Paper
Separation of benzene and hexane by solvent extraction with 1-alkyl-3-methylimidazolium bis{(trifluoromethyl)sulfonyl}amide ionic liquids: effect of the alkyl-substituent length.
Published Jan 30, 2007 · A. Arce, M. Earle, H. Rodríguez
The journal of physical chemistry. B
195
Citations
3
Influential Citations
Abstract
The influence of the alkyl-substituent chain in 1-alkyl-3-methylimidazolium bis{(trifluoromethyl)sulfonyl}amide ionic liquids ([C(n)mim][NTf(2)], where n is the length of a linear alkyl chain) as solvents for the separation of benzene and hexane by liquid extraction was investigated. The liquid-liquid equilibrium (LLE) at 25 degrees C for the ternary systems ([C(n)mim][NTf(2)] + hexane + benzene), with n taking the values 4, 8, 10, and 12, were determined. These data were analyzed and compared to those previously reported for the system ([C(2)mim][NTf(2)] + hexane + benzene). The results show that short alkyl chains on the imidazolium cation of the ionic liquid lead to a better extractive separation of benzene and hexane, and reveal the influence of the relative degree of ordering in the ionic liquids on the extraction parameters.
Short alkyl chains in 1-alkyl-3-methylimidazolium bis-(trifluoromethyl)sulfonyl-amide ionic liquids lead to better extraction of benzene and hexane, with the relative degree of ordering also influencing extraction parameters.
Sign up to use Study Snapshot
Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.
Full text analysis coming soon...