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Journal ArticleDOI

High-pressure vapor-liquid equilibrium with a UNIFAC-based equation of state

Søren Dahl, +1 more
- 01 Dec 1990 - 
- Vol. 36, Iss: 12, pp 1829-1836
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TLDR
In this paper, the ability of the mixing rules proposed by Michelsen to predict high-pressure phase equilibrium, when used in combination with the parameter table of modified UNIFAC, was investigated.
Abstract
Recent procedures developed by Heidemann (1990) and by Michelsen (1990a, b) enable us to formally incorporate excess Gibbs energy model parameters into a fully consistent equation of state, cith accurate reproduction of the behavior of the excess Gibbs energy model at atmospheric pressure. This paper investigates the ability of the mixing rules proposed by Michelsen to predict high-pressure phase equilibrium, when used in combination with the parameter table of modified UNIFAC. Considering that a group contribution method is used for the excess Gibbs energy and that model parameters are extrapolated over a 200 K temperature interval, quite satisfactory results are obtained for the mixtures investigated.

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Isothermal Vapor–Liquid Equilibrium of the Binary Mixture Difluoromethane (R32) + Octafluoropropane (R218) at Temperatures from 253.150 to 283.150 K

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