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5.1 It is normal for some of the combustion products of an internal combustion engine to penetrate into the engine lubricant and be retained in it.5.2 When an engine is run for a period of time and then stored over a long period of time, the by-products of combustion might be retained in the oil in a liquefied state.5.3 Under these circumstances, precipitates can form that impair the filterability of the oil the next time the engine is run.5.4 This test method subjects the test oil and the new oil to the same treatments such that the loss of filterability can be determined. The four water treatment levels may be tested individually, all four simultaneously, or any combination of multiple water treatment levels.5.5 Reference oils, on which the data obtained by this test method is known, are available.5.6 This test method requires that a reference oil also be tested and results reported. Two oils are available, one known to give a low and one known to give a high data value for this test method.NOTE 1: When the new oil test results are to be offered as candidate oil test results for a specification, such as Specification D4485, the specification will state maximum allowable loss of filterability (flow reduction) of the test oil as compared to the new oil.1.1 This test method covers the determination of the tendency of an oil to form a precipitate that can plug an oil filter. It simulates a problem that may be encountered in a new engine run for a short period of time, followed by a long period of storage with some water in the oil.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 It is normal for some of the combustion products of an internal combustion engine to penetrate into the engine lubricant and be retained in it.5.2 When an engine is run for a period of time and then stored over a long period of time, the by-products of combustion might be retained in the oil in a liquefied state.5.3 Under these circumstances, precipitates can form that impair the filterability of the oil the next time the engine is run.5.4 This test method subjects the test oil and the new oil to the same treatments such that the loss of filterability can be determined.5.5 Reference oils, on which the data obtained by this test method is known, are available.5.6 This test method requires that a reference oil also be tested and results reported. Two oils are available, one known to give a low and one known to give a high data value for this test method.NOTE 1: When the new oil test results are to be offered as candidate oil test results for a specification, such as Specification D4485, the specification will state maximum allowable loss of filterability (flow reduction) of the test oil as compared to the new oil.1.1 This test method covers the determination of the tendency of an oil to form a precipitate that can plug an oil filter. It simulates a problem that may be encountered in a new engine run for a short period of time, followed by a long period of storage with some water in the oil.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Aircraft turbine lubricants, upon standing at low temperatures for prolonged periods of time, may show an increase in kinematic viscosity. This increase may cause lubrication problems in aircraft engines. Thus, this test method is used to ensure that the kinematic viscosity does not exceed the maximum kinematic viscosity in certain specifications for aircraft turbine lubricants.1.1 This test method covers the determination of the kinematic viscosity of aircraft turbine lubricants at low temperature, and the percent change of viscosity after a 3 h and a 72 h standing period at low temperature.1.1.1 The range of kinematic viscosities covered by this test method is from 7700 mm2/s to 14 000 mm2/s at –40 °C and from 7000 mm2/s to 17 500 mm2/s at –51 °C. The precision has only been determined for those materials, kinematic viscosity ranges, and temperatures as shown in the precision section. Kinematic viscosities and percent change of viscosity may be measured and reported at other temperatures and other thermal soak period intervals as agreed by the contracting parties.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.2.1 The SI unit used in this test method for Kinematic Viscosity is mm2/s. For user reference, 1 mm2/s = 10-6 m2/s = 1 cSt.1.3 Warning—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use caution when handling mercury and mercury-containing products. See the applicable product Safety Data Sheet (SDS) for additional information. The potential exists that selling mercury or mercury-containing products, or both, is prohibited by local or national law. Users must determine legality of sales in their location.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 Section 7.1.5 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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4.1 This practice summarizes a method that may be used to accelerate the oxidation of UHMWPE components using elevated temperature and elevated oxygen pressure. Under real-time conditions, such as shelf aging and implantation, oxidative changes to UHMWPE after sterilization using high-energy radiation may take months or years to produce changes that may result in deleterious mechanical performance. The method outlined in this practice permits the evaluation of oxidative stability in a relatively short period of time (for example, weeks).4.2 This practice may also be used to oxidize UHMWPE test specimens and joint replacement components prior to characterization of their physical, chemical, and mechanical properties. In particular, this practice may be used for accelerated aging of UHMWPE components prior to evaluation in a hip or knee joint wear simulator as outlined in Guide F1714 (hip wear), Guide F1715 (knee wear), ISO 14242 (hip wear), or ISO 14243 (knee wear), or combination thereof.1.1 It is the intent of this practice to permit an investigator to evaluate the oxidative stability of UHMWPE materials as a function of processing and sterilization method. This practice describes a laboratory procedure for accelerated aging of ultra-high molecular weight polyethylene (UHMWPE) specimens and components for total joint prostheses. The UHMWPE is aged at elevated temperature and at elevated oxygen pressure, to accelerate oxidation of the material and thereby allow for the evaluation of its long-term chemical and mechanical stability.1.2 Although the accelerated aging method described by this practice will permit an investigator to compare the oxidative stability of different UHMWPE materials, it is recognized that this method may not precisely simulate the degradative mechanisms for an implant during real-time shelf aging and implantation.1.3 The accelerated aging method specified herein has been validated based on oxidation levels exhibited by certain shelf-aged UHMWPE components packaged in air and sterilized with gamma radiation. The method has not been shown to be representative of shelf aging when the UHMWPE is packaged in an environment other than air. For example, this practice has not been directly correlated with the shelf life of components that have been sealed in a low-oxygen package, such as nitrogen. This practice is not intended to simulate any change that may occur in UHMWPE following implantation.1.4 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to inch-pound units that are for information only and are not considered standard.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, 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 guide is not intended to measure the precise temperature range for dispensing and curing product under all the possible substrate and environmental factors but to provide a basis for benchmarking a foam sealant product under specific laboratory conditions.5.2 The product user is encouraged to evaluate each application and determine suitability for actual use.1.1 This guide covers the general effects of temperature from the aerosol foam sealant (either polyurethane or latex types) under the use temperatures.1.2 The guide is intended to estimate the observed product dispensing characteristics and foam quality of aerosol foam dispensed or cured, or both, at specific temperatures and standard conditions.1.3 Such foam sealants are primarily intended to reduce air movement in and out of building enclosures.1.4 Currently two main foam sealant types are applicable to this standard: single component polyurethane and latex.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 There are no other known test methods specific for measuring the product temperature range for aerosol foam sealant.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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1 Scope This part of ISO 10993 specifies test methods for the assessment of the local effects of an implant material on living tissue, at both the macroscopic and microscopic level. The test specimen is implanted into a site and tissue appropriate f

定价: 546元 / 折扣价: 465

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5.1 The test requirements specified herein have been established for use in evaluating the forced-entry resistance characteristics of assemblies to be used in commercial, residential, schools, government, and other institutional installations where the risk of a single person active shooter attack is present.5.2 The procedures of this test method are intended to evaluate the ability to create an opening of sufficient size to permit passage of a test shape through it.5.3 The procedure presented herein is based on post-event examination and are not intended to be used to establish or confirm the absolute prevention of forced entries.1.1 This test method sets forth the requirements and testing procedures to test forced-entry-resistant building components, construction components, and specialty security equipment. This test method is intended primarily for manufacturers to test and rate their windows, doors, modular panels, glazings, and similar products to ensure that all manufactured products meet the necessary requirements for forced-entry protection after sustaining an active shooter assault.1.2 This test method is currently designed to simulate an active shooter weakening the system with repetitive shots followed by mechanically driven impact to simulate forced entry.1.3 This test method is not to be used for ballistic resistant glazing rating. Test projectiles are permitted to perforate the entire specimen. The test projectile firings are intended to simulate actions taken by an assailant to aid in the ability to gain entry to a facility.1.4 This is a laboratory test to be performed on full systems and therefore not applicable for field testing.1.5 All tests are executed on the exterior surface of the fenestration.1.6 Systems are required to be tested as complete units in a test frame or fielded conditions. Mulled systems must be tested in the mulled condition. Test results only apply to the component or system as tested. Once a system is tested and deemed to satisfy the requirements of this test method, no design change can be made without a retest except those that qualify under Annex A1 Substitution Criteria.1.7 Components (such as glazing, door leaves, etc.) may be tested in accordance with Appendix X1, receiving a capability statement for the component, but not a system rating per this standard.1.8 Window and door systems shall be rated to at least a minimum level of Test Methods F476, F588, or F842, or combinations thereof, as appropriate prior to commencing this test evaluation. This test does not dual certify to the above mentioned standards.1.9 The values stated in this standard are SI units with the exception of the nominal descriptors for tools.1.10 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.1.11 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 Even so-called high-purity water will contain contaminants. While not always present, these contaminants may contribute one or more of the following: dissolved active ionic substances such as calcium, magnesium, sodium, potassium, manganese, ammonium, bicarbonates, sulfates, nitrates, chloride and fluoride ions, ferric and ferrous ions, and silicates; dissolved organic substances such as pesticides, herbicides, plasticizers, styrene monomers, deionization resin material; and colloidal suspensions such as silica. While this test method facilitates the monitoring of these contaminants in high-purity water, in real time, with one instrument, this test method is not capable of identifying the various sources of residue contamination or detecting dissolved gases or suspended particles.5.2 This test method is calibrated using weighed amounts of an artificial contaminant (potassium chloride). The density of potassium chloride is reasonably typical of contaminants found in high-purity water; however, the response of this test method is clearly based on a response to potassium chloride. The response to actual contaminants found in high-purity water may differ from the test method's calibration. This test method is not different from many other analytical test methods in this respect.5.3 Together with other monitoring methods, this test method is useful for diagnosing sources of RAE in ultra-pure water systems. In particular, this test method can be used to detect leakages such as colloidal silica breakthrough from the effluent of a primary anion or mixed-bed deionizer. In addition, this test method has been used to measure the rinse-up time for new liquid filters and has been adapted for batch-type sampling (this adaptation is not described in this test method).5.4 Obtaining an immediate indication of contamination in high-purity water has significance to those industries using high-purity water for manufacturing components; production can be halted immediately to correct a contamination problem. The emerging nano-particle technology industry will also benefit from this information.1.1 This test method covers the determination of dissolved organic and inorganic matter and colloidal material found in high-purity water used in the semiconductor, and related industries. This material is referred to as residue after evaporation (RAE). The range of the test method is from 0.001 μg/L (ppb) to 60 μg/L (ppb).1.2 This test method uses a continuous, real time monitoring technique to measure the concentration of RAE. A pressurized sample of high-purity water is supplied to the test method's apparatus continuously through ultra-clean fittings and tubing. Contaminants from the atmosphere are therefore prevented from entering the sample. General information on the test method and a literature review on the continuous measurement of RAE has been published.21.3 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to inch-pound units that are provided for information only and are not considered standard.1.4 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 hazards statements, see Section 8.1.5 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 used to determine the vulcanization characteristics of (vulcanizable) rubber compounds under selected test conditions of strain and frequency which do not significantly affect the cured dynamic properties. In the same test, this test method also will measure the dynamic properties of the vulcanizate at temperatures significantly below the cure temperature. These lower temperature measurements are necessary in order to more effectively relate to rubber product service conditions.5.2 This test method may be used for quality control in rubber manufacturing processes and for research and development testing of rubber compounds containing curatives. This test method also may be used for evaluating cure and dynamic property differences resulting from the use of different compounding ingredients.5.3 For additional information regarding the significance of dynamic testing of vulcanized rubber, the reader may wish to reference Guide D5992.1.1 This test method covers the use of a rotorless oscillating shear rheometer for measuring after cure dynamic properties at predetermined temperature(s) below the cure temperature.1.2 Specified cure conditions that approximate a “static cure” also are covered to minimize effects on cured rubber compound dynamic properties. This test method is not intended to replace Test Method D5289.1.3 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 Warning—Compounds based on silicone or fluoroelastomers may have high levels of thermal contraction or poor adhesion to the dies when cooled after the cure portion of this test method, causing slippage during strain sweeps. If this occurs, the results will not be reliable.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 Glass fiber reinforcing meshes are used to strengthen EIFS. The reinforcing meshes are embedded into base coats that contain portland cement, which potentially exposes the glass fibers in the reinforcing meshes to weakening by the action of alkali. The breaking force following alkali exposure as determined by this method, is a factor used to comparatively evaluate the alkali resistance of EIFS glass fiber reinforcing meshes in the laboratory.5.2 This test method does not purport to simulate the conditions that may be encountered in service. The performance of an EIFS is a function of many factors, such as proper installation, rigidity of supporting construction and resistance of the EIFS to deterioration by other causes.1.1 This test method covers procedures for determining the breaking force of glass fiber mesh following their conditioning in an alkali solution. The method is applicable to glass fiber mesh used in Class PB Exterior Insulation and Finish Systems (EIFS) with base coats that contain portland cement as an ingredient.1.2 Breaking force is expressed both as force per unit width of mesh and as a percentage of the breaking force of the mesh that has not been exposed to alkali conditioning.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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5.1 The purpose of this practice is to provide data that can be used for comparison and evaluation of the accuracy of different CAS systems.5.2 The use of CAS systems and robotic tracking systems is becoming increasingly common and requires a degree of trust by the user that the data provided by the system meets necessary accuracy requirements. In order to evaluate the potential use of these systems, and to make informed decisions about suitability of a system for a given procedure, objective performance data of such systems are necessary. While the end user will ultimately want to know the accuracy parameters of a system under clinical application, the first step must be to characterize the digitization accuracy of the tracking subsystem in a controlled environment under controlled conditions.5.3 In order to make comparisons within and between systems, a standardized way of measuring and reporting point accuracy is needed. Parameters such as coordinate system, units of measure, terminology, and operational conditions must be standardized.1.1 This standard will measure the effects on the accuracy of computer assisted surgery (CAS) systems of the environmental influences caused by equipment utilized for bone preparation during the intended clinical application for the system. The environmental vibration effect covered in this standard will include mechanical vibration from: cutting saw (sagittal or reciprocating), burrs, drills, and impact loading. The change in accuracy from detaching and re-attaching or disturbing a restrained connection that does not by design require repeating the registration process of a reference base will also be measured.1.2 It should be noted that one system may need to undergo multiple iterations (one for each clinical application) of this standard to document its accuracy during different clinical applications since each procedure may have different exposure to outside forces given the surgical procedure variability from one procedure to the next.1.3 All units of measure will be reported as millimeters for 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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4.1 The final appearance of an installed floor depends upon several factors. These include but are not limited to size and squareness in the case of tiles/planks, the quality of joint cut, the quality and preparation of the subfloor and the skill of the installer. Long term appearance of the installed floor is also dependent on but not limited to the ability of the tile/plank to resist shrinkage due to internal stress relief. This test method is used to measure the ability of the floor to retain its original dimensions following exposure to heat, simulating a long service life at reasonable and expected temperatures.1.1 This test method covers the determination of the change in linear dimensions of resilient floor tile/plank products after exposure to heat and reconditioning to ambient temperature.1.2 This test method allows one to also measure curling that can occur after a specimen has been exposed to heat and reconditioned back to ambient temperature.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 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 evaluates the edge binding assembly used to determine how well the two external elements along the mattress edge, essentially, the edge tape and FR sewing thread, behave after exposure to an open flame and a hot air oven. These data can be used to confirm that either the mattress or foundation, or both will pass when tested using 16 CFR1633. Evaluation of raw material components is a vital and ongoing part of any manufacturing operation, especially when each item can contribute to the technical performance of the final product.5.2 Inherently flame resistant (FR) sewing thread is used as shown in Fig. 1, Fig. 2, and Fig. 3 to secure and encapsulate the following elements:FIG. 1 Mattress Edge Bound Sample – ProfileFIG. 2 Before Trimming – ProfileFIG. 3 After Trimming – Profile5.2.1 Test method measures the behavior of mattress edge binding tape that joins and closes the assembly of either the mattress or the box spring foundation, or both, and sewing thread during and after exposure to an open flame ignition source.5.2.2 Test method can be used to determine if the encapsulated multilayer assembly of mattress cover, fire barrier, and foam (when used) work together to prevent entry of open flame to mattress interior.5.3 Flame resistance of the components used to close the perimeter of a mattress is an important factor in limiting the potential of a bedding fire by preventing the chance for seam failure.5.4 Data which show a correlation of behavior for both the sewing thread and edge binding tape, when tested as a subassembly according to this test method, and also when tested using a full scale composite mattress burn test, such as 16 CFR 1633, can provide the manufacturer with important information. These data can be valuable when selecting components to be used in the manufacture of its products which are designed to use mattress edge binding and sewing thread.5.5 The level of performance required for these components is (1) that they do not support the afterflame, and (2) that these components demonstrate post flame exposure characteristics which contribute to retaining the structural integrity of the subassembly.5.6 In case of a dispute arising from differences in reported results when using this test method for acceptance testing of commercial shipments, the purchaser and the supplier should conduct comparative tests to determine if there is a statistical bias between their laboratories. Competent statistical assistance is recommended for the investigation of bias. As a minimum, the two parties should take a group of test specimens which are as homogeneous as possible and which are from a lot of material of the type in question. The test specimens should then be sent to each laboratory for testing. The average results from the two laboratories should be compared using Student's t-test and an acceptable probability level chosen by the two parties before testing is begun. If a bias is found, either its cause must be found and corrected or the purchaser and the supplier must agree to interpret future test results with consideration of known bias.1.1 This test method measures the flammability characteristics of mattress edge bindings and sewing threads during and after exposure to an open flame ignition source.1.1.1 This test method is used to evaluate these components either independently or in combination for use in mattresses designed with a fire barrier fabric.1.1.1.1 The test method is used to evaluate mattress edge binding and sewing thread when the design requires the use of these components.1.1.2 This test method can be used as a screening test method to determine how sewing thread and mattress edge binding component combinations will perform.1.2 This standard is used to measure and describe the response of materials, products, or assemblies to heat and flame 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 Fire testing of products and materials is inherently hazardous, and adequate safeguards for personnel and property shall be employed in conducting these tests.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 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.1.5 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 provides a means of measuring the water retention of flat specimens of rigid thermal insulation as a result of immersion in water and exposure to drying conditions.1.1 This test method determines the amount of water retained (excluding surface water) by flat specimens of rigid thermal insulations after immersion and exposure to drying conditions. This test method is intended to be used for the characterization of materials in the laboratory. It is not intended to simulate any particular environmental condition potentially encountered in building construction applications.1.2 This test method does not address all the possible mechanisms of water intake and retention and related phenomena for rigid thermal insulations. It relates only to those conditions outlined in 1.1. Determination of moisture accumulation in thermal insulations due to partial immersion, water vapor transmission, internal condensation, freeze-thaw cycling, or a combination of these effects requires different test procedures.1.3 This test method does not address or attempt to quantify the drainage characteristics of materials.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 are not necessarily exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems has the potential to result in non-conformance with the standard.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.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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