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The kinetics of transesterification in blends of liquid crystalline copolyester and polycarbonate

dc.citation.epage727en_US
dc.citation.issue3en_US
dc.citation.spage717en_US
dc.citation.volume40en_US
dc.citation.woscount11
dc.contributor.authorHo, JCen_US
dc.contributor.authorWei, KHen_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.date.accessioned2014-12-08T15:46:55Z
dc.date.available2014-12-08T15:46:55Z
dc.date.issued1999-02-01en_US
dc.description.abstractThe kinetics of transesterification in blends of thermotropic copoly(oxybenzoate-ethylene terephthalate) and polycarbonate at melt state were analysed quantitatively with C-13 nuclear magnetic resonance, and were then modelled by a phenomenological equation. It was found that the activation energy for the transesterification reaction between the poly(oxybenzoate) segment in copoly(oxybenzoate-ethylene terephthalate) and polycarbonate was more than twice that for the transesterification reaction between the poly(ethylene terephthalate) segment and polycarbonate (i.e. 94.6 versus 41.8 kcal/mol). This is probably due to the stronger chemical bond in oxybenzoate-oxybenzoate that in ethylene-terephthalate. Additionally, owing to the rigid-rod nature of the poly(oxybenzoate) segment, the frequency factor in the transesterification reaction in poly(oxybenzoate) segment and polycarbonate is much higher than that in poly(ethylene terephthalate) segment and polycarbonate (i.e. 10(36) versus 10(14) min(-1)). (C) 1998 Elsevier Science Ltd. All rights reserved.en_US
dc.identifier.issn0032-3861en_US
dc.identifier.journalPOLYMERen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/31533
dc.identifier.wosnumberWOS:000076800000020
dc.language.isoen_USen_US
dc.subjectthermotropic copolymers blendsen_US
dc.subjectkineticsen_US
dc.subjecttransesterificationen_US
dc.titleThe kinetics of transesterification in blends of liquid crystalline copolyester and polycarbonateen_US
dc.typeArticleen_US

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