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ASTM E826-14

(Practice)

Standard Practice for Testing Homogeneity of a Metal Lot or Batch in Solid Form by Spark Atomic Emission Spectrometry (Withdrawn 2023)

Standard Practice for Testing Homogeneity of a Metal Lot or Batch in Solid Form by Spark Atomic Emission Spectrometry (Withdrawn 2023)

SIGNIFICANCE AND USE
5.1 The purpose of this practice is to evaluate the homogeneity of a lot of material selected as a candidate for development as a reference material or certified reference material, or for a L/B selected for some other purpose (see Appendix X1 – Appendix X4 for examples).  
5.2 This practice is applicable to the testing of samples taken at various stages during production. For example, continuous cast materials, ingots, rolled bars, wire, etc., could be sampled at various stages during the production process and tested.
SCOPE
1.1 This practice is suitable for testing the homogeneity of a metal lot or batch (L/B) in solid form by spark atomic emission spectrometry (Spark-AES). It is compliant with ISO Guide 35—Certification of Reference Materials: General and Statistical Principles. It is primarily intended for use in the development of reference materials but may be used in any other application where a L/B is to be tested for homogeneity. It is designed to provide a combined study of within-unit and between-unit homogeneity of such a L/B.  
1.2 This practice is designed primarily to test for elemental homogeneity of a metal L/B by Spark-AES. However, it can be adapted for use with other instrumental techniques such as X-ray fluorescence spectrometry (XRF) or atomic absorption spectrometry (AAS).Note 1—This practice is not limited to elemental analysis or techniques. This practice can be applied to any property that can be measured, for example, the property of hardness as measured by the Rockwell technique.  
1.3 The criteria for acceptance of the test specimens must be previously determined. That is, the maximum acceptable level of heterogeneity must be determined on the basis of the intended use of the L/B.  
1.4 It is assumed that the analyst is trained in Spark-AES techniques including the specimen preparation procedures needed to make specimens ready for measurements. It is further assumed that the analyst is versed in and has access to computer-based data capture and analysis. The methodology of this practice is best utilized in a computer based spreadsheet.  
1.5 This practice can be applied to one or more elements in a specimen provided the signal-to-background ratio is not a limiting factor.  
1.6 This practice includes methods to correct for systematic drift of the instrument with time. (Warning—If drift occurs, erroneous conclusions will be obtained from the data analysis.)  
1.7 This practice also includes methods to refine estimates of composition and uncertainty through the use of a type standard or multiple calibrants.  
1.8 It further provides a means of reducing a nonhomogeneous set to a homogeneous subset.  
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 and health practices and determine the applicability of regulatory limitations prior to use.
WITHDRAWN RATIONALE
This practice is suitable for testing the homogeneity of a metal lot or batch (L/B) in solid form by spark atomic emission spectrometry (Spark-AES). It is compliant with ISO Guide 35—Certification of Reference Materials: General and Statistical Principles. It is primarily intended for use in the development of reference materials but may be used in any other application where a L/B is to be tested for homogeneity. It is designed to provide a combined study of within-unit and between-unit homogeneity of such a L/B.
Formerly under the jurisdiction of Committee E01 on Analytical Chemistry for Metals, Ores, and Related Materials, this practice was withdrawn in January 2023 in accordance with section 10.6.3 of the Regulations Governing ASTM Technical Committees, which requires that standards shall be updated by the end of the eighth year since the last approval date.

General Information

Status
Withdrawn
Publication Date
31-Mar-2014
Withdrawal Date
05-Jan-2023
ICS
77.040.99 - Other methods of testing of metals
Technical Committee
E01 - Analytical Chemistry for Metals, Ores, and Related Materials
Drafting Committee
E01.22 - Laboratory Quality
Current Stage
Ref Project

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ASTM E826-14 - Standard Practice for Testing Homogeneity of a Metal Lot or Batch in Solid Form by Spark Atomic Emission Spectrometry (Withdrawn 2023)ASTM E826-14 - Standard Practice for Testing Homogeneity of a Metal Lot or Batch in Solid Form by Spark Atomic Emission Spectrometry (Withdrawn 2023)
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ASTM E826-14 - Standard Practice for Testing Homogeneity of a Metal Lot or Batch in Solid Form by Spark Atomic Emission Spectrometry (Withdrawn 2023)
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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Contact ASTM International (www.astm.org) for the latest information
Designation: E826 − 14
Standard Practice for
Testing Homogeneity of a Metal Lot or Batch in Solid Form
1
by Spark Atomic Emission Spectrometry
This standard is issued under the fixed designation E826; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision.Anumber in parentheses indicates the year of last reapproval.A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope 1.7 This practice also includes methods to refine estimates
of composition and uncertainty through the use of a type
1.1 Thispracticeissuitablefortestingthehomogeneityofa
standard or multiple calibrants.
metallotorbatch(L/B)insolidformbysparkatomicemission
spectrometry (Spark-AES). It is compliant with ISO Guide
1.8 It further provides a means of reducing a nonhomoge-
35—Certification of Reference Materials: General and Statis-
neous set to a homogeneous subset.
tical Principles. It is primarily intended for use in the devel-
1.9 This standard does not purport to address all of the
opment of reference materials but may be used in any other
safety concerns, if any, associated with its use. It is the
application where a L/B is to be tested for homogeneity. It is
responsibility of the user of this standard to establish appro-
designed to provide a combined study of within-unit and
priate safety and health practices and determine the applica-
between-unit homogeneity of such a L/B.
bility of regulatory limitations prior to use.
1.2 This practice is designed primarily to test for elemental
homogeneityofametalL/BbySpark-AES.However,itcanbe
2. Referenced Documents
adapted for use with other instrumental techniques such as
2
X-ray fluorescence spectrometry (XRF) or atomic absorption
2.1 ASTM Standards:
spectrometry (AAS).
E135Terminology Relating to Analytical Chemistry for
NOTE 1—This practice is not limited to elemental analysis or tech-
Metals, Ores, and Related Materials
niques.Thispracticecanbeappliedtoanypropertythatcanbemeasured,
E177Practice for Use of the Terms Precision and Bias in
for example, the property of hardness as measured by the Rockwell
ASTM Test Methods
technique.
E178Practice for Dealing With Outlying Observations
1.3 Thecriteriaforacceptanceofthetestspecimensmustbe
E634Practice for Sampling of Zinc and Zinc Alloys by
previously determined. That is, the maximum acceptable level
Spark Atomic Emission Spectrometry
of heterogeneity must be determined on the basis of the
E716Practices for Sampling and Sample Preparation of
intended use of the L/B.
Aluminum and Aluminum Alloys for Determination of
1.4 It is assumed that the analyst is trained in Spark-AES
Chemical Composition by Spectrochemical Analysis
techniques including the specimen preparation procedures
E1329PracticeforVerificationandUseofControlChartsin
needed to make specimens ready for measurements. It is
Spectrochemical Analysis
further assumed that the analyst is versed in and has access to
E1601Practice for Conducting an Interlaboratory Study to
computer-baseddatacaptureandanalysis.Themethodologyof
Evaluate the Performance of an Analytical Method
this practice is best utilized in a computer based spreadsheet.
E1806Practice for Sampling Steel and Iron for Determina-
1.5 This practice can be applied to one or more elements in
tion of Chemical Composition
a specimen provided the signal-to-background ratio is not a
3
2.2 ISO Standard:
limiting factor.
ISO Guide 35Certification of Reference Materials: General
1.6 This practice includes methods to correct for systematic
and Statistical Principles
drift of the instrument with time. (Warning—If drift occurs,
erroneousconclusionswillbeobtainedfromthedataanalysis.)
2
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
1
This practice is under the jurisdiction ofASTM Committee E01 on Analytical contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
ChemistryforMetals,Ores,andRelatedMaterialsandisthedirectresponsibilityof Standards volume information, refer to the standard’s Document Summary page on
Subcommittee E01.22 on Laboratory Quality. the ASTM website.
3
Current edition approved April 1, 2014. Published June 2014. Originally Available from International Organization for Standardization (ISO), 1, ch. de
approved in 1981. Last previous edition approved in 2013 as E826–08 (2013). la Voie-Creuse, Case postale 56, CH-1211, Geneva 20, Switzerland, http://
DOI: 10.1520/E0826-14. www.iso.ch.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

---------------------- Page: 1 ----------------------
E826 − 14
3. Terminology 4.4 This practice requires that there be an absence of
outliers in the data (Practice E178). (Warning—The use of
3.1 De
...

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Standard Practice for Testing Homogeneity of a Metal Lot or Batch in Solid Form by Spark Atomic Emission Spectrometry

SIGNIFICANCE AND USE
5.1 The purpose of this practice is to evaluate the homogeneity of a lot of material selected as a candidate for development as a reference material or certified reference material, or for a L/B selected for some other purpose (see Appendix X1-Appendix X4 for examples).  
5.2 This practice is applicable to the testing of samples taken at various stages during production. For example, continuous cast materials, ingots, rolled bars, wire, etc., could be sampled at various stages during the production process and tested.
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1.1 This practice is suitable for testing the homogeneity of a metal lot or batch (L/B) in solid form by spark atomic emission spectrometry (Spark-AES). It is compliant with ISO Guide 35—Certification of Reference Materials: General and Statistical Principles. It is primarily intended for use in the development of reference materials but may be used in any other application where a L/B is to be tested for homogeneity. It is designed to provide a combined study of within-unit and between-unit homogeneity of such a L/B.  
1.2 This practice is designed primarily to test for elemental homogeneity of a metal L/B by Spark-AES. However, it can be adapted for use with other instrumental techniques such as X-ray fluorescence spectrometry (XRF) or atomic absorption spectrometry (AAS).Note 1—This practice is not limited to elemental analysis or techniques. This practice can be applied to any property that can be measured, for example, the property of hardness as measured by the Rockwell technique.  
1.3 The criteria for acceptance of the test specimens must be previously determined. That is, the maximum acceptable level of heterogeneity must be determined on the basis of the intended use of the L/B.  
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1.5 This practice can be applied to one or more elements in a specimen provided the signal-to-background ratio is not a limiting factor.  
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1.8 It further provides a means of reducing a nonhomogeneous set to a homogeneous subset.  
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 and health practices and determine the applicability of regulatory limitations prior to use.

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SIGNIFICANCE AND USE
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The equipment and procedures described in this guide may also be suitable for identifying or segregating, or both, scrap metals.
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ASTM A1033-18(2023)(Practice)
Standard Practice for Quantitative Measurement and Reporting of Hypoeutectoid Carbon and Low-Alloy Steel Phase Transformations

SIGNIFICANCE AND USE
5.1 This practice is used to provide steel phase transformation data required for use in numerical models for the prediction of microstructures, properties, and distortion during steel manufacturing, forging, casting, heat treatment, and welding. Alternatively, the practice provides end users of steel and fabricated steel products the phase transformation data required for selecting steel grades for a given application by determining the microstructure resulting from a prescribed thermal cycle.  
5.1.1 There are available several computer models designed to predict the microstructures, mechanical properties, and distortion of steels as a function of thermal processing cycle. Their use is predicated on the availability of accurate and consistent thermal and transformation strain data. Strain, both thermal and transformation, developed during thermal cycling is the parameter used in predicting both microstructure and properties, and for estimating distortion. It should be noted that these models are undergoing continued development. This process is aimed, among other things, at establishing a direct link between discrete values of strain and specific microstructure constituents in steels. This practice describes a standardized method for measuring strain during a defined thermal cycle.  
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5.1.3 This practice is suitable for providing the data needed for the construction of transformation diagrams that depict the microstructures developed during the thermal processing of steels as functions of time and temperature. Such diagrams provide a qualitative assessment of the effects of changes in thermal cycle on steel microstructure. Appendix X2 describes ...
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Standard Guide for Investigating the Effects of Helium in Irradiated Metals

ABSTRACT
This guide presents the simulation procedure which would provide advice for conducting experiments to investigate the effects of helium on the properties of irradiated metals where the technique for introducing the helium differs in someway from the actual mechanism of introduction of helium in service. Simulation techniques considered for introducing helium shall include charged particle implantation, exposure to α-emitting radioisotopes, and tritium decay techniques. Procedures for the analysis of helium content and helium distribution within the specimen are also recommended. The two other methods for introducing helium into irradiated materials namely, the enhancement of helium production in nickel-bearing alloys by spectral tailoring in mixed-spectrum fission reactors, and the isotopic tailoring in both fast and mixed-spectrum fission reactors, are not covered in this guide. Dual ion beam techniques for simultaneously implanting helium and generating displacement damage are also not included here.
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4.1 Helium is introduced into metals as a consequence of nuclear reactions, such as (n, α), or by the injection of helium into metals from the plasma in fusion reactors. The characterization of the effect of helium on the properties of metals using direct irradiation methods may be impractical because of the time required to perform the irradiation or the lack of a radiation facility, as in the case of the fusion reactor. Simulation techniques can accelerate the research by identifying and isolating major effects caused by the presence of helium. The word ‘simulation’ is used here in a broad sense to imply an approximation of the relevant irradiation environment. There are many complex interactions between the helium produced during irradiation and other irradiation effects, so care must be exercised to ensure that the effects being studied are a suitable approximation of the real effect. By way of illustration, details of helium introduction, especially the implantation temperature, may determine the subsequent distribution of the helium (that is, dispersed atomistically, in small clusters in bubbles, etc.).
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ABSTRACT
These test methods cover the detection of detrimental intermetallic phase in duplex austenitic/ferritic stainless steel to the extent that toughness and corrosion resistance is affected significantly. These test methods will not necessarily detect losses of toughness or corrosion resistance attributable to other causes. Test method A-sodium hydroxide etch test, test method B-Charpy impact test, and test method C-ferric chloride corrosion test shall be made for classification of structures of duplex stainless steels.
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1.2 Duplex (austenitic-ferritic) stainless steels are susceptible to the formation of intermetallic compounds during exposures in the temperature range from approximately 600 to 1750 °F (320 to 955 °C). The speed of these precipitation reactions is a function of composition and thermal or thermomechanical history of each individual piece. The presence of these phases is detrimental to toughness and corrosion resistance.  
1.3 Correct heat treatment of duplex stainless steels can eliminate these detrimental phases. Rapid cooling of the product provides the maximum resistance to formation of detrimental phases by subsequent thermal exposures.  
1.4 Compliance with the chemical and mechanical requirements for the applicable product specification does not necessarily indicate the absence of detrimental phases in the product.  
1.5 These test methods include the following:  
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1.7 The tests do not determine the precise nature of the detrimental phase but rather the presence or absence of an intermetallic phase to the extent that it is detrimental to the toughness and corrosion resistance of the material.  
1.8 Examples of the correlation of thermal exposures, the occurrence of intermetallic phases, and the degradation of toughness and corrosion resistance are given in Appendix X1 and Appendix X2.  
1.9 The values stated in either inch-pound or SI units are to be regarded as the standard. The values given in parentheses are for information only.  
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Standard Test Methods for Characterizing Duplex Grain Sizes

SIGNIFICANCE AND USE
5.1 Duplex grain size may occur in some metals and alloys as a result of their thermomechanical processing history. For comparison of mechanical properties with metallurgical features, or for specification purposes, it may be important to be able to characterize grain size in such materials. Assigning an average grain size value to a duplex grain size specimen does not adequately characterize the appearance of that specimen, and may even misrepresent its appearance. For example, averaging two distinctly different grain sizes may result in reporting a size that does not actually exist anywhere in the specimen.  
5.2 These test methods may be applied to specimens or products containing randomly intermingled grains of two or more significantly different sizes (henceforth referred to as random duplex grain size). Examples of random duplex grain sizes include: isolated coarse grains in a matrix of much finer grains, extremely wide distributions of grain sizes, and bimodal distributions of grain size.  
5.3 These test methods may also be applied to specimens or products containing grains of two or more significantly different sizes, but distributed in topologically varying patterns (henceforth referred to as topological duplex grain sizes). Examples of topological duplex grain sizes include: systematic variation of grain size across the section of a product, necklace structures, banded structures, and germinative grain growth in selected areas of critical strain.  
5.4 These test methods may be applied to specimens or products regardless of their state of recrystallization.  
5.5 Because these test methods describe deviations from a single, log-normal distribution of grain sizes, and characterize patterns of variation in grain size, the total specimen cross-section must be evaluated.  
5.6 These test methods are limited to duplex grain sizes as identifiable within a single polished and etched metallurgical specimen. If duplex grain size is suspected in a product too ...
SCOPE
1.1 These test methods provide simple guidelines for deciding whether a duplex grain size exists. The test methods separate duplex grain sizes into one of two distinct classes, then into specific types within those classes, and provide systems for grain size characterization of each type.  
1.2 Units—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 may involve hazardous materials, operations, and equipment. This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 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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ASTM E1245-03(2023)(Practice)
Standard Practice for Determining the Inclusion or Second-Phase Constituent Content of Metals by Automatic Image Analysis

SIGNIFICANCE AND USE
5.1 This practice is used to assess the indigenous inclusions or second-phase constituents of metals using basic stereological procedures performed by automatic image analyzers.  
5.2 This practice is not suitable for assessing the exogenous inclusions in steels and other metals. Because of the sporadic, unpredictable nature of the distribution of exogenous inclusions, other methods involving complete inspection, for example, ultrasonics, must be used to locate their presence. The exact nature of the exogenous material can then be determined by sectioning into the suspect region followed by serial, step-wise grinding to expose the exogenous matter for identification and individual measurement. Direct size measurement rather than application of stereological methods is employed.  
5.3 Because the characteristics of the indigenous inclusion population vary within a given lot of material due to the influence of compositional fluctuations, solidification conditions and processing, the lot must be sampled statistically to assess its inclusion content. The largest lot sampled is the heat lot but smaller lots, for example, the product of an ingot, within the heat may be sampled as a separate lot. The sampling of a given lot must be adequate for the lot size and characteristics.  
5.4 The practice is suitable for assessment of the indigenous inclusions in any steel (or other metal) product regardless of its size or shape as long as enough different fields can be measured to obtain reasonable statistical confidence in the data. Because the specifics of the manufacture of the product do influence the morphological characteristics of the inclusions, the report should state the relevant manufacturing details, that is, data regarding the deformation history of the product.  
5.5 To compare the inclusion measurement results from different lots of the same or similar types of steels, or other metals, a standard sampling scheme should be adopted such as described in Test Method...
SCOPE
1.1 This practice describes a procedure for obtaining stereological measurements that describe basic characteristics of the morphology of indigenous inclusions in steels and other metals using automatic image analysis. The practice can be applied to provide such data for any discrete second phase.  
Note 1: Stereological measurement methods are used in this practice to assess the average characteristics of inclusions or other second-phase particles on a longitudinal plane-of-polish. This information, by itself, does not produce a three-dimensional description of these constituents in space as deformation processes cause rotation and alignment of these constituents in a preferred manner. Development of such information requires measurements on three orthogonal planes and is beyond the scope of this practice.  
1.2 This practice specifically addresses the problem of producing stereological data when the features of the constituents to be measured make attainment of statistically reliable data difficult.  
1.3 This practice deals only with the recommended test methods and nothing in it should be construed as defining or establishing limits of acceptability.  
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ASTM E228-22(Test Method)
Standard Test Method for Linear Thermal Expansion of Solid Materials With a Push-Rod Dilatometer

SIGNIFICANCE AND USE
5.1 Coefficients of linear thermal expansion are required for design purposes and are used, for example, to determine dimensional behavior of structures subject to temperature changes, or thermal stresses that can occur and cause failure of a solid artifact composed of different materials when it is subjected to a temperature excursion.  
5.2 This test method is a reliable method of determining the linear thermal expansion of solid materials.  
5.3 For accurate determinations of thermal expansion, it is absolutely necessary that the dilatometer be calibrated by using a reference material that has a known and reproducible thermal expansion. The appendix contains information relating to reference materials in current general use.  
5.4 The measurement of thermal expansion involves two parameters: change of length and change of temperature, both of them equally important. Neglecting proper and accurate temperature measurement will inevitably result in increased uncertainties in the final data.  
5.5 The test method can be used for research, development, specification acceptance, quality control (QC) and quality assurance (QA).
SCOPE
1.1 This test method covers the determination of the linear thermal expansion of rigid solid materials using push-rod dilatometers. This method is applicable over any practical temperature range where a device can be constructed to satisfy the performance requirements set forth in this standard.
Note 1: Initially, this method was developed for vitreous silica dilatometers operating over a temperature range of –180 °C to 900 °C. The concepts and principles have been amply documented in the literature to be equally applicable for operating at higher temperatures. The precision and bias of these systems is believed to be of the same order as that for silica systems up to 900 °C. However, their precision and bias have not yet been established over the relevant total range of temperature due to the lack of well-characterized reference materials and the need for interlaboratory comparisons.  
1.2 For this purpose, a rigid solid is defined as a material that, at test temperature and under the stresses imposed by instrumentation, has a negligible creep or elastic strain rate, or both, thus insignificantly affecting the precision of thermal-length change measurements. This includes, as examples, metals, ceramics, refractories, glasses, rocks and minerals, graphites, plastics, cements, cured mortars, woods, and a variety of composites.  
1.3 The precision of this comparative test method is higher than that of other push-rod dilatometry techniques (for example, Test Method D696) and thermomechanical analysis (for example, Test Method E831) but is significantly lower than that of absolute methods such as interferometry (for example, Test Method E289). It is generally applicable to materials having absolute linear expansion coefficients exceeding 0.5 μm/(m·°C) for a 1000 °C range, and under special circumstances can be used for lower expansion materials when special precautions are used to ensure that the produced expansion of the specimen falls within the capabilities of the measuring system. In such cases, a sufficiently long specimen was found to meet the specification.  
1.4 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Or...

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ASTM
ASTM E975-22(Test Method)
Standard Test Method for X-Ray Determination of Retained Austenite in Steel with Near Random Crystallographic Orientation

SIGNIFICANCE AND USE
2.1 Significance—Retained austenite with a near random crystallographic orientation is found in the microstructure of heat-treated low-alloy, high-strength steels that have medium (0.40 weight %) or higher carbon contents. Although the presence of retained austenite may not be evident in the microstructure, and may not affect the bulk mechanical properties such as hardness of the steel, the transformation of retained austenite to martensite during service can affect the performance of the steel.  
2.2 Use—The measurement of retained austenite can be included in low-alloy steel development programs to determine its effect on mechanical properties. Retained austenite can be measured on a companion specimen or test section that is included in a heat-treated lot of steel as part of a quality control practice. The measurement of retained austenite in steels from service can be included in studies of material performance.
SCOPE
1.1 This test method covers the determination of retained austenite phase in steel using integrated intensities (area under peak above background) of X-ray diffraction peaks using chromium  Kα  or molybdenum Kα  X-radiation.  
1.2 The method applies to carbon and alloy steels with near random crystallographic orientations of both ferrite and austenite phases.  
1.3 This test method is valid for retained austenite contents from 1 % by volume and above.  
1.4 If possible, X-ray diffraction peak interference from other crystalline phases such as carbides should be eliminated from the ferrite and austenite peak intensities.  
1.5 Substantial alloy contents in steel cause some change in peak intensities which have not been considered in this method. Application of this method to steels with total alloy contents exceeding 15 weight % should be done with care. If necessary, the users can calculate the theoretical correction factors to account for changes in volume of the unit cells for austenite and ferrite resulting from variations in chemical composition.  
1.6 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.  
1.7 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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