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5.1 In form-fill operations, sealed areas of packages are frequently subject to disruptive forces while still hot. If the hot seals have inadequate resistance to these forces, breakage can occur during the packaging process. These test methods measure hot seal strength and can be used to characterize and rank materials in their ability to perform in commercial applications where this quality is critical.1.1 These two test methods cover laboratory measurement of the strength of heatseals formed between thermoplastic surfaces of flexible webs, immediately after a seal has been made and before it cools to ambient temperature (hot tack strength).1.2 These test methods are restricted to instrumented hot tack testing, requiring a testing machine that automatically heatseals a specimen and immediately determines strength of the hot seal at a precisely measured time after conclusion of the sealing cycle. An additional prerequisite is that the operator shall have no influence on the test after the sealing sequence has begun. These test methods do not cover non-instrumented manual procedures employing springs, levers, pulleys and weights, where test results can be influenced by operator technique.1.3 Two variations of the instrumented hot tack test are described in these test methods, differing primarily in two respects: (a) rate of grip separation during testing of the sealed specimen, and (b) whether the testing machine generates the cooling curve of the material under test, or instead makes a measurement of the maximum force observed following a set delay time. Both test methods may be used to test all materials within the scope of these test methods and within the range and capacity of the machine employed. They are described in Section 4.1.4 SI units are preferred and shall be used in referee decisions. Values stated herein in inch-pound units are to be regarded separately and may not be exact equivalents to SI units. Therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.1.5 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. The operator of the equipment is to be aware of pinch points as the seal jaws come together to make a seal, hot surfaces of the jaws, and sharp instruments used to cut specimens. It is recommended that the operator review safety precautions from the equipment supplier.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 Vapor pressure is an important physical property of liquid spark-ignition engine fuels. It provides an indication of how a fuel will perform under different operating conditions. For example, vapor pressure is a factor in determining whether a fuel will cause vapor lock at high ambient temperature or at high altitude, or will provide easy starting at low ambient temperature.5.2 Petroleum product specifications generally include vapor pressure limits to ensure products of suitable volatility performance.NOTE 3: Vapor pressure of fuels is regulated by various government agencies.1.1 This test method covers and is applicable to gasolines and gasoline-oxygenate blends with a vapor pressure range from 35 kPa to 100 kPa (5 psi to 15 psi) (see Note 2). This test method, a modification of Test Method D323 (Reid Method), provides two procedures to determine the vapor pressure (Note 1) of gasoline and gasoline-oxygenate blends.NOTE 1: Because the external atmospheric pressure is counteracted by the atmospheric pressure initially present in the air chamber, this vapor pressure is an absolute pressure at 37.8 °C (100 °F) in kilopascals (pounds-force per square inch). This vapor pressure differs from the true vapor pressure of the sample due to some small vaporization of the sample and air in the confined space.NOTE 2: Vapor pressure of gasoline or gasoline-oxygenate blends below 35 kPa (5 psi) or greater than 100 kPa (15 psi) can be determined with this test method but the precision and bias (Section 11) do not apply. For materials with a vapor pressure greater than 100 kPa (15 psi), use a 0 kPa to 200 kPa (0 psi to 30 psi) gauge as specified in the annex of Test Method D323.1.2 Some gasoline-oxygenate blends may show a haze when cooled to 0 °C to 1 °C. If a haze is observed in 9.4, it shall be indicated in the reporting of results. The precision and bias statements for hazy samples have not been determined (see Note 7).1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific warnings are given in 7.5, 8.4.1, 8.5.1, 9.1, A1.1, and A1.1.3.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The mass of particulates present in a fuel is a significant factor, along with the size and nature of the individual particles, in the rapidity with which fuel system filters and other small orifices in fuel systems can become plugged. This test method provides a means of assessing the mass of particulates present in a fuel sample.5.2 The test method can be used in specifications and purchase documents as a means of controlling particulate contamination levels in the fuels purchased.1.1 This test method covers the determination of the mass of particulate contamination in B100 biodiesel in accordance with Specification D6751 and BXX blends that are prepared against all No. 1 and No. 2 grade fuels allowed within Specifications D396 and D975.NOTE 1: Middle distillate fuels with flash points less than 38 °C have been ignited by discharges of static electricity when the fuels have been filtered through inadequately bonded or grounded glass fiber filter systems. See Guide D4865 for a more detailed discussion of static electricity formation and discharge.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 This test is designed to be used as a rapid measure of the overall relative corrosivity of Ethanol Fuel Blends (Specification D5798) and Denatured Fuel Ethanol (Specification D4806) to iron (steel).5.2 The test can be used to compare corrosion inhibitor dosage levels and effectiveness of various corrosion inhibitors as they pertain to protecting iron (steel) materials from corrosion.1.1 This test method measures the ability of inhibited and uninhibited Ethanol Fuel Blends defined by Specification D5798 and Denatured Fuel Ethanol defined by Specification D4806 to resist corrosion of iron should water become mixed with the fuel, using an accelerated laboratory test method. Corrosion ratings are reported based on a visual, numbered rating scale.1.2 The values stated in SI units are to be regarded as standard. The values 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. Specific hazard statements are given in Sections 7 and 8.1.4 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 A knowledge of the hydrocarbon composition of the middle distillates, including the biodiesel blends is useful in following the effect of changes in process variables, diagnosing the source of plant upsets, and in evaluating the effect of changes in composition on product performance properties. The total aromatics content and polycyclic aromatics content are also important to evaluate the quality of diesel fuels/biodiesel blends. It requires an appropriate analytical method to make such determinations for diesel fuel/biodiesel blends production process and quality control.5.2 This test method provides a comprehensive analytical strategy for the determination of the total aromatics contents, polycyclic aromatics contents and the detail hydrocarbon composition of diesel fuel/biodiesel blends to ensure compliance with certain specifications or regulations.5.3 Test Method D2425 is applicable to the determination of the detailed hydrocarbon composition in middle distillates, however, the pre-separation procedure of elution chromatography is time-consuming and not eco-friendly. By combining with the separation procedures described in Test Method D8144, the dual column GC-MS system proposed in this method can determine the total aromatic hydrocarbon contents, polycyclic aromatic hydrocarbon contents and detailed hydrocarbon composition of diesel fuel/biodiesel blends simultaneously. The content of FAME in biodiesel blends can also be determined by GC. It is demonstrated to be time-saving and eco-friendly for the quality control of diesel fuel and biodiesel blends.1.1 This test method covers an analytical scheme using the gas chromatography/mass spectrometry (GC-MS) to determine the hydrocarbon types present in middle distillates 170 °C to 365 °C boiling range, 5 % to 95 % by volume as determined by Test Method D86, including biodiesel blends with up to 20 % by volume of fatty acid methyl ester (FAME). The detailed hydrocarbon composition, total aromatic hydrocarbon and polycyclic aromatic hydrocarbon contents can be determined. The hydrocarbon types include: paraffins, noncondensed cycloparaffins, condensed dicycloparaffins, condensed tricycloparaffins, alkylbenzenes, indans or tetralins, or both, CnH2n-10 (indenes, etc.), naphthalenes, CnH2n-14 (acenaphthenes, etc.), CnH2n-16 (acenaphthylenes, etc.), and tricyclic aromatics. The content of FAME in biodiesel blends can also be determined by GC.1.2 The values stated in acceptable SI units are to be regarded as the 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 Typically, denatured fuel ethanol is added to gasoline blendstocks after production. For laboratories to test a sample that is similar to the finished fuel available in the market, it is important to provide a laboratory practice that standardizes the preparation of a blend of denatured fuel ethanol and gasoline blendstock.5.2 The laboratory blend shall be prepared volumetrically to yield a fuel similar to that produced for consumer use.5.3 When applicable, blends shall meet requirements of CFR 40.80, Subpart D—Reformulated Gasoline.1.1 This practice covers and provides instructions on making a volumetric blend of denatured fuel ethanol with gasoline blendstocks, such as a reformulated gasoline blendstock for oxygenate blending (RBOB) or a conventional gasoline blendstock for oxygenate blending (CBOB).1.2 This practice does not preclude the use of automated volumetric blending systems.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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