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5.1 This test method is used to determine the presence and quantity of carbonate in a soil or soft rock specimen in terms of the calcite equivalent. The method is generally intended for use as an index of approximate carbonate content to assist with characterizing marine soils, but can be used for other soils and soft rock. Other test methods exist (such as Method C25 and Test Method D3042) to evaluate calcium carbonate equivalency for purposes of characterizing use of calcareous materials as soil modifiers or agricultural lining materials.5.1.1 Calcium carbonates (CaCO3) are known cementing agents, are water soluble at pH < 7, and are soft on the Mohs' scale compared to other soil minerals.5.2 This test method has limitations as follows:5.2.1 If low carbonate contents (calcite equivalents) are measured, the user does not know whether the soil is low in carbonate content or contains cerrusite, witherite, and the like, which are carbonate species whose reactions with hydrochloric acid are either very slow or limited.5.2.2 Testing times may be extensive (longer than 1 hour) for some carbonate species (such as dolomite) if calcite equivalents within about 1 % are required.5.2.3 The effects of specimen grain size, duration of testing, pH and specimen mass are discussed in the literature.3NOTE 1: The quality of the result produced by this standard 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/sampling/inspection, etc. Users of this standard are cautioned that compliance with Practice D3740 does not in itself assure reliable results. Reliable results depend on many factors; Practice D3740 provides a means of evaluating some of those factors.1.1 This test method covers the determination of carbonate content of soils and soft rock which can be readily broken down by mechanical effort. It is a gasometric method that uses a simple portable apparatus. Results should be clearly stated as the calcite equivalent in percent because different carbonate species cover a wide range of percent calcite equivalent as shown below for a number of carbonates:Species Cation CalciteEquivalent, %Magnesite Mg 117.0Dolomite Ca, Mg 108.6Calcite Ca 100.0Aragonite Ca 100.0Rhodocrosite Mn 87.1Siderite Fe 86.4Smithsonite Zn 79.8Witherite Ba 50.7Cerrusite Pb 37.5For example, a 100 % dolomite would be expected to yield 108.6 % calcite equivalent while 100 % siderite would yield only 86.4 % calcite equivalent. Calcite and aragonite reactions will typically complete within about 10 minutes. This method does not distinguish between the carbonate species and such determination must be made using quantitative chemical analysis methods such as atomic absorption.1.2 Units—The values stated in SI units are to be regarded as standard. The values given in parentheses are provided for information only and are not considered standard. Reporting of test results in units other than SI shall not be regarded as nonconformance with this standard1.3 All observed and calculated values shall conform to the guidelines for significant digits and rounding established in Practice D6026.1.3.1 The procedures used to specify how data are collected/recorded or calculated, in this standard are regarded as the industry standard. In addition, they are representative of the significant digits that generally should be retained. The procedures used do not consider material variation, purpose for obtaining the data, special purpose studies, or any considerations for the user's objectives; and it is common practice to increase or reduce significant digits of reported data to be commensurate with these considerations. It is beyond the scope of this standard to consider significant digits used in analytical methods for engineering design.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 is a standard procedure for determining the resistance to water penetration during rapid cyclic pulses of dynamic air pressure differences. The air-pressure differences acting across a building envelope vary greatly. These factors should be fully considered prior to specifying the test pressure difference to be used.5.2 The median test pressure used in this test method is defined as the specified test pressure supplied by the user and related to the maximum positive building design pressure. This test method departs from the format of other ASTM water penetration resistance test methods based on a maximum test pressure related to a maximum positive building design pressure.5.3 As the specified or median test pressure is increased, the maximum test pressure in this procedure is also increased to 1.5 times the specification median test pressure. This higher maximum test pressure may not be representative of actual building service conditions. For this reason the maximum recommended median test pressure is 480 Pa (10 psf), which corresponds to a maximum test pressure of 720 Pa (15 psf).5.4 The pulsed pressure of this test method may act to pump water past dry seals and breather systems of units incorporating these features, thereby making the test method more severe than a static pressure test method. On the other hand, the low pressure portions of the pressure cycles of this test method may allow weep systems and drainage dams to dissipate water from units incorporating these features, thereby making the test method less severe than a static pressure test method.NOTE 1: In applying the results of tests by this test method, note that the performance of a wall or its components, or both, may be a function of proper installation and adjustment. In service, the performance will also depend on the rigidity of supporting construction and on the resistance of components to deterioration by various causes, (vibration, thermal expansion and contraction, and so forth). It is difficult to accurately simulate the actual complex wetting conditions that can be encountered in service, with large wind-blown water drops, increasing water drop impact pressures with increasing wind velocity and lateral or upward moving air and water. Some designs are more sensitive than others to this upward moving water.NOTE 2: This test does not identify unobservable liquid water which may penetrate into the test specimen.1.1 This test method covers the determination of the resistance of exterior windows, skylights, and doors to water penetration when water is applied to the outdoor face and exposed edges simultaneously with a rapid pulsed air pressure at the outdoor face higher than the pressure at the indoor face.1.2 This test method is applicable to windows, skylights, or doors alone. Those interested in testing curtain walls to rapid pulsed air pressure differences should use AAMA 501.1-94.1.3 This test method addresses water penetration through a manufactured assembly. Water that penetrates the assembly, but does not result in a failure as defined herein, may have adverse effects on the performance of contained materials such as sealants and insulating or laminated glass. This test method does not address these issues.1.4 The proper use of this test method requires a knowledge of the principles of pressure measurement.1.5 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM F2238-20 Standard Test Method for Performance of Rapid Cook Ovens Active 发布日期 :  1970-01-01 实施日期 : 

5.1 The energy input rate test is used to confirm that the rapid cook oven is operating properly prior to further testing.5.2 Preheat energy and time can be useful to food service operators to manage power demands and to know how quickly the rapid cook oven can be ready for operation.5.3 Idle energy rate and pilot energy rate can be used to estimate energy consumption during non-cooking periods.5.4 Cooking-energy efficiency is a precise indicator of a rapid cook oven's energy performance while cooking a typical food product. If energy performance information is desired using a food product other than the specified test food, the test method could be adapted and applied. Energy performance information allows an end user to better understand the operating characteristics of a rapid cook oven.5.5 Production capacity information can help an end user to better understand the production capabilities of a rapid cook oven as it is used to cook a typical food product and this could help in specifying the proper size and quantity of equipment. If production information is desired using a food product other than the specified test food, the test method could be adapted and applied.1.1 This test method evaluates the energy consumption and cooking performance of rapid cook ovens. The food service operator can use this evaluation to select a rapid cook oven and understand its energy consumption.1.2 This test method is applicable to gas and electric rapid cook ovens.1.3 The rapid cook oven can be evaluated with respect to the following (where applicable):1.3.1 Energy input rate (see 10.2),1.3.2 Preheat energy consumption and time (see 10.3),1.3.3 Idle energy rate (see 10.4),1.3.4 Pilot energy rate (if applicable) (see 10.5), and1.3.5 Cooking-energy efficiency, cooking energy rate, and production capacity (see 10.6).1.4 The values stated in inch-pound units are to be regarded as standard. No other units of measurement are included in this standard.1.5 This test method may involve hazardous materials, operations, and equipment. This test method 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 test method 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 Thermogravimetry is useful in determining the dynamic functional effect of temperature on the amount of volatile materials leaving a specimen as the latter is heated progressively to higher temperatures. TGA can be useful for process control, process development, material evaluation, and for identification and quality control in specifications.5.2 The thermal stability of a material can be associated with the degree and time rate of mass loss as a function of temperature. TGA curves can, therefore, be used as a preliminary screen method in the evaluation of relative behavior of insulating materials of the same generic family.5.3 The functional temperature-life relationship of an insulating material in any given application depends on a number of service and environmental factors. Therefore, the information obtained from TGA curves is not adequate by itself to describe the thermal capability of an insulating material.5.4 Refer to the Appendix for further discussion of the interpretation of TGA data.1.1 This test method outlines a procedure for obtaining thermogravimetric (TGA) data on solid polymeric materials intended for use as electrical insulating materials.1.2 Do not use this standard to quantify an estimate of the long-term thermal capability for any electrical insulating material. If a relationship exists between TGA and the long-term thermal capabilities of a material, then that fact must be established and made public, preferably by comparing data between a candidate and another material known to display similar failure modes.1.3 The values stated in SI units are the 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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5.1 Storage stability depends on complex interactions. It varies with feedstock type and source, and the processing used. The rate of degradation may not change uniformly with temperature. Chemical reactions may lead to a change in color followed by the formation of soluble gums and insoluble sediments. Insoluble sediments may overload filters, and plug nozzles and injectors.5.2 This test method, which does not require the test sample to be heated, uses a portable apparatus and allows tests to be carried out on site or in the laboratory to give a result within 35 min.5.3 The potential beneficial effects of stability additives in fuels may not be recognized by this test method. Therefore, the actual storage stability of middle distillate fuels with stability additives may not be correctly indicated by these test results.5.4 The unstable reactive compounds (phenalenes and phenalenones) detected by this test method may be present in fuels containing catalytically cracked or straight run materials and can affect the potential instability of the fuel.5.5 If this test method is used by any party for a rapid assessment of stability, it is the responsibility of parties concerned to decide whether or not this procedure yields meaningful results.5.6 Interpretation of results and correlation with other test methods is given in Appendix X1.1.1 This test method covers a procedure3 for the rapid determination of phenalenes and phenalenones in middle distillate fuels, including marine, automotive, heating, and gas turbine fuel such as those specified in Specifications D396, D975, D2069, and D2880. Phenalenes and phenalenones affect the potential instability of fuels, leading to fuel degradation products during storage, which may cause performance problems.1.2 This test method is applicable to both dyed and undyed fuels at all points in the distribution chain from refinery to end-user. It is not applicable to fuels containing residual oil. The portable apparatus allows the whole test to be conducted on site or in a laboratory and does not require the test sample to be heated.1.3 This test method is suitable for testing samples with a relative absorbance of up to 5.00 absorbance units (AU).NOTE 1: The precision of the test method has been established on relative absorbance up to 1.00 AU. For relative absorbance above 1.00 AU the precision may not apply.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 Excessive levels of hydrogen sulfide in the vapor phase above residual fuel oils in storage tanks can result in health hazards, violation of local occupational health and safety regulations, and public complaint. An additional concern is corrosion that can be caused by the presence of H2S during refining or other activities. Control measures to maintain safe levels of H2S require a precise method for the measurement of potentially hazardous levels of H2S in fuel oils. (Warning—Safety. Hydrogen sulfide (H2S) is a very dangerous, toxic, explosive and flammable, colorless and transparent gas which can be found in crude oil and can be formed during the manufacture of the fuel at the refinery and can be released during handling, storage, and distribution. At very low concentrations, the gas has the characteristic smell of rotten eggs. However, at higher concentrations, it causes a loss of smell, headaches, and dizziness, and at very high concentrations, it causes instantaneous death. It is strongly recommended that personnel involved in the testing for hydrogen sulfide are aware of the hazards of vapor-phase H2S and have in place appropriate processes and procedures to manage the risk of exposure.)5.2 This test method was developed so refiners, fuel terminal operators, and independent testing laboratory personnel can rapidly and precisely measure the amount of H2S in residual fuel oils and distillate blend stocks, with a minimum of training, in a wide range of locations.5.3 Test Method D5705 provides a simple and consistent field test method for the rapid determination of H2S in the residual fuel oils vapor phase. However it does not necessarily simulate the vapor phase H2S concentration of a fuel storage tank nor does it provide any indication of the liquid phase H2S concentration.5.4 Test Method D6021 does measure the H2S concentration of H2S in the liquid phase, however it requires a laboratory and a skilled operator to perform the complex procedure and calculations, and does not offer any reproducibility data. This test method (D7621) offers a 15 min automated test, simplicity, full precision, and a degree of portability.5.5 H2S concentrations in the liquid and vapor phase attempt to reach equilibrium in a static system. However, this equilibrium and the related liquid and vapor concentrations can vary greatly depending on temperature and the chemical composition of the liquid phase. The equilibrium of the vapor phase is disrupted the moment a vent or access point is opened to collect a sample.1.1 This test method covers procedures (A and B) for the determination of the hydrogen sulfide (H2S) content of fuel oils such as marine residual fuels and blend stocks, with viscosity up to 3000 mm2s-1 at 50 °C, and marine distillate fuels, as measured in the liquid phase.NOTE 1: Specification fuels falling within the scope of this test method are: ASTM Specification D396, MIL-DTL-16884, and ISO 8217.1.2 Procedure A has been shown to eliminate interferences such as thiols (mercaptans) and alkyl sulfides. Procedure B can give elevated results if such interferences are present (see Annex A2).NOTE 2: A procedure for measuring the amount of hydrogen sulfide in crude oil can be found in Appendix X1. Full precision for Appendix X1 has not yet been determined.1.3 Valid ranges for the precision are given in Table 2 and Table 3. Measurements can be made outside these ranges however precision has not been determined.1.4 Samples containing FAME do not affect the measurement of hydrogen sulfide by this test method.1.5 The values stated in SI units are to be regarded as standard. Non-SI units given in parentheses are for information only.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This specification covers packaged, dry, cementitious mortar or concrete materials for rapid repairs to hardened hydraulic-cement concrete pavements and structures. Materials that contain organic compounds, such as bitumens, epoxy resins, and polyesters, as the principal binder are not included. Packaged, dry, concrete material contains aggregate of which at least 5% by mass of the total mixture is retained. Packaged, dry, mortar material contains aggregate of which less than 5% by mass of the total mixture is retained. Aqueous solutions, aqueous emulsions or dispersions may be included as components of the packaged materials. Aggregates must be included as a component of the packaged materials. Both packaged dry concrete and mortar shall be mechanically mixed with the use of a mixing liquid. Different test methods shall be performed in order to determine the following properties: compressive strength, length change, scaling resistance, and slant shear bond strength.1.1 This specification covers packaged, dry, cementitious mortar or concrete materials for rapid repairs to hardened hydraulic-cement concrete pavements and structures. Materials that contain organic compounds, such as bitumens, epoxy resins, and polymers, as the principal binder are not included.1.1.1 Packaged, dry, concrete material contains aggregate of which at least 5 % by mass of the total mixture is retained on a 9.5-mm [3/8-in.] sieve.1.1.2 Packaged, dry, mortar material contains aggregate of which less than 5 % by mass of the total mixture is retained on a 9.5-mm [3/8-in.] sieve.1.2 Aqueous solutions, aqueous emulsions or dispersions may be included as components of the packaged materials. The manufacturer may specify that these liquids are to replace some or all of the mixing water.1.3 Aggregates must be included as a component of the packaged materials. The manufacturer may recommend job site addition of specific amounts and types of additional aggregates to his product for some uses. However, such reformulated products are not within the scope of this specification.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 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.1.5 The following safety hazards caveat pertains to the test methods portion of this specification: 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 Riprap and armor material are composed of pieces of natural rock or manmade material that are placed on construction projects, shorelines, streambeds, bridge abutments, pilings and other structures to minimize the effects of erosion. The ability of rock or manmade material to withstand deterioration from weathering affects both the effectiveness of the project and its cost. The specific gravity and absorption provide useful information that can be used in evaluating possible deterioration of rock or manmade material.5.2 Test specimens equal in size to the proposed design size would provide the best correlations between laboratory tests and actual field performance; however, this is usually neither practical nor economically feasible.5.3 This test method has been used to evaluate different types of rocks and manmade material. There have been rare occasions when test results have provided data that have not agreed with the durability of rock or manmade material under actual field conditions.5.4 The results of this test is not to be used as the sole basis for determination of durability, but should be used in conjunction with the results of other tests.Note 1—The quality of the result produced by this standard is dependent upon 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/sampling/inspection/etc. Users of this standard are cautioned that compliance with Practice D3740 does not in itself assure reliable results. Reliable results depend on many factors; Practice D3740 provides a means of evaluation some of those factors1.1 This test method covers the determination of the rapid specific gravity of rock or man-made materials for erosion control.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 All observed and calculated values shall conform to the guidelines for significant digits and rounding established in Practice D6026, unless superseded by this standard.1.3.1 For purposes of comparing measured or calculated value(s) with specified limits, the measured or calculated value(s) shall be rounded to the nearest decimal or significant digits in the specified limits.1.3.2 The procedures used to specify how data are collected/recorded or calculated, in this standard are regarded as the industry standard. In addition, they are representative of the significant digits that generally should be retained. The procedures used do not consider material variation, purpose for obtaining the data, special purpose studies, or any considerations for the user’s objectives; and it is common practice to increase or reduce significant digits of reported data to be commensurate with these considerations. It is beyond the scope of this standard to consider significant digits used in analytical methods for engineering design.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 This test method is for the rapid assessment of the static segregation resistance of self-consolidating concrete.5.2 The method is useful for rapid assessment of the static segregation resistance of self-consolidating concrete during mixture development in the laboratory as well as prior to placement of the mixture in the field. Test Method C1610/C1610M for static segregation of SCC is not sufficiently rapid, and the non-mandatory Visual Stability Index as determined through the procedure described in Appendix X1 of Test Method C1611/C1611M is highly subjective and qualitative.5.3 Appendix X1 provides non-mandatory criteria that may be used to indicate the degree of static segregation resistance of self-consolidating concrete mixtures.1.1 This test method covers the rapid assessment of static segregation resistance of normal-weight self-consolidating concrete (SCC). The test does not measure static segregation resistance directly, but provides an assessment of whether static segregation is likely to occur.1.2 The test apparatus and protocol were developed based on tests with SCC mixtures containing saturated surface dry (SSD) coarse aggregates ranging in relative density from 2.67 to 2.79 and in nominal maximum size from 9.5 mm to 25 mm. For SCC mixtures outside these ranges, testing is recommended to establish a correlation between penetration depth and static segregation measured in accordance with Test Method C1610/C1610M. This test method shall not be used to assess the static segregation resistance of self-consolidating concrete containing lightweight aggregates or heavyweight aggregates without prior testing to establish a correlation.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 The text of this standard references notes and footnotes that provide explanatory material. These notes and footnotes shall not be considered as requirements of 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. (Warning—Fresh hydraulic cementitious mixtures are caustic and may cause chemical burns to skin and tissue upon prolonged exposure.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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