Vapour?Liquid Equilibria in the Polystyrene + Toluene System at Higher Concentrations of Solvent

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985858%3A_____%2F15%3A00444044" target="_blank" >RIV/67985858:_____/15:00444044 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.15255/CABEQ.2015.2183" target="_blank" >http://dx.doi.org/10.15255/CABEQ.2015.2183</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.15255/CABEQ.2015.2183" target="_blank" >10.15255/CABEQ.2015.2183</a>

Result language
angličtina
Original language name
Vapour?Liquid Equilibria in the Polystyrene + Toluene System at Higher Concentrations of Solvent
Original language description
Vapour?liquid equilibria (VLE) were determined in the polystyrene + toluene system under isothermal conditions at 363.15, 373.15, and 383.15 K using an improved all-glass microebulliometer with circulation of the liquid phase for the dynamic measurementof total pressure over liquid mixtures. The experimental data were correlated using the UNIQUAC-free volume model. Additionally, the applicability of three known predictive models was tested. It was found that both the GC-Flory equation of state and theUNIFAC-vdW-FV model provide better prediction of VLE than the Entropic-FV model, which very slightly underestimates the experimental data for the system studied.
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CF - Physical chemistry and theoretical chemistry
OECD FORD branch
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Project
<a href="/en/project/GA15-19542S" target="_blank" >GA15-19542S: Thermodynamics of polymer solutions: experiments meet theory and vice versa</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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