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本文(EN 14104-2003 en Fat and oil derivatives - Fatty Acid Methyl Esters (FAME) - Determination of acid value《脂肪和油的衍生物 脂肪酸甲基酯(FAME) 酸值的测定》.pdf)为本站会员(fuellot230)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!

EN 14104-2003 en Fat and oil derivatives - Fatty Acid Methyl Esters (FAME) - Determination of acid value《脂肪和油的衍生物 脂肪酸甲基酯(FAME) 酸值的测定》.pdf

1、BRITISH STANDARD BS EN 14104:2003 Fat and oil derivatives Fatty Acid Methyl Esters (FAME) Determination of acid value The European Standard EN 14104:2003 has the status of a British Standard ICS 67.200.10 BS EN 14104:2003 This British Standard was published under the authority of the Standards Polic

2、y and Strategy Committee on 13 May 2003 BSI 13 May 2003 ISBN 0 580 41836 7 National foreword This British Standard is the official English language version of EN 14104:2003. The UK participation in its preparation was entrusted to Technical Committee AW/307, Animal and vegetables fats and oils, whic

3、h has the responsibility to: A list of organizations represented on this committee can be obtained on request to its secretary. Cross-references The British Standards which implement international or European publications referred to in this document may be found in the BSI Catalogue under the secti

4、on entitled “International Standards Correspondence Index”, or by using the “Search” facility of the BSI Electronic Catalogue or of British Standards Online. This publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application. Co

5、mpliance with a British Standard does not of itself confer immunity from legal obligations. aid enquirers to understand 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 rela

6、ted international and European developments and promulgate them in the UK. Summary of pages This document comprises a front cover, an inside front cover, the EN title page, pages 2 to 9 and a back cover. The BSI copyright notice displayed in this document indicates when the document was last issued.

7、 Amendments issued since publication Amd. No. Date CommentsEUROPEANSTANDARD NORMEEUROPENNE EUROPISCHENORM EN14104 April2003 ICS67.200.10 Englishversion FatandoilderivativesFattyAcidMethylEsters(FAME) Determinationofacidvalue ProduitsdrivsdescorpsgrasEstersmthyliques dacidesgras(EMAG)Dterminationdeli

8、ndicedacide ErzeugnisseauspflanzlichenundtierischenFettenund lenFettsureMethylester(FAME)Bestimmungder Surezahl ThisEuropeanStandardwasapprovedbyCENon2January2003. CENmembersareboundtocomplywiththeCEN/CENELECInternalRegulationswhichstipulatetheconditionsforgivingthisEurope an Standardthestatusofanat

9、ionalstandardwithoutanyalteration.Uptodatelistsandbibliographicalreferencesconcernings uchnational standardsmaybeobtainedonapplicationtotheManagementCentreortoanyCENmember. ThisEuropeanStandardexistsinthreeofficialversions(English,French,German).Aversioninanyotherlanguagemadebytra nslation underther

10、esponsibilityofaCENmemberintoitsownlanguageandnotifiedtotheManagementCentrehasthesamestatusasthe official versions. CENmembersarethenationalstandardsbodiesofAustria,Belgium,CzechRepublic,Denmark,Finland,France,Germany,Greece, Hungary,Iceland,Ireland,Italy,Luxembourg,Malta,Netherlands,Norway,Portugal

11、,Slovakia,Spain,Sweden,SwitzerlandandUn ited Kingdom. EUROPEANCOMMITTEEFORSTANDARDIZATION COMITEUROPENDENORMALISATION EUROPISCHESKOMITEEFRNORMUNG ManagementCentre:ruedeStassart,36B1050Brussels 2003CEN Allrightsofexploitationinanyformandbyanymeansreserved worldwideforCENnationalMembers. Ref.No.EN1410

12、4:2003EEN14104:2003(E) 2 Foreword Thisdocument(EN14104:2003)hasbeenpreparedbyTechnicalCommitteeCEN/TC307“Oilseeds,vegetable andanimalfatsandoilsandtheirbyproductsMethodsofsamplingandanalysis“,thesecretariatofwhichisheld byAFNOR. ThisEuropeanStandardshallbegiventhestatusofanationalstandard,eitherbypu

13、blicationofanidenticaltextor byendorsement,atthelatestbyOctober2003andconflictingnationalstandardsshallbewithdrawnatthelatestby October2003. ThisdocumenthasbeenpreparedunderMandateM/245onFattyAcidMethylester(FAME)giventoCENbythe EuropeanCommissionandtheEuropeanFreeTradeAssociation. AnnexAisinformati

14、ve. AccordingtotheCEN/CENELECInternalRegulations,thenationalstandardsorganizationsofthefollowing countriesareboundtoimplementthisEuropeanStandard:Austria,Belgium,CzechRepublic,Denmark,Finland, France,Germany,Greece,Hungary,Iceland,Ireland,Italy,Luxembourg,Malta,Netherlands,Norway,Portugal, Slovakia,

15、Spain,Sweden,SwitzerlandandtheUnitedKingdom.EN14104:2003(E) 3 Introduction ThisEuropeanStandardisbasedontheENISO6601whichwasspecificallyadaptedforthedeterminationof acidvalueoffattyacidmethylesters(FAME).EN14104:2003(E) 4 1Scope ThisEuropeanStandardspecifiesonetitrimetricmethodforthedeterminationofa

16、cidvalueinlightcolouredFatty AcidMethylEsters,hereinafterreferredasFAME. Itallowsthedeterminationofacidvaluewithinarangeof0,10mgKOH/gto1,00mgKOH/g. 2 Normativereferences ThisEuropeanStandardincorporatesbydatedorundatedreference,provisionsfromotherpublications.These normativereferencesarecitedattheap

17、propriateplacesinthetext,andthepublicationsarelistedhereafter.For datedreferences,subsequentamendmentstoorrevisionsofanyofthesepublicationsapplytothisEuropean Standardonlywhenincorporatedinitbyamendmentorrevision.Forundatedreferencesthelatesteditionofthe publicationreferredtoapplies(includingamendme

18、nts). ENISO661, AnimalandvegetablefatsandoilsPreparationoftestsample(ISO661:1989). ENISO3696, WaterforanalyticallaboratoryuseSpecificationandtestmethods(ISO3696:1987). 3 Termsanddefinitions ForthepurposesofthisEuropeanStandard,thefollowingtermanddefinitionapply. 3.1 acidvalue numberofmilligramsofpot

19、assiumhydroxiderequiredtoneutralisethefreefattyacidspresentin1gofFAME, whendeterminedinaccordancewiththeprocedurespecifiedinthisEuropeanStandard Acidvalueisexpressedinmilligramsofpotassiumhydroxidepergramofsample. NOTE Ifthesamplecontainsmineralacidstheseare,byconventiondeterminedasapartoftotalacidv

20、alue.Thismethod doesnotallowtodistinguishbetweenweak(fromfreefattyacids)andstrong(frommineralacids,ifpresent)acidity. 4Principle Atestportionisdissolvedinamixedsolventandtitratedwithadilutedsolutionofpotassiumhydroxide,using phenolphthaleinasanindicatorinordertodetectthetitrationendpoint. 5Reagents

21、Useonlyreagentsofrecognisedanalyticalgradeandwaterofgrade3inaccordancewithENISO3696. 5.1 Diethylether and95% ethanol,1+1mixturebyvolume. WARNING Diethyletherisveryflammableandmayformexplosiveperoxides.Usewithgreatcaution. Neutralise,justbeforeuse,byaddingthepotassiumhydroxidesolution(5.2)inthepresen

22、ceof0,3 mlof phenolphthaleinalcoholicsolution(5.3)per100mlofsolventmixture. Ifitisnotpossibletousediethylether,amixedsolventmaybeusedasfollows: tolueneand95%( V/V)ethanol,1+1mixturebyvolume; tolueneand99%( V/V)2propanol,1+1mixturebyvolume.EN14104:2003(E) 5 Themixedsolventcanbereplacedby99%( V/V)2pro

23、panol. NOTE Largervolumesofsolventmixtureandindicatormaybenecessaryfordarkcolouredsamples. 5.2 Potassiumhydroxide ,standardvolumetricsolutioninethanol: mol/l 1 0 (KOH) , = c Theethanolicpotassiumhydroxidesolutioncanbereplacedbyaqueouspotassiumorsodiumhydroxidesolutions, butonlyifthevolumeofwaterintr

24、oduceddoesnotleadtophaseseparation. 5.2.1 Preparationofthesolution Dissolveapproximately7gofpotassiumhydroxidepelletsinethanolanddiluteto1000mlwiththesamesolvent. NOTE 2propanolcanbeusedinsteadofethanol. Weigh,tothenearest0,0002g,0,15gofbenzoicacidhavingminimumpurity99,9%( m/m),oranotherprimary stan

25、dard,ina150mlbeakeranddissolvein50mlof4methylpentan2one(5.4).UseapHmetertofollowtitration andtodetecttheendpoint,startthestirrerandtitratewiththepotassiumhydroxidesolutiontotheequivalence point. 5.2.2 Calculationofthesolutionconcentration Theconcentrationofthepotassiumhydroxidesolution,expressedinmo

26、lesperlitre,(whenbenzoicacidisused),is givenby: 0 0 1 , 122 000 1 V m where m 0 isthemass,reportedingrams,ofbenzoicacidused; V 0 isthevolume,inmillilitres,ofpotassiumhydroxidesolutionusedtoreachtheendpoint. NOTE1 Intheaboveandlatermathematicalexpressions,thesymbolrepresentsthenumericalvaluesofthequa

27、ntities. NOTE2 Potassiumhydroxidestandardisedsolutionsarecommerciallyavailableandsuitableforuse. Usesolutionpreparedatleast5dayspreviouslyanddecantedintoabrownglassbottle,fittedwitharubber stopperprovidedwithathermometerneededfortemperaturecorrection(see10).Thesolutionshallbecolourless orstrawyellow

28、.Ifthebottleisconnectedtotheburette,provisionshallbemadetopreventintakeofcarbon dioxide,forexamplebyusingatubefilledwithgranularsodalime. 5.3 Phenolphthalein,10g/lsolutionin95%Ethanol. 5.4 4Methylpentan2one neutralizedjustbeforeusebyaddingthepotassiumhydroxidesolution(5.2)using thepHmeter(6.3). 6App

29、aratus Usuallaboratoryequipmentand,inparticular: 6.1 Microburette,10mlcapacity,graduatedin0,02mlsubdivisions. 6.2 Analyticalbalance ,capableofweighingwithanaccuracyof 0,05gorless.EN14104:2003(E) 6 6.3 pHmeter ,equippedwithglassandcalomelelectrodes. 7Sampling Samplingisnotpartofthemethodspecifiedinth

30、isEuropeanStandard.Arecommendedsamplingmethodisgiven inENISO55552. Itisimportantthatalaboratoryreceivesasample,whichistrulyrepresentativeandhasnotbeendamagedor changedduringtransportationandstorage. 8 Preparationoftestsample PreparethetestsampleinaccordancewithENISO661.Thetestsampleshallnotbeheateda

31、nd/orfiltered. 9Procedure 9.1 Testportion Takeapproximately20gofthetestsample. Weighthetestportionintoa250mlconicalflask. 9.2Determination 9.2.1 Dissolvethetestportion(9.1)in100mlofpreviouslyneutralisedsolventmixture(5.1). Titrate,whilstswirlingthesolution,withthepotassiumhydroxidesolution(5.2)tothe

32、endpointwhentheadditionof asingledropproducesaslight,butdefinitecolourchangepersistingforatleast15s. 9.2.2 Ifthesolutionbecomesturbidduringtitration,addasufficientquantityofthemixedsolvent(5.1)togivea clearsolution. 10Calculation Theacidvalueisreportedas: m c V 1 , 56 where V isthevolume,inmillilitr

33、es,ofstandardvolumetricpotassiumhydroxidesolutionused; c istheexactconcentration,inmolesperlitre,ofthestandardvolumetricpotassiumhydroxidesolution used; m isthemass,ingrams,ofthetestportion; 56,1isthemolecularmassofpotassiumhydroxide. ResultsareexpressedasmgKOH/gsampleandshallberoundedtotheseconddec

34、imaldigit.EN14104:2003(E) 7 NOTE Theconcentrationoftheethanolicsodiumorpotassiumhydroxidesolutionvarieswithtemperatureanditmaybe usefultousethefollowingcorrection: ) ( 0011 , 0 1 0 t t V V t - - = where V isthecorrectedvolume,inmillilitres,ofthestandardsodiumorpotassiumhydroxidesolution; V t isthevo

35、lume,inmillilitres,ofthestandardsodiumorpotassiumhydroxidesolutionmeasuredattemperature t; t isthetemperatureatwhichthedeterminationwascarriedout,indegreesCelsius; t 0 isthetemperature,indegreesCelsius,atwhichtheconcentrationofthestandardsodiumorpotassiumhydroxide solutionwasdetermined. 11Precision

36、11.1 Interlaboratorytest DetailsofinterlaboratorytestaregiveninannexA.Thevaluesderivedfromthesetestsmaynotbeapplicableto concentrationrangesandmatricesotherthanthosegiven. 11.2Repeatability Theabsolutedifferencebetweentwoindependentsingletestresults,obtainedusingthesamemethodonidentical testmaterial

37、inthesamelaboratorybythesameoperatorusingthesameequipmentwithinashortintervaloftime, shallnotbegreaterthan0,02mgKOH/gmorethanonceoutof20determinations. 11.3Reproducibility Theabsolutedifferencebetweentwosingletestresults,obtainedusingthesamemethodonidenticaltestmaterial indifferentlaboratorieswithdi

38、fferentoperatorsusingdifferentequipment,shallnotbegreaterthan0,06mgKOH/g morethanonceoutof20determinations. 12 Testreport Thetestreportshallspecify: allinformationnecessaryforthecompleteidentificationofthesample; thesamplingmethodusedifknown; thetestmethodused,withreferencetothisEuropeanstandard; al

39、loperatingdetailsnotspecifiedinthisEuropeanStandard,orregardedasoptional,togetherwithdetailsof anyincidentswhichmayhaveinfluencedthetestresult(s); thetestresult(s)obtained,oriftherepeatabilityhasbeenchecked,thefinalquotedresultobtained.EN14104:2003(E) 8 Annex A (informative) Resultsofaninterlaborato

40、rytrial AEuropeancollaborativetestinvolving15laboratoriesin5countrieswascarriedouton5samples: Sample1: FAMEpreparedfromsunfloweroil; Sample2: FAMEpreparedfromrapeseedoil; Sample3: FAMEpreparedfromrapeseedoil; Sample4: FAMEpreparedfromsunflowerandrapeseedoils(75%sunflower); Sample5: FAMEpreparedfromr

41、apeseedoil. ThetestwasorganizedbyCENTC307/WG1in1998andtheresultsobtainedweresubjectedtostatistical analysisinaccordancewithENISO42593togivetheprecisiondatashowninTableA.1. TableA.1 S a m p l e 12345 Nofparticipatinglaboratories 15 15 15 15 15 Nofparticipatinglaboratoriesaftereliminatingoutliers 14 1

42、5 14 15 14 Meanvalue (mgKOH/g) 0,512 0,359 0,882 0,151 0,682 Repeatabilitystandarddeviation(mgKOH/g) 0,004 0,004 0,006 0,003 0,008 Reproducibilitystandarddeviation(mgKOH/g) 0,016 0,022 0,020 0,017 0,017 Repeatabilitylimit, r(mgKOH/g) 0,013 0,011 0,019 0,009 0,024 Reproducibilitylimit R(mgKOH/g) 0,04

43、8 0,067 0,062 0,051 0,052EN14104:2003(E) 9 Bibliography 1 ENISO660, AnimalandvegetablefatsandoilsDeterminationofacidvalueandacidity(ISO660:1996). 2 ENISO5555, AnimalandvegetablefatsandoilsSampling(ISO5555:2001). 3 ENISO4259, PetroleumproductsDeterminationandapplicationofprecisiondatainrelationtomethodsof test(ISO4259:1992/Cor1:1993 ).BS EN 14104:2003 BSI 389 Chiswick High Road London W4 4AL BSI British Standards Institution BSI is the independent national bo

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