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5.1 Porous articles (often textiles) are often treated with antimicrobial agents to reduce the growth of microorganisms during use, in storage, or while waiting to be laundered, or both. Additionally, antimicrobial agents are added to reduce or control the overall microbial growth on porous articles that may affect the material’s odor, visual, chemical or physical integrity, or both.5.2 Antimicrobial textile test methods that measure the antimicrobial behavior of treated textiles do exist but they are often specific for one type of antimicrobial agent or are designed to or may artificially (not expected in real life) promote the release of some specific antibacterial agents over others. This test method is designed to be able to measure the antimicrobial activity from all common antimicrobial agents used to treat porous articles, including textiles, without giving either positive or negative bias to one type of chemistry or product over another.5.3 In an effort to avoid excessive use or abuse of antimicrobial agents in the environment, it is important to understand if untreated porous articles are susceptible to microbial contamination and growth. In this test method, a small amount of nutrients is added to each test sample in order to promote some microbial growth on susceptible test samples but not enough to overwhelm potential antimicrobial agents that may be effective in real life situations. Furthermore, low levels of nutrients allow investigators to add soiling agents that may be more reflective of a specific treated product’s end use or expected performance.5.4 Very specific parameters are identified within this method to limit any variability that may be seen between laboratories. Identifying and clarifying potential variables found in other guides or methods used in the industry will allow for better reproducibility and repeatability between and within laboratories.5.5 This test method provides the foundation for conducting tests on porous antibacterial treated articles. Modifications of this method that simulate intended use, durability and compatibility of the treated article should be outlined to ensure an accurate assessment of antimicrobial activity with each particular biocide that substantiates end use claims made for the article. A list of these typical modifications and current test methods for textiles can be found in Guide E2922.5.6 This test method is appropriate for porous materials such as textiles, paper, or similar porous materials. It is intended to measure the antibacterial properties of such materials. In most instances, further studies will be required to support and substantiate actual claims being made for the performance of treated materials in practice or as part of a regulatory process.5.7 This test method or indicated modifications may be used to determine antimicrobial activity as indicated in 5.6 or may be used as a routine bioassay in standard quality control programs.1.1 To determine the bactericidal or bacteriostatic properties of porous articles treated with an active biocidal agent, samples of porous treated materials, such as textiles or paper, are inoculated with a defined suspension of microorganisms and then incubated. The changes in numbers of the bacterial populations on the treated article are compared with untreated articles either over designated time or they are compared to the initial bacterial population at “zero time” for the treated article to measure antibacterial properties.1.2 This test method is used for measuring the quantitative antibacterial activity of porous materials that have been treated with a biocide to inhibit the growth of bacteria on the treated materials. This method may also be used to measure the ability of the treated material to inhibit the growth of a microorganism. It can measure both bactericidal and bacteriostatic activity.1.3 This test method shall be performed by individuals experienced and adept in microbiological procedures and in facilities suitable for the handling of the microorganisms under test.1.4 This test method 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.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 to be used when a quantitative measurement of the alkali durability of a ceramic-glass enamel is needed. The test is applicable to glass coated with fired enamels where exposure to strong alkalis, or alkalis at elevated temperatures might be encountered in service.5.2 This test method is intended to be an accelerated, destructive test. Results can be used as an indicator of the relative durability of a particular enamel.1.1 This test method covers the determination of the resistance of a fired ceramic-glass enamel to a 10 % alkali solution held near its boiling point for 2 h.1.2 This test method is not applicable to large tempered glass sheets or specimens larger than 9 by 9 cm.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 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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4.1 Although Test Method D4017 is widely used for the determination of water in paints and related materials, this method may overcome some of the variability found in the Karl Fischer method.4.2 Control of water content is often important in controlling the performance of paints, and it is critical in determining volatile organic compound (VOC) content when VOC content is measured by difference from total volatile matter and water content as required in certain federal and state regulations.1.1 This test method describes the determination of the total water content of paints using a calcium hydride reaction test kit, or water content between 2 and 85 % water.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method is fully quantitative and it also avoids any loss of viable organisms through wash off, making it possible to produce statistically valid data using many fewer test and control carriers than other quantitative methods based on most probable numbers (MPN).5.2 The design of the carriers makes it possible to place into each a precisely measured volume of the test suspension. The use of the threaded stir bars allows for efficient recovery of the inoculum even after its exposure for several hours to strong fixatives such as glutaraldehyde.5.3 The membrane filtration step allows processing of the entire eluate from the test carriers and therefore the capture and subsequent detection of even low numbers of viable organisms that may be present.5.4 This test can be performed with or without a soil load to determine the effect of such loading on microbicide performance. Consult the target regulatory agency on the need, type(s), and acceptable level(s) of soil load prior to testing. One type of soil load (Quantitative Disk Carrier Test Method E2197) to consider for this test is a mixture of three types of proteins (high molecular weight proteins, low molecular weight peptides, and mucous material) to represent the body secretions, excretions, or other extraneous substances that chemical microbicides may encounter under field conditions. It is suitable for working with the various test organisms included here. The components of the soil load are readily available and subject to much less variability than animal sera.5.5 If distilled water or other diluent is not to be specified on the product label, the diluent for the test substance is assumed to be tap water. Since the quality of tap water varies considerably both geographically and temporally, this test method incorporates the use of water with a specified and documented level of hardness to prepare use-dilutions of test substance that require dilution in water before use. Consult the target regulatory agency regarding the use and level of water hardness prior to testing.1.1 This test method is designed for use in product development and for the generation of product potency data. This test method permits the loading of each carrier with a known volume of the test organism. The incorporation of controls can also determine the initial load of colony forming units (CFU) of organisms on the test carriers and any loss in CFU after the mandatory drying of the inoculum.1.2 This test method is designed to have survivors and also to be used with a performance standard. The surviving microorganisms on each test carrier are compared to the mean of no less than three control carriers to determine if the performance standard has been met. To allow proper statistical evaluation of results, the size of the test inoculum should be sufficiently large to take into account both the performance standard and the experimental variation in the results. For example, if an arbitrary performance standard of 6-log10 reduction in the viability titer of the test organism is used, and an inoculum size of 107 CFU, then theoretically a maximum of ten survivors per carrier is permitted; however, because of experimental variability, the exact target may need to be higher than 106 CFU/carrier, thus fewer survivors would be permitted.1.3 This test method should be performed by persons with training in microbiology and in facilities designed and equipped for work with infectious agents at the appropriate biosafety level (3).1.4 In this test method, SI units are used for all applications, except for distance, in which case inches are used and SI units follow.1.5 It is the responsibility of the investigator to determine whether Good Laboratory Practice Regulations (GLPs) are required and to follow them where appropriate (40 CFR Part 160 for EPA submissions and 21 CFR Part 58 for FDA submissions).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 This test method allows the determination of 241Am in a plutonium solution without separation of the americium from the plutonium. It is generally applicable to any solution containing 241Am.5.2 The 241Am in solid plutonium materials may be determined when these materials are dissolved (see Practice C1168).5.3 When the plutonium solution contains unacceptable levels of fission products or other materials, this method may be used following a tri-n-octylphosphine oxide (TOPO) extraction, ion exchange or other similar separation techniques (see Test Methods C758 and C759).5.4 This test method is less subject to interferences from plutonium than alpha counting since the energy of the gamma ray used for the analysis is better resolved from other gamma rays than the alpha particle energies used for alpha counting.5.5 The minimal sample preparation reduces the amount of sample handling and exposure to the analyst.5.6 This test method is applicable only to homogeneous solutions. This test method is not suitable for solutions containing solids.5.7 Solutions containing 241Am at concentrations as little as 1 × 10−5 g/L may be analyzed using this method. The lower limit depends on the detector used and the counting geometry. Solutions containing high concentrations may be analyzed following an appropriate dilution.1.1 This test method covers the quantitative determination of 241Am by gamma-ray spectrometry in plutonium nitrate solution samples that do not contain significant amounts of radioactive fission products or other high specific activity gamma-ray emitters.1.2 This test method can be used to determine the 241Am in samples of plutonium metal, oxide and other solid forms, when the solid is appropriately sampled and dissolved.1.3 The values stated in SI units are to be regarded as standard. Additionally, the non-SI units of electron volts, kiloelectron volts, and liters 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 This practice is used to provide steel phase transformation data required for use in numerical models for the prediction of microstructures, properties, and distortion during steel manufacturing, forging, casting, heat treatment, and welding. Alternatively, the practice provides end users of steel and fabricated steel products the phase transformation data required for selecting steel grades for a given application by determining the microstructure resulting from a prescribed thermal cycle.5.1.1 There are available several computer models designed to predict the microstructures, mechanical properties, and distortion of steels as a function of thermal processing cycle. Their use is predicated on the availability of accurate and consistent thermal and transformation strain data. Strain, both thermal and transformation, developed during thermal cycling is the parameter used in predicting both microstructure and properties, and for estimating distortion. It should be noted that these models are undergoing continued development. This process is aimed, among other things, at establishing a direct link between discrete values of strain and specific microstructure constituents in steels. This practice describes a standardized method for measuring strain during a defined thermal cycle.5.1.2 This practice is suitable for providing data for computer models used in the control of steel manufacturing, forging, casting, heat-treating, and welding processes. It is also useful in providing data for the prediction of microstructures and properties to assist in steel alloy selection for end-use applications.5.1.3 This practice is suitable for providing the data needed for the construction of transformation diagrams that depict the microstructures developed during the thermal processing of steels as functions of time and temperature. Such diagrams provide a qualitative assessment of the effects of changes in thermal cycle on steel microstructure. Appendix X2 describes construction of these diagrams.5.2 It should be recognized that thermal and transformation strains, which develop in steels during thermal cycling, are sensitive to chemical composition. Thus, anisotropy in chemical composition can result in variability in strain, and can affect the results of strain determinations, especially determination of volumetric strain. Strains determined during cooling are sensitive to the grain size of austenite, which is determined by the heating cycle. The most consistent results are obtained when austenite grain size is maintained between ASTM grain sizes of 5 to 8. Finally, the eutectoid carbon content is defined as 0.8 % for carbon steels. Additions of alloying elements can change this value, along with Ac1 and Ac3 temperatures. Heating cycles need to be employed, as described below, to ensure complete formation of austenite preceding strain measurements during cooling.1.1 This practice covers the determination of hypoeutectoid steel phase transformation behavior by using high-speed dilatometry techniques for measuring linear dimensional change as a function of time and temperature, and reporting the results as linear strain in either a numerical or graphical format.1.2 The practice is applicable to high-speed dilatometry equipment capable of programmable thermal profiles and with digital data storage and output capability.1.3 This practice is applicable to the determination of steel phase transformation behavior under both isothermal and continuous cooling conditions.1.4 This practice includes requirements for obtaining metallographic information to be used as a supplement to the dilatometry measurements.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.

定价： 646元 加购物车

定价： 590元 加购物车

定价： 590元 加购物车