2011
DOI: 10.1016/j.jct.2010.11.013
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Extraction of toluene from aliphatic compounds using an ionic liquid as solvent: Influence of the alkane on the (liquid+liquid) equilibrium

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Cited by 39 publications
(17 citation statements)
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“…Effect of the anion on the (a) selectivity and (b) distribution factor in mole fraction basis and (c) distribution factor in mass fraction basis versus composition of toluene in the upper raffinate phase for the heptane + toluene + [emim] + cation-based ionic liquids systems. Solid symbols, 298.15 K; open symbols, 313.15 K. (Solid black square) [Tf 2 N] − ; (open black square) [Tf 2 N] − ; (solid blue circle) [DEP] − ; (solid green diamond) [OAc] − ; (open orange triangle) [CH 3 SO 3 ] − ; (open purple star) [CF 3 SO 3 ] − ; (cross) [CHF 2 CF 2 SO 3 ] − ; (solid red inverted triangle) [ESO 4 ] − ; (open red inverted triangle) [ESO 4 ] − ; (×) [SCN] − ; (asterisk) [DCA] − ; (dash) [TCM] − ; and (black square with line) sulfolane …”
Section: Liquid–liquid Separation Of Aromatic From Aliphatics Using I...mentioning
confidence: 99%
See 1 more Smart Citation
“…Effect of the anion on the (a) selectivity and (b) distribution factor in mole fraction basis and (c) distribution factor in mass fraction basis versus composition of toluene in the upper raffinate phase for the heptane + toluene + [emim] + cation-based ionic liquids systems. Solid symbols, 298.15 K; open symbols, 313.15 K. (Solid black square) [Tf 2 N] − ; (open black square) [Tf 2 N] − ; (solid blue circle) [DEP] − ; (solid green diamond) [OAc] − ; (open orange triangle) [CH 3 SO 3 ] − ; (open purple star) [CF 3 SO 3 ] − ; (cross) [CHF 2 CF 2 SO 3 ] − ; (solid red inverted triangle) [ESO 4 ] − ; (open red inverted triangle) [ESO 4 ] − ; (×) [SCN] − ; (asterisk) [DCA] − ; (dash) [TCM] − ; and (black square with line) sulfolane …”
Section: Liquid–liquid Separation Of Aromatic From Aliphatics Using I...mentioning
confidence: 99%
“…Liquid–liquid phase equilibrium, capacity, and selectivity have been reported for several combinations of aliphatics and aromatics using ionic liquids as the extraction solvent. Among the ionic liquids studied, the cations used are mostly imidazolium , and pyridinium. ,,, A few studies use pyrrolidinium, ammonium, ,, morpholinium, and other cations, , while the most investigated ionic liquid anion is bis­(trifluoromethylsulfonyl)­imide ([Tf 2 N] − ). In addition, aromatic extractions have been performed with ionic liquid mixtures in an attempt to improve both selectivity and capacity. In some cases, infinite dilution activity coefficients of aromatic and aliphatic compounds in ionic liquids have been used as a first pass evaluation of the suitability of a particular ionic liquid for aliphatic–aromatic separation. …”
Section: Introductionmentioning
confidence: 99%
“…From Figure , it is concluded that for the systems with hexane, DES 2 shows comparable values of distribution coefficients to [EMim]­[ESO 4 ], [EMpy]­[ESO 4 ], and [BMim]­[MSO 4 ] in the whole investigated concentration range of toluene in the system. However, DES 1 shows less attractive distribution coefficients compared to the other solvents.…”
Section: Results and Discussionmentioning
confidence: 86%
“…Ionic liquids , (ILs) were investigated as a replacement for the organic solvents in extractive desulfurization, , denitrification, , or dearomatization. , This novel solvent captured the attention of many researchers due to the ease of tuning its properties, low volatility, and high extraction efficiency. However, the toxicity, poor biodegradability, high cost, and difficulty in synthesizing ILs restricted their commercial use as extractive solvents …”
Section: Introductionmentioning
confidence: 99%