Isobaric vapor–liquid equilibria for ethanol–water system containing different ionic liquids at atmospheric pressure |
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| Institution: | 1. College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China;2. College of Chemical and Environmental Engineering, Shandong University of Science and Technology, Qingdao 266590, China;1. College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China;2. College of Chemical and Environmental Engineering, Shandong University of Science and Technology, Qingdao 266590, China;1. College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China;2. Faculty of Chemistry, Kim Il Sung University, Pyongyang 999093, Democratic People''s Republic of Korea;1. School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China;2. Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan |
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| Abstract: | Isobaric vapor–liquid equilibrium (VLE) data for ethanol–water systems containing ionic liquids (ILs) 1-methyl-3-methylimidazolium dimethylphosphate (MMIM]DMP]), 1-ethyl-3-methylimidazolium diethylphosphate (EMIM]DEP]), 1-butyl-3-methylimidazolium bromide (BMIM]Br]), 1-butyl-3-methylimidazolium chloride (BMIM]Cl]) and 1-butyl-3-methylimidazolium hexafluorophosphate (BMIM]PF6]) at atmospheric pressure (101.32 kPa) were measured with a circulation still. The results showed that the VLE of ethanol–water systems in the presence of different ILs was obviously different from that of the IL-free system. All ILs studied showed a salting-out effect, which gave rise to a change of the relative volatility of ethanol, and even to an elimination of the azeotropic point. It was found that the salting-out effect followed the order of BMIM]Cl] > BMIM]Br] > BMIM]PF6] and MMIM]DMP] > EMIM]DEP], which was ascribed to the preferential solvation ability of the ions resulting from the dissociation of the IL. |
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