Liquid–Liquid Equilibrium for Ternary System Water + Cyclohexane + Acetic Acid at (303.2 to 333.2) K

2013 ◽  
Vol 58 (12) ◽  
pp. 3489-3493 ◽  
Author(s):  
Fuqiong Lei ◽  
Qinbo Wang ◽  
Xing Gong ◽  
Binwei Shen ◽  
Bingyan Mao ◽  
...  
2010 ◽  
Vol 293 (1) ◽  
pp. 73-78 ◽  
Author(s):  
Song Hu ◽  
Qing-lin Chen ◽  
Bing-jian Zhang ◽  
Yuan-lan Liang ◽  
Xue-nong Gao

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.


2000 ◽  
Vol 45 (2) ◽  
pp. 301-303 ◽  
Author(s):  
Adel S. Aljimaz ◽  
Mohamed S. H. Fandary ◽  
Jasem A. Alkandary ◽  
Mohamed A. Fahim

1973 ◽  
Vol 28 (10) ◽  
pp. 1740-1742 ◽  
Author(s):  
R. Haase ◽  
M. Pehlke ◽  
K.-H. Dücker

Vapour pressures and vapour compositions of the liquid system water + acetic acid have been measured at 25 °C, 30 °C, 35 °C, 40 °C, and 45 °C in the whole range of compositions. The dimerization of acetic acid in the vapour being taken into account, the molar excess Gibbs function ḠE is derived from the measurements. Earlier measurements of the molar excess enthalpy HE are combined with the -GE values to give the molar excess entropy SE. The “symmetry rule” (Haase, 1951) concerning the composition dependence of ḠE, -HE, and S̄E has been confirmed.


1996 ◽  
Vol 41 (3) ◽  
pp. 562-565 ◽  
Author(s):  
Mohamed A. Fahim ◽  
Shaheen A. Al-Muhtaseb ◽  
Inas M. Al-Nashef

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