HEAL DSpace

Catalyzed solid-state polyamidation

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dc.contributor.author Vouyiouka, SN en
dc.contributor.author Papaspyrides, CD en
dc.contributor.author Pfaendner, R en
dc.date.accessioned 2014-03-01T01:23:41Z
dc.date.available 2014-03-01T01:23:41Z
dc.date.issued 2006 en
dc.identifier.issn 1438-7492 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/17093
dc.subject Catalysts en
dc.subject Nylon 6,6 en
dc.subject Phosphorus-containing compounds en
dc.subject Polyamides en
dc.subject Solid-state polymerization en
dc.subject.classification Materials Science, Multidisciplinary en
dc.subject.classification Polymer Science en
dc.subject.other Catalysis en
dc.subject.other Catalyst activity en
dc.subject.other Chemical modification en
dc.subject.other Extruders en
dc.subject.other Phosphorus compounds en
dc.subject.other Polycondensation en
dc.subject.other Catalytic performance en
dc.subject.other Nylon 6,6 en
dc.subject.other Solid-state polymerization en
dc.subject.other Polyamides en
dc.title Catalyzed solid-state polyamidation en
heal.type journalArticle en
heal.identifier.primary 10.1002/mame.200600254 en
heal.identifier.secondary http://dx.doi.org/10.1002/mame.200600254 en
heal.language English en
heal.publicationDate 2006 en
heal.abstract The current study is focused on key experiments on catalyzed SSP, examining the effect of selected phosphonates on the overall process rate. Catalyst incorporation was achieved through melt blending in a single screw extruder, providing a suitable and homogenous starting material for the reaction in the solid phase. More specifically, the post-polycondensation runs were performed in a fixed bed reactor under flowing nitrogen at 160 and 200 °C. The additives used were found to catalyze the reaction in the solid phase, resulting even in tripling the solution relativeviscosity after 4 h of SSP, Differences in the catalytic performance of the added materials were observed and correlated to the catalysts properties and morphology. An indicative potential catalysis mechanism is suggested, in which reactivity enhancement through partial attachment of the phosphorus compounds on the polyamide chain is the key step. Finally, the kinetics of the process were examined based on a power-law rate expression, which was further modified so as to relate the apparent SSP rate constant with the phosphorus concentration. © 2006 WILEY-VCH Verlag GmbH & Co. KGaA. en
heal.publisher WILEY-V C H VERLAG GMBH en
heal.journalName Macromolecular Materials and Engineering en
dc.identifier.doi 10.1002/mame.200600254 en
dc.identifier.isi ISI:000243314400005 en
dc.identifier.volume 291 en
dc.identifier.issue 12 en
dc.identifier.spage 1503 en
dc.identifier.epage 1512 en


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