聚对苯二甲酸-共-丁二酸丁二醇酯(pbst)的成核剂和共聚改性研究

聚对苯二甲酸-共-丁二酸丁二醇酯(pbst)的成核剂和共聚改性研究

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时间:2018-11-10

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1、东华大学硕士学位论文摘要synthesizedfromthestartingmaterialsofterephthalicacid(PTA),succinicacid(SA),1,4-butanediol(1,4-BD)inthepresenceoftetraisopropoxidetitanium(TTiPO)asthebulkpolycondensationcatalystandkaolin,talcandsilicaasthenucleatingagent.Angletestofthepreparedcopolyestersshowedthatincr

2、easedasthenucleatingagentisadded,thehydrophilicwouldworsebeforetheygetbetter,amongthem,thekaolinmodifiedcopolyesterhydrophilicchangedobviously.WAXDresultsindicatedthatthecrystalstructuresofthemodifiedcopolyestershavenotchanged,theaddednucleatingagentimprovedthecrystallinityofcopoly

3、esterssystem,perfectedthecrystalstructures.ContraststretchingbeforeandafterthemodificationofPBSTpolyesterswide—angletestresults,showedthatpolyestersinducedorientation,thepositionsofthecharacteristicpeaksdidnotchange,andpartsofthediffractionpeaksgraduallyrushedintowidepeakor‘‘should

4、erpeak”.ThestudiesontheisothermalcrystallizationkineticsofnucleatingagentmodifiedPBSTcopolyestersshowedthatnucleatingagentsignificantlyimprovedthecrystallizationrateofPBST,embodiedintheexothermicpeakswidthdecreased,therelativecrystallinityvariationcurvesslopeincreasedobviously,semi

5、crystallinetime(ill2)decreased.Basedontheanalysisandcomparisonofthreekindsofnucleatingagentandmodifiedcopolyestertestresults,itwouldbeknownthatthebestadditiveamountrespectivelykaolinadditionis2.5%,thetalcpowderis2%,thesilicais0.5%and2%.revealedthatthemodifiedcopolyesterisothermalcr

6、ystallizationexothermicpeakwidthofthesmallest,leastsemicrystallinetime(tl/2),thecrystallizationrateisoptimal.Themechanicalpropertiestestshowedthatnucleatingagentwassignificantlyimprovedthetensilefracturestrengthofcopolyesters.ComprehensivecomparisonfoundthatthemodifiedPBSTcopolyest

7、erswithkaolinhasoptimalperformance,boththermo-dynamicperformance,andthebestadditiveamountiSlwt%.Aserisofaliphatic—aromaticPBSTcopolyesterwithdifferentqualitypercentageoffourthmonomer,respectively,O.25%,O.5%,0.75%,1.0%,1.2.5%,wereefficientlysynthesizedfromthestartingmaterialsofPTA,S

8、A,1,4-BDinthepresenceofTTi

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