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本文(ASTM E1351-2001(2006) Standard Practice for Production and Evaluation of Field Metallographic Replicas《现场金相复制品的生产和评定标准实施规范》.pdf)为本站会员(inwarn120)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM E1351-2001(2006) Standard Practice for Production and Evaluation of Field Metallographic Replicas《现场金相复制品的生产和评定标准实施规范》.pdf

1、Designation: E 1351 01 (Reapproved 2006)Standard Practice forProduction and Evaluation of Field Metallographic Replicas1This standard is issued under the fixed designation E 1351; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the

2、 year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.INTRODUCTIONReplication is a nondestructive sampling procedure which records and preserves the topography ofa metallogra

3、phic specimen as a negative relief on a plastic film. The microstructural replica can beexamined using a light microscope (LM) or scanning electron microscope (SEM) for subsequentanalysis. Specimens examined in the SEM are vacuum coated with vaporized carbon or a suitablemetal to provide contrast an

4、d conductivity. The convenience of the replication process makes itsuitable for obtaining microstructures from field locations for subsequent examination and analysis ina laboratory. The proper preparation of the test surface and of the replica itself is of paramountimportance and must receive caref

5、ul attention. Because of the diversity of metallographic equipmentavailable and the wide range of environments in which replication is conducted, the preparation ofreplicas of high quality should be viewed as a skilled process for which there exists a variety oftechniques that achieve satisfactory r

6、esults.This practice presents some guidelines on the preparation of metallic surfaces and production ofreplicas and guidelines on evaluation of replica quality. It does not attempt to limit the variations intechnique developed by skilled metallographers, each of which may produce acceptable replicas

7、.1. Scope1.1 This practice covers recognized methods for the prepa-ration and evaluation of cellulose acetate or plastic filmreplicas which have been obtained from metallographicallyprepared surfaces. It is designed for the evaluation of replicasto ensure that all significant features of a metallogr

8、aphicallyprepared surface have been duplicated and preserved on thereplica with sufficient detail to permit both LM and SEMexamination with optimum resolution and sensitivity.1.2 This practice may be used as a controlling document incommercial situations.1.3 The values stated in SI units are to be r

9、egarded as thestandard. Inch-pound units given in parentheses are for infor-mation only.1.4 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices

10、 and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2A 335/A 335M Specification for Seamless Ferritic Alloy-Steel Pipe for High-Temperature ServiceE3 Guide for Preparation of Metallographic SpecimensE7 Terminology Relating to Metallograp

11、hyE 407 Practice for Microetching Metals and Alloys3. Terminology3.1 DefinitionsFor definitions of terms used in this prac-tice, refer to Terminology E7.4. Significance and Use4.1 Replication is a nondestructive sampling procedure thatrecords and preserves the topography of a metallographicallyprepa

12、red surface as a negative relief on a plastic film (replica).The replica permits the examination and analysis of themetallographically prepared surface on the LM or SEM.4.2 Enhancement procedures for improving replica contrastfor microscopic examination are utilized and sometimes nec-essary (see 8.1

13、).1This practice is under the jurisdiction of ASTM Committee E04 on Metallog-raphy and is the direct responsibility of Subcommittee E04.01 on Preparation ofSamples.Current edition approved Oct. 1, 2006. Published October 20062. Originallyapproved in 1990. Last previous edition approved in 2001 as E

14、1351 01.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive,

15、 PO Box C700, West Conshohocken, PA 19428-2959, United States.NOTE 1It is recommended that the purchaser of a field replicationservice specify that each replicator demonstrate proficiency by providingfield prepared replica metallography and direct LM and SEM comparisonto laboratory prepared samples

16、of an identical material by grade andservice exposure.5. Evaluation Methods5.1 A suitable replica should accurately reproduce all themicrostructural features present on the surface that was repli-cated.5.2 No visible loss of resolution is permitted over thenormal range of magnifications on the LM as

17、 shown in Figs.1-3.5.3 The resolution of the structural detail in the replicashould exceed 0.1 m to permit SEM examination at highmagnifications (up to 50003). See Figs. 4-6.6. Metal Surface Preparation6.1 If magnetic particle testing was previously used on thework-piece, demagnetize the piece befor

18、e beginning surfacepreparation.6.2 Surface preparation may be accomplished using manual,mechanical, or electrolytic polishing methods.NOTE 2Electrolytic preparation always carries the risk of pitting, andof enlarging existing voids such as creep cavities and porosity.6.3 Prepare the surface to be re

19、plicated using the methodssuggested in Methods E3modified for field use, as appropri-ate, in such a way as to obtain a surface free of deformation,scratches, polishing defects, etch pits, and other artifacts whichmay obscure the true microstructural features.NOTE 3The presence of decarburization can

20、 be detected with aportable hardness tester during the grinding steps. Further grinding toreach a surface free of decarburization can be monitored with the hardnesstester. A replica may also be made on the decarburized surface, if it servesthe purpose of the investigation.6.4 Do not remove any preci

21、pitates, carbides, nonmetallicinclusions such as oxides and sulfides during the polishing oretching operations.6.5 Etching procedures for surface metallographic examina-tion should be performed in accordance with Practice E 407.6.6 The quality of the surface preparation should be con-trolled by the

22、use of a portable field microscope.6.7 To prevent possible contamination of any components,the etched area should be prepared carefully and thoroughlywashed after replication.7. Replication Technique7.1 In general, a replicated area of 12 by 18 mm (0.5 by 0.75in.) is satisfactory.7.2 A replica is pr

23、oduced by one of the two methodsdescribed below. All methods produce acceptable replicas.7.2.1 A replica may be produced by wetting one side of asheet of plastic film with a suitable solvent, such as acetone ormethyl acetate, and applying the wetted side of the film to theprepared metal surface.7.2.

24、2 Alternatively, a replica may be produced by wettingthe prepared metallic surface with a suitable solvent, such asacetone or methyl acetate, and applying the strip of plastic film(usually cellulose acetate) to the wet surface. The film ispressed against the surface for several seconds to ensureadhe

25、rance.7.2.3 Apply a rubber-based replicating compound to theprepared metal surface. Cover with the materials carrier paper,then use a roller to spread the compound into a uniformly thinlayer under the paper.7.3 The replica shall be prepared as soon as possible afterspecimen preparation of the origin

26、al surface is completed, tominimize transfer of post-preparation oxidation and contami-nation to the replicating film.FIG. 1 Example of Replica Microstructure at 1003 LM. Material: See Specification A 335/A 335M, Grade P22. Etchant: 2 % NitalE 1351 01 (2006)27.4 After the film has dried, remove the

27、replica and perma-nently mount on a rigid slide to facilitate analysis of the replicaand to protect it from damage during subsequent transport andstorage. The mounting may be accomplished using a double-sided adhesive tape, either applied to the back side of the driedreplica film while it remains on

28、 the prepared surface or appliedto the slide before transferring the replica on the tape surface.Using the rounded end of a glass rod to apply the replica on thetape is usually beneficial in reducing air bubbles and ensuringa flat replica. Some metallographers prefer to coat the back sideof the repl

29、ica with an opaque substance such as black paint orink prior to applying tape to improve the contrast when thereplica is subsequently examined.7.5 Place identification on the slide, and store it in a durableslide container for safe, contamination-free transfer to theexamination laboratory.8. Replica

30、 Examination8.1 To enhance contrast of the replica for microscopicexamination at low magnifications on the LM, the replica mayFIG. 2 Example of Replica Microstructure at 4003 LM. Material: See Specification A 335/A 335M, Grade P22. Etchant: 2 % NitalFIG. 3 Example of Replica Microstructure at 10003

31、LM. Material: See Specification A 335/A 335M, Grade P22. Etchant: 2 % NitalE 1351 01 (2006)3be placed on an underlying polished surface, such as a mirror,which acts as a reflector. In addition, using a coating of blackink or paint on the back side of the replica can improve thecontrast. In some case

32、s, the use of interference illuminationwill also improve contrast; however, optimum contrast for bothLM and SEM can be achieved by coating the replica surfacewith a thin, highly reflective metallic layer material normallydeposited in a vacuum coating unit. Aluminum, carbon, andchromium have been fou

33、nd to be satisfactory coatings forreplicas to be evaluated by LM. If the replica is to be examinedin the SEM, however, gold, which yields optimum contrast, ispreferable. ASTM STP 547 is the suggested guide for electronmetallographic techniques.38.2 The coating is generally applied at a 45 angle topr

34、ovide a light to shadow length of 1 to 1. The coatingthickness should be no greater than that required to provide fullcontrast in the replicated microstructure when examined in theLM and to prevent charging of the film when examined in the3Manual on Electron Metallography Techniques, ASTM STP 547, A

35、STM, 1973.FIG. 4 Example of Replica Microstructure at 10003 SEM. Material: See Specification A 335/A 335M, Grade P22. Etchant: 2 % NitalFIG. 5 Example of Replica Microstructure at 20003 SEM. Material: See Specification A 335/A 335M, Grade P22. Etchant: 2 % NitalE 1351 01 (2006)4SEM. Documentation of

36、 the structural features of interestshould then be made at the appropriate magnifications with theLM or SEM.9. Replica SurfaceNOTE 4Examples of replicated microstructures, (Specification A 335/A 335M steel, Grade P22 shown, with 2 % Nital etch. This materialexhibits a wide range of microstructures,

37、not all of which are shown here.)9.1 High quality replicas must meet the criteria listed inSection 5.9.2 No folds or permanent deformation shall be allowed todevelop in the replica film during processing.9.3 Microstructural features should be clearly developedover an area of at least 6 mm (0.25 in.)

38、 in diameter.9.4 Replicas taken at weldments should accurately recordthe base metal, weld metal, and heat-affected-zone microstruc-ture along the fusion line for a distance of at least 13 mm (0.5in.).9.5 All microstructural features shall be accurately renderedand photographic documentation shall be

39、 obtainable over therange of magnifications normally used for replica evaluation:50 to 1000X for LM and 500 to 5000X for SEM.9.6 All grain boundaries, grain boundary precipitates,cracks and cavities should be easily identified.9.7 Precipitates and inclusions contained in the material thatare greater

40、 than 0.1 m should be accurately recorded on thereplica. In addition, neither precipitates, such as primary andsecondary carbides and carbonitrides, nor nonmetallic inclu-sions, such as oxides and sulfides, shall be dislodged duringpolishing or etching regardless of their size.10. Documentation10.1

41、Photomicrographic documentation of microstructuralfeatures shall be obtainable over the normal range of magnifi-cation: 50 to 1000X LM and 500 to 5000X SEM.10.2 Each replica be adequately identified. Minimum iden-tification should include the job or other identification number,the name, the presence

42、 and characteristics of any coatingapplied to either side of the replica, and the name of thepreparer.10.3 A statement shall be made on the conformance ornon-conformance of the replica to this practice.10.4 Replicas shall remain attached to their carrier slides,and shall be stored in dust-free biolo

43、gical slide cases, withproper indexing to permit retrieval where required for record.11. Precision and Bias11.1 It is not possible to specify the precision or bias of thispractice because no quantitative results are produced. How-ever, all quantitative results produced through the examinationof repl

44、icas can be influenced by the replication process.12. Keywords12.1 replica; replicationFIG. 6 Example of Replica Microstructure at 50003 SEM. Material: See Specification A 335/A 335M, Grade P22. Etchant: 2 % NitalE 1351 01 (2006)5ASTM International takes no position respecting the validity of any pa

45、tent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revisio

46、n at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your com

47、ments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyright

48、ed by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org).E 1351 01 (2006)6

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