BS 6043-2 4-2000 Methods of sampling and test for carbonaceous materials used in aluminium manufacture - Electrode coke - Analysis by X-ray fluorescence spectroscopy《制铝工业用含碳材料的取样和试.pdf

《BS 6043-2 4-2000 Methods of sampling and test for carbonaceous materials used in aluminium manufacture - Electrode coke - Analysis by X-ray fluorescence spectroscopy《制铝工业用含碳材料的取样和试.pdf》由会员分享，可在线阅读，更多相关《BS 6043-2 4-2000 Methods of sampling and test for carbonaceous materials used in aluminium manufacture - Electrode coke - Analysis by X-ray fluorescence spectroscopy《制铝工业用含碳材料的取样和试.pdf（18页珍藏版）》请在麦多课文档分享上搜索。

1、| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | BRITISH STANDARD BS 6043-2.4:2000 ISO 1298

2、0:2000 ICS 71.100.10; 75.160.10 NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAW Methods of sampling and test for carbonaceous materials used in aluminium manufacture Part 2: Electrode coke Section 2.4: Analysis by X-ray flourescence spectroscopyThis British Standard, having be

3、en prepared under the direction of the Sector Committee for Materials and Chemicals, was published under the authority of the Standards Committee and comes into effect on 15 August 2000 BSI 08-2000 ISBN 0 580 36316 3 BS 6043-2.4:2000 Amendments issued since publication Amd. No. Date Comments Nationa

4、l foreword This British Standard reproduces verbatim ISO 12980:2000 and implements it as the UK national standard. The UK participation in its preparation was entrusted to Technical Committee CII/24, Raw materials for the aluminium industry, which has the responsibility to: aid enquirers to understa

5、nd the text; present to the responsible international/European committee any enquiries on the interpretation, or proposals for change, and keep the UK interests informed; monitor related international and European developments and promulgate them in the UK. A list of organizations represented on thi

6、s committee can be obtained on request to its secretary. Cross-references The British Standards which implement international publications referred to in this document may be found in the BSI Standards Catalogue under the section entitled “International Standards Correspondence Index”, or by using t

7、he “Find” facility of the BSI Standards Electronic Catalogue. A British Standard does not purport to include all the necessary provisions of a contract. Users of British Standards are responsible for their correct application. Compliance with a British Standard does not of itself confer immunity fro

8、m legal obligations. Summary of pages This document comprises a front cover, an inside front cover, the ISO title page, pages ii to v, a blank page, pages 1 to 9 and a back cover. The BSI copyright notice displayed in this document indicates when the document was last issued.Referencenumber ISO12980

9、:2000(E) INTERNATIONAL STANDARD ISO 12980 Firstedition 2000-04-01 Carbonaceousmaterialsusedin theproductionofaluminiumGreencoke andcalcinedcokeforelectrodes AnalysisusinganX-rayfluorescence method Produits carbons utiliss pour la production de laluminium Coke calcin et coke cru pour lectrodes Analys

10、e par fluorescence aux rayons XISO12980:2000(E) ii ISO12980:2000(E)iii Contents Page Foreword.iv Introduction.v 1 Scope1 2 Normativereference1 3 Principle1 4 Apparatusandmaterials.2 5 Samplingandtestspecimenpreparation.2 6 Procedure.3 7 Expressionofresults8 8 Precision.8 9 Testreport9ISO12980:2000(E

11、) iv Foreword ISO(theInternationalOrganizationforStandardization)isaworldwidefederationofnationalstandardsbodies(ISO memberbodies).TheworkofpreparingInternationalStandardsisnormallycarriedoutthroughISOtechnical committees.Eachmemberbodyinterestedinasubjectforwhichatechnicalcommitteehasbeenestablishe

12、dhas therighttoberepresentedonthatcommittee.Internationalorganizations,governmentalandnon-governmental,in liaisonwithISO,alsotakepartinthework.ISOcollaboratescloselywiththeInternationalElectrotechnical Commission(IEC)onallmattersofelectrotechnicalstandardization. InternationalStandardsaredraftedinac

13、cordancewiththerulesgivenintheISO/IECDirectives,Part3. DraftInternationalStandardsadoptedbythetechnicalcommitteesarecirculatedtothememberbodiesforvoting. PublicationasanInternationalStandardrequiresapprovalbyatleast75%ofthememberbodiescastingavote. Attentionisdrawntothepossibilitythatsomeoftheelemen

14、tsofthisInternationalStandardmaybethesubjectof patentrights.ISOshallnotbeheldresponsibleforidentifyinganyorallsuchpatentrights. InternationalStandardISO12980waspreparedbyTechnicalCommitteeISO/TC47, Chemistry, Subcommittee SC7, Aluminium oxide, cryolite, aluminium fluoride, sodium fluoride, carbonace

15、ous products for the aluminium industry.ISO12980:2000(E)v Introduction Thedeterminationoftheelementalimpuritiesisimportantforreasonsofmetalqualityandanodeconsumption. ThisInternationalStandardrefersonlytopetroleumcokealthoughtheprinciplesdescribedarevalidforpitch, anthracite,graphiteorelectrodemater

16、ials.Asthesamplepreparationand/orthemassfractionrangesforthese othermaterialsarequitedifferentitisintendedthatspecificstandardmethodswillbepublishedforeachmaterial.INTERNATIONALSTANDARD ISO12980:2000(E)1 Carbonaceousmaterialsusedintheproductionofaluminium GreencokeandcalcinedcokeforelectrodesAnalysi

17、susingan X-rayfluorescencemethod 1 Scope ThisInternationalStandardspecifiesanX-rayfluorescencemethodforthedeterminationofelementalimpuritiesin greenandcalcinedpetroleumcokesusedforthemanufactureofanodes.Theseanodesareusedintheproduction ofaluminium. 2 Normativereference Thefollowingnormativedocument

18、containsprovisionswhich,throughreferenceinthistext,constituteprovisionsof thisInternationalStandard.Fordatedreferences,subsequentamendmentsto,orrevisionsof,anyofthesethis publicationsdonotapply.However,partiestoagreementsbasedonthisInternationalStandardareencouragedto investigatethepossibilityofappl

19、yingthemostrecenteditionofthenormativedocumentindicatedbelow.For undatedreferences,thelatesteditionofthenormativedocumentreferredtoapplies.MembersofISOandIEC maintainregistersofcurrentlyvalidInternationalStandards. ISO6375, Carbonaceous materials for the production of aluminium Coke for electrodes S

20、ampling. 3Principle ApressedtabletofpulverizedcokeandorganicbinderisirradiatedbyX-raysfromatargetthinwindowX-raytube. TheX-raytubescanbechromium,rhodiumorscandiumdependingonwhichelementsaretobedetermined. Irradiationofthetestspecimencausesejectionandrearrangementoforbitalelectronsresultingintheemiss

21、ionof secondaryradiationwithacharacteristicwavelengthforeachelement. Thissecondaryradiationisreflected,ontothedetectorsystem,byacrystal,whichissetataspecificangletothe secondaryradiation.OnlyspecificradiationwhichobeysBraggslawreachesthedetectorsystem. n =2d sin (1) where n istheorderofthediffractio

22、n; istheX-raywavelength; d istheinterplanardistanceinthecrystal; sin istheanglesettingofthecrystal. Theintensitiesofthespecificsecondaryradiationarecalculatedintomassfractionsaccordingtogivencalibration curves.ISO12980:2000(E) 2 4 Apparatusandmaterials 4.1 X-rayfluorescencespectrometer,equippedwitht

23、hefollowingcrystals:LiF 200 (lithiumfluoride,reflecting plane200),PE(pentaerythiol),PX1(syntheticW-Si),Ge,TIAP(thalliumacidphthalate)andLSM(layeredsynthetic microstructure).ForinstrumentsequippedwithasidewindowX-raytube,ascandiumtubeisadvantageousfor lightelements.Forinstrumentsequippedwithanendwind

24、owX-raytube,arhodiumtubeoffersoptimumsensitivity. 4.2 Swinging-discmill,withtungsten-carbidegrindingdevices. 4.3 Organicbinder,suitableforpressed-tabletpreparation.Thebindershallnotcontainanyoftheelementsto beanalysed.SuitablebindersareHoechstwachsGorstearicacid. 4.4 Tabletpress,capableofprovidinga2

25、0-tonneload. 4.5 Appropriatesampleholders,forexamplealuminiumdishesorbrassringswiththedimensionsasshownin Figure1. 4.6 Detectorgas,consistingof90%argonand10%methane. 4.7 Calibrationstandards,commerciallyavailableandcertifiedcoveringtherangeofmassfractiongivenin clause6.5. 4.8 Referencesamples(RS),co

26、mmerciallyavailableandcertifiedwithappropriatemassfractionsforall elements.(See6.4.2) Dimensionsinmillimetres Figure1Dimensionsofsampleholder 5 Samplingandtestspecimenpreparation 5.1 Sampling SamplingshallbeinaccordancewiththerequirementsofISO6375. 5.2 Testspecimenpreparation Crushthesampleintosuffi

27、cientlysmallparticlessoastopassitthrougha4mmsieve.Drytoconstantmassat 120C.Millthesampleofcrushedmaterialintosufficientlysmallparticlessoastopassitthrougha63 msieve. Mixapproximately30gofthissievedmaterialwithapproximately5gofbinderandremillfor20s.Crushany remaininglumpswithaspatula. Iftoomanylumpsa

28、reformedinthismixture,repeattheaboveprocedurewithasmallerquantityofbinder,for example4g.Whenasmallerquantityofbinderisused,testittoseeifthecalibrationsampleandothersamples givepressedtabletsstrongenoughtowithstandtheprocedure.Repeattheaboveprocedureuntilasuitable quantityofbinderhasbeenaddedtoprovid

29、eanacceptablemixtureforpressingatablet.ISO12980:2000(E)3 Placethematerialintotheselectedsampleholder. NOTE Aluminiumdishesarepreferred,butbrassringsmayalsobeused. Placethefilledsampleholderinthepressandpressat20tfor20s. Forthebestresults,thetestspecimenshouldbeatleast4mmthick. 6 Procedure 6.1 Measur

30、ementconditions Themeasurementconditionsareapparatus-dependentbuttheindicationsinTable1canserveasguidelines. Normallynolineoverlappingwillbeexperiencediftheseconditionsareusedforthemeasurementofpetroleum coke. Table1Typicalmeasurementconditionsforthedifferentelements Element line Na K Al K Si K S K

31、Ca K V K Fe K Ni K Crystal LSM a or PX1 PEorPX1 PEorPX1 PEorGe LiF 200 LiF 200 LiF 200 LiF 200 Counter F b F F FFFFF Exposure, totaltime,s 100 20 20 10 10 20 30 20 Collimator coarse coarse coarse medium fine fine fine fine kV 40 40 40 40 40 40 60 60 mA 60 60 60 60 60 60 40 40 Angle 28 PE:145,1 PX1:1

32、9,5 PE:109,2 PX1:16,6 PE:75,8 PX1:110,9 113,1 76,9 57,5 48,7 Offsetangle c 2 1 1 1 F=flowcounter a Layeredsyntheticmicrostructurewith2dvaluearound5nm. b A1 mor2 mflowcounterwindowisrequired. c Backgroundmeasurementangles( offsetangles). 6.2 Intensitiesandbackgroundcorrections ThenetpeakintensityI,ex

33、pressedasthenumberofcountspersecond,oftheelementofinterestiscalculatedas thedifferencebetweenthemeasuredpeakintensityoftheelementandthebackgroundintensityatthepeakangle inaccordancewithequations(4)and(5).SeeFigure2. I=I p I b (2) where I p isthecountrate,expressedasthenumberofcountspersecond,attheel

34、ementposition(2 ); I b isthebackgroundcountrate,expressedasthenumberofcountspersecond,attheelementposition (2 );ISO12980:2000(E) 4 and I=I p C 1 I b1 C 2 I b2 (3) where I b1 iscountrate,expressedasthenumberofcountspersecond,atthenegative( offsetangleofthe backgroundposition; I b2 iscountrate,express

35、edasthenumberofcountspersecond,atthepositive( offsetangleofthe backgroundposition; C d dd 1 2 12 C d dd 2 1 12 where d 2 isthedifferencebetweenthepositive( offsetangleofthebackgroundpositionand2 ; d 1 isthedifferencenegative( offsetangleofthebackgroundpositionand2 ; togivethenetcountrateI. Figure2In

36、tensitiesandbackgroundcorrectionsISO12980:2000(E)5 6.3 Countingtime Theminimumcountingtimeisthetimenecessarytoachieveanetcountingerror(2 % ) net whichislessthanthe desiredprecisionforthemeasurement. Assumethatthepartofthecountingerrorintherepeatability( 4 )ofthismethodisabout50%. Chooseareferencemat

37、erialhavinganelementmassfractioninthemiddleoftherangegivenin6.5.1.Measure thecountingrate.Calculatetheminimumcountingtimeforeachelementbyusingequation(4). t= 100 2 1 % pb F H G G I K J J II 2 (4) Where t isthetotalcountingtimeforthepeaksandbackground; I p ismeasuredpeakintensity,expressedasthenumber

38、ofcountspersecond; I b isthebackgroundintensity,expressedasthenumberofcountspersecond; 2 % istherelativetargetedprecision,expressedasapercentage,atthe95%probabilitylevel. ForNa,take2%astherelativetargetedprecisionfor2 % .Forotherelements,take1%for2 % . Thisequationrequiresthatthedistributionofthecou

39、ntingtimeatpeakandbackgroundfollowtheequationbelow: t t I I p b p b = (5) where t p isthecountingtimeforthepeak; t b isthecountingtimeforthebackground. NOTE Additionalcheckssuchasmonitorsamplesarerecommended,andwilldependontheageandstateofthe equipment.Adescriptionisgivenin6.4.1. 6.4 Driftdetectionb

40、yuseofamonitorsample 6.4.1 Driftdetection Anydriftinthenetcountratecanbedetectedbyusingamonitorstandardduringthecalibrationprocedureand duringthemeasurementofunknownsamples. Calculatethedriftfactorf d foreachelementbytheratio f I I d = 1 n (6) where I 1 istheintensityofmonitorstandardduringthecalibr

41、ationprocedure; I n istheintensityofmonitorstandardwhenunknownsamplesaremeasured.ISO12980:2000(E) 6 Ifthedriftfactordoesnotliewithintherepeatabilityrange(see7.1)thisindicatesthatamajorchange,orproblem hasoccurredintheX-rayequipment.ChecktheX-rayequipment,rectifyasnecessaryandrecalibrate. 6.4.2 Selec

42、tionandpreparationofmonitorstandards Amonitorstandardcanbepreparedasdescribedbelowor,alternatively,useareferencesample(RS),with appropriatemassfractionsforallelements. Monitorstandardscanbepreparedincopperdishes,withdimensionsaccordingtotheactualsampleholderas showninFigure1. Selectappropriatecompon

43、entsforthemonitorsample,weighthemintothedesiredproportions,mixthemcarefully andfusethemat1200Cina(Pt+5%Au)-crucible(atypicalrecipeisgiveninTable2). Allowtocool,crushthemeltandmeltagain.Repeatthisprocedureoncemore,thenfinelygrindthemeltinthe swinging-discmill.Placethepowderinathinlayerinthecopperdish

44、andheatonagasburneruntiltheenamel softensandadherestothecopper.Repeatthisprocedureuntilalayerof0,5mminthecopperdishiscreated.A typicalrecipeformonitorstandardsisshowninTable2.Asuitableamountis5g. Table2Typicalmonitorrecipe S V Ni Na Ca Al Fe Si Li 2 B 4 O 7 90% K 2 SO 4 8% V 2 O 5 0,3% NiO 0,3% Na 2

45、 CO 3 0,2% CaO 0,2% Al 2 O 3 0,2% Fe 2 O 3 0,3% SiO 2 0,3% Itispreferablethatthemonitorstandardgivessomewhathigherintensitiesthanthetestsamples. Thebestresultsareobtainedwhenthemassfractionsofthedifferentelementsarechoseninsuchawaythatthe monitorintensitiesare10timesto20timesthemeanintensitiesmeasur

46、edonthecalibrationstandards. Takethemonitorsample,asdescribedabove,ortheappropriatereferencesamplethatistobeusedasamonitor, andprepareaccordingto5.2. Aftercalibration,inordertodetermineitsnominalmassfraction,testthehomogeneityofthemonitorstandard. IftheactualvalueofthemonitorRSliesoutsidetherepeatab

47、ilityrange(see7.1)whenanalysingunknown samples,analyseanewRS.Iftheresultsstillexceedthetolerancemassfraction,recalibratetheequipment. 6.5 Calibration 6.5.1 Referencematerialselection ThecertifiedreferencematerialsareselectedinordertocovertherangeofimpuritiesgiveninTable3. Table3Massfractionrangeofth

48、ereferencematerials Elements S % V g/g Ni g/g Na g/g Ca g/g Al g/g Fe g/g Si g/g Massfraction range 0,5to5 20to500 20to500 20to200 20to200 20to500 20to500 20to500ISO12980:2000(E)7 Certifiedcalibrationstandardsshallhavebeencertifiedbyinterlaboratorytestinginaccordancewithwetchemical methods. Preparet

49、hesereferencematerialsinaccordancewith5.2. Sulfurisresponsibleforanabsorptioneffect;thereforereferencematerialsshowinghighandlowelementalmass fractionsandwithhighandlowsulfurcontentshallbeavailabletocorrectforthiseffect. 6.5.2 Calculationofthecalibrationline Inthecalibrationgraph(seeanexampleinFigure3)thenetcountrate(I)orthecountrateratio(monitorsample) isgivenonthey-axis,whilethechemicalmassfraction(w)isgivenonthex-axis.Thecalibrationlineisfixedb