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dc.contributor.authorKuo, SWen_US
dc.contributor.authorLiu, WPen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:40:38Z-
dc.date.available2014-12-08T15:40:38Z-
dc.date.issued2003-07-15en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma0341824en_US
dc.identifier.urihttp://hdl.handle.net/11536/27713-
dc.description.abstractA series of poly(vinylphenol-co-acetoxystyrene) (PVPh-co-PAS) copolymers were prepared by partial hydrolyses of poly(acetoxystyrene) (PAS) in acidic and basic solutions. Higher glass transition temperature, higher fraction of hydrogen-bonded carbonyl group, and higher interassociation equilibrium constant were observed for copolymers with same composition prepared from the acidic hydrolysis than from the basic hydrolysis because the sequence distribution of the former is relatively more random than the latter. Infrared spectra provide positive evidence in terms of sequence distribution, glass transition temperature, and hydrogen-bonding strength in poly(vinylphenol-co-acetoxystyrene) by prepared these two hydrolysis methods.en_US
dc.language.isoen_USen_US
dc.titleEffect of hydrolysis on the strength of hydrogen bonds and T-g of poly(vinylphenol-co-acetoxystyrene)en_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma0341824en_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume36en_US
dc.citation.issue14en_US
dc.citation.spage5165en_US
dc.citation.epage5173en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000184120900022-
dc.citation.woscount12-
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