Partition coefficients of 51 organic compounds in two ionic liquids (IL), 1-ethyl-3-methylimidazolium dicyanamide and trimethylhexylammonium bis((trifluoromethyl)sulfonyl)amide, were measured using inverse gas chromatography from (322.5 to 352.5) K. These partition coefficients were converted into water-to-IL partition coefficients using the corresponding gas-to-water partition coefficients. Both sets of partition coefficients were analyzed using the Abraham solvation parameter model with cation-specific and anionspecific equation coefficients. The derived equations correlated the experimental gas-to-IL and water-to-IL partition coefficient data to within (0.12 and 0.14) log units, respectively.
In this work, (1)H and (31)P NMR spectroscopy were used to study the interactions between thiophene or benzene with three imidazolium based ionic liquids (ILs): 1-butyl-3-methylimidazolium tetrafluoroborate, 1,3-dimethylimidazolium methylphosphonate, and 1-butyl-3-methylimidazolium thiocyanate. NMR study indicates that solubility of thiophene or benzene in ionic liquid strongly depends on the structure of the ionic liquid. Structural organizations of such systems have been proposed. From these results, liquid-liquid equilibria (LLE) measurements of ternary mixtures containing benzene or thiophene with n-heptane and these ILs were carried out at 298.15 K in order to check the ability of these ILs to act as extractive solvents.
Activity coefficients at infinite dilution γ ∞ of organic compounds in the ionic liquid (IL) trihexyl(tetradecyl)phosphonium bis(trifluoromethylsulfonyl)imide were determined using inverse gas chromatography at three temperatures, T ) (302.45, 322.35, and 342.45) K. Linear free energy relationship (LFER) correlations have been obtained for describing the gas-to-IL and water-to-IL partition coefficients.
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