Photocatalytic Oxidation Mechanism of As(III) on TiO2: Unique Role of As(III) as a Charge Recombinant Species

Abstract

Using TiO2 photocatalyst, arsenile, As(III), can be rapidly oxidized to arsenate, As(V), which is less toxic and less mobile in the aquatic environment. Therefore, the TiO2/UV process can be employed as an efficient pretreatment method for arsenic contaminated water. Since we first reported in 2002 that the superoxide (or hydroperoxyl radical) plays the role of main oxidant of As(III) in the TiO2/UV process, there has been much debate over the true identity of the major photooxidant among superoxides, holes, and OH radicals. The key issue is centered on why the much stronger OH racicals cannot oxidize As(III), and it has been proposed that the unique role of As(III) as an external charge recombination center on the UV-excited TiO2 particle is responsible for this e;:centric mechanism. Although the proposed mechanism has been supported by many experimental evidences, doubts on it were not clearly removed. In this study, we provided direct and undisputed evidence to support the role of As(III) in the c large recombination dynamics using time-resolved transient absorption spectroscopy. The presence of As(III) indeed mediated the charge recombination in TiO2. Under this condition, the role of the OH radical is suppressed because of the null cycle, and the weaker oxidant, superoxide, should prevail. The role of the superoxide has been previously doubted on the basis of the observation that the addition of excess formic ac d (hole scavenger that should enhance the production of superoxides) inhibited the photocatalytic oxidation of As(III). However, this study proved that this was due to the photogeneration of reducing radicals (HCO2 center dot) that recycle As(V)/As(IV) back to As(III). It was also demonstrated that the 4-chlorophenol/TiO2 system under visible light that cannot generate neither OH radicals nor valence band holes converted As(III) to As(V) through the superoxide pathway.