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dc.contributor.authorTseng, FPen_US
dc.contributor.authorChang, FCen_US
dc.contributor.authorLin, SFen_US
dc.contributor.authorLin, JJen_US
dc.date.accessioned2014-12-08T15:46:02Z-
dc.date.available2014-12-08T15:46:02Z-
dc.date.issued1999-11-28en_US
dc.identifier.issn0021-8995en_US
dc.identifier.urihttp://hdl.handle.net/11536/30957-
dc.identifier.urihttp://dx.doi.org/10.1002/(SICI)1097-4628(19991128)74:9<2196en_US
dc.description.abstractPhenol/dicyclopentadiene adducts were prepared from the BF3-catalyzed reaction of p-nonylphenol and dicyclopentadiene at molar ratios of 2 : 1 and 3 : 2. These dicyclopentadiene-derived novolac products contain tricyclodecane and multiple phenol functionalities. In curing with diglycidyl ether of bisphenol A, the polymer properties were compared with those cured with formaldehyde novolac or Jeffamine D-400 amine. When p-nonylphenol/dicyclopentadiene adducts were mixed with other commercially available curing agents such as Jeffamine D-400 amine, the tricyclodecane functionality was introduced into the resulting epoxy network. The flexibility of the cured resin was improved due to the presence of the tricyclodecane moiety in the polymer structure. (C) 1999 John Wiley & Sons, Inc.en_US
dc.language.isoen_USen_US
dc.subjectphenolen_US
dc.subjectdicyclopentadieneen_US
dc.subjectJeffamineen_US
dc.subjectepoxy curingen_US
dc.titlePreparation and epoxy curing of p-nonylphenol/dicyclopentadiene adductsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/(SICI)1097-4628(19991128)74:9<2196en_US
dc.identifier.journalJOURNAL OF APPLIED POLYMER SCIENCEen_US
dc.citation.volume74en_US
dc.citation.issue9en_US
dc.citation.spage2196en_US
dc.citation.epage2206en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000082931700009-
dc.citation.woscount7-
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