Photocatalytic Activation of Permanganate for the Highly Efficient Oxidation of Micropollutant

Activation of permanganate (Mn(VII)) by generating intermediate manganese species (Mnint, i.e., Mn(V) and Mn(III)) has been demonstrated to be an efficient way to enhance the oxidative ability of Mn(VII). In this work, it was found that the addition of indium oxide (In2O3) could significantly enhance the visible light response of Mn(VII) (Vis/In2O3/Mn(VII)) by selecting flumequine (FLU) as a representative compound. The presence of In2O3 enhanced the degradation of FLU by the Vis/Mn(VII) process with the pseudo first-order rate constant increasing by around 30 folds. Intermediate Mnint (Mn(V) and Mn(III)) and hydroxyl radicals (•OH) were identified as the major oxidants in the Vis/In2O3/Mn(VII) process, and •OH outcompeted that of Mnint under alkaline conditions. The scavenge of photogenerated e- by Mn(VII) played a critical role in the generation of Mnint, while the reaction of photogenerated h+ with H2O contributed to the generation of •OH. The degradation efficiency of FLU showed a negative relationship with the increase of solution pH, likely due to the electrostatic repulsion between the deprotonated FLU and negatively charged In2O3 surfaces. Increasing Mn(VII) or In2O3 dosages enhanced the degradation of FLU by elevating the concentrations of reactive species. The presence of chloride, bicarbonate, and humic acid slightly inhibited FLU degradation by the Vis/In2O3/Mn(VII) process, due to their competitive scavenging of reactive species. Good stability and reusability of the In2O3 catalyst were obtained. This work proposed a new activation pathway for Mn(VII) and provided a novel approach for the treatment of emerging contaminants in aqueous environments.