5.1 This practice provides a means for the users of ASTM Committee D02 standards to monitor the drift in sensed temperature of liquid-in-glass thermometer (LiG), and digital contact thermometers (DCT). Digital contact thermometers are sometimes referred to as portable electronic thermometers (PET) or simply digital thermometers.5.2 This practice is not suitable for determining the accuracy or calibration of a temperature-measuring device as the error in the ice bath temperature can be greater than 0.02 °C. For greater accuracy, the user should use Practice E563 to prepare the ice bath.5.3 The ice point is a common practical industrial reference point of thermometry. The ice point is relatively simple to realize and provides a readily available natural fixed-point reference temperature.5.4 This practice only checks the measurement drift at a single temperature. It will not detect a change in measurement response with change in temperature. Temperature-measuring devices should be recalibrated at set intervals. See device supplier for recommendations.5.5 This practice provides a technique to determine minimum immersion depth of the sensing probe of the thermometer using an ice bath. The minimum immersion depth determined by this practice may change when the differential temperature differs significantly from the conditions described. A greater differential will likely increase the minimum immersion depth.1.1 This practice describes two procedures for use with temperature measurement devices. Methodology is described for determining minimum immersion depth for thermal sensors, in particular RTDs or similar temperature sensors. Included is a procedure for consistently preparing a reference bath for the purpose of monitoring measurement drift of thermal sensors such as liquid-in-glass or digital contact thermometers.1.2 This practice focuses on temperature measurement drift in a laboratory. If the user requires greater measurement accuracy, then they should follow the instructions in Practice E563.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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6.1 This test method provides a means of measuring the water absorption of flat or cylindrical specimens of thermal insulation materials under isothermal conditions as a result of direct immersion in liquid water. It is intended for quality control and product and material specifications.6.2 The procedure to be used: A, B, or C as well as any exceptions shall be noted in material specifications citing this test method.6.3 Repeatability has been established only for one type and size of material at one immersion duration.NOTE 1: Specifications referring to this test method are encouraged to establish repeatability for specific materials, immersion duration, and dimensions for inclusion in this test method.1.1 This test method determines the amount of water retained (excluding surface water) by flat or cylindrical specimens of thermal insulations after these materials have been fully immersed in liquid water for a prescribed time interval under isothermal 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 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, 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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1.1 This test method covers determination of the corrosive effects of water-soluble aluminum cleaners (nonetching type) on aluminum or aluminum alloys, under conditions of total immersion, by quantitative measurement of weight change or by qualitative visual determination of change. The test is designed for the determination of corrosion characteristics of the cleaner and not for determination of the life of the cleaner. 1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Material Safety Data Sheets are available for reagents and materials. Review them for hazards prior to usage.

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4.1 The useful life of photovoltaic modules deployed in marine applications (such as floating aids-to-navigation) may depend on the ability to withstand repeated exposure to salt atmosphere, immersion in seawater, and the temperature changes associated with seawater splash falling on modules operating in sunlight. The effects of these exposures may be physical or electrical changes in the module, or both.4.2 This test method describes a procedure for positioning the test specimen, conducting a cyclical combined pressure, immersion, and temperature (PIT) test, and reporting the results. It also references methods for conducting module electrical performance and insulation integrity tests.4.3 Data generated by this test method may be used to evaluate and compare the effects of a simulated marine environment on test specimens. This test method requires recording of visible effects as well as electrical performance.4.3.1 Effects on modules may vary from none to significant changes. Some physical changes in the module may be visible when there are no apparent electrical changes in the module. Similarly, electrical changes may occur with no visible changes in the module.1.1 This test method provides a procedure for determining the ability of photovoltaic modules to withstand repeated immersion or splash exposure by seawater as might be encountered when installed in a marine environment, such as a floating aid-to-navigation. A combined environmental cycling exposure with modules repeatedly submerged in simulated saltwater at varying temperatures and under repetitive pressurization provides an accelerated basis for evaluation of aging effects of a marine environment on module materials and construction.1.2 This test method defines photovoltaic module test specimens and requirements for positioning modules for test, references suitable methods for determining changes in electrical performance and characteristics, and specifies parameters which must be recorded and reported.1.3 This test method does not establish pass or fail levels. The determination of acceptable or unacceptable results is beyond the scope of this test method.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this 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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4.1 This practice provides a standard immersion procedure for investigating the chemical resistance of a geosynthetic to a liquid waste, leachate, or chemical in a laboratory environment. The conditions specified in this practice are intended both to provide a basis of standardization and to serve as a guide for those wishing to compare or investigate the chemical resistance of a geosynthetic material(s) in a laboratory environment. Practice D5496 can be used should the user need to assess the performance of a geosynthetic in field conditions.4.2 This practice is not intended to establish, by itself, the behavior of geosynthetics when exposed to liquids. Such behavior, referred to as chemical resistance, can be defined only in terms of specific chemical solutions and methods of testing and evaluation criteria selected by the user.1.1 This practice covers laboratory immersion procedures for the testing of geosynthetics for chemical resistance to liquid wastes, prepared chemical solutions, and leachates derived from solid wastes.1.2 This standard is not applicable to some geosynthetics such as geosynthetic clay liners (GCLs), because of their composite nature requiring a confining pressure during immersion. However, individual geosynthetic components of the GCL can be tested.1.3 This standard was originally developed to supplement and expand EPA 9090 to include all geosynthetics. EPA 9090 has not been updated since 1992.1.4 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.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. For specific hazards statements, see Section 7.1.6 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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3.1 This test method gives the rubber technologist two means to evaluate the effect of liquids on rubber vulcanizates or rubbery materials. Volatile, nonvolatile, and other liquids that require pressure to maintain a liquid state may be used. Data obtained on rubbery materials exposed to liquids by this method may be used to predict their behavior in applications involving similar exposure. These changes in length have been found to be useful for specifications but do not necessarily indicate changes for design purposes.1.1 This test method covers a technique to measure the effect of immersion liquids on rubber vulcanizates or rubbery materials. Change in specimen geometry and dimensions are observed through the transparent walls of the tube containing the specimen immersed in the liquid. Although it may be employed with any liquid, it is especially applicable to liquids that are so volatile that they must be maintained under pressure during the period of immersion.1.2 This test method differs from Test Method D471 in that volume changes are approximated from observed dimensional changes rather than being calculated directly.1.3 The values stated in SI units are to be regarded as the standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method uses elevated temperature in an attempt to accelerate the degradation of a sealant and its adhesion to a substrate. This test method is an accelerated method and will only be a predictor of long-term durability if the actual service temperature is significantly lower than the elevated test temperature.5.2 This test method can be used as an indicator of longevity but direct correlation to actual use will be difficult for many applications.5.3 The correlation of data from this test method to applications where the sealant joint will have wet and dry cycles will be difficult since, with some sealants on some substrates, adhesion that is lost during wet periods is regained during dry periods.5.4 This test method is performed in a hot liquid and may be considered an acceleration of deterioration of the sealant or the sealant's adhesion to a substrate. Compared to how the sealant will be used in some applications, in some cases, this test may be less severe than the actual application. The benefit from the use of this test method will depend on the comparison of the conditions of this test to the actual conditions of use (temperature, duration, nature of substrate, composition of the liquid).5.5 To determine the ability of a sealant to perform in a given application; modification of this procedure will often be required and is permissible, as mutually agreed upon by interested parties.1.1 This test method covers a laboratory procedure that assists in determining the durability of a sealant and its adhesion to a substrate while continuously immersed in a liquid. This method tests the influence of a liquid on the sealant and its adhesion to a substrate. It does not test the added influence of constant stress from hydrostatic pressure that is often present with sealants used in submerged and below-grade applications, nor does it test the added influence of stress from joint movement while immersed. This method also does not (in its standard form) test the added influence of acids or caustics or other materials that may be in the liquid, in many applications.1.2 The values stated in SI units are to be regarded as the standard. The inch-pound given in parentheses are provided for information only.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The purpose of these tests is to obtain, by means of simple apparatus, reliable and easy to determine values of liquid water transport for capillary active materials expressed in suitable units. These values are for use as part of the material properties in hygrothermal analysis tools for building envelope design and forensic studies. As the topic of liquid transport phenomena in porous materials is very complex, Appendix X1 in ISO 15148 shows some more detailed background information.1.1 This test method defines a procedure to determine the water absorption coefficient of a material by partial submersion. The scope is to evaluate the rate of absorption of water due to capillary forces for building materials in contact with normal or driving rain above grade. The procedure is typically suitable mainly for masonry material, plaster, or a coating in combination with a substrate; but it can also be used for insulation materials. This test method is designed to be used only on homogeneous materials and does not apply to materials that are composites or non-homogeneous (for example, Faced Rigid Closed-cell Insulation). It is not within the scope of this standard to determine liquid uptake phenomena in below-grade applications. The water absorption coefficient is mainly used as an input datum for numerical simulation of the combined heat and moisture transport in building envelopes for design and forensic investigation purposes.1.2 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system 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. However, derived results can be converted from one system to the other using appropriate conversion factors (see Table 1).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 Thermoplastic moldings contain residual stresses due to differential cooling rates through the thickness of the molding. Changes in residual stress have been found to occur with time after molding due to stress relaxation. Many part performance parameters as well as part failures are affected by the level of residual stress present in a part. Residual stresses cause shrinkage, warpage, and a decrease in environmental stress crack resistance. This practice estimates the relative magnitude of residual stresses in parts produced from the series of sulfone plastics (SP), namely polysulfone (PSU), polyethersulfone (PESU), and polyphenylsulfone (PPSU) materials.5.2 No direct correlation has been established between the results of the determination of residual stresses by this practice and part performance properties. For this reason, this practice is not recommended as a substitute for other tests, nor is it intended for use in purchasing specifications for parts. Despite this limitation, this practice does yield information of value in indicating the presence of residual stresses and the relative quality of plastic parts.5.3 Residual stresses cannot be easily calculated, hence it is important to have an experimental method, such as this practice, to estimate residual stresses.5.4 This practice is useful for extruders and molders who wish to evaluate residual stresses in SP parts. This can be accomplished by visual examination after immersion in one or more chemical reagents to evaluate whether or not cracking occurs. Stresses will relax after molding or extrusion. Accordingly, both immersion in the test medium and visual examination must be made at identical times and conditions after processing, if comparing parts. It is important to note the differences in part history. Thus, this technique is suitable as an indication for quality of plastic processing.5.5 The practice is useful primarily for indicating residual stresses near the surface.1.1 This practice covers the evaluation of residual stresses in extruded profile or molded SP parts. The presence and relative magnitude of residual stresses are indicated by the crazing of the specimen part upon immersion in one or more of a series of chemical reagents. The specified chemical reagents were previously calibrated by use of Environmental Stress Cracking (ESC) techniques to cause crazing in sulfone plastics (SP) at specified stress levels.1.2 This practice applies only to unfilled injection molding and extrusion grade materials of high molecular weight as indicated by the following melt flow rates: PSU 9 g/10 min, max., PESU 30 g/10 m, max, and PPSU 25 g/10 min, max. Lower molecular weight (higher melt flow) materials will craze at lower stress levels than indicated in Tables 1-3. (See Specification D6394 for melt flow rate conditions.)TABLE 1 Liquid Reagents for Residual Stress Test for PSUMixture Mixture Composition Critical Stress, MPa (psi)% by volume Ethanol % by volume Ethyl Acetate1 50 50 15.2 (2200)2 43 57 12.1 (1750)3 37 63 9.0 (1300)4 25 75 5.5 (800)TABLE 2 Liquid Reagents for Residual Stress Test for PESUMixture Mixture Composition Critical Stress, MPa (psi)% by volume Ethanol % by volume MEK1 50 50 17.9 (2600)2 40 60 10.3 (1500)3 20 80 6.9 (1000)4 0 100 5.9 (850)TABLE 3 Liquid Reagents for Residual Stress Test for PPSUMixture Mixture Composition Critical Stress, MPa (psi)% by volume Ethanol % by volume MEK1 50 50 22.8 (3300)2 25 75 13.8 (2000)3 10 90 9.0 (1300)4 0 100 8.0 (1150)1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.NOTE 1: There is no known ISO equivalent 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 Protective coatings are used on metallic and concrete storage and processing vessels, shipping containers, dams and rail cars to protect the substrate from corrosive attack and to protect stored materials (cargo) from contamination. This method provides a means to assess the ability of a protective coating to resist degradation by chemicals and to protect the liquid cargo from contamination by either the substrate or coating, based on visual observations. Other measures of degradation, such as changes in weight or dimensions of the coating material, or chemical changes to the cargo, may be used to assess this protective ability as mutually agreed upon between contracting parties. Simple chemical-resistance evaluations of the lining materials may be performed more conveniently by other pertinent methods as a prescreening test for this procedure in accordance with Test Methods C267 and D471.4.2 This practice covers three approaches to conducting evaluations of a lining coating material’s fitness for purpose.4.2.1 Method A—Evaluation of specimens under conditions of constant temperature at atmospheric pressure (that is, without a thermal gradient).4.2.2 Method B—Evaluation of specimens under conditions which provide a temperature gradient across the sample.4.2.3 Method C—Evaluation of specimens under conditions of constant temperature and increased pressure (that is, without a thermal gradient).1.1 This practice establishes procedures for the evaluation of the resistance of industrial protective coatings to immersion in chemicals.1.2 Linings are a particular type of coating intended for protection of substrates from corrosion as a result of continuous or intermittent fluid immersion.1.3 The values stated in SI units are to be regarded as the standard. The values given in parenthesis are 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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4.1 Corrosion testing by its very nature precludes complete standardization. This standard, rather than a standardized procedure, is presented as a guide so that some of the pitfalls of such testing may be avoided.4.2 Experience has shown that all metals and alloys do not respond alike to the many factors that affect corrosion and that accelerated corrosion tests give indicative results only, or may even be entirely misleading. It is impractical to propose an inflexible standard laboratory corrosion testing procedure for general use, except for material qualification tests where standardization is required. One purpose for this guide is to promote better correlation of results in the future and the reduction of conflicting reports through a more detailed recording of meaningful factors and conditions.4.3 In designing any corrosion test, consideration should be given to the various factors discussed in this guide, because these factors have been found to affect the results obtained.1.1 This guide covers and describes the factors that influence laboratory immersion corrosion tests, particularly mass loss tests. These factors include apparatus, sampling, test specimen, test conditions (test solution composition, temperature, gas sparging, fluid motion, solution volume, method of supporting test specimens, duration of test), methods of cleaning test specimens, interpretation of results, and calculation of corrosion rates. This guide also emphasizes the importance of recording all pertinent data and provides a checklist for reporting test data.1.2 The specific evaluation of localized attack, environmentally assisted cracking, and effects of solution flow are not within the scope of this guide.1.3 This guide is intended to be used by those designing laboratory immersion tests who may not be familiar with all of the variables to consider and the pitfalls that could be encountered when designing and conducting this kind of testing. It should be used as a reference to ensure that the test will allow generation of data relevant to the application with the minimum of interferences.1.4 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.1.5 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 Safety-related service water system (SWS) components are designed to provide adequate cooling to equipment essential to the safe operation and shutdown of the plant. Linings in these systems are installed to maintain the integrity of the system components by preventing corrosion and erosion of the metal materials of construction. Linings on SWS surfaces upstream of components, including heat exchangers, orifice plates, strainers, and valves, the detachment of which may affect safe-plant operation or shutdown, may be considered safety-related, depending on plant-specific licensing commitments and design bases.5.2 The testing presented in this guide is used to provide reasonable assurance that the linings, when properly applied, will be suitable for the intended service by preventing corrosion and erosion for some extended period of time. Additionally, the test data derived allows development of schedules, methods, and techniques for assessing the condition of the lining materials (see Guide D7167). The ultimate objective of the testing is to avoid lining failures that could result in blockage of equipment, such as piping or heat transfer components, preventing the system or component from performing its intended safety function.5.3 It is expected that this guide will be used by:5.3.1 Lining manufacturers for comparing specific products and systems and to establish a qualification basis for recommended linings and5.3.2 End users seeking a consistent design basis for candidate coating systems.5.4 In the event of conflict, users of this guide must recognize that the licensee's plant-specific quality assurance program and licensing commitments shall prevail with respect to the selection process for and qualification of CSL III lining materials.5.5 Operating experience has shown that the most severe operating conditions with respect to heat exchanger linings occur on pass partitions. A phenomenon known as the “cold wall effect” accelerates moisture permeation through a coating applied to the warmer side of a partition that separates fluids at two different temperatures. The thickness and permeability of the lining are key variables affecting the ability of a lining to withstand cold wall blistering.5.5.1 This effect is particularly pronounced when the separated fluids are water, though the effect will occur when only air is on the other side, for example, an outdoor tank filled with warm liquid. A heat exchanger pass partition represents geometry uniquely vulnerable to the water-to-water maximized temperature differentials (ΔTs) that drive the cold wall effect.5.5.2 Pass partitions separate relatively cold incoming cooling water from the discharge water warmed by the heat exchanger's thermal duty. Improperly designed coatings will exhibit moisture permeation to the substrate accelerated by the cold-wall effect. Many instances of premature pass partition warm-side blistering have been noted in the nuclear industry. Such degradation has also been seen on lined cover plate and channel barrel segments that reflect water-to-air configurations.5.6 Large water-to-water ΔTs are known to be the most severe design condition. The test device used to replicate ΔT configurations is known as an “Atlas cell.” Atlas cell testing is governed by industry standard test methodologies (Test Method C868 and NACE TM0174). A lining proven suitable for the most severe hypothesized ΔT would also be suitable for service on other waterside surfaces.5.7 Plant cooling water varies in composition and temperature seasonally. For purposes of standardization, demineralized water is used in Atlas cell exposures rather than raw plant water. It is generally accepted in polymeric coatings technology that low-conductivity water (deionized or demineralized) is more aggressive with respect to its ability to permeate linings than raw water. Thus, stipulating use of low-conductivity water as the test medium is considered conservative.1.1 This guide establishes procedures for evaluating lining system test specimens under simulated operating conditions.1.2 Lining systems to be tested in accordance with this guide are intended for use in both new construction and for refurbishing existing systems or components.1.3 The lining systems evaluated in accordance with this guide are expected to be applied to metal substrates comprising water-wetted (that is, continuous or intermittent immersion) surfaces in systems that may include:1.3.1 Service water piping upstream of safety-related components,1.3.2 Service water pump internals (draft tube, volutes, and diffusers),1.3.3 Service water heat exchanger channels, pass partitions, tubesheets, end bells, and covers,1.3.4 Service water strainers, and1.3.5 Refueling water storage tanks and refuel cavity water storage tanks.1.4 This guide anticipates that the lining systems to be tested include liquid-grade and paste-grade polymeric materials. Sheet type lining materials, such as rubber, are excluded from the scope of this guide.1.5 Because of the specialized nature of these tests and the desire in many cases to simulate to some degree the expected service environment, the creation of a standard practice is not practical. This standard gives guidance in setting up tests and specifies test procedures and reporting requirements that can be followed even with differing materials, specimen preparation methods, and test facilities.1.6 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.1.7 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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5.1 The measurement of apparent attenuation in materials is useful in applications such as the comparison of heat treatments of different lots of material or the assessment of the degradation of materials due to environment.5.2 Several different modes of wave vibration can be propagated in solids. This practice is concerned with the attenuation associated with longitudinal waves introduced into the specimen by the immersion method.5.3 This practice allows for the comparison of the apparent attenuations of geometrically similar specimens.5.4 For the determination of apparent attenuation, the procedures described herein are valid only for measurements in the far field of the ultrasonic beam.1.1 This practice describes a procedure for measuring the apparent attenuation of ultrasound in materials or components with flat, parallel surfaces using conventional pulse-echo ultrasonic flaw detection equipment in which reflected indications are displayed in an A-scan presentation.1.2 The measurement procedure is readily adaptable for the determination of relative attenuation between materials. For absolute (true) attenuation measurements, indicative of the intrinsic nature of the material, it is necessary to correct for specimen geometry, sound beam divergence, instrumentation, and procedural effects. These results can be obtained with more specialized ultrasonic equipment and techniques.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 may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.1.4 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 3.5 % NaCl alternate immersion procedure is a general, all-purpose procedure that produces valid comparisons for most metals, particularly when specimens are exposed at high levels of applied stress or stress intensity.4.2 While the alternate immersion test is an accelerated test and is considered to be representative of certain natural conditions, it is not intended to predict performance in specialized chemical environments in which a different mode of cracking may be operative. For example, it does not predict the performance of aluminum alloys in highly acidic environments such as heated inhibited red fuming nitric acid (IRFNA). For such cases, the results of the alternate immersion test are of doubtful significance until a relationship has been established between it and anticipated service environments.4.3 While this practice is applicable in some degree to all metals, it is not equally discriminative of all alloys, even within the same metal system. Consequently, information should be established to allow comparisons of performances of the alloy of interest in the alternate immersion test and in natural environments.NOTE 2: The alternate immersion concept can be useful for exposure of corrosion specimens in other solutions because the procedure and apparatus provide a controlled set of conditions. Details of this are beyond the scope of this practice.1.1 This practice covers procedures for making alternate immersion stress corrosion tests in 3.5 % sodium chloride (NaCl) (Note 1). It is primarily for tests of aluminum alloys (Test Method G47) and ferrous alloys, but may be used for other metals exhibiting susceptibility to chloride ions. It sets forth the environmental conditions of the test and the means for controlling them.NOTE 1: Alternate immersion stress corrosion exposures are sometimes made in substitute ocean water (without heavy metals) prepared in accordance with Practice D1141. The general requirements of this present practice are also applicable to such exposures except that the reagents used, the solution concentration, and the solution pH should be as specified in Practice D1141.1.2 This practice can be used for both stressed and unstressed corrosion specimens. Historically, it has been used for stress-corrosion cracking testing, but is often used for other forms of corrosion, such as uniform, pitting, intergranular, and galvanic.1.3 This practice is intended for alloy development and for applications where the alternate immersion test is to serve as a control test on the quality of successive lots of the same material. Therefore, strict test conditions are stipulated for maximum assurance that variations in results are attributable to variations in the material being tested.1.4 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.1.5 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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3.1 This practice not only provides information on the accumulated effects of corrosion at specific time periods under a given set of conditions, but also provides information on the initial rate of corrosion of virgin metal, the corrosion rate of metal per unit time after long exposure, and the initial corrosion rate of virgin metal after long exposure of the corroding fluid to metal. The test also provides a means of determining the direction corrosion will take with time, although causes for increase or decrease in the corrosiveness and corrodibility of media and metal (such as passive film formation or destruction, depletion of corrosive contaminate, and so forth) as a function of time are not given.1.1 This practice covers the determination of the corrosiveness of tank-type aircraft maintenance chemicals on aircraft metals and the corrodibility of metals in these maintenance chemicals with time. The determination is made under conditions of total immersion by a combination of weight change measurements and visual qualitative determinations of change.1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.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. For specific precautions, see Section 6.1.4 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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