Activity coefficients for NH4Cl in 2-PrOH/water mixed solvent and some thermodynamic correlations for NH4Cl in ROH/water mixed solvents (R = Me, Et, 1-Pr and 2-Pr)

In this work the results concerning the determination of the activity coefficients for NH4Cl in 2-PrOH/water mixed solvents, along with some thermodynamic correlations concerning the resulting osmotic coefficients and excess Gibbs free energies for this electrolyte in different ROH/water mixed solvent systems (where R = Me, Et, 1-Pr and 2-Pr) are presented. These electrolytic systems were modeled using the Pitzer ion-interaction model and based on the experimental electromotive force (emf) data, of the following galvanic cell: AgCl | N H 4 Cl ( m ) , H 2 O ( 100 − w % ) , ROH ( w % ) | N H 4 + ISE , at 298.15 K. The results concern the previous and new collected experimental data using NH4+ ion-selective PVC membrane and Ag/AgCl electrodes for different mass fraction percents ( w ) of alcohol in water (with w = 0 , 10 , 20 , and   30 % , and R = Me, Et, 1-Pr, and R = 2-Pr, respectively). The thermodynamic behavior of these electrolyte systems were determined over the molality ranging from dilute solution to near salt saturation, or to phase separation (e.g. R = 2-Pr) in these mixed solvent systems. The non-ideal behavior of these electrolyte systems were satisfactorily correlated in term of the linear dependence of the Pitzer ion-interaction parameters on the dielectric constant of the solvents, and also in term of the ion association phenomenon related to the Pitzer electrostatic interaction terms in the second virial coefficient for the used electrolytic systems.