TERNARY NaCl+LiCl+H2O MIXED ELECTROLYTE SYSTEM: DETERMINATION OF ACTIVITY COEFFICIENTS BASED ON POTENTIOMETRIC METHOD
Farzad Deyhimi, Mojgan Sabzehzari, Zohreh Karimzadeh
Abstract
Farzad Deyhimi, Mojgan Sabzehzari, Zohreh Karimzadeh
Abstract
The mean activity coefficients for NaCl in a ternary electrolyte system were determined by the potentiometric method, at 25°C, using a solvent polymeric (PVC) sodium-selective membrane electrode (Na+ ISE), containing N,N′-dibenzyl-N,N′-diphenyl-1,2-phenylenedioxydiacetamide as ionophore, and combined with an Ag/AgCl electrode. The potentiometric measurements were performed at the same ionic strengths in different series of mixed salt solutions, each characterized by a fixed salt molal ratio r (where r = m1/m2 = 1, 10, 50, 100). The nonideal behavior of the ternary NaCl(m1) + LiCl(m2) + H2O electrolyte system was described based on the Pitzer ion-interaction model for mixed salts over the ionic strength ranging from 0.01 up to about 4 mol/kg. Two- and three-particle Pitzer interaction parameters for a mixed electrolyte system were determined based on potentiometric data, and the critical role of potentiometric selectivity coefficient (K 12) of ISE as limiting factor in the potentiometric measurements was analyzed.
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The mean activity coefficients for NaCl in a ternary electrolyte system were determined by the potentiometric method, at 25°C, using a solvent polymeric (PVC) sodium-selective membrane electrode (Na+ ISE), containing N,N′-dibenzyl-N,N′-diphenyl-1,2-phenylenedioxydiacetamide as ionophore, and combined with an Ag/AgCl electrode. The potentiometric measurements were performed at the same ionic strengths in different series of mixed salt solutions, each characterized by a fixed salt molal ratio r (where r = m1/m2 = 1, 10, 50, 100). The nonideal behavior of the ternary NaCl(m1) + LiCl(m2) + H2O electrolyte system was described based on the Pitzer ion-interaction model for mixed salts over the ionic strength ranging from 0.01 up to about 4 mol/kg. Two- and three-particle Pitzer interaction parameters for a mixed electrolyte system were determined based on potentiometric data, and the critical role of potentiometric selectivity coefficient (K 12) of ISE as limiting factor in the potentiometric measurements was analyzed.
Key concepts: Potentiometric titration, Chemistry, Electrolyte, Activity coefficient, Ternary operation, Molality, Electroanalytical method, Ionic strength