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Glass transition and molecular dynamics in poly(dimethylsiloxane)/silica nanocomposites

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dc.contributor.author Fragiadakis, D en
dc.contributor.author Pissis, P en
dc.contributor.author Bokobza, L en
dc.date.accessioned 2014-03-01T01:22:26Z
dc.date.available 2014-03-01T01:22:26Z
dc.date.issued 2005 en
dc.identifier.issn 0032-3861 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/16572
dc.subject Cooperativity en
dc.subject Glass transition en
dc.subject Nanocomposites en
dc.subject.classification Polymer Science en
dc.subject.other Crystallization en
dc.subject.other Dielectric relaxation en
dc.subject.other Differential scanning calorimetry en
dc.subject.other Electric currents en
dc.subject.other Glass transition en
dc.subject.other Molecular dynamics en
dc.subject.other Nanostructured materials en
dc.subject.other Natural frequencies en
dc.subject.other Surface chemistry en
dc.subject.other Synthesis (chemical) en
dc.subject.other Broadband dielectric relaxation spectroscopy en
dc.subject.other Depolarization currents en
dc.subject.other Filler interface en
dc.subject.other Poly(dimethylsiloxane) en
dc.subject.other Silica en
dc.subject.other polymer en
dc.title Glass transition and molecular dynamics in poly(dimethylsiloxane)/silica nanocomposites en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.polymer.2005.05.080 en
heal.identifier.secondary http://dx.doi.org/10.1016/j.polymer.2005.05.080 en
heal.language English en
heal.publicationDate 2005 en
heal.abstract The molecular dynamics of a series of poly(dimethylsiloxane) networks filled with silica nanoparticles synthesized in situ was investigated using thermally stimulated depolarization currents, broadband dielectric relaxation spectroscopy and differential scanning calorimetry. The techniques used cover together a broad frequency range (10(-3)-10(9) Hz), thus allowing to gain a more complete understanding of the effects of the nanoparticles on the chain dynamics. In addition to the a relaxation associated with the glass transition of the polymer matrix, we observe in dielectric measurements a slower a relaxation which is assigned to polymer chains close to the polymer/filler interface whose mobility is restricted due to interactions with the filler surface. The thickness of the interfacial layer is estimated to be about 2.1-2.4 nm. Differential scanning calorimetry shows a change in the shape of the glass transition step, as well as a decrease in both the degree of crystallinity and the crystallization rate by the addition of silica. (c) 2005 Elsevier Ltd. All rights reserved. en
heal.publisher ELSEVIER SCI LTD en
heal.journalName Polymer en
dc.identifier.doi 10.1016/j.polymer.2005.05.080 en
dc.identifier.isi ISI:000230714200020 en
dc.identifier.volume 46 en
dc.identifier.issue 16 en
dc.identifier.spage 6001 en
dc.identifier.epage 6008 en


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