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Fluid Phase Equilibria, Vol.301, No.2, 257-266, 2011
Correlations for describing gas-to-ionic liquid partitioning at 323 K based on ion-specific equation coefficient and group contribution versions of the Abraham model
Chromatographic retention measurements were measured for a wide range of solutes on 1-methy1-3-ethylimidazolium tris(pentafluoroethyl)trifluorophosphate, ([MEIm](+)[FAP](-)), and 1-(3-hydroxypropyl)pyridinium tris(pentafluoroethyl)trifluorophosphate, ([1-PrOHPy](+)[FAP](-)), stationary phases at 323 K. The measured retention factors were combined with published infinite dilution activity coefficient, gas solubility data and retention factor data to yield gas-to-anhydrous ionic liquid (IL) partition coefficients at 323 K for 2349 different solute-IL combinations. The compiled partition coefficient data were analyzed using the ion-specific equation coefficient and the functional group contribution versions of the Abraham salvation parameter model. Ion-specific equation coefficients were calculated for 25 cations and 14 anions. In addition, values were calculated for 14 cation functional groups and 14 anions. The calculated ion-specific equation coefficients and calculated functional group values described the experimental 323 K partition coefficient data to within standard deviations of 0.10 and 0.13 log units, respectively. (C) 2010 Elsevier B.V. All rights reserved.
Keywords:Room temperature ionic liquids;Linear free energy relationships;Activity coefficients;Group contribution methods;Gas chromatographic retention factors;Partition coefficients