Fluid Phase Equilibria | 2019

Phase equilibrium measurements and thermodynamic modeling of {CO2 + diethyl succinate + cosolvent} systems

 
 
 
 
 

Abstract


Abstract This work reports experimental phase equilibrium data for the binary systems {CO2(1)\xa0+\xa0diethyl succinate(2)} and {CO2(1)\xa0+\xa0ethyl acetate(2)}, and for the ternary systems {CO2(1)\xa0+\xa0diethyl succinate(2)\xa0+\xa0ethanol(3)} and {CO2(1)\xa0+\xa0diethyl succinate(2)\xa0+\xa0ethyl acetate(3)}. The experiments for the binary system {CO2(1)\xa0+\xa0diethyl succinate(2)} were carried out at temperatures ranging from 308\xa0K to 358\xa0K, and temperatures ranging from 303\xa0K to 343\xa0K for {CO2(1)\xa0+\xa0ethyl acetate(2)} as well as for all ternary systems. Only vapor-liquid equilibria were observed for all systems. The experimental measurements were carried out in a high-pressure variable-volume view cell containing a movable piston, which allows pressure control inside the cell. Binary and ternary systems were modeled with the Peng-Robinson cubic equation of state with the van der Waals quadratic mixing rule (vdW2). The presence of a cosolvent (ethanol and ethyl acetate) decreased the saturation pressures of either bubble or dew points compared to the binary system CO2\xa0+\xa0diethyl succinate, increasing the solubility of diethyl succinate in CO2.

Volume 502
Pages 112285
DOI 10.1016/J.FLUID.2019.112285
Language English
Journal Fluid Phase Equilibria

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