Phase equilibria of poly(ethylene-co-vinyl acetate) copolymers in subcritical and supercritical ethylene and ethylene-vinyl acetate mixtures

被引:38
作者
Folie, B
Gregg, C
Luft, G
Radosz, M
机构
[1] EXXON RES & ENGN CO, CORP RES, ANNANDALE, NJ 08801 USA
[2] TH DARMSTADT, INST CHEM TECHNOL, D-64287 DARMSTADT, GERMANY
[3] LOUISIANA STATE UNIV, DEPT CHEM ENGN, BATON ROUGE, LA 70803 USA
关键词
D O I
10.1016/0378-3812(95)02981-8
中图分类号
O414.1 [热力学];
学科分类号
摘要
Experimental high-pressure phase equilibrium data (cloud point and coexistence data) are reported for solutions of commercial poly(ethylene-co-vinyl acetate) samples in supercritical ethylene and ethylene-vinyl acetate (VA) mixtures, These data are correlated with an equation of state rooted in statistical associating fluid theory (SAFT). SAFT captures the effects of polymer MW, incorporated VA%, and free VA on the cloud point pressure, and on the size of the fluid-liquid miscibility gap, over a broad range of temperatures (50-250 degrees C) and polymer concentrations. Free VA is found to behave as a cosolvent (lowering the cloud point pressure), except at low temperatures (< 100 degrees C) and with low VA-containing copolymers, in which case free VA, if present in large excess (> 70 wt.%), behaves as a polar antisolvent due to favorable self-interactions among the free VA molecules, SAFT predicts a shift in the phase transition type, from upper-critical-solution-temperature (UCST), to upper-lower-critical-solution-temperature (U-LCST) with increasing flee VA in the monomer mixture.
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页码:11 / 37
页数:27
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