文摘
The solubilities of C2H4 and CO2 and the interactions of polar and nonpolar solutes with the novel ionic liquids(ILs) 1-butyronitrile-3-methylimidazolium bis(trifluoromethylsulfonyl) imidate (CpMIm[NTf2]), 1-butyronitrile-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl) imidate (CpMMIm[NTf2]), 1-butyronitrile-3-methylimidazolium dicyanamide (CpMIm[N(CN)2]), 1-butyronitrile-2,3-dimethylimidazolium dicyanamide (CpMMIm[N(CN)2]), 1-butyl-3-methylimidazolium palmitate (BMIm[n-C16H33COO]), and 1-butyl-3-methylimidazoliumstearate (BMIm[n-C18H35COO]) were studied by gas chromatography at infinite dilution at T = (303.15, 313.15,323.15, and 333.15) K. Henry's law constant kH of C2H4 and CO2 gas, infinite dilution activity coefficient ,molar enthalpies of solution solH, and partial molar excess enthalpies of solution HE and of Gibbs energiesGE were determined for polar and nonpolar solutes in these novel ILs. Compared with the 1,3-dialkylimidazoliumILs, cyano functional group substitution on the alkyl chain results in a remarkable decrease of the interactions ofhydrocarbons. BMIm[n-C16H31OO] and BMIm[n-C18H35OO] demonstrate strong solubilization for both polar andnonpolar solutes. Straight lines of ln Vg versus 1/T and ln versus 1/T were obtained for the majority of solutesin the temperature range. BMIm[NTf2] and 1-octyl-3-methylimidazolium tetrafluoroborate (OMIm[BF4]) showmuch better solubility for thiophene and are better solvents for the separations of thiophene from hydrocarbons.