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Molecular dynamics in nanostructured polyimide-silica hybrid materials and their thermal stability

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dc.contributor.author Bershtein, VA en
dc.contributor.author Egorova, LM en
dc.contributor.author Yakushev, PN en
dc.contributor.author Pissis, P en
dc.contributor.author Sysel, P en
dc.contributor.author Brozova, L en
dc.date.accessioned 2014-03-01T01:18:04Z
dc.date.available 2014-03-01T01:18:04Z
dc.date.issued 2002 en
dc.identifier.issn 0887-6266 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/14779
dc.subject nanocomposites en
dc.subject polyimides en
dc.subject molecular dynamics en
dc.subject glass transition en
dc.subject thermal properties en
dc.subject.classification Polymer Science en
dc.subject.other SOL-GEL PROCESS en
dc.subject.other CREEP RATE SPECTROSCOPY en
dc.subject.other GLASS-TRANSITION en
dc.subject.other LASER INTERFEROMETER en
dc.subject.other POLYMER HYBRIDS en
dc.subject.other LIQUIDS en
dc.subject.other RELAXATION en
dc.subject.other FILMS en
dc.subject.other POLYSTYRENE en
dc.subject.other MEMBRANES en
dc.title Molecular dynamics in nanostructured polyimide-silica hybrid materials and their thermal stability en
heal.type journalArticle en
heal.identifier.primary 10.1002/polb.10162 en
heal.identifier.secondary http://dx.doi.org/10.1002/polb.10162 en
heal.language English en
heal.publicationDate 2002 en
heal.abstract Molecular motion and thermal stability in two series of nanophase-separated polyimide-silica (PI-SiO2) hybrid materials with chemically bound components were studied. The hybrids were synthesized from p-aminophenyltrimethoxysilane-terminated poly(amic acid)s as PI precursors and tetramethoxysilane as a silica precursor via a sol-gel process. The hybrids differed in their PI chemical structure and chain length (number-average molecular weight = 5.000, 7.500, or 10.000) and in their SiO2 content, which ranged from 0 to 50 wt %. Differential scanning calorimetry, laser-interferometric creep rate spectroscopy, and thermally stimulated depolarization current techniques were used for studying the dynamics from 100 to 650 K and from 10(-3) to 10(-2) Hz. Comparative thermogravimetric measurements were also carried out from 300 to 900 K. Silica nano- or submicrodomains that formed affected PI dynamics in two opposite directions. Because of the loosening of the molecular packing of PI chains confined to nanometer-scale spaces between silica constraints, an enhancement of small-scale motion, mostly at temperatures below the beta-relaxation region, occurred. However, a partial or total suppression of segmental motion could be observed above the beta-relaxation temperature, drastically so for the shortest PI chains at elevated silica contents and within or close to the glass-transition range, because of the covalent anchoring of chain ends to silica domains. Large changes in thermal stability, including a 2.5-fold increase in the apparent activation energy of degradation, were observed in the hybrids studied. A greater than 100 degreesC rise in long-term thermal stability could be predicted for some hybrids with respect to pure PI. (C) 2002 Wiley Periodicals, Inc. en
heal.publisher JOHN WILEY & SONS INC en
heal.journalName JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS en
dc.identifier.doi 10.1002/polb.10162 en
dc.identifier.isi ISI:000175073800014 en
dc.identifier.volume 40 en
dc.identifier.issue 10 en
dc.identifier.spage 1056 en
dc.identifier.epage 1069 en


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