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Conformational motions in immiscible blends of polycarbonate and styrene-acrylonitrile copolymers

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dc.contributor.author Belloch, GP en
dc.contributor.author Sanchez, MS en
dc.contributor.author Ribelles, JLG en
dc.contributor.author Pradas, MM en
dc.contributor.author Duenas, JMM en
dc.contributor.author Pissis, P en
dc.date.accessioned 2014-03-01T01:14:28Z
dc.date.available 2014-03-01T01:14:28Z
dc.date.issued 1999 en
dc.identifier.issn 0032-3888 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/13092
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-0032627913&partnerID=40&md5=97902aeb2fd2e5db98e03688bbcdec74 en
dc.subject.classification Engineering, Chemical en
dc.subject.classification Polymer Science en
dc.subject.other Annealing en
dc.subject.other Chemical bonds en
dc.subject.other Copolymers en
dc.subject.other Dielectric relaxation en
dc.subject.other Ethanol en
dc.subject.other Glass transition en
dc.subject.other Molecular weight en
dc.subject.other Numerical methods en
dc.subject.other Oligomers en
dc.subject.other Phase composition en
dc.subject.other Polycarbonates en
dc.subject.other Precipitation (chemical) en
dc.subject.other Conformational motions en
dc.subject.other Polymer chains en
dc.subject.other Styrene acrylonitrile copolymers en
dc.subject.other Polymer blends en
dc.title Conformational motions in immiscible blends of polycarbonate and styrene-acrylonitrile copolymers en
heal.type journalArticle en
heal.language English en
heal.publicationDate 1999 en
heal.abstract Blends of commercial bisphenol-A-polycarbonate and styrene-acrylonitrile copolymers were prepared by precipitation in ethanol from the solution in methylene chloride in order to eliminate the low molecular weight substances contained in the commercial polymers, specially the oligomers contained in commercial SAN copolymers. Two glass transitions appear in the DSC thermograms of the blend at the same temperatures as in the pure components which, in principle, indicates that the blend consists of two phases formed by pure PC and pure SAN. In order to detect small changes in the glass transition process that could be indicative of different mobility of the polymer chains in the blend with respect to the pure polymers, blends of different compositions were subjected to different thermal treatments that included annealing at temperatures below both glass transitions, and then the DSC thermograms were recorded. A broadening in the peaks shown by the c(p)(T) curves measured on annealed samples in the zone of the PC transition is detected while no significant differences are shown by the glass transition of the SAN phase of the blend with respect to pure SAN copolymer. Dielectric relaxation experiments in the frequency domain (from 100 to 3.10(6)Hz) were carried out on the blends. The dielectric relaxation spectrum in the zone of the SAN main relaxation process was fitted with the stretched exponential equation showing no significant differences between the blends and the pure SAN copolymer. The region of the main relaxation process of PC was not analyzed due to the small polar activity of PC and the overlapping with the relaxation of the SAN phase. en
heal.publisher Soc Plast Eng, Brookfield, CT, United States en
heal.journalName Polymer Engineering and Science en
dc.identifier.isi ISI:000080246000008 en
dc.identifier.volume 39 en
dc.identifier.issue 4 en
dc.identifier.spage 688 en
dc.identifier.epage 698 en


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