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Received March 20, 2016
Accepted May 14, 2016
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The selectivity of imidazolium-based ionic liquids with different anions to BTX aromatics in hexane at 298.15 K and atmospheric pressure
Department of Chemical Engineering, Chungnam National University, 220 Gung-dong, Yuseong-gu, Daejeon 34134, Korea
sjpark@cnu.ac.kr
Korean Journal of Chemical Engineering, October 2016, 33(10), 2982-2989(8), 10.1007/s11814-016-0140-4
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Abstract
The selectivity of alkyl-substituted imidazolium cation-based ionic liquids (ILs) with different anion: Tf2N, PF6, Tf2N and BF4, namely 1-Butyl-3-methylimidazolium bis(trifluoromethyl sulfonyl)imide ([BMIM][Tf2N]), 1-Butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]), 1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide ([EMIM][Tf2N]), 1-Methyl-3-octyl imidazolium tetrafluoroborate ([OMIM][BF4]), was tested for the extraction of benzene, toluene and p-xylene(BTX) aromatics with hexane mixtures. Liquid-liquid equilibrium (LLE) data were determined for the six ternary mixtures {hexane (1)+BTX (2)+ILs (3)} at 298.15 K and atmospheric pressure. In addition, binary LLE data from 293.15 K to 318.15 K are also reported for the system {hexane (1)+[BMIM][Tf2N] (2)}. The ternary experimental LLE data were satisfactorily correlated with the NRTL activity coefficient model. The degree of consistency of the tie lines was estimated by using the Othmer-Tobias equation, for which a good linear correlation coefficient (R2) was obtained. As a result, the selectivity of ILs as potential solvents for the extraction of BTX from aliphatic components was found to be much higher than unity and PF6 anion showed higher selectivity compared to other anions.
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Othmer DF, Tobias PE, Ind. Eng. Chem., 34, 693 (1942)
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Yang SK, Wang YJ, Qi XH, Wang HX, Fluid Phase Equilib., 367, 69 (2014)
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Aralaguppi MI, Jadar CV, Aminabhavi TM, J. Chem. Eng. Data, 44, 446 (1999)
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Singh G, Kumar A, Indian J. Chem., 47, 495 (2008)
Arce A, Rodil E, Soto A, J. Solution Chem., 35, 63 (2006)
Laesecke A, Fortin TJ, Splettt JD, Energy Fuels, 26(3), 1844 (2012)
Fortin TJ, Laesecke A, Freund M, Outcalt S, J. Chem. Thermodyn., 57, 276 (2013)
Chirico RD, Frenkel M, Magee JW, Diky V, Muzny CD, Kazakov AF, Kroenlein K, Abdulagatov I, Hardin GR, Acree WE, Brenneke JF, Brown PL, Cummings PT, de Loos TW, Friend DG, Goodwin ARH, Hansen LD, Haynes WM, Koga N, Mandelis A, Marsh KN, Mathias PM, McCabe , J. Chem. Eng. Data, 58(10), 2699 (2013)
Jeong IY, You SH, Park SJ, Fluid Phase Equilib., 378, 93 (2014)
Hwang IC, Park SJ, Fluid Phase Equilib., 301(1), 18 (2011)
Treybal RE, Liquid Extraction, 2nd Ed., McGraw-Hill press: New York (1963).
Mukhopadhyay M, Dongaonkar KR, Ind. Eng. Chem. Process Des. Dev., 22, 521 (1983)
Renon H, Prausnitz JM, AIChE J., 14, 135 (1968)
You SH, Jeong IY, Park SJ, Fluid Phase Equilib., 389, 9 (2015)
Gonzalez EJ, Calvar N, Gomez E, Dominguez A, Fluid Phase Equilib., 303(2), 174 (2011)