BS EN 13926-2003 Surface active agents - Alkoxylated derivatives - Determination of hydroxyl value - N-methyl imidazole method《表面活性剂 烷氧基衍生物 羟基值的测定 N-甲基咪唑法》.pdf

《BS EN 13926-2003 Surface active agents - Alkoxylated derivatives - Determination of hydroxyl value - N-methyl imidazole method《表面活性剂 烷氧基衍生物 羟基值的测定 N-甲基咪唑法》.pdf》由会员分享，可在线阅读，更多相关《BS EN 13926-2003 Surface active agents - Alkoxylated derivatives - Determination of hydroxyl value - N-methyl imidazole method《表面活性剂 烷氧基衍生物 羟基值的测定 N-甲基咪唑法》.pdf（16页珍藏版）》请在麦多课文档分享上搜索。

1、BRITISH STANDARD BS EN 13926:2003 Surface active agents Alkoxylated derivatives Determination of hydroxyl value N-methyl imidazole method The European Standard EN 13926:2003 has the status of a British Standard ICS 71.100.40 BS EN 13926:2003 This British Standard was published under the authority of

2、 the Standards Policy and Strategy Committee on 20 March 2003 BSI 20 March 2003 ISBN 0 580 41461 2 National foreword This British Standard is the official English language version of EN 13926:2003. The UK participation in its preparation was entrusted to Technical Committee CII/34, Methods of test f

3、or surface active agents, which 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

4、 BSI Catalogue under the section 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 f

5、or its correct application. Compliance 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 in

6、terests informed; monitor related 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 13 and a back cover. The BSI copyright date displayed in this document indicates when

7、the document was last issued. Amendments issued since publication Amd. No. Date CommentsEUROPEANSTANDARD NORMEEUROPENNE EUROPISCHENORM EN13926 March2003 ICS71.100.40 Englishversion SurfaceactiveagentsAlkoxylatedderivativesDetermination ofhydroxylvalueNmethylimidazolemethod AgentsdesurfaceDrivsalkylo

8、xylsDterminationde lindicedhydroxyleMthodelaNmthylimidazole GrenzflchenaktiveStoffeAlkoxylierteDerivate BestimmungderHydroxylzahlNMethylimidazol Verfahren ThisEuropeanStandardwasapprovedbyCENon29November2002. CENmembersareboundtocomplywiththeCEN/CENELECInternalRegulationswhichstipulatetheconditionsf

9、orgivingthisEurope an Standardthestatusofanationalstandardwithoutanyalteration.Uptodatelistsandbibliographicalreferencesconcernings uchnational standardsmaybeobtainedonapplicationtotheManagementCentreortoanyCENmember. ThisEuropeanStandardexistsinthreeofficialversions(English,French,German).Aversioni

10、nanyotherlanguagemadebytra nslation undertheresponsibilityofaCENmemberintoitsownlanguageandnotifiedtotheManagementCentrehasthesamestatusasthe official versions. CENmembersarethenationalstandardsbodiesofAustria,Belgium,CzechRepublic,Denmark,Finland,France,Germany,Greece, Hungary,Iceland,Ireland,Italy

11、,Luxembourg,Malta,Netherlands,Norway,Portugal,Slovakia,Spain,Sweden,SwitzerlandandUn ited Kingdom. EUROPEANCOMMITTEEFORSTANDARDIZATION COMITEUROPENDENORMALISATION EUROPISCHESKOMITEEFRNORMUNG ManagementCentre:ruedeStassart,36B1050Brussels 2003CEN Allrightsofexploitationinanyformandbyanymeansreserved

12、worldwideforCENnationalMembers. Ref.No.EN13926:2003EEN13926:2003(E) 2 Contents page Foreword3 1 Scope 4 2 Normativereferences 4 3 Termanddefinition. .4 4 Principle4 5 Reagents.4 6 Apparatus .5 7 Sampling.5 8 Procedure .5 9 Expressionofresults . .6 10 Precision.8 11 Testreport 8 AnnexA (informative)

13、Resultsofinterlaboratorytest9 AnnexB (informative) Exampleforpotentiometricoperatingparameters.11 AnnexC (informative) Exampleforatypicaltitrationcurveanditsderivative .12 Bibliography 13EN13926:2003(E) 3 Foreword Thisdocument(EN13926:2003)hasbeenpreparedbyTechnicalCommitteeCEN/TC276“Surfaceactiveag

14、ents“, thesecretariatofwhichisheldbyAFNOR. ThisEuropeanStandardshallbegiventhestatusofanationalstandard,eitherbypublicationofanidenticaltextor byendorsement,atthelatestbySeptember2003,andconflictingnationalstandardsshallbewithdrawnatthe latestbySeptember2003. AnnexesA,B,andCareinformative. According

15、totheCEN/CENELECInternalRegulations,thenationalstandardsorganizationsofthefollowing countriesareboundtoimplementthisEuropeanStandard:Austria,Belgium,CzechRepublic,Denmark,Finland, France,Germany,Greece,Hungary,Iceland,Ireland,Italy,Luxembourg,Malta,Netherlands,Norway,Portugal, Slovakia,Spain,Sweden,

16、SwitzerlandandtheUnitedKingdom.EN13926:2003(E) 4 1Scope ThisEuropeanStandardspecifiesamethodforthedeterminationofhydroxylvalueofaliphaticandalicyclic hydroxylcompoundssuchaspolyols,sorbitanesters,plasticisersandsurfaceactiveagentalcoholsand alkoxylateswithhydroxylvaluesgreaterthan20mgKOH/g. 2 Normat

17、ivereferences ThisEuropeanStandardincorporatesbydatedorundatedreference,provisionsfromotherpublications.These normativereferencesarecitedattheappropriateplacesinthetext,andthepublicationsarelistedhereafter.For datedreferences,subsequentamendmentstoorrevisionsofanyofthesepublicationsapplytothisEurope

18、an Standardonlywhenincorporatedinitbyamendmentorrevision.Forundatedreferencesthelatesteditionofthe publicationreferredtoapplies(includingamendments). ISO607, SurfaceactiveagentsanddetergentsMethodsofsampledivision. ISO4314, SurfaceactiveagentsDeterminationoffreealkalinityorfreeacidityTitrimetricmeth

19、od. 3 Termanddefinition ForthepurposesofthisEuropeanStandard,thefollowingtermanddefinitionapply. 3.1 hydroxylvalue I(OH) numberofmilligramsofpotassiumhydroxideneededtoneutralizetheaceticacidrequiredtoesterifythehydroxyl groupsin1gofthematerial,orthenumberofmilligramsofpotassiumhydroxidecorresponding

20、tothehydroxyl groupsin1gofthematerial 4Principle Aknownmassoftestsampleisesterifiedwithanexcessofaceticanhydride/tetrahydrofuransolutionusing Nmethylimidazoleasacatalyst.Theexcessofaceticanhydrideishydrolysedandthentheformedaceticacid istitratedpotentiometricallywithethanolicpotassiumhydroxidestanda

21、rdvolumetricsolution.Thehydroxylvalueis calculatedfromthedifferenceintitrationvolumesofablanktestandthetestsample. 5Reagents 5.1 General Duringtheanalysis,unlessotherwisespecified,useonlyreagentsofrecognizedanalyticalgradeandhavebeen checkedinadvanceastonotinterferewiththeanalyticalresults. WARNINGT

22、etrahydrofuranandNmethylimidazolebeinghazardouschemicals,alltheoperationsshall beconductedunderawellventilatedfumehood. 5.2 Tetrahydrofuran,C 4 H 8 O. 5.3 Aceticanhydride ,C 4 H 6 O 3 . 5.4 Nmethylimidazole ,C 4 H 6 N 2 . 5.5 Potassiumhydrogenphthalate , C 8 H 5 O 4 K, w(C 8 H 5 O 4 K)=99%driedat(10

23、5 1)C.EN13926:2003(E) 5 5.6 Ethanol,C 2 H 5 OH. 5.7 Potassiumhydroxidestandardvolumetricsolutioninethanol , c(KOH)=0,5mol/l. Weigh66,0gofpotassiumhydroxidewithapurityof85%( m/m)tothenearest0,1ganddissolveitin250ml freshlyboiledwater.Thentransferthesolutionintoa2lvolumetricflaskandcompletetothemarkwi

24、thethanol (5.6).Allowthesolutiontostandfor24hbeforestandardization. 5.8 Acetylationreagent Carefullymix92mloftetrahydrofuran(5.2)and8mlofaceticanhydride(5.3).Thissolutionisstableforuptoone month. 6Apparatus 6.1 General Ordinarylaboratoryapparatusandthefollowing. 6.2 Potentiometer,comprisingatitrator

25、withacombinedglass/calomelelectrode,automaticburetteassembly andamagneticstirrer. 6.3 Waterbath ,capableofmaintainingatemperatureof(45 1)C. 6.4 Aircooler ,withalengthof1m. 6.5 Analyticalbalance ,withanaccurateto0,0001g. 7Sampling SamplethematerialtobetestedandstoreinaccordancewithISO607. 8Procedure

26、8.1 Standardizationoftheethanolicpotassiumhydroxidestandardvolumetricsolution Weighapproximately1gofdriedpotassiumhydrogenphthalate(5.5)tothenearest0,1mgintoa150mlbeaker anddissolveitin80mloffreshlyboiledwater. Immersetheelectrodeandamagneticstirbarintothebeaker,stirandtitratewiththepotentiometer(6.

27、2)withthe ethanolicpotassiumhydroxidestandardvolumetricsolution(5.7). Recordthevolume V o oftheethanolicpotassiumhydroxidestandardvolumetricsolution(5.7)atthefirstinflection point. Carryoutthestandardizationintriplicate. 8.2 Testportion Calculatethequantityofthelaboratorysampletobeweighed, m,express

28、edingrams,bytheequation(1): () E OH 168 I m = (1)EN13926:2003(E) 6 where I(OH) E istheexpectedhydroxylvalue,inmilligramsKOHpergramofthematerial. 8.3Determination Fillthecalculatedmassofthetestportion(8.2), m,weighedtothenearest0,1mgandnotexceeding10gintoa cleandry150mlstopperedconicalflask. Introduc

29、ewithapipette10mloftheacetylationreagent(5.8). Add2mlofNmethylimidazole(5.4)intotheflaskanddissolvethetestportion. Stopuptheflaskorconnecttheaircooler(6.4). Placetheflaskinawaterbath(6.3)at45Cfor15min. Attheendofthereactiontime,add10 mlofwater(takingcareofwashingthestopperortheaircooler). Homogenise

30、andallowtostandfor2min. Introducetheelectrodeandamagneticstirbarintotheflask,addenoughethanoltocoverthetipoftheelectrode. Titratewiththepotentiometer(6.2)withtheethanolicpotassiumhydroxidestandardvolumetricsolution(5.7)and notethevolume (V 1 )atthefirstinflectionpoint. Performthelaboratorysampleanal

31、ysisinduplicate. 8.4Blank tests Carryouttwoblanktestsatthesametimeatthedetermination,usingthesamereagents,butwithoutthetest portionandnotethevolumeatthefirstinflectionas V 2 . 9 Expressionofresults 9.1 Standardisationfactoroftheethanolicpotassiumhydroxidestandardvolumetricsolution Thestandardisation

32、factor, f,oftheethanolicpotassiumhydroxidestandardvolumetricsolution(5.6)iscalculated bytheequation(2): c M V w m f = 0 0 0 10 (2) where m o isthemassofpotassiumhydrogenphthalate(5.5),ingrams; w o isthepurityofpotassiumhydrogenphthalate(5.5),inpercent( m/m); V o isthevolumeoftheethanolicpotassiumhyd

33、roxidestandardvolumetricsolution(5.7)usedforthe standardisation(8.1),inmillilitres; M isthemolarmassofpotassiumhydrogenphthalate(5.5), M(C 8 H 5 O 4 K)=204,23g/mol; c istheconcentrationoftheethanolicpotassiumhydroxidestandardvolumetricsolution(5.7), c(KOH)=0,5mol/l.EN13926:2003(E) 7 Takeasthestandar

34、dizationfactorthemeanofthreetitrationsperformedaccordingto8.1. 9.2 Hydroxylvalue Theexperimentalhydroxylvalue, I(OH) o ,inmilligramsofKOHpergramofthetestportion,iscalculatedbythe equation(3): ()( ) m f c V V I o 11 56 OH 1 2 , - = (3) where V 2 isthemeanvolumeoftheethanolicpotassiumhydroxidestandard

35、volumetricsolution(5.7)usedfor theblanktests(see8.4),inmillilitres; V 1 isthevolumeoftheethanolicpotassiumhydroxidestandardvolumetricsolution(5.7)usedforthe determination(see8.3),inmillilitres; c istheconcentrationoftheethanolicpotassiumhydroxidestandardvolumetricsolution(5.7), c(KOH)=0,5mol/l; f is

36、themeanofstandardisationfactorofethanolicpotassiumhydroxidethestandardvolumetric solution(5.7)from9.1; m isthemassofthetestportion(see8.3),ingrams. Forsamplescontainingfreeacidity,thehydroxylvalue, I(OH),iscalculatedbytheequation(4): ()()AV I I o + = OH OH (4) where () o I OH istheexperimentalhydrox

37、ylvalue,inmilligramsofKOHpergramofthetestportion; AV istheacidityvalueofthesampleinaccordancewithISO4314orequivalent,inmilligramsofKOHper gramofthetestportion. Forsamplescontainingfreealkalinity,thehydroxylvalue, I(OH),iscalculatedbytheequation(5): ()() BV I I - = o OH OH (5) where I(OH) o istheexpe

38、rimentalhydroxylvalue,inmilligramsofKOHpergramofthetestportion; BV isthealkalinityvalueofthesampleinaccordancewithISO4314orequivalent,inmilligramsofKOH pergramofthetestportion.EN13926:2003(E) 8 10Precision 10.1 Repeatabilitylimit Theabsolutedifferencebetweentwoindependentsingletestresults,obtainedus

39、ingthesamemethodonidentical testmaterialinthesamelaboratorybythesameoperatorusingthesameequipmentwithinashortintervaloftime, willnotexceedtherepeatabilitylimit, r, inmorethan5%ofcases. TypicalprecisiondataobtainedinaringtestaregiveninannexA. 10.2Reproducibilitylimit Theabsolutedifferencebetweentwoin

40、dependentsingletestresults,obtainedusingthesamemethodonidentical testmaterialindifferentlaboratoriesbydifferentoperatorsusingdifferentequipment,willnotexceedthe reproducibilitylimit, R,inmorethan5%ofcases. TypicalprecisiondataobtainedinaringtestaregiveninannexA. 11 Testreport Thetestreportshallinclu

41、dethefollowinginformation: a) allinformationnecessaryforthecompleteidentificationofthesample; b) areferencetothisEuropeanStandard; c) thetestresults; d) detailsofanyoperationsnotspecifiedinthisEuropeanStandard,andanyoperationsregardedasoptional,as wellasanyincidentslikelytohaveaffectedtheresults.EN1

42、3926:2003(E) 9 Annex A (informative) Resultsofinterlaboratorytest TheinterlaboratorytestwascarriedoutbyCESIO/AISEin1998.Theprecisiondatawereevaluatedinaccordance withISO 57252.Foursampleswereanalysedfourtimesby13 laboratories.Thesesamplesareshownin TableA.1. TableA.1Testsamples Sample Designation A

43、Isotridecanole+7EO B Sorbitanmonolaurate C PO/EOblockcopolymer D Laurylalcohol TheringtestresultsaregiveninTablesA.2andA.3. TableA.2Resultsofinterlaboratorytestconcerningtheexperimentalhydroxylvalues, I(OH) o Designation SampleA SampleB SampleC SampleD Numberoflaboratoriesparticipating 12 13 13 13 Numberoflaboratoriesnoteliminated 12 9 9 12 Totalnumberofvalues(withoutoutliers) 48 36 36 48 Meanvalue,inmgKOH/g 116,34 339,18 49,18 299,93 Repeatabilitystandarddeviation, s r ,inmgKOH/g 0,944 1,42 0,35 2,65 Repeatabilitylimit ,r :( r =2,8x s r