Alternative formalism for the evaluation of the activity coefficients on ternary electrolyte solutions from osmotic coefficient data

2021 ◽  
pp. 113169
Author(s):  
Francisco J. Passamonti ◽  
María R. Gennero de Chialvo ◽  
Abel C. Chialvo
1990 ◽  
Vol 68 (2) ◽  
pp. 294-297 ◽  
Author(s):  
Ch. Venkateswarlu ◽  
J. Ananthaswamy

The activity coefficients of NaCl in the NaCl–NiCl2–H2O system were estimated at 25, 35, and 45 °C and total ionic strengths of 0.5, 1.0, 2.0, and 3.0 m by an EMF method using a Na-ion selective electrode and a silver–silver chloride reference electrode. The Harned coefficients were calculated at all the temperatures studied. At 25 °C the data were analysed using the Pitzer formalism. The osmotic coefficients and the excess free energies of mixing were also calculated at 25 °C. Keywords: activity coefficients, sodium chloride, nickel chloride, Pitzer equations, thermodynamics.


2004 ◽  
Vol 6 (1) ◽  
pp. 124-128 ◽  
Author(s):  
Francesco Malatesta ◽  
Chiara Fagiolini ◽  
Roberto Franceschi

1976 ◽  
Vol 54 (1) ◽  
pp. 9-11 ◽  
Author(s):  
Chai-Fu Pan

In non-associated dilute aqueous electrolyte solutions, the deviation from ideality is principally attributed to the interionic interactions and hydration of ions. Stokes and Robinson combined Bjerrum's thermodynamic treatment of ion–solvent interactions with Debye–Hückel treatment of interionic interactions to obtain a two-parameter equation. In very dilute regions, the Stokes and Robinson's equation reduces to a much simpler form, i.e.[Formula: see text]Activity coefficients of an electrolyte at lower concentrations, say up to 0.1 m, can be calculated from the equation provided suitable values of &([a-z]+); and h are available. Solutions of hydrogen chloride and sodium chloride were chosen as examples. The results agree with the existing data very satisfactorily.


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