Thermochemical and Ionic Speciation Modeling of the Aqueous Sulfuric Acid System Up to 6 Molal and 0-100 °C

Fuentes, Aldo N. N.; Casas, Jesus M.

Abstract

Sulfuric acid (H2SO4) is one of the most widely used chemicals, acting as a reagent in several industries and metallurgy. The chemical behavior in aqueous solutions can be as strong or weak if the acid concentration is low or high, respectively. The aim of this work is the estimation of the thermodynamic properties and to predict the speciation, density and ionic conductivity of aqueous sulfuric acid solutions up to 6 molal and 0-100 degrees C, using the Pitzer model adapted to include the interaction parameters of sulfate complexes as HSO4- and H2SO40. A thermodynamic model that includes a set of aqueous species, components, equilibrium reactions, activity coefficients, and mass balances was defined as a function of temperature. The parameters of the equilibrium constants for HSO4- and H2SO40, the Equation of State (EOS) HKFmoRR for solution density, the Casteel-Amis relationship for ionic conductivity, and the Pitzer model for water activity were combined by coupling of the optimization software PEST with the hydro-geochemical code PHREEQC. The Pitzer model was calibrated and resulting in a standard deviation of water activity adjustment of 0.7%. Sulfuric acid distributes in water forming common anions, cations, and neutral species as SO42- , HSO4-, H+, and H2SO40, where the association of sulfate increase with both electrolyte concentration and temperature. The solution density and ionic conductivity calculations were in good agreement with experimental data, presenting a standard deviation of adjustment of 0.2 and 4.8%, respectively, over the temperature and concentration ranges studied.

Más información

Título según WOS: Thermochemical and Ionic Speciation Modeling of the Aqueous Sulfuric Acid System Up to 6 Molal and 0-100 °C
Título de la Revista: JOURNAL OF SOLUTION CHEMISTRY
Volumen: 52
Número: 10
Editorial: SPRINGER/PLENUM PUBLISHERS
Fecha de publicación: 2023
Página de inicio: 1176
Página final: 1193
DOI:

10.1007/s10953-023-01304-0

Notas: ISI