Crystallization and unusual rheological behavior in poly(ethylene oxide)–clay nanocomposites
Type
ArticleKAUST Grant Number
KUS-C1-018-02Date
2011-05Permanent link to this record
http://hdl.handle.net/10754/597908
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We report a systematic study of the crystallization and rheological behavior of poly(ethylene oxide) (PEO)-clay nanocomposites. To that end a series of nanocomposites based on PEOs of different molecular weight (103 < MW < 105 g/mol) and clay surface modifier was synthesized and characterized. Incorporation of organoclays with polar (MMT-OH) or aromatic groups (MMT-Ar) suppresses the crystallization of polymer chains in low MW PEO, but does not significantly affect the crystallization of high MW matrices. In addition, the relative complex viscosity of the nanocomposites based on low MW PEO increases significantly, but the effect is less pronounced at higher MWs. The viscosity increases in the series MMT-Alk < MMT-OH < MMT-Ar. In contrast to the neat PEO which exhibits a monotonic decrease of viscosity with temperature, all nanocomposites show an increase after a certain temperature. This is the first report of such dramatic enhancements in the viscoelasticity of nanocomposites, which are reversible, are based on a simple polymer matrix and are true in a wide temperature range. © 2011 Elsevier Ltd. All rights reserved.Citation
Kelarakis A, Giannelis EP (2011) Crystallization and unusual rheological behavior in poly(ethylene oxide)–clay nanocomposites. Polymer 52: 2221–2227. Available: http://dx.doi.org/10.1016/j.polymer.2011.03.031.Sponsors
This material is based on work supported as part of the Energy Materials Center at Cornell, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Award Number DE-SC0001086. This publication is based on work supported in part by Award No. KUS-C1-018-02, made by King Abdullah University of Science and Technology (KAUST).Publisher
Elsevier BVJournal
Polymerae974a485f413a2113503eed53cd6c53
10.1016/j.polymer.2011.03.031