On the selection of optimum thermodynamic conditions for the GAS process

被引:21
作者
de la Fuente, JC
Shariati, A
Peters, CJ
机构
[1] Delft Univ Technol, Fac Appl Sci, Lab Phys Chem & Mol Thermodynam, NL-2628 BL Delft, Netherlands
[2] Univ Tecn Federico Santa Maria, Dept Proc Quim, Valparaiso, Chile
关键词
GAS process; volume expansion; phase behavior; thermodynamic modeling; equation of state;
D O I
10.1016/j.supflu.2004.01.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, the new definition of the relative molar volume change as recently proposed by de la Fuente Badilla et al. [J. Supercrit. Fluids 17 (2000) 13] has been further investigated. Simulation results show that, according to this new definition, each solvent shows a distinguished molar volume change behavior for a given anti-solvent. In addition, it is shown that the pressure, at which the curve of the relative molar volume change has a minimum, exactly coincides with the pressure at which almost all the solute precipitates in a very narrow pressure window. The results also indicate that the thermodynamically suitable operating temperature should be close, but below the critical temperature of the anti-solvent. Based on these findings, a thermodynamic strategy is proposed to select the proper combination sol vent-anti-solvent for a given solute and the optimum operating conditions as well. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 61
页数:7
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