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CORRELATION AND PREDICTION OF HENRY CONSTANTS FOR LIQUIDS AND GASES IN 5 INDUSTRIALLY IMPORTANT POLYMERS USING A CS-TYPE CORRELATION-BASED ON THE VAN-DER-WAALS-EQUATION OF STATE - COMPARISON WITH OTHER PREDICTIVE MODELS

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dc.contributor.author BITHAS, S en
dc.contributor.author KONTOGEORGIS, GM en
dc.contributor.author KALOSPIROS, N en
dc.contributor.author FREDENSLUND, A en
dc.contributor.author TASSIOS, DP en
dc.date.accessioned 2014-03-01T01:43:50Z
dc.date.available 2014-03-01T01:43:50Z
dc.date.issued 1995 en
dc.identifier.issn 0378-3812 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/24221
dc.subject THEORY en
dc.subject APPLICATION en
dc.subject EQUATION OF STATE en
dc.subject CUBIC en
dc.subject ACTIVITY COEFFICIENT MODELS en
dc.subject POLYMER SOLUTIONS en
dc.subject HENRY CONSTANTS en
dc.subject CORRESPONDING STATES en
dc.subject.classification Thermodynamics en
dc.subject.classification Chemistry, Physical en
dc.subject.classification Engineering, Chemical en
dc.subject.other HARD-CHAIN THEORY en
dc.subject.other UNIFAC-FV MODEL en
dc.subject.other MOLTEN POLYMERS en
dc.subject.other THERMODYNAMIC PROPERTIES en
dc.subject.other SOLUBILITY PARAMETERS en
dc.subject.other POLY(ETHYLENE OXIDE) en
dc.subject.other SOLVENT INTERACTIONS en
dc.subject.other POLY(DIMETHYLSILOXANE) SOLUTIONS en
dc.subject.other POLYVINYL ACETATE) en
dc.subject.other INFINITE-DILUTION en
dc.title CORRELATION AND PREDICTION OF HENRY CONSTANTS FOR LIQUIDS AND GASES IN 5 INDUSTRIALLY IMPORTANT POLYMERS USING A CS-TYPE CORRELATION-BASED ON THE VAN-DER-WAALS-EQUATION OF STATE - COMPARISON WITH OTHER PREDICTIVE MODELS en
heal.type journalArticle en
heal.language English en
heal.publicationDate 1995 en
heal.abstract A simple two-parameter corresponding states-type method for the prediction of Henry constants of gases and liquid solvents in polymer solutions recently presented in the literature is thoroughly evaluated here and compared with the predictions of other models used for polymers. The corresponding states-type method is based on the van der Waals equation of state which has been recently extended to mixtures including polymers. Results are presented for systems containing five polymers in a variety of gases and nonpolar and polar liquid solutes. It is shown that agreement between experimental and calculated Henry constants is, in most cases, quite good and that the estimations with the new method compare favorably with the UNIFAC-FV and Entropic-FV activity coefficient models, the GC-Flory liquid-phase equation of state while they are somewhat better than the Group Contribution Lattice-Fluid (GCLF) equation of state. The proposed method is currently limited to five polymers but it is applicable to supercritical solvents, where the two activity coefficient models and the GC-Flory equation of state cannot be used. en
heal.publisher ELSEVIER SCIENCE BV en
heal.journalName FLUID PHASE EQUILIBRIA en
dc.identifier.isi ISI:A1995TK19500006 en
dc.identifier.volume 113 en
dc.identifier.issue 1-2 en
dc.identifier.spage 79 en
dc.identifier.epage 102 en


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