ASTM D5702-95
(Practice)Standard Practice for Field Sampling of Coating Films for Analysis for Heavy Metals
Standard Practice for Field Sampling of Coating Films for Analysis for Heavy Metals
SCOPE
1.1 This practice covers a method to control the removal of samples of coating films from substrates for subsequent laboratory analysis for heavy metal content on a mass basis. This technique can be used in the field, the fabricating shop, or laboratory.
1.2 The values stated in SI units are to be regarded as the standard. The values 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific hazard information, see Section 5, Note 1 and Note 3.
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NOTICE: This standard has either been superseded and replaced by a new version or discontinued.
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Designation: D 5702 – 95
AMERICAN SOCIETY FOR TESTING AND MATERIALS
100 Barr Harbor Dr., West Conshohocken, PA 19428
Reprinted from the Annual Book of ASTM Standards. Copyright ASTM
Standard Practice for
Field Sampling of Coating Films for Analysis for Heavy
Metals
This standard is issued under the fixed designation D 5702; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
1. Scope D 3335; however, since the analysis is based on the weight of
the specimen, the removal of the sample must be properly
1.1 This practice covers a method to control the removal of
controlled to improve the reliability of the test results. The
samples of coating films from substrates for subsequent labo-
number and location of samples to be removed must also be
ratory analysis for heavy metal content on a mass basis. This
determined to characterize properly the extent of the presence
technique can be used in the field, the fabricating shop, or
of hazardous materials, if any, on a structure.
laboratory.
1.2 The values stated in inch-pound units are to be regarded
4. Materials and Equipment
as the standard. The values in parentheses are for information
4.1 Sample Collection Container—A clean plastic bag or
only.
rigid container comprised of a material such as polyethylene
1.3 This standard does not purport to address all of the
that will not contaminate the sample.
safety concerns, if any, associated with its use. It is the
4.2 Straight Edge or Ruler.
responsibility of the user of this standard to establish appro-
4.3 Knife or Chisel, cleaned and sharpened, for removing
priate safety and health practices and determine the applica-
paint samples.
bility of regulatory limitations prior to use. For specific hazard
4.4 Dry Film Thickness Gage, for measuring total coating
information, see Section 5, Note 1 and Note 2.
thickness.
2. Referenced Documents
5. Procedure
2.1 ASTM Standards:
5.1 Select a sufficient number of areas for coating removal
D 1186 Test Methods for Nondestructive Measurement of
that properly characterize the coatings on the structure.
Dry Film Thickness of Nonmagnetic Coatings Applied to
5.1.1 Selection may be based on painting history, knowl-
a Ferrous Base
edge of previously applied coatings, prior touch-up and re-
D 1400 Test Method for Nondestructive Measurement of
painting programs, and other such factors.
Dry Film Thickness of Nonconductive Coatings Applied to
2 5.1.2 Select areas that properly characterize the range of
a Nonferrous Metal Base
thickness found. Dry film thickness can be measured in
D 3335 Test Method for Low Concentrations of Lead,
accordance with Test Methods D 1186, D 1400, or D 4138.
Cadmium, and Cobalt in Paint by Atomic Absorption
5.1.3 Remove a minimum of three samples.
Spectroscopy
5.2 At each sample site, clean the surface of dirt, dust, or
D 4138 Test Method for Measurement of Dry Film Thick-
3 debris.
ness of Protective Coating Systems by Destructive Means
NOTE 1—Hazardous materials can be present in surface debris and
3. Significance and Use
chalk which may be removed during cleaning. Thus, consideration should
be given to collecting this surface debris and chalk for analysis.
3.1 Prior to beginning a project that involves the removal,
cutting, grinding, or burning of paint, it is necessary to
5.3 At each sample site, use a knife and straight edge to
determine if the coating contains hazardous materials, such as
scribe the perimeter of a square that measures 1 in. (25 mm) on
lead, as certain
...
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SIGNIFICANCE AND USE
3.1 Prior to beginning a project that involves the removal, cutting, grinding, or burning of paint, it is necessary to determine if the coating contains hazardous metals, such as lead. If it does, certain requirements for worker and environmental protection may need to be imposed. The presence and quantity of hazardous metals in a paint can be determined through laboratory analysis. Proper sampling protocol is needed to assure the laboratory results represent the actual amount of heavy metal in the coating. The number and location of samples to be removed must also be determined to characterize properly the extent of the presence of hazardous materials, if any, on a structure.
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1.1 This practice covers a method to control the removal of samples of coating films from substrates for subsequent laboratory analysis for heavy metal content on a mass basis. This technique can be used in the field, the fabricating shop, or laboratory.
1.2 The values stated in SI units are to be regarded as the standard. The values in parentheses are for information only.
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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 The Hi-Vol sampler is commonly used for the collection of the airborne particulate component of the atmosphere. Some physical and chemical parameters of the collected particulate matter are dependent upon the physical characteristics of the collection system and the choice of filter media. A variety of options available for the Hi-Vol sampler give it broad versatility and allow the user to develop information about the size and quantity of airborne particulate material and, using subsequent chemical analytical techniques, information about the chemical properties of the particulate matter.
5.2 This test method presents techniques that when uniformly applied, provide measurements suitable for intersite comparisons.
5.3 This test method measures the atmosphere presented to the sampler with good precision, but the actual dust levels in the atmosphere can vary widely from one location to another. This means that sampler location may be of paramount importance, and may impose far greater variability of results than any lack of precision in the method of measurement. In particular, localized dust sources may exert a major influence over a very limited area immediately adjacent to such sources. Examples include unpaved streets, vehicle traffic on roadways with a surface film of dust, building demolition and construction activity, or nearby industrial plants with dust emissions. In some cases, dust levels measured close to such sources may be several times the community wide levels exclusive of such localized effects (see Practice D1357).
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1.1 This test method provides for sampling a large volume of atmosphere, 1600 m3 to 2400 m3 (55 000 ft3 to 85 000 ft3), by means of a high flow-rate vacuum pump at a rate of 1.13 m3/min to 1.70 m3/min (40 ft3/min to 60 ft3/min) (1-4).2
1.2 This flow rate allows suspended particles having diameters of less than 100 μm (stokes equivalent diameter) to be collected. However, the collection efficiencies for particles larger than 20 μm decreases with increasing particle size and it varies widely with the angle of the wind with respect to the roof ridge of the sampler shelter and with increasing speed (5). When glass fiber filters are used, particles within the size range of 100 μm to 0.1 μm diameters or less are ordinarily collected.
1.3 The upper limit of mass loading will be determined by plugging of the filter medium with sample material, which causes a significant decrease in flow rate (see 6.4). For very dusty atmospheres, shorter sampling periods will be necessary. The minimum amount of particulate matter detectable by this method is 3 mg (95 % confidence level). When the sampler is operated at an average flow rate of 1.70 m3/min (60 ft3/min) for 24 h, this is equivalent to 1 μg/m3 to 2 μg/m3 (3).
1.4 The sample that is collected may be subjected to further analyses by a variety of methods for specific constituents.
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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.
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5.1 This test method is applicable to the measurement of airborne asbestos in a wide range of ambient air situations and for detailed evaluation of any atmosphere for asbestos structures. Most fibers in ambient atmospheres are not asbestos, and therefore, there is a requirement for fibers to be identified. Most of the airborne asbestos fibers in ambient atmospheres have diameters below the resolution limit of the light microscope. This test method is based on transmission electron microscopy, which has adequate resolution to allow detection of small thin fibers and is currently the only technique capable of unequivocal identification of the majority of individual fibers of asbestos. Asbestos is often found, not as single fibers, but as very complex, aggregated structures, which may or may not also be aggregated with other particles. The fibers found suspended in an ambient atmosphere can often be identified unequivocally if sufficient measurement effort is expended. However, if each fiber were to be identified in this way, the analysis would become prohibitively expensive. Because of instrumental deficiencies or because of the nature of the particulate matter, some fibers cannot be positively identified as asbestos even though the measurements all indicate that they could be asbestos. Therefore, subjective factors contribute to this measurement, and consequently, a very precise definition of the procedure for identification and enumeration of asbestos fibers is required. The method defined in this test method is designed to provide a description of the nature, numerical concentration, and sizes of asbestos-containing particles found in an air sample. The test method is necessarily complex because the structures observed are frequently very complex. The method of data recording specified in the test method is designed to allow reevaluation of the structure-counting data as new applications for measurements are developed. All of the feasible specimen preparation techn...
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1.1 This test method2 is an analytical procedure using transmission electron microscopy (TEM) for the determination of the concentration of asbestos structures in ambient atmospheres and includes measurement of the dimension of structures and of the asbestos fibers found in the structures from which aspect ratios are calculated.
1.1.1 This test method allows determination of the type(s) of asbestos fibers present.
1.1.2 This test method cannot always discriminate between individual fibers of the asbestos and non-asbestos analogues of the same amphibole mineral.
1.2 This test method is suitable for determination of asbestos in both ambient (outdoor) and building atmospheres.
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6.1 Manufacturers increasingly are being asked or required to demonstrate that vapor-phase emissions of chemicals of concern from their products under normal use conditions comply with various voluntary or regulatory acceptance criteria. This process typically requires manufacturers to have their products periodically tested for VOC emissions by independent laboratories using designated reference test methods (for example, Test Method D6007, ISO 16000-9, and ISO 16000-10). To ensure continuing compliance, manufacturers may opt to, or be required to, implement screening tests at the production level.
6.2 Reference methods for testing chemical emissions from products are rigorous and typically are too time-consuming and impractical for routine emission screening in a production environment.
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6.4 This practice can also be used to monitor the quality of raw materials for manufacturing processes.
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1.1 This practice describes a micro-scale chamber apparatus and associated procedures for rapidly screening materials and products for their vapor-phase emissions of volatile organic compounds (VOCs) including formaldehyde and other carbonyl compounds. It is intended to complement, not replace reference methods for measuring chemical emissions for example, small-scale chamber tests (Guide D5116) and emission cell tests (Practice D7143).
1.2 This practice is suitable for use in and outside of laboratories, in manufacturing sites and in field locations with access to electrical power.
1.3 Compatible material/product types that may be tested in the micro-scale chamber apparatus include rigid materials, dried or cured paints and coatings, compressible products, and small, irregularly-shaped components such as polymer beads.
1.4 This practice describes tests to correlate emission results obtained from the micro-scale chamber with results obtained from VOC emission reference methods (for example, Guide D5116, Test Method D6007, Practice D7143, and ISO 16000-9 and ISO 16000-10).
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1.6 Gas sample collection and chemical analysis are dependent upon the nature of the VOCs targeted and are beyond the scope of this practice. However, the procedures described in Test Method D7339, Practice D6196 and ISO 16000-6 for analysis of VOCs and in Test Method D5197 and ISO 16000-3 for analysis of formaldehyde and other carbonyl compounds are applicable to this practice.
1.7 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
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6.1 SPF insulation is applied and formed onsite, which creates unique challenges for measuring product emissions. This test method provides a way to measure post-application chemical emissions from SPF insulation.
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6.3 Emission data may be used in product development, manufacturing quality control and comparison of field samples.
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1.1 This test method is used to identify and to measure the emissions of volatile organic compounds (VOCs) emitted from samples of cured spray polyurethane foam (SPF) insulation using micro-scale environmental test chambers combined with specific air sampling and analytical methods for VOCs.
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1.2.1 Samples for formaldehyde and other low-molecular weight carbonyl compounds are collected on treated silica gel cartridges and are analyzed by high performance liquid chromatography (HPLC) as described in Test Method D5197 and ISO 16000-3.
1.2.2 Samples for other VOCs are collected on multi-sorbent samplers and are analyzed by thermal-desorption gas chromatography / mass spectrometry (TD-GC/MS) as described in U.S. EPA Compendium Method TO-17 and ISO 16000-6.
1.3 This test method is intended specifically for SPF insulation products. Compatible product types include two component, high pressure and two-component, low pressure formulations of open-cell and closed-cell SPF insulation.
1.4 VOCs that can be sampled and analyzed by this test method generally include organic blowing agents such as 1,1,1,3,3-pentafluoropropane, formaldehyde and other carbonyl compounds, residual solvents, and some amine catalysts. Emissions of some organic flame retardants can be measured after 24 h with this method, such as tris (chloroisopropyl) phosphate (TCPP).
1.5 This test method does not cover the sampling and analysis of methylene diphenyl diisocyanate (MDI) or other isocyanates.
1.6 Area-specific and mass-specific emission rates are quantified at the elapsed times and chamber conditions as specified in 13.2 and 13.3 of this test method.
1.7 This test method is used to identify emitted compounds and to estimate their emission factors at specific times. The emission factors are based on specified conditions, therefore, use of the data to predict emissions in other environments may not be appropriate and is beyond the scope of this test method. The results may not be representative of other test conditions or comparable with other test methods.
1.8 This test method is primarily intended for freshly applied, SPF insulation samples that are sprayed and packaged as described in Practice D7859. The measurement of emissions during spray application and within the first hour following application is outside of the scope of this test method.
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SIGNIFICANCE AND USE
5.1 Studies of indoor air problems are often iterative in nature. A thorough engineering evaluation of a building (1-4)3 is sometimes sufficient to identify likely causes of indoor air problems. When these investigations and subsequent remedial measures are not sufficient to solve a problem, more intensive investigations may be necessary.
5.2 This guide provides the basis for determining when probability sampling methods are needed to achieve statistically defensible inferences regarding the goals of a study of indoor air quality. The need for probability sampling methods in a study of indoor air quality depends on the specific objectives of the study. Such methods may be needed to select a sample of people to be asked questions, examined medically, or monitored for personal exposures. They may also be needed to select a sample of locations in space and time to be monitored for environmental contaminants.
5.3 This guide identifies several potential obstacles to proper implementation of probability sampling methods in studies of indoor air quality in buildings and presents procedures that overcome those obstacles or at least minimize their impact.
5.4 Although this guide specifically addresses sampling people or locations across time within a building, it also provides important guidance for studying populations of buildings. The guidance in this document is fully applicable to sampling locations to determine environmental quality or sampling people to determine environmental effects within each building in the sample selected from a larger population of buildings.
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1.1 This guide covers criteria for determining when probability sampling methods should be used to select locations for placement of environmental monitoring equipment in a building or to select a sample of building occupants for questionnaire administration for a study of indoor air quality. Some of the basic probability sampling methods that are applicable for these types of studies are introduced.
1.2 Probability sampling refers to statistical sampling methods that select units for observation with known probabilities (including probabilities equal to one for a census) so that statistically defensible inferences are supported from the sample to the entire population of units that had a positive probability of being selected into the sample.
1.3 This guide describes those situations in which probability sampling methods are needed for a scientific study of the indoor air quality in a building. For those situations for which probability sampling methods are recommended, guidance is provided on how to implement probability sampling methods, including obstacles that may arise. Examples of their application are provided for selected situations. Because some indoor air quality investigations may require application of complex, multistage, survey sampling procedures and because this standard is a guide rather than a practice, the references in Appendix X1 are recommended for guidance on appropriate probability sampling methods, rather than including expositions of such methods in this guide.
1.4 This standard does not address non-probability sampling approaches. Non-probability sampling approaches may be needed, such as worst-case sampling, range finding sampling, and screening sampling as inputs to help guide and inform probability sampling methods.
1.5 Units—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 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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SIGNIFICANCE AND USE
5.1 Effects of Air Change—Air change often accounts for a significant portion of the heating or air-conditioning load of a building. It also affects the moisture and contaminant balances in the building. Moisture-laden air passing through the building envelope can permit condensation and cause material degradation. An appropriate level of ventilation is required in all buildings; one should consult ASHRAE Standard 62 to determine the ventilation requirements of a building.
5.2 Prediction of Air Change—Air change depends on the size and distribution of air leakage sites, pressure differences induced by wind and temperature, mechanical system operation, and occupant behavior. Air change may be calculated from this information, however, many of the needed parameters are difficult to determine. Tracer gas testing permits direct measurement of air change.
5.3 Utility of Measurement—Measurements of air change provide useful information about ventilation and air leakage. Measurements in buildings with the ventilation system closed are used to determine whether natural air leakage rates are higher than specified. Measurements with the ventilation system in operation are used to determine whether the air change meets or exceeds requirements.
5.4 Known Conditions—Knowledge of the factors that affect air change makes measurement more meaningful. Relating building response to wind and temperature requires repetition of the test under varying meteorological conditions. Relating building response to the ventilation system or to occupant behavior requires controlled variation of these factors.
5.5 Applicability of Results—The values for air change obtained by the techniques used in this test method apply to the specific conditions prevailing at the time of the measurement. Air change values for the same building will differ if the prevailing wind and temperature conditions have changed, if the operation of the building is different, or if the envelope changes between m...
SCOPE
1.1 This test method covers techniques using tracer gas dilution for determining a single zone's air change with the outdoors, as induced by weather conditions and by mechanical ventilation. These techniques are: (1) concentration decay, (2) constant injection, and (3) constant concentration.
1.2 This test method is restricted to a single tracer gas.
1.3 The associated data analysis assumes that one can characterize the tracer gas concentration within the zone with a single value. The zone shall be a building, vehicle, test cell, or any conforming enclosure.
1.4 Use of this test method requires a knowledge of the principles of gas analysis and instrumentation. Correct use of the formulas presented here requires consistent use of units, especially those of time.
1.5 Determination of the contribution to air change by individual components of the zone enclosure is beyond the scope of this test method.
1.6 The results from this test method pertain only to those conditions of weather and zonal operation that prevailed during the measurement. The use of the results from this test to predict air change under other conditions is beyond the scope of this test method.
1.7 The text of this test method references notes and footnotes which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered requirements of this test method.
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.
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SIGNIFICANCE AND USE
5.1 Many regulators, industrial processes, and other stakeholders require determination of NMOC in atmospheres.
5.2 Accurate measurements of ambient NMOC concentrations are critical in devising air pollution control strategies and in assessing control effectiveness because NMOCs are primary precursors of atmospheric ozone and other oxidants (7, 8).
5.2.1 The NMOC concentrations typically found at urban sites may range up to 1 ppm C to 3 ppm C or higher. In order to determine transport of precursors into an area monitoring site, measurement of NMOC upwind of the site may be necessary. Rural NMOC concentrations originating from areas free from NMOC sources are likely to be less than a few tenths of 1 ppm C.
5.3 Conventional test methods based upon gas chromatography and qualitative and quantitative species evaluation are relatively time consuming, sometimes difficult and expensive in staff time and resources, and are not needed when only a measurement of NMOC is desired. The test method described requires only a simple, cryogenic pre-concentration procedure followed by direct detection with an FID. This test method provides a sensitive and accurate measurement of ambient total NMOC concentrations where speciated data are not required. Typical uses of this standard test method are as follows.
5.4 An application of the test method is the monitoring of the cleanliness of canisters.
5.5 Another use of the test method is the screening of canister samples prior to analysis.
5.6 Collection of ambient air samples in pressurized canisters provides the following advantages:
5.6.1 Convenient collection of integrated ambient samples over a specific time period,
5.6.2 Capability of remote sampling with subsequent central laboratory analysis,
5.6.3 Ability to ship and store samples, if necessary,
5.6.4 Unattended sample collection,
5.6.5 Analysis of samples from multiple sites with one analytical system,
5.6.6 Collection of replicate samples for ...
SCOPE
1.1 This test method2 presents a procedure for sampling and determination of non-methane organic compounds (NMOC) in ambient, indoor, or workplace atmospheres.
1.2 This test method describes the collection of integrated whole air samples in silanized or other passivated stainless steel canisters, and their subsequent laboratory analysis.
1.2.1 This test method describes a procedure for sampling in canisters at final pressures above atmospheric pressure (pressurized sampling).
1.3 This test method employs a cryogenic trapping procedure for concentration of the NMOC prior to analysis.
1.4 This test method describes the determination of the NMOC by the flame ionization detection (FID), without the use of gas chromatographic columns and other procedures necessary for species separation.
1.5 The range of this test method is from 20 ppb C to 10 000 ppb C (1, 2).3
1.6 This test method has a larger uncertainty for some halogenated or oxygenated hydrocarbons than for simple hydrocarbons or aromatic compounds. This is especially true if there are high concentrations of chlorocarbons or chlorofluorocarbons present.
1.7 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to inch-pound units that are provided for information only and are not considered standard.
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.
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SIGNIFICANCE AND USE
3.1 Prior to beginning a project that involves the removal, cutting, grinding, or burning of paint, it is necessary to determine if the coating contains hazardous metals, such as lead. If it does, certain requirements for worker and environmental protection may need to be imposed. The presence and quantity of hazardous metals in a paint can be determined through laboratory analysis. Proper sampling protocol is needed to assure the laboratory results represent the actual amount of heavy metal in the coating. The number and location of samples to be removed must also be determined to characterize properly the extent of the presence of hazardous materials, if any, on a structure.
SCOPE
1.1 This practice covers a method to control the removal of samples of coating films from substrates for subsequent laboratory analysis for heavy metal content on a mass basis. This technique can be used in the field, the fabricating shop, or laboratory.
1.2 The values stated in SI units are to be regarded as the standard. The values 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. For specific hazard information, see Section 5, Note 1, and Note 3.
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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SIGNIFICANCE AND USE
5.1 This test method can be used to measure the level of mercury in any gaseous fuel (as defined by Terminology D4150) for purposes such as determining compliance with regulations, studying the effect of various abatement procedures on mercury emissions, checking the validity of direct instrumental measurements, and verifying that mercury concentrations are below those required for gaseous fuel processing and operations.
5.2 Adsorption of the mercury on gold-coated sorbent can remove interferences associated with the direct measurement of mercury in the presence of high concentrations of organic compounds. It preconcentrates the mercury before analysis, thereby offering measurement of ultra-low average concentrations in a gas stream over a long time span. It avoids the cumbersome use of liquid spargers with on-site sampling and eliminates contamination problems associated with the use of potassium permanganate solutions.5,6,7
SCOPE
1.1 This test method covers the determination of total mercury in gaseous fuels at concentrations down to 0.5 ng/m3. It includes separate procedures for both sampling and atomic absorption spectrophotometric determination of mercury. This procedure detects both inorganic and organic forms of mercury.
1.2 Units—The values stated in SI units are to be regarded as the standard.
1.3 Warning—Mercury has been designated by many regulatory agencies as a hazardous material that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Caution should be taken when handling mercury and mercury containing products. See the applicable product Safety Data Sheet (SDS) for additional information. Users should be aware that selling mercury or mercury containing products, or both, into your state or country may be prohibited by law.
1.4 This standard does not purport to address all of the safety concerns 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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