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5.1 Interlaminar delamination growth can be a critical failure mode in laminated CMC structures. Knowledge of the resistance to interlaminar delamination growth of a laminated CMC is essential for material development and selection, and for CMC component design. (See (1-8)3 which give GIc values of 20 J/m2 to 800 J/m2 for different CMC and carbon-carbon composite systems at ambient temperatures.)5.2 Conducting this test produces multiple values of GIc which are traditionally plotted against the delamination length at which that value was measured (see Fig. 2). The specific data of value to the test requestor will depend on the end use that motivated testing.5.2.1 The first increment of growth, initiated from a pre-implanted insert or machined notch, is sometimes described as the non-precracked (NPC) toughness. NPC toughness may be of interest, as it can represent manufacturing or processing defects, such as foreign object debris in a laminate or an error during machining.5.2.2 The next increment of growth, initiated from the sharp crack tip assumed to be present after the first increment, is sometimes defined as the precracked (PC) toughness. PC toughness may be of interest, as it is more representative of the resistance to delamination growth from a naturally occurring or damage-induced delamination.5.2.3 The remaining increments of growth, collectively forming an R-curve, provide information on how GIc evolves as the delamination advances. In unidirectional tape laminates, the R-curve is often increasing due to bridging of nested fibers across the delamination plane, artificially increasing GIc. For 2-D woven laminates for which there is little interply nesting, the R-curve may be flat.5.2.4 The increments of growth in which the R-curve is flat, and GIc has reached a steady state value defined as GIR, may be of interest and may also useful in design and analysis.5.3 This test method for measurement of GIc of CMC materials can serve the following purposes:5.3.1 To establish quantitatively the effect of CMC material variables (fiber interface coatings, matrix structure and porosity, fiber architecture, processing and environmental variables, conditioning/exposure treatments, etc.) on GIc and the interlaminar crack growth and damage mechanisms of a particular CMC material;5.3.2 To determine if a CMC material shows R-curve behavior where GIc changes with crack extension or reaches a stable value at a given amount of delamination growth. Fig. 2 shows R-curve behavior for a SiC-SiC composite (1);5.3.3 To develop delamination failure criteria and design allowables for CMC damage tolerance, durability or reliability analyses, and life prediction;NOTE 3: Test data can only reliably be used for this purpose if there is confidence that the test is yielding a material property and not a structural, geometry-dependent, property.5.3.4 To compare quantitatively the relative values of GIc for different CMC materials with different constituents and material properties, reinforcement architectures, processing parameters, or environmental exposure conditions; and5.3.5 To compare quantitatively the values of GIc obtained from different batches of a specific CMC material, to perform lot acceptance quality control, to use as a material screening criterion, or to assess batch variability.1.1 This test method describes the experimental methods and procedures for the determination of the critical mode I interlaminar strain energy release rate of continuous fiber- reinforced ceramic matrix composite (CMC) materials in terms of GIc. This property is also sometimes described as the mode I fracture toughness or the mode I fracture resistance.1.2 This test method applies primarily to ceramic matrix composite materials with a 2-D laminate structure, consisting of lay-ups of continuous ceramic fibers, in unidirectional tape or 2-D woven fabric architectures, within a brittle ceramic matrix.1.3 This test method determines the elastic strain energy released per unit of new surface area created as a delamination grows at the interlaminar interface between two lamina or plies. The term delamination is used in this test method to specifically refer to this type of growth, while the term crack is a more general term that can also refer to matrix cracking, intralaminar delamination growth, or fiber fracture.1.4 This test method uses a double cantilever beam (DCB) specimen to determine the critical mode I interlaminar strain energy release rate (GIc). A DCB test method has been standardized for polymer matrix composites (PMCs) under Test Method D5528. This test method addresses a similar procedure, but with modifications to account for the different physical properties, reinforcement architectures, stress-strain response, and failure mechanisms of CMCs compared to PMCs.1.5 This test is written for ambient temperature and atmospheric test conditions, but the test method can also be used for elevated temperature or environmental exposure testing with the use of an appropriate environmental test chamber, measurement equipment for controlling and measuring the chamber temperature, humidity, and atmosphere, high temperature gripping fixtures, and modified equipment for measuring delamination growth.1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6.1 Values expressed in this test method are in accordance with the International System of Units (SI) and IEEE/ASTM SI 10.1.7 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. Specific hazard statements are given in Section 8.1.8 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 Bacteria that exist in biofilms are phenotypically different from suspended cells of the same genotype. Research has shown that biofilm bacteria are more difficult to kill than suspended bacteria (5, 7). Laboratory biofilms are engineered in growth reactors designed to produce a specific biofilm type. Altering system parameters will correspondingly result in a change in the biofilm. For example, research has shown that biofilm grown under high shear is more difficult to kill than biofilm grown under low shear (5, 8). The purpose of this test method is to direct a user in the laboratory study of a Pseudomonas aeruginosa biofilm by clearly defining each system parameter. This test method will enable an investigator to grow, sample, and analyze a Pseudomonas aeruginosa biofilm grown under high shear. The biofilm generated in the CDC Biofilm Reactor is also suitable for efficacy testing. After the 48 h growth phase is complete, the user may add the treatment in situ or remove the coupons and treat them individually.1.1 This test method specifies the operational parameters required to grow a reproducible (1)2 Pseudomonas aeruginosa ATCC 700888 biofilm under high shear. The resulting biofilm is representative of generalized situations where biofilm exists under high shear rather than being representative of one particular environment.1.2 This test method uses the Centers for Disease Control and Prevention (CDC) Biofilm Reactor. The CDC Biofilm Reactor is a continuously stirred tank reactor (CSTR) with high wall shear. Although it was originally designed to model a potable water system for the evaluation of Legionella pneumophila (2), the reactor is versatile and may also be used for growing and/or characterizing biofilm of varying species (3-5).1.3 This test method describes how to sample and analyze biofilm for viable cells. Biofilm population density is recorded as log10 colony forming units per surface area.1.4 Basic microbiology training is required to perform this test method.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health 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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5.1 This test method is intended for the determination of the radiant heat resistance value of a material, a combination of materials, or a comparison of different materials used in flame-resistant clothing for workers exposed to radiant thermal hazards.5.2 This test method evaluates a material's heat transfer properties when exposed to a continuous and constant radiant heat source. Air movement at the face of the specimen and around the calorimeter can affect the measured heat transferred due to forced convective heat losses. Minimizing the air movement around the specimen and test apparatus will aid in the repeatability of the results.5.3 This test method maintains the specimen in a static, vertical position and does not involve movement, except that resulting from the exposure.5.4 This test method specifies two standard sets of exposure conditions: 21 kW/m2 (0.5 cal/cm2s) and 84 kW/m2 (2.0 cal/cm2s). Either can be used.5.4.1 If a different set of exposure conditions is used, it is likely that different results will be obtained.5.4.2 The optional use of other conditions representative of the expected hazard, in addition to the standard set of exposure conditions, is permitted. However, the exposure conditions used must be reported with the results along with a determination of the exposure energy level stability.5.5 This test method does not predict skin burn injury from the standardized radiant heat exposure.NOTE 4: See Appendix X4 for additional information regarding this test method and predicted skin burn injury.1.1 This test method rates the non-steady state thermal resistance or insulating characteristics of flame resistant clothing materials subjected to a continuous, standardized radiant heat exposure.1.1.1 This test method is not applicable to clothing materials that are not flame resistant.NOTE 1: The determination of a clothing material's flame resistance shall be made prior to testing and done in accordance with the applicable performance standard, specification standard, or both, for the clothing material's end use.1.1.2 This test method does not predict skin burn injury from the standardized radiant heat exposure, as it does not account for the thermal energy contained in the test specimen after the exposure has ceased.NOTE 2: See Appendix X4 for additional information regarding this test method and predicted skin burn injury.1.2 This test method is used to measure and describe the response of materials, products, or assemblies to heat under controlled conditions, but does not by itself incorporate all factors required for fire hazard or fire risk assessment of the materials, products, or assemblies under actual fire conditions.1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to inch-pound or other units that are commonly used for thermal testing.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 allows for the measurement of the torque retention properties of container/continuous thread closure systems of various designs, materials, and manufacture, and is suitable for package development and engineering evaluation.5.2 Each test method can be used for the evaluation of non child resistant container/continuous thread closure systems under controlled conditions such as when the application torque is known and the applied downward force to the closure is zero or for Type I, style “A” push down and turn child resistant container/continuous thread closure systems under controlled conditions such as when the application torque and the applied downward force to the closure is known.5.3 This test method measures torque retention properties of container/continuous thread closure systems with the use of an automated transducer based torque meter operating at a known rotational velocity (rpm) or known torque ramp.5.4 This test method is intended for measurement of dry torque only.1.1 These test methods evaluate the torque retention of continuous thread closures on containers with matching finishes, for predetermined environmental conditions over time. Methods are defined for both Type I, style “A” push down and turn Type II2 child resistant and non child resistant type closures.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.NOTE 1: The SI unit system is the recommended system.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 CEDI devices can be used to produce deionized water from feeds of pretreated water. This test method permits the relatively rapid measurement of key performance capabilities of CEDI devices using standard sets of conditions. The data obtained can be analyzed to provide information on whether changes may have occurred in operating characteristics of the device independently of any variability in feed water characteristics or operating conditions. Under specific circumstances, this test method may also provide sufficient information for plant design.1.1 This test method covers the determination of the operating characteristics of continuous electrodeionization (CEDI) devices using synthetic feed solutions and is not necessarily applicable to natural waters. This test method is a procedure applicable to solutions with a conductivity range from approximately 50 μS/cm to 1000 μS/cm.1.2 This test method covers the determination of operating characteristics under standard test conditions of CEDI devices where the electrically active transfer media therein is predominantly unregenerated. This results in more rapid achievement of steady state and shorter test time than when performing a test which requires the active media be predominantly regenerated.1.3 This test method is not necessarily indicative of the following:1.3.1 Long-term performance on feed waters containing foulants or sparingly soluble solutes, or both,1.3.2 Performance on feeds of brackish water, sea water, or other high-salinity feeds,1.3.3 Performance on synthetic industrial feed solutions, pharmaceuticals, or process solutions of foods and beverages, or,1.3.4 Performance on feed waters less than 50 μS/cm, particularly performance relating to organic solutes, colloidal or particulate matter, or biological or microbial matter.1.4 This test method, subject to the limitations previously described, can be applied as either an aid to predict expected deionization performance for a given feed water quality, or as a test method to determine whether performance of a given device has changed over some period of time. It is ultimately, however, the user's responsibility to ensure the validity of this test method for their specific applications.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Some process catalysts used in refining can be poisoned when trace amounts of sulfur bearing materials are contained in the feedstocks. There are also government regulations as to how much sulfur is permitted to be present in commercial transportation fuels. This test method can be used to determine sulfur in process and downstream distribution streams. It can also be used for purposes of screening and quality control of finished hydrocarbon fuel products.1.1 This test method covers the determination of total sulfur in liquid hydrocarbon based fuel with a final boiling point of up to 450 °C. It is applicable to analysis of natural, processed and final product materials containing sulfur in the range of 4.0 mg/kg to 830 mg/kg (see Note 1).NOTE 1: For liquid hydrocarbons containing less than 4.0 mg/kg total sulfur or more than 830 mg/kg total sulfur, Test Method D5453 may be more appropriate.1.2 This test method is applicable for total sulfur determination in liquid hydrocarbons containing less than 0.35 % (m/m) halogen(s).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. For specific hazard statements, see 4.1, 8.3, and Section 9.1.5 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 intended for use in the laboratory or in the field to evaluate the cleanliness of distillate fuels, and liquid biofuels, such as biodiesel and diesel blends. This specific test method and the precision statement applies to off-line analysis.NOTE 5: These PCMs can be used for high pressure on-line applications as well, however the repeatability (r) and reproducibility (R) for on-line application were not established.5.2 An increase in particulate counts can indicate a change in the fuel condition caused for example by contamination during storage or transfer. Potential causes of particulates formation during storage could be “fuel-degradation products,” as described in Specification D975, Appendix X3.5.3 High levels of particles can cause filter blockages (especially when the particles are close in size to the filter porosity rating) and have a serious impact on the life of pumps, injectors, pistons, and other moving parts. Knowledge of particle size in relation to the metallurgy can provide vital information, especially if the hardness of particles is also known from other sources.5.4 This test method specifies a minimum requirement for reporting measurements in particle size bands (A1.2.1). Some specific applications may require measurements in other particle size bands. The particle count from the test should be carefully interpreted by the user as it can potentially over-state risk of abrasive damage or filter blocking due to counting water droplets as well as hard dirt particles.5.5 In situations where there is a requirement for the calibration of the apparatus to be solely in accordance with ISO 11171, Test Methods D7619, IP 565, or IP 577 may be used.1.1 This test method uses specific particle contamination monitors (PCMs) to count and measure the size of dispersed dirt particles, water droplets and other particulates, in middle distillate fuel, in the overall range from 4 µm to 70 µm and in the size bands ≥4 µm, ≥6 µm, ≥14 µm, and ≥30 µm.NOTE 1: The term particle contamination monitor, as used in this test method, is the same as that defined in ISO 21018-4; an instrument that automatically measures the concentrations of particles suspended in a fluid at certain sizes and cannot be calibrated in accordance with ISO 11171 whose output may be as a particle size distribution at limited sizes or as a contamination code.1.2 This test method has interim repeatability precision only, see Section 14 for more information.NOTE 2: ASTM specification fuels falling within the scope of this test method include Specifications: D975, D1655, D3699, D7467, MIL-DTL-83133, MIL-DTL-5624, and distillate grades of D396 and D2880.NOTE 3: For the purposes of this test method, water droplets are counted as particles, and agglomerated particles are detected and counted as a single larger particle. Dirt includes microbial particulates. Although the projected area of a particle is measured, this is expressed as the diameter of a circle for the purposes of this test method. The detector is unable to distinguish between dirt and water particles.NOTE 4: This test method may be used for particle sizes bands up to 70 µm, however the interim repeatability has only been determined for the size bands ≥4 µm, ≥6 µm, and ≥14 µm. All measurements are counts per millilitre.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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5.1 CEDI devices can be used to produce deionized water from feeds of pretreated water. This test method permits the measurement of key performance capabilities of CEDI devices using a standard set of conditions. The data obtained can be analyzed to provide information on whether changes may have occurred in operating characteristics of the device independently of any variability in feed water characteristics or operating conditions. Under specific circumstances, this test method may also provide sufficient information for plant design.1.1 This test method covers the determination of the operating characteristics of continuous electrodeionization (CEDI) devices, indicative of deionization performance when a device is applied to production of highly deionized water from the product water of a reverse osmosis system. This test method is a procedure applicable to feed waters containing carbonic acid or dissolved silica, or both, and other solutes, with a conductivity range of approximately 2 to 100 microsiemens-cm-1.1.2 This test method covers the determination of operating characteristics under standard test conditions of CEDI devices where the electrically active transfer media therein is predominantly regenerated.1.3 This test method is not necessarily indicative of:1.3.1 Long term performance on feed waters containing foulants or sparingly soluble solutes, or both;1.3.2 Performance on feeds of brackish water, sea water, or other high salinity feeds;1.3.3 Performance on synthetic industrial feed solutions, pharmaceuticals, or process solutions of foods and beverages; or1.3.4 Performance on feed waters less than 2 μS/cm, particularly performance relating to organic solutes, colloidal or particulate matter, or biological or microbial matter.1.4 This test method, subject to the limitations described, can be applied as either an aid to predict expected deionization performance for a given feed water quality, or as a method to determine whether performance of a given device has changed over some period of time. It is ultimately, however, the user’s responsibility to ensure the validity of this test method for their specific applications.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This specification deals with continuous grain flow carbon and alloy steel crankshaft forgings intended for medium speed diesel and natural gas engines. The steel used in the manufacture of the forgings is required to be vacuum degassed. Heat treatment, which may be done either before or after rough machining, shall consist of normalizing followed by tempering at a subcritical temperature, or austenitizing, liquid quenching and subcritical tempering. Charpy impact and tensile tests, which shall be performed at a frequency of one test per heat treatment load, shall be used to evaluate tensile strength, yield strength, elongation, reduction of area, and Brinell hardness requirements of forgings. Chemical composition requirements shall also be examined by heat analysis. Grain size tests and non-destructive magnetic particle examinations shall be conducted as well. When required by the purchaser, crankshafts may be surface hardened in designated areas for the purposes of enhanced wear resistance and fatigue strength.1.1 This specification covers continuous grain flow forged carbon and alloy steel crankshafts for medium speed diesel and natural gas engines.1.2 The steel used in the manufacture of the forgings is required to be vacuum degassed.1.3 The choice of steel composition grade for a given strength class is normally made by the forging supplier, unless otherwise specified by the purchaser.1.4 Provision is made for treatment of designated surfaces of the crankshaft to provide enhanced fatigue strength, or wear resistance, or both.1.5 Except as specifically required in this specification, all provisions of Specification A788/A788M apply.1.6 Unless the order specifies the applicable “M” specification designation, the material shall be furnished to the inch-pound units.1.7 The values stated in either inch-pound units or SI (metric) units are to be regarded separately as standard. Within the text and tables the SI units are shown in brackets. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.1.8 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 Continuous fiber-reinforced ceramic composites are candidate materials for structural applications requiring high degrees of wear, erosion, corrosion resistance, and damage tolerance at high temperatures.5.2 The 1D and 2D CFCCs are highly anisotropic and their transthickness tensile and interlaminar shear strength are lower than their in-plane tensile and in-plane shear strength, respectively.5.3 Shear tests provide information on the strength and deformation of materials under shear stresses.5.4 This test method may be used for material development, material comparison, quality assurance, characterization, and design data generation.5.5 For quality control purposes, results derived from standardized shear test specimens may be considered indicative of the response of the material from which they were taken for given primary processing conditions and post-processing heat treatments.1.1 This test method addresses the uniaxial compression of a double-notched test specimen to determine interlaminar shear strength of continuous fiber-reinforced ceramic composites (CFCCs) at elevated temperatures. Failure of the test specimen occurs by interlaminar shear between two centrally located notches machined halfway through the thickness of the test specimen and spaced a fixed distance apart on opposing faces (see Fig. 1). Test specimen preparation methods and requirements, testing modes (force or displacement control), testing rates (force rate or displacement rate), data collection, and reporting procedures are addressed.FIG. 1 Schematic of Uniaxial Compression of Double-Notched Test Specimen for the Determination of Interlaminar Shear Strength of CFCCs1.2 This test method is used for testing advanced ceramic or glass matrix composites with continuous fiber reinforcement having a laminated structure such as in unidirectional (1D) or bidirectional (2D) fiber architecture (lay-ups of unidirectional plies or stacked fabric). This test method does not address composites with nonlaminated structures, such as (3D) fiber architecture or discontinuous fiber-reinforced, whisker-reinforced, or particulate-reinforced ceramics.1.3 Values expressed in this test method are in accordance with the International System of Units (SI) and IEEE/ASTM SI 10.1.4 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 precautionary statements are noted in 8.1 and 8.2.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This test method covers the procedures for the standard practice of performing magnetic particle examination of continuous grain flow crankshaft forgings intended for medium speed diesel engines. Crankshafts shall be divided into four zones of decreasing operational stress, each of which have been designated its own set of acceptance criteria. Zone 1, which consists of the major critical areas, includes the crankpin journals, main bearing journals, and oil holes. Zone 2, which consists of the minor critical areas, includes the balance of the fillet radii of the crankpin and main bearing journals not included in Zone 1. Zone 3, which comprises the journal running surfaces, includes the remainder of the crankpin and main bearing journal surfaces not covered by Zones 1 and 2. Finally, Zone 4 comprises all other remaining areas, including the crankpin web surfaces, and flange faces and periphery. Dimpling technique may be used to remove unwanted visual or magnetic particle indications.1.1 This specification covers the magnetic particle examination of forged continuous grain flow (CGF) crankshafts intended for medium speed diesel engines.1.2 For the purpose of magnetic particle indication assessment, the crankshaft is divided into four zones of decreasing operational stress. Acceptance criteria have been set for each zone.1.3 The engines to which these crankshafts are fitted are commonly used for diesel electric locomotives, marine propulsion, and power generation. Engines fueled by natural gas also fall into this medium speed category.1.4 Specification A983/A983M is a product specification that covers the manufacture of CGF crankshafts.1.5 The values stated in either inch-pound units or SI units are to be regarded separately as standard. Within the text, the SI units are shown in brackets. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.1.6 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 The continuous grading temperatures and continuous grade are used for informational purposes only and shall not be used for the sale or purchase of asphalt binders. The continuous grading temperatures and continuous grade may be used for forensic or research studies and when producing, blending, modifying, or otherwise evaluating asphalt binders. This guide is applicable to Specification D6373, Tables 1 and 2.NOTE 1: The quality of the results produced by this standard are dependent on the competence of the personnel performing the procedure and the capability, calibration, and maintenance of the equipment used. Agencies that meet the criteria of Specification D3666 are generally considered capable of competent and objective testing, sampling, inspection, etc. Users of this standard are cautioned that compliance with Specification D3666 alone does not completely ensure reliable results. Reliable results depend on many factors; following the suggestions of Specification D3666 or some similar acceptable guideline provides a means of evaluating and controlling some of those factors.1.1 This practice is used to estimate the continuous grading temperatures and continuous grade for an asphalt binder graded in accordance with the requirements specified in Specification D6373.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 The text of this standard references notes and footnotes which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered as requirements of the standard.1.4 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 CFMEs are used to measure skid resistance on runways, roads, and various other trafficked surfaces. These tests may comprise operational testing, performed to obtain an immediate assessment of skid resistance in current conditions or routine testing in standardized conditions which include the application of a precise amount of water in front of the test tire.5.2 Standard test speeds and nominal water film thicknesses are according to national or international agency standards, the type of CFME, and the test application. Some examples of typical applications are given in Appendix X1.1.1 This test method covers the measurement of the skid resistance of a pavement or other trafficked surface using the continuous reading, fixed-slip technique.1.2 This test method covers braked wheel measurements obtained with less than 100 % slip. It does not cover side force measurements.1.3 This test method provides a record of the skid resistance along the whole length of one track of the test surface and enables averages to be obtained for specified test segments.1.4 This test method is used to measure skid resistance on a wide variety of surfaces in a wide variety of circumstances. Consequently, there are many different designs of continuous reading, fixed-slip measuring equipment (CFME) and as many different test procedures governing their use.1.5 This test method does not attempt to detail these different equipment and procedures but does set out the essential common principles.1.6 CFMEs function by creating and measuring a frictional force between a test tire operating at a selected slip and the test surface. Different types of CFME do not necessarily create the same frictional force between their particular test tire and a common test surface and do not necessarily use the same method to measure this frictional force.1.7 CFME measurements are obtained at a selected steady test speed. This speed may vary according to the application.1.8 The test surface may be contaminated or clean and dry. If it is clean and dry, a measured amount of water is normally deposited on the surface just in front of the test wheel.1.9 The measuring apparatus may be built into a vehicle, built into a trailer that is towed by a vehicle, or built into a device that is manually pushed.1.10 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in nonconformance with the standard.1.11 This standard may involve hazardous materials, operations, and equipment. 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. Safety precautionary information is contained in Section 7.1.12 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 Vegetative biofilm bacteria are phenotypically different from suspended cells of the same genotype. Biofilm growth reactors are engineered to produce biofilms with specific characteristics. Altering either the engineered system or operating conditions will modify those characteristics.5.2 The purpose of this test method is to direct a user in how to grow, sample, and analyze a P. aeruginosa biofilm under low fluid shear and close to the air/liquid interface using the DFR. The P. aeruginosa biofilm that grows has a smooth appearance that varies across the coupon surface and is loosely attached. Microscopically, the biofilm is sheet-like with few architectural details. This laboratory biofilm could represent those found on produce sprayers, on food processing conveyor belts, on catheters, in lungs with cystic fibrosis, and oral biofilms, for example. The biofilm generated in the DFR is also suitable for efficacy testing. After the 54 h growth phase is complete, the user may add the treatment in situ or harvest the coupons and treat them individually. Research has shown that P. aeruginosa biofilms grown in the DFR were less tolerant to disinfection than biofilms grown under high shear conditions.51.1 This test method specifies the operational parameters required to grow a repeatable2 Pseudomonas aeruginosa biofilm close to the air/liquid interface in a reactor with a continuous flow of nutrients under low fluid shear conditions. The resulting biofilm is representative of generalized situations where biofilm exists at the air/liquid interface under low fluid shear rather than representative of one particular environment.1.2 This test method uses the drip flow biofilm reactor. The drip flow biofilm reactor (DFR) is a plug flow reactor with laminar flow resulting in low fluid shear. The reactor is versatile and may also be used for growing and/or characterizing biofilms of different species, although this will require changing the operational parameters to optimize the method based upon the growth requirements of the new organism.1.3 This test method describes how to sample and analyze biofilm for viable cells. Biofilm population density is recorded as log colony forming units per surface area.1.4 Basic microbiology training is required to perform this test method.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Proton exchange membranes (PEM) used in fuel cells are susceptible to contamination from a number of species that can be found in hydrogen. It is critical that these contaminants be measured and verified to be present at or below the amounts stated in SAE J2719 and ISO 14687 to ensure both fuel cell longevity and optimum efficiency. Contaminant concentrations as low as single-figure ppb(v) for some species can seriously compromise the life span and efficiency of PEM fuel cells. The presence of contaminants in fuel-cell-grade hydrogen can, in some cases, have a permanent adverse impact on fuel cell efficiency and usability. It is critical to monitor the concentration of key contaminants in hydrogen during the production phase through to delivery of the fuel to a fuel cell vehicle or other PEM fuel cell application. In ISO 14687, the upper limits for the contaminants are specified. Refer to SAE J2719 (see 2.3) for specific national and regional requirements. For hydrogen fuel that is transported and delivered as a cryogenic liquid, there is additional risk of introducing impurities during transport and delivery operations. For instance, moisture can build up over time in liquid transfer lines, critical control components, and long-term storage facilities, which can lead to ice buildup within the system and subsequent blockages that pose a safety risk or the introduction of contaminants into the gas stream upon evaporation of the liquid. Users are reminded to consult Practice D7265 for critical thermophysical properties such as the ortho/para hydrogen spin isomer inversion that can lead to additional hazards in liquid hydrogen usage.1.1 This test method describes contaminant determination in fuel cell grade hydrogen as specified in relevant ASTM and ISO standards using cavity ring-down spectroscopy (CRDS). This standard test method is for the measurement of one or multiple contaminants including, but not limited to, water (H2O), oxygen (O2), methane (CH4), carbon dioxide (CO2), carbon monoxide (CO), ammonia (NH3), and formaldehyde (H2CO), henceforth referred to as “analyte.”1.2 This test method applies to CRDS analyzers with one or multiple sensor modules (see 6.2 for definition). This test method describes sampling apparatus design, operating procedures, and quality control procedures required to obtain the stated levels of precision and accuracy.1.3 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.1.4 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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