Abstract. In industrial wastewater, arsenic is most often present in the trivalent state. An analysis of existing purification methods shows that in all cases, with a few exceptions, the most complete removal of arsenic is observed from solutions in which it is in the pentavalent state. This is explained by the significantly lower solubility of arsenates of heavy and alkaline earth metals compared to the corresponding arsenites. The chemical oxidation of As(III) in the following systems was studied: As(III)-H2SO4-H2O, As(III)-MeSO4-H2O, As(III)–H2SO4–MeSO4–H2O (where Me is Cu, Ni, Co, Mn, Zn). The influence of temperature, the amount of transition metal ions, the duration of the experiment, and the concentration of sulfuric acid on the degree of transition of As(III) to As(V) was studied. The effect of catalytic oxidation of As(III) in sulfuric acid solutions was discovered. The maximum degree of oxidation of trivalent arsenic (55-60%) is observed when transition metal salts are introduced into an arsenic solution in the presence of a platinum plate. It has been established that the nature of the studied transition metal salts (Cu2+, Ni2+, Co2+, Mn2+, Zn2+), process duration and temperature do not have a significant effect on the degree of As(III) conversion. The results obtained largely explain the predominance of pentavalent forms of arsenic in production solutions of non-ferrous metallurgy. Key words: copper electrolyte, arsenic, transition metals, catalytic role, instant oxidation effect, activated oxygen.
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