Activity Coefficients of Aqueous Solutions of NaOH and KOH in Wide Concentration and Temperature Ranges

1996 ◽  
Vol 61 (11) ◽  
pp. 1549-1562 ◽  
Author(s):  
Jan Balej

Up to now, there exist a quite wide temperature interval between 70 or 80 and 150 °C with no sufficiently reliable experimental data of mean activity coefficients for aqueous NaOH as well as KOH solutions. In order to fill this gap, it was tried to derive suitable correlation equations for this quantity in dependence on the molality (for NaOH in the range mNaOH = 2-25 mol kg-1, for KOH in the range mKOH = 2-18 mol kg-1) and temperature (in the range 0-200 °C for both kinds of solutions) on the basis of the available data of this quantity and with the use of the previously derived correlation equations for the water activity in aqueous solutions of NaOH and KOH under the same conditions. The comparison between the calculated and experimental data was discussed.

2013 ◽  
Vol 6 (2) ◽  
pp. 163-167
Author(s):  
Jan Balej

Abstract Solubility data of the conversion system 2NH4+ - 2Na+ - S2O82- - SO42- - H2O at 20 °C and 30 °C for the partial pseudoternary systems Na2S2O8-(NH4)2SO4-H2O, (NH4)2S2O8-Na2SO4-H2O, Na2S2O8-NaNH4SO4-H2O and (NH4)2S2O8-NaNH4SO4-H2O have been correlated using the relative activity coefficient expansion of the crystallizing component. The obtained correlation equations have been used for the calculation of mean activity coefficients of ammonium and sodium peroxodisulfates in their saturated solutions of the mentioned pseudoternary systems.


2020 ◽  
Vol 77 (4) ◽  
pp. 141-168
Author(s):  
Silvia M. Calderón ◽  
Jussi Malila ◽  
Nønne L. Prisle

AbstractWe introduce the CMC based Ionic Surfactant Activity model (CISA) to calculate activity coefficients in ternary aqueous solutions of an ionic surfactant and an inorganic salt. The surfactant can be either anionic or cationic and in the present development, the surfactant and inorganic salts share a common counterion. CISA incorporates micellization into the Pitzer–Debye–Hückel (PDH) framework for activities of mixed electrolyte solutions. To reduce computing requirements, a parametrization of the critical micelle concentration (CMC) is used to estimate the degree of micellization instead of explicit equilibrium calculations. For both binary and ternary systems, CISA only requires binary experimentally-based parameters to describe water–ion interactions and temperature–composition dependency of the CMC. The CISA model is intended in particular for atmospheric applications, where higher-order solution interaction parameters are typically not constrained by experiments and the description must be reliable across a wide range of compositions. We evaluate the model against experimental activity data for binary aqueous solutions of ionic surfactants sodium octanoate and sodium decanoate, as common components of atmospheric aerosols, and sodium dodecylsulfate, the most commonly used model compound for atmospheric surfactants. Capabilities of the CISA model to describe ternary systems are tested for the water–sodium decanoate–sodium chloride system, a common surrogate for marine background cloud condensation nuclei and to our knowledge the only atmospherically relevant system for which ternary activity data is available. For these systems, CISA is able to provide continuous predictions of activity coefficients both below and above CMC and in all cases gives an improved description of the water activity above the CMC, compared to the alternative model of Burchfield and Wolley [J. Phys. Chem., 88(10), 2149–2155 (1984)]. The water activity is a key parameter governing the formation and equilibrium growth of cloud droplets. The CISA model can be extended from the current form to include the effect of other inorganic salts with the existing database of binary PDH parameters and using appropriate mixing rules to account for ion specificity in the micellization process.


1995 ◽  
Vol 60 (4) ◽  
pp. 537-544 ◽  
Author(s):  
Vladislav Holba ◽  
Marcela Hanková

The solubilities of tris(ethylenediamine)chromium(III) and hexa(urea)chromium(III) hexacyanoferrates(III) in aqueous solutions of different supporting electrolytes as well as in binary mixtures of water with methanol, tert-butyl alcohol and acetonitrile were measured at 25 °C. The experimental data have been used to evaluate the activity coefficients of the saturating salts in water and their Gibbs energies of transfer from water into the binary mixtures investigated.


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