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5.1 EIFS are barrier-type systems that must be weatherproofed to prevent the passage of moisture, air, dust, heat, and cold from entering a structure.5.2 This test method is intended to determine the adhesion properties of the sealant with the EIFS substrate as determined by its tensile adhesive properties for dry, wet, frozen, heat-aged, and artificial weather-aged conditions.1.1 This test method describes a laboratory procedure for measuring tensile adhesion properties of sealants to exterior insulation and finish systems (EIFS) under dry, wet, frozen, heat-aged, and artificial weather-aged conditions.1.2 The committee with jurisdiction over this standard is not aware of any comparable standards published by other organizations.1.3 The values stated in SI units are to be regarded as the standard. The inch-pound values given in parentheses are provided for information only.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This guide supersedes the slope guidelines of Appendix X1 of Specification D 312.Hot-applied roofing asphalt serves both as the waterproofing agent and adhesive for construction of built-up roofing membranes. There are many variables that may affect the performance of BUR membranes. This guide provides general specification guidelines for the asphalt only.1.1 The purpose of this guide is to provide advice for the selection of asphalt used in the construction of built-up roofing (BUR). This guide does not address the use of asphalt in waterproofing, cold-applied, or modified bituminous roofing.1.2 Reinforcements considered for use with roofing asphalt include ply sheets, (see Specifications D 226, D 2178, and D 5726), base sheets (see Specifications D 2626, D 4601, and D 4897), and cap sheets (see Specification D 3909). They consist of glass, organic, or synthetic fibers.1.3 The use of asphalt in the placement of vapor retarders and rigid roof insulation also is addressed.

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5.1 This test method is based on Test Method F903 for measuring resistance of chemical protective clothing materials to penetration by liquids. This test method is normally used to evaluate specimens from individual finished items of protective clothing and individual samples of materials that are candidates for items of protective clothing.5.1.1 Finished items of protective clothing include gloves, arm shields, aprons, gowns, coveralls, hoods, and boots.5.1.2 The phrase “specimens from finished items” encompasses seamed and other discontinuous regions as well as the usual continuous regions of protective clothing items.5.2 Medical protective clothing materials are intended to be a barrier to blood, body fluids, and other potentially infectious materials. Many factors can affect the wetting and penetration characteristics of body fluids, such as surface tension, viscosity, and polarity of the fluid, as well as the structure and relative hydrophilicity or hydrophobicity of the materials. The surface tension range for blood and body fluids (excluding saliva) is approximately 0.042 to 0.060 N/m (1) .7 To help simulate the wetting characteristics of blood and body fluids, the surface tension of the synthetic blood is adjusted to approximate the lower end of this surface tension range. The resulting surface tension of the synthetic blood is approximately 0.042 ± 0.002 N/m.5.3 The synthetic blood mixture is prepared with a red dye to aid in visual detection and a thickening agent to simulate the flow characteristics of blood.5.4 Part of the protocol in Procedures A and B in Table 1 for exposing the protective clothing material specimens with synthetic blood involves pressurization of the test cell to 13.8 kPa [2 psig]. This hydrostatic pressure has been documented to discriminate between protective clothing material performance and to correlate with visual penetration results that are obtained with a human factors validation (2). Some studies, however, suggest that mechanical pressures exceeding 345 kPa [50 psig] can occur during clinical use (3, 4). Therefore, it is important to understand that this test method does not simulate all the physical stresses and pressures that are exerted on protective clothing garments during actual use. This test method is offered to identify those protective clothing materials that warrant further evaluation with a microbiological challenge.5.5 Since this test method uses visual observation rather than analytical measurements for determination of penetration, use this test method as a preliminary evaluation for possible penetration of blood and other body fluids. Perform subsequent testing with a microbiological challenge and analytical technique using Test Method F1671.NOTE 1: No viral resistance claims can be made based on this test method, as materials can pass the test method and fail Test Method F1671.5.6 Testing without considering degradation by physical, chemical, and thermal stresses which could negatively impact the performance of the protective barrier could lead to a false sense of security. Consider tests which assess the impact of storage conditions and shelf life for disposable products, and the effects of laundering and sterilization for reusable products. The integrity of the protective barrier can also be compromised during use by such effects as flexing and abrasion (5) . It is also possible that prewetting by contaminating materials such as alcohol and perspiration can also compromise the integrity of the protective barrier. If these conditions are of concern, evaluate the performance of protective clothing materials for synthetic blood penetration following an appropriate preconditioning technique representative of the expected conditions of use.5.7 While this test method involves a qualitative determination of the protective clothing material resistance to penetration by synthetic blood under specific test conditions, it is possible to use this test method as a material quality control or assurance procedure.5.7.1 If this procedure is used for quality control, perform proper statistical design and analysis of the data when more than three specimens are tested. This type of analysis includes, but is not limited to, the number of individual specimens tested, the average percent passing or failing, or both, with a standard deviation. Data reported in this way helps to establish confidence limits concerning product performance. Examples of acceptable sampling plans are found in references such as MIL-STD-105, ANSI/ASQC Z1.4, and ISO 2859-1.1.1 This test method is used to evaluate the resistance of materials used in protective clothing to penetration by synthetic blood under conditions of continuous liquid contact. Protective clothing pass/fail determinations are based on visual detection of synthetic blood penetration.1.1.1 This test method is not always effective in testing protective clothing materials having thick, inner liners which readily absorb the synthetic blood.1.2 This test method is a means for selecting protective clothing materials for subsequent testing with a more sophisticated barrier test as described in Test Method F1671.1.3 This test method does not apply to all forms or conditions of blood-borne pathogen exposure. Users of the test method must review modes for work/clothing exposure and assess the appropriateness of this test method for their specific application.1.4 This test method addresses only the performance of materials or certain material constructions (for example, seams) used in protective clothing. This test method does not address the design, overall construction and components, or interfaces of garments, or other factors which may affect the overall protection offered by the protective clothing.1.5 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.1.6 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 performance requirements for helmets used by downhill mountain bicycle riders. Studies have shown higher risk to the head and face for this sport as compared to recreational street riding; hence, this specification requires greater impact protection and provides performance criteria for chin bars on full-face helmets, but does not require full-face helmets. Retention system tests shall be performed before impact testing. The helmet can be impacted anywhere on or above the test line with the curbstone anvil in any horizontal orientation. The ambient test helmet shall be subjected to the chin bar impact test.1.1 This specification covers performance requirements for helmets used by downhill mountain bicycle riders. Studies have shown higher risk to the head and face for this sport as compared to recreational street riding; hence, this specification requires greater impact protection and provides performance criteria for chin bars on full-face helmets, but does not require full-face helmets. This specification recognizes the desirability of lightweight construction and ventilation; however, it is a performance specification and is not intended to restrict design.1.2 All testing and requirements of this specification shall be in accordance with Test Methods F1446, except where noted herein.1.3 Partial utilization of this standard is prohibited. Any statement of compliance with this specification must be a certification that the product meets all of the requirements of this specification in its entirety. A product that fails to meet any one of the requirements of this specification is considered to have failed this standard, and should not be sold with any indication that it meets parts of this standard.1.4 Headgear designed to comply with this and other standards may proclaim uses as certified by the manufacturer.1.5 This standard is subject to revision at any time by ASTM. It must be reviewed every five years and if not revised either reapproved or withdrawn. References to the standard must include the version date. No references to a version that has been replaced or withdrawn shall be placed on any product or its packaging manufactured more than 24 months after the effective revision or withdrawal date. Go to astm.org to verify the latest version of this standard.1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.7 The following safety caveat applies to the chemical, mechanical, or physical, or a combination thereof, test methods described herein and is meant specifically for those performing the tests (in an effort to provide them with notice to take the appropriate precautions when conducting the tests): This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Viscosity values at the shear rate and temperature of this test method have been indicated to be related to the viscosity providing hydrodynamic lubrication in automotive and heavy duty engines in severe service.75.2 The viscosities of engine oils under such high temperatures and shear rates are also related to their effects on fuel efficiency and the importance of high shear rate, high temperature viscosity has been addressed in a number of publications and presentations.71.1 This test method covers the laboratory determination of the viscosity of engine oils at 150 °C and 1.0·106 s−1 using a viscometer having a slightly tapered rotor and stator called the Tapered Bearing Simulator (TBS) Viscometer.21.2 The Newtonian calibration oils used to establish this test method range from approximately 1.2 mPa·s to 7.7 mPa·s at 150 °C. The precision has only been determined for the viscosity range 1.47 mPa·s to 5.09 mPa·s at 150 °C for the materials listed in the precision section.1.3 The non-Newtonian reference oil used to establish the shear rate of 1.0·106 s−1 for this test method has a viscosity closely held to 3.55 mPa·s at 150 °C by using the absolute viscometry of the TBS.1.4 Manual, semi-automated, and fully automated TBS viscometers were used in developing the precision statement for this test method.1.5 Application to petroleum products such as base oils and formulated engine oils was determined in preparing the viscometric information for this test method.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 This test method uses the milliPascal·second (mPa·s) as the unit of viscosity. This unit is equivalent to the centipoise (cP).1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This practice covers the design, material grouping classification, and manufacture of wire image quality indicators (IQI) used to indicate the quality of radiologic images. This practice, applicable to X-ray and gamma-ray radiology, covers the use of wire penetrameters as the controlling image quality indicator for the material thickness range from 6.4 to 152 mm [0.25 to 6.0 in.]. The alloy group(s) of the material, the thickness or thickness range of the material, and the applicable IQI's that represent the required IQI thickness(s) and alloy(s) shall be considered when selecting IQI's.1.1 This practice2 covers the design, material grouping classification, and manufacture of wire image quality indicators (IQI) used to indicate the quality of radiographic images.1.2 This practice is applicable to X-ray and gamma-ray radiography.1.3 This practice covers the use of wire penetrameters as the controlling image quality indicator for the material thickness range from 6.4 to 152 mm (0.25 to 6.0 in.).1.4 The values stated in inch-pound units are to be regarded as 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.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method is based on Test Method F903 for measuring resistance of chemical protective clothing materials to penetration by liquids. This test method is normally used to evaluate specimens from individual finished items of protective clothing and individual samples of materials that are candidates for items of protective clothing.5.1.1 Finished items of protective clothing include gloves, arm shields, aprons, gowns, coveralls, hoods, and boots.5.1.2 The phrase “specimens from finished items” encompasses seamed and other discontinuous regions, as well as the usual continuous regions of protective clothing items.5.2 It is known that body fluids penetrating protective clothing materials are likely to carry microbiological contaminants; however, visual detection methods are not sensitive enough to detect minute amounts of liquid containing microorganisms (1-3).7 This test method uses media containing Phi-X174 Bacteriophage. The visual detection technique of this test method is supplemented with a biologically based assay capable of detecting virus under the specified test conditions.5.3 Test Method F1670/F1670M allows the screening of protective clothing materials for resistance to penetration with synthetic blood as a challenge liquid. Test Method F1670/F1670M uses the same penetration test cell and technique, but exposes material specimens to synthetic blood with visual detection of liquid penetration. Materials passing Test Method F1670/F1670M should then be tested against bacteriophage penetration using this test method to verify performance.5.4 This test method has been specifically designed for measuring penetration of a surrogate microbe for Hepatitis (B and C) and the Human Immunodeficiency Viruses. The surrogate, Phi-X174 Bacteriophage, used in this test method is similar to HCV in size and shape but also serves as a surrogate for HBV and HIV. Inferences about protection from other pathogens must be assessed on a case-by-case basis.5.5 Part of the protocol in Procedures A and B in Table 1 for exposing the protective clothing material specimens to the Phi-X174 Bacteriophage challenge suspension involves pressurization of the penetration cell to 13.8 kPa [2 psig]. This hydrostatic pressure has been documented to discriminate between protective clothing material performance and correlate with visual penetration results that are obtained with a human factors validation (4). Some studies, however, suggest that mechanical pressures exceeding 345 kPa [50 psig] can occur during actual clinical use (5, 6). Therefore, it is important to understand that this test method does not simulate all the physical stresses and pressures that might be exerted on protective clothing materials during actual use.5.6 Medical protective clothing materials are intended to be a barrier to blood, body fluids, and other potentially infectious materials. Many factors can affect the wetting and penetration characteristics of body fluids, such as surface tension, viscosity, and polarity of the fluids, as well as the structure and relative hydrophilicity or hydrophobicity of the materials. The surface tension range for blood and body fluids (excluding saliva) is approximately 0.042 to 0.060 N/m (7). To help simulate the wetting characteristics of blood and body fluids, the surface tension of the Phi-X174 Bacteriophage challenge suspension is adjusted to approximate the lower end of this surface tension range. This is accomplished by adding surfactant to the Phi-X174 Bacteriophage nutrient broth. The resulting surface tension of the Phi-X174 Bacteriophage challenge suspension is approximately 0.042 ± 0.002 N/m.5.7 Testing prior to degradation by physical, chemical, and thermal stresses which could negatively impact the performance of the protective material could lead to a false sense of security. Additional tests should be considered that assess the impact of storage conditions and shelf life on disposable products and the impact of laundering and sterilization on reusable products. The integrity of the protective barrier may also be compromised during use by such effects as flexing and abrasion (8). Prewetting agents, such as alcohol, and contaminating agents, such as perspiration, may also compromise the integrity of the protective barrier. If these conditions are of concern, the performance of protective clothing materials should be evaluated for Phi-X174 Bacteriophage penetration following an appropriate preconditioning technique representative of the expected conditions of use.5.8 This test method involves a sensitive assay procedure for determining protective clothing material resistance to penetration by a surrogate microbe. Because of the length of time required to complete this method, it may not be suitable for use as a material or protective clothing quality control or quality assurance procedure.5.9 If this procedure is used for quality control or to support broad product claims concerning the viral-resistant properties of materials used in protective clothing, proper statistical design and analysis of larger data sets than those specified in this test method should be performed.8 Examples of acceptable sampling plans can be found in MIL-STD-105, ANSI/ASQ Z1.4, and ISO 2859-1.5.10 This test method requires a working knowledge of basic microbiological techniques (9).1.1 This test method is used to measure the resistance of materials used in protective clothing to penetration by blood-borne pathogens using a surrogate microbe under conditions of continuous liquid contact. Protective clothing material pass/fail determinations are based on the detection of viral penetration.1.1.1 This test method is not always effective in testing protective clothing materials having thick, inner liners which readily absorb the liquid assay fluid.1.2 This test method does not apply to all forms or conditions of blood-borne pathogen exposure. Users of the test method should review modes for worker/clothing exposure and assess the appropriateness of this test method for their specific applications.1.3 This test method has been specifically defined for modeling the viral penetration of Hepatitis (B and C) and Human Immunodeficiency Viruses transmitted in blood and other potentially infectious body fluids. Inferences for protection from other pathogens must be assessed on a case-by-case basis.1.4 This test method addresses only the performance of materials or certain material constructions (for example, seams) used in protective clothing and determined to be viral resistant. This test method does not address the design, overall construction and components, or interfaces of garments or other factors which may affect the overall protection offered by the protective clothing.1.5 The values stated in SI units or in other units shall be regarded separately as standard. The values stated in each system must be used independently of the other, without combining values in any way.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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1.1 This specification is applicable to the use of plastic lumber materials and of wood-plastic composite materials, and no other plastic composite materials, used as exterior wall coverings, as part of an exterior wall assembly.1.2 This specification is not applicable to the use of plastic lumber materials or of wood-plastic composite materials contained in exterior wall assemblies when not used as part of the exterior wall covering.1.3 This specification is not applicable to the use of any of the following types of materials:(a) poly(vinyl chloride) (PVC) siding (see Specification D3679, for standard vinyl siding, or Specification D7793, for insulated vinyl siding),(b) polypropylene siding (see Specification D7254),(c) wood (including lumber, plywood, engineered wood, coated wood, or painted wood).1.4 This specification is not applicable to the use of plastic lumber materials or of wood-plastic composite materials in any application other than the one addressed in 1.1. In particular, this specification is not applicable to the use of plastic lumber materials or of wood-plastic composite materials as exterior deck boards, stair treads, handrails, guards, or soffits.1.5 The values stated in inch-pound units are to be regarded as standard. Any 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.NOTE 1: There is no known ISO equivalent to this standard.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 practice is intended primarily for the testing of flat panel composites and sandwich core panels to an acceptance criteria most typically specified in a purchase order or other contractual document.5.2 Basis of Application—There are areas in this practice that require agreement between the cognizant engineering organization and the supplier, or specific direction from the cognizant engineering organization.1.1 This practice establishes two procedures for ultrasonic testing (UT) of flat panel composites and flat sandwich core panels (parallel surfaces). Typical as-fabricated lay-ups include uniaxial, cross ply and angle ply laminates; as well as honeycomb sandwich core materials. These procedures can be used throughout the life cycle of the materials; product and process design optimization, on line process control, after manufacture inspection, and in service inspection. Contact methods such as angle-beam techniques using shear waves, or surface-beam techniques using Lamb waves, are not discussed.1.2 Ultrasonic testing is a common subsurface method for detection of laminar oriented discontinuities. Two techniques can be considered based on panel surface accessibility; pulse echo for one sided and through transmission (bubblers/squirters) for two sided. As used in this practice, both require the use of a pulsed straight-beam ultrasonic longitudinal wave followed by observing indications of either the reflected (pulse-echo) or received (through transmission) wave. The general types of anomalies detected by both techniques include foreign materials, delamination, disbond/un-bond, fiber de-bonding, inclusions, porosity, and voids.1.3 This practice provides two ultrasonic test procedures. Each has its own merits and requirements for inspection and shall be selected as agreed upon in a contractual document.1.3.1 Test Procedure A, Pulse Echo (non-contacting and contacting), is at a minimum a single transducer transmitting and receiving a longitudinal wave in the range of 0.5 to 20 MHz (see Fig. 1). This procedure requires access to only one side of the specimen. This procedure can be conducted by automated or manual means. Automated and manual test results may be imaged or recorded.FIG. 1 Test Procedure A, Pulse Echo Apparatus Set-up1.3.2 Test Procedure B, Through Transmission, is a combination of two transducers. One transmits a longitudinal wave and the other receives the longitudinal wave in the range of 0.5 MHz to 20 MHz (see Fig. 2). This procedure requires access to both sides of the specimen. This procedure is automated and the examination results are recorded.FIG. 2 Test Procedure B, Through Transmission Apparatus Set-up1.4 This practice does not specify accept-reject criteria.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, 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 Method Considerations—The objective of most groundwater sampling programs is to obtain samples that are similar in composition to that of the formation water near the well screen. The low-flow purging and sampling method uses the stabilization of indicator parameters to determine when the pump discharge is considered to represent a flow-weighted average of the formation water. Measurements of operational parameters are used to determine potential sampling bias (for example, artifactual turbidity and increased temperature) that may have been introduced by pumping operations and to ensure that the sample is representative of formation water. The low-flow purge rate minimizes lowering of the ambient groundwater level and thereby minimizes potential entrainment of blank-riser pipe (and potentially stagnant) water above or below the screen into the screened-zone of the well. This sampling method assumes that the well has been properly designed and constructed as described in Practices D5092/D5092M and D6725/D6725M, adequately developed as described in Guide D5521/D5521M, and has received proper well maintenance and rehabilitation as described in Guide D5978/D5978M (see Note 1).NOTE 1: This Standard is not intended to replace or supersede any regulatory requirements, standard operating procedure (SOP), quality assurance project plan (QAPP), ground water sampling and analysis plan (GWSAP) or site-specific regulatory permit requirements. The procedures described in this Standard may be used in conjunction with regulatory requirements, SOPs, QAPPs, GWSAPs or permits where allowed by the authority with jurisdiction.5.2 Applicability—Low-flow purging and sampling may be used in a monitoring well that can be pumped at a constant low-flow rate without continuously increasing drawdown in the well (2). If a well cannot be purged without continuously increasing drawdown even at very low pumping rates (for example, 50 – 100 mL/min), the well should not be sampled using this sampling method as described in this standard; a passive sampling method, as described in Guide D7929, may be considered as an alternative.5.3 Target Analytes—Low-flow purging and sampling can be used to collect samples for all categories of aqueous-phase contaminants and naturally-occurring analytes. It is particularly well suited for use where it is desirable to sample aqueous-phase constituents that may sorb or partition to particulate matter, because the method minimizes the potential for artifactual turbidity compared with high flow/high volume purging using a pump, bailer, or inertial-lift device (9-12).1.1 This practice describes the method of low-flow purging and sampling used to collect groundwater samples from wells to assess groundwater quality.1.2 The purpose of this procedure is to collect groundwater samples that represent a flow-weighted average of solute and colloid concentrations transported through the formation near the well screen under ambient conditions. Samples collected using this method can be analyzed for groundwater contaminants and/or naturally occurring analytes.1.3 This practice is generally not suitable for use in wells with very low-yields and cannot be conducted using grab sampling or inertial lift devices. This practice is not suitable for use in wells with non-aqueous phase liquids.1.4 Units—The values stated in SI units are to be regarded as standard. The values given in parentheses are approximate mathematical conversions to inch-pound units that are provided for information only and are not considered standard.1.5 This practice offers a set of instructions for performing one or more specific operations. This document cannot replace education or experience and should be used in conjunction with professional judgment. Not all aspects of this practice may be applicable in all circumstances. This ASTM standard is not intended to represent or replace the standard of care by which the adequacy of a given professional service must be judged, nor should this document be applied without consideration of a project's many unique aspects. The word “standard” in the title means only that the document has been approved through the ASTM consensus process.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 Coagulated pentane insolubles can include oil-insoluble materials, some oil-insoluble resinous matter originating from oil or additive degradation, soot from incomplete diesel fuel combustion, or a combination of all three.5.2 A significant change in coagulated pentane insolubles indicates a change in oil, and this could lead to lubrication system problems.5.3 Coagulated pentane insolubles measurements can also assist in evaluating the performance characteristics of a used oil or in determining the cause of equipment failure.5.4 High values of coagulated pentane insolubles have been associated with plugged oil filters, leading to opening of the bypass valve and circulation of unfiltered oil in the engine. This can lead to increased piston deposits, increased bearing wear, and premature engine failure.1.1 This test method covers the determination of coagulated pentane insolubles in used lubricating oils by a paper filtration method.1.2 This test method was originally developed by the Fuels, Lubricants, and Environmental Committee (FL&E) of the Locomotive Maintenance Officer’s Association (LMOA).21.3 This test method is used primary for testing used diesel engine oils from railroad locomotive service. It may be applied to other samples types but precision, bias, and significance have not been determined for samples other than used railroad locomotive diesel engine oils.1.4 This test method, in general, does not correlate with Test Method D893 on Insolubles in Lubricating Oils, since it uses separation by centrifugation and a more concentrated solution of anti-coagulant.1.5 The correlation between this test method and Appendix A4 (Enhanced Thermal Gravimetric Analysis (TGA) Procedure) in Test Method D5967 has not been investigated.1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see 7.2, 7.3, and 7.4.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

定价: 590元 / 折扣价: 502 加购物车

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This specification covers flexible, preformed sheet membrane materials to be used as vapor retarders in contact with soil or granular fill under concrete slabs. The specified tests are conducted on new materials and materials that have been conditioned or exposed to simulate potential service conditions. The membranes are classified into 3 classes. The materials shall be subject to tests for water vapor permeance, tensile strength, and puncture resistance. Under special conditions, the material shall also conform to the required flame spread, permeance after soil poison petroleum vehicle exposure, and permeance after exposure to ultraviolet light.1.1 This specification covers flexible, preformed sheet membrane materials to be used as vapor retarders in contact with soil or granular fill under concrete slabs.1.1.1 This specification does not cover bituminous vapor retarders. See Specification E1993/E1993M for information on bituminous vapor retarders.1.2 The specified tests are conducted on new materials and materials that have been conditioned or exposed to simulate potential service conditions.1.3 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

定价: 515元 / 折扣价: 438 加购物车

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