化学和树脂干胶的先驱体制备过程文档格式.docx
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化学和树脂干胶的先驱体制备过程文档格式.docx
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Polymerizablecomplex(PC)methodseemstobetheeasiestandthemostelegantvariationofsol–gelmethods.Thesimplestimplementationofthistechniquerequiresonlyinexpensivechemicals,abeaker,astirrer,ahotplateandafurnace.Itisnotsensitivetothepresenceofwater(fortherareexceptions);
itdoesnotrequireinertatmosphere,andevenwithoutcarefulcontrolofgelprocessingtimeandconditions,oneshouldbestillabletoobtainsamplesofoutstandinghomogeneity.Itisthecombinationofthesefactorsthatexplainsthegrowingpopularityofthepolymerizablecomplexmethodforthesynthesisofferroelectric,superconducting,ferromagnetic,CMR,photocatalytic,fuelcell,electrode,catalyticandothercomplexoxidematerials.
TheoriginofthepolymerizablecomplexmethodisdatedbacktothePechinipatent(Pechini,1967)onfabricationofthinfilmcapacitorsbyutilizingmultifunctionalorganicacidscapableofchelatingmetalionsintothestablecomplexesandadiol,whichservesasasolventduringcomplexformationstepandlaterparticipatesinthepolyesterificationreactiontoformthree-dimensionalpolymernetworkwithincorporatedmetalcomplexesmixed,asassumed,ontheatomicscale.TheessentialstepsofthepolymerizablecomplexmethodarepresentedinFigure4-1.Suitablemetalsaltsareintroducedintotheethyleneglycol(EG)afterdissolutionofcitricacid(CA),whichisaddedinalargeexcesstoformmetal-citratecomplex.Thenthetemperatureshouldbeincreasedto100–130°
Ctospeeduptheformationofpolyesterduetothereactionbetweenfreecitricacidandethyleneglycol.Aftertheformationofplastic-likegel,thetemperatureisincreasedfurthertoremovetheexcessofethyleneglycol.Theobtainedrelativelyhardsubstanceshouldbetreatedat450–600°
Ctooxidizeorganiccompounds.Precursorpowdersthusobtainedcontainamixtureofhomogeneouslydistributedmetaloxides,carbonatesorsometimesanintermediatesinglephasecompoundwiththeproperstoichiometryofthemetalions.
Thebasicideaofthisapproachistouseinsitupolymerizationofmonomersspeciallyintroducedintosolutioninadditiontotherequiredmetalcations.ThistechniqueisknownasPechinimethod(Pechini,1967).Thebackgroundoftheproposedapproachisesterificationreactionbetweenglycolandmultifunctionalcarboxylicacid.Forcontinuousgrowthofthepolymerchaintheexistenceofatleasttwofunctionalgroupsinamonomerisimportant.Theviscosityofthesolutiondrasticallyincreasesduringthepolymerchainaugmentation(Fig.4-2).AsonecouldnoticeformFigure4-2,constructedfromthereporteddata(Arima,1996;
Kakihana,1997),thenatureofthecationsaffectstherateofviscosityincrease,whichindicatesthatmetalionsplayanimportantroleincross-linkingthepolymerchainsbymeansofcomplexformation.Thisviscosityincreaseisoftenreferredtoasa“gelation”.Probablyitwouldbemoreaccuratetousetheword“inspissation”toreflectthenatureandconditionsofthepolyesterificationreaction;
however,inthischapterwewillfollowtheestablishedterminology.Duringthefirststageofthepolymergrowththesolutionprovidesnecessaryenvironmenttopreventcationsegregation,andlater,therelativelyrigidpolymernetworktrapscationsandpreservestheinitialhomogeneityofthesolution.TheoriginalPechinipatentstatestheimportanceofthecarboxylicacid,whichcanformastablechelatecomplexsuchascitricacidandthepolyhydroxyalcohol,whichisliquidbelow100°
Candmayservesimultaneouslyasamonomerandasasolvent.Afterthepolymerizationiscompletedandtheexcessofsolventisevaporated,thepolymermatrixofgelistobeoxidizedyieldingaerogelwhichiscomposedofoxidesandcarbonates.
Figure4-1.Schemeofpolymericgelmethod.
Figure4-2.Viscosityincreaseofthemetal-citricacid-ethyleneglycolsystemasafunctionofreactiontime.
Sincethepublicationoftheoriginalpatent,thepolymerizablecomplexmethodwasintensivelystudied,sometimesremarkablymodifiedtomeettheparticularsyntheticneedsortoovercometheobstaclesthatmayariseduringthesynthesis.Inthepastfewyearsitbecamemorecommontorefertopolymerizablecomplexmethodas“Pechinimethod”,“modifiedPechinimethod”,“liquidmixtechnique”,etc.Inthischapterwewillalsofollowthewell-establishedcustomwheneverwewilldiscusssynthesisemployingcitricacidandethyleneglycolasessentialreagents.InadditiontothatwewilldiscussthesynthesistechniquesdevelopedfromPechinimethodthatcanbeclassifiedaspolymerizablecomplexmethod(Kakihana,1996,1999a)sincetheypossesstwodistinctivefeatures:
formationofstablemetalcomplexinthesolutionandpreservingatomicscalehomogeneityachievedinthesolutionbyuseofpolymertohindertheionsmobilityandpreventsegregation.
Chemistry
ComparedtotheknowledgebaseonthepracticaluseofPechinimethodforsynthesisofdifferentoxidematerials,relativelylittleisknownaboutchemistryofthistechnique.Mostofthefundamentalstudiesoncitricacidanditsmetalcomplexeswerecarriedoutin60and70s—eitherbeforePechinipublicationorrightafteritwhenpolymerizablecomplexmethodhasnotdeservedmuchattentionyet.Thereforemostoftheresultsarenotdirectlyrelatedtopolymerizablecomplexmethod.MorerecentstudiesonthechemistryofPechinimethodoftenwerecarriedoutbymaterialscientistswithnecessarychemistrybackgroundandfocusedonveryspecificquestionsornarrowsetofparticularproblems.Wewillattempttosummarizetheavailableinformationandcreateageneral(andhopefullyuseful)pictureofthechemistryinvolvedinthismethod.
Precursors
InthetypicalsynthesisofoxidematerialsbyPechini-typeprocess,solublemetalnitrates,acetates,chlorides,carbonates,isopropoxidesorothersuitablemetalcompoundsaredissolvedintheCA–EGsolution.Citricacidisrelativelystrongmultifunctionalorganicacid.Theacidityofthemiddlecarboxylicgroup(–mCOOH)isenhancedby–OHgroupattachedtoternarycarbonatom.Methylenegroups,ontheotherhand,provideadestabilizingeffect;
howeveritisreducedbytheneighboringterminalcarboxylicgroups(–tCOOH).ThereforemiddlecarboxylicgroupinwatersolutionlosesH+veryeasily(pK1=2.91)(Harris,1976)andpHofcitricacidaqueoussolutionisusuallyintherangeof0–2dependingonconcentration.Theterminalcarboxylicgroupsarelessacidic(pK2=4.36andpK3=5.74)(Harris,1976)andthedissociationbecomessubstantialathigherpH.AtveryhighpHthehydroxygroupofcitricacidmaybecomedeprotonated(pK4=10.96)(Grigor’eva,1975).Onemayalsonoticethatlocationof–OHgroupisfavorablefortheformationofhydrogenbondsbetweencarboxylicgroupsandhydroxygroup,whichshouldstabilizethecarboxylicion.Whatisimportant,isthatsuchaskeletonisresponsiblefortheformationofstablefive-andsix-memberringsinmetalcitratecomplexes.
Citricacidiswellsolubleinethyleneglycol,whichprovidesawiderangeofCA:
EGratiosforthePechinimethod,andmakesitpossibletotunetheconditionsofsynthesisforeachparticularsystem.Chemicalinteractionbetweencitricacidandethyleneglycoloccursatroomtemperaturewithoutanytreatmentofthesolution.Ofcourse,thisinteractionisnotcompleteandchemicalequilibriumisstronglyshiftedtowardfreecitricacidandethyleneglycol,however13C-NMRspectrumunambiguouslyprovesesterformation(Kakihana,1999a;
Fang,2001).Thequalityofthefinalpowderdependsontheextenttowhichthemolecular-scalehomogeneityachievedinthesolutionmaybepreservedintheprocessofpolymerformationandpyrolysisofthepolymerresin.ForthepurposeofoxidepowderssynthesiscitricacidandethyleneglycolratiointhePechiniprocessseemstobefarfromtheoptimalvalue.Figure4-3summarizestheresultsoftheinvestigationofCA–EGsystembehaviorduringgelation,solventremovalandthermaldecompositionoforganicmatrixconductedbyTaiandLessing(1992a,1992b).TherangeofCAconcentrationsfrom50to60%seemstobethemostappropriateforthecomplexoxidepowderspreparationsinceitprovidesthemaximumviscosityoftheobtainedgel.Strongfoamingisanadditionalfactorthatpreventssegregationduringthermaldecompositionofthepolymer.Mildburningwouldguaranteerelativelylowtemperatureinsideoftheprecursorand,consequently,relativelyslowgraingrowth.Oneshouldkeepinmind,however,thatesterformationisareversibleprocess.
Theequilibriuminthisreactioncanbeshiftedtowardpolyesterbyeitherincreaseofastartingreagentconcentrationorbyaproductremovalfromthereactionmedium.OnthecitricacidrichsideonewouldberestrictedbytheCAsolubilityinethyleneglycol(Fig.4-3).Frompracticalviewpoint,highviscosityoftheconcentratedCAsolutionwillslowdownthedissolutionofmetalsaltsand,inaddition,theprecipitationofcitricacidmightoccurwhilepH,temperatureormetalsaltconcentration(ionicstrength)willchangeduringtheprocessing.AnotherreasontouseexcessofEGisconnectedwithaneedtoremovewaterfromthereactionmixture.Inthiscase,thevaporwillcontainethyleneglycolasamajorfractionthatwillbeprogressivelyremovedfromthereaction.However,thecompleteremovaloftheexcessofEGrarelyoccursduringpolyesterificationandtheuseof20%citricacidconcentrationrequiresrelativelylongheattreatmenttoeliminateunreactedglycol.TheboilingpointofEGisthelowestamongdials,sothechoiceofethyleneglycolasasolventandasamonomeristhemostconvenien
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- 关 键 词:
- 化学 树脂 先驱 体制 过程
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