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ASTM F1459-06

(Test Method)

Standard Test Method for Determination of the Susceptibility of Metallic Materials to Hydrogen Gas Embrittlement (HGE)

Standard Test Method for Determination of the Susceptibility of Metallic Materials to Hydrogen Gas Embrittlement (HGE)

SIGNIFICANCE AND USE
This test method will provide a guide for the choice of metallic materials for applications in high pressure hydrogen gas.
The value of the PHe/PH2 ratio will be a relative indication of the severity of degradation of the mechanical properties to be expected in hydrogen.
SCOPE
1.1 This test method covers the quantitative determination of the susceptibility of metallic materials to hydrogen embrittlement, when exposed to high pressure gaseous hydrogen.
1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.
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.

General Information

Status
Historical
Publication Date
31-Mar-2006
ICS
77.040.99 - Other methods of testing of metals
Technical Committee
F07 - Aerospace and Aircraft
Drafting Committee
F07.04 - Hydrogen Embrittlement
Current Stage
Ref Project

Relations

Replaces
ASTM F1459-93(1998)e1 - Standard Test Method for Determination of the Susceptibility of Metallic Materials to Gaseous Hydrogen Embrittlement
Effective Date
01-Apr-2006
Replaced By
ASTM F1459-06(2012) - Standard Test Method for Determination of the Susceptibility of Metallic Materials to Hydrogen Gas Embrittlement (HGE)
Effective Date
01-Jun-2012
Referred By
ASTM F519-18 - Standard Test Method for Mechanical Hydrogen Embrittlement Evaluation of Plating/Coating Processes and Service Environments
Effective Date
01-Apr-2006
Referred By
ASTM B650-95(2023) - Standard Specification for Electrodeposited Engineering Chromium Coatings on Ferrous Substrates
Effective Date
01-Apr-2006

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ASTM F1459-06 - Standard Test Method for Determination of the Susceptibility of Metallic Materials to Hydrogen Gas Embrittlement (HGE)ASTM F1459-06 - Standard Test Method for Determination of the Susceptibility of Metallic Materials to Hydrogen Gas Embrittlement (HGE)
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ASTM F1459-06 - Standard Test Method for Determination of the Susceptibility of Metallic Materials to Hydrogen Gas Embrittlement (HGE)
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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:F1459–06
Standard Test Method for
Determination of the Susceptibility of Metallic Materials to
1
Hydrogen Gas Embrittlement (HGE)
This standard is issued under the fixed designation F1459; 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 4. Significance and Use
1.1 This test method covers the quantitative determination 4.1 This test method will provide a guide for the choice of
of the susceptibility of metallic materials to hydrogen em- metallic materials for applications in high pressure hydrogen
brittlement, when exposed to high pressure gaseous hydrogen. gas.
1.2 The values stated in SI units are to be regarded as the 4.2 The value of the P /P ratio will be a relative
He H2
standard. The values given in parentheses are for information indication of the severity of degradation of the mechanical
only. properties to be expected in hydrogen.
1.3 This standard does not purport to address all of the
5. Apparatus
safety concerns, if any, associated with its use. It is the
responsibility of the user of this standard to establish appro- 5.1 A basic test system shall consist of the following items:
5.1.1 Test Cell, consists of two flanges as shown schemati-
priate safety and health practices and determine the applica-
bility of regulatory limitations prior to use. cally in Fig. 1.
5.1.1.1 The test cell shall befabricated from materials such
2. Referenced Documents
as 316 stainless steel in the annealed condition that are not
2.1 ASTM Standards: susceptible to HGE (3, 4).
E384 Test Method for Microindentation Hardness of Mate- 5.1.1.2 The seals shall be elastomer O-rings for helium
rials testing and hydrogen testing at rates of 10 bar/min (145
psig/min) or higher. For hydrogen tests at a lower rate, indium
3. Summary of Test Method
O-rings shall be used.
3.1 Athin disk metallic specimen is subjected to an increas- 5.1.1.3 An evaluation port (Item 1 in Fig. 1) on the lower
ing gas pressure at constant rate until failure (bursting or
flangeisusedtocheckgaspurityandadjustpressurizationrate.
cracking of the disk). The embrittlement of the material can be 5.1.2 The test cell is pressurized with hydrogen or helium
evaluated by comparing the rupture pressures of identical disk
throughapneumaticsystem.Fig.2schematicallyillustratesthe
specimens in hydrogen (P ) and in a reference inert gas such pneumatic system.
H2
2
as helium (P ) (1, 2).
5.1.2.1 The pressurization rate shall be adjustable in the
He
3.2 The ratio P /P can be used to evaluate the suscepti- system.Athrottle valve is used to adjust the pressurization rate
He H2
bility of the metallic material to gaseous hydrogen embrittle-
in Fig. 2.
ment. The ratio is dependent on the pressurization rate.Aratio
6. Gases
of 1 or less indicates the material is not susceptible to hydrogen
embrittlement.Aratio greater than 1 indicates that the material 6.1 Helium, purity 99.995 minimum, 6000-psig (41 400-
is susceptible to hydrogen embrittlement and the susceptibility kPa) or higher pressure source.
increases as the ratio increases. 6.2 Hydrogen, purity 99.995 minimum, 6000-psig (41 400-
kPa) or higher pressure source.
1
This test method is under the jurisdiction of ASTM Committee F07 on
7. Specimen Preparation
Aerospace and Aircraft and is the direct responsibility of Subcommittee F07.04 on
7.1 Fifteen (15) specimens with identical dimensions and
Hydrogen Embrittlement.
Current edition approved April 1, 2006. Published May 2006. Originally
temper conditions shall be prepared for each test program. Six
´1
approved in 1993. Last previous edition approved in 1998 as F1459 – 93 (1998) .
(6) specimens are to be tested in helium and nine (9) specimens
DOI: 10.1520/F1459-06.
2
The boldface numbers in parentheses refer to the list of references at the end of
this standard.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
1

---------------------- Page: 1 ----------------------
F1459–06
1
7.3 The disk specimen shall have a flatness of less than ⁄10
1
mm ( ⁄254 in.) deflection.
7.4 The surface of the disk specimen shall be free of oxides.
The surface roughness Ra shall be 0.001 mm (40 µin.) or less.
7.5 The disk specimen shall be prepared by a method that
does not alter mechanical properties of the material at the edge
of the specimen. Microhardness testing should be conducted
per Test Method E384 at the outer edge of the specimen
(outside the tested area) to ensure it is as a means of confirming
that the mechanical properties were not altered.
7.6 The specimens shall be cleaned, free of grease
...

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SIGNIFICANCE AND USE
4.1 This test method will provide a guide for the choice of metallic materials for applications in high pressure hydrogen gas.  
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SIGNIFICANCE AND USE
3.1 Applications of Macroetching:  
3.1.1 Macroetching is used to reveal the heterogeneity of metals and alloys. Metallographic specimens and chemical analyses will provide the necessary detailed information about specific localities, but they cannot give data about variation from one place to another unless an inordinate number of specimens are taken.  
3.1.2 Macroetching, on the other hand, will provide information on variations in (1) structure, such as grain size, flow lines, columnar structure, dendrites, and so forth; (2) variations in chemical composition as evidenced by segregation, carbide and ferrite banding, coring, inclusions, and depth of carburization or decarburization. The information provided about variations in chemical composition is strictly qualitative but the location of extremes in segregation will be shown. Chemical analyses or other means of determining the chemical composition would have to be performed to determine the extent of variation. Macroetching will also show the presence of discontinuities and voids, such as seams, laps, porosity, flakes, bursts, extrusion rupture, cracks, and so forth.  
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3.1.4 Macroetching is used extensively for quality control in the steel industry, to determine the tone of a heat in billets with respect to inclusions, segregation, and structure. Forge shops, in addition, use macroetching to reveal flow...
SCOPE
1.1 These procedures describe the methods of macroetching metals and alloys to reveal their macrostructure.  
1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to the International System (SI) units that are provided for information only and are not considered standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
For specific warning statements, see 6.2, 7.1, 8.1.3, 8.2.1, 8.8.3, 8.10.1.1, and 8.13.2. It is further recommended to review the guidance in Guide E2014.  
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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Standard Practice for Microetching Metals and Alloys

SIGNIFICANCE AND USE
5.1 This practice lists recommended methods and solutions for the etching of specimens for metallographic examination. Solutions are listed that highlight the phases and constituents present in most major alloy systems.
SCOPE
1.1 This practice covers chemical solutions and procedures to be used in etching metals and alloys for microscopic examination. Safety precautions and miscellaneous information are also included.  
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ASTM E45-18a(2023)(Test Method)
Standard Test Methods for Determining the Inclusion Content of Steel

SIGNIFICANCE AND USE
4.1 These test methods cover four macroscopic and five microscopic test methods (manual and image analysis) for describing the inclusion content of steel and procedures for expressing test results.  
4.2 Inclusions are characterized by size, shape, concentration, and distribution rather than chemical composition. Although compositions are not identified, Microscopic methods place inclusions into one of several composition-related categories (sulfides, oxides, and silicates—the last as a type of oxide). Paragraph 11.1.1 describes a metallographic technique to facilitate inclusion discrimination. Only those inclusions present at the test surface can be detected.  
4.3 The macroscopic test methods evaluate larger surface areas than microscopic test methods and because examination is visual or at low magnifications, these methods are best suited for detecting larger inclusions. Macroscopic methods are not suitable for detecting inclusions smaller than about 0.40 mm (1/64 in.) in length and the methods do not discriminate inclusions by type.  
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1.4 These test methods deal only with recommended test methods and nothing in them should be construed as defining or establishing limits of acceptability for any grade of steel.  
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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.  
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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.
SIGNIFICANCE AND USE
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.).
SCOPE
1.1 This guide provides advice for conducting experiments to investigate the effects of helium on the properties of metals where the technique for introducing the helium differs in some way from the actual mechanism of introduction of helium in service. Techniques considered for introducing helium may 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.  
1.2 Three other methods for introducing helium into irradiated materials are not covered in this guide. They are: (1) the enhancement of helium production in nickel-bearing alloys by spectral tailoring in mixed-spectrum fission reactors, (2) a related technique that uses a thin layer of NiAl on the specimen surface to inject helium, and (3) isotopic tailoring in both fast and mixed-spectrum fission reactors. These techniques are described in Refs (1-6).2 Dual ion beam techniques (7) for simultaneously implanting helium and generating displacement damage are also not included here. This latter method is discussed in Practice E521.  
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1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
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Standard Test Methods for Detecting Detrimental Intermetallic Phase in Duplex Austenitic/Ferritic Stainless Steels

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.
SCOPE
1.1 The purpose of these test methods is to allow detection of the presence of intermetallic phases in certain duplex stainless steels as listed in Table 1, Table 2, and Table 3 to the extent that toughness or corrosion resistance is affected significantly. These test methods will not necessarily detect losses of toughness or corrosion resistance attributable to other causes. Similar test methods for other duplex stainless steels are described in Test Method A1084, but the procedures described in this standard differ significantly from Test Methods A, B, and C in A1084.  
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:  
1.5.1 Test Method A—Sodium Hydroxide Etch Test for Classification of Etch Structures of Duplex Stainless Steels (Sections 3 – 7).  
1.5.2 Test Method B—Charpy Impact Test for Classification of Structures of Duplex Stainless Steels (Sections 8 – 13).  
1.5.3 Test Method C—Ferric Chloride Corrosion Test for Classification of Structures of Duplex Stainless Steels (Sections 14 – 20).  
1.6 The presence of detrimental intermetallic phases is readily detected in all three tests, provided that a sample of appropriate location and orientation is selected. Because the occurrence of intermetallic phases is a function of temperature and cooling rate, it is essential that the tests be applied to the region of the material experiencing the conditions most likely to promote the formation of an intermetallic phase. In the case of common heat treatment, this region will be that which cooled most slowly. Except for rapidly cooled material, it may be necessary to sample from a location determined to be the most slowly cooled for the material piece to be characterized.  
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.  
1.10 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.  
1.11 This internat...

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ASTM E1181-02(2023)(Test Method)
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.  
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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.  
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.  
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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ASTM
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...

  • Standard
    10 pages
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  • Standard
    10 pages
    English language
    sale 15% off