Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, MS | en_US |
dc.contributor.author | Su, YF | en_US |
dc.contributor.author | Ma, CCM | en_US |
dc.contributor.author | Chen, JL | en_US |
dc.contributor.author | Lu, MS | en_US |
dc.contributor.author | Chang, FC | en_US |
dc.date.accessioned | 2014-12-08T15:02:27Z | - |
dc.date.available | 2014-12-08T15:02:27Z | - |
dc.date.issued | 1996-08-01 | en_US |
dc.identifier.issn | 0032-3861 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/1126 | - |
dc.description.abstract | Infrared 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.iso | en_US | en_US |
dc.subject | epoxy | en_US |
dc.subject | blend | en_US |
dc.subject | polycarbonate | en_US |
dc.title | Transesterification and cyclization of polycarbonate-epoxy blends cured with anhydride | en_US |
dc.type | Article | en_US |
dc.identifier.journal | POLYMER | en_US |
dc.citation.volume | 37 | en_US |
dc.citation.issue | 17 | en_US |
dc.citation.spage | 3899 | en_US |
dc.citation.epage | 3905 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
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