Herrador M Angeles, González A Gustavo
Department of Analytical Chemistry, Facultad de Quimica, University of Seville, 41012 Seville, Spain.
Talanta. 2002 Mar 11;56(4):769-75. doi: 10.1016/s0039-9140(01)00607-5.
Non ideality of acetonitrile-water mixtures was studied from data on the excess of molar volumes and viscosities. pH and autoprotolisis constants were evaluated at the standard state of the mixed solvent from titrations of a strong acid with a strong base. In order to illustrate the evaluation of the aqueous ionisation constant of water insoluble compounds from pH titrations in ACN-water mixtures, a typical insoluble arylpropionic acid, ketoprofen, was chosen. Ketoprofen was titrated in mixtures from 10 to 70% w/w of acetonitrile against a strong base. From the titration data, the ionisation constant of ketoprofen was evaluated at the standard state of the solvent mixture (pK(a)()). Aqueous pK(a) was determined by extrapolation, as the intercept of the plot of pK(a)() versus ACN mole fraction.