Liquid−Liquid Equilibrium Data for Systems Containing Vegetable Oils, Anhydrous Ethanol, and Hexane at (313.15, 318.15, and 328.15) K

2009 ◽  
Vol 54 (6) ◽  
pp. 1850-1859 ◽  
Author(s):  
Marcelo Lanza ◽  
Guilherme Sanaiotti ◽  
Eduardo A. C. Batista ◽  
Ronei J. Poppi ◽  
Antonio J. A. Meirelles
2009 ◽  
Vol 54 (8) ◽  
pp. 2174-2181 ◽  
Author(s):  
Wagner L. Priamo ◽  
Marcelo Lanza ◽  
Antonio J. A. Meirelles ◽  
Eduardo A. C. Batista

2019 ◽  
Vol 64 (5) ◽  
pp. 2153-2162 ◽  
Author(s):  
Simone Shiozawa ◽  
Marcela C. Ferreira ◽  
Daniel Gonçalves ◽  
Antonio J. A. Meirelles ◽  
Eduardo A. C. Batista

2009 ◽  
Vol 54 (8) ◽  
pp. 2182-2188 ◽  
Author(s):  
Irede Dalmolin ◽  
Marcelo Lanza ◽  
Antonio J. A. Meirelles ◽  
Eduardo A. C. Batista

2010 ◽  
Vol 55 (7) ◽  
pp. 2416-2423 ◽  
Author(s):  
César A. S. da Silva ◽  
Guilherme Sanaiotti ◽  
Marcelo Lanza ◽  
Antonio J. A. Meirelles ◽  
Eduardo A. C. Batista

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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