5.1 DPGBE and EGBE have a variety of residential and industrial applications such as cleaning formulations, surface coatings, inks, and cosmetics. These analytes may be released into the environment at levels that may be harmful to aquatic life.5.2 This test method has been investigated for use with reagent and sea water.1.1 This test method covers the determination of dipropylene glycol monobutyl ether (DPGBE) and ethylene glycol monobutyl ether (EGBE) in sea water by direct injection using liquid chromatography (LC) and detection with tandem mass spectrometry (MS/MS). These analytes are qualitatively and quantitatively determined by this test method. This test method adheres to selected reaction monitoring (SRM) mass spectrometry.1.2 The detection verification level (DVL) and reporting range for DPGBE and EGBE are listed in Table 1.1.2.1 The DVL is required to be at a concentration at least 3 times below the reporting limit (RL) and have a signal/noise ratio greater than 3:1. Fig. 1 and Fig. 2 display the signal/noise ratio of the single reaction monitoring (SRM) transition.FIG. 1 Detection Verification Level Signal/Noise RatioFIG. 2 Reporting Level (Calibration Standard) Signal/Noise Ratio1.2.2 The reporting limit is the concentration of the Level 1 calibration standard as shown in Table 4 for DPGBE and EGBE, taking into account the 20 % sample preparation dilution factor.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 Separation and identification of stabilizers used in the manufacture of polyethylene are necessary in order to correlate performance properties with polymer composition.5.2 The BHT extraction procedure is made effective by the insolubility of the polymer sample in solvents generally used for gas chromatographic analysis.1.1 This test method describes a procedure for the determination of butylated hydroxy toluene (BHT) (2,6-di-t-butyl-4-methyl-hydroxybenzene) in polymers of ethylene and ethylene-vinyl acetate (EVA) copolymers by solvent extraction followed by gas chromatographic analysis. Detection of the compound is achieved by flame ionization, and quantitative analysis is obtained by use of internal or external standards, as described in Practices E260, E355, and E594.1.2 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 and health practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 9.NOTE 1: There is no known ISO equivalent for this test method.

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1.1 This specification covers the requirements for a prediluted aqueous ethylene glycol base low-silicate engine coolant (50 volume percent minimum) for cooling systems of heavy-duty engines. When used without further dilution, this product will function effectively during both summer and winter to provide protection from corrosion, freezing at least to -36.7°C (-34.0°F), and boiling at least to 108°C (226°F). 1.2 Prediluted coolant meeting this specification requires both an initial charge of a supplemental coolant additive (SCA) and regular maintenance doses of an SCA to continue the protection in certain operating heavy-duty engine cooling systems, particularly those of the wet cylinder liner-in-block design. The SCA additions are defined by and are the primary responsibility of the engine or vehicle manufacturer. If they provide no instructions, follow the SCA supplier's recommended instructions. 1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only. 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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5.1 Rock for erosion control consists of individual pieces of natural quarried stone or large boulders and cobbles. The ability of these individual pieces of stone to resist deterioration due to weathering action affects the stability of the integral placement of rock for erosion control and hence, the stability of construction projects, structures, shorelines, and stream banks.5.2 Deterioration of stone in this test is one indicator that similar samples exposed to wet/dry and freeze/thaw cycles may break down in a water-soaked environment condition in service.5.3 This test method was developed to be used in conjunction with additional test methods listed in Practice D4992. This test method provides a quantitative value indicating potential resistance to weathering; however, the results of this test method are not to be used as the sole basis for the determination of rock durability.NOTE 1: The quality of the result produced by this standard is dependent upon the competence of the personnel performing it, and the suitability of the equipment and facilities used. Agencies that meet the criteria of Practice D3740 are generally considered capable of competent and objective testing/sampling/inspection/etc. Users of this standard are cautioned that compliance with Practice D3740 does not in itself assure reliable results. Reliable results depend on many factors; Practice D3740 provides a means of evaluation some of those factors.1.1 This test method covers the testing for and quantitative determination of the presence of swelling clays of the smectite group in rock for erosion control. The test particles are intended to be representative of erosion control rock and its durability. The test is appropriate for breakwater stone, armor stone, riprap and gabion sized rock materials.1.2 Ethylene glycol is one of the materials that react with swelling clays to form an organoclay complex having a larger basal spacing than that of the clay mineral itself. Rock containing swelling clay of the smectite group will be expected to undergo expansive breakdown upon soaking in ethylene glycol. If the amount, distribution, state of expansion, and ability to take up glycol is such as to cause such breakdown to occur, it may be expected that similar breakdown may occur of similar rock samples exposed, for longer times, to wetting and drying or freezing and thawing in a water-soaked condition in service.1.3 The prepared size of the rock specimens may eliminate some of the internal features present in the gross structure. The test specimens may not be representative of the quality of the larger rock samples used in construction. Careful examination of the rock source and proper sampling are essential in minimizing this limitation.1.3.1 The test is time intensive and requires over two weeks to complete the sample preparation, testing and analysis portions of the procedure.1.4 The use of reclaimed concrete and materials other than natural rock is beyond the scope of this test method.1.5 Units—The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard. Reporting of test results in units other than SI shall not be regarded as nonconformance with this standard.1.5.1 The gravitational system of inch-pound units is used when dealing with inch-pound units. In this system, the pound (lbf) represents a unit of force (weight), while the unit for mass is slugs. The slug unit is not given unless dynamic (F=ma) calculations are involved.1.5.2 The SI units presented for apparatus are substitutions of the inch-pound units, other similar SI units should be acceptable providing they meet the technical requirements established by the inch-pound apparatus.1.5.3 It is common practice in the engineering/construction profession to concurrently use pounds to represent both a unit of mass (lbm) and force (lbf). This practice implicitly combines two separate systems of units: the absolute and the gravitational systems. It is scientifically undesirable to combine the use of two separate sets of inch-pound units within a single standard. As stated, this standard includes the gravitational system of inch-pound units and does not use/present the slug unit for mass. However, the use of balances or scales recording pounds of mass (lbm) or recording density in lbm/ft3 shall not be regarded as nonconformance with this standard.1.5.4 Calculations are done using only one set of units; either SI or gravitational inch pound. Other units are permissible provided appropriate conversion factors are used to maintain consistency of units throughout the calculations, and similar significant digits or resolution, or both are maintained.1.6 All observed and calculated values shall conform to the guidelines for significant digits and rounding established in Practice D6026, unless superseded by this standard.1.6.1 For purposes of comparing measured or calculated value(s) with specified limits, the measured or calculated value(s) shall be rounded to the nearest decimal or significant digits in the specified limits.1.6.2 The procedures used to specify how data are collected/recorded or calculated, in this standard are regarded as the industry standard. In addition, they are representative of the significant digits that generally should be retained. The procedures used do not consider material variation, purpose for obtaining the data, special purpose studies, or any considerations for the user’s objectives; and it is common practice to increase or reduce significant digits of reported data to be commensurate with these considerations. It is beyond the scope of this standard to consider significant digits used in analytical methods for engineering design.1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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1.1 This specification covers flexible sheet made from ethylene propylene diene terpolymer (EPDM) geomembrane intended for use in geotechnical and geoenvironmental applications. The tests and property limits used to characterize the sheet are values to ensure minimum quality for the intended use. The vulcanized rubber sheet may be non-reinforced, fabric or scrim reinforced.1.2 In-place geomembrane design criteria, such as field seaming strength and material compatibility, among others, are factors that must be considered but are beyond the scope of this specification.1.3 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.1.4 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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This specification establishes the properties and requirements for ethylene glycol for use in the preparation of surface coatings. The material shall be appropriately sampled and tested, and shall conform to the following specified requirements: apparent specific gravity; color (Pt-Co units); distillation range (initial boiling point and dry point); water content; acidity as acetic acid; diethylene glycol content; and iron content.1.1 This specification covers ethylene glycol for use in the preparation of surface coatings.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 The following applies to all specified limits in this standard; for purposes of determining conformance with this standard, an observed value or a calculated value shall be rounded off “to the nearest unit” in the last right-hand digit used in expressing the specification limit, in accordance with the rounding-off method of Practice E29.1.4 For specific hazard information and guidance, consult the supplier's Material Safety Data Sheet.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The freezing point of an engine coolant indicates the coolant freeze protection.5.2 The freezing point of an engine coolant may be used to determine the approximate glycol content, provided the glycol type is known.5.3 Freezing point as measured by Test Method D1177 or approved alternative method is a requirement in Specifications D3306 and D6210.5.4 This test method provides results that are equivalent to Test Method D1177 and expresses results to the nearest 0.1 °C with improved reproducibility over Test Method D1177.5.5 This test method determines the freezing point in a shorter period of time than Test Method D1177.5.6 This test method removes most of the operator time and judgement required by Test Method D1177.1.1 This test method covers the determination of the freezing point of an aqueous engine coolant solution.1.2 This test method is designed to cover ethylene glycol base coolants up to a maximum concentration of 60 % (v/v) in water; however, the ASTM interlaboratory study mentioned in 12.2 has only demonstrated the test method with samples having a concentration range of 40 % to 60 % (v/v) water.NOTE 1: Where solutions of specific concentrations are to be tested, they shall be prepared from representative samples as directed in Practice D1176. Secondary phases separating on dilution need not be separated.NOTE 2: The products may also be marketed in a ready-to-use form (prediluted).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. Some specific hazards statements are given in 7.3.1.5 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 Leakage of aqueous engine coolant into the crank case weakens the ability of the oil to lubricate. If ethylene glycol is present, it promotes varnish and deposit formation. This test method is designed for early detection to prevent coolant from accumulating and seriously damaging the engine.1.1 This test method covers the determination of ethylene glycol as a contaminant in used engine oil. This test method is designed to quantitate ethylene glycol in the range from 5 mass ppm to 200 mass ppm.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 Section 7.NOTE 1: A qualitative determination of glycol-base antifreeze is provided in Test Methods D2982. Procedure A is sensitive to about 100 ppm.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 This test method covers the determination of the dissolved gases methane, ethane, ethylene, and propane in drinking, waste, and ground waters, including domestic wells; whether naturally occurring or resulting from commercial activities, dissolved gases can be hazardous both to the environment and humans. Due to increased scrutiny of dissolved gases, developing a valid method for the testing of dissolved gases in water has become more imperative. Static headspace sampling is generally applicable for sampling these compounds. However, as these compounds are extremely volatile, a closed sampling system is recommended. This test method can be used for quantitatively determining dissolved gases in ground, waste, and drinking waters.5.2 This test method is suitable for analysis of domestic drinking water samples from residential and commercial water supply wells prior to oil and gas exploration activities to form a baseline for monitoring potential impacts during exploration; development, including hydraulic fracturing; operation; closure; and reclamation of nearby oil and gas production and injection wells.1.1 This test method covers the determination of the dissolved gases methane, ethane, ethylene, and propane in drinking, waste, and ground waters, including domestic wells whether naturally occurring or resulting from commercial activities, or both. This test method has an analytical range from 10 µg/L to 11 000 µg/L for methane, and 10 µg/L to 5000 µg/L for ethane, ethylene, and propane. If a sample has a dissolved gas concentration above the calibration range, the sample would require dilution. Other analytical ranges may be used as long as the instrument calibration encompasses the desired range and demonstrates adequate linearity.1.2 This test method is applicable to samples collected at a nominal ambient pressure. Samples collected under high pressures, that is, above ambient pressure, may not be accurately analyzed using this method.1.3 This test method is applicable to a variety of dissolved gases; however, for the present standard, only methane, ethane, ethylene, and propane were validated. In order to validate for a gas not listed in this method, the analyst would need to establish the saturation concentration of the new gas, and establish a valid curve, method detection limits, and demonstration of capability following the procedures outlined in this method.1.4 It is the analyst’s responsibility to ensure the validity of this test method for dissolved gases other than methane, ethane, ethylene, and propane and other sample matrices.1.5 Units—The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.1.6 A single laboratory study was done in order to establish precision and bias for the surrogate (see Section 16).1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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3.1 Either test method may be used to determine the concentrations of diethylene glycol in ethylene glycol. The concentrations of the components are obtained by a normalization technique, based on the assumption that all components are eluted under the conditions used. If all components should not be eluted, the calculated concentrations will be erroneously high, with the major component showing the most significant absolute error. Since water is not detected by these procedures, the results are on a water-free basis. Water may be determined in accordance with the applicable sections of Test Methods E202 and the gas chromatographic results corrected for the water concentration.3.2 Both test methods are currently in industrial use. Test Method A is the simpler of the two test methods because it does not require the preparation of derivatives prior to gas chromatographic analysis. The results obtained by Test Method A are slightly more accurate than those obtained by Test Method B. With respect to precision there is no significant difference between the two test methods. Test Method B has been reported to be suitable also for the analysis of a wide variety of glycol ethers, but this use is beyond the scope of this standard.1.1 These test methods are intended primarily for the analysis of mixtures of ethylene and diethylene glycols in which the diethylene glycol concentration is 0.1 % or less. Both test methods should be applicable to higher concentrations of diethylene glycol, but precision and bias estimates have been obtained only for 0.05 to 0.1 % diethylene glycol.NOTE 1: Test Methods E202 describe another gas chromatographic test method applicable to mixtures of ethylene, diethylene, and triethylene glycols and mixtures of propylene, dipropylene, and tripropylene glycols in which one of the glycols is the principal component and the other two are present in concentrations of 0.1 to 1 % each.NOTE 2: Test Method E2409 describes another gas chromatographic test method for the determination of glycol impurities in mono-, di-, tri- and tetraethylene glycol (MEG, DEG, TEG and TeEG) in the range of 5 to 3000 μg/g.1.2 The two test methods are given as follows:  SectionsTest Method A—Nonderivative Method 5 to 13Test Method B—Derivative Method 14 to 221.3 Review the current Safety Data Sheets (SDS) for detailed information concerning toxicity, first aid procedures, and safety precautions for chemicals used in this standard.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard with the exception of foot-pound units for apparatus descriptions.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. For a specific warning statement, see 15.1.5.

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4.1 High-purity ethylene is required as a feedstock for some manufacturing processes and the presence of trace amounts of certain hydrocarbon impurities can have deleterious effects. This test method is suitable for setting specifications, for use as an internal quality control tool, and for use in development or research work.4.2 This test method does not detect such impurities as H2O, CO, CO2, and alcohols that may be present in the sample. Hydrocarbons higher than n-decane cannot be analyzed by this test method, if present in the sample. Test Method D2504 addresses the analysis of noncondensable gases and Test Method D2505 addresses the analysis of CO2. Guide D5234 describes all potential impurities present in ethylene. These standards should be consulted when determining the total concentration of impurities in ethylene.1.1 This test method covers the determination of methane, ethane, propane, propene, acetylene, iso-butane, propadiene, butane, trans-2-butene, butene-1, isobutene, cis-2-butene, methyl acetylene and 1,3-butadiene in high-purity ethylene. The purity of the ethylene can be calculated by subtracting the total percentage of all impurities from 100.00 %. Since this test method does not determine all possible impurities such as CO, CO2, H2O, alcohols, nitrogen oxides, and carbonyl sulfide, as well as hydrocarbons higher than decane, additional tests may be necessary to fully characterize the ethylene sample.1.2 Data are reported in this test method as ppmV (parts per million by gaseous volume) and ppmMol (parts per million Mol). This test method was evaluated in an interlaboratory cooperative study in the concentration range of 4 ppmV to 340 ppmV (2 mg/kg to 204 mg/kg). The participants in the interlaboratory cooperative study reported the data in non-SI units. Wherever possible, SI units are included.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 The inherent viscosity is relatable to the composition and molecular weight of a polyester resin. It must be controlled so that the processability and end properties of the resin remain in a desired range.1.1 This test method is for the determination of the inherent viscosity of poly(ethylene terephthalate) (PET) soluble at 0.50 % concentration in a 60/40 phenol/1,1,2,2-tetrachloroethane solution by means of a glass capillary viscometer. Highly crystalline forms of PET that are not soluble in this solvent mixture will require a different procedure.1.2 The inherent viscosity values obtained by this test method are comparable with those obtained using differential viscometry described in Test Method D5225.1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.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. Specific hazards statements are given in Section 8.1.4.1 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 and/or mercury containing products into your state or country may be prohibited by lawNOTE 1: This standard and ISO 1628-5 address the same subject matter, but differ in technical content. This ISO standard gives an option of solvents for PET. Solvent specified in this ASTM test method is one of the options in the ISO method. ISO also uses Type 1C Ubbelohde viscometer, rather than the 1B, and reports viscosity number, rather than inherent viscosity.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 Measurements of EO content correlate to polyol reactivity (as related to primary hydroxyl content), linearity of foam rise, and hydrophilicity of the polyol and final product.1.1 Test Method A—Proton Nuclear Magnetic Resonance Spectroscopy (1H NMR) measures polymerized ethylene oxide (EO) content of ethylene oxide (EO) propylene oxide (PO) polyether polyols used in flexible polyurethane foams and non-foams. It is suitable for diols initiated from glycols of EO or PO containing EO percentages >5. For triols initiated with glycerol (glycerin) and trimethylolpropane, an uncorrected EO value is obtained since both initiators have protons that contribute to the EO measurement.1.2 Test Method B—Carbon-13 Nuclear Magnetic Resonance Spectroscopy (13C NMR) measures the polymerized EO content of EO-PO polyether polyols used in flexible polyurethane foams and non-foams. It is suitable for diols and triols made from the commonly used initiators and containing EO percentages >5.1.3 The values stated in SI units are to be regarded as 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.NOTE 1: There is no known ISO equivalent to this standard.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Many important properties of crosslinked ethylene plastics vary with the gel content. Hence, determination of the gel content provides a means of both controlling the process and rating the quality of finished products.5.2 Extraction tests permit verification of the proper gel content of any given crosslinked ethylene plastic and they also permit comparison between different crosslinked ethylene plastics, including those containing fillers, provided that, for the latter, the following conditions are met:5.2.1 The filler is not soluble in either decahydronaphthalene or xylenes at the extraction temperature.5.2.2 The amount of filler present in the compound either is known or will be determined by other means.5.2.3 Sufficient crosslinking has been achieved to prevent migration of filler during the extraction. Usually it has been found that, at extraction levels up to 50 %, the extractant remains clear and free of filler.5.3 A suitable antioxidant is added to the extractant to inhibit possible oxidative degradation at the extraction temperatures.5.4 Before proceeding with this test method, reference shall be made to the specification of the material being tested. Any test specimen preparation, conditioning, dimensions, or testing parameters, or a combination thereof, covered in the materials specification shall take precedence over those mentioned in this test method. If there are no material specifications, then the default conditions apply.1.1 The gel content (insoluble fraction) produced in ethylene plastics by crosslinking is determined by extracting with solvents such as decahydronaphthalene or xylenes. The methods described herein are applicable to crosslinked ethylene plastics of all densities, including those containing fillers, and all provide corrections for the inert fillers present in some of those compounds.1.2 Test Method A, which permits most complete extraction in least time, is to be used for referee tests, but two alternative nonreferee Test Methods B and C are also described. Test Method B differs from the referee test method only in sample preparation; that is, it requires use of shavings taken at selected points in cable insulation, for example, rather than the ground sample required by the referee test method. Because the shaved particles are larger, less total surface per sample is exposed to the extractant, so this test method ordinarily yields extraction values about 1 to 2 % lower than the referee method. Test Method C requires that a specimen in one piece be extracted in xylenes at a constant temperature of 110°C. At this temperature and with a one-piece specimen, even less extraction occurs (from 3 to 9 % less than the referee test method), this method permits swell ratio (a measure of the degree of crosslinking in the gel phase) be determined.1.3 Extraction tests are made on articles of any shape. They have been particularly useful for electrical insulations since specimens can be selected from those portions of the insulation most susceptible to insufficient crosslinking.1.4 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.NOTE 1: This test method is equivalent to ISO 10147, Method B. It is not equivalent to ISO 10147 in any other measurement or section.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. Specific precautionary statements are given in Sections 6, 9, and 24.

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4.1 This test method provides for the quantitative determination of inorganic chloride (chloride ion) in monoethylene glycol (MEG), diethylene glycol (DEG) and triethylene glycol (TEG) using ion chromatography with conductivity detection. The analysis time is less than 5 min with little or no sample preparation required. Conductivity detection is a universal detection mode and is linear over the range of the method. Acceptable levels of chloride in polyester-grade and low-conductivity-grade MEG vary with the manufacturer’s specifications but are normally in the low mg/kg range. Knowledge of the chloride content in polyester-grade and low-conductivity-grade MEG is required to establish whether the MEG product meets specification requirements.4.2 Glycols have high viscosities and a dilution with high quality deionized water may be required depending on the capability of the autosampler, if used, to deliver the injection. All standards and samples, whether diluted or not should be treated in the same manner.1.1 This test method covers the determination of inorganic chloride (chloride ion) in monoethylene glycol (MEG), diethylene glycol (DEG) and triethylene glycol (TEG) in the range of 0.01 to 1.0 mg/kg by ion chromatography (IC).1.2 Ethylene glycol can be analyzed directly by this test method without any sample preparation or diluted with high quality deionized water if an autosampler is used and dilution is necessary (that is, 50:50 or other suitable ratio).1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3.1 The exception is the additional information of (psi) in 9.3.3, 11.1.1, and 11.2.1.1.4 Review the current Safety Data Sheets (SDS) for detailed information concerning toxicity, first-aid procedures and safety precautions.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 to determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Section 9.

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