Anoxic oxidation of As(III) during Fe(II)-induced goethite recrystallization: Evidence and importance of Fe(IV) intermediate

Abstract

Under anoxic conditions, aqueous Fe(II) (Fe(II)_aq)-induced recrystallization of iron (oxyhydr)oxides changes the speciation and geochemical cycle of trace elements in environments. Oxidation of trace element, i.e., As(III), driven by Fe(II)_aq-iron (oxyhydr)oxides interactions under anoxic condition was observed previously, but the oxidative species and involved mechanisms are remained unknown. In the present study, we explored the formed oxidative intermediates during Fe(II)_aq-induced recrystallization of goethite under anoxic conditions. The methyl phenyl sulfoxide-based probe experiment suggested the featured oxidation by Fe(IV) species in Fe(II)_aq-goethite system. Both the Mössbauer spectra and X-ray absorption near edge structure spectroscopic evidenced the generation and quenching of Fe(IV) intermediate. It was proved that the interfacial electron exchange between Fe(II)_aq and Fe(III) of goethite initiated the generation of Fe(IV). After transferring electrons to goethite, Fe(II)_aq was transformed to labile Fe(III), which was then transformed to Fe(IV) via a proton-coupled electron transfer process. This highly reactive transient Fe(IV) could quickly react with reductive species, i.e. Fe(II) or As(III). Considering the ubiquitous occurrence of Fe(II)-iron (oxyhydr)oxides reactions under anoxic conditions, our findings are expected to provide new insight into the anoxic oxidative transformation processes of matters in non-surface environments on earth.

Keywords: Anoxic oxidation; Electron and atom exchange; Fe(IV) intermediate; Proton-coupled electron transfer; Stable Fe isotope.