Modeling pVT Properties and Vapor-Liquid Equilibrium of Ionic Liquids Using Cubic-plus-association Equation of State

被引:0
作者
Ma Jun
Li Jinlong
Fan Dongfu
Peng Changjun [1 ]
Liu Honglai
Hu Ying
机构
[1] E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
cubic-plus-association; equation of state; ionic liquids; vapor-liquid equilibrium; EXTENDED PRESSURE RANGE; THERMODYNAMIC PROPERTIES; BINARY-SYSTEMS; ACTIVITY-COEFFICIENTS; 1-BUTYL-3-METHYLIMIDAZOLIUM HEXAFLUOROPHOSPHATE; SOLUBILITY BEHAVIOR; EXCESS-ENTHALPIES; PHASE-BEHAVIOR; CATION-ANION; N-ALCOHOLS;
D O I
暂无
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Combining Peng-Robinson (PR) equation of state (EoS) with an association model derived from shield-sticky method (SSM) by Liu et al., a new cubic-plus-association (CPA) EoS is proposed to describe the thermodynamic properties of pure ionic liquids (ILs) and their mixtures. The new molecular parameters for 25 ILs are obtained by fitting the experimental density data over a wide temperature and pressure range, and the overall average deviation is 0.22%. The model parameter b for homologous ILs shows a good linear relationship with their molecular mass, so the number of model parameters is reduced effectively. Using one temperature-independent binary adjustable parameter k(ij), satisfactory correlations of vapor-liquid equilibria (VLE) for binary mixtures of ILs + non-associating solvents and + associating solvents are obtained with the overall average deviation of vapor pressure 2.91% and 7.01%, respectively. In addition, VLE results for ILs + non-associating mixtures from CPA, lattice-fluid (LF) and square-well chain fluids with variable range (SWCF-VR) EoSs are compared.
引用
收藏
页码:1009 / 1016
页数:8
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