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Enhancing hydroxyl radical production from cathodic ozone reduction during the ozone-electrolysis process with
Xiangyu Li1, Gang Yu1, Yujue Wang1
1School of Environment, Beijing Key Laboratory for Emerging Organic Contaminants Control, State Key Joint Laboratory of Environmental Simulation and Pollution Control, Tsinghua University, Beijing, 100084, China.
Abstract:
In this study, a flow-through ozone-electrolysis (O3-electrolysis) process was developed by combining ozonation with an electrolysis using a porous reactive electrochemical membrane (REM) cathode. Due to the convection-enhanced mass transport and fast radial diffusion inside the small pores of REM cathodes, the rate of cathodic O3 reduction to ozonide radicals (O3•-) was significantly enhanced, while the further cathodic O3•- reduction to oxygen was inhibited during the flow-through O3-electrolysis process compared to the conventional mixed-tank O3-electrolysis process. Consequently, more hydroxyl radicals (•OH) were formed from O3•- decay in water during the flow-through O3-electrolysis process than the mixed-tank O3-electrolysis process. Corresponding to the higher •OH yields from cathodic O3 reduction, the flow-through O3-electrolysis process substantially enhanced the abatement kinetics and efficiency of para-benzoic acid (pCBA, a model compound of ozone-resistant micropollutant) in a groundwater than conventional ozonation and the mixed-tank O3-electrolysis process. These results suggest that the flow-through O3-electrolysis process may provide a competitive treatment technology for micropollutant abatement in water treatment.
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