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dc.contributor.authorKuo, SWen_US
dc.contributor.authorHuang, WJen_US
dc.contributor.authorHuang, CFen_US
dc.contributor.authorChan, SCen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:39:01Z-
dc.date.available2014-12-08T15:39:01Z-
dc.date.issued2004-06-01en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma035417een_US
dc.identifier.urihttp://hdl.handle.net/11536/26710-
dc.description.abstractThe binary poly(acetoxystyrene)/poly(ethylene oxide) (PAS/PEO) blend system is fully miscible, as evidenced by a single glass transition temperature over a full range of compositions when analyzed by differential scanning calorimetry analysis, as a result of weak C-(HO)-O-... hydrogen-bonding interactions between the carbonyl groups of PAS and the methylene groups of PEO. One- and two-dimensional correlation spectroscopies provide positive evidence for this specific interaction between the two polymers. In addition, a negative polymer-polymer interaction parameter "chi(12)" was calculated using the Flory-Huggins equation based on the melting depression of PEO. The presence of an amorphous PAS phase results in a reduction in the spherulite growth rate of PEO. Both the values of nucleation constant and the surface free energy of chain folding of PEO decrease with increasing PAS content, which indicates that the crystallization ability of PEO increases correspondingly.en_US
dc.language.isoen_USen_US
dc.titleMiscibility, specific interactions, and spherulite growth rates of binary poly(acetoxystyrene)/poly(ethylene oxide) blendsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma035417een_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume37en_US
dc.citation.issue11en_US
dc.citation.spage4164en_US
dc.citation.epage4173en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000221688600033-
dc.citation.woscount35-
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