Optimized titania nanotubes photoanode mediated photoelectrochemical oxidation of ammonia in highly chlorinated wastewater via Cl-based radicals.

Efficient removal of low-concentration ammonia from chlorinated wastewater is a challenge for decentralized wastewater treatment due to its notorious environmental effect and lethal influence on aquaculture. Photoelectrocatalytic (PEC) oxidation process is considered as an efficient and environment-friendly approach, whereas a low-cost and stable photoanode is crucial. In this study, TiO nanotubes (TNTs) photoanode (Ar-TNT-500 °C) with excellent physicochemical and photoelectrochemical properties was prepared by optimizing the parameters of anodization, including the voltage/times of anodization and the atmosphere/temperature of heat treatment. During the synthesis, the electrochemical and heat treatment processes promoted the formation of oxygen vacancies (O) on the TNTs surface and enhanced its electrocatalytic activity. The optimized Ar-TNT-500 °C photoanode could selectively convert ammonia to N (86%) and a small amount of nitrate (14%). Radical quenching and probe experiments confirmed that the ClO produced by rapid quenching of OH and Cl by free chlorine dominated the selective degradation of ammonia in the synergistic process of photocatalysis and electrocatalysis. The cycle of chlorine-based radicals (ClO and Cl) and Cl provided a continuous and efficient ammonia oxidation system, because chlorine-based radicals could efficiently and selectively oxidize ammonia and reduce the production of toxic (per) chlorate.