1954
DOI: 10.1021/ja01651a110
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Determination of Thermodynamic Equilibrium Constants in Mixed Solvents

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Cited by 53 publications
(28 citation statements)
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“…The glass electrode was equilibrated in a well-stirred PG-water mixture containing an inert electrolyte. The effects of variations in the asymmetry potential, liquid junction potential, activity coefficient, sodium ion error and dissolved carbon dioxide on the response of the glass electrode were accounted for in the form of correction factor (Gonzalez et al, 1986;Van Uitert and Haas, 1953).…”
Section: Apparatusmentioning
confidence: 99%
“…The glass electrode was equilibrated in a well-stirred PG-water mixture containing an inert electrolyte. The effects of variations in the asymmetry potential, liquid junction potential, activity coefficient, sodium ion error and dissolved carbon dioxide on the response of the glass electrode were accounted for in the form of correction factor (Gonzalez et al, 1986;Van Uitert and Haas, 1953).…”
Section: Apparatusmentioning
confidence: 99%
“…Hence the difference between the experimentally observed pH in solvent medium and the pH calculated based on the concentrations of the ingredients is used as factor that accounts for all the above parameters. This factor is named as correction factor in complex equilibria [31]. The correction factor is subtracted from pH meter dial reading.…”
Section: Methodsmentioning
confidence: 99%
“…The binary excess quantity of density for the 2-PE+TMS system is not taken into account, since it is supposed that the characteristics of both solvents are similar. The excess quantity of density for other binary solvents in a mixed solvent, A P~,~, is empirically correlated as follows : (10) where Tg1,2,3 has the same formulation as eqn (9), and 4t…”
Section: Density and Viscositymentioning
confidence: 99%