71.080 - Organic chemicals
ICS 71.080 Details
Organic chemicals
Organische Chemikalien
Chimie organique
Organske kemikalije
General Information
Frequently Asked Questions
ICS 71.080 is a classification code in the International Classification for Standards (ICS) system. It covers "Organic chemicals". The ICS is a hierarchical classification system used to organize international, regional, and national standards, facilitating the search and identification of standards across different fields.
There are 1687 standards classified under ICS 71.080 (Organic chemicals). These standards are published by international and regional standardization bodies including ISO, IEC, CEN, CENELEC, and ETSI.
The International Classification for Standards (ICS) is a hierarchical classification system maintained by ISO to organize standards and related documents. It uses a three-level structure with field (2 digits), group (3 digits), and sub-group (2 digits) codes. The ICS helps users find standards by subject area and enables statistical analysis of standards development activities.
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This document specifies a test method for determination of aldehydes in propylene oxide by liquid chromatography. This document is applicable to the determination of aldehydes in propylene oxide for industrial use, including formaldehyde, acetaldehyde, propionaldehyde and acrolein. The concentration for each aldehyde ranges from 0,5 mg/kg to 100 mg/kg.
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This document specifies a test method for the determination of propylene oxide and trace impurities in propylene oxide for industrial use by gas chromatography. This document is suitable for the determination of propylene oxide which is produced by ethylbenzene co-oxidation (PO/SM), isobutane co-oxidation (PO/TBA), cumene co-oxidation (CHPPO), hydrogen peroxide oxidation (HPPO) and chlorohydrin. This document is applicable for determination of propylene oxide with a purity ≥ 99,70 % and impurity content ≥ 0,000 3 %.
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This document specifies general requirements for basic chemicals and raw materials of basic chemicals resulting from chemical recycling of organic materials. This document does not provide specific requirements for materials covered by other ISO technical committees.
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This document specifies a method for determining the total acidity, calculated as acetic acid, of ethanol to be used in petrol blends. It is applicable to ethanol having total acid contents of between 0,003 % (m/m) and 0,015 % (m/m).
NOTE For the purposes of this document, the terms "% (m/m)" and "% (V/V)" are used to represent the mass fraction and the volume fraction, respectively.
WARNING - Use of this document can involve hazardous materials, operations and equipment. This document does not purport to address all of the safety problems associated with its use. It is the responsibility of the user of this document to take appropriate measures to ensure the safety and health of personnel prior to the application of the document, and to fulfil statutory and regulatory restrictions for this purpose.
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SIGNIFICANCE AND USE
5.1 N-methylcarbamates and n-methylcarbomoyloximes are used in agriculture as insecticides and herbicides. They are sometimes found in both surface and ground waters and can be toxic to animals and plants at moderate to high concentrations. The manufacturing precursors and degradation products may be equally as hazardous to the environment.
SCOPE
1.1 This is a high-performance liquid chromatographic (HPLC) test method applicable to the determination of certain n-methylcarbamoyloximes and n-methylcarbamates in ground water and finished drinking water (1).2 This test method is applicable to any carbamate analyte that can be hydrolyzed to a primary amine. The following compounds have been validated using this test method:
Analyte
Chemical Abstract Services
Registry Number A
Aldicarb
116-06-3
Aldicarb sulfone
1646-88-4
Aldicarb sulfoxide
1646-87-3
Baygon
114-26-1
Carbaryl
63-25-2
Carbofuran
1563-66-2
3-Hydroxycarbofuran
16655-82-6
Methiocarb
2032-65-7
Methomyl
16752-77-5
Oxamyl
23135-22-0
1.2 This test method has been validated in a collaborative round-robin study (2) and estimated detection limits (EDLs) have been determined for the analytes listed in 1.1 (Table 1). Observed detection limits may vary between ground waters, depending on the nature of interferences in the sample matrix and the specific instrumentation used.
1.3 This test method is restricted to use by, or under the supervision of, analysts experienced in both the use of liquid chromatography and the interpretation of liquid chromatograms. Each analyst should demonstrate an ability to generate acceptable results with this test method using the procedure described in 12.3.
1.4 When this test method is used to analyze unfamiliar samples for any or all of the analytes listed in 1.1, analyte identifications should be confirmed by at least one additional qualitative technique.
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Additional guidance on laboratory safety is available and suitable references for the information are provided (3-5).
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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SIGNIFICANCE AND USE
5.1 This test method is useful for the analysis of drinking water and groundwaters. Other waters may be analyzed by this test method, see 1.2.
5.2 EDB and DBCP have been widely used as soil fumigants. EDB is also used as a lead scavenger in leaded gasolines. These compounds are very water soluble and are often found in groundwater and drinking water. Since they are highly toxic and are suspected carcinogens, there is concern about the potential health impact of even extremely low concentrations in potable water.
SCOPE
1.1 This test method covers the determination of 1,2-dibromoethane (commonly referred to as ethylene dibromide or EDB) and 1,2-dibromo-3-chloropropane (commonly referred to as DBCP) in water at a minimum detection level of 0.010 μg/L by liquid-liquid extraction combined with gas-liquid chromatography. This test method is applicable to the analysis of drinking waters and groundwaters. It is not recommended for wastewaters, due to the potential for interferences from high concentrations of other extractable organics. Similar information can be found in EPA Method 504.
1.2 This test method was used successfully with reagent water and groundwater. It is the user's responsibility to ensure the validity of this test method for waters of untested matrices.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Sections 6 and 9.
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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SIGNIFICANCE AND USE
4.1 The presence of 4-CBA and p-TOL in PTA used for the production of polyester is undesirable because they can affect the PET quality (such as contribute to fiber breaks), the polymerization process, and 4-CBA imparts coloration to the polymer due to thermal instability.
4.2 Determining the amount of 4-CBA and p-TOL remaining from the manufacture of PTA is often required. This test method is suitable for setting specifications and for use as an internal quality control tool where these products are produced or are used.
SCOPE
1.1 This test method covers the determination of the 4-Carboxybenzaldehyde (4-CBA) and p-Toluic acid (p-TOL) in purified terephthalic acid (PTA) by reverse phase high performance liquid chromatography (HPLC). This method is applicable for 4-CBA and p- TOL with an upper limit of 500 mg/kg, respectively, but may be applicable to a wider range.
1.2 In determining the conformance of the test results using this method to applicable specification, results shall be rounded off in accordance with the rounding-off method of Practice E29.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.For specific hazard statements, see Section 7.
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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SIGNIFICANCE AND USE
4.1 This is a revision of the method for measuring rosin acids content combines the three major ways of determining the rosin acids content of pine chemicals products into a single method.
4.1.1 For materials containing less than 15 % rosin, the modified Glidden procedure has gained acceptance. For materials containing more than 15 % rosin the modified Wolfe Method is preferred. The modified Wolfe and modified Glidden procedures differ only in their details. They have been combined here into a single procedure. This procedure can be run using either a potentiometer or an internal indicator to determine the end point of the titration. Use of a potentiometer is preferred and is the referee method. Use of an internal indicator is the principal alternative method. They will be referred to as the Potentiometric Method and the Internal Indicator Method.
SCOPE
1.1 These test methods cover the determination of rosin acids in tall oil, tall oil fatty acid, tall oil rosin, and other pine chemicals products.
1.2 These test methods may not be applicable to adducts or derivatives of rosin, fatty acid, or other pine chemicals products.
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.
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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SIGNIFICANCE AND USE
4.1 Perfluoroalkyl and polyfluoroalkyl substances (PFAS) are a family of more than 4700 synthetic organic chemicals. PFAS can withstand high temperatures and survive highly corrosive environments. They are used in the manufacture of coatings, surface treatments, and specialty chemicals in cookware, carpets, food packaging, clothing, cosmetics, and other common consumer products. PFAS also have many industrial applications and are an active ingredient in certain types of fire-fighting foams (aqueous film-forming foams, or AFFF). PFAS coatings resist oil, grease, and water. PFAS are persistent compounds. Therefore, PFAS should be considered for purposes of managing investigation-derived waste where PFAS is known or suspected to be present in environmental media.
4.1.1 PFAS are emerging contaminants for which environmental regulations and guidance are dynamic and are being developed simultaneously at federal, state, local, and international levels as more is learned about their characteristics, environmental fate, and management/treatment. Therefore, site-specific rules, regulations, and guidance should be evaluated for options and restrictions on management of PFAS investigation-derived waste. For example, the Massachusetts Department of Environmental Protection has determined that PFAS wastes are “hazardous materials” subject to the Massachusetts Oil and Hazardous Material Release Prevention and Response Act (M.G.L. Chapter 21E) and the Massachusetts Contingency Plan. Other states and jurisdictions may have or will develop and implement similar determinations that affect the on-site management, storage, and labeling and off-site transportation requirements for PFAS investigation-derived waste.
4.1.2 Given the characteristics and persistence of PFAS compounds, PFAS investigation-derived waste presents special handling and treatment/disposal considerations. EPA recently issued Interim Guidance on the Destruction and Disposal of Perfluoralkyl and Polyfluoralky...
SCOPE
1.1 Existing guidance on the management of investigation-derived waste is focused upon cuttings, purge water, personal protective equipment, and other miscellaneous solid waste generated at property that may be impacted by the release of hazardous materials and hazardous substances. These hazardous substances include, but are not limited to, heavy metals, petroleum, petroleum byproducts, solvents, polycyclic aromatic hydrocarbons, organic and inorganic corrosives, radioactive material, and explosives. Guidance on the management of investigation derived waste generated at sites that may be impacted by releases of perfluoroalkyl and polyfluoroalkyl substances (PFAS) is limited. This standard guide addresses this deficiency
1.2 This guide describes best practices for managing investigation-derived waste associated with PFAS that are consistent with federal and state policies and regulations at the date of issuance. The user is advised to determine if new regulations or rules have been promulgated by the state, federal, or tribal regulatory agency having jurisdiction over the property.
1.3 This guide describes considerations to prevent the unintended and unauthorized disposal of liquid investigation-derived waste that may contain PFAS into wastewater treatment plants or systems that are not permitted to receive these waste streams.
1.4 This guide describes considerations to prevent the unintended and unauthorized disposal of solid investigation-derived waste that may contain PFAS into landfills or other solid waste disposal facilities that are not permitted to receive these waste streams.
1.5 This guide describes several stormwater pollution prevention best management practices applicable to investigation-derived waste.
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,...
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SIGNIFICANCE AND USE
4.1 This test method is suitable for determining the quantity of aldehydes, both for quality control and quality assurance of the product.
SCOPE
1.1 This test method covers the wet chemical determination of aldehydes in styrene monomer. Aldehydes are calculated and reported as benzaldehyde.
1.2 This test method is applicable to samples with aldehyde concentrations to 0.030 mass%. The limit of detection (LOD) is 0.0006 mass% and the limit of quantitation (LOQ) is 0.002 mass% based on the data in 13.1.
1.3 In determining conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
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. For specific hazard statements, see 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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SIGNIFICANCE AND USE
4.1 Organic and inorganic chlorine compounds can have a deleterious effect on equipment and reactions in processes involving aromatic hydrocarbons.
4.2 Maximum chloride levels are often specified for process streams and for aromatic hydrocarbon products.
SCOPE
1.1 This test method covers the determination of total chloride (organic and inorganic) in liquid aromatic hydrocarbons and cyclohexane.
1.2 The test method is applicable to samples with chloride concentrations of 1 mg/kg to 25 mg/kg.
1.3 Bromides and iodides, if present, will be calculated as chlorides.
1.4 Materials, such as styrene, that are polymerized by sodium biphenyl reagent cannot be analyzed by this test method.
1.5 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For a specific hazard statement, see Section 7.
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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SIGNIFICANCE AND USE
4.1 This test method is applicable to the determination of trace amounts of aldehydes and ketones in aqueous solutions and a wide variety of organic solvents.
SCOPE
1.1 This test method covers the determination of total carbonyl in the range from 0.5 μg to 50 μg calculated as CO.
1.2 This test method is intended to be general and does not include steps for sample preparation.
1.3 Acetals that hydrolyze under the conditions of the test are also determined.
1.4 Carbonyl derivatives such as acetals and imines that are easily hydrolyzed may be determined by an alternative procedure.
1.5 The developed color is not stable and must be measured within a specified period.
Note 1: Other test methods for the determination of traces of carbonyl compounds are given in Test Methods D1089, D1612, D2119, and D2191.
1.6 Review the current appropriate Safety Data Sheets (SDS) for detailed information concerning toxicity, first aid procedures, and safety precautions.
1.7 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.8 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
1.9 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 7 and Section 8.
1.10 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
4.1 The coulometric technique is especially suited for determining low concentrations of water in organic liquids that would yield small titers by the Karl Fischer volumetric procedure. The precision and accuracy of the coulometric technique decreases for concentrations of water much greater than 2.0 % because of the difficulty in measuring the small size of sample required. The test method assumes 100 % efficiency of coulombs in iodine production. Provision is made for verifying this efficiency. (See Table 1 and Note 5.)
SCOPE
1.1 This test method covers the determination of water from 0 % to 2.0 % mass in most liquid organic chemicals, with Karl Fischer reagent, using an automated coulometric titration procedure. Use of this test method is not applicable for liquefied gas products such as Liquid Petroleum Gas (LPG), Butane, Propane, Liquid Natural Gas (LNG), etc.
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 Review the current Safety Data Sheets (SDS) for detailed information concerning toxicity, first-aid procedures, handling, and safety precautions.
1.4 This standard does not purport to address all of the safety problems, 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.
1.5 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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SIGNIFICANCE AND USE
4.1 This test method is suitable for determining the quantity of aldehydes, both for quality control and quality assurance of the product.
SCOPE
1.1 This test method covers the wet chemical determination of total aldehydes in styrene monomer. Total aldehydes are calculated and reported as benzaldehyde.
1.2 This test method is applicable to samples with aldehyde concentrations to 0.013 mass%. The Limit of Detection (LOD) is 0.0006 mass% and the Limit of Quantification (LOQ) is 0.0020 mass%. The LOD and LOQ were calculated based on the data in Table 1.
1.3 In determining conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
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. For specific hazard statements, see 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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ABSTRACT
This specification covers ethylbenzene. Different tests shall be conducted in order to determine the following properties of ethylbenzene: purity, benzene content, toluene content, xylene content, cumene content, diethylbenzene content, chloride content, sulfur content, and color.
SCOPE
1.1 This specification covers ethylbenzene.
1.2 The following applies to all specified limits in this specification for purposes of determining conformance with this specification, 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measure are included in this specification.
1.4 Consult current OSHA regulations, supplier’s Safety Data Sheet for all materials, and local regulations used in this 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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SIGNIFICANCE AND USE
2.1 This test method is intended for use in the determination of the acidity as free fatty acids in the absence of ammonium or triethanolamine soaps in sulfonated and sulfated oils for the purpose of quality assurance.
SCOPE
1.1 This test method covers the determination of the acidity as free fatty acids existing in a sample of sulfonated or sulfated oil, or both, by titrating the sample dissolved in a solvent. It is not applicable in the presence of ammonium or triethanolamine soaps or salts or other compounds that do not react neutral to phenolphthalein when dissolved in alcohol.
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 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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SIGNIFICANCE AND USE
5.1 Furanic compounds are generated by the degradation of cellulosic materials used in the solid insulation systems of electrical equipment.
5.2 Furanic compounds which are oil soluble to an appreciable degree will migrate into the insulating liquid.
5.3 High concentrations or unusual increases in the concentrations of furanic compounds in oil may indicate cellulose degradation from aging or incipient fault conditions. Testing for furanic compounds may be used to complement dissolved gas in oil analysis as performed in accordance with Test Method D3612.
SCOPE
1.1 This test method covers the determination in electrical insulating liquids of products of the degradation of cellulosic materials such as paper, pressboard, and cotton materials typically found as insulating materials in electrical equipment. These degradation products are substituted furan derivatives, commonly referred to as furanic compounds or furans. This test method allows either liquid/liquid or solid phase extraction (SPE) of the furanic compounds from the sample matrix followed by analysis for specific furanic compounds by HPLC or direct injection for analysis of specific furanic compounds by HPLC.
1.2 The individual furanic compounds that may be identified and quantified include the following:
5-hydroxymethyl-2-furaldehyde
furfuryl alcohol
2-furaldehyde
2-acetylfuran
5-methyl-2-furaldehyde
1.3 The direct injection method generally has a higher limit of detection, especially for furfuryl alcohol. Greater interference for furfuryl alcohol may be expected when using the direct injection method as opposed to extraction methods.
1.4 This test method has been used to successfully test for furanic compounds in mineral insulating oil, silicone fluid, high fire point electrical insulating oils of mineral origin, askarels, and perchloroethylene-based dielectric fluids.
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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SIGNIFICANCE AND USE
4.1 This guide is intended to provide information on the likely composition of propylene concentrates and on probable ways to test them. Since there are currently no ASTM test methods for determining all components of interest, this guide provides information on other potentially available test methods.
4.2 Although this guide is not to be used for specifications, it can provide a starting point for parties to develop mutually agreed upon specifications which meet their respective requirements. It can also be used as a starting point in finding suitable test methods for determining various components of propylene.
SCOPE
1.1 This guide covers a list of the major grades of propylene concentrates produced in North America. It includes possible components and test methods, both ASTM and other, either actually used, or believed to be in use, to test for these properties. This guide is not intended to be used or construed as a set of specifications for any grade of propylene concentrate.
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 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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SIGNIFICANCE AND USE
5.1 This procedure describes a rapid and sensitive method for estimating the stability reserve of an oil. The stability reserve is estimated in terms of a separability number, where a low value of the separability number indicates that there is a stability reserve within the oil. When the separability number is between 0 to 5, the oil can be considered to have a high stability reserve and asphaltenes are not likely to flocculate. If the separability number is between 5 to 10, the stability reserve in the oil will be much lower. However, asphaltenes are, in this case, not likely to flocculate as long as the oil is not exposed to any worse conditions, such as storing, aging, and heating. If the separability number is above 10, the stability reserve of the oil is very low and asphaltenes will easily flocculate, or have already started to flocculate.
5.2 This test method can be used by refiners and users of oils, for which this test method is applicable, to estimate the stability reserves of their oils. Hence, this test method can be used by refineries to control and optimize their refinery processes. Consumers of oils can use this test method to estimate the stability reserve of their oils before, during, and after storage.
FIG. 1 Schematic Representation of a Typical Measurement Using an Optical Scanning Device
5.3 This test method is not intended for predicting whether oils are compatible before mixing, but can be used for determining the separability number of already blended oils. However, oils that show a low separability number are more likely to be compatible with other oils than are oils with high separability numbers.
SCOPE
1.1 This test method covers the quantitative measurement, either in the laboratory or in the field, of how easily asphaltene-containing heavy fuel oils diluted in toluene phase separate upon addition of heptane. This is measured as a separability number (%) by the use of an optical scanning device.
1.2 The test method is limited to asphaltene-containing heavy fuel oils. ASTM specification fuels that generally fall within the scope of this test method are Specification D396, Grade Nos. 4, 5, and 6, Specification D975, Grade No. 4-D, and Specification D2880, Grade Nos. 3-GT and 4-GT. Refinery fractions from which such blended fuels are made also fall within the scope of this test method.
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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SIGNIFICANCE AND USE
4.1 This guide provides standard terminology for use in identifying and describing the different chemical forms of cyanide. The complex nature of cyanide chemistry, existence of numerous distinct chemical forms as well as the various regulatory distinctions that may be made can lead to confusion in technical discussions on cyanide and in the selection of appropriate methods for its analysis. This guide is intended to provide clarification and a common framework of terms and definitions to facilitate discussions and referencing different cyanide chemical species and groups of cyanide compounds.
4.2 The use of such common terminology is particularly important from an environmental perspective because certain forms of cyanide are considered to be toxic. Therefore, their release into the environment is regulated by federal and state agencies. Thus a general understanding of cyanide chemistry and species definitions is needed for proper wastewater management and testing.
SCOPE
1.1 This guide defines guidance based on a consensus of viewpoints for interpretation of test results to identify various chemical forms of cyanide. It is intended to provide a general understanding of the chemical nature of distinct cyanide species as related to chemical analysis and environmental fate and transport.
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 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 Organic as well as inorganic chlorine compounds can prove harmful to equipment and reactions in processes involving hydrocarbons.
5.2 Maximum chloride levels are often specified for process streams and for hydrocarbon products.
5.3 Organic chloride species are potentially damaging to refinery processes. Hydrochloric acid can be produced in hydrotreating or reforming reactors and this acid accumulates in condensing regions of the refinery.
SCOPE
1.1 This test method covers the determination of organic chloride in aromatic hydrocarbons, their derivatives, and related chemicals.
1.2 This test method is applicable to samples with chloride concentrations to 25 mg/kg. The limit of detection (LOD) is 0.2 mg/kg and the limit of quantitation (LOQ) is 0.7 mg/kg. With careful analytical technique or the measurement of replicates, or both, this method can be used to successfully analyze concentrations below the LOD.
Note 1: The maximum is the highest concentration from the interlaboratory study and the LOD and LOQ were calculated from Performance Testing Program (PTP) data. See Table 1.
1.3 This test method is preferred over Test Method D5194 for products, such as styrene, that are polymerized by the sodium biphenyl reagent.
1.4 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
1.5 Organic chloride values of samples containing inorganic chlorides will be biased high due to partial recovery of inorganic species during combustion. Interference from inorganic species can be reduced by water washing the sample before analysis. This does not apply to water soluble samples.
1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see 7.3 and Section 9.
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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SIGNIFICANCE AND USE
5.1 This test method is one of a number of tests conducted on heavy hydrocarbon mixtures to characterize these materials for a refiner or a purchaser. It provides an estimate of the yields of fractions of various boiling ranges.
5.2 The fractions made by this test method can be used alone or in combination with other fractions to produce samples for analytical studies and quality evaluations.
5.3 Residues to be used in the manufacture of asphalt can also be made but may not always be suitable. The long heat soaking that occurs in this test method may alter some of the properties.
Note 1: While the practice of reblending distillates with residue can be done to produce a lighter residue, it is not recommended because it produces blends with irregular properties.
5.4 Details of cutpoints must be mutually agreed upon before the test begins.
5.5 This is a complex procedure involving many interacting variables. It is most important that at the time of first use of a new apparatus, its components be checked as detailed in Annex A1 and Annex A2 and that the location of the vapor temperature sensor be verified as detailed in 6.5.3 and Fig. 1.
SCOPE
1.1 This test method covers the procedure for distillation of heavy hydrocarbon mixtures having initial boiling points greater than 150 °C (300 °F), such as heavy crude oils, petroleum distillates, residues, and synthetic mixtures. It employs a potstill with a low pressure drop entrainment separator operated under total takeoff conditions. Distillation conditions and equipment performance criteria are specified and typical apparatus is illustrated.
1.2 This test method details the procedures for the production of distillate fractions of standardized quality in the gas oil and lubricating oil range as well as the production of standard residue. In addition, it provides for the determination of standard distillation curves to the highest atmospheric equivalent temperature possible by conventional distillation.
1.3 The maximum achievable atmospheric equivalent temperature (AET) is dependent upon the heat tolerance of the charge. For most samples, a temperature up to 565 °C (1050 °F) can be attained. This maximum will be significantly lower for heat sensitive samples (for example, heavy residues) and might be somewhat higher for nonheat sensitive samples.
1.4 The recommended distillation method for crude oils up to cutpoint 400 °C (752 °F) AET is Test Method D2892. This test method can be used for heavy crude oils with initial boiling points greater than 150 °C (302 °F). However, distillation curves and fraction qualities obtained by these methods are not comparable.
1.5 This test method contains the following annexes:
1.5.1 Annex A1—Test Method for Determination of Temperature Response Time,
1.5.2 Annex A2—Practice for Calibration of Sensors,
1.5.3 Annex A3—Test Method for Dehydration of a Wet Sample of Oil,
1.5.4 Annex A4—Practice for Conversion of Observed Vapor Temperature to Atmospheric Equivalent Temperature (AET), and
1.5.5 Annex A5—Test Method for Determination of Wettage.
1.6 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warnings, see 6.5.4.2, 6.5.6.3, 6.9.3, 9.5, 9.7, and A2.3.1.3.
1.8 WARNING—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use Caution when handling mercury and mercury-containing...
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SIGNIFICANCE AND USE
5.1 This test method can be used for determining polymer concentrations in styrene monomer.
5.2 This test method will not detect dimers and trimers.
5.3 This test method can be used for plant control and for specification analysis.
SCOPE
1.1 These test methods cover the determination of the polymer content of styrene monomer. It should be noted, however, that dimers and trimers are not measured by these test methods.
1.2 Test Method A, which is based on the use of a spectrophotometer or photometer, is intended for the quantitative determination of the polymer content of styrene monomer in concentrations up to 15 mg/kg. Samples containing more than 15 mg/kg of polymer must be suitably diluted before measurement. The limit of detection (LOD) is 1.2 mg/kg and the limit of quantitation (LOQ) is 4.0 mg/kg. LOD and LOQ were calculated using the last sample in Table 1.
1.3 Test Method B is a rapid visual procedure that is intended for the approximate evaluation of polymer to a maximum concentration of 1.0 mass %. Samples having a polymer content of 1.0 mass % or greater should be suitably diluted prior to measurement.
1.4 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Section 9.
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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ABSTRACT
This specification covers dimethyl ether (DME) for use as a fuel in engines specifically designed or modified for DME and for blending with liquefied petroleum gas. It is intended for use by DME manufacturers, purpose-built engine developers, in contracts for the purchase of DME for fuel purposes, and for the guidance of consumers of this type of fuel. This specification includes chemical composition and other requirements, sampling, and test methods.
SCOPE
1.1 This specification covers dimethyl ether (DME) for use as a fuel in engines specifically designed or modified for DME and for blending with liquefied petroleum gas (LPG). This specification is for use by manufacturers of dimethyl ether, by engine developers of purpose-built engines, in contracts for the purchase of DME for fuel purposes, and for the guidance of consumers of this type of fuel.
Note 1: The generation and dissipation of static electricity can create problems in the handling of DME. For more information on the subject, see Guide D4865.
1.2 The values stated in SI units are to be regarded as standard. Units 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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This document specifies a procedure for the determination of dry residue in ethanol by gravimetric (desiccation) method in the range (10 to 25) mg/100 ml.
NOTE In an interlaboratory study [2] the method described has been tested at levels down to 3,5 mg/100 ml, but the precision appeared to be insufficient at such low levels.
WARNING - Use of this document can involve hazardous equipment, materials and operations. This method does not purport to address to all of the safety problems associated with its use. It is the responsibility of the user of this document to take appropriate measures to ensure the safety and health of personnel prior to the application of the document, and to fulfil statutory and regulatory restrictions for this purpose.
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ABSTRACT
This specification covers technical grade ethylene dichloride. Technical grade ethylene dichloride shall conform to the requirements prescribed. The color, ethylene dichloride content, specific gravity, acidity, and water content shall be tested to meet the requirements prescribed.
SCOPE
1.1 This specification covers technical grade ethylene dichloride.
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 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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ABSTRACT
This specification covers reclaimed methylene chloride used in various industries for noncritical applications. Tests for specific gravity, acidity, water content, appearance, color, nonvolatile residue, chloride content, assay, and 1,1,1-trichloroethane content shall be performed and shall conform to the requirements specified.
SCOPE
1.1 This specification covers the grade of methylene chloride typically needed in various industries for noncritical applications, such as in paint stripping formulations. It may be used as a reference document by purchasers or by persons establishing in-house methylene chloride recovery programs.
1.2 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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ABSTRACT
This specification covers solvents based on stabilized normal-propyl bromide (nPB) for use in vapor degreasing. The standard also includes a separate specification for technicalgraden-propyl bromide. Blends and azeotropic mixtures of stabilized nPB for vapor-degreasing shall be blended from nPB meeting the specification for technical-grade nPB. Vapor-degreasing solvents based on stabilized normalpropyl bromide shall conform to the requirements of different properties such as boiling point, acidity, water content, appearance, color, free halogen, nonvolatile residue, acid acceptance, and aluminum corrosion at reflux. Blends and azeotropic mixtures of stabilized nPB with other materials for use in vapor degreasing shall be prepared from technical-grade nPB which shall conform also to requirements of different properties such as: specific gravity, boiling point, acidity, water content, appearance, color, free halogen, nonvolatile residue, normal-propyl bromide content, and iso-propyl bromide content.
SCOPE
1.1 This standard covers solvents based on stabilized normal-propyl bromide (nPB) for use in vapor degreasing. The standard also includes a separate specification for technical-grade n-propyl bromide.
1.2 Blends and azeotropic mixtures of stabilized nPB for vapor-degreasing shall be blended from nPB meeting the specification for technical-grade nPB.
Note 1: Guide D3844, Practice D4276, and MNL22 provide additional important information on vapor degreasing and solvent properties.
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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This document specifies a spectrometric method for the determination of the absorbance at a wavelength of 290 nm of caprolactam for industrial use.
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This document specifies a spectrometric method of determining the colour, expressed in Hazen units, of a 50 % aqueous caprolactam solution as a measure of coloured impurities content of the sample.
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This document describes the procedures and the precautions to be taken in drawing representative samples of ethylene in the liquid phase stored at -100 °C and in the gaseous phase, for the purpose of their analysis. Annex A sets out a diagrammatic representation of a system for the disposal of the portion of the sample which is not used in the analysis.
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ABSTRACT
This specification covers glacial acrylic acid (99.0% grade) for use in paint, varnish, lacquer and related products. The properties of the material shall be determined in accordance with the following test methods: purity; water; color; inhibitor; and dimer.
SCOPE
1.1 This specification covers glacial acrylic acid2 (99.0 % grade) for use in paint, varnish, lacquer and related products.
1.2 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 For hazard information and guidance, see the supplier’s Safety Data Sheet.
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Section 6.
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 This test method is suitable for setting specifications on the materials referenced in Table 1 and for use as an internal quality control tool where cyclohexane is produced or is used in a manufacturing process. It may also be used in development or research work involving cyclohexane.
5.2 This test method is useful in determining the purity of cyclohexane with normal impurities present. If extremely high boiling or unusual impurities are present in the cyclohexane, this test method would not necessarily detect them and the purity calculation would be erroneous.
SCOPE
1.1 This test method covers the determination of the purity of cyclohexane by gas chromatography.
1.2 This test method is applicable to the measurement of impurities in Table 1. This test method is applicable to samples with concentrations to 400 mg/kg, but may be applicable to a wider range. The limit of detection (LOD) is 1 mg/kg and the limit of quantitation (LOQ) is 3 mg/kg for benzene.
Note 1: The LOD and LOQ were calculated from the ILS data for benzene.
1.3 The following applies for the purposes of determining the conformance of the test results using this test method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
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. For specific hazard statements, see 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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SIGNIFICANCE AND USE
4.1 This test method provides a measurement of commonly found impurities in commercially available methyl isobutyl ketone. The measurement of these impurities and the results thereof can individually or when totaled and subtracted from 100 (assay) be used for specification acceptance.
SCOPE
1.1 This test method covers the determination of the purity of methyl isobutyl ketone (MIBK) by gas chromatography and in addition provides a means for measuring certain impurities such as methyl isobutyl carbinol which are of interest. Impurities such as water and acidity are measured by other appropriate ASTM procedures and the results are used to normalize the chromatographic value.
1.2 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 round-off method of Practice E29.
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.
1.5 For specific hazard information and guidance, see the supplier’s Safety Data Sheet for the materials listed in this test method.
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
4.1 This test method provides a measurement of acidity (as formic acid) in formaldehyde solutions. The results of these measurements can be used for specification acceptance.
SCOPE
1.1 This test method covers the determination of the acidity of commercially available formaldehyde solutions.
1.2 For purposes of determining conformance of an observed or a calculated value using this test method to relevant specifications, test result(s) 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 For hazard information and guidance, see the supplier’s Safety Data Sheet.
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 hazard statements are given in Section 7.
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
4.1 Water-insoluble materials present in a solvent expected to be completely water miscible may interfere with many uses of the solvent. This test method provides a measure of the miscibility of water-soluble solvents with a polar medium-water. It also provides a qualitative indication of the presence or absence of water-immiscible contaminants.
4.2 The results of this test method may be used in assessing compliance with a specification. Prior to agreeing to this test method as the basis of a specification requirement, it may be desirable that the interpretation of what constitutes cloudiness or turbidity be agreed upon between the supplier and the purchaser.
SCOPE
1.1 This test method covers the determination of the miscibility of water-soluble solvents with water. While written specifically for testing acetone, isopropyl alcohol (isopropanol), and methyl alcohol (methanol), the method is suitable for testing most water-soluble solvents.
1.2 This test method serves to detect water-immiscible contaminants qualitatively; the level of detection of these impurities varies widely with both the type of solvent and the type of impurity.
1.3 The level of detection of water-insoluble materials depends upon the solvent tested and the type of impurity or impurities present, that is paraffin, olefin, aromatic, high molecular weight alcohol, or ketone, etc. There is, therefore, no specific level of impurity detected by this procedure.
Note 1: This test method is normally performed at ambient, but other temperatures may be used as specified by the consumer and supplier.
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 For specific hazard information and guidance, consult the supplier’s Safety Data Sheet for materials listed in this test method.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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ABSTRACT
This specification details the properties and requirements for isobutyl acetate. The specimens shall be sampled, go through chemical tests and conform accordingly to specified values of the following requirements: apparent specific gravity; color (Pt-Co units) distillation (initial boiling point and dry point); nonvolatile matter content; water content; acidity (free acid as acetic acid); and purity.
SCOPE
1.1 This specification covers isobutyl acetate (95 % grade).
1.2 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 For specific hazard information and guidance, see the supplier’s Safety Data Sheet for material listed in this specification.
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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ABSTRACT
This specification covers isophorone volatile solvents used in paints, varnishes, lacquers, and related products. Isoprophone should conform to the specified requirements on apparent specific gravity, color, distillation, purity, acidity as acetic acid, and water content.
SCOPE
1.1 This specification covers isophorone2 (98 % grade) for use in paint, varnish, lacquer, and related products.
1.2 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 For specific hazard information and guidance, see the supplier’s Safety Data Sheet for materials listed in this 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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SIGNIFICANCE AND USE
4.1 This test method provides a measurement of alkalinity in acetone. The results of this measurement can be used for specification acceptance.
SCOPE
1.1 This test method covers the determination in acetone of alkalinity calculated as ammonia (NH3).
1.2 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 For specific hazard information and guidance, consult the supplier’s Safety Data Sheet.
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 hazard statements are given in Section 7.
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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ABSTRACT
This specification covers dipropylene glycol monomethyl ether (DPM). Dipropylene glycol monomethyl ether shall conform to the requirements specified for the following: (1) assay content, (2) distillation range defined by the initial boiling point and dry point, (3) apparent specific gravity, (4) platinum-cobalt scale color, (5) water content, and (6) acidity (free acid as acetic acid). The sampling and test methods to determine conformance to the specified properties are given.
SCOPE
1.1 This specification covers dipropylene glycol monomethyl ether (DPM).
Note 1: Dipropylene glycol monomethyl ether (DPM) is a mixture of isomers, the predominant isomer being 1-(2-methoxy-1-methylethoxy)-2-propanol.
1.2 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 For specific hazard information and guidance, consult the supplier’s Safety Data Sheet for materials listed in 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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ABSTRACT
This specification covers glacial acetic acid for use in paint, varnish, lacquer, and related products. Glacial acetic acid shall be tested for purity, freezing point, color, water content, iron content, acetaldehyde content, and formic acid content, and shall conform to the requirements of the specification. Test methods, sampling, and packaging shall be in accordance with ASTM standard methods.
SCOPE
1.1 This specification covers glacial (99.8 %) acetic acid for use in paint, varnish, lacquer, and related products.
1.2 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.
1.3 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.
1.5 For specific hazard information and guidance, see the supplier’s Safety Data Sheet for materials listed in this specification.
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
4.1 This procedure is designed to determine the purity of the two ketones, methyl isoamyl ketone and methyl amyl ketone, and to obtain the concentration of their various impurities, several of which are critical in the application of these solvents.
SCOPE
1.1 This test method covers the determination of the purity of methyl amyl ketone and methyl isoamyl ketone. In addition, the method determines total ketones and various impurities which may include acetone, isopropyl alcohol, methyl propyl ketone, methyl isobutyl ketone, methyl butyl ketone, methyl isobutyl carbinol, mesityl oxide, methyl isoamyl ketone, methyl butyl carbinol, methyl amyl ketone, and diisobutyl ketone.
1.2 Water and acid cannot be determined by this test method. They must be determined by other appropriate ASTM procedures, and the results used to normalize the chromatographic data.
1.3 For purposes of determining conformance of an observed or a calculated value using this test method to relevant specifications, test result(s) 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 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.5 For hazard information and guidance, see the supplier’s Safety Data Sheet.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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This document describes the procedures and precautions to be taken in drawing representative samples of propylene and butadiene, in the liquid phase, for the purpose of their analysis. Annex A sets out a diagrammatic representation of a system for the disposal of the portion of the sample not used in the analysis. Annexes B, C and D show the sequence of operations for filling a sampling cylinder in non-closed and closed sampling apparatus.
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ABSTRACT
This specification establishes the testing and requirements of four types of engine coolant grade ethylene glycol and propylene glycol, including virgin glycols and those derived from the recycling of vehicle engine coolants and industrial source glycols. Types EG-1 and PG-1 cover glycols with sufficiently low limits on components to allow a blended coolant to meet most OEM (Original Equipment Manufacturer) specifications. These types will probably be virgin materials, although redistillation could produce a sufficiently pure product. Types EG-2 and PG-2 cover glycol that will be suitable for many coolants, and can either be redistilled or virgin. The commercial products shall be suitably sampled and tested, and shall conform accordingly to specified values of the following physical and chemical properties: clarity; color (Pt/Co scale); relative density; pH by volume in distilled water; acidity as acetic acid; composition by mass of individual glycols (including ethylene glycol, propylene glycol, dipropylene glycol, and others); total composition by mass of all glycols; water content; glycol ester content; and the maximum content for nitrites, nitrates, phosphates, silicon, chloride, sulfate, boron, aluminum, calcium, copper, iron, magnesium, lead, zinc, and iron.
SCOPE
1.1 This specification covers commercial products, engine coolant grade ethylene glycol and propylene glycol, including virgin glycols and those derived from the recycling of vehicle engine coolants and industrial source glycols.
1.2 Types EG-1 and PG-1 cover glycols with sufficiently low limits on components to allow a blended coolant to meet most OEM (Original Equipment Manufacturer) specifications. These types will probably be virgin materials, although redistillation could produce a sufficiently pure product. Types EG-2 and PG-2 cover glycol that will be suitable for many coolants. These types can be either redistilled or virgin.
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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ABSTRACT
This specification covers a grade of o-xylene identified as ortho-Xylene 980. O-xylene 980 shall be tested and sampled in accordance with standard test methods and practices and shall conform to the following requirements: purity; non-aromatic hydrocarbons; p-xylene plus m-xylene; C9 and heavier aromatics; cumene; bromine index; appearance which shall be a clear liquid, free of sediment and haze; color in the platinum-cobalt scale; and distillation range.
SCOPE
1.1 This specification covers a grade of o-xylene identified as ortho-Xylene 980.
1.2 The following applies to all specified limits in this specification: for purposes of determining conformance with this specification, 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.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 Consult current OSHA regulations and supplier’s Safety Data Sheets, and local regulations for all materials used in this specification.
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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SIGNIFICANCE AND USE
5.1 Autoignition, by its very nature, is dependent on the chemical and physical properties of the material and the method and apparatus employed for its determination. The autoignition temperature by a given method does not necessarily represent the minimum temperature at which a given material will self-ignite in air. The volume of the vessel used is particularly important since lower autoignition temperatures will be achieved in larger vessels. (See Appendix X2.) Vessel material can also be an important factor.
5.2 The temperatures determined by this test method are those at which air oxidation leads to ignition. These temperatures can be expected to vary with the test pressure and oxygen concentration.
5.3 This test method is not designed for evaluating materials which are capable of exothermic decomposition. For such materials, ignition is dependent upon the thermal and kinetic properties of the decomposition, the mass of the sample, and the heat transfer characteristics of the system.
5.4 This test method can be employed for solid chemicals which melt and vaporize or which readily sublime at the test temperature. No condensed phase, liquid or solid, should be present when ignition occurs.
5.5 This test method is not designed to measure the autoignition temperature of materials which are solids or liquids at the test temperature (for example, wood, paper, cotton, plastics, and high-boiling point chemicals). Such materials will thermally degrade in the flask and the accumulated degradation products may ignite.
5.6 This test method can be used, with appropriate modifications, for chemicals that are gaseous at atmospheric temperature and pressure.
5.7 This test method was developed primarily for liquid chemicals but has been employed to test readily vaporized solids. Responsibility for extension of this test method to solids of unknown thermal stability, boiling point, or degradation characteristics rests with the operator.
SCOPE
1.1 This test method covers the determination of hot- and cool-flame autoignition temperatures of a liquid chemical in air at atmospheric pressure in a uniformly heated vessel.
Note 1: Within certain limitations, this test method can also be used to determine the autoignition temperature of solid chemicals which readily melt and vaporize at temperatures below the test temperature and for chemicals that are gaseous at atmospheric pressure and temperature.
Note 2: After a round robin study, Test Method D2155 was discontinued, and replaced by Test Method E659 in 1978. See also Appendix X2.
1.2 This standard 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 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.
1.3 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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SIGNIFICANCE AND USE
5.1 The aniline point (or mixed aniline point) is useful as an aid in the characterization of pure hydrocarbons and in the analysis of hydrocarbon mixtures. Aromatic hydrocarbons exhibit the lowest, and paraffins the highest values. Cycloparaffins and olefins exhibit values that lie between those for paraffins and aromatics. In homologous series the aniline points increase with increasing molecular weight. Although it occasionally is used in combination with other physical properties in correlative methods for hydrocarbon analysis, the aniline point is most often used to provide an estimate of the aromatic hydrocarbon content of mixtures.
SCOPE
1.1 These test methods cover the determination of the aniline point of petroleum products and hydrocarbon solvents. Test Method A is suitable for transparent samples with an initial boiling point above room temperature and where the aniline point is below the bubble point and above the solidification point of the aniline-sample mixture. Test Method B, a thin-film method, is suitable for samples too dark for testing by Test Method A. Test Methods C and D are for samples that may vaporize appreciably at the aniline point. Test Method D is particularly suitable where only small quantities of sample are available. Test Method E describes a procedure using an automatic apparatus suitable for the range covered by Test Methods A and B.
1.2 These test methods also cover the determination of the mixed aniline point of petroleum products and hydrocarbon solvents having aniline points below the temperature at which aniline will crystallize from the aniline-sample mixture.
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 WARNING—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use caution when handling mercury and mercury-containing products. See the applicable product Safety Data Sheet (SDS) for additional information. The potential exists that selling mercury or mercury-containing products, or both, is prohibited by local or national law. Users must determine legality of sales in their location.
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 warning statements are given in Section 7.
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 Determining the type and amount of hydrocarbon impurities remaining from the manufacture of toluene, mixed xylenes, p-xylene, o-xylene, ethylbenzene, benzene, and styrene used as chemical intermediates and solvents is often required. This test method is suitable for setting specifications and for use as an internal quality control tool where these products are produced or are used. Typical impurities are: alkanes containing 1 to 10 carbons atoms, benzene, toluene, ethylbenzene (EB), xylenes, and aromatic hydrocarbons containing nine carbon atoms or more.
5.2 This method may not detect all components and there may be unknown components that would be assigned inappropriate correction factors and thus, the results may not be absolute.
SCOPE
1.1 This test method covers the determination of total nonaromatic hydrocarbons and monocyclic aromatic hydrocarbons in benzene, toluene, ethylbenzene, p-xylene, o-xylene, styrene and mixed xylenes by gas chromatography. The purity of benzene, toluene, ethylbenzene, p-xylene, o-xylene, styrene and mixed xylenes is also calculated. Similar test methods, using the internal standard calibration technique and the external standard calibration technique, are Test Methods D2360, D5060, D5135, and D5917 respectively.
1.2 The limit of detection (LOD) is 0.0002 mass % and limit of quantitation (LOQ) is 0.0006 mass % for impurities in toluene, mixed xylenes, p-xylene, o-xylene, ethylbenzene, benzene, and styrene.
1.3 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
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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SIGNIFICANCE AND USE
5.1 This test method is useful for benzene purity on the basis of impurities normally present in benzene and may be used for final product inspections and process control.
5.2 This test method will detect the following impurities: toluene, methylcyclopentane, n-hexane, 2-methylhexane, cyclohexane, cyclopentane, 2-methylpentane, 2,3-dimethylpentane, 3-methylhexane, n-heptane, methylcyclohexane, ethylcyclopentane, 2,4-dimethylhexane, trimethylpentane, and others where specific impurity standards are available. Absolute purity cannot be accurately determined if unknown impurities are present.
SCOPE
1.1 This test method covers the determination of specific impurities in, and the purity of benzene for cyclohexane feedstock by gas chromatography.
1.2 This test method has been found applicable to benzene in the range from 99 % to 100 % purity and to impurities at concentrations of 2 mg/kg to 10 000 mg/kg. The limit of detection (LOD) is 2 mg/kg for an impurity and the limit of quantitation (LOQ) is 6 mg/kg for an impurity.
1.3 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
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. For specific hazard statements, see 7.2 and 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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SIGNIFICANCE AND USE
5.1 The total fluorine, chlorine, and sulfur contained in aromatic hydrocarbon matrices can contribute to emissions, be harmful to many catalytic chemical processes, and lead to corrosion. This test method can be used to determine total sulfur and halogens in aromatic hydrocarbons and their mixtures. The results can be used for compliance determinations when acceptable to a regulatory authority using performance based criteria.
SCOPE
1.1 This test method covers the individual determination of total fluorine, chlorine, and sulfur in aromatic hydrocarbons and their mixtures. Samples containing 0.10 mg/kg to 10 mg/kg of each element can be analyzed.
1.2 This method can be applied to sample concentrations outside the range of the scope by dilution of the sample in an appropriate solvent to bring the total concentrations of fluorine, chlorine, and sulfur within the range covered by the test method. However, it is the responsibility of the analyst to verify the solubility of the sample in the solvent and that the diluted sample results conform to the precision and accuracy of the method.
1.2.1 Special considerations must be made in order to attain detection limits below 1.0 mg/kg in a sample. The instrument must be clean and properly maintained to address potential sources of contamination, or carryover, or both. Multiple sequential injections shall be completed until a stable background is attained. A stable background is considered to be achieved when the analysis of a minimum of three consecutive system blanks have area counts equal to or less than 5 % RSD for the anions of interest.
1.3 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
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. See Section 9.
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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