4.5 Article

Separation of azeotropic mixtures (ethanol and water) enhanced by deep eutectic solvents

Journal

FLUID PHASE EQUILIBRIA
Volume 448, Issue -, Pages 128-134

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.fluid.2017.03.010

Keywords

Vapor-liquid equilibrium (VLE); Deep eutectic solvents (DESs); Ionic liquids (ILs); Azeotropic mixture; Extractive distillation

Funding

  1. National Natural Science Foundation of China [21476204, 21676243]
  2. Zhejiang Provincial Natural Science Foundation of China [LZ14B060002]
  3. Zhejiang Province Collaborative Innovation Center of Agricultural Biological Resources Biochemical Manufacturing Open Fund [2016KF0023]
  4. Zhejiang University of Science and Technology Research Fund

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The distillation of azeotropic mixtures is commonly and widely performed in the pharmaceutical, petroleum, and chemical industries. Deep eutectic solvents (DESs) are environmentally-friendly entrainers that have many properties similar to ionic liquids (ILs) but are also simple in preparation and cheap in price. Also, the ethanol/water system is a typical industrial azeotropic mixture. In this work, the relative volatility of ethanol and water at the azeotropic point was increased from 1.00 to 4.70 with 0-51.0 mass % ChCl/urea (1:2, mol/mol), with ChCl/urea showing a remarkable entrainer performance in this separation. Isobaric vapor liquid equilibrium (VLE) data of four systems, water + ethanol, water + ChCl/urea, ethanol + ChCl/urea, and water + ethanol + ChCl/urea (at 10, 20, and 30 mass%), were determined using a modified Othmer equilibrium still at 10132 kPa. After addition of ChCl/urea, the ethanol + water mixture's azeotropic point was eliminated. The parameters of the nonrandom two-liquid (NRTL) model for these systems were calculated and the predicted values for these systems were found to fit the experimental VLE data quite well. (C) 2017 Elsevier B.V. All rights reserved.

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