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) 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, and photocatalytic degradation of methyl orange (a refractory dye, with O 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.
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http://dx.doi.org/10.1016/j.jhazmat.2020.122670 | DOI Listing |
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