完整後設資料紀錄
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dc.contributor.authorLin, MSen_US
dc.contributor.authorLee, STen_US
dc.date.accessioned2019-04-02T06:00:51Z-
dc.date.available2019-04-02T06:00:51Z-
dc.date.issued1997-01-01en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0032-3861(96)00484-3en_US
dc.identifier.urihttp://hdl.handle.net/11536/149417-
dc.description.abstractFully interpenetrating polymer networks (fully IPNs) based on diglycidyl ether of bisphenol A (DGEBA) and ethylene dimethacrylate (EDMA) were prepared using isophronediamine and benzoyl peroxide as curing agents. Semi-interpenetrating polymer networks (semi-IPNs) based on DGEBA and 2-hydroxyethyl methacrylate (HEMA) were also prepared using the same curing agents. The average activation energies of transition for both these IPNs were calculated from rheometric dynamic spectroscopy (r.d.s.) data, which indicated higher values for the fully IPNs than the corresponding semi-IPNs. The more acrylic the interpenetrating polymer network (both fully and semi-IPNs) contained the lower the activation energy of transition. Broadened tan 6 peaks were observed for compatible materials, implying an enhanced cracking energy absorption. RDS data also revealed a maximum half-width of tan 6 at 30% of EDMA for the fully IPNs and at 25% of HEMA for the semi-IPNs. Beyond these compositions, decreased impact resistance and lower tensile modulus and elongation values were observed for these materials, presumably because of microphase-separation. Copyright (C) 1996 Elsevier Science Ltd.en_US
dc.language.isoen_USen_US
dc.subjectmechanical behavioursen_US
dc.subjectfully IPNen_US
dc.subjectsemi-IPNen_US
dc.subjectimpact resistanceen_US
dc.titleMechanical behaviours of fully and semi-interpenetrating polymer networks based on epoxy and acrylicsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0032-3861(96)00484-3en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume38en_US
dc.citation.spage53en_US
dc.citation.epage58en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1997WB71600008en_US
dc.citation.woscount42en_US
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