Photo-oxidation is a potential pathway for the transformation of Cr(III) to Cr(VI) in natural environments. In this study, the Cr(III)-citrate complex (Cr(III)-cit) was prepared and its speciation was determined by high performance liquid chromatography (HPLC). Results showed that Cr(III)-cit existed in [Cr(III)-H-cit](+) and [Cr(III)-cit] species in a pH range of 3-5, in [Cr(III)-cit] only from pH 6-8, in [Cr(III)-cit] and [Cr(III)-OH-cit](-) from pH 9-11, and only in [Cr(III)-OH-cit](-) at pH 12. Additional experiments were conducted in batch systems with pHs of 5 to 12 at 25 °C, where aqueous Cr(III) and Cr(III)-cit were fully exposed to light from medium pressure mercury lamps and a xenon lamp mimicking solar light irradiation. Results demonstrated that oxidation of Cr(III) in Cr(III)-cit was much faster than that in aqueous Cr(III). Rates of Cr(III) photo-oxidation were not sensitive to pH in the range from 7 to 9 but increased significantly with further increases in pH, which was consistent with the distribution of Cr(III) forms. It appeared that [Cr(III)-cit-OH](-) was the most photochemically active form and Cr(II), resulting from a ligand-to-metal charge-transfer (LMCT) pathway after light absorption, was a precursor of the oxidation of Cr(III) to Cr(VI). Both dissolved oxygen and the hydroxyl radical ((•)OH), an intermediate, served as oxidants and facilitated the oxidation of Cr(II) to Cr(VI) via a multiple step pathway. The photoproduction of (•)OH was detected by HPLC using benzene as a probe, supporting the proposed reaction mechanism.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.