Simultaneous prediction of the critical and sub-critical phase behavior in mixtures using equation of state I. Carbon dioxide-alkanols

被引:74
作者
Polishuk, I
Wisniak, J
Segura, H
机构
[1] Ben Gurion Univ Negev, Dept Chem Engn, IL-84105 Beer Sheva, Israel
[2] Univ Concepcion, Dept Chem Engn, Concepcion, Chile
基金
以色列科学基金会;
关键词
phase equilibria; supercritical fluid; carbon dioxide; alkanols; parameter identification; equation of state;
D O I
10.1016/S0009-2509(01)00307-4
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The present study is a step towards solving the problem of predicting the properties of a mixture in the entire PTx range, without resource to experimental data. Vapor-liquid phase equilibria and liquid-liquid equilibria are shown to be closely related. A novel semi-predictive approach (SPA) is introduced. It involves estimation of the binary adjustable parameters for a certain member of a homologous series using the Quantitative Global Phase Diagram method, and their implementation for predicting the data of other homologs. This approach has been combined with the equations of state (EOSs) of Peng-Robinson, Trebble-Bishnoi-Salim, and a four-parameter EOS (C4EOS), as described by Polishuk et al. (Chem. Eng. Sci. 55 (2000) 5705) for predicting data of carbon dioxide-alkanols. It is demonstrated that different isomeric configurations of alkanols do not affect the reliability of SPA. The predicted results exhibit the behavior characteristic for many series of alkanols, however, they are not accurate for carbon dioxide-methanol because of weak chemical interactions present in this system. C4EOS is more reliable predicting the topology of phase behavior, the critical, and the bubble-point lines. However, it is less exact for predicting the gas phase composition. The available experimental and theoretical results for carbon dioxide-alkanols are reviewed. The predictions of SPA usually exhibit a significant advantage over other methods that do not predict but correlate the data. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:6485 / 6510
页数:26
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