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Solubility of CO 2 in [1- n -butylthiolanium][Tf 2 N]+toluene mixtures: liquid–liquid phase split separation and modelling
Author(s) -
Roberto I. Canales,
Michael Lübben,
María GonzálezMiquel,
Joan F. Brennecke
Publication year - 2015
Publication title -
philosophical transactions of the royal society a mathematical physical and engineering sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.074
H-Index - 169
eISSN - 1471-2962
pISSN - 1364-503X
DOI - 10.1098/rsta.2015.0011
Subject(s) - ionic liquid , imide , solubility , toluene , phosphonium , ternary operation , chemistry , materials science , inorganic chemistry , organic chemistry , catalysis , computer science , programming language
Carbon dioxide has been shown to be an effective antisolvent gas for separating organic compounds from ionic liquids (ILs) by inducing a liquid–vapour to liquid–liquid–vapour transition. Using carbon dioxide, toluene can be separated from imidazolium, phosphonium and pyridinum cation-based ILs with the bis(trifluoromethylsulfonyl)imide anion, which is relatively hydrophobic and has a high toluene solubility. A new IL with relatively low viscosity is tested here for the same toluene separation process: 1-n -butylthiolanium bis(trifluoromethylsulfonyl)imide. Carbon dioxide solubility in binary and ternary systems containing toluene and 1-n -butylthiolanium bis(trifluoromethylsulfonyl)imide is measured at 298.15 and 313.15 K up to 7.4 MPa. Solubility behaviour in this IL is similar to imidazolium-based ILs with the same anion. However, phase split pressures are lower when 1-n -butylthiolanium bis (trifluoromethylsulfonyl)imide is used instead of 1-n -hexyl-3-methylimidazolium bis(trifluoromethylsu- lfonyl)imide at the same conditions of temperature and initial composition of toluene in the IL. Solubility data are modelled with the conductor-like screening model for real solvents combined with the Soave–Redlich–Kwong equation of state, which provides good qualitative results.

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