Dynamics and mechanisms of arsenite oxidation by freshwater lake sediments

Abstract

There has been increasing concern over As in freshwater environments from sources such as arsenical pesticides, smelters, coal-fired power plants, and erosion caused by intensive land use. Arsenic in the reduced state, As (III) (arsenite), is much more toxic, more soluble and mobile, than when in the oxidized state, As (V) (arsenate). This paper summarizes the dynamics and mechanisms involved in the oxidation of As (III) to As (V) by freshwater lake sediments. Sediments from selected freshwater lakes in southern Saskatchewan oxidize As (III) to As (V) predominantly through an abiotic process. Solution analysis of As (III) and As (V) by colorimetry, and examination of the oxidation state of surface-sorbed As species by X-ray photoelectron spectroscopy, indicate that Mn present in the sediment is the primary electron acceptor in the oxidation of As (III). The transformation of As (III) to As (V) by carbonate and silicate minerals, common in sediments, is not evident. The heat of activation, ΔH_a, for the depletion (oxidation plus sorption) of As (III) by the sediments, varies from 3.3 to 8.5 kcal mole⁻¹, indicating that the process is predominantly diffusion-controlled. The Mn present in a series of particle size fractions ( < 2– > 20 µm) of the sediments may potentially detoxify As (III) in aquatic systems, by converting it to As (V).