Phase behavior of LCST and UCST solutions of branchy copolymers

experiment and SAFT modelling

Shean Jer Chen, Ioannis Economou, Maciej Radosz

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Phase boundaries for a series of poly(ethylene-propylene) copolymers having uniform structure but differing in molecular weight, from 800 to nearly 100,000, in various solvents are determined experimentally up to 200°C and 600 bar. Propylene, 1-butene, and 1-hexene are used as solvents. A free-volume sensitive LCST is found near the solvent critical point and an energy sensitive UCST is found away from the solvent critical point. The effect of supercritical ethylene on the phase behavior of these systems is investigated. Statistical Associating Fluid Theory (SAFT) is used to model the phase behavior of these systems. SAFT was chosen because the parameters for the polymers can be calculated from generalized correlations based on the polymer molecular weight. SAFT is able to correlate the experimental data accurately using only one binary interaction parameter that is polymer molecular weight dependent. In addition, calculations are shown using the polymer solution theory of Flory and Patterson.

Original languageEnglish
Pages (from-to)391-398
Number of pages8
JournalFluid Phase Equilibria
Volume83
Issue numberC
DOIs
Publication statusPublished - 1993
Externally publishedYes

Fingerprint

Phase behavior
copolymers
Copolymers
molecular weight
Polymers
Fluids
fluids
Molecular weight
polymers
propylene
Propylene
critical point
Ethylene
ethylene
Experiments
hexenes
Free volume
butenes
Phase boundaries
Polymer solutions

Keywords

  • equation of state
  • experiments
  • perturbation theory
  • polymer
  • supercritical fluid

ASJC Scopus subject areas

  • Fluid Flow and Transfer Processes
  • Physical and Theoretical Chemistry

Cite this

Phase behavior of LCST and UCST solutions of branchy copolymers : experiment and SAFT modelling. / Chen, Shean Jer; Economou, Ioannis; Radosz, Maciej.

In: Fluid Phase Equilibria, Vol. 83, No. C, 1993, p. 391-398.

Research output: Contribution to journalArticle

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