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5.1 This test method measures the amount of unfixed chrome in Wet Blue. Results may vary according to the age of the Wet Blue.1.1 This test method covers the procedures to analyze and calculate unfixed chrome concentrations in Wet Blue.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 Many petroleum products, and some non-petroleum materials, are used as lubricants and the correct operation of the equipment depends upon the appropriate viscosity of the liquid being used. In addition, the viscosity of many petroleum fuels is important for the estimation of optimum storage, handling, and operational conditions. Thus, the accurate determination of viscosity is essential to many product specifications.5.2 Density is a fundamental physical property that can be used in conjunction with other properties to characterize both the light and heavy fractions of petroleum and petroleum products.5.3 Determination of the density or relative density of petroleum and its products is necessary for the conversion of measured volumes to volumes at the standard temperature of 15 °C.1.1 This test method covers and specifies a procedure for the concurrent measurement of both the dynamic viscosity, η, and the density, ρ, of liquid petroleum products and crude oils, both transparent and opaque. The kinematic viscosity, ν, can be obtained by dividing the dynamic viscosity, η, by the density, ρ, obtained at the same test temperature.1.2 The result obtained from this test method is dependent upon the behavior of the sample and is intended for application to liquids for which primarily the shear stress and shear rate are proportional (Newtonian flow behavior).1.3 The precision has only been determined for those materials, viscosity ranges, density ranges, and temperatures as indicated in Section 15 on Precision and Bias. The test method can be applied to a wider range of materials, viscosity, density, and temperature. For materials not listed in Section 15 on Precision and Bias, the precision and bias may not be applicable.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 to 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 Mean particle diameters defined according to the Moment-Ratio (M-R) system are derived from ratios between two moments of a particle size distribution.1.1 The purpose of this practice is to present procedures for calculating mean sizes and standard deviations of size distributions given as histogram data (see Practice E1617). The particle size is assumed to be the diameter of an equivalent sphere, for example, equivalent (area/surface/volume/perimeter) diameter.1.2 The mean sizes/diameters are defined according to the Moment-Ratio (M-R) definition system.2,3,41.3 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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5.1 In the design and operation of reverse osmosis and nanofiltration installations, it is important to predict the CaSO4, SrSO4, and BaSO4 scaling properties of the concentrate stream. Because of the increase in total dissolved solids and the increase in concentration of the scaling salts, the scaling properties of the concentrate stream will be quite different from those of the feed solution. This practice permits the calculation of the scaling potential for the concentrate stream from the feed water analyses and the reverse osmosis or nanofiltration operating parameters.5.2 Scaling by CaSO4, SrSO4, and BaSO4 will adversely affect the reverse osmosis or nanofiltration performance. This practice gives various procedures for the prevention of scaling.1.1 This practice covers the calculation and adjustment of calcium, strontium, and barium sulfates for the concentrate stream of a reverse osmosis or nanofiltration system. The calculations are used to determine the need for scale control in the operation and design of reverse osmosis and nanofiltration installations. This practice is applicable for all types of reverse osmosis devices (tubular, spiral wound, and hollow fiber) and nanofiltration devices.1.2 This practice is applicable to both brackish waters and seawaters.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 international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This practice is intended to provide a method that will yield uniformity of calculations used in making, matching, or controlling colors of objects. This uniformity is accomplished by providing a method for calculation of weighting factors for tristimulus integration consistent with the methods utilized to obtain the weighting factors for common illuminant-observer combinations contained in Practice E308.5.2 This practice should be utilized by persons desiring to calculate a set of weighting factors for tristimulus integration who have custom source, or illuminant spectral power distributions, or custom observer response functions.1.1 This practice describes the method to be used for calculating tables of weighting factors for tristimulus integration using custom spectral power distributions of illuminants or sources, or custom color-matching functions.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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4.1 The true vapor pressure of a distillate fuel is a relative measurement, both of the tendency of the most volatile portion of the fuel to gasify, and of the restraining pressure required to prevent gasification of the most volatile portion. Thus the measurement is of importance when a fuel is to be utilized in applications where no gasification may be tolerated, and temperature-pressure conditions are expected to be near the true vapor pressure of the fuel.1.1 This test method describes the calculation of true vapor pressures of petroleum distillate fuels for which distillation data may be obtained in accordance with Test Method D86 without reaching a decomposition point prior to obtaining 90 % by volume distilled.1.2 The test method may be used to calculate vapor pressures at temperatures between the 0 % equilibrium flash temperature and the critical temperature of the fuel. Provision is included for obtaining a calculated critical temperature for fuels for which it is not known.1.3 Critical pressure-temperature data are usually not available for petroleum fuels. However, if both the critical pressure and critical temperature are known, the values shall be used as the coordinates in Fig. 1 to establish a critical point to be used instead of the focal point established as described in 6.5.4; and the calculations described in 6.5 through 6.5.4 are not required. If either a determined true boiling point or determined equilibrium flash vaporization temperature at 0 % distilled at atmospheric pressure is known, the determined value shall be used to establish the lower limit of the bubble-point line referred to in 6.4.FIG. 1 Test Method D86 Distillation Temperature and Equalization Flash Vaporization Temperature Pressure Conversion Chart1.4 The method is not reliable for distillate fuels having a boiling range of less than 100 °F (38 °C) between the Test Method D86 10 % by volume and 90 % by volume distilled temperatures.1.5 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.1.6 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 The carbon distribution and ring content serve to express the gross composition of the heavier fractions of petroleum. These data can be used as an adjunct to the bulk properties in monitoring the manufacture of lubricating oil base stocks by distillation, solvent refining or hydrogenation, or both, and in comparing the composition of stocks from different crude sources. Furthermore, the data can often be correlated with critical product performance properties.1.1 This test method covers the calculation of the carbon distribution and ring content (Note 1) of olefin-free petroleum oils from measurements of refractive index, density, and molecular weight (n-d-M).2 This test method should not be applied to oils whose compositions are outside the following ranges:1.1.1 In terms of carbon distribution—up to 75 % carbon atoms in ring structure; percentage in aromatic rings not larger than 1.5 times the percentage in naphthenic rings.1.1.2 In terms of ring content—up to four rings per molecule with not more than half of them aromatic. A correction must be applied for oils containing significant quantities of sulfur.NOTE 1: The composition of complex petroleum fractions is often expressed in terms of the proportions of aromatic rings (RA), naphthene rings (RN), and paraffin chains (CP) that would comprise a hypothetical mean molecule. Alternatively, the composition may be expressed in terms of a carbon distribution, that is, the percentage of the total number of carbon atoms that are present in aromatic ring structures (% CA), naphthene ring structures (% CN), and paraffin chains (% Cp).1.2 The values stated in SI units are to be regarded as the standard.1.2.1 Exception—The values 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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3.1 This practice may be used to determine non-protein or non-nitrogen containing organic matter in leather which is not extractable with water or hexane. Examples would be vegetable tannins and acrylic lubricants.1.1 This practice covers the determination of the combined tannin and nonextractable organic resins and the degree of tannage of all types of vegetable-tanned leather and leather with organic retannages. This practice does not apply to wet blue.1.2 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 Heat capacities obtained by this method are those at atmospheric pressure. However, because the temperature range is low, the calculated values are similar to saturated liquid heat capacities in the temperature-pressure range required for most engineering design.1.1 This test method covers the calculation of liquid heat capacity, Btu/lb · °F (kJ/kg · K), at atmospheric pressure, of petroleum fuels for which distillation data may be obtained in accordance with Test Method D86 without reaching a decomposition point prior to obtaining 90 % by volume distilled.1.2 This test method is not applicable at temperatures less than 0 °F (−18 °C) and greater than 60 °F (16 °C) above the volumetric average boiling point of the fuel.1.3 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 The viscosity-gravity constant (VGC) is a useful function for the approximate characterization of the viscous fractions of petroleum.2 It is relatively insensitive to molecular weight and is related to a fluids composition as expressed in terms of certain structural elements. Values of VGC near 0.800 indicate samples of paraffinic character, while values close to 1.00 indicate a preponderance of aromatic structures. Like other indicators of hydrocarbon composition, the VGC should not be indiscriminately applied to residual oils, asphaltic materials, or samples containing appreciable quantities of nonhydrocarbons.1.1 This test method covers the calculation of the viscosity-gravity constant (VGC) of petroleum oils2 having viscosities in excess of 5.5 mm2/s at 40 °C (104 °F) and in excess of 0.8 mm2/s at 100 °C (212 °F).1.2 Annex A1 describes a method for calculating the VGC from Saybolt (SUS) viscosity and relative density.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3.1 The SI unit of kinematic viscosity is mm2/s.1.3.2 Exception—Fahrenheit temperature units are used in this practice because they are accepted by industry for the type of legacy conversions described in this practice.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 Permanent Shear Stability Index (PSSI) is a measure of the loss of viscosity, due to shearing, contributed by a specified additive.NOTE 2: For example, a PSSI of 50 means the additive will lose 50 % of the viscosity it contributes to the finished oil.5.2 The selection of appropriate base fluids and additive concentrations to be used in test oils is left to individual operators or companies. These choices will depend on the intended application for the additive.NOTE 3: PSSI may depend more strongly on base fluid, additive concentration, additive chemistry, and the presence of other additives for base fluids of unusual composition (for example, esters) or if additives outside the common range of chemistries and concentrations are used. Caution should be exercised when interpreting results from different sources.1.1 This practice specifies the procedure for the calculation of Permanent Shear Stability Index (PSSI) of an additive using viscosities before and after a shearing procedure.1.2 PSSI is calculated for a single blend component and can then be used to estimate the effects of that component on finished lubricant blends.1.3 This practice is applicable to many products and may use data from many different test methods. The calculation is presented in its most general form in order not to restrict its 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 Each power reactor has a specific DEX value that is their technical requirement limit. These values may vary from about 200 to about 900 μCi/g based upon the height of their plant vent, the location of the site boundary, the calculated reactor coolant activity for a condition of 1 % fuel defects, and general atmospheric modeling that is ascribed to that particular plant site. Should the DEX measured activity exceed the technical requirement limit, the plant enters an LCO requiring action on plant operation by the operators.5.2 The determination of DEX is performed in a similar manner to that used in determining DEI, except that the calculation of DEX is based on the acute dose to the whole body and considers the noble gases 85mKr, 85Kr, 87Kr, 88Kr, 131mXe, 133mXe, 133Xe, 135mXe, 135Xe, and 138Xe which are significant in terms of contribution to whole body dose.5.3 It is important to note that only fission gases are included in this calculation, and only the ones noted in Table 1. For example 83mKr is not included even though its half-life is 1.86 hours. The reason for this is that this radionuclide cannot be easily determined by gamma spectrometry (low energy X-rays at 32 and 9 keV) and its dose consequence is vanishingly small compared to the other, more prevalent krypton radionuclides.5.4 Activity from 41Ar, 19F, 16N, and 11C, all of which predominantly will be in gaseous forms in the RCS, are not included in this calculation.5.5 If a specific noble-gas radionuclide is not detected, it should be assumed to be present at the minimum-detectable activity. The determination of dose-equivalent Xe-133 shall be performed using effective dose-conversion factors for air submersion listed in Table III.1 of EPA Federal Guidance Report No. 12,3 or the average gamma-disintegration energies as provided in ICRP Publication 38 (“Radionuclide Transformations”) or similar source.1.1 This practice applies to the calculation of the dose equivalent to 133Xe in the reactor coolant of nuclear power reactors resulting from the radioactivity of all noble gas fission products.1.2 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 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 density/unit weight of a cohesionless soil may be determined by various in-place methods in the field or by the measurement of physical dimensions and masses by laboratory soil specimens. The dry density/unit weight of a cohesionless soil does not necessarily, by itself, reveal whether the soil is loose or dense.5.2 Relative density/unit weight expresses the degree of compactness of a cohesionless soil with respect to the loosest and densest condition as defined by standard laboratory procedures. Only when viewed against the possible range of variation, in terms of relative density/unit weight, can the dry density/unit weight be related to the compaction effort used to place the soil in a compacted fill or indicate volume change and stress-strain tendencies of soil when subjected to external loading.5.3 An absolute minimum density/unit weight is not necessarily obtained by these test methods.NOTE 1: In addition, there are published data to indicate that these test methods have a high degree of variability.4 However, the variability can be greatly reduced by careful calibration of equipment, and careful attention to proper test procedure and technique.5.4 The use of the standard molds (6.2.1) has been found to be satisfactory for most soils requiring minimum index density/unit weight testing. Special molds (6.2.2) shall only be used when the test results are to be applied in conjunction with design or special studies and there is not enough soil to use the standard molds. Such test results should be applied with caution, as minimum index densities/unit weights obtained with the special molds may not agree with those that would be obtained using the standard molds.NOTE 2: The quality of the result produced by this standard is dependent on the competence of the personnel performing it, and the suitability of the equipment and facilities used. Agencies that meet the criteria of Practice D3740, generally, are considered capable of competent and objective testing/sampling/inspection/etc. Users of this standard are cautioned that compliance with Practice D3740 does not in itself assure reliable results. Reliable results depend on many factors; Practice D3740 provides a means of evaluating some of those factors.1.1 These test methods cover the determination of the minimum-index dry density/unit weight of cohesionless, free-draining soils. The adjective “dry” before density or unit weight is omitted in the title and remaining portions of this standards to be be consistent with the applicable definitions given in Section 3 on Terminology.1.2 System of Units: 1.2.1 The testing apparatus described in this standard has been developed and manufactured using values in the gravimetric or inch-pound system. Therefore, test apparatus dimensions and mass given in inch-pound units are regarded as the standard.1.2.2 It is common practice in the engineering profession to concurrently use pounds to represent both a unit of mass (lbm) and a unit of force (lbf). This implicitly combines two separate systems of units; that is, the absolute system and the gravitational system. It is scientifically undesirable to combine the use of two separate sets of inch-pound units within a single standard. This test method has been written using the gravitational system of units when dealing with the inch-pound system. In this system, the pound (lbf) represents a unit of force (weight). However, balances or scales measure mass; and weight must be calculated. In the inch-pound system, it is common to assume that 1 lbf is equal to 1 lbm. While reporting density is not regarded as nonconformance with this standard, unit weights should be calculated and reported since the results may be used to determine force or stress.1.2.3 The terms density and unit weight are often used interchangeably. Density is mass per unit volume, whereas unit weight is force per unit volume. In this standard, density is given only in SI units. After the density has been determined, the unit weight is calculated in SI or inch-pound units, or both.1.3 Three alternative methods are provided to determine the minimum index density/unit weight, as follows:1.3.1 Method A—Using a funnel pouring device or a hand scoop to place material in mold.1.3.2 Method B—Depositing material into a mold by extracting a soil filled tube.1.3.3 Method C 2—Depositing material by inverting a graduated cylinder.1.4 The method to be used should be specified by the agency requesting the test. If no method is specified, the provisions of Method A shall govern. Test Method A is the preferred procedure for determining minimum index density/unit weight as used in conjunction with the procedures of Test Methods D4253. Methods B and C are provided for guidance of testing used in conjunction with special studies, especially where there is not enough material available to use a 0.100 ft3 (2830 cm3) or 0.500 ft3 (14 200 cm3) mold as required by Method A.1.5 These test methods are applicable to soils that may contain up to 15 %, by dry mass, of soil particles passing a No. 200 (75-μm) sieve, provided they still have cohesionless, free-draining characteristics (nominal sieve dimensions are in accordance with Specification E11).1.5.1 Method A is applicable to soils in which 100 %, by dry mass, of soil particles pass a 3-in. (75-mm) sieve and which may contain up to 30 %, by dry mass, of soil particles retained on a 11/2-inch (37.5-mm) sieve.1.5.2 Method B is applicable to soils in which 100 %, by dry mass, of soil particles pass a 3/4-inch (19.0-mm) sieve.1.5.3 Method C is applicable only to fine and medium sands in which 100 %, by dry mass, of soil particles pass a 3/8-in. (9.5-mm) sieve and which may contain up to 10 %, by dry mass, of soil particles retained on a No. 10 (2.00-mm) sieve.1.5.4 Soils, for the purposes of these test methods, shall be regarded as naturally occurring cohesionless soils, processed particles, or composites or mixtures of natural soils, or mixtures of natural and processed particles, provided they are free-draining.1.6 All observed and calculated values shall conform to the guidelines for significant digits and rounding established in Practice D6026.1.6.1 For purposes of comparing a measured or calculated value(s) to specified limits, the measured or calculated value(s) shall be rounded to the nearest decimal or significant digits in the specified limits.1.6.2 The procedures used to specify how data are collected/recorded or calculated in this standard are regarded as the industry standard. In addition, they are representative of the significant digits that generally should be retained. The procedures used do not consider material variation, purpose for obtaining the data, special purpose studies, or any considerations for the user’s objectives; and it is common practice to increase or reduce significant digits of reported data to be commensurate with these considerations. It is beyond the scope of this standard to consider significant digits used in analysis methods for engineering design.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 and health practices and determine the applicability of regulatory limitations prior to use.

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