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ASTM D816-06(2023) Standard Test Methods for Rubber Cements Active 发布日期 :  1970-01-01 实施日期 : 

4.1 These tests are used as a means of classifying, evaluating, and controlling cement compositions. Adhesion strength in tension, shear, and in a peeling mode are necessary where rubber materials are used in various engineering applications where forces are encountered both normal to the adhesion plane and parallel to the plane of the adhesive interface.1.1 These test methods cover tests to measure the properties of adhesives, commonly called rubber cements, that may be applied in plastic or fluid form and that are manufactured from natural rubber, reclaimed rubber, synthetic elastomers, or combinations of these materials. All tests are not to be considered as applicable to a particular type of adhesive nor is every test included that may be applicable to a particular type. The tests do provide standard procedures for evaluating the more important properties of the usual adhesives ordinarily classed as rubber cements.1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, 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 WPPO composition is useful in optimization of process variables, diagnosing unit performance, and in evaluating the effect of changes in waste plastic composition on WPPO performance properties.5.1.1 Aromatics and olefin hydrocarbon type analysis, including sub-classes, may be useful for evaluating suitability of WPPO as a feedstock for further processing.1.1 This test method covers a standard procedure for the determination of hydrocarbon types (saturates, olefins, styrenes, aromatics and polyaromatics) of waste plastic process oil (WPPO) from chemical or thermal processes using gas chromatography and vacuum ultraviolet absorption spectroscopy detection (GC-VUV).1.1.1 This test method is applicable for plastic recycling and circular schemes including wide range density material from polyethylene and polypropylene.1.1.2 The test method is applicable to waste plastic process oil having a final boiling point of 545 °C or lower at atmospheric pressure as measured by this test or Test Method D2887. This test method is limited to samples having a boiling range greater than 36 °C, and having a vapor pressure sufficiently low to permit sampling at ambient temperature.1.1.3 WPPOs with initial boiling points less than nC5 (36 °C) and final boiling point less than nC15 (271 °C) may be analyzed by Test Method D8369.1.1.4 Appendix X3 is applicable to waste plastic process oils that are predominantly hydrocarbons in the boiling range of pentane, nC5 (36 °C) to tetrahexacontane, nC64 (629 °C).1.2 Concentrations of group type totals are determined by percent mass or percent volume. The applicable working ranges are as follows:Total Aromatics %Mass 1 to 50Monoaromatics %Mass 1 to 50Diaromatics %Mass 1 to 15Tri-plus aromatics %Mass 0.5 to 5PAH %Mass 0.5 to 15Saturates %Mass 5 to 99Olefins %Mass 1 to 80Conjugated diolefins %Mass 0.2 to 5Styrenes %Mass 0.2 to 5The final precision concentration ranges will be defined by a future ILS.1.2.1 Saturates totals are the result of the summation of normal paraffins, isoparaffins, and naphthenes.1.2.2 Aromatics are the summation of monoaromatic and polyaromatic group types. Polyaromatic totals are the result of the summation of diaromatic and tri-plus aromatic group types.1.2.3 Olefin totals are the result of the sum of mono-olefins, conjugated diolefins, non-conjugated diolefins, and cyclic olefins.1.2.4 Styrenes totals are the sum of styrene and alkylated styrenes. Styrenes are classified separately, neither as aromatic nor olefin.1.3 Waste plastic process oil containing mixed plastic types such as polyethylene terephthalate PET and polyvinyl chloride or other material may yield compounds including hetero-compounds that are not speciated by this test method.1.4 Individual components are typically not baseline separated by the procedure described in this test method. The coelutions are resolved at the detector using VUV absorbance spectra and deconvolution algorithms.1.5 This test method may apply to other process oils from sources such as tires and bio-mass boiling between pentane (36 °C) and tetratetracontane (545 °C), but has not been extensively tested for such applications.1.6 Units—The values stated in SI units are to be regarded as standard. No other units of measurement, other than the boiling point of normal paraffins (°F) in Table 2 and Table X.3.1, 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.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 This test method is used by athletic footwear manufacturers and others, both as a tool for development of athletic shoe cushioning systems and as a test of the general cushioning characteristics of athletic footwear products, materials and components. Adherence to the requirements and recommendations of this test method will provide repeatable results that can be compared among laboratories.5.2 Data obtained by these procedures are indicative of the impact attenuation of athletic shoe cushioning systems under the specific conditions employed.5.3 This test method is designed to provide data on the force versus displacement response of athletic footwear cushioning systems under essentially uniaxial impact loads at rates that are similar to those of heel and forefoot impacts during different athletic activities.5.4 The peak or maximum values of force, acceleration, displacement, and strain are dependent on the total impact energy applied to the specimen. These values are normalized to provide comparative results for a reference value of total energy input.5.5 Impact attenuation outcomes are strongly dependent on initial conditions (impact mass, impact velocity, contact area, etc.) and on specimen size and the specimen’s prior history of compressive loading. Therefore results should be compared only for specimens of the same nominal size and prior conditioning.Note 1—Impact test outcomes have been found to correlate with in-vivo loads (peak ground reaction force, peak plantar pressure, lower extremity acceleration) experienced by runners. Relationships between test outcomes and subjective perceptions of cushioning have also been found. However, there is no direct evidence of a correlation between scores on this test method and the probability of injury among users of a particular athletic footwear product.1.1 This test method describes the use of a gravity-driven impact test to measure certain impact attenuation characteristics of cushioning systems and cushioning materials employed in the soles of athletic shoes.1.2 This test method uses an 8.5 kg mass dropped from a height of 30-70 mm to generate force-time profiles that are comparable to those observed during heel and forefoot impacts during walking, running and jump landings.1.3 This test method is intended for use on the heel and or forefoot regions of whole, intact athletic shoe cushioning systems. An athletic shoe cushioning system is defined as all of the layers of material between the wearer's foot and the ground surface that are normally considered a part of the shoe. This may include any of the following components: outsole or other abrasion resistant outer layer, a midsole of compliant cushioning materials or structures forming an intermediate layer, an insole, insole board, or other material layers overlying the midsole, parts of the upper and heel counter reinforcement which extend beneath the foot, and an insock, sockliner or other cushioning layers, either fixed or removable, inside the shoe.1.4 This test method may also be employed in to measure the impact attenuation of cushioning system components and cushioning material specimens.1.5 This test method is not intended for use as a test of shoes classified by the manufacturer as children's shoes.1.6 The type, size or dimensions and thickness of the specimen, the total energy input and prior conditioning shall qualify test results obtained by this test method.1.6.1 The range of tests results is limited by the calibrated range of the test device’s force transducer. Combinations of thin specimens, high specimen stiffness and high total energy input may produce forces that exceed the transducer’s capacity and are hence not measurable. In practice, the specified force transducer range (10 kN) accommodates more than 99 % of typical shoe soles and cushioning material specimens that are 7 mm or more in thickness at a total energy input of 5 Joules.1.6.2 The nominal value of the total energy input applied by this test method is 5 J for shoes, such as running shoes, which are subject to moderate impacts during normal use. Total energy inputs of 7.0 J and 3.0 J may be used for shoes (e.g basketball shoes) which are subject to higher impact loads during normal use. Other values of total energy input may be used, if they are stated in the report.1.6.3 Results from tests performed with different total energy inputs or with different masses are not directly comparable.1.6.4 Specimen thickness has a significant effect on impact attenuation outcomes. Consequently, results from tests of material specimens of different thicknesses cannot be directly compared.1.6.5 The impact attenuation of cushioning materials may change over time and with use (e.g. wear or durability testing) or prior conditioning (e.g. from previous tests). Consequently, test results obtained using this test method shall be qualified by the age and prior conditioning of the samples.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 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 This test method is intended to evaluate the penetration and permeation resistance for complete ensembles to vapors from chemical warfare agents and other chemical substances.5.1.1 This test method differs from Test Method F1052 by providing an evaluation of ensembles worn on human test subjects and measuring the inward leakage of a chemical agent vapor simulant as it would be absorbed by the wearer’s skin. Test Method F1052 is not applicable to the range of protective ensembles that are evaluated by this test method.5.1.2 This test method differs from Test Method F1359/F1359M by using a chemical agent vapor simulant as compared to a liquid challenge and in the use of human test subjects. This test method further provides a quantitative assessment of inward leakage for the chemical agent vapor simulant.5.1.3 The use of this test method to determine the inward leakage of other chemical vapor threats must be evaluated on a case-by-case basis.5.2 This test method is applied to complete ensembles consisting of a suit or garment in combination with gloves, footwear, respirators, and interface devices.5.2.1 This test method permits any combination or configuration of ensemble elements and components, including ensembles where the respirator covers the face or head.5.2.2 This test method accommodates protective ensembles or protective clothing having any combination of the following characteristics:(1) The protective ensemble or clothing is constructed of air-permeable, semipermeable, or impermeable fabrics,(2) The protective ensemble or clothing is of a single or multi-layered design, or(3) The protective ensemble or clothing is constructed of inert or sorptive fabrics.5.3 MeS has been used as a simulant for chemical warfare agents. MeS is primarily a simulant for distilled mustard (HD) with a similar vapor pressure, density, and water solubility. The use of MeS in vapor form does not simulate all agents or hazardous substances to which ensemble wearers are potentially exposed.5.4 The principal results of this test are physiological protective dosage factors that indicate the relative effectiveness of the ensemble in preventing the inward leakage of the chemical agent vapor simulant and its consequent dosage to the wearer’s skin as determined by the use and placement of personal adsorbent devices (PAD) on human test subjects.5.4.1 Specific information on inward leakage of chemical agent vapor simulant is provided by local physiological protective dosage factors for individual PAD locations to assist in determining possible points of entry of the chemical agent vapor simulant into the ensemble.5.4.2 The determination of the local physiological protective dosage factors is based on ratio of the outside exposure dosage to the inside exposure dosage on the wearer’s skin at specific locations of the body and accounts for the specific susceptibility of the average human’s skin at those locations to the effects of blister agent, distilled mustard using the onset of symptoms exposure dosages (OSED) at different points on the body. The specific OSED values used in this test method are based on the exposure concentration of distilled mustard that causes threshold effects to the average individual human in the form of reversible skin ulceration and blistering (1).55.4.3 The body locations chosen for the placement of PADs were chosen to represent the range of body areas on the human body, with preference to those body areas generally near interfaces found in common two-piece ensembles with separate respirator, gloves, and footwear. Additional locations are permitted to be used for the placement of PAD where there are specific areas of interest for evaluating the inward leakage of the chemical agent vapor simulant.NOTE 1: Common interface areas for protective ensemble include the hood to respirator facemask, clothing or suit closure, upper torso garment to lower torso garment, garment sleeve to glove, and garment pant cuff to footwear.5.4.4 An assessment of the vapor penetration and permeation resistance for the entire ensemble is provided by the determination of a systemic physiological protective dosage factor. The same PAD data are used in a body region hazard analysis to determine the overall physiological protective dosage factor accounting for the areas of the body represented by the location, and the relative effects of the nerve agent, VX. A systemic analysis assists in the evaluation for those chemical agents, such as nerve agents, affecting the human body through a cumulative dose absorbed by the skin (2).5.4.5 Examples of analyses applying PAD data for the assessment of ensemble inward leakage resistance are provided in NFPA 1971, Standard on Protective Ensemble for Structural and Proximity Fire Fighting, and NFPA 1994, Standard on Protective Ensemble for CBRN Terrorism Incidents.5.4.6 The general procedures in this test method are based on Test Operations Procedure (TOP 10-2-022), Man-In-Simulant Test (MIST)—Chemical Vapor Testing of Chemical/ Biological Protective Suits.5.5 The human subject activities simulate possible causes of changes in ensemble vapor barrier during expected activities. These activities are primarily based on stationary activities provided in Part A of Practices F1154 and are intended to create movements that are likely to affect the integrity of the ensemble and its interface areas. Additional activities (such as dragging a dummy and climbing a ladder) have been added to simulate activities that might be used by first responders during emergency events such as rescuing victims from a terrorism incident involving chemical agents. The test method permits the modification of the activity protocol to simulate the specific needs of the protective ensemble application.5.6 The length of the human subject exposure to the chemical agent vapor simulant is set at 30 min in the test chamber with a 5-min decontamination period. This test duration is intended to replicate a possible exposure of a first responder during a terrorism incident involving chemical agents. If a self-contained breathing apparatus is used, a 60-min rated respirator must be used or provisions made for supplemental umbilical air (through a supplied air system). The test method permits the adjustment of the exposure period to simulate the specific needs of the protective ensemble application.5.7 Test results generated by this test method are specific to the ensemble being evaluated. Changing any part of the ensemble necessitates a new set of testing for the modified ensemble.5.8 Additional information on man-in-simulant testing is provided in (3).1.1 This test method specifies the test equipment and procedures for conducting tests to estimate the entry of chemical agent vapor simulant through protective ensembles while worn by test subjects.1.2 This test method permits the evaluation of protective ensembles consisting of protective garments or suits, gloves, footwear, respirators, and interface devices.1.3 The results of this test method yield local physiological protective dosage factors at individual locations of the human body as well as a systemic physiological protective dosage factor for the entire ensemble.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 spiral contractometer, properly used, will give reproducible results (see 9.5) over a wide range of stress values. Internal stress limits with this method can be specified for use by both the purchaser and the producer of plated or electroformed parts.5.2 Plating with large tensile stresses will reduce the fatigue strength of a product made from high-strength steel. Maximum stress limits can be specified to minimize this. Other properties affected by stress include corrosion resistance, dimensional stability, cracking, and peeling.5.3 In control of electroforming solutions, the effects of stress are more widely recognized, and the control of stress is usually necessary to obtain a usable electroform. Internal stress limits can be determined and specified for production control.5.4 Internal stress values obtained by the spiral contractometer do not necessarily reflect the internal stress values found on a part plated in the same solution. Internal stress varies with many factors, such as coating thickness, preparation of substrate, current density, and temperature, as well as the solution composition. Closer correlation is achieved when the test conditions match those used to coat the part.1.1 This test method covers the use of the spiral contractometer for measuring the internal stress of metallic coatings as produced from plating solutions on a helical cathode. The test method can be used with electrolytic and autocatalytic deposits.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 non-conformance 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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5.1 The deformation and end point of a cone corresponds to a certain heat-work condition due to the effects of time, temperature, and atmosphere.5.2 The precision of this test method is subject to many variables that are difficult to control. Therefore, an experienced operator may be necessary where PCE values are being utilized for specification purposes.5.3 PCE values are used to classify fireclay and high-alumina refractories.5.4 This is an effective method of identifying fireclay variations, mining control, and developing raw material specifications.5.5 Although not recommended, this test method is sometimes applied to materials other than fireclay and high alumina. Such practice should be limited to in-house laboratories and never be used for specification purposes.1.1 This test method covers the determination of the pyrometric cone equivalent (PCE) of fire clay, fireclay brick, high-alumina brick, and silica fire clay refractory mortar by comparison of test cones with standard pyrometric cones under the conditions prescribed in this test method.1.2 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.1.2.1 Exceptions—Certain weights are in SI units with inch-pound in parentheses. Also, certain figures have SI units without parentheses. These SI units are to be regarded as 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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ASTM D1293-18 Standard Test Methods for pH of Water Active 发布日期 :  1970-01-01 实施日期 : 

5.1 The pH of water is a critical parameter affecting the solubility of trace minerals, the ability of the water to form scale or to cause metallic corrosion, and the suitability of the water to sustain living organisms. It is a defined scale, based on a system of buffer solutions2 with assigned values. In pure water at 25°C, pH 7.0 is the neutral point, but this varies with temperature and the ionic strength of the sample.5 Pure water in equilibrium with air has a pH of about 5.5, and most natural uncontaminated waters range between pH 6 and pH 9.1.1 These test methods cover the determination of pH by electrometric measurement using the glass electrode as the sensor. Two test methods are given as follows:  SectionsTest Method A—Precise Laboratory Measurement  8 to 15Test Method B—Routine or Continuous Measurement 16 to 241.2 Test Method A covers the precise measurement of pH in water utilizing at least two of seven standard reference buffer solutions for instrument standardization.1.3 Test Method B covers the routine measurement of pH in water and is especially useful for continuous monitoring. Two buffers are used to standardize the instrument under controlled parameters, but the conditions are somewhat less restrictive than those in Test Method A. For on-line measurement, also see Test Method D6569 which provides more detail.1.4 Both test methods are based on the pH scale established by NIST (formerly NBS) Standard Reference Materials.21.5 Neither test method is considered to be adequate for measurement of pH in water whose conductivity is less than about 5 μS/cm. Refer to Test Methods D5128 and D5464.1.6 Precision and bias data were obtained using buffer solutions only. It is the user's responsibility to assure the validity of these test methods for untested types of water.1.7 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to inch-pound units that are provided for information only and are not considered standard.1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.9 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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ASTM D2510-22 Standard Test Method for Adhesion of Solid Film Lubricants Active 发布日期 :  1970-01-01 实施日期 : 

5.1 Effective solid film lubricant coatings must adhere to surfaces to provide adequate lubrication in applications with restricted access where fluid lubricants cannot easily be replenished. Loss of coating adhesion results in metal to metal contact causing significant wear of contacting surfaces. Adhesion is critical to the performance of the solid film lubricant. Examples of solid film lubricant applications include fasteners, bearings and sliding members in automotive, aircraft, and aerospace hardware.5.2 This test method is intended to determine the adhesion of solid film lubricant coatings when submitted to contact with water and other fluids. Results of this test provide an indication of the suitability of the lubricant coating in applications where contact with water or other fluids is likely.1.1 This test method2 covers the measurement of the adhesion characteristics of dry solid film lubricants.1.2 The values stated in SI units are to be regarded as standard.1.2.1 Exception—The values given in parentheses are provided 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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ASTM D2901-99 Standard Test Method for Cement Content of Freshly Mixed Soil-Cement (Withdrawn 2006) Withdrawn, No replacement 发布日期 :  1970-01-01 实施日期 : 

1.1 This test method covers determination of the cement content of samples of freshly-mixed soil-cement. 1.2 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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4.1 Products are exposed to complex dynamic stresses in the transportation environment. The determination of the resonant frequencies of the product may aid the packaging designer in determining the proper packaging system to provide adequate protection for the product, as well as providing an understanding of the complex interactions between the components of the product as they relate to expected transportation vibration inputs.1.1 These test methods cover the determination of resonances of unpackaged products and components of unpackaged products by means of vertical linear motion at the surface on which the product is mounted for test. Two alternate test methods are presented:Test Method A—Resonance Search Using Sinusoidal Vibration, andTest Method B—Resonance Search Using Random Vibration.NOTE 1: The two test methods are not necessarily equivalent and may not produce the same results. It is possible that tests using random vibration may be more representative of the transport environment and may be conducted more quickly than sine tests.1.2 This information may be used to examine the response of products to vibration for product design purposes, or for the design of a container or interior package that will minimize transportation vibration inputs at these critical frequencies, when these products resonances are within the expected transportation environment frequency range. Since vibration damage is most likely to occur at product resonant frequencies, these resonances may be thought of as potential product fragility points.1.3 Information obtained from the optional dwell test methods may be used to assess the fatigue characteristics of the resonating components and for product modification. This may become necessary if the response of a product would require design of an impractical or excessively costly shipping container.1.4 These test methods do not necessarily simulate the vibration effects that the product will encounter in its operational or in-use environment. Other, more suitable test procedures should be used for this purpose.1.5 Test levels given in these test methods represent the correlation of the best information currently available from research investigation and from experience in the use of these test methods. If more applicable or accurate data are available, they should be substituted.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. See Section 6 for specific precautionary statements.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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4.1 Identification of a brackish water, seawater, or brine is determined by comparison of the concentrations of their dissolved constituents. The results are used to evaluate the origin of the water, determine if it is a possible pollutant or determine if it is a commercial source of a valuable constituent such as iodine or bromine.1.1 These test methods2 cover the determination of soluble iodide and bromide ions, or both, in brackish water, seawater, and brines. Four test methods are given as follows:1.1.1 Test Method A for both Iodide and Bromide Ions—Volumetric, for concentrations from 0.2 mg/L to 2000 mg/L iodide and from 5 mg/L to 6500 mg/L bromide (Sections 7 – 15).1.1.2 Test Method B for Iodide Ion—Colorimetric, for concentrations from 0.2 mg/L to 2000 mg/L iodide (Sections 16 – 25).1.1.3 Test Method C for Iodide Ion—Selective electrode, for concentrations from 1 mg/L to 2000 mg/L iodide (Sections 26 – 34).1.1.4 Test Method D for Bromide Ion—Colorimetric, for concentrations from 40 mg/L to 6500 mg/L bromide (Sections 35 – 44).1.2 Test Method A is intended for use on all brackish waters, seawaters, and brines that contain appreciable amounts of iodide or bromide ions or both. Test Methods B, C, and D, because of their rapidity and sensitivity, are recommended for the analysis of brackish waters, seawaters, and brines in the field and in the laboratory.1.3 Samples containing from 0.2 mg/L to 2000 mg/L of iodide or 5 mg/L to 6500 mg/L of bromide may be analyzed by these methods.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 precautionary statements, see 20.2 and 39.2.1.6 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 This test method provides a simple means of characterizing the important rheological properties and viscosity of thermoplastic polymers using very small amounts of material (approximately 25 to 50 mm in diameter by 1 to 3 mm in thickness ... approximately 3 to 5 g). Data are generally used for quality control, research and development, and establishment of optimum processing conditions.5.2 Dynamic mechanical testing provides a sensitive method for determining molten polymer properties by measuring the elastic and loss moduli as a function of frequency, strain, temperature, or time. Plots of viscosity, storage, and loss moduli, and tan delta as a function of the aforementioned process parameters provide graphical representation indicative of molecular weight, molecular weight distribution, effects of chain branching, and melt-processability for specified conditions.5.2.1 Observed data are specific to experimental conditions. Reporting in full (as described in this test method) the conditions under which the data was obtained is essential to assist users with interpreting the data an reconciling apparent or perceived discrepancies.5.3 Values obtained in this test method can be used to assess the following:5.3.1 Complex viscosity of the polymer melt as a function of dynamic oscillation,5.3.2 Processing viscosity, minimum as well as changes in viscosity as a function of experimental parameters,5.3.3 Effects of processing treatment,5.3.4 Relative polymer behavioral properties, including viscosity and damping, and5.3.5 Effects of formulation additives that might affect processability or performance.5.4 Before proceeding with this test method, refer to the specification for the material being tested. Any test specimen preparation, conditioning, dimensions, or testing parameters, or combination thereof, covered in the relevant ASTM materials specification shall take precedence over those mentioned in the test method. If there are no relevant ASTM material specifications, then the default conditions apply.1.1 This test method outlines the use of dynamic mechanical instrumentation in determining and reporting the rheological properties of thermoplastic resins and other types of molten polymers. The method is useful for determining the complex viscosity and other significant viscoelastic characteristics of such materials as a function of frequency, strain amplitude, temperature, and time. It is known that fillers and other additives influence rheological properties.1.2 It incorporates a laboratory test method for determining the relevant rheological properties of a polymer melt subjected to various oscillatory deformations on an instrument of the type commonly referred to as a mechanical or dynamic spectrometer.1.3 This test method is intended to provide a means of determining the rheological properties of molten polymers, such as thermoplastics and thermoplastic elastomers over a range of temperatures by nonresonant, forced-vibration techniques. Plots of modulus, viscosity, and tan delta as a function of dynamic oscillation (frequency), strain amplitude, temperature, and time are indicative of the viscoelastic properties of a molten polymer.1.4 This test method is valid for a wide range of frequencies, typically from 0.01 Hz to 100 Hz.1.5 This test method is intended for homogenous and heterogeneous molten polymeric systems and composite formulations containing chemical additives, including fillers, reinforcements, stabilizers, plasticizers, flame retardants, impact modifiers, processing aids, and other important chemical additives often incorporated into a polymeric system for specific functional properties, and which could affect the processability and functional performance. These polymeric material systems have molten viscosities typically less than 106 Pa·s (107 poise).1.6 Test data obtained by this test method are relevant and appropriate for use in engineering design.1.7 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.NOTE 1: This test method is equivalent to ISO 6721, Part 10.1.9 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.

定价: 590元 / 折扣价: 502 加购物车

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3.1 This test method is designed to measure the load required to tear leather through two holes in the test specimen. Tanners and leather buyers have found that this test gives an indication of the resistance of leather to tearing. It is of particular value in estimating the durability of leather to withstand tearing stresses encountered in the manufacture of shoes, garments, and upholstered products. The thickness of the specimen and direction of tear relative to the backbone will affect the uniformity of the test results. This test method may not apply when the conditions of the test employed differ widely from those specified in the test method.1.1 This test method is intended for use in determining the stitch tearing resistance of leather using a double hole tear. It is particularly applicable to lightweight leathers. This test method does not apply to wet blue.1.2 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.1.3 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.

定价: 515元 / 折扣价: 438 加购物车

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5.1 Results of this test method are used to predict displacements in rock mass caused by loads from a structure or from underground construction for the load range that the device can apply. It is one of several tests that should be performed.5.2 Because the jack can apply directed loads, this test method can be performed to provide an estimate of anisotropy.5.3 In theory, the analysis of test data is straight forward; the modulus estimate requires a record of applied hydraulic pressure versus borehole diameter change, and a knowledge of the rock's Poisson's ratio. In practice, the above procedure, using the original theoretical formula, frequently has resulted in computing a material modulus that was demonstrably too low.5.4 For analyzing the test data it is assumed that the rock mass is linearly elastic, isotropic, and homogeneous. Within these assumptions, this test method can provide useful data for rock masses for which equivalent continuous properties cannot be found or estimated.NOTE 1: Notwithstanding the statements on precision and bias contained in this test method; the precision of this test method is dependent on the competence of the personnel performing it, and the suitability of the equipment and facilities used. Agencies that meet the criteria of Practice D3740 are generally considered capable of competent and objective testing. Users of this test method are cautioned that compliance with Practice D3740 does not in itself assure reliable testing. Reliable testing depends on many factors; Practice D3740 provides a means of evaluating some of those factors.1.1 This test method covers the estimation of in situ modulus of a rock mass at various depths and orientations. Information on time-dependent deformation may also be obtained.1.2 This test method covers testing in an N size drill hole and is more relevant to a borehole jack device designed for “hard rock” than for soft rock.1.3 All observed and calculated values shall conform to the guidelines for significant digits and rounding established in Practice D6026.1.3.1 The method used to specify how data are collected, calculated, or recorded in this standard is not directly related to the accuracy to which the data can be applied in design or other uses, or both. How one applies the results obtained using this standard is beyond its scope.1.4 The values stated in SI units are to be regarded as the standard. The values given in parentheses are mathematical conversions to inch-pound units that are provided for information only and are not considered standard.1.5 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.

定价: 590元 / 折扣价: 502 加购物车

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5.1 Procedure A is designed to produce moisture diffusion material property data that may be used as follows:5.1.1 To determine approximate exposure times for coupon conditioning in Procedures B-E, Y, and Z;5.1.2 As input to moisture prediction analysis computer codes; or5.1.3 For making qualitative decisions on material selection or performance under environmental exposure to various forms of moisture.5.2 Procedures B-E are designed to condition test coupons to a specified environmental condition or equilibrium state prior to other material property testing (including, but not limited to, mechanical testing).5.3 Procedures Y-Z are designed to determine the loss of moisture content due to removal of a test coupon from the conditioning chamber (such as for strain gauge bonding) or due to heating of the test coupon prior to and during mechanical loading.5.4 A single pair of tests on thin and thick specimens using Procedure A provides the moisture diffusivity constant, Dz, and the moisture equilibrium content, Mm, at the given moisture exposure level and temperature. Multiple tests at differing temperatures are required to establish the dependence of Dz on temperature. Multiple tests at differing moisture exposure levels are required to establish the dependence of Mm on moisture exposure level.NOTE 1: For many polymer matrix composites, the moisture diffusivity is usually only weakly related to relative humidity and is often assumed to be a function only of temperature, usually following an Arrhenius-type exponential relation with inverse absolute temperature. For many of these materials, moisture equilibrium content is only weakly related to temperature and is usually assumed to be a function only of relative humidity (1).5.5 Vapor-exposure testing shall be used to condition the specimen when the in-service environmental condition is a vapor such as humid air. Immersion in a liquid bath should be used to simulate vapor exposure only when apparent absorption properties are desired for qualitative purposes. Properties determined in the latter manner shall be reported as apparent properties.NOTE 2: For many polymer matrix composites, the moisture absorption properties under atmospheric humid conditions are generally not equivalent to exposure either to liquid immersion or to pressurized steam. These latter environments may have different material diffusion characteristics.1.1 This test method covers a procedure for the determination of moisture absorption or desorption properties in the through-the-thickness direction for single-phase Fickian solid materials in flat or curved panel form. Also covered are procedures for conditioning test coupons prior to use in other test methods; either to an essentially moisture-free state, to equilibrium in a standard laboratory atmosphere environment, or to equilibrium in a non-laboratory environment. Also included are procedures for determining the moisture loss during elevated temperature testing, as well as moisture loss resulting from thermal exposure after removal from the conditioning environment, such as during strain gauge bonding. While intended primarily for laminated polymer matrix composite materials, these procedures are also applicable to other materials that satisfy the assumptions of 1.2.1.2 The calculation of the through-the-thickness moisture diffusivity constant in Procedure A assumes a single-phase Fickian material with constant moisture absorption properties through the thickness of the specimen. The validity of the equations used in Procedure A for evaluating the moisture diffusivity constant in a material of previously unknown moisture absorption behavior is uncertain prior to the test, as the test results themselves determine if the material follows the single-phase Fickian diffusion model. A reinforced polymer matrix composite material tested below its glass-transition temperature typically meets this requirement, although two-phase matrices such as toughened epoxies may require a multi-phase moisture absorption model. While the test procedures themselves may be used for multi-phase materials, the calculations used to determine the moisture diffusivity constant in Procedure A are applicable only to single-phase materials. Other examples of materials and test conditions that may not meet the requirements are discussed in Section 6.1.3 The evaluation by Procedure A of the moisture equilibrium content material property does not assume, and is therefore not limited to, single-phase Fickian diffusion behavior.1.4 The procedures used by this test method may be performed, and the resulting data reduced, by suitable automatic equipment.1.5 This test method is consistent with the recommendations of CMH-17 Rev G (1),2 which describes the desirable attributes of a conditioning and moisture property determination procedure.1.6 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.1.6.1 Within the text, the inch-pound units are shown in brackets.1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

定价: 646元 / 折扣价: 550 加购物车

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