This specification covers forged alloy steel lifting components and welded coupling and master links for Grade 80 and Grade 100 alloy chain slings. The steel materials shall be melt processed either by electric process or oxygen blown process. The steel shall be fully killed and shall conform to the required austenitic grain size. Product analysis shall be performed on and the steel specimens shall conform to the required chemical compositions of nickel, chromium, molybdenum, phosphorus and sulfur. Proof tests shall be performed and the materials shall conform to the required values of working load and breaking force. Deformation test, breaking force test and fatigue test shall be performed on the steel materials.1.1 This specification covers the requirements for forged alloy steel lifting components and welded coupling and master links for Grade 80 and Grade 100 alloy chain slings as described in Specification A906/A906M.1.2 Two grades of components and welded links are covered:1.2.1 Grade 80.1.2.2 Grade 100.1.3 This specification is a performance standard. Other standards apply to use of these products. Some of these standards are: OSHA 1910.184, ASME B30.9, and ASME B30.10.1.4 The values stated in either inch-pound units or SI units are to be regarded separately as standard. Within the text, the SI units are shown in brackets. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.1.5 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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4.1 This guide attempts to detail specific areas of concern regarding the attachment of geomembranes to structures. Components of the geomembrane attachment are addressed as to the type and use of each component.4.2 Although this guide does not address all aspects of geomembrane attachments, the user of this guide may note important objectives and design issues of each component of the geomembrane. All these objectives and design issues may or may not be required to obtain an appropriate geomembrane attachment. By describing these areas of concern, it is hoped that the user of this guide will be able to design geomembrane attachments, develop specifications or construct geomembrane attachments, or both, which fulfill the requirements of its design intent.1.1 This guide covers procedures that can be employed to mechanically attach fabricated geomembranes to structures, pipes, etc.1.2 This guide does not address all problems or situations a geomembrane installer or design engineer may face in the attachment of geomembranes to structures, pipes, etc. The sole purpose of this standard guide is to point out typical problems with geomembrane attachments and clearly state objectives of each component of the geomembrane attachment(s).1.3 This guide has been generated for geomembrane application(s); however, a geomembrane installer or design engineer, or both, may find portions of this guide applicable to other geosynthetics.1.4 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This specification covers coal tar adhesive with or without polymer modification suitable for brush, spray, squeegee and trowel application to coal tar built up and coal tar modified bitumen membrane roofings and flashings. The adhesive shall be classified as: Type I and Type II. Coal tar adhesive shall consist of a processed coal tar base, volatile solvents, mineral stabilizers, with or without polymer modifiers excluding asbestos, mixed to a smooth consistency. The following test methods shall be performed to conform with the requirements of the material: nonvolatile matter; water; ash; lap shear strength; and peel strength.1.1 This specification covers coal tar adhesive with or without polymer modification suitable for brush, spray, squeegee, and trowel application to coal tar built-up and coal tar modified bitumen membrane roofings and flashings.1.2 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in nonconformance with the 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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4.1 This test method is designed to determine the water content of various rubber accelerators. Since 2-mercaptobenzothiazole sulfenamide is hydrolytically unstable, the residual water content is an important characteristic.1.1 This test method covers a procedure for the determination of water in 2-mercaptobenzothiazole sulfenamide accelerators by a Karl Fischer coulometric titration.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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This specification covers pads of repositionable, colored, note paper. Each sheet has a strip of pressure-sensitive adhesive on the back side. A hand-operated steel roller shall be used in the manufacture of the pads and a cylindrical mandrel shall be used for flagging test of the pads. A minimum average of determined sheets of paper shall be assembled in the form of a pad. No individual pad shall contain less than a certain number of sheets. The pad of paper and a backing sheet shall be securely fastened together by means of the repositionable, pressure-sensitive adhesive coating. The paper to be used in the manufacture of the pad shall be determined by its basis weight and thickness. In order to determine the sheets' overall performance, the following properties shall be tested: writing quality, sheet removal, multiple sheet lift, fiber pull, initial flagging, and repositionable flagging. The sheets of pad paper shall be clean and free from dirt, foreign matter, holes, tears, wrinkles, and other defects which might affect appearance or serviceability. The sheets shall be uniform with respect to color and formation. Pads shall be square cut with smooth, clean edges.1.1 This specification covers pads of repositionable, colored, note paper. Each sheet has a strip of pressure-sensitive adhesive on the back side.1.2 The values stated in either SI or inch-pound units are to be regarded separately as standard. The values stated in each system are not exact equivalents; therefore, each system must be used independently, without combining values in any way.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 test method covers the determination of gross leaks in flexible packaging containing a headspace gas by bubble emission. A vacuum chamber shall be any transparent container capable of withstanding approximately one atmosphere pressure differential, fitted with a vacuum-tight cover. A vacuum gage, an inlet tube from a source of vacuum, and an outlet tube to the atmosphere shall be connected to the chamber cover. Use an immersion fluid which does not degrade the package being tested. The test sample and test fluid shall be at equilibrium with normal room temperature. The procedures for testing are presented in details.1.1 This test method covers the determination of gross leaks in flexible packaging containing a headspace gas. Test sensitivity is limited to 1 × 10−5 atm cm3/s (1 × 10−6 Pa m3/s) or even less sensitive as indicated in a recent interlaboratory test (reported in Section 12).1.2 Small leaks may not be detected by this procedure. Viscoelastic effects on the products, or entrapped air, become significant and prevent passage through small openings. Positive pressure inside the pouch after the vacuum is drawn may force the product to plug small leaks. The size of the leak that can be detected is dependent upon the products contained, the nature of the packaging material, and the test parameters selected.1.3 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered 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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This guide assists potential users in understanding the issues related to the accuracy of non-contacting strain measurement systems and to provide a common framework for quantitative comparison of optical systems. The output from a non-contacting optical strain and deformation measurement system is generally divided into optical data and image analysis data. Each non-contacting optical strain measurement system must be evaluated to determine reliable estimates for the accuracy of the resulting Derived Data.1.1 The purpose of this document is to assist potential users in understanding the issues related to the accuracy of non-contacting strain measurement systems and to provide a common framework for quantitative comparison of optical systems. The output from a non-contacting optical strain and deformation measurement system is generally divided into optical data and image analysis data. Optical data contains information related to specimen strains and the image analysis process converts the encoded optical information into strain data. The enclosed document describes potential sources of error in the strain data and describes general methods for quantifying the error and estimating the accuracy of the measurements when applying non-contacting methods to the study of events for which the optical integration time is much smaller than the inverse of the maximum temporal frequency in the encoded data (that is, events that can be regarded as static during the integration time). A brief application of the approach, along with specific examples defining the various terms, is given in the Appendix.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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5.1 Environmental tobacco smoke consists of both vapor- and particle-phase components. Due to the nature of vapor and particulate phases, they rarely correlate well, and an accurate assessment of ETS levels in indoor air requires determining good tracers of both phases. Among the attributes of an ideal ETS tracer, one critical characteristic is that the tracer should “remain in a fairly consistent ratio to the individual contaminant of interest or category of contaminants of interest (for example, suspended particulates) under a range of environmental conditions...” (2). The UVPM and FPM fulfill this requirement, staying in a constant ratio to RSP from tobacco smoke under a variety of ventilation conditions and sampling durations. Solanesol (a C45 isoprenoid alcohol specific to tobacco), determined in accordance with Test Method D6271, is an ETS tracer or marker that also meets this requirement. In contrast, nicotine (a component of the ETS vapor phase) does not remain in a consistent ratio to ETS-PM (3). 5.2 To be able to quantify the contribution of ETS to RSP is important because RSP is not specific to tobacco smoke. The RSP are a necessary indicator of overall air quality; the Occupational Safety and Health Administration (OSHA) has previously set a PEL (permissible exposure level) for respirable dust in the workplace of 5000 μg/m3. However, the RSP emanate from numerous sources (4) and have been shown to be an inappropriate tracer of ETS (5-13). In the test methods described herein, UVPM and FPM are used as more selective markers to estimate more accurately the contribution of ETS to RSP (5-7, 9-18). Of the available ETS particulate phase markers (UVPM, FPM, and solanesol), all are currently used and relied upon in investigations of indoor air quality, although UVPM and FPM can overestimate the contribution of tobacco smoke to RSP due to potential interference from nontobacco combustion sources. Solanesol, because it is tobacco-specific and ETS particle phase-specific, may be the best indicator of the ETS particulate phase contribution to RSP (9-13, 19-21). Refer to Test Method D6271 for the protocol on determining solanesol. 1.1 These test methods pertain to the sampling/analysis of respirable suspended particles (RSP) and the estimation of the RSP fraction attributable to environmental tobacco smoke (ETS). These test methods are based on collection of total RSP on a membrane filter, extracting the collected material in methanol, and measuring total ultraviolet absorbance or fluorescence, or both, of this extract. The corresponding methods of estimation are termed ultraviolet particulate matter (UVPM) and fluorescent particulate matter (FPM), respectively. 1.2 These test methods are compatible with, but do not require the determination of solanesol, which is also used to estimate the contribution of ETS to RSP (see Test Method D6271). 1.3 The sampling components consist of a preweighed, 1.0-μm pore size polytetrafluoroethylene (PTFE) membrane filter in a filter cassette connected on the inlet end to a particle size separating device and, on the outlet end, to a sampling pump. These test methods are applicable to personal and area sampling. 1.4 These test methods are limited in sample duration only by the capacity of the membrane filter (about 2000 μg). These test methods have been evaluated up to a 24-h sample duration with a minimum sample duration of at least 1 h. 1.5 Limits of detection (LOD) and quantitation (LOQ) for the UVPM test method at a sampling rate of 2 L/min are, respectively, 2.5 μg/m3 and 8.3 μg/m3 for a 1-h sample duration and 0.3 μg/m3 and 1.0 μg/m 3 for an 8-h sample duration. The LOD and LOQ for the FPM test method at a sampling rate of 2 L/min are, respectively, 1.4 μg/m 3 and 4.7 μg/m3 for a 1-h sample duration and 0.2 μg/m3 and 0.6 μg/m3 for an 8-h sample duration. 1.6 Units—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 and health practices and determine the applicability of regulatory limitations prior to use. Specific precautionary information is given in 13.6. 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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5.1 The method of excitation simulates, to a practical degree, the operation of a magnetic core in a self-saturating magnetic amplifier. The properties measured are related to the quality of performance of the cores in magnetic amplifiers and are useful for the specification of materials for such cores.1.1 This test method covers the determination of the magnetic performance of fully processed cores for magnetic amplifier-type applications.1.2 Tests may be conducted at excitation frequencies of 60 Hz, 400 Hz, 1600 Hz, or higher frequencies.1.3 Permissible core sizes for this test method are limited only by the available power supplies and the range and sensitivity of the instrumentation.1.4 At specified values of full-wave sinusoidal-current excitation, Hmax, this test method provides procedures of determining the corresponding value of maximum induction, Bmax.1.5 At specified values of half-wave sinusoidal-current excitation, this test method provides procedures for determining the residual induction, Br.1.6 At increased specified values of half-wave sinusoidal-current excitation, this test method provides procedures for determining the dc reverse biasing magnetic field strength, H1, required to reset the induction in the core material past Br to a value where the total induction change, ΔB1, becomes approximately one third of the induction change, 2 Bp. It also provides procedures for determining the additional dc reset magnetic field strength, ΔH, which, combined with H1, is the value required to reset the induction in the core material past Br to a value where the total induction change, ΔB2, becomes approximately two thirds of the induction change 2 Bp.1.7 This test method specifies procedures for determining core gain from the corresponding biasing and induction changes, ΔH and ΔB.1.8 This test method covers test procedures and requirements for evaluation of finished cores which are to be used in magnetic-amplifier-type applications. It is not a test for basic-material magnetic properties.1.9 This test method shall be used in conjunction with Practice A34/A34M.1.10 Explanations of symbols and abbreviated definitions appear in the text of this test method. The official symbols and definitions are listed in Terminology A340.1.11 The values and equations stated in customary (cgs-emu and inch-pound) or SI units are to be regarded separately as standard. Within this test method, SI units are shown in brackets. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in nonconformance with this test method.1.12 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.1.13 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 IgE-mediated allergic reactions to protein allergens in Hevea natural rubber latex derived from the Hevea brasiliensis tree emerged in the 1990s as a concern with occasional allergic manifestations. Symptoms encompassing hives, uriticaria, rhinitis, asthma and anaphylaxis have all been reported in latex allergic individuals exposed to products derived from Hevea natural rubber latex.5.2 Since no safe level of Hevea latex allergen exposure is known, avoidance is the primary mode of treating latex allergy.5.3 As a result of investigations conducted by many scientists across the world, fourteen latex allergens have so far been identified and categorized by the Allergen Nomenclature Sub-Committee of the International Union of Immunological Societies (IUIS) as Hev b 1 to Hev b 13 (Table 1) (see Specification D1193). Reported sensitization rates for these allergenic Hev b proteins vary among the many reports as a result of differences in the study populations, IgE antibody assay methods and the quality of the Hev b allergens used as calibrators and quality control reagents in the analysis. Most studies, however, agree that Hev b 1 and Hev b 3 are important allergens for individuals (for example, children with spina bifida) who are exposed through mucosal contact as a result of multiple surgeries or latex catheter use for an extended period of time. Additionally, investigators performing sensitization studies also agree that Hev b 5 and Hev b 6.02 are important allergens that may elicit sensitization in genetically-predisposed individuals who are exposed to Hevea natural rubber latex (2-4). On the basis of these clinical studies, assays for these four allergenic proteins (that is, Hev b 1, Hev b 3, Hev b 5 and Hev b 6.02) have been developed and they are thus the subject of this standard. Adoption of immunoenzymetric assay reagents and standard proteins needed to quantify other latex allergens (other than Hev b 1, 3, 5, and 6.02) in extracts of Hevea natural rubber latex products will require separate documentation and validation.(A) PR = pathogenesis-related.5.3.1 From the historical context, a number of assays have been developed to quantify the level of protein, antigen and allergen in Hevea natural rubber latex containing products (see Practices D4483 and D4678).5.3.2 The modified Lowry assay for total protein, Test Method D5712, was the first assay of this type. It assesses the level of total protein as an indirect indicator of allergenicity of latex-containing products. This assay does not discriminate between the allergenic and non-allergenic proteins.5.3.3 The second assay to be developed involved the use of human latex-specific IgE antibody in a competitive inhibition immunoassay format to estimate the overall allergenic potency of a Hevea natural rubber product extract (5, 6). The extract is incubated with human serum containing latex-specific IgE antibody and then this mixture is incubated with a solid phase latex allergosorbent. Latex allergenic proteins, if they are present, bind to the latex-specific IgE antibody in solution and they thus inhibit IgE antibody binding onto the latex allergosorbent. Allergosorbent bound IgE is then quantified and the extent of competitive inhibition of IgE binding is a measure of latex allergens. While this assay provides an estimate of the allergenicity or level of Hevea natural rubber allergens extractable from a product, difficulty in procuring reproducible lots of latex specific IgE containing human serum has precluded widespread use of this assay. For this reason, this assay has not been put forth as an ASTM standard.5.3.4 A third assay design is similar to the human IgE based competitive inhibition immunoassay, but it employs rabbit antiserum instead of human serum containing IgE anti-latex. The competitive inhibition enzyme linked immunosorbent assay (ELISA) has been adopted as Test Method D6499. It measures latex proteins that elicit immune responses, but it cannot distinguish between latex allergens (IgE inducing) from non-allergenic antigens (non-IgE inducing).5.3.5 The most recent assay, which is the subject of this standard, is the two-site immunoenzymetric assay (IEMA) which uses an insolubilized capture antibody to bind one of Hev b allergenic proteins from a latex product extract, and a second enzyme labeled detection antibody to detect bound allergens. Optical density responses are interpolated from reference curves constructed with known allergens. The performance characteristics of the reagents used in immunoenzymetric assays for Hev b 1, 3, 5 and 6.02 were investigated in the international collaborative study associated with the development of this standard and results are provided in Sections 15 through 17.1.1 This test method covers an immunological method known as an immunoenzymetric assay to quantify the amount of 4 principal Hevea brasiliensis [Hev b] allergenic proteins [Hev b 1, Hev b 3, Hev b 5 and Hev b 6.02] in Hevea natural rubber and its products2 derived from latex using monoclonal antibodies specific for epitopes on these proteins. Since these assays quantify the levels of only 4 of the known 14 officially acknowledged allergens potentially present in Hevea natural rubber latex containing products, the sum of the four allergen levels shall be viewed as an indicator of the allergen burden and not as a measure of the total allergen content that can be released from the product.1.2 For the purpose of this test method, the range of allergenic protein will be measured in terms of nanogram to microgram quantities per gram or unit surface area of a Hevea natural rubber containing product.1.3 The test method is not designed to evaluate the potential of Hevea natural rubber containing materials to induce or elicit Type I (IgE-mediated) hypersensitivity reactions.1.4 This test method should be used under controlled laboratory conditions to detect and quantify the level of 4 allergenic proteins found in Hevea natural rubber containing products. It should not be used to describe, appraise or assess the hazard or risk of these Hevea natural rubber containing materials or products under actual in use conditions.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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