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5.1 For PM materials containing less than two percent porosity, a density measurement may be used to determine if the part has been densified, either overall or in a critical region, to the degree required for the intended application. Density alone cannot be used for evaluating the degree of densification because chemical composition and heat treatment affect the pore-free density.5.2 For cemented carbides, a density measurement is normally used to determine if there is any significant deviation in composition of the carbide grade. For straight tungsten carbide-cobalt grades, the relationship is straightforward. For complex carbide grades (for example, grades containing tantalum carbide or titanium carbide, or both, in addition to tungsten carbide-cobalt), the situation is more complicated. If the measured density is beyond the specified limits, the composition is outside of the specified limits. A measured density within the specified limits does not ensure correct composition; compensation between two or more constituents could result in the expected density with the wrong composition. Density alone cannot be used for evaluating a cemented carbide grade.1.1 This test method covers the determination of density for powder metallurgy (PM) materials containing less than two percent porosity and for cemented carbides. This test method is based on the water displacement method.NOTE 1: A test specimen that gains mass when immersed in water indicates the specimen contains surface-connected porosity. Unsealed surface porosity will absorb water and result in calculated density values higher than the true value. This test method is not applicable if this problem occurs, and Test Methods B962 should be used instead.1.2 Units—With the exception of the values for density and the mass used to determine density, for which the use of the gram per cubic centimetre (g/cm3) and gram (g) units is the long-standing industry practice, the values 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.1.3 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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AbstractThese test methods cover the standard procedures and related calculations for determining the saturated hydraulic conductivity, water retention, porosity, and bulk density of sand-based root zone mixtures used in the construction and topdressing of golf course putting greens including United States Golf Association (USGA) recommended greens, golf course tees, sand-based sports fields, and other highly trafficked turfgrass areas. These test methods are not designed for use with fine or medium textured soils such as sandy loams and loams. Test Method A is used to determine the saturated hydraulic conductivity by maintaining water flow through the core at a constant hydraulic head until a steady flow rate is achieved, at which time aliquots of the outflow are collected. Test Method B, on the other hand, is used to determine water retention and bulk density. Water retention is obtained at a soil suction, wherein water is extracted from a prepared core by means of a tension table or other water extraction apparatus. And when equilibrium is achieved after the core has been oven dried, the weight is recorded. Bulk density is, then, calculated from the mix or sand dry weight and volume. Test Method C is used to calculate the total porosity from the bulk density and particle density. And lastly, Test Method D is used to calculate the capillary and air-filled porosities. Capillary porosity is calculated from the bulk density and water retention information, while, the air-filled or aeration porosity is calculated from the difference of the total and capillary porosities.1.1 These test methods cover the measurements of saturated hydraulic conductivity, water retention, porosity (including distribution of capillary and air-filled porosity at a known soil suction), and bulk density on sand-based root zone mixes to be used for construction and topdressing of golf course putting greens including United States Golf Association (USGA) recommended greens, golf course tees, sand-based sports fields, or other highly trafficked turfgrass areas. These test methods are designed for sand-based mixes and are not intended for use with fine or medium textured soils, for example, sandy loams and loams.1.2 The values stated in SI units are to be regarded as the standard. The inch-pound units 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.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 Gold coatings are often specified for the contacts of separable electrical connectors and other devices. Electrodeposits are the form of gold that is most used on contacts, although it is also employed as inlay or clad metal and as weldments on the contact surface. The intrinsic nobility of gold enables it to resist the formation of insulating oxide films that could interfere with reliable contact operation.5.2 Palladium coatings are sometimes specified as alternatives to gold on electrical contacts and similar electrical component surfaces, both as electrodeposits and as inlay or clad metal. This test method is particularly suitable for determining porosity in palladium coatings, since the reactive atmosphere that is used does not attack the palladium if the specified test conditions are followed. In contrast, palladium coatings are attacked by nitric acid (HNO3) and other strong oxidizing agents, so that Test Method B735 cannot be used for determining the porosity in such coatings.5.3 In order for these coatings to function as intended, porosity, cracks, and other defects in the coating that expose base-metal substrates and underplates must be minimal or absent, except in those cases where it is feasible to use the contacts in structures that shield the surface from the environment or where corrosion inhibiting surface treatments for the deposit are employed. The level of porosity in the coating that may be tolerable depends on the severity of the environment to the underplate or substrate, design factors for the contact device like the force with which it is mated, circuit parameters, and the reliability of contact operation that it is necessary to maintain. Also, when present, the location of pores on the surface is important. If the pores are few in number and are outside of the zone of contact of the mating surfaces, their presence can often be tolerated.5.4 Methods for determining pores on a contact surface are most suitable if they enable their precise location and numbers to be determined. Contact surfaces are often curved or irregular in shape, and testing methods should be suitable for them. In addition, the severity of porosity-determining tests may vary from procedures capable of detecting all porosity to procedures that detect only highly porous conditions.5.5 The present test method is capable of detecting virtually all porosity or other defects that could participate in corrosion reactions with the substrate or underplate. The test is rapid, simple, and inexpensive. In addition, it can be used on contacts having complex geometry such as pin-socket contacts (although with deep recesses it is preferred that the contact structures be opened to permit reaction of the sulfur dioxide with the interior significant surfaces).5.6 The relationship of porosity levels revealed by particular tests to contact behavior must be made by the user of these tests through practical experience or by judgment. Thus, absence of porosity in the coating may be a requirement for some applications, while a few pores in the contact zone may be acceptable for others.5.7 This test is considered destructive in that it reveals the presence of porosity by contaminating the surface with corrosion products and by undercutting the coating at pore sites or at the boundaries of the unplated areas. Any parts exposed to this test shall not be placed in service.5.8 This test is intended to be used for quantitative descriptions of porosity (such as number of pores per unit area or per contact) only on coatings that have a pore density sufficiently low that the corrosion sites are well separated and can be readily resolved. As a general guideline this can be achieved for pore densities up to about 100/cm2. Above this value the tests are useful for the qualitative detection and comparisons of porosity.5.9 For these purposes, the measurement area, or significant surface, shall be defined as those portions of the surface that are essential to the serviceability or function of the part, such as its contact properties, or which can be the source of corrosion products or tarnish films that interfere with the function of the part. The significant surfaces shall be indicated on the drawings of the parts, or by the provision of suitably marked samples.1.1 This test method covers equipment and methods for determining the porosity of gold and palladium coatings, particularly electrodeposits and clad metals used on electrical contacts.1.2 This test method is designed to show whether the porosity level is less or greater than some value which by experience is considered by the user to be acceptable for the intended application.1.3 A variety of other porosity testing methods are described in the literature. 2, 3 Other porosity test methods are B735, B741, B798, and B809. An ASTM Guide to the selection of porosity tests for electrodeposits and related metallic coatings is available as Guide B765.1.4 The values stated in SI units are to be regarded as 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 become familiar with all hazards including those identified in the appropriate Material Safety Data Sheet (MSDS) for this product/material as provided by the manufacturer, to establish appropriate safety, health, and environmental practices, and determine the applicability of regulatory limitations prior to use. For specific hazards, see Section 6.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method is used to determine the mechanical properties in flexure of engineered ceramic components with multiple longitudinal hollow channels, commonly described as “honeycomb” channel architectures. The components generally have 30 % or more porosity and the cross-sectional dimensions of the honeycomb channels are on the order of 1 mm or greater.5.2 The experimental data and calculated strength values from this test method are used for material and structural development, product characterization, design data, quality control, and engineering/production specifications.NOTE 1: Flexure testing is the preferred method for determining the nominal “tensile fracture” strength of these components, as compared to a compression (crushing) test. A nominal tensile strength is required, because these materials commonly fail in tension under thermal gradient stresses. A true tensile test is difficult to perform on these honeycomb specimens because of gripping and alignment challenges.5.3 The mechanical properties determined by this test method are both material and architecture dependent, because the mechanical response and strength of the porous test specimens are determined by a combination of inherent material properties and microstructure and the architecture of the channel porosity [porosity fraction/relative density, channel geometry (shape, dimensions, cell wall thickness, etc.), anisotropy and uniformity, etc.] in the specimen. Comparison of test data must consider both differences in material/composition properties as well as differences in channel porosity architecture between individual specimens and differences between and within specimen lots.5.4 Test Method A is a user-defined specimen geometry with a choice of four-point or three-point flexure testing geometries. It is not possible to define a single fixed specimen geometry for flexure testing of honeycombs, because of the wide range of honeycomb architectures and cell sizes and considerations of specimen size, cell shapes, pitch, porosity size, crush strength, and shear strength. As a general rule, the experimenter will have to define a suitable test specimen geometry for the particular honeycomb structure of interest, considering composition, architecture, cell size, mechanical properties, and specimen limitations and using the following guidelines. Details on specimen geometry definition are given in 9.2.5.4.1 Four-point flexure (Test Method A1) is strongly preferred and recommended for testing and characterization purposes. (From Test Method C1161 section 4.5: “The three-point test configuration exposes only a very small portion of the specimen to the maximum stress. Therefore, three-point flexural strengths are likely to be much greater than four-point flexural strengths. Three-point flexure has some advantages. It uses simpler test fixtures, it is easier to adapt to high temperature and fracture toughness testing, and it is sometimes helpful in Weibull statistical studies. However, four-point flexure is preferred and recommended for most characterization purposes.”)5.4.2 The three-point flexure test configuration (Test Method A2) may be used for specimens which are not suitable for 4-point testing, with the clear understanding that 3-point loading exposes only a very small portion of the specimen to the maximum stress, as compared to the much larger maximum stress volume in a 4-point loading configuration. Therefore, 3-point flexural strengths are likely to be greater than 4-point flexural strengths, based on statistical flaw distribution factors.5.5 Test Method B (with a specified specimen size and a 4-point-1/4 point flexure loading geometry) is widely used in industry for cordierite and silicon carbide honeycomb structures with small cell size (cell pitch ~2 mm). Test Method B is provided as a standard test geometry that provides a baseline specimen size for honeycomb structures with appropriate properties and cell size with the benefit of experimental repeatability, reproducibility and comparability. (See 9.3 for details on Test Method B.)NOTE 2: Specific fixture and specimen configurations were chosen for Test Method B to provide a balance between practical configurations and linear cell count effect limits and to permit ready comparison of data without the need for Weibull-size scaling.5.6 The calculation of the flexure stress in these porous specimens is based on small deflection elastic beam theory with assumptions that (1) the material properties are isotropic and homogeneous, (2) the moduli of elasticity in tension and compression are identical, and (3) the material is linearly elastic. If the porous material in the walls of the honeycomb is not specifically anisotropic in microstructure, it is also assumed that the microstructure of the wall material is uniform and isotropic. To understand the effects of some of these assumptions, see Baratta et al. (6).NOTE 3: These assumptions may limit the application of the test to comparative type testing such as used for material development, quality control, and flexure specifications. Such comparative testing requires consistent and standardized test conditions both for specimen geometry and porosity architecture, as well as experimental conditions—loading geometries, strain rates, and atmospheric/test conditions.5.7 Three flexure strength values (defined in Section 3 and calculated in Section 11) may be calculated in this test method. They are the nominal beam strength, the wall fracture strength, and the honeycomb structure strength.5.7.1 Nominal Beam Strength—The first approach to calculating a flexure strength is to make the simplifying assumption that the specimen acts as a uniform homogeneous material that reacts as a continuum. Based on these assumptions, a nominal beam strength SNB can be calculated using the standard flexure strength equations with the specimen dimensions and the breaking force. (See Section 11.)5.7.1.1 A linear cell count effect (specimen size-cell count effect) has been noted in research on the flexure strength of ceramic honeycomb test specimens (7, 8). If the cell size is too large with respect to the specimen dimensions and if the linear cell count (the integer number of cells along the shortest cross-sectional dimension) is too low (<15), channel porosity has a geometric effect on the moment of inertia that produces an artificially high value for the nominal beam strength. (See Appendix X1.) With the standard elastic beam equations the strength value is overestimated, because the true moment of inertia of the open cell structure is not accounted for in the calculation.5.7.1.2 This overestimate becomes increasingly larger for specimens with lower linear cell counts. The linear cell count has to be 15 or greater for the calculated nominal beam strength, SNB, to be within a 10 % overestimate of the wall fracture strength SWF.NOTE 4: The study by Webb, Widjaja, and Helfinstine (7) showed that for cells with a square cross section a minimum linear cell count of 15 should be maintained to minimize linear cell count effects on the calculated nominal beam strength. (This study is summarized in Appendix X1.)5.7.1.3 For those smaller test specimens (where the linear cell count is between 2 and 15), equations for wall fracture strength and honeycomb structure strength are given in Section 11. These equations are used to calculate a more accurate value for the flexure strength of the honeycomb, as compared to the calculated nominal beam strength.5.7.2 Wall Fracture Strength, SWF, is calculated using the true moment of inertia of the honeycomb architecture, based on the geometry, dimensions, cell wall thickness, and linear count of the channels in the honeycomb structure. The wall fracture strength is a calculation of the true failure stress in the outer fiber surface of the specimen. (Appendix X1 describes the calculation as cited in the Webb, Widjaja, and Helfinstine (7) report). Section 11 on calculations gives the formula for calculating the moment of inertia for test specimens with square honeycomb channels and uniform cell wall thickness.NOTE 5: The moment of inertia formula given in Section 11 and Appendix X1 is only applicable to square cell geometries. It is not suitable for rectangular, circular, hexagonal, or triangular geometries. Formulas for those geometries have to be developed from geometric analysis and first principles.5.7.3 Honeycomb Structure Strength, SHS, is calculated from the wall fracture strength SWF. This calculation gives a flexure strength value which is independent of specimen-cell size geometry effects. The honeycomb structure strength value can be used for comparison of different specimen geometries with different channel sizes. It also gives a flexure strength value that can be used for stress models that assume continuum strength. (See Appendix X1.) Section 11 on calculations gives the formula for calculating the honeycomb structure strength for test specimens with square honeycomb channels and uniform cell wall thickness.5.7.4 The following recommendations are made for calculating a flexure strength for the ceramic honeycomb test specimens.5.7.4.1 For flexure test specimens where the linear cell count is 15 or greater, the nominal beam strength SNB calculation and the honeycomb structure strength SHS are roughly equivalent in value (within 10 %). The nominal beam strength SNB calculation can be used considering this variability.5.7.4.2 For flexure test specimens where the linear cell count is between 5 and 15, the nominal beam strength SNB calculation may produce a 10 % to 20 % overvalue. The SNB value should be used with caution.5.7.4.3 For flexure test specimens where the linear cell count is less than 5, the nominal beam strength SNB calculation may produce a 20 % to 100 % overvalue. It is recommended that the honeycomb structure strength SHS be calculated and used as a more accurate flexure strength number.5.7.4.4 If specimen availability and test configuration permit, test specimens with a linear cell count of 15 or greater are preferred to reduce the specimen linear cell count effect on nominal beam strength SNB to less than 10 %.5.8 Flexure test data for porous ceramics will have a statistical distribution, which may be analyzed and described by Weibull statistics, per Practice C1239.5.9 This flexure test can be used as a characterization tool to assess the effects of fabrication variables, geometry and microstructure variations, and environmental exposure on the mechanical properties of the honeycombs. The effect of these variables is assessed by flexure testing a specimen set in a baseline condition and then testing a second set of specimens with defined changes in geometry or fabrication methods or after controlled environmental exposure.5.9.1 Geometry and microstructure variations would include variations in cell geometry (shape dimensions, cell wall thickness, and count) and wall porosity (percent, size, shape, morphology, etc.).5.9.2 Fabrication process variations would include forming parameters, drying and binder burn-out conditions, sintering conditions, heat treatments, variations in coatings, etc.5.9.3 Environmental conditioning would include extended exposure at different temperatures and different corrosive atmospheres (including steam).5.10 This flexure test may be used to assess the thermal shock resistance of the honeycomb ceramics, as described in Test Method C1525.5.11 The flexure test is not the preferred method for determining the Young's modulus of these porous structures. (For this reason, the deflection of the flexure test bar is not commonly measured in this test.) Young's modulus measurements by sonic resonance (Test Method C1198) or by impulse excitation (Test Method C1259) give more reliable and repeatable data.5.12 It is beyond the scope of this standard to require fractographic analysis at the present time. Fractographic analysis for critical flaws in porous honeycomb ceramics is extremely difficult and of very uncertain value.1.1 This test method covers the determination of the flexural strength (modulus of rupture in bending) at ambient conditions of advanced ceramic structures with 2-dimensional honeycomb channel architectures.1.2 The test method is focused on engineered ceramic components with longitudinal hollow channels, commonly called “honeycomb” channels (see Fig. 1). The components generally have 30 % or more porosity and the cross-sectional dimensions of the honeycomb channels are on the order of 1 mm or greater. Ceramics with these honeycomb structures are used in a wide range of applications (catalytic conversion supports (1),2 high temperature filters (2, 3), combustion burner plates (4), energy absorption and damping (5), etc.). The honeycomb ceramics can be made in a range of ceramic compositions—alumina, cordierite, zirconia, spinel, mullite, silicon carbide, silicon nitride, graphite, and carbon. The components are produced in a variety of geometries (blocks, plates, cylinders, rods, rings).FIG. 1 General Schematics of Typical Honeycomb Ceramic Structures1.3 The test method describes two test specimen geometries for determining the flexural strength (modulus of rupture) for a porous honeycomb ceramic test specimen (see Fig. 2):FIG. 2 Flexure Loading ConfigurationsL = Outer Span Length (for Test Method A, L = User defined; for Test Method B, L = 90 mm)NOTE 1: 4-Point-1/4 Loading for Test Methods A1 and B.NOTE 2: 3-Point Loading for Test Method A2.1.3.1 Test Method A—A 4-point or 3-point bending test with user-defined specimen geometries, and1.3.2 Test Method B—A 4-point-1/4 point bending test with a defined rectangular specimen geometry (13 mm × 25 mm × > 116 mm) and a 90 mm outer support span geometry suitable for cordierite and silicon carbide honeycombs with small cell sizes.1.4 The test specimens are stressed to failure and the breaking force value, specimen and cell dimensions, and loading geometry data are used to calculate a nominal beam strength, a wall fracture strength, and a honeycomb structure strength.1.5 Test results are used for material and structural development, product characterization, design data, quality control, and engineering/production specifications.1.6 The test method is meant for ceramic materials that are linear-elastic to failure in tension. The test method is not applicable to polymer or metallic porous structures that fail in an elastomeric or an elastic-ductile manner.1.7 The test method is defined for ambient testing temperatures. No directions are provided for testing at elevated or cryogenic temperatures.1.8 The values stated in SI units are to be regarded as standard (IEEE/ASTM SI 10). English units are sparsely used in this standard for product definitions and tool descriptions, per the cited references and common practice in the US automotive industry.1.9 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.1.10 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 Apparent porosity, water absorption, apparent specific gravity, and bulk density are primary properties of refractory shapes. These properties are widely used in the evaluation and comparison of product quality and as part of the criteria for selection and use of refractory products in a variety of industrial applications. These test methods are used for determining any or all of these properties and are particularly useful for testing hydratable products.3.2 These test methods are primary standard methods that are suitable for use in quality control, research and development, establishing criteria for and evaluating compliance with specifications, and providing data for design purposes.3.3 Fundamental assumptions inherent in these test methods are:3.3.1 The test specimens conform to the requirements for size, configuration, and original faces,3.3.2 The open pores of the test specimens are fully impregnated with liquid during the vacuum-pressure treatment, and3.3.3 The blotting of the saturated test specimens is performed as specified in a consistent and uniform manner to avoid withdrawing liquid from the pores.3.3.4 Deviation from any of these assumptions adversely affects the test results.3.4 In laboratory studies involving castable specimen, a bias was noted between formed 2 in. by 2 in. by 2 in. (50 mm by 50 mm by 50 mm) and specimens quartered from larger 9 in. by 4.5 in. by 2.5 in. (228 mm by 114 mm by 64 mm) cast specimens. Additionally, an error in the apparent porosity determination was found on castables whenever the specimens were heated to 1500 °F (816 °C) and then exposed to water as a saturation media. The error was attributed to reactivity of cement with water and subsequent re-hydration of cement phases. The higher the cement level of the castable, the greater the error noted. It was concluded that an error in porosity values could occur for refractory materials having a potential to form hydrated species with water. Testing under the same conditions in kerosene produced results that were believed to be more accurate, but the data suggested that the kerosene might not have saturated the open pores of cast specimen as readily as water.33.5 Certain precautions must be exercised in interpreting and using results from these test methods. All four property values are interrelated by at least two of the three base data values generated during testing. Thus, an error in any base data value will cause an error in at least three of the property values for a given test specimen. Certain of the properties, that is, apparent specific gravity and bulk density, are functions of other factors such as product composition, compositional variability within the same product, impervious porosity, and total porosity. Generalizations on or comparisons of property values should be judiciously made between like products tested by these test methods or with full recognition of potentially inherent differences between the products being compared or the test method used.3.6 When a liquid other than water is used, such as types of kerosene or mineral spirits, specific gravity must be known by either determination or monitoring on a controlled basis. Specific gravity will change due to different grades of liquids, evaporation, or contamination with dirt or foreign material. The test should not be run if the liquid becomes dirty, foamy, or changes color, because foreign particles can block pores and prevent impregnation of the sample.1.1 These test methods cover the determination of the following properties of refractory shapes:1.1.1 Apparent porosity,1.1.2 Liquid absorption,1.1.3 Apparent specific gravity, and1.1.4 Bulk density.1.2 These test methods are applicable to all refractory shapes except those that chemically react with both water and mineral spirits. When testing a material capable of hydration or other chemical reaction with water but which does not chemically react with mineral spirits, mineral spirits is substituted for water and appropriate corrections for the density differences are applied when making calculations.1.3 Units—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.1.3.1 Exception—The apparatus used in this standard is only available in SI units.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.NOTE 1: Test Methods C20 cover procedures for testing properties of refractories that are not attacked by water.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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3.1 Apparent porosity, water absorption, apparent specific gravity, and bulk density are primary properties of burned refractory brick and shapes. These properties are widely used in the evaluation and comparison of product quality and as part of the criteria for selection and use of refractory products in a variety of industrial applications. These test methods are used for determining any or all of these properties.3.2 These test methods are primary standard methods which are suitable for use in quality control, research and development, establishing criteria for and evaluating compliance with specifications, and providing data for design purposes.3.3 Fundamental assumptions inherent in these test methods are that the test specimens are not attacked by water, the test specimens conform to the requirements for size, configuration, and original faces, the open pores of the test specimens are fully impregnated with water during the boiling treatment, and the blotting of the saturated test specimens is performed as specified in a consistent and uniform manner to avoid withdrawing water from the pores. Deviation from any of these assumptions adversely affects the test results.3.4 In laboratory studies involving castable specimens, a bias was noted between formed 2 by 2 by 2 in. (50 by 50 by 50 mm) and specimens that were quartered from larger 9 by 4.5 by 2.5 (228 by 114 by 64 mm) cast specimens. Additionally, an error in the apparent porosity determination on castables was found whenever the specimens were heated to 1500 °F (816 °C) and then exposed to water as a saturation media (Test Methods C830). The error was attributed to reactivity of cement with water and subsequent re-hydration of cement phases. The higher the cement level of the castable, the greater the error noted. It was concluded that an error in porosity values could occur for refractory materials having a potential to form hydrated species with water.33.5 Certain precautions must be exercised in interpreting and using results from these test methods. All four property values are interrelated by at least two of the three base data values generated during testing. Thus, an error in any base data value will cause an error in at least three of the property values for a given test specimen. Certain of the properties, that is, apparent specific gravity and bulk density, are functions of other factors such as product composition, compositional variability within the same product, impervious porosity, and total porosity. Generalizations on or comparisons of property values should only be judiciously made between like products tested by these test methods or with full recognition of potentially inherent differences between the products being compared or the test method used.1.1 These test methods cover the determination of the following properties of burned refractory brick:1.1.1 Apparent porosity,1.1.2 Water absorption,1.1.3 Apparent specific gravity, and1.1.4 Bulk density.1.2 These test methods are not applicable to refractories attacked by water.1.3 The values stated in inch-pound units are to be regarded as the standard. The values given in parentheses 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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