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Polyamide solid state polymerization: Evaluation of pertinent kinetic models

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dc.contributor.author Vouyiouka, SN en
dc.contributor.author Papaspyrides, CD en
dc.contributor.author Weber, J en
dc.contributor.author Marks, D en
dc.date.accessioned 2014-03-01T01:22:57Z
dc.date.available 2014-03-01T01:22:57Z
dc.date.issued 2005 en
dc.identifier.issn 0021-8995 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/16736
dc.subject Activation energy en
dc.subject Kinetics (polym.) en
dc.subject Nylon en
dc.subject Solid-state polymerization en
dc.subject.classification Polymer Science en
dc.subject.other Kinetics (polym.) en
dc.subject.other Melt polymerization en
dc.subject.other Semicrystalline polymers en
dc.subject.other Solid-state polymerization en
dc.subject.other Activation energy en
dc.subject.other Chemical activation en
dc.subject.other Concentration (process) en
dc.subject.other Diffusion en
dc.subject.other Molecular weight en
dc.subject.other Polyethylene terephthalates en
dc.subject.other Rate constants en
dc.subject.other Resins en
dc.subject.other Vacuum en
dc.subject.other Polymerization en
dc.subject.other polymer en
dc.title Polyamide solid state polymerization: Evaluation of pertinent kinetic models en
heal.type journalArticle en
heal.identifier.primary 10.1002/app.21811 en
heal.identifier.secondary http://dx.doi.org/10.1002/app.21811 en
heal.language English en
heal.publicationDate 2005 en
heal.abstract Nylon 6,6 resins, in the form of pellets, were solid state polymerized in the temperature range of 160-200 degrees C in a fixed-bed reactor under flowing nitrogen for times of 0-4 h. The kinetics of the solid state polymerization (SSP) of nylon 6,6 were examined by the evaluation of pertinent rate expressions and the selection of the most suitable one for describing the apparent overall process. The Flory-theory-based kinetic models were the most effective both for this study's data and for data previously published on SSP of different polyamides. Accordingly, SSP rate constants and activation energies were derived, and process parameters, such as the temperature and time, were investigated. (c) 2005 Wiley Periodicals, Inc. en
heal.publisher JOHN WILEY & SONS INC en
heal.journalName Journal of Applied Polymer Science en
dc.identifier.doi 10.1002/app.21811 en
dc.identifier.isi ISI:000229386800030 en
dc.identifier.volume 97 en
dc.identifier.issue 2 en
dc.identifier.spage 671 en
dc.identifier.epage 681 en


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