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Rubber-toughening of polycarbonate-nylon blends

dc.citation.epage290en_US
dc.citation.spage279en_US
dc.citation.volume252en_US
dc.contributor.authorChang, FCen_US
dc.contributor.authorChou, DCen_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:02:56Z
dc.date.available2014-12-08T15:02:56Z
dc.date.issued1996en_US
dc.description.abstractIncompatible and brittle polymer blends of polycarbonate (PC) and nylon-6 [polyamide (PA)] have been compatibilized with high-molecular-weight bisphenol A epoxy resin and toughened by reactive and unreactive core-shell rubbers. The epoxy resin has proved to be an effective, reactive, in situ compatibilizer for the incompatible PC-PA blends. Rubber particles in the PC-PA blends can be controlled so as to be distributed in either PC, PA, or both phases. Unreactive methyl methacrylate-butadiene-styrene (MBS) rubber is more compatible with PC than with PA and tends to reside in the PC phase and near the PC-PA interface. Reactive MBS rubber containing maleic anhydride and methacrylic acid (MBS-MA) can react with nylon end groups, and the resulting nylon-linked rubber particles are retained within the nylon phase. Rubber distributed in the PC phase is more effective in toughening the PC-PA blends than that distributed in the nylon phase. Rubber-toughening of blends with PC as a matrix is more efficient than in blends with nylon as a matrix.en_US
dc.identifier.isbn0-8412-3151-6en_US
dc.identifier.issn0065-2393en_US
dc.identifier.journalTOUGHENED PLASTICS II: NOVEL APPROACHES IN SCIENCE AND ENGINEERINGen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/1542
dc.identifier.wosnumberWOS:A1996BG72Q00018
dc.language.isoen_USen_US
dc.titleRubber-toughening of polycarbonate-nylon blendsen_US
dc.typeArticle; Proceedings Paperen_US

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