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dc.contributor.authorLin, MSen_US
dc.contributor.authorWang, MWen_US
dc.date.accessioned2014-12-08T15:45:59Z-
dc.date.available2014-12-08T15:45:59Z-
dc.date.issued1999-12-01en_US
dc.identifier.issn0959-8103en_US
dc.identifier.urihttp://hdl.handle.net/11536/30934-
dc.description.abstractInterpenetrating polymer networks (IPN) based on diglycidyl ether of bisphenol-A (DGEBA) and bishenol-A diacrylate (BADA) in weight ratios of 100/0, 50/50, and 0/100 were blended and were cured simultaneously by using benzoyl peroxide (BPO) and 4,4'-methylenedianiline (MDA) as curing agents. Kinetic study during IPN formation was carried out at 65, 70, 75 and 80 degrees C. Absorbance changes at 1623.3 cm(-1) and 914 cm(-1) relating to concentration changes of C=C and epoxide were monitored with Fourier-transform infrared spectroscopy (FTIR). The epoxide cure kinetic data revealed a combination of non-catalytic bimolecular reaction and a catalyzed termolecular reaction, while the C=C cure kinetic data fitted a first-order reaction. The calculated kinetic parameters indicated decreased rate constants and increased activation energies of the IPN compared with those of the individual components. Presumably, chain entanglements between the two networks provide a sterically hindered environment for the cure reactions and vitrification restrains the chain mobility, accounting for the kinetic parameters. (C) 1999 Society of Chemical Industry.en_US
dc.language.isoen_USen_US
dc.subjectIPNen_US
dc.subjectkineticsen_US
dc.subjectdecreased rate constantsen_US
dc.subjectincreased activation energyen_US
dc.titleKinetic study on epoxy bisphenol-A diacrylate IPN formationen_US
dc.typeArticleen_US
dc.identifier.journalPOLYMER INTERNATIONALen_US
dc.citation.volume48en_US
dc.citation.issue12en_US
dc.citation.spage1237en_US
dc.citation.epage1243en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000084033000008-
dc.citation.woscount9-
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