Abstract

The solubility of dilute SO2 in aqueous HCl and NaCl solutions was determined at 298.15 K as a function of ionic strength up to 3 mol·L-1, in the partial pressure range between (0.075 and 1.8) kPa. Measurements were carried out by a saturation method using a laboratory batch reactor. Equations to correlate the apparent Henry's law constant, Hm, and the apparent first dissociation constant, Km1, were obtained as a function of ionic strength. Comparisons between experimental results and theoretical predictions were also made. A model based on the classical Sechenov equation was tested, and a new value for the SO2 gas-specific parameter was obtained to calculate Hm. Two different models were considered for calculating the activity coefficients to determine Km1. An extended version of the Debye−Huckel theory described the experimental results for ionic strengths below 0.1 mol·L-1. The Pitzer model was in good agreement with the experimental data in the ionic strength range between (0 and 3) mol·L-1. The close...

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