Published December 2015 | Version v1
Journal article

Ionic liquid 1-hexyl-3-methylimidazolium hexafluorophosphate, an efficient solvent for extraction of acetone from aqueous solutions

  • 1. Department of Applied Chemistry, Bu-Ali Sina University, Hamedan 65174 (Iran, Islamic Republic of)
  • 2. Department of Chemical and Chemical Engineering, Malek-Ashtar University of Technology, 3454 Tehran (Iran, Islamic Republic of)
  • 3. Department of Inorganic Chemistry, Bu-Ali Sina University, Hamedan 65174 (Iran, Islamic Republic of)

Description

Highlights: • The use of HMIMPF6 as a green ionic was feasible in the extraction of acetone from water. • The binodal curves were determined by cloud point measurement method. • High level separation factor of acetone between the ionic liquid and water were achieved. • The thermodynamic properties of HMIMPF6 were obtained by the Density Functional Theory calculations. • The NRTL and UNIQUAC models were applied satisfactorily to correlate the equilibrium data. - Abstract: (Liquid + liquid) equilibrium (LLE) of the chemical system of {water + acetone + 1-Hexyl-3-methylimidazolium hexafluorophosphate (HMIMPF6) ionic liquid} was studied at different temperatures of (293.2, 298.2 and 303.2) K and under atmospheric pressure of 81.5 kPa. The results show that HMIMPF6 provides the acetone distribution coefficient and separation factor values within (0.8813 to 1.2351) and (3.0 to 54.4), respectively; indicating the high capability of the ionic liquid for extraction of acetone from aqueous solutions. In most cases, acetone solubility in the ionic liquid is higher than in water, especially at higher solute concentrations. Meanwhile, higher separation factor is relevant to the lower temperature due to lower (water + ionic liquid) miscibility. The consistency of tie line data, at each temperature, was examined with Othmer–Tobias correlation. The values were nicely reproduced with the well-known NRTL and UNIQUAC models. Accordingly, the required thermodynamic properties of HMIMPF6 were obtained by the Density Functional Theory (DFT) calculations, carried out at the M06/6-311++G∗∗ level of theory. The root mean square deviations (RMSD) between experimental and model concentration values were 0.0192 and 0.0255, respectively; indicating close agreement of the both models.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jct.2015.08.027

Additional details

Identifiers

DOI
10.1016/j.jct.2015.08.027;
PII
S0021-9614(15)00309-2;

Publishing Information

Journal Title
Journal of Chemical Thermodynamics
Journal Volume
91
Journal Page Range
p. 404-413
ISSN
0021-9614
CODEN
JCTDAF

Optional Information

Copyright
Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.