Kinetics of Molecular Chlorine Release during Photochemical Ozonation of Acidic Chloride Solutions

The kinetics of the release of molecular chlorine during the oxidation of the chloride ion in acidified aqueous solutions (pH ≤2) under the action of ozone and UV radiation with a wavelength of 254 nm has been studied. In contrast to the dark reaction of O3 with Cl–(aq), the photochemical reaction gives significant yields of Cl2 relative to the starting O3, reaching 70% in weakly acidic solutions at pH 2. At increased acidity (pH ≤0.1), the Cl2 yields during the photochemical and dark ozonation are closer. The combined action of ozone and UV irradiation on the oxidation of Cl–(aq) is achieved due to the generation of free hydroxyl OH radicals and hydrogen peroxide H2O2 during the photolysis of O3 in an aqueous medium. Due to the interaction with OH radicals, the oxidation of chloride ions is accelerated, and in the “O3–Cl–(aq)–hν (254 nm)” system there is an additional source of active free radicals capable of participating in the oxidation of Cl–(aq), the nature of which cannot be explained based on the known mechanisms of chemical processes in similar systems. Hydrogen peroxide inhibits the oxidation of Cl–(aq), since it effectively interacts with Cl2 and other chlorine compounds in the nonnegative oxidation states and reduces them to the chloride ion.