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Articles

Measurement and correlation of liquid–liquid equilibria for water + ethanol + mixed solvents (dichloromethane or chloroform + diethyl ether) at T = 293.15 K

, &
Pages 245-257 | Received 03 Jun 2015, Accepted 11 Jul 2015, Published online: 18 Aug 2015
 

Abstract

Liquid–liquid equilibrium (LLE) data for the quaternary systems (water + ethanol + dichloromethane (DCM) or chloroform (CHCl3) + diethyl ether (DEE)) were experimentally investigated at 293.15 K. The thermodynamic consistency of the data was performed using the Othmer–Tobias and Hand plots. The experimental tie-line data were correlated using the non-random, two-liquid (NRTL) model. As a result, the comparison of the extracting capabilities of the mixed solvents with respect to the distribution coefficients and separation factors showed that the (50% DCM +50% DEE) system had a higher separation factor for the (water + ethanol + DCM + DEE) system. On the other hand, the (50% CHCl3 +50% DEE) system had a higher separation factor for the (water + ethanol + CHCl3 + DEE) system. The last solvent (50% CHCl3 +50% DEE) was found to be the best solvent, with a positive synergistic effect on DEE, high separation factor, and very low solubility in water.

Acknowledgements

The authors would like to thank Mr Laiadi Djemoui, Mr Merzougui Abedalkarim, Mrs Naili Radia and Mrs Ben Mechich Hayet for technical support.

Nomenclature

List of symbols

DCM=

Dichloromethane

DEE=

Diethyl ether

CHCl3=

Chloroform

A=

NRTL binary interaction parameter

a1, b1=

Othmer–Tobias equation constants

a2, b2=

Hand equation constants

F=

Objective function

T=

Temperature

w=

Mass fraction

x=

Mole fraction

Super/subscripts

R2=

regression coefficient

nD=

refractive index

D1=

distribution coefficient of water

D2=

distribution coefficient of ethanol

S=

Separation factor

Lit=

Literature

Exp=

Experimental

i, j=

Components

Min=

Minimal

NRTL=

non-random, two-liquid

RMSE=

root mean square error

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