4.1 The use of the body measurement information in Table 1 and Table 2 will assist manufacturers in developing patterns and garments that are consistent with the current anthropometric characteristics of the population of interest. This practice should, in turn, reduce or minimize consumer confusion and dissatisfaction related to apparel sizing (also refer to ISO 3635 Size Designation Procedures).FIG. 1 Form Front View 2-6 Little KidsFIG. 2 Form Quarter View 2-6 Little KidsFIG. 3 Form Side View 2-6 Little KidsFIG. 4 Form Back View 2-6 Little Kids1.1 These tables list body measurements of little kids’ figure type regular sizes 2-6. Although these are body measurements, they can be used as a baseline in designing apparel for little kids in this size range when considering such factors as fabric type, ease for body movement, styling, and fit.1.2 These tables list body measurements for the complete range of little kids regular sizing.1.3 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 The use of the body measurement information in Tables 1–2 will assist manufacturers in developing patterns and garments that are consistent with the current anthropometric characteristics of the population of interest. This practice should in turn reduce or minimize consumer confusion and dissatisfaction related to apparel sizing. (Also refer to ISO 3635 Size Designation Procedures).4.2 Three-dimensional avatars depicting each of the girls’ sizes on certain measures, were created by Alvanon, Inc. and included in this standard to assist manufacturers in visualizing the posture, shape, and proportions generated by the measurements charts in the accompanying Tables. (See Figs. 1–4.)1.1 These tables list body measurements of big girl’s figure Type Regular sizes 7 through 20. Although these are body measurements, they can be used as a baseline in designing apparel for girls in this size range when considering such factors as fabric type ease for body movement, styling, and fit.1.2 These tables list body measurements for the complete range of big girl’s regular sizing.1.3 The values stated in either acceptable SI units or inch units shall be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system must be used independently of the other, without combining values in any way.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 use of the body measurement information in Tables 1–2 will assist manufacturers in developing patterns and garments that are consistent with the current anthropometric characteristics of the population of interest. This practice should in turn reduce or minimize consumer confusion and dissatisfaction related to apparel sizing. (Also refer to ISO 3635 Size Designation Procedures).4.2 Three-dimensional avatars depicting each of the big boys’ sizes on certain measures, were created by Alvanon, Inc. and included in this standard to assist manufacturers in visualizing the posture, shape, and proportions generated by the measurements charts in the accompanying Tables. (See Figs. 1–4.)1.1 These tables list body measurements of big boy’s regular figure Type sizes 7 through 20. Although these are body measurements, they can be used as a baseline in designing apparel for boys regular in this size range when considering such factors as fabric type ease for body movement, styling, and fit.1.2 These tables list body measurements for the complete range of big boy’s sizing.1.3 The values stated in either acceptable SI units or inch units shall be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system must be used independently of the other, without combining values in any way.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 degree of deacetylation of chitosan, as well at the molar mass and molar mass distribution, determines the functionality of chitosan in an application. For instance, functional and biological effects are highly dependent upon the composition and molar mass of the polymer.4.2 This test method describes procedures for measurement of molar mass of chitosan chlorides and glutamates, and chitosan base, although it in principle applies to any chitosan salt. The measured molar mass is that for chitosan acetate, since the mobile phase contains acetate as counter ion. This value can further be converted into the corresponding molar mass for the chitosan as a base, or the parent salt form (chloride or glutamate).4.3 Light scattering is one of very few methods available for the determination of absolute molar mass and structure, and it is applicable over the broadest range of molar masses of any method. Combining light scattering detection with size exclusion chromatography (SEC), which sorts molecules according to size, gives the ability to analyze polydisperse samples, as well as obtaining information on branching and molecular conformation. This means that both the number-average and mass-average values for molar mass and size may be obtained for most samples. Furthermore, one has the ability to calculate the distributions of the molar masses and sizes.4.4 Multi-angle laser light scattering (MALS) is a technique where measurements of scattered light are made simultaneously over a range of different angles. MALS detection can be used to obtain information on molecular size, since this parameter is determined by the angular variation of the scattered light. Molar mass may in principle be determined by detecting scattered light at a single low angle (LALLS). However, advantages with MALS as compared to LALLS are: (1) less noise at larger angles, (2) precision of measurements is improved by detecting at several angles, and (3) the ability to detect angular variation allows determination of size, branching, aggregation, and molecular conformation.4.5 Size exclusion chromatography uses columns, which are typically packed with polymer particles containing a network of uniform pores into which solute and solvent molecules can diffuse. While in the pores, molecules are effectively trapped and removed from the flow of the mobile phase. The average residence time in the pores depends upon the size of the solute molecules. Molecules that are larger than the average pore size of the packing are excluded and experience virtually no retention; these are eluted first, in the void volume of the column. Molecules, which may penetrate the pores will have a larger volume available for diffusion, they will be retained in the column for a time dependent upon their molecular size, with smaller molecules eluting after larger molecules.4.6 For polyelectrolytes, dialysis against the elution buffer has been suggested, in order to eliminate Donnan-type artifacts in the molar mass determination by light scattering (1, 2).5 However, in the present method, the size exclusion chromatography step preceding the light scatter detection is an efficient substitute for a dialysis step. The sample is separated on SEC columns with large excess of elution buffer for 30 to 40 min, and it is therefore in full equilibrium with the elution buffer when it reaches the MALS detector.1.1 This test method covers the determination of the molar mass of chitosan and chitosan salts intended for use in biomedical and pharmaceutical applications as well as in tissue engineered medical products (TEMPs) by size exclusion chromatography with multi-angle laser light scattering detection (SEC-MALS). A guide for the characterization of chitosan salts has been published as Guide F2103.1.2 Chitosan and chitosan salts used in TEMPs should be well characterized, including the molar mass and polydispersity (molar mass distribution) in order to ensure uniformity and correct functionality in the final product. This test method will assist end users in choosing the correct chitosan for their particular application. Chitosan may have utility as a scaffold or matrix material for TEMPs, in cell and tissue encapsulation applications, and in drug delivery formulations.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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4.1 The composition and sequential structure of alginate, as well as the molar mass and molar mass distribution, determines the functionality of alginate in an application. For instance, the gelling properties of an alginate are highly dependent upon the composition and molar mass of the polymer.4.2 Light scattering is one of very few methods available for the determination of absolute molar mass and structure, and it is applicable over the broadest range of molar masses of any method. Combining light scattering detection with size exclusion chromatography (SEC), which sorts molecules according to size, gives the ability to analyze polydisperse samples, as well as to obtain information on branching and molecular conformation. This means that both the number-average and mass-average values for molar mass and size may be obtained for most samples. Furthermore, one has the ability to calculate the distributions of the molar masses and sizes.4.3 Multi-angle laser light scattering (MALS) is a technique where measurements are made simultaneously over a range of different angles and used to determine the scattering at 0°, which directly relates to molecular weight. MALS detection can be used to obtain information on molecular size, since this parameter is determined by the angular variation of the scattered light. This can be related to branching, aggregation, and molecular conformation. Molar mass can also be determined by detecting scattered light at a single low angle (LALS) and assuming that this is not significantly different from the scattering at 0°.4.4 Size exclusion chromatography uses columns, which are typically packed with polymer particles containing a network of uniform pores into which solute and solvent molecules can diffuse. While in the pores, molecules are effectively trapped and removed from the flow of the mobile phase. The average residence time in the pores depends upon the size of the solute molecules. Molecules that are larger than the average pore size of the packing are excluded and experience virtually no retention; these are eluted first, in the void volume of the column. Molecules which penetrate the pores will have a larger volume available for diffusion; their retention will depend on their molecular size, with the smaller molecules eluting last.4.5 For polyelectrolytes, dialysis against the elution buffer has been suggested, in order to eliminate Donnan-type artifacts in the molar mass determination by light scattering (1, 2).6 However, in the present method, the size exclusion chromatography step preceding the light scatter detection is an efficient substitute for a dialysis step. The sample is separated on SEC columns with large excess of elution buffer for 30 to 40 min, and it is therefore in full equilibrium with the elution buffer when it reaches the MALS detector.1.1 This test method covers the determination of the molar mass (typically expressed as grams/mole) of sodium alginate intended for use in biomedical and pharmaceutical applications as well as in tissue-engineered medical products (TEMPs) by size exclusion chromatography with multi-angle laser light scattering detection (SEC-MALS). A guide for the characterization of alginate has been published as Guide F2064.1.2 Alginate used in TEMPs should be well characterized, including the molar mass and polydispersity (molar mass distribution) in order to ensure uniformity and correct functionality in the final product. This test method will assist end users in choosing the correct alginate for their particular application. Alginate may have utility as a scaffold or matrix material for TEMPs, in cell and tissue encapsulation applications, and in drug delivery formulations.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 and health practices and determine the applicability of regulatory limitations prior to use.

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5.1 Workability is one of the main factors that influence the compaction quality and ultimately the performance of asphalt pavement. This method uses the relative rotation measured by the wireless particle-size sensor to evaluate the workability of the asphalt mixture.5.2 This test method is used to generate information concerning the workability of an asphalt mixture. Workability characteristics, in turn, can give users insight as to how the mixture will handle and compact in the field.5.3 This method is used to evaluate workability of the mix in a situation where it is being used for research or mix design. It is not intended to be a quality control (QC) evaluation.5.4 This test method can be used to evaluate conventional and modified asphalt mixtures to achieve the best workability at an appropriate compaction temperature. The test method can be used to determine the compaction temperature and optimal dosage rate of additives or modifiers to achieve the best workability for the modified asphalt mixtures, such as polymer modified, crumb rubber modified, waste plastic modified, etc.5.5 This test method is appropriate for laboratory-produced mixtures and plant-produced mixtures, regardless of the type or grade of the binder, the type or gradation of the aggregates, and whether RAP, WMA additives, or other modifiers are used in the asphalt mixture.NOTE 1: The quality of the results produced by this standard is dependent on the competence of the personnel performing the procedure and the capability, calibration, and maintenance of the equipment used. Agencies that meet the criteria of Specification D3666 are generally considered capable of competent and objective testing, sampling, inspection, etc. Users of this standard are cautioned that compliance with Specification D3666 alone does not completely ensure reliable results. Reliable results depend on many factors; following the suggestions of Specification D3666 or some similar acceptable guideline provides a means of evaluating and controlling some of those factors.1.1 This test method covers the determination of relative rotation to evaluate the workability of asphalt mixture during compaction using a wireless particle-size sensor. It is applicable to asphalt mixture being compacted using the Superpave Gyratory Compactor (SGC).1.2 This test method is appropriate for use to determine the relative rotation of laboratory-produced and plant-produced asphalt mixtures, regardless of the type or gradation of the aggregates, and whether reclaimed asphalt pavement (RAP), warm mix asphalt (WMA) additives, or any type of modifiers are used in the asphalt mixture.1.3 Units—The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.1.4 The text of this standard references notes and footnotes which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered requirements of the standard.1.5 Since a complete precision and bias statement for this standard has not been developed, the test method is to be used for research and informational purposes only. Therefore, this standard should not be used for acceptance or rejection of a material for purchasing purposes.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 One of the factors affecting the image quality of a radiographic image is geometric unsharpness. The degree of geometric unsharpness is dependent upon the focal spot size of the radiation source, the distance between the source and the object to be radiographed, the distance between the object to be radiographed and the image plane (film, imaging plate, Digital Detector Array (DDA), or radioscopic detector). This test method allows the user to determine the effective focal spot size (dimensions) of the X-ray source. This result can then be used to establish source to object and object to image detector distances appropriate for maintaining the desired degree of geometric unsharpness or maximum magnification possible, or both, for a given radiographic imaging application. The accuracy of this method is dependent upon the spatial resolution of the imaging system, magnification, and signal-to-noise of the resultant images.1.1 The image quality and the resolution of X-ray images highly depend on the characteristics of the focal spot. The imaging qualities of the focal spot are based on its two dimensional intensity distribution as seen from the imaging place.1.2 This test method provides instructions for determining the effecting size (dimensions) of mini and micro focal spots of industrial X-ray tubes. It is based on the European standard, EN 12543–5, Non-destructive testing - Characteristics of focal spots in industrial X-ray systems for use in non-destructive testing - Part 5: Measurement of the effective focal spot size of mini and micro focus X-ray tubes.1.3 This standard specifies a method for the measurement of effective focal spot dimensions from 5 up to 300 μm of X-ray systems up to and including 225 kV tube voltage, by means of radiographs of edges. Larger focal spots should be measured using Test Method E1165 Standard Test Method for Measurement of Focal Spots of Industrial X-Ray Tubes by Pinhole Imaging.1.4 The same procedure can be used at higher kilovoltages by agreement, but the accuracy of the measurement may be poorer.1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 This practice supports test methods designed to evaluate the performance of fluid-filter media, for example, Practice F796 wherein particle size distributions are addressed and at the same time this practice provides a means to compare size measurements obtained from several different types of instruments.4.2 The factor for converting one kind of diameter scale to another is only valid for the specific test particles studied.1.1 This practice provides a procedure for comparing the sizes of nonspherical particles in a test sample determined with different types of automatic particle counters, which operate on different measuring principles.1.2 A scale factor is obtained by which, in the examination of a given powder, the size scale of one instrument may be multiplied to agree with the size scale of another.1.3 The practice considers rigid particles, free of fibers, of the kind used in studies of filtration, such as: commercially available test standards of quartz or alumina, or fly ash, or some powdered chemical reagent, such as iron oxide or calcium sulfate.1.4 Three kinds of automatic particle counters are considered:1.4.1 Image analyzers, which view stationary particles under the microscope and, in this practice, measure the longest end-to-end distance of an individual particle.1.4.2 Optical counters, which measure the area of a shadow cast by a particle as it passes by a window; and1.4.3 Electrical resistance counters, which measure the volume of a particle as it passes through an orifice in an electrically conductive liquid.1.5 This practice also considers the use of instruments that provide sedimentation analyses, which is to say provide measures of the particle mass distribution as a function of Stokes diameter. The practice provides a way to convert mass distribution into number distribution so that the meaning of Stokes diameter can be related to the diameter measured by the instruments in 1.4.1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this 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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4.1 These criteria6 and procedures provide a uniform base for analysis of liquid drop data.1.1 This practice gives procedures for determining appropriate sample size, size class widths, characteristic drop sizes, and dispersion measure of drop size distribution. The accuracy of and correction procedures for measurements of drops using particular equipment are not part of this practice. Attention is drawn to the types of sampling (spatial, flux-sensitive, or neither) with a note on conversion required (methods not specified). The data are assumed to be counts by drop size. The drop size is assumed to be the diameter of a sphere of equivalent volume.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 The analysis applies to all liquid drop distributions except where specific restrictions are stated.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 It is important to recognize that the results obtained by this test method or any other method for particle size determination utilizing different physical principles may disagree. The results are strongly influenced by physical principles employed by each method of particle size analysis. The results of any particle sizing method should be used only in a relative sense and should not be regarded as absolute when comparing results obtained by other methods. Particularly for fine materials (that is, average particle size < 20 μm), significant differences are often observed for laser light scattering instruments of different manufacturers. These differences include lasers of different wavelengths, detector configuration, and the algorithms used to convert scattering to particle size distribution. Therefore, comparison of results from different instruments may be misleading.35.2 Light scattering theories (Fraunhofer Diffraction4 and Mie Scattering5) that are used for determination of particle size have been available for many years. Several manufacturers of testing equipment now have units based on these principles. Although each type of testing equipment utilizes the same basic principles for light scattering as a function of particle size, different assumptions pertinent to application of the theory and different models for converting light measurements to particle size, may lead to different results for each instrument. Furthermore, any particles which are outside the size measurement range of the instrument will be ignored, causing an increase in the reported percentages within the detectable range. A particle size distribution which ends abruptly at the detection limit of the instrument may indicate that particles outside the range are present. Therefore, use of this test method cannot guarantee directly comparable results from different types of instruments.5.3 This test method can be used to determine particle size distributions of catalysts, supports, and catalytic raw materials for specifications, manufacturing control, and research and development work.5.4 For fine materials (that is, average particle size < 20 μm), it is critical that Mie Scattering Theory be applied. This involves entering an “optical model” consisting of the “real” and “imaginary” refractive indices of the solid at the wavelength of the laser. The “imaginary” refractive index is also referred to as the “absorbance,” as it has a value of zero for transparent materials such as glass beads. For common materials and naturally occurring minerals (for example, kaolin), these values are known and published, and usually included in the manufacturer’s instrument manual (for example, as an appendix). For example, kaolinite measured at 589.3 nm has a “real” refractive index of 1.55. The absorbance (imaginary component) for minerals and metal oxides is normally taken as 0.001, 0.01 or 0.1. Many of the published values were measured at 589.3 nm (sodium light) but often values at other wavelengths are also given. Extrapolation, interpolation, or estimation to the wavelength of the laser being used can therefore be made.61.1 This test method covers the determination of the particle size distribution of catalyst, catalyst carrier, and catalytic raw material particles and is one of several found valuable for the measurement of particle size. The range of average particle sizes investigated was from 1 to 300 μm equivalent spherical diameter. The technique is capable of measuring particles above and below this range. The angle and intensity of laser light scattered by the particles are selectively measured to permit calculation of a volume distribution using light-scattering techniques.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This practice provides a way to estimate the average grain size of polycrystalline materials. It is based on EBSD measurements of crystallographic orientation which are inherently quantitative in nature. This method has specific advantage over traditional optical grain size measurements in some materials, where it is difficult to find appropriate metallographic preparation procedures to adequately delineate grain boundaries.1.1 This practice is used to determine grain size from measurements of grain areas from automated electron backscatter diffraction (EBSD) scans of polycrystalline materials.1.2 The intent of this practice is to standardize operation of an automated EBSD instrument to measure ASTM G directly from crystal orientation. The guidelines and caveats of E112 apply here, but the focus of this standard is on EBSD practice.1.3 This practice is only applicable to fully recrystallized materials.1.4 This practice is applicable to any crystalline material which produces EBSD patterns of sufficient quality that a high percentage of the patterns can be reliably indexed using automated indexing software.1.5 The practice is applicable to any type of grain structure or grain size distribution.1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this 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 Manufacturers and users of alumina powders will find this test method useful to determine the particle size distribution of these materials for product specification, quality control, and research and development testing.1.1 This test method covers the determination of the particle size distribution of alumina in the range from 0.1 to 20 μm having a median particle diameter from 0.5 to 5.0 μm.1.2 The procedure described in this test method may be successfully applied to other ceramic powders in this general size range. It is the responsibility of the user to determine the applicability of this test method to other material.1.3 The values stated in SI units are to 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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4.1 This test method concerns the sieving of coal into designated size fractions for the purpose of characterizing the material as to its particle size distribution for further processing or for commercial purposes. This is covered in Part A of this standard. Raw, as well as prepared (crushed, cleaned, or screened), coals can be tested by this test method.4.2 This test method is applicable for all types of coals, except for pulverized coals (see Method D197) such as fed into steam boilers. Low rank coals, that is, lignites, subbituminous, and high volatile bituminous C, must be dried with caution and handled with care to minimize deterioration or size degradation during sieving.4.3 This test method is applicable for the wet or dry-sieving of coal at sizes from 200 mm [8 in.] to 38 μm [No. 400 U.S.A. Standard]. Methods for sizing materials below 38 μm are outside the scope of this test method.NOTE 2: The sizing of material that passes the 38 μm sieve is normally performed by optical microscopy, sedimentation, centrifugation, light scattering or obfuscation, surface area measurement, or other such methods. Subsieve techniques are also used sometimes.4.4 This test method also concerns the designation of a coal sample as to its upper (nominal top-size) and lower (nominal bottom-size) limiting sizes for the purpose of characterizing the material for further processing or for commercial purposes. This is covered in Part B of this test method. Anthracite coal is further designated by a one word descriptive term (see 14.4).4.5 Enough material may not be collected by this test method to meet subsequent test procedures, such as washability analyses (Test Method D4371).1.1 This test method covers procedures for determining the sieve analysis of coal and designating the size of coal from sieve analysis data. Raw as well as prepared (crushed, cleaned or screened) coals can be tested by this test method.1.2 This test method explains how to designate coal sizes from the results of sieve analysis data in order to represent the condition of the coal as sold. In the case of special mixtures or coals with noncontinuous ranges of sizes, a sufficiently complete sieve analysis must be made to properly describe the size distribution.1.3 This test method is not applicable for determining the sieve analysis nor for designating the size of pulverized coal. (See Note 1.) Size fractions down to and including 38 μm [No. 400 U.S.A. Standard Series] can be treated by the methods discussed in this test method. Methods for handling size fractions below 38 μm [No. 400] will be developed by this committee.NOTE 1: For powdered or pulverized coal as is fired into steam boilers, refer to Test Method D197.1.4 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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4.1 This practice is of value (1) to the producer of fine particles as a means of reporting particle characteristics with respect to quality control and (2) to the buyer to assure that the particle size and particle size distribution meet his requirements.1.1 This practice for reporting the fineness characteristics of pigments is designed to apply in most cases where well-known methods for determining these particle size characteristics in the subsieve range are employed, such as microscopic, sedimentation, and turbidimetric methods; and partially to absorption and permeability methods.1.2 Laminar, plate-like pigments and composite pigments having a definite bimodal distribution are not considered within the scope of this practice.1.3 Parameters—The fineness characteristics are reported in the following three parameters:1.3.1 Particle Size Parameter.1.3.2 Coarseness Parameter—A parameter descriptive of the coarseness character of the pigment, making use of a limiting value in the subsieve range similar to that used in the sieve ranges.1.3.3 Dispersion Parameter—A parameter descriptive of the uniformity of the particle size distribution.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 This practice is primarily intended for use by associations, third-party grading agencies, technical societies and other groups that develop national design standards and use recommendations for round timber piles.4.2 This practice provides procedures for establishing compression parallel to grain and bending stresses for round timber piles including: sampling of material for testing; methods of test and property calculation procedures; distribution analysis of test data; procedures for determining adjustments for critical section location; pile oversize, load sharing and treatment; and procedures for deriving allowable stresses.4.3 In using allowable stresses established under this practice, factors specific to each end use which may affect the performance of the pile system shall be considered by the designer. Such factors include the location of the critical section, the bearing capacity of the soil, the ability of the pile to withstand driving forces, the properties of the cap or load distributive element tying piles together and the loading and conditions of service.1.1 This practice contains procedures for establishing allowable compression parallel to grain and bending stresses for round timbers used for piling, based on results from full-size tests.NOTE 1: Allowable stresses for compression perpendicular to grain and shear properties are established in accordance with the provisions of Practice D2899.1.2 Stresses established under this practice are applicable to piles conforming to the size, quality, straightness, spiral grain, knot, shake and split provisions of Specification D25.1.3 A commentary on the practice is available from ASTM International.1.4 The values stated in inch-pound 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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