Effective blockage of chloride ion quenching and chlorinated by-product generation in photocatalytic wastewater treatment

Photocatalytic degradation of pollutants in high salinity wastewater usually shows extremely low activities and produces highly toxic by-products, often related to the presence of excess chloride ion (Cl − ). Herein, we report for the first time that involvement of Cl − (quenching active species and generating chlorinated by-products) could be effectively blocked during photocatalytic processes. Based on a comprehensive investigation of its mechanism, we found that Cl − could quench superoxide radicals ( O 2 − ) through a cyclic indirect quenching model with holes (h + ) and hydroxyl radicals ( OH) quenching as "initiators". Thus, scavenging h + and OH could successfully block the chain reactions between Cl − and O 2 − , and photocatalytic degradation of methyl orange (a refractory dye, with O 2 − as dominant attacking species) could be enhanced by nearly 50 times, even when Cl − content was up to 10 wt%. More importantly, both HPLC-MS analyses and DFT calculation validated that, by blocking its quenching effect, Cl − could be successfully excluded from the pollutant degradation processes, thus preventing the generation of toxic chlorinated by-products. This work provides new insights into control of chlorinated by-products and proposes feasible strategies to extend photocatalytic technology in high salinity wastewater.