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dc.contributor.authorLi, MSen_US
dc.contributor.authorSu, YFen_US
dc.contributor.authorMa, CCMen_US
dc.contributor.authorChen, JLen_US
dc.contributor.authorLu, MSen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2019-04-02T05:58:32Z-
dc.date.available2019-04-02T05:58:32Z-
dc.date.issued1996-08-01en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/0032-3861(96)00215-7en_US
dc.identifier.urihttp://hdl.handle.net/11536/149285-
dc.description.abstractInfrared spectra have been investigated to study the curing mechanisms of polycarbonate-epoxy blends using anhydride as a hardener catalysed by tertiary amine. Due to a significant difference in the reaction, curing reactions of the system can be considered as two sequential stages: (1) an anionic alternating copolymerization of cyclic anhydride and epoxy resin, and (2) a homopolymerization of oxirane initiated by a quaternary ammonium salt zwitter ion. The transesterification/cyclization of carbonate groups proceeds in the later stage if the oxirane is still available. Degrees of transesterification/cyclization and homopolymerization are higher when a higher epoxy/anhydride ratio is used. This study positively confirms the mechanism of transesterification/cyclization proceeding through a zwitter ion. The zwitter ion is formed from epoxide and tertiary amine, which attacks the carbonate group. Copyright (C) 1996 Elsevier Science Ltd.en_US
dc.language.isoen_USen_US
dc.subjectepoxyen_US
dc.subjectblenden_US
dc.subjectpolycarbonateen_US
dc.titleTransesterification and cyclization of polycarbonate-epoxy blends cured with anhydrideen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/0032-3861(96)00215-7en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume37en_US
dc.citation.spage3899en_US
dc.citation.epage3905en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1996VD68600015en_US
dc.citation.woscount4en_US
Appears in Collections:Articles