Abiotic oxidation of arsenite in natural and engineered systems: Mechanisms and related controversies over the last two decades (1999-2020)

Abstract

Abiotic oxidation of toxic As(III) to As(V) is being deemed as a necessary step for the overall arsenic decontamination in both natural and engineered systems. Direct oxidation of As(III) by chemical oxidants, such as ozone, permanganate, ferrate, chlorine and chloramine, or naturally occurring minerals like Mn, Fe oxides, seems straightforward. Both O₂ and H₂O₂ are ineffective for arsenite oxidation, but they can be activated by reducing substances like Fe²⁺, Fe⁰ to increase the oxidation rates. Photo-induced oxidation of As(III) has been demonstrated effective in Fe complexes or minerals, NO₃^-/NO₂^-, dissolved organic matter (DOM), peroxygens and TiO₂ systems. Although a variety of oxidation methods have been developed over the past two decades, there remain many scientific and technical challenges that must be overcome before the rapid progress in basic knowledge can be translated into environmental benefits. To better understand the trends in the existing data and to identify the knowledge gaps, this review describes in detail the complicated mechanisms for As(III) oxidation by various methods and emphasizes on the conflicting data and explanation. Some prevailing concerns and challenges in the sphere of As(III) oxidation are also pointed out so as to appeal to researchers for further investigations.

Keywords: Arsenic; Direct oxidation; Electron transfer; Photooxidation; Reactive oxygen species.