTM E1226-19 Standard Test Method for Explosibility of Dust Clouds Active 发布日期 :  1970-01-01 实施日期 : 

5.1 This test method provides a procedure for performing laboratory tests to evaluate deflagration parameters of dusts.5.2 The data developed by this test method may be used for the purpose of sizing deflagration vents in conjunction with the nomographs and equations published in NFPA 68, ISO 6184/1, or VDI 3673.5.3 The values obtained by this testing technique are specific to the sample tested and the method used and are not to be considered intrinsic material constants.5.4 For dusts with low KSt values, discrepancies have been observed between tests in 20-L and 1-m3 chambers. A strong ignitor may overdrive a 20-L chamber, as discussed in Test Method E1515 and Refs (1-4).8 Conversely, more recent testing has shown that some metal dusts can be prone to underdriving in the 20-L chamber, exhibiting significantly lower KSt values than in a 1-m3 chamber (5). Ref (6) provides supporting calculations showing that a test vessel of at least 1-m3 of volume is necessary to obtain the maximum explosibility index for a burning dust cloud having an abnormally high flame temperature. In these two overdriving and underdriving scenarios described above, it is therefore recommended to perform tests in 1-m3 or larger calibrated test vessels in order to measure dusts explosibility parameters accurately.NOTE 5: Ref (2) concluded that dusts with KSt values below 45 bar m/s when measured in a 20-L chamber with a 10 000-J ignitor, may not be explosible when tested in a 1-m3 chamber with a 10 000-J ignitor. Ref (2) and unpublished testing has also shown that in some cases the KSt values measured in the 20-L chamber can be lower than those measured in the 1-m3 chamber. Refs (1) and (3) found that for some dusts, it was necessary to use lower ignition energy in the 20-L chamber in order to match MEC or MIC test data in a 1-m3 chamber. If a dust has measurable (nonzero) Pmax and KSt values with a 5000 or 10 000-J ignitor when tested in a 20-L chamber but no measurable Pmax and KSt values with tests conducted using an ignition source less than or equal to 2500 J, it may be helpful to test the material in a larger chamber such as a 1-m3 chamber using at least a 10 000-J ignition source to further characterize the material’s explosibility in dust cloud form.1.1 Purpose. The purpose of this test method is to provide standard test methods for characterizing the “explosibility” of dust clouds in two ways, first by determining if a dust is “explosible,” meaning a cloud of dust dispersed in air is capable of propagating a deflagration, which could cause a flash fire or explosion; or, if explosible, determining the degree of “explosibility,” meaning the potential explosion hazard of a dust cloud as characterized by the dust explosibility parameters, maximum explosion pressure, Pmax; maximum rate of pressure rise, (dP/dt)max; and explosibility index, KSt.1.2 Limitations. Results obtained by the application of the methods of this standard pertain only to certain combustion characteristics of dispersed dust clouds. No inference should be drawn from such results relating to the combustion characteristics of dusts in other forms or conditions (for example, ignition temperature or spark ignition energy of dust clouds, ignition properties of dust layers on hot surfaces, ignition of bulk dust in heated environments, etc.)1.3 Use. It is intended that results obtained by application of this test be used as elements of a dust hazard analysis (DHA) that takes into account other pertinent risk factors; and in the specification of explosion prevention systems (see, for example NFPA 68, NFPA 69, and NFPA 652) when used in conjunction with approved or recognized design methods by those skilled in the art.NOTE 1: Historically, the evaluation of the deflagration parameters of maximum pressure and maximum rate of pressure rise has been performed using a 1.2-L Hartmann Apparatus. Test Method E789, which describes this method, has been withdrawn. The use of data obtained from the test method in the design of explosion protection systems is not recommended.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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6.1 Method—It is possible that electrical insulation in service will fail as a result of tracking, erosion, or a combination of both, if exposed to high relative humidity and contamination environments. This is particularly true of organic insulations in outdoor applications where the surface of the insulation becomes contaminated by deposits of moisture and dirt, for example, coal dust or salt spray. This test method is an accelerated test that simulates extremely severe outdoor contamination. It is believed that the most severe conditions likely to be encountered in outdoor service in the United States will be relatively mild compared to the conditions specified in this test method.6.2 Test Results—Materials can be classified by this test method as tracking-resistant, tracking-affected, or tracking-susceptible. The exact test values for these categories as they apply to specific uses will be specified in the appropriate material specifications, but guideline figures are suggested in Note 4. Tracking-resistant materials, unless erosion failure occurs first, have the potential to last many hundreds of hours (Note 5). Erosion, though it is possible that it will progress laterally, generally results in a failure perpendicular to the specimen surface. Therefore, compare only specimens of the same nominal thickness for resistance to tracking-induced erosion. Estimate the extent of erosion from measurements of the depth of penetration of the erosion. Place materials that are not tracking-susceptible in three broad categories—erosion-resistant, erosion-affected, and erosion-susceptible. When the standard thickness specimen is tested, the following times to failure typify the categories (Note 6):Erosion-susceptible 5 h to 50 hErosion-affected 50 h to 200 hErosion-resistant over 200 hNOTE 4: Tracking-susceptible materials usually fail within 5 h. Tracking-affected materials usually fail before about 100 h.NOTE 5: This information is derived from the individual experiences of eight laboratories using this test method since its publication as a suggested test method in June 1957, and from the results of an organized test program among these laboratories.NOTE 6: In a normal distribution approximately 68 % of all test values are included within ±1 standard deviation of the mean.6.3 Interpretation of Test Results—This test method provides information that allows classification as described in 6.2. The comparison of materials within the same group is likely to be ambiguous unless three or more replicate specimens are tested. When the test method is used for specification purposes, do not establish simple minimum values without consideration of the large variance to be expected in test results. It is recommended that quality levels and specification minima be determined by statistical techniques.1.1 This test method is intended to differentiate solid electrical insulating materials with respect to their resistance to the action of electric arcs produced by conduction through surface films of a specified contaminant containing moisture. Test Methods D2302, D2303, D3638, and D5288 are also useful to evaluate materials.1.2 Units—The values stated in SI units are the standard. The inch-pound units in parentheses are for information only. 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.NOTE 1: There is no equivalent ISO standard.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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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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5.1 Human exposure to toxic metals and metalloids present in surface dust can result from dermal contact with or ingestion of contaminated dust. Also, inhalation exposure can result from disturbing dust particles from contaminated surfaces. Thus, standardized methods for the collection and analysis of metals and metalloids in surface dust samples are needed in order to evaluate the potential for human exposure to toxic elements.5.2 This practice involves the use of sampling equipment to collect surface dust samples that may contain toxic metals and metalloids, and is intended for use by qualified technical professionals.5.3 This practice allows for the subsequent determination of collected elemental concentrations on an area (loading) or mass concentration basis, or both.5.4 Because particle losses can occur due to collection of dust onto the inner surfaces of the nozzle, the length of the collection nozzle is specified in order that such losses are comparable from one sample to another.5.5 This practice is suitable for the collection of surface dust samples from, for example: (a) soft, porous surfaces such as carpet or upholstery; (b) hard, rough surfaces such as concrete or roughened wood; (c) confined areas that cannot be easily sampled by other means (such as wipe sampling as described in Practice D6966). A companion sampling technique that may be used for collection of surface dust from hard, smooth surfaces is wipe sampling (Practice D6966). A companion vacuum sampling technique that may be used for sampling carpets is described in Practice D5438.5.6 Procedures presented in this practice are intended to provide a standardized method for dust collection from surfaces that cannot be reliably sampled using wipe collection methods (for example, Practice D6966). Additionally, the procedure described uses equipment that is readily available and in common use for other environmental and occupational hygiene sampling applications.5.7 The entire contents of the filter holder, that is, the filter plus collected dust, is targeted for subsequent analysis for metals and metalloids content. An internal capsule is used if gravimetric analysis is necessary.1.1 This practice covers the micro-vacuum collection of surface dust for subsequent determination of metals and metalloids. The primary intended application is for sampling from soft, rough, or porous surfaces.1.2 Micro-vacuum sampling is carried out using a collection nozzle attached to a filter holder (sampling cassette) that is connected to an air sampling pump.1.3 This practice allows for the subsequent determination of metals and metalloids on a loading basis (mass of element(s) per unit area sampled), or on a concentration basis (mass of element(s) per unit mass of sample collected), or both.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 Limitations—Due to a number of physical factors inherent in the micro-vacuum sampling method, analytical results for vacuum dust samples are not likely to reflect the total dust contained within the sampling area prior to sample collection. Indeed, dust collection will generally be biased towards smaller, less dense dust particles. Nevertheless, the use of this standard practice will generate data that are consistent and comparable between operators performing micro-vacuum collection at a variety of sampling locations and sites.21.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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1.1 This specification covers requirements for premoistened wipe materials that are used to collect settled dusts on surfaces for the subsequent determination of beryllium.1.2 For wipe materials used for the determination of lead in surface dust, refer to Specification E1792. This is mentioned to insure that users of wipes recognize that there is some relationship between 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 specification contains notes that are explanatory and are not part of the mandatory requirements of the specification.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method covers the determination of respirable dust concentration in workplace atmospheres.5.2 Variations of the test method are in world-wide use for determining compliance relative to occupational exposure levels.5.3 The test method may be used to verify dust control measures.5.4 The test method may also be applied in research into health effects of dust in an occupational setting.1.1 This test method provides details for the determination of respirable dust concentration defined in terms of international convention in a range from 0.5 mg/m3 to 10 mg/m3 in workplace atmospheres, depending on sampling time. Specifics are given for sampling and analysis using any one of a number of commercially available cyclone samplers.1.2 The limitations on the test method are a minimum weight of 0.1 mg of dust on the filter, and a maximum loading dependent on sampler type and time of sampling. The test method may be used at higher loadings if the flow rate can be maintained constant.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 test method contains notes that are explanatory and are not part of the mandatory requirements of the method.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 Beryllium is an important analyte in industrial hygiene because of the risk of exposed workers developing Chronic Beryllium Disease (CBD). CBD is a granulomatous lung disease that is caused by the body’s immune system response to inhaled dust or fumes containing beryllium, a human carcinogen (2). Surface wipe samples and air filter samples are collected to monitor the workplace. This practice addresses the problem of spurious results caused by the presence of interfering elements in the solution analyzed. The practice has been evaluated for all elements having emission spectra near the 313.042 and 313.107 nm beryllium lines, as well as elements of general concern including aluminum, calcium, iron and lead. Below is a table listing each possible spectrally interfering element:Cerium Chromium Hafnium MolybdenumNiobium Thorium Titanium ThuliumUranium Vanadium Uranium   Measurement of beryllium on the order of 1 ppb (0.003 µg Be/100 cm2 wipe sample) has been successfully accomplished in the presence of spectrally interfering elements on the order of hundreds of ppm. This method has been validated on matrices containing 10 mg of each of the above elements. In some cases including interferents such as chromium and calcium, the single 2 mL beryllium extraction chromatography resin can handle >100 mg of total dissolved solids and still deliver >90 % beryllium yield. Should the matrix contain greater amounts of contaminants, additional resin may be used or, more likely, a combination of different resins may be used. (3,4).1.1 This practice covers the separation of beryllium from other metals and metalloids in acid solutions, by extraction chromatography, for subsequent determination of beryllium by atomic spectroscopy techniques such as inductively coupled plasma atomic emission spectroscopy (ICP-AES).1.2 This practice is applicable to samples of settled dust that have been collected in accordance with Practices D6966 or D7296.1.3 This practice is compatible with a wide variety of acid digestion techniques used in digesting settled dust samples, such as those described in Test Method D7035.1.4 This practice is appropriate for the preparation of settled dust samples where an unacceptable bias is suspected or known because of spectral interferences caused by other metals or metalloids present in the sample. This practice may also be appropriate for the analysis of other types of samples.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 and health practices and determine the applicability of regulatory limitations prior to use.

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4.1 This practice provides the basic criteria to be used by accreditation bodies and others in evaluating the qualifications of laboratories engaged in the testing of lead in paint, or settled dust, or airborne particulates, or soil, or combination thereof, taken from and around buildings and related structures. The criteria in this practice shall be supplemented by additional specific criteria and requirements, when appropriate; for example, when necessary to be in accordance with federal, state, or local government regulations.4.2 The accreditation is for organizations and not individuals.4.3 The practice is intended to provide objective information on the capabilities needed by laboratories to determine lead in paint, dust, airborne particulates, and soil taken from and around buildings and related structures. It is not intended to be used to compare one laboratory with another.4.4 This practice is also intended for use by laboratories in the development and implementation of their management systems and for use to request or perform an evaluation of in-house facilities in accordance with this practice.1.1 This practice covers the qualifications, including minimum requirements for personnel and equipment, duties, responsibilities, and services of laboratories engaged in the determination of lead in paint, or settled dust, or airborne particulates, or soil, or any combination thereof, taken from and around buildings and related structures.1.2 This practice has been developed consistent with Guides E548 and E994, to supplement ISO/IEC 17025.1.3 This practice contains notes that are explanatory and are not part of the mandatory requirements of the practice.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 Molding and extruding plastic pellets require dust free, dry pellets to prevent processing problems. Plastic producers try to remove the dust and streamers with dust removal systems prior to packaging and loading. How to accurately measure dust and streamer content in plastic pellets is an important quality control issue.5.2 Particle size analysis is used to determine a percentage of particle size distribution from a representative sample of the whole. In terms of size analysis concerning plastic pellets, sieving is used to determine the dust content in the range of 500 to 2000 micron. Test Method D1921, Test Method B, is used to determine this type of particle sizing.5.3 After dry sieve analysis, particles smaller than 500 microns need to be analyzed by wet method. A fresh sample shall be used for wet analysis. This test method allows washing down the fines attached to the pellets by electrostatic forces.5.4 The wet analysis provides accurate quantification of small to large amounts of fines, negating static effects, and eliminating detrimental effects of mechanical agitation. A wet analysis must be employed to accurately quantify lower PPM dust levels in plastic pellets.1.1 This test method measures the amount of fine particles adhered on plastic pellets or granules in which they are commonly produced and supplied. The lower limit of this test method is restricted only by the porosity of the filter disc used to capture the particle size being quantified.1.2 The wet analysis technique allows for separation and collection of statically charged particles by liquid wash and filtration methods. This must be performed under standard laboratory conditions.1.3 The values stated in SI units are to be regarded as standard.1.4 This test method describes an essential practice to check the quality of plastics once the production cycle is terminated and to evaluate the performance of pellet cleaning systems or of the special pneumatic conveying systems for the distinct size fractions below 500 micron only.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.NOTE 1: There is no known ISO equivalent to this standard.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This practice is intended for the digestion of metals and metalloids in airborne dust and dust wipe samples collected during various activities performed in and around workplaces, buildings and related structures.5.2 This practice is applicable to the digestion of airborne dust and dust wipe samples collected in accordance with Test Method D4532, Guide D6062, Practice D7144 or Guide E1370 for airborne dust, and Practices D6966, D7296, D7822, or E1728 using wipes that may or may not conform to Specifications D7707 or E1792.5.2.1 This practice is applicable to the digestion of airborne dust sample filters that have been removed from their sampling cassettes which have been wiped to collect all dust adhering to the side walls and included in the hard-walled containers as part of the collected samples.5.2.2 This practice is applicable to the digestion of airborne dust samples that use acid-soluble cellulosic air sampling capsules with the entire contents of the cassettes transferred to hard-walled containers.5.2.3 This practice is applicable to the digestion of settled dust samples collected using wipe materials in hard-walled containers.5.3 Digestates prepared according to this practice are intended to be analyzed for metal and metalloid concentrations using spectrometric techniques such as inductively coupled plasma mass spectrometry (ICP-MS), inductively coupled plasma optical emission spectrometry (ICP-OES), graphite furnace atomic absorption spectrometry (GFAAS), and flame atomic absorption spectrometry (FAAS) (see Test Methods D4185, D6785, D7035, D7439, E1613, E3193, and E3203), or for lead using electrochemical techniques such as anodic stripping voltammetry (see Practice E2051), or for beryllium using optical fluorescence detection (see Test Method D7202).5.4 Laboratories developing in-house test methods using this procedure shall determine precision and bias in accordance with the principles laid down by their accrediting agency.1.1 This practice covers the digestion of airborne and surface dust samples (collected using air and wipe sampling practices) and associated quality control (QC) samples for the determination of metals and metalloids by means of a mixture of dilute ammonium bifluoride and nitric acid.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This practice contains notes which are explanatory and not part of mandatory requirements of the standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

定价: 590元 / 折扣价: 502 加购物车

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