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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

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.  
5.1.2 This practice is suitable for providing data for computer models used in the control of steel manufacturing, forging, casting, heat-treating, and welding processes. It is also useful in providing data for the prediction of microstructures and properties to assist in steel alloy selection for end-use applications.  
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 ...
SCOPE
1.1 This practice covers the determination of hypoeutectoid steel phase transformation behavior by using high-speed dilatometry techniques for measuring linear dimensional change as a function of time and temperature, and reporting the results as linear strain in either a numerical or graphical format.  
1.2 The practice is applicable to high-speed dilatometry equipment capable of programmable thermal profiles and with digital data storage and output capability.  
1.3 This practice is applicable to the determination of steel phase transformation behavior under both isothermal and continuous cooling conditions.  
1.4 This practice includes requirements for obtaining metallographic information to be used as a supplement to the dilatometry measurements.  
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.

General Information

Status
Published
Publication Date
31-Aug-2023
ICS
77.040.99 - Other methods of testing of metals
Technical Committee
A01 - Steel, Stainless Steel and Related Alloys
Drafting Committee
A01.13 - Mechanical and Chemical Testing and Processing Methods of Steel Products and Processes
Current Stage
Ref Project

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ASTM A1033-18(2023) - Standard Practice for Quantitative Measurement and Reporting of Hypoeutectoid Carbon and Low-Alloy Steel Phase TransformationsASTM A1033-18(2023) - Standard Practice for Quantitative Measurement and Reporting of Hypoeutectoid Carbon and Low-Alloy Steel Phase Transformations
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ASTM A1033-18(2023) - Standard Practice for Quantitative Measurement and Reporting of Hypoeutectoid Carbon and Low-Alloy Steel Phase Transformations
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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.
Designation: A1033 − 18 (Reapproved 2023)
Standard Practice for
Quantitative Measurement and Reporting of Hypoeutectoid
1
Carbon and Low-Alloy Steel Phase Transformations
This standard is issued under the fixed designation A1033; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope 2. Referenced Documents
2
2.1 ASTM Standards:
1.1 This practice covers the determination of hypoeutectoid
steel phase transformation behavior by using high-speed E3 Guide for Preparation of Metallographic Specimens
E112 Test Methods for Determining Average Grain Size
dilatometry techniques for measuring linear dimensional
change as a function of time and temperature, and reporting the E407 Practice for Microetching Metals and Alloys
results as linear strain in either a numerical or graphical format.
3. Terminology
1.2 The practice is applicable to high-speed dilatometry
3.1 Definitions of Terms Specific to This Standard:
equipment capable of programmable thermal profiles and with
3.1.1 diametrical linear engineering strain—the strain, ei-
digital data storage and output capability.
ther thermal or resulting from phase transformation, that is
1.3 This practice is applicable to the determination of steel
determined from a change in diameter as a result of a change
phase transformation behavior under both isothermal and
in temperature, or over a period of time, and which is expressed
continuous cooling conditions.
as follows:
1.4 This practice includes requirements for obtaining met-
e 5 Δd/d 5 ~d 2 d !/d
D 0 1 0 0
allographic information to be used as a supplement to the
3.1.2 hypoeutectoid steel—a term used to describe a group
dilatometry measurements.
of carbon steels with a carbon content less than the eutectoid
composition (0.8 % by weight).
1.5 The values stated in SI units are to be regarded as
standard. No other units of measurement are included in this
3.1.3 longitudinal linear engineering strain—the strain, ei-
standard.
ther thermal or resulting from phase transformation, that is
determined from a change in length as a result of a change in
1.6 This standard does not purport to address all of the
temperature, or over a period of time, and which is expressed
safety concerns, if any, associated with its use. It is the
as follows:
responsibility of the user of this standard to establish appro-
priate safety, health, and environmental practices and deter-
e 5 Δl/L 5 l 2 l /l
~ !
L 0 1 0 0
mine the applicability of regulatory limitations prior to use.
3.1.4 steel phase transformation—during heating, the crys-
1.7 This international standard was developed in accor-
tallographic transformation from ferrite, pearlite, bainite, mar-
dance with internationally recognized principles on standard-
tensite or combinations of these constituents to austenite.
ization established in the Decision on Principles for the
During cooling, the crystallographic transformation from aus-
Development of International Standards, Guides and Recom-
tenite to ferrite, pearlite, bainite, or martensite or a combination
mendations issued by the World Trade Organization Technical
thereof.
Barriers to Trade (TBT) Committee.
3.1.5 volumetric engineering strain—the strain, either ther-
mal or resulting from phase transformation, that is determined
from a change in volume as a result of a change in temperature,
1
This practice is under the jurisdiction of ASTM Committee A01 on Steel,
or over a period of time, and which is expressed as follows:
Stainless Steel and Related Alloys and is the direct responsibility of Subcommittee
A01.13 on Mechanical and Chemical Testing and Processing Methods of Steel
2
Products and Processes. For referenced ASTM standards, visit the ASTM website, www.astm.org, or
Current edition approved Sept. 1, 2023. Published September 2023. Originally contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
approved in 2004. Last previous edition approved in 2018 as A1033 – 18. DOI: Standards volume information, refer to the standard’s Document Summary page on
10.1520/A1033-18R23. the ASTM website.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

---------------------- Page: 1 ----------------------
A1033 − 18 (2023)
e 5 Δv/v 5 v 2 v /v link between discrete values of strain and specific microstruc-
~ !
V 0 1 0 0
e '3e '3e
ture constituents in steels. This practice describes a standard-
V L
...

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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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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.  
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5.4 These test methods may be applied to specimens or products regardless of their state of recrystallization.  
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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.  
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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.  
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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.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
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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.  
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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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ASTM
ASTM E96/E96M-22ae1(Test Method)
Standard Test Methods for Gravimetric Determination of Water Vapor Transmission Rate of Materials

SIGNIFICANCE AND USE
5.1 The purpose of these tests is to obtain, by means of simple apparatus, reliable values for water vapor transfer rate through materials, expressed in suitable units.  
5.2 A WVTR value obtained in one method under one set of test conditions is not necessarily indicative of the value that would be obtained using the other method or under a different set of conditions. See Appendix X3 for discussion of determining dependency of WVTR on different relative humidity (at a given temperature).  
5.3 Commonly used test conditions are listed in Appendix X1, but given the caution in 5.2, the selection of test conditions other than those listed, and which closely approach exposure conditions of material in actual use, is allowed. Where tests are conducted for classification or compliance purposes, environmental conditions are typically defined in product standard specifications.
SCOPE
1.1 These test methods cover the determination of water vapor transmission rate (WVTR) of materials, such as, but not limited to, paper, plastic films, other sheet materials, coatings, foams, fiberboards, gypsum and plaster products, wood products, and plastics. Two basic methods, the Desiccant Method and the Water Method, are provided for the measurement of WVTR. In these tests, the desired temperature and side-to-side humidity conditions, with resultant vapor drive through the specimen, are used. The test conditions employed are at the discretion of the user, but in all cases, are reported with the results.  
1.2 The values stated in either Inch-Pound or SI units are to be regarded separately as standard. The values stated in each system are not necessarily exact equivalents; therefore, each system shall be used independently of the other. Derived results are converted from one system to the other using appropriate conversion factors (see Table 1).  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM
ASTM G142-98(2022)(Test Method)
Standard Test Method for Determination of Susceptibility of Metals to Embrittlement in Hydrogen Containing Environments at High Pressure, High Temperature, or Both

SIGNIFICANCE AND USE
5.1 This test method provides a reliable prediction of the resistance or susceptibility, or both, to loss of material strength and ductility as a result of exposure to hydrogen-containing gaseous environments. This test method is applicable over a broad range of pressures, temperatures, and gaseous environments. The results from this test method can be used to evaluate the effects of material composition, processing, and heat treatment as well as the effects of changes in environment composition, temperature, and pressure. These results may or may not correlate with service experience for particular applications. Furthermore, this test method may not be suitable for the evaluation of high temperature hydrogen attack in steels unless suitable exposure time at the test conditions has taken place prior to the initiation of tensile testing to allow for the development of internal blistering, decarburization or cracking, or both.
SCOPE
1.1 This test method covers a procedure for determination of tensile properties of metals in high pressure or high temperature, or both, gaseous hydrogen-containing environments. It includes accommodations for the testing of either smooth or notched specimens.  
1.2 This test method applies to all materials and product forms including, but not restricted to, wrought and cast materials.  
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.  
1.4 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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