Effect of mono-, di- and tri-ethanolammonium tetrafluoroborate protonic ionic liquids on the volatility of water, ethanol, and methanol

• Published in: Fluid phase equilibria 2011-04, Vol.303 (1), p.103-110
• Main Authors: Shen, Chong, Li, Xue-mei, Lu, Ying-zhou, Li, Chun-xi
• Format: Article
• Language: English
• Subjects: Activity coefficient; Activity coefficients; Binary systems; Chemistry; Deviation; Ethanol; Ethyl alcohol; Exact sciences and technology; General and physical chemistry; Mathematical models; Methyl alcohol; NRTL model; Phase equilibria; Protonic ionic liquid; Solvents; Vapor pressure
• ISSN: 0378-3812; 1879-0224
• DOI: 10.1016/j.fluid.2011.01.009

► Vapor pressure data for nine binary systems {solvent + ionic liquid} were measured. ► Water, ethanol, methanol, and ethanolammonium-based tetrafluoroborate were studied. ► The vapor pressure data can be well correlated by NRTL model. ► The activity coefficients of solvents were calculated by NRTL model. ► The vapor pressure lowering degree follows the order of water > methanol > ethanol. Vapor pressure data were measured for nine binary systems containing water, ethanol, or methanol with one of three protonic ionic liquids (PILs), viz. mono-, di- and tri-ethanolammonium tetrafluoroborate ([HMEA][BF 4], [HDEA][BF 4], and [HTEA][BF 4]), at varying temperatures and PIL-contents using a quasi-static ebulliometer. The vapor pressure data were correlated by NRTL model with an overall average absolute relative deviation (AARD) of 0.0175. It is showed that the effect of PILs on the vapor pressure lowering of solvents follows the order of [HMEA][BF 4] > [HDEA][BF 4] > [HTEA][BF 4], and the vapor pressure lowering degree follows the order of water > methanol > ethanol. Besides, the activity coefficients of solvent for binary system {solvent + PIL} at fixed PIL mole fraction of 0.10 were calculated using the regressed NRTL parameters. The results indicate that three PILs can give rise to a negative deviation from the Raoult's law for water and methanol and a positive deviation for ethanol to a varying degree, leading to the variation of relative volatility of a solvent.