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dc.contributor.authorChen, JLen_US
dc.contributor.authorHuang, HMen_US
dc.contributor.authorLi, MSen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:47:04Z-
dc.date.available2014-12-08T15:47:04Z-
dc.date.issued1999-01-03en_US
dc.identifier.issn0021-8995en_US
dc.identifier.urihttp://hdl.handle.net/11536/31584-
dc.description.abstractTransesterification has been investigated in poly(epsilon-caprolactone) (PCL)-epoxy blends. In the hot melt process, the hydroxyl on diglycidyl ether of bisphenol-il (DGEBA) monomers is too low to give a noticeable transesterification reaction. In the postcure process, model reactions reveal that the hydroxyls from a ring-opening reaction are able to react with the esters of PCL. In the meantime, the PCL molecular weight decrease and its distribution becomes broader. Nuclear magnetic resonance spectra reveal that fraction of the tertiary hydroxyls converts to secondary hydroxyls. In the cured DGEBA-3,3'-dimethylmethylene-di(cyclohexylamine)-PCL blend, a homogeneous morphology is achieved. PCL segments are grafted onto the epoxy network after postcuring and result in the lower T-g observed in the differential scanning calorimetry thermogram. A higher transesterification extent also results in broader transition peaks by dynamic mechanical analysis. (C) 1999 John Wiley & Sons, Inc.en_US
dc.language.isoen_USen_US
dc.subjectepoxyen_US
dc.subjectpoly(epsilon-caprolactone)en_US
dc.subjecttransesterificationen_US
dc.titleTransesterification in homogeneous poly(epsilon-caprolactone)-epoxy blendsen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF APPLIED POLYMER SCIENCEen_US
dc.citation.volume71en_US
dc.citation.issue1en_US
dc.citation.spage75en_US
dc.citation.epage82en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000077039300010-
dc.citation.woscount14-
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