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dc.contributor.authorHuang, JMen_US
dc.contributor.authorChu, PPen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:45:36Z-
dc.date.available2014-12-08T15:45:36Z-
dc.date.issued2000-03-01en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0032-3861(99)00329-8en_US
dc.identifier.urihttp://hdl.handle.net/11536/30673-
dc.description.abstractConformational conversion and molecular dynamics of the amorphous poly(ethylene terephthalate) (PET) annealed above T-g were investigated by C-13 high-resolution solid-state NMR and differential scanning calorimetry (DSC). Rapid increase in the PET trans content and crystallinity were observed near the onset crystallization temperature (congruent to 120 degrees C). By comparing both changes in conformation and crystallinity during thermal annealing, we found that the trans conformer increases continuously while the degree of crystallinity levels off during the later stage of annealing. The H-1 spin-lattice relaxation time in the rotating frame (T-1 rho(H)) correlates linearly with PET crystallinity but less well with the trans content. A three-domain model containing crystalline (all trans), constrained noncrystalline (trans rich) and amorphous (gauche rich) phases satisfactorily explains the relationship among the PET conformation, crystallinity and annealing conditions. This study complements the prior study of molecular motion by T-1 rho(C), and illustrates the importance of the trans conformer to induce PET crystallization. (C) 1999 Elsevier Science Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectpoly(ethylene terephthalate)en_US
dc.subjectsolid-state NMRen_US
dc.subjectcrystallinityen_US
dc.titleConformational changes and molecular motion of poly(ethylene terephthalate) annealed above glass transition temperatureen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0032-3861(99)00329-8en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume41en_US
dc.citation.issue5en_US
dc.citation.spage1741en_US
dc.citation.epage1748en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000084608400011-
dc.citation.woscount38-
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