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dc.contributor.authorKuo, SWen_US
dc.contributor.authorHuang, WJen_US
dc.contributor.authorHuang, SBen_US
dc.contributor.authorKao, HCen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:40:01Z-
dc.date.available2014-12-08T15:40:01Z-
dc.date.issued2003-12-01en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.polymer.2003.10.007en_US
dc.identifier.urihttp://hdl.handle.net/11536/27344-
dc.description.abstractIn this paper, we report the preparation of in situ blends of metallocence polyethylene (mPE) with montmorillonite (clay). The polymerization activity of polyethylene decreases upon increasing the amount of the clay feed. The mPE nanocomposites still possess their original melting and crystallization temperatures, but the melting and crystallization enthalpies decrease upon increasing the clay content. In addition, the polymer interaction parameter between mPE and exfoliated clay sheets was calculated to be -0.204 based on a modified Kim-Bae equilibrium melting depression equation. All of the isothermal crystallization kinetics data fit well to the Avrami crystallization equation. We found that increasing the clay content results in a faster rate of crystallization, but pure mPE still crystallizes the fastest. Using a small amount of pretreated clay results in a more homogeneous and finer dispersion of the clay in the polymer matrix, as determined by wide-angle X-ray diffraction and transmission electron microscopy analyses. Both the values of T-1rho(H) in the solid-state NMR spectra of the fast and slow components show increment upon increasing the clay content, which indicates that either the mobile phase tends to increase its rigidity in the clay-containing system. (C) 2003 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectmetallocence polyethyleneen_US
dc.subjectclayen_US
dc.subjectnanocompositesen_US
dc.titleSyntheses and characterizations of in situ blended metallocence polyethylene/clay nanocompositesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.polymer.2003.10.007en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume44en_US
dc.citation.issue25en_US
dc.citation.spage7709en_US
dc.citation.epage7719en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000186550500017-
dc.citation.woscount50-
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