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5.1 Abrasion resistance is a performance factor of paramount importance for many rubber products, such as tires, conveyor belts, power transmission belts, hoses, footwear, and floor covering. A test capable of measuring resistance to abrasion of rubber, including uniformity of wear behavior under abrasive/frictional service conditions is therefore highly desirable.5.2 This test method may be used to estimate the relative abrasion resistance of different rubbers. Since conditions of abrasive wear in service are complex and vary widely, no direct correlation between this accelerated test and actual performance can be assumed.5.3 This test method is suitable for comparative testing, quality control, specification compliance testing, referee purposes, and research and development work.1.1 This test method covers the measurement of abrasion resistance of rubbers (vulcanized thermoset rubbers and thermoplastic elastomers) that are subject to abrasive/frictional wear in actual service. The abrasion resistance is measured by simultaneously moving 4 test pieces across the surface of abrasive sheets in a soft lissajous movement, and is expressed as volume loss in cubic millimeters where a smaller number indicates better abrasion resistance.1.2 Test results obtained by this test method shall not be assumed to represent the wear behavior of rubber products in actual service.1.3 Results obtained by this test have shown to be similar to those obtained using Test Method D5963 and ISO 4649.1.4 The values stated in SI units are to be regarded as the standard. The values in parentheses are for information only.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 A knowledge of the composition of hydrocarbon refinery streams is useful for process control and quality assurance.5.2 Aromatics in gasoline are soon to be limited by federal mandate. This test method can be used to provide such information.1.1 This test method covers the determination of paraffins, naphthenes, and aromatics by carbon number in low olefinic hydrocarbon streams having final boiling points of 200 °C or less. Hydrocarbons with boiling points greater than 200 °C and less than 270 °C are reported as a single group. Olefins, if present, are hydrogenated and the resultant saturates are included in the paraffin and naphthene distribution. Aromatics boiling at C9 and above are reported as a single aromatic group.1.2 This test method is not intended to determine individual components except for benzene and toluene that are the only C6 and C7 aromatics, respectively, and cyclopentane that is the only C5 naphthene. The lower limit of detection for a single hydrocarbon component or group is 0.05 % by mass.1.3 This test method is applicable to hydrocarbon mixtures including virgin, catalytically converted, thermally converted, alkylated and blended naphtha.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4.1 The abbreviation for SI unit “coulomb” is “C”.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 8 and Table 1.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Multi-axis force measuring platforms are used to measure the ground reaction forces produced at the interface between a subject's foot or shoe and the supporting ground surface. These platforms are used in various settings ranging from research laboratories to healthcare facilities. The use of force platforms has become particularly important in gait analysis where clinical evaluations have become a billable clinical service.5.2 Of particular importance is the application of force platforms in the treatment of cerebral palsy (CP) (1, 2).3 An estimated 8000 to 10 000 infants born each year will develop CP (3) while today’s affected population is over 764 000 patients (4). Quantitative gait analysis, using force platforms and motion capture systems, provides a valuable tool in evaluating the pathomechanics of children with CP. This type of mechanical evaluation provides a quantitative basis for treating neuromuscular conditions. In other words, surgical decisions are in part guided by information gained from the use of force platform measurements (5, 6).5.3 Another application is treatment of spina bifida. According to the Gait and Clinical Movement Analysis Society (GCMAS) (7), an instrumented gait analysis is the standard of expert care for children with gait abnormalities secondary to spina bifida. The main objective of diagnostic gait analysis is to define the pathological consequences of neural tube defects as they relate to gait. The use of instrumented gait analysis allows physicians to determine which surgical or non-surgical interventions would provide the best outcome.5.4 More recently, force platforms have been used for pre- and post-surgical evaluation of TKA (total knee arthroplasty) and THA (total hip arthroplasty) patients. Such data provides an objective measure of the mechanical outcome of the surgical procedure.5.5 In addition to the clinical applications there are numerous medical and human performance research activities which rely on accurate measurement of ground reaction forces by using multi-axis force platform measurement instruments.5.6 As a standards organization, ASTM has historically provided excellent standards for the calibration of force transducers and force-measuring instrumentation. Force platforms, however, are different from force transducers. Force platforms typically provide a large active working surface, whereas force transducers provide more or less a single point of interaction with the load-applying environment. Moreover, force platforms typically provide six-axis measurements and are expected to be used in environments causing multi-axial loading.1.1 This standard recommends practices for performance verification of multi-axis force platforms commonly used for measuring ground reaction forces during gait, balance, and other activities.1.1.1 This standard provides a method to quantify the relationship between applied input force and force platform output signals across the manufacturer’s defined spatial working surface and specified force operating range.1.1.2 This standard provides definitions of the critical parameters necessary to quantify the behavior of multi-axis force measuring platforms and the methods to measure the parameters.1.1.3 This standard presents methods for the quantification of spatially distributed errors and absolute measuring performance of the force platform at discrete spatial intervals and discrete force levels on the working surface of the platform.1.1.4 This standard further defines certain important derived parameters, notably COP (center of pressure) and methods to quantify and report the measuring performance of such derived parameters at spatial intervals and force levels across the working range of the force platform.1.1.5 This standard defines the requirements for a report suitable to characterize the force platform’s performance and provide traceable documentation to be distributed by the manufacturer or calibration facility to the users of such platforms.1.1.6 Dynamic characteristics and applications where the force platform is incorporated in other equipment, such as instrumented treadmills and stairs, are beyond the scope of this standard.1.1.7 This standard is written for purposes of multi-axis force platform verification. However, the methods and procedures are applicable to calibration of force platforms by manufacturers.1.2 The values stated in SI units are to be regarded as the standard. Other metric and inch-pound values are regarded as equivalent when required.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 guide on the proper collection of emission and discharge wastes from glycol dehydrators is applicable to any natural gas industry and supplier that operates glycol dehydration units and that needs to identify which glycol units may have emissions above regulatory levels.The emission and discharge sampling methods discussed in this guide are not regulatory standards. Standard protocols have been developed by the Gas Research Institute (3) and other gas associations (4) and some state regulatory agencies such as the Louisiana Department of Environmental Quality (LDEQ) (5) and the Texas Natural Resource Conservation Commission (TNRCC) (6) are accepting these data. This guide is not intended to instruct the user on how to perform the sampling using these protocols, but to make the user aware of certain practical considerations generally associated with sampling these waste streams.1.1 Purpose This guide covers the proper collection of field emission and discharge data associated with glycol dehydration units used in the natural gas production, processing, transmission, storage, and distribution industries.1.2 Background:1.2.1 Increasing regulatory pressure has made emissions of benzene, toluene, ethylbenzene, and xylene isomers (collectively known as BTEX) and volatile organic compounds (VOCs) from the still vent of glycol dehydration units a major concern of the natural gas industry. The Clean Air Act Amendments (CAAA) of 1990 have been the impetus for air toxics regulations, and several states are regulating or are considering regulating emissions from glycol units (1). Liquid and solid waste discharges are exempt from Subtitle C (hazardous waste) regulation under the Resource Conservation and Recovery Act (RCRA), but may be regulated in the future (2).1.2.2 Measurement of the waste streams from dehydrators is important to determine which units may have emissions above levels of regulatory concern. Measurements of air emissions from glycol dehydration units have been made from a variety of sampling points using different sampling protocols and analytical techniques since no standard methods have been developed by the United States Environmental Protection Agency (USEPA) or state regulatory agencies. Standard sampling methods do not exist for the liquid and solid waste streams since they are exempt from RCRA Subtitle C. The lack of standard protocols has meant that variations of this approach can result in very different emissions measurements (3).1.2.3 Providing guidance on the collection of field emission and discharge data will allow the natural gas industry to quantify emissions and apply appropriate controls to comply with regulations.1.3 Summary--This guide has several parts and an annex. Section 1 is . Section 2 is Terminology that has definitions of terms commonly used with relation to glycol dehydration units in the natural gas industry. Section 3 is of this guide. Section 4 is a process description of glycol dehydration units. Section 5 is a discussion of the waste streams associated with glycol dehydrators. Section 6 presents the Approaches for Collecting Air Emission Data, while Sections 7 and 8 present the approaches for collecting liquid and solid waste discharge data, respectively. The annex includes a standard operating procedure (SOP) for the rich/lean glycol sampling method discussed in this guide.1.4 The values stated in either inch-pound or SI units are to be regarded separately as the standard. The values given in parentheses are for information only.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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1.1 This specification covers bridge bearings that consist of an unconfined polyether urethane rotational element subjected to compression loads, along with a resisting mechanism to transmit shear and/or tension loads through the bearing. For expansion and/or contraction applications, an additional stainless steel flat surface slides against a carbon steel plate faced with sheet polytetrafluoroethylene (PTFE). The function of the bearing is to transfer loads and to accommodate any relative movement, including rotation between a bridge superstructure and its supporting structure, or both.1.2 The requirements stated in this specification are the minimums necessary for the manufacture of quality bearing devices. It may be necessary to increase these minimum values due to other design or construction conditions.1.3 The values stated in inch-pound 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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5.1 This test method provides for the following measurements and evaluations:5.1.1 Movement capacity of the perimeter fire barrier.5.1.2 Loadbearing capacity of the perimeter joint protection is optional.5.1.3 Ability of the perimeter fire barrier to resist the passage of flames and hot gases.5.1.4 Transmission of heat through the perimeter fire barrier.5.2 This test method does not provide the following:5.2.1 Evaluation of the degree to which the perimeter fire barrier contributes to the fire hazard by generation of smoke, toxic gases, or other products of combustion,5.2.2 Measurement of the degree of control or limitation of the passage of smoke or products of combustion through the perimeter fire barrier,NOTE 1: This test method does not measure the quantity of smoke or hot gases through the floor assembly, the wall assembly, or the perimeter joint protection.5.2.3 Measurement of flame spread over the surface of the perimeter fire barrier,NOTE 2: The information in 5.2.1 through 5.2.3 are determined by other suitable fire test methods. For example, Test Method E84 is used to determine 5.2.3.5.2.4 Durability of the test specimen under actual service conditions, including the effects of cycled temperature,5.2.5 Effects of a load on the movement cycling of the perimeter fire barrier established by this test method,5.2.6 Rotational, vertical, and horizontal shear capabilities of the test specimen,5.2.7 Any other attributes of the test specimen, such as wear resistance, chemical resistance, air infiltration, water-tightness, and so forth, and5.2.8 A measurement of the capability of the test specimen to resist:5.2.8.1 Flame propagation over the exterior faces of the test specimen,5.2.8.2 Spread of flame within the combustible core component of the exterior wall assembly from one story to the next,NOTE 3: Some exterior wall assemblies are made from sandwich panels, which use EPS foam or other similar materials that are combustible.5.2.8.3 Spread of flame over the interior surface (room side) of the test specimen from one story to the next, andNOTE 4: While it is a failure to have fire on the interior surface of the observation room, this test method does not provide a measurement of that flame spread.5.2.8.4 Lateral spread of flame from the compartment of fire origin to adjacent spaces.NOTE 5: The exterior wall assembly, floor assembly, and perimeter joint protection are individual components. The capabilities of individual components are not part of this specific test method's Conditions of Compliance.5.3 In this test method, the test specimens are subjected to one or more specific test conditions. When different test conditions are substituted or the end-use conditions are changed, it is not always possible by, or from, this test method to predict changes to the characteristics measured.5.4 This test method is not intended to be used as the only test method in the selection of a perimeter fire barrier. It is not intended as a specification for all attributes required by a perimeter fire barrier, or any of its individual components, in order for a perimeter fire barrier to be used in a particular application.1.1 This test method measures the performance of the perimeter fire barrier and its ability to maintain a seal to prevent fire spread during the deflection and deformation of the exterior wall assembly and floor assembly during the fire test, while resisting fire exposure from an interior compartment fire as well as from the flame plume emitted from the window burner below. The end point of the fire-resistance test is the period of time elapsing before the first condition of compliance is reached as the perimeter fire barrier is subjected to a time-temperature fire exposure.1.2 The fire exposure conditions used are those specified by this test method for the first 30 min of exposure and then conform to the Test Methods E119 time-temperature curve for the remainder of the test in the test room.1.3 This test method specifies the heating conditions, methods of test, and criteria for evaluation of the ability of a perimeter fire barrier to maintain the fire resistance where a floor and exterior wall assembly are juxtaposed to a perimeter joint.1.4 Test results establish the performance of perimeter fire barriers during the fire-exposure period and shall not be construed as having determined the suitability of perimeter fire barriers for use after that exposure.1.5 This test method does not provide quantitative information about the perimeter fire barrier relative to the rate of leakage of smoke or gases or both. While it requires that such phenomena be noted and reported when describing the general behavior of perimeter fire barrier during the fire-resistance test, such phenomena are not part of the conditions of compliance.1.6 Potentially important factors and fire characteristics not addressed by this test method include, but are not limited to:1.6.1 The performance of the perimeter fire barrier constructed with components other than those tested, and1.6.2 The cyclic movement capabilities of perimeter fire barriers other than the cycling conditions tested.1.7 This test method is used to measure and describe the response of materials, products or assemblies to heat and flame under controlled conditions but does not by itself incorporate all factors required for the fire-hazard or fire-risk assessment of the materials, products, or assemblies under actual fire conditions.1.8 Units—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.1.9 The text of this test method references notes and footnotes which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered as requirements of the standard.1.10 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.1.11 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 The degree of deacetylation of chitosan, as well at the molar mass and molar mass distribution, determines the functionality of chitosan in an application. For instance, functional and biological effects are highly dependent upon the composition and molar mass of the polymer.4.2 This test method describes procedures for measurement of molar mass of chitosan chlorides and glutamates, and chitosan base, although it in principle applies to any chitosan salt. The measured molar mass is that for chitosan acetate, since the mobile phase contains acetate as counter ion. This value can further be converted into the corresponding molar mass for the chitosan as a base, or the parent salt form (chloride or glutamate).4.3 Light scattering is one of very few methods available for the determination of absolute molar mass and structure, and it is applicable over the broadest range of molar masses of any method. Combining light scattering detection with size exclusion chromatography (SEC), which sorts molecules according to size, gives the ability to analyze polydisperse samples, as well as obtaining information on branching and molecular conformation. This means that both the number-average and mass-average values for molar mass and size may be obtained for most samples. Furthermore, one has the ability to calculate the distributions of the molar masses and sizes.4.4 Multi-angle laser light scattering (MALS) is a technique where measurements of scattered light are made simultaneously over a range of different angles. MALS detection can be used to obtain information on molecular size, since this parameter is determined by the angular variation of the scattered light. Molar mass may in principle be determined by detecting scattered light at a single low angle (LALLS). However, advantages with MALS as compared to LALLS are: (1) less noise at larger angles, (2) precision of measurements is improved by detecting at several angles, and (3) the ability to detect angular variation allows determination of size, branching, aggregation, and molecular conformation.4.5 Size exclusion chromatography uses columns, which are typically packed with polymer particles containing a network of uniform pores into which solute and solvent molecules can diffuse. While in the pores, molecules are effectively trapped and removed from the flow of the mobile phase. The average residence time in the pores depends upon the size of the solute molecules. Molecules that are larger than the average pore size of the packing are excluded and experience virtually no retention; these are eluted first, in the void volume of the column. Molecules, which may penetrate the pores will have a larger volume available for diffusion, they will be retained in the column for a time dependent upon their molecular size, with smaller molecules eluting after larger molecules.4.6 For polyelectrolytes, dialysis against the elution buffer has been suggested, in order to eliminate Donnan-type artifacts in the molar mass determination by light scattering (1, 2).5 However, in the present method, the size exclusion chromatography step preceding the light scatter detection is an efficient substitute for a dialysis step. The sample is separated on SEC columns with large excess of elution buffer for 30 to 40 min, and it is therefore in full equilibrium with the elution buffer when it reaches the MALS detector.1.1 This test method covers the determination of the molar mass of chitosan and chitosan salts intended for use in biomedical and pharmaceutical applications as well as in tissue engineered medical products (TEMPs) by size exclusion chromatography with multi-angle laser light scattering detection (SEC-MALS). A guide for the characterization of chitosan salts has been published as Guide F2103.1.2 Chitosan and chitosan salts used in TEMPs should be well characterized, including the molar mass and polydispersity (molar mass distribution) in order to ensure uniformity and correct functionality in the final product. This test method will assist end users in choosing the correct chitosan for their particular application. Chitosan may have utility as a scaffold or matrix material for TEMPs, in cell and tissue encapsulation applications, and in drug delivery formulations.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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4.1 The composition and sequential structure of alginate, as well as the molar mass and molar mass distribution, determines the functionality of alginate in an application. For instance, the gelling properties of an alginate are highly dependent upon the composition and molar mass of the polymer.4.2 Light scattering is one of very few methods available for the determination of absolute molar mass and structure, and it is applicable over the broadest range of molar masses of any method. Combining light scattering detection with size exclusion chromatography (SEC), which sorts molecules according to size, gives the ability to analyze polydisperse samples, as well as to obtain information on branching and molecular conformation. This means that both the number-average and mass-average values for molar mass and size may be obtained for most samples. Furthermore, one has the ability to calculate the distributions of the molar masses and sizes.4.3 Multi-angle laser light scattering (MALS) is a technique where measurements are made simultaneously over a range of different angles and used to determine the scattering at 0°, which directly relates to molecular weight. MALS detection can be used to obtain information on molecular size, since this parameter is determined by the angular variation of the scattered light. This can be related to branching, aggregation, and molecular conformation. Molar mass can also be determined by detecting scattered light at a single low angle (LALS) and assuming that this is not significantly different from the scattering at 0°.4.4 Size exclusion chromatography uses columns, which are typically packed with polymer particles containing a network of uniform pores into which solute and solvent molecules can diffuse. While in the pores, molecules are effectively trapped and removed from the flow of the mobile phase. The average residence time in the pores depends upon the size of the solute molecules. Molecules that are larger than the average pore size of the packing are excluded and experience virtually no retention; these are eluted first, in the void volume of the column. Molecules which penetrate the pores will have a larger volume available for diffusion; their retention will depend on their molecular size, with the smaller molecules eluting last.4.5 For polyelectrolytes, dialysis against the elution buffer has been suggested, in order to eliminate Donnan-type artifacts in the molar mass determination by light scattering (1, 2).6 However, in the present method, the size exclusion chromatography step preceding the light scatter detection is an efficient substitute for a dialysis step. The sample is separated on SEC columns with large excess of elution buffer for 30 to 40 min, and it is therefore in full equilibrium with the elution buffer when it reaches the MALS detector.1.1 This test method covers the determination of the molar mass (typically expressed as grams/mole) of sodium alginate intended for use in biomedical and pharmaceutical applications as well as in tissue-engineered medical products (TEMPs) by size exclusion chromatography with multi-angle laser light scattering detection (SEC-MALS). A guide for the characterization of alginate has been published as Guide F2064.1.2 Alginate used in TEMPs should be well characterized, including the molar mass and polydispersity (molar mass distribution) in order to ensure uniformity and correct functionality in the final product. This test method will assist end users in choosing the correct alginate for their particular application. Alginate may have utility as a scaffold or matrix material for TEMPs, in cell and tissue encapsulation applications, and in drug delivery formulations.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 and health practices and determine the applicability of regulatory limitations prior to use.

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5.1 Uranium hexafluoride used to produce nuclear-reactor fuel must meet certain criteria for its isotopic composition. This test method may be used to help determine if sample materials meet the criteria described in Specifications C787 and C996.1.1 This test method covers a quantitative test method applicable to determining the mass percent of uranium isotopes in uranium hexafluoride (UF6) samples. This method as described is for concentrations of 235U between 0.1 and 10 mass %, and 234U and 236U between 0.0001 and 0.1 mass %.1.2 This test method is for laboratory analysis by a gas mass spectrometer with a multi-collector.1.3 This standard complements Test Methods C761, the double-standard method for gas mass spectrometers using a single collector, by providing a method for spectrometers using a multi-collector.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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4.1 This classification is intended to encourage uniformity in reporting properties of MLS and Metal Layer gaskets, to provide a common language for communications between producers and users, and to guide engineers and designers in the application and construction of commercially available gaskets.(A) This classification may also be used to classify Single Layer Steel (SLS) Gaskets.(B) Refer to Specification A666 or Specification A109/A109M for Stainless Steel and Low Carbon Steel, respectively. Other metals not referenced in the table or not covered by Specification A666 or Specification A109/A109M must be defined by the producer/user (that is, H – High Temperature Alloy).(C) Refer to Practice D1418 for general information regarding rubber coating types and use Classification D2000 to define the physical properties of the rubber. This physical property information is typically specified on the gasket drawing or the customer specification, or both.(D) Coated side as specified on part drawing.4.2 Suffix Table 2 is provided to allow hardness designation for Active, Inactive, or Load Stoppers.4.2.1 If suffixes are not to be used, only the basic callout from Table 1 is required. If a suffix is used for 1 layer, it must be specified for all layers, even if a “0” is used. It cannot be assumed that hardnesses of like layers are the same; if used, all layers must be specified separately. The first layer specified must be indicated on the part drawing. To use a hardness call-out, at the end of the base callout leave a space followed by the “HR” suffix with a series of suffix numbers to specify the hardnesses for each layer.4.2.1.1 Example: ASTM F2325, A32ANBW11 HR252—Example from Table 1 modified to add hardness requirement for the three metal layers. Active layers 1 and 3 are designated to be the same, 1/4 hard steel. Stopper layer 2 is designated to be full hard steel.1.1 This classification covers a means for specifying Multi-Layer Steel (MLS) and other Metal Layer Gaskets for Transportation Applications by application and construction. These structures are composed of one or more steel or metal layers of material, which may have coatings or embossments. Commercial materials designated as composite or enveloped gaskets are excluded from this classification and are covered by Classification F868 and Practice F336, respectively.1.2 Since all of the properties that contribute to gasket performance are not included, use of this classification as a basis for selecting an MLS or Metal Layer gasket is limited.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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Plans for sampling and analysis of nuclear material are designed with two purposes in mind: the first is related to material accountability and the second to material specifications. For the accounting of special nuclear material, sampling and analysis plans should be established to determine the quantity of special nuclear material held in inventory, shipped between buyers and sellers, or discarded. Likewise, material specification requires the determination of the quantity of nuclear material present. Inevitably there is uncertainty associated with such measurements. This practice presents a tool for developing sampling plans that control the random error component of this uncertainty. Precision and accuracy statements are highly desirable, if not required, to qualify measurement methods. This practice relates to“ precision” that is generally a statement on the random error component of uncertainty. 1.1 This practice provides an aid in designing a sampling and analysis plan for the purpose of minimizing random error in the measurement of the amount of nuclear material in a lot consisting of several containers. The problem addressed is the selection of the number of containers to be sampled, the number of samples to be taken from each sampled container, and the number of aliquot analyses to be performed on each sample. 1.2 This practice provides examples for application as well as the necessary development for understanding the statistics involved. The uniqueness of most situations does not allow presentation of step-by-step procedures for designing sampling plans. It is recommended that a statistician experienced in materials sampling be consulted when developing such plans. 1.3 The values stated in SI units are to be regarded as the standard. 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 and health practices and determine the applicability of regulatory limitations prior to use.

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5.1 This specification sets forth minimum standard requirements for use in local codes and ordinances relating to public, multi-family, residential, and commercial outdoor play areas or zones and their environments.5.2 This specification does not have the effect of law, nor is it intended to supersede local codes and ordinances of a more restrictive nature.5.3 Playgrounds that intentionally incorporate water into the play area are exempt from this specification.1.1 This specification provides the recommended minimum requirements for denoting various types of fences/barriers for the protection of children's outdoor play spaces in public, commercial, and multi-family residential use locations. This specification excludes individual single family residential use play equipment locations. Interior fences located in a play area that has a perimeter fence established shall only have to comply with the latch height requirement indicated in 7.6.2.1.2 This specification provides for the safety of occupants in play areas or zones as it pertains to vehicular intrusion as well as other participant intrusion, and for children containment or entry/exit. This specification has the intent to also keep children inside a predetermined area in an effort to enhance supervision; to keep children from running out of the area into water and other hazards; to minimize the likelihood of facial lacerations on low gate and fence hardware; to minimize the likelihood of abduction; and to restrict access to railroads, highways, roads, and other such hazards.1.3 This specification does not choose the product components for the fence system, the choice of which should be made by the operators of the play space and their specification writers or drafters based upon their determination of the merits of the products that could be used.1.4 The values stated in inch-pound units are to be regarded as standard. The SI values given in parentheses are for information only.1.5 This specification does not purport to address the aspect of safety within a play area or zone. It is the responsibility of the user of this specification to establish appropriate safety practices as related to the play area and determine the applicability of regulatory requirements 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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4.1 The breaking strength and elongation of the strand are determined by one or more tensile tests in which fracture of the specimen ideally occurs in the free span.4.2 Mechanical properties of the strand will be negatively affected if proper care is not taken to prevent damage such as severe bending, abrasion, or nicking of the strand during sampling.4.3 Premature failure of the test specimens may result if there is appreciable notching, cutting, or bending of the specimen by the gripping devices of the testing machine.4.4 Errors in testing will result if the wires constituting the strand are not loaded uniformly.4.5 The mechanical properties of the strand will be materially affected by excessive heating during test specimen collection or preparation.1.1 These test methods describe procedures for testing the mechanical properties of multi-wire steel prestressing strand.1.2 These test methods are intended for use in evaluating specific strand properties prescribed in specifications for multi-wire steel prestressing strand, but they do not quantify acceptance criteria specified in the applicable specification for the strand being tested.1.3 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.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The test method is capable of measuring uranium isotopic abundances of 234U, 235U, 236U, and 238U as required by Specifications C787 and C996.1.1 This test method covers the isotopic abundance analysis of 234U, 235U, 236U, and 238U in samples of hydrolysed uranium hexafluoride (UF6) by inductively coupled plasma source, multicollector, mass spectrometry (ICP-MC-MS). The method applies to material with  235U abundance in the range of 0.2 to 6 % mass. This test method is also described in ASTM STP 1344.1.2 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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5.1 The determination of the tensile force-elongation values of geogrids provides index property values. This test method shall be used for quality control and acceptance testing of commercial shipments of geogrids.5.2 In cases of dispute arising from differences in reported test results when using this test method for acceptance testing of commercial shipments, the purchaser and supplier should conduct comparative tests to determine if there is a statistical bias between their laboratories. Competent statistical assistance is recommended for the investigation of bias. As a minimum, the two parties should take a group of test specimens which are as homogeneous as possible and which are from a lot of material of the type in question. The test specimens should then be randomly assigned in equal numbers to each laboratory for testing. The average results from the two laboratories should be compared using Student's t-test for unpaired data and an acceptable probability level chosen by the two parties before the testing began. If a bias is found, either its cause must be found and corrected or the purchaser and supplier must agree to interpret future test results in light of the known bias.5.3 All geogrids can be tested by any of these methods. Some modification of techniques may be necessary for a given geogrid depending upon its physical makeup. Special adaptations may be necessary with strong geogrids, multiple layered geogrids, or geogrids that tend to slip in the clamps or those which tend to be damaged by the clamps.1.1 This test method covers the determination of the tensile strength properties of geogrids by subjecting strips of varying width to tensile loading.1.2 Three alternative procedures are provided to determine the tensile strength, as follows:1.2.1 Method A—Testing a single geogrid rib in tension (N or lbf).1.2.2 Method B—Testing multiple geogrid ribs in tension (kN/m or lbf/ft).1.2.3 Method C—Testing multiple layers of multiple geogrid ribs in tension (kN/m or lbf/ft).1.3 This test method is intended for quality control and conformance testing of geogrids.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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