ASTM E768-1999(2010)e1 6376 Standard Guide for Preparing and Evaluating Specimens for Automatic Inclusion Assessment of Steel《用于制备和评估钢铁自动纳入评估标本的标准指南》.pdf

《ASTM E768-1999(2010)e1 6376 Standard Guide for Preparing and Evaluating Specimens for Automatic Inclusion Assessment of Steel《用于制备和评估钢铁自动纳入评估标本的标准指南》.pdf》由会员分享，可在线阅读，更多相关《ASTM E768-1999(2010)e1 6376 Standard Guide for Preparing and Evaluating Specimens for Automatic Inclusion Assessment of Steel《用于制备和评估钢铁自动纳入评估标本的标准指南》.pdf（5页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E768 99 (Reapproved 2010)1Standard Guide forPreparing and Evaluating Specimens for AutomaticInclusion Assessment of Steel1This standard is issued under the fixed designation E768; the number immediately following the designation indicates the year oforiginal adoption or, in the case of

2、revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1NOTEFootnote 1 was editorially corrected in May 2016.1. Scope1.1 This guide2covers two preparation methods

3、for steelmetallographic specimens that will be analyzed for nonmetallicinclusions with automatic image analysis (AIA) equipment.The two methods of preparation are offered as acceptedmethods used to retain nonmetallic inclusions in steel. Thisguide does not limit the user to these methods.1.2 A proce

4、dure to test the suitability of the preparedspecimen for AIA inclusion work, using differential interfer-ence contrast (DIC), is presented.1.3 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.2. Referenced Documents2.1 ASTM Stand

5、ards:3E3 Guide for Preparation of Metallographic SpecimensE7 Terminology Relating to MetallographyE45 Test Methods for Determining the Inclusion Content ofSteelE883 Guide for ReflectedLight PhotomicrographyE1122 Practice for Obtaining JK Inclusion Ratings UsingAutomatic Image Analysis (Withdrawn 200

6、6)4E1245 Practice for Determining the Inclusion or Second-Phase Constituent Content of Metals by Automatic ImageAnalysis2.2 ASTM Adjuncts:5ADJE0768 Differential Interference Contrast Magnification100X and 500X (6 micrographs)3. Terminology3.1 Definitions:3.1.1 For definitions used in this practice,

7、refer to Termi-nology E7.3.1.2 differential interference contrast microscopya com-prehensive definition appears in Guide E883, paragraph 11.8.3.2 Definitions of Terms Specific to This Standard:3.2.1 rigid grinding diska non-fabric support surface,such as a composite of metal/ceramic or metal/polymer

8、,charged with an abrasive (usually 6 to 15-m diamondparticles), and used as the fine grinding operation in a metal-lographic preparation procedure.4. Significance and Use4.1 Inclusion ratings done either manually using Test Meth-ods E45 or automatically using Practice E1122 or E1245 areinfluenced by

9、 the quality of specimen preparation. This guideprovides examples of proven specimen preparation methodsthat retain inclusions in polished steel specimens.4.2 This guide provides a procedure to determine if theprepared specimens are of suitable quality for subsequentrating of inclusions. None of the

10、se methods should be con-strued as defining or establishing specific procedures or limitsof acceptability for any steel grade.5. Preparation Methods5.1 Background:5.1.1 The inclusions in the plane of polish must be fullypreserved and clearly visible. Preparation should not produceexcessive relief ar

11、ound the perimeter of the inclusions thatwould exaggerate the size and number of inclusions on theplane of polish. In many cases, the preparation of specimens1This guide is under the jurisdiction ofASTM Committee E04 on Metallographyand is the direct responsibility of Subcommittee E04.01 on Specimen

12、 Preparation.Current edition approved Nov. 1, 2010. Published January 2011. Originallyapproved in 1980. Last previous edition approved in 2005 as E76899(2005). DOI:10.1520/E0768-99R10.2Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Report

13、 RR:E04-1002.3For 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.4The last approved version of this historical st

14、andard is referenced onwww.astm.org.5A colored plate, consisting of six micrographs that illustrate the use of DIC indetermining a properly prepared sample (at 100x and 500x), is available fromASTM Headquarters. Order Adjuct: ADJE0768.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700,

15、 West Conshohocken, PA 19428-2959. United States1for inclusion rating is more readily performed after thespecimens have been hardened by a suitable heat treatmentprocedure (austenize, quench to fully martensitic structure,temper at a relatively low temperature).5.1.2 Cleanliness is an important cons

16、ideration in all stagesof specimen preparation.5.1.2.1 Heat-treated specimens should be wire brushed orshot blasted or have the surface ground to remove adherentscale.5.1.2.2 After completing the grinding steps and beforeperforming the polishing steps, the specimens and specimenholders must be clean

17、ed to prevent contamination of the nextpreparation step. Cleaning the specimens and specimen holdersbetween each grinding step can eliminate contamination ofcoarse abrasives to the following finer preparation step.5.1.2.3 After the preparation is complete, swab the surfacecarefully with cotton and a

18、 water/soap solution containing acorrosion inhibitor such as a machine coolant or ethyl alcoholsolution to remove any films or other debris that wouldinterfere with the inclusion rating.5.1.2.4 It is advisable to perform the inclusion analysis assoon as possible after preparation to minimize stainin

19、g or otherproblems that can affect the analysis.5.1.3 The two methods that follow have been found to bereliable procedures for retaining inclusions in steel and achiev-ing the desired results when evaluated by DIC. There are othermethods that will result in a quality specimen as revealed byDIC. Each

20、 laboratory should develop preparation proceduresfor their materials so that the prepared surfaces meet therequirements presented in 6 of this guide.5.1.4 As described in Prractice E3, the specimens may besectioned and mounted to ease handling during preparation. Itis advisable to use a mounting med

21、ium that is hard enough topreserve edges and maintain flatness.5.1.5 Abrasive grit size designations in this guide areexpressed in theAmerican National Standards Institute (ANSI)or Coated Abrasives Manufacturers Institute (CAMI) systemunits with the corresponding Federation of European AbrasiveProce

22、dure (FEPA) numbers in parentheses. Table 1 provides acorrelation between these two systems and the approximatemedian particle diameter for a given grit size in micrometres.5.1.6 Most preparation systems apply pressure on the speci-mens being processed. The best pressure to be used for eachpreparati

23、on step should be determined experimentally. Conver-sions between applied force and pressure are discussed in theAppendix X1.NOTE 1Care must be taken to protect the polished specimen surfacefrom scratches or contaminants when using a specimen leveling device.5.2 Silicon Carbide Procedure:5.2.1 A sum

24、mary of the silicon carbide procedure can befound in Table 2.5.2.2 When using a semi-automatic polishing equipment,grinding and polishing should be performed using approxi-mately 18 kPa pressure per specimen. (For a specimen holdercontaining six 32-mm mounts, a force of approximately 87 Nmust be app

25、lied (see X1.4.2).5.2.2.1 Low pressures are recommended to ensure theretention of an assortment of inclusion types found in a varietyof steel grades. The relatively low pressures suggested in thisprocedure will not necessarily result in a satisfactory polish foretching and the further evaluation of

26、the specimens generalmicrostructure. The pressures used in the following rigid diskprocedure are more likely to result in a surface more satisfac-tory for revealing general microstructures.5.2.3 Grind the specimens on ANSI 80 grit (P80 FEPA)silicon carbide paper to ensure all sectioning artifacts an

27、ddeformation damage have been removed and the entire speci-men surface is co-planar to the grinding surface.NOTE 2If the sectioning method resulted in a smooth face and littledeformation damage, and if after securing the specimens in a fixture forpolishing, the entire surface of interest is co-plana

28、r to the grinding surface,then finer grit papers, such as ANSI 180 to 240 (P180 to P240 FEPA) canbe used for the initial grinding step.5.2.3.1 An adequate flow of water should remove all loos-ened abrasive and grinding debris from the paper during thegrinding procedure. The flow of water should ensu

29、re thespecimen is kept cool during grinding.5.2.4 Continue grinding through the sequence of siliconcarbide papers listed in Table 2. It may be necessary to cleanthe samples between every grinding step to prevent contami-nation of the next preparation step.5.2.5 After completing the entire grinding o

30、peration, cleanthe specimens thoroughly, using ethyl alcohol and cotton, thenrinse and dry. Ultrasonic cleaning can be used.5.2.5.1 The use of a soap and water solution in an ultrasoniccleaner can attack non-metallic inclusions in some carbon andlow alloy steels, leading to an exaggeration in the in

31、clusionsapparent size. Adding an inhibitor (such as that used as amachining coolant) may reduce this size exaggeration.5.2.6 Polish the specimens using 3-m diamond abrasive ona low nap cloth, such as woven wool, for 50 s. Clean and drythe specimens as described in 5.2.5.TABLE 1 Comparison of ANSI (C

32、AMI) versus FEPA versusMedian Diameter of Grit Size in MicrometersANSIA(CAMI)BFEPACApproximate MedianDiameter(m)60 P60 25080 P80 180100 P100 150120 P120 125150 P150 90180 P180 75220 P220 63240 P240 58.5P280 52.2280 P320 46.2320 P360 40.5P400 35.0360 P500 30.2400 P600 25.8P800 21.8500 P1000 18.3600 P

33、1200 15.3800 P2400 8.41200 P4000D3.0AANSI - American National Standards InstituteBCAMI - Coated Abrasives Manufacturers InstituteCFEPA - Federation of European Abrasive ProducersDNot a FEPA designationE768 99 (2010)125.2.7 Polish the specimens using a 1-m diamond abrasiveon a high nap cloth for 50 s

34、. Clean and dry the specimens asdescribed in 5.2.5.5.2.8 A final manual polishing step may be added, using0.25-m diamond abrasive on a low nap cloth for 10 to 20 s,using relatively high pressure. Clean and dry the specimens asdescribed in 5.2.5.5.2.8.1 Ultrasonic cleaning is not recommended after th

35、efinal manual or automatic polishing step. Ultrasonic cleaningcan cause cavitation damage, ultimately distorting the inclu-sion sizes.NOTE 3Depending on the material, it may be advisable to avoid waterafter polishing.5.3 Rigid Grinding Disk Procedure:5.3.1 Asummary of the rigid grinding disk procedu

36、re can befound in Table 3.5.3.2 Semi-automatic grinding equipment is required, withspecimens contained in a circular fixture for the entire proce-dure. For 5.3.2 5.3.5, a pressure of 42 kPa should be appliedper specimen. (For a specimen holder containing six 32-mmcircular mounts, a force of approxim

37、ately 203 N must beapplied (see X1.4.3).5.3.3 Grind for at least 15 s after achieving a co-planarcondition, using a 150-grit alumina grinding stone at 1450 rpmor 80-grit (P80 FEPA) alumina/zirconia grinding paper at 300rpm.5.3.3.1 An adequate flow of water should remove all loos-ened abrasive and gr

38、inding debris from the paper during thegrinding procedure. The flow of water should ensure thespecimen is kept cool during grinding.TABLE 2 Preparation Method I Silicon Carbide Abrasive Paper GrindingSurface Coolent/LubricantAbrasive Size/TypeANSIAFEPABTime(seconds)ForceCnewtons lbsSurfaceSpeedRPMRe

39、lative RotationPlanar GrindingPaper Water 80 P80 grit SIC 60 14 2 300 ComplementaryDFine GrindingPaper Water 120 P120 grit SIC 14 2 300 ComplementaryPaper Water 240 P240 grit SIC 60 14 2 300 ComplementaryPaper Water 320 P500 grit SIC 60 14 2 300 ComplimentaryPaper Water 400 P600 grit SIC 60 14 2 300

40、 ComplementaryPaper Water 600 P1200 grit SIC 60 14 2 300 ComplimentaryPaper Water 800P2400 grit SIC 60 14 2 300 ComplementaryRough PolishingNAP free cloth Extending fluid 3 m diamond 50 14 2 150 ComplementaryFinal PolishingLow nap cloth Extending fluid 1 m diamond 50 14 2 150 ComplementaryOptional P

41、olishing (manual)Low nap cloth Extending fluid 1 m diamond 50 relatively high NA NAEAAmerican National Standards Institute (ANSI) designation of grit size.BFederation of European Producers of Abrasives (FEPA) designation of grit size.CForce per 3-mm (1.25-in.) diameter specimen.DComplementary rotati

42、on, surface and specimens spin in same direction.ESince this optional step is completed manually, these two categories are not applicable.TABLE 3 Preparation Method II - Rigid Grinding Disk ProcedureSurface Coolant/LubricantAbrasive Size/Type ANSIAFEPABTime - seconds ForceCnewtons lbsSurface SpeedRP

43、MRelative RotationPlanar GrindingAlumina/zirconia paper Water 80 P80 grit 15 34 8 300 ComplementaryDOrAlumina grinding stone Water 150 P150 grit 15 34 8 1450 ComplementaryFine GrindingRigid grinding disk Alcohol/glycol 9 m diamond 180 34 8 150 ComplementaryRough PolishingNapless or stiff napped clot

44、h Alcohol/glycol 3 m diamond 240 34 8 150 ComplementaryFinal PolishingSoft short napped cloth Alcohol/glycol 1 m diamond 120 34 8 150 ComplementaryOptional PolishingPorous Synthetic Cloth Water Alkaline Colloidal Silica orAcidic Colloidal AluminaE90 100 23 150 ComplementaryAAmerican National Standar

45、ds Institute (ANSI) designation of grit size.BFederation of European Producers of Abrasives (FEPA) designation of grit size.CForce per 32-mm (1.25-in.) diameter specimen.DComplementary rotation surface, and specimens spin in same direction.EWater is substituted for the colloidal oxide during the las

46、t 20 s.E768 99 (2010)135.3.3.2 It may be necessary to clean the samples betweenevery grinding step to prevent contamination of the nextpreparation step.5.3.4 Finish grind using 9-m diamond on a rigid grindingdisk for3mat150rpm, using an alcohol/glycol lubricant.Clean the specimens and fixture thorou

47、ghly (ultrasonic clean-ing is helpful) with alcohol and cotton, then dry with forced air.5.3.4.1 The use of a soap and water solution in an ultrasoniccleaner can attack non-metallic inclusions in some carbon andlow alloy steels, leading to an exaggeration in the inclusionsapparent size. Adding an in

48、hibitor (such as that used as amachining coolant) may reduce this size exaggeration.5.3.5 Rough polish using 3-m diamond on a napless cloth(silk or non-woven chemotextile) or a low nap cloth (wovenwool) for 4 min at 150 rpm using alcohol/glycol lubricant.Clean as in 5.3.4.5.3.6 Final polish using 1-

49、m diamond on a high nap clothfor 2 min at 150 rpm, using alcohol/glycol lubricant. Clean asin 5.3.4.5.3.6.1 Ultrasonic cleaning is not recommended after thefinal polishing step. Ultrasonic cleaning can cause cavitationdamage, ultimately distorting the inclusion sizes.5.3.7 An optional oxide-polishing step, using a poroussynthetic cloth with either alkaline colloidal silica or acidiccolloidal alumina, may be used if necessary to eliminate finescratches. The conditions are 90 s at 150 rpm, 100 N, wi