Liquid–liquid equilibrium data for ternary mixtures composed of n-hexane, benzene and acetonitrile at (298.15, 308.15, and 318.15)K

2014 ◽  
Vol 367 ◽  
pp. 69-73 ◽  
Author(s):  
Shengkai Yang ◽  
Yujie Wang ◽  
Xinhua Qi ◽  
Jiuxia Wang
2013 ◽  
Vol 634-638 ◽  
pp. 1022-1025 ◽  
Author(s):  
Heng De Li ◽  
Cheng Huang ◽  
Xiao Zhong Ma ◽  
Yu Qing Feng

Liquid-liquid equilibrium tie-line data were examined at atmospheric pressure and at 298.15 K for ternary mixtures of (water + methanol + linalool) as well as (water + ethanol + linalool). The distribution ratios of alcohol between organic and aqueous phases are discussed. The immiscible area of (water + methanol + linalool) system is wider than that for the ethanol system. The experimental liquid–liquid equilibrium data were satisfactorily fitted by means of an extended UNIQUAC model.


2011 ◽  
Vol 396-398 ◽  
pp. 908-911
Author(s):  
Heng De Li ◽  
Tian Fei Zhang ◽  
Yan Yan ◽  
Lin Chen ◽  
Ling Ling Hu

Liquid-liquid equilibrium tie-line data were examined for ternary mixtures of (water + methanol + geraniol) and (water + ethanol + geraniol) at 298.15 K. The distribution ratios of alcohol between organic and aqueous phases are discussed. The immiscible area of (water + methanol + geraniol) system is wider than that for the ethanol system. The experimental liquid–liquid equilibrium data have been satisfactorily represented by using an extended UNIQUAC model.


2008 ◽  
Vol 59 (5) ◽  
Author(s):  
Viorel Feroiu ◽  
Dan Geana ◽  
Catinca Secuianu

Vapour � liquid equilibrium, thermodynamic and volumetric properties were predicted for three pure hydrofluorocarbons: difluoromethane (R32), pentafluoroethane (R125) and 1,1,1,2 � tetrafluoroethane (R134a) as well as for binary and ternary mixtures of these refrigerants. Three cubic equations of state GEOS3C, SRK (Soave � Redlich � Kwong) and PR (Peng � Robinson) were used. A wide comparison with literature experimental data was made. For the refrigerant mixtures, classical van der Waals mixing rules without interaction parameters were used. The GEOS3C equation, with three parameters estimated by matching several points on the saturation curve (vapor pressure and corresponding liquid volumes), compares favorably to other equations in literature, being simple enough for applications.


1983 ◽  
Vol 48 (9) ◽  
pp. 2446-2453 ◽  
Author(s):  
Jan Linek

Isothermal vapour-liquid equilibrium data at 65, 73 and 80 °C and isobaric ones at 101.3 kPa were measured in the tetrachloromethane-sec-butyl alcohol system. A modified circulation still of the Gillespie type was used for the measurements. Under the conditions of measurement, the system exhibits positive deviations from Raoult's law and minimum boiling-point azeotropes. The experimental data were fitted to a number of correlation equations, the most suitable being the Wilson equation.


1989 ◽  
Vol 54 (11) ◽  
pp. 2840-2847 ◽  
Author(s):  
Ivona Malijevská ◽  
Alena Maštalková ◽  
Marie Sýsová

Isobaric equilibrium data (P = 101.3 kPa) for the system cyclohexane-acetic acid-propionic acid have been measured by two different analytical techniques. Activity coefficients calculated by simultaneous solving of equations for the chemical and phase equilibria were subjected to a consistency test based on inaccuracies determined from the error propagation law, and were correlated by Wilson’s equation. The activity coefficients measured were compared with those calculated from binary vapour-liquid equilibrium data and with values predicted by the UNIFAC method.


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