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Calculation of critical lines of hydrocarbon/water systems by extrapolating mixing rules fitted to subcritical equilibrium data

机译:通过外推适合亚临界平衡数据的混合规则,计算碳氢化合物/水系统的临界线

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The phase behavior of water/hydrocarbon mixtures in a wide range of pressures is important for various applications ranging from reservoir engineering to environmental engineering. In this work, mutual solubility and critical loci of hydrocarbon/water systems are calculated using the Peng-Robinson-Stryjek-Vera cubic equation of state with four mixing rules: (1) van der Waals mixing rules with one binary interaction parameter (vdW-1). (2) van der Waals mixing rules with asymmetric composition dependent binary interaction parameter (vdW-A), (3) Wong-Sandler mixing rules (WS) and (4) second-order modified Huron-Vidal mixing rules (MHV2). It was found that the parameters obtained from correlating liquid-liquid equilibria using different mixing rules would lead to prediction of completely different forms of critical behavior. Unusual branches of critical loci were found with WS and MHV2 mixing rules. Therefore, equation of states models must be used with extreme caution when applied for predicting phase behavior over wide ranges of temperatures and pressures. (C) 2004 Elsevier B.V. All rights reserved.
机译:水/烃混合物在很大压力范围内的相行为对于从油藏工程到环境工程的各种应用都很重要。在这项工作中,使用具有四个混合规则的Peng-Robinson-Stryjek-Vera立方状态方程,计算了烃/水系统的互溶度和临界位点:(1)具有一个二元相互作用参数(vdW- 1)。 (2)具有不对称成分相关的二元相互作用参数(vdW-A)的范德华混合规则,(3)Wong-Sandler混合规则(WS)和(4)二阶修改的Huron-Vidal混合规则(MHV2)。已经发现,使用不同的混合规则通过将液-液平衡相关联而获得的参数将导致预测完全不同形式的临界行为。使用WS和MHV2混合规则发现了关键基因座的异常分支。因此,当将状态方程模型用于在宽范围的温度和压力范围内预测相态时,必须格外谨慎。 (C)2004 Elsevier B.V.保留所有权利。

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