THE DISSOCIATION CONSTANT OF ACETIC ACID AND THE ACTIVITY COEFFICIENTS OF THE IONS IN CERTAIN ACETATE SOLUTIONS1

1928 ◽  
Vol 50 (3) ◽  
pp. 696-714 ◽  
Author(s):  
Edwin J. Cohn ◽  
Francis F. Heyroth ◽  
Miriam F. Menkin
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.


1932 ◽  
Vol 54 (4) ◽  
pp. 1350-1357 ◽  
Author(s):  
Herbert S. Harned ◽  
Russell W. Ehlers

Nature ◽  
1933 ◽  
Vol 131 (3297) ◽  
pp. 27-28
Author(s):  
A. I. VOGEL ◽  
G. H. JEFFERY

1991 ◽  
Vol 69 (12) ◽  
pp. 2117-2121 ◽  
Author(s):  
T. S. Banipal ◽  
B. S. Lark ◽  
S. Singh

Total vapour pressures for binary mixtures containing acetic acid, propionic acid, isobutyric acid, and trimethylacetic acid with acetonitrile have been measured for the entire composition range at 298.15 and 318.15 K using a static manometric method. All systems show positive deviations from Raoult's law, enhanced by both an increase in temperature and an increase in the methylation of acetic acid. Activity coefficients have been calculated by taking into consideration the dimerization of these carboxylic acids in the vapour phase. TSE values obtained from GE and earlier reported HE values are found to be negative for acetic acid, about zero for propionic and isobutyric acids, and positive for trimethylacetic acid for the whole composition range. The results have been interpreted in terms of various contributions such as depolymerization, heteromolecular dipole–dipole interactions, and the increasing dimerization constant and steric hindrance with increase of complexity of the acid. Key words: excess Gibbs energy, carboxylic acids, acetonitrile, activity coefficients


1972 ◽  
Vol 129 (1) ◽  
pp. 203-208 ◽  
Author(s):  
Henry B. F. Dixon

Valylhistidine (Val-His) reacts with glucose (Glc) in a mixture of pyridine and acetic acid to form glucosylvalylhistidine (Glc-Val-His). The pK of the α-amino group is thereby lowered to about 5.6 as judged by electrophoretic mobility. The reaction: [Formula: see text] also occurs in an aqueous solution of pyridine and acetic acid of pH6.2 at 50°C, in which it exhibits a half-time of about 30h and a dissociation constant of about 0.3m. Isoleucyltyrosine and glucose react similarly in aqueous solution. The Glc-Val-His has the chromatographic, electrophoretic and chemical properties reported by Holmquist & Schroeder (1966a) for the substance released by proteolysis from the N-terminus of the β-chains of haemoglobin AIc; the value of the dissociation constant means that the concentration of haemoglobin AIc found naturally could be explained by reaction of haemoglobin A with the blood glucose.


1986 ◽  
Vol 51 (12) ◽  
pp. 2665-2674 ◽  
Author(s):  
Ivona Malijevská ◽  
Helena Perničková ◽  
Karel Ledvinka ◽  
Bohuslav Doležal

Results of measurement of vapour-liquid equilibria in the benzene-propionic acid-acetic acid ternary system at normal pressure are presented. The activity coefficients were, within the framework of inaccuracies determined on the basis of the law of error propagation, subjected to a test of consistency and correlated by the Wilson equation. The experimental values of activity coefficients are compared with the values calculated on the basis of the Wilson equation with its constants obtained both from the ternary and from the binary data and with the values estimated by the UNIFAC method.


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