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dc.contributor.authorKuo, SWen_US
dc.contributor.authorHuang, CFen_US
dc.contributor.authorTung, PHen_US
dc.contributor.authorHuang, WJen_US
dc.contributor.authorHuang, JMen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:18:12Z-
dc.date.available2014-12-08T15:18:12Z-
dc.date.issued2005-10-24en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.polymer.2005.07.044en_US
dc.identifier.urihttp://hdl.handle.net/11536/13157-
dc.description.abstractWe have synthesized a series of block copolymers of poly(2,6-dimethyl- 1,4-phenylene oxide) and polystyrene (PPO-b-PS copolymer) by atom transfer radical polymerization. The PS content in these copolymer systems was determined by using infrared spectroscopy, thermal gravimetric analysis, and solution and solid-state NMR spectroscopy; good correlations exist between these characterization methods. DSC analyses indicated that the PPO-b-PS copolymers have higher glass transition temperatures than do their corresponding PPO/PS blends. Our FTIR and solid-state NMR spectroscopic analyses suggest that the PPO-b-PS copolymers possess stronger specific interactions that are responsible for the observed relatively higher values of T-g. We found one single dynamic relaxation from the dynamic mechanical analysis, which implies dynamic homogeneity exists in the PPO-b-PS copolymer; this result is consistent with the one single proton spin-lattice relaxation time observed in the rotating frame [T-1 rho(H)] during solid state NMR spectroscopic analysis. In addition, the 2D FTIR spectroscopy reveals evidence for the stronger interactions between segments of PPO and PS through the formation of pi-cation complexes. (c) 2005 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectATRPen_US
dc.subjectblock copolymeren_US
dc.subjectspecific interactionsen_US
dc.titleSynthesis, thermal properties, and specific interactions of high T-g increase in poly(2,6-dimethyl-1,4-phenylene oxide)-block-polystyrene copolymersen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.polymer.2005.07.044en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume46en_US
dc.citation.issue22en_US
dc.citation.spage9348en_US
dc.citation.epage9361en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000232642300014-
dc.citation.woscount26-
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