Prediction of the solubility and gas-liquid equilibria for gas-water and light hydrocarbon-water systems at high temperatures and pressures with a group contribution equation of state

被引:35
作者
Li, JD
Vanderbeken, I
Ye, SY
Carrier, H
Xans, P
机构
[1] UNIV PAU & PAYS ADOUR,LAB HAUTE PRESS,F-64000 PAU,FRANCE
[2] TSING HUA UNIV,DEPT CHEM ENGN,BEIJING 100084,PEOPLES R CHINA
关键词
theory; vapour-liquid equilibria; equation of state; excess function; method of calculation; activity coefficient; MODIFIED UNIFAC MODEL; PSRK;
D O I
10.1016/S0378-3812(96)03234-7
中图分类号
O414.1 [热力学];
学科分类号
摘要
A group contribution equation of state has been proposed. The model is based on the Weidlich-Gmehling modified UNIFAC and Soave-Redlich-Kwong equation of state, in which the modified Huron-Vidal excess Gibbs free energy mixing rule is used, the residual term of the modified UNIFAC is changed a little and the combinatorial term is improved. Nine interaction parameters between gas groups CO2, CO, N-2, H-2, H2S, CH4, C2H6, C3H8, C4H10 and water are fitted. The model parameters have been used to predict solubility and gas-liquid equilibria for seven gas-water, and thirty-nine light hydrocarbon-water data sets in large temperature and pressure ranges (278-637 K, 1-1972 bar). The predicted results are in good agreement with the experiments, which makes it possible that the real phase behavior at high temperatures and pressures for gas-water and light hydrocarbon-water systems which are of interest to petroleum and natural gas exploitation industries, can be predicted reliably. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:107 / 118
页数:12
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