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- W3136995287 abstract "It is highly concerned to explore heterogeneous catalysts of metal oxides to remove NH4+-N in the wastewater, in which NH4+-N can be greatly oxidized as gaseous nitrogen in the mild reaction conditions. Herein, the high-efficient catalyst cobalt oxide modified by Mg was prepared, and the structures of catalyst were thoroughly characterized by SEM, XRD, ICP, Raman and ESR. Furthermore, the reaction kinetics of ammonia and affecting ammonia removal factors were investigated. In addition, the mechanism of catalytic ozonation for degrading NH4+ to gaseous nitrogen was also clarified. At the condition of 30 °C, initial pH = 8.0 and catalyst dosage of 2.0 g/L, 30.00 mg/L NH4+-N (source: NH4Cl) was almost completely oxidized and TN removal efficiency was 84.26% after 60 min. The degradation of ammonia and the conversion of Cl− both followed pseudo-zero kinetics. The presence of SO42−, CO32− and PO43− inhibited the degradation of ammonia with the order: SO42− < CO32− < PO43−, while the coexistence of Br− greatly promoted the ammonia conversion to gas. It was assumed that ozone transfers an oxygen atom to the Cl− ion at the active site on the catalyst surface, producing ClO− ions to form intermediates, which further oxidized NH4+-N to NO2−, NO3− and other gaseous nitrogen compounds. These results achieved might encourage the development of novel heterogeneous catalysts to active O3 for indirect oxidation of ammonia to gaseous nitrogen effectively." @default.
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- W3136995287 date "2021-08-01" @default.
- W3136995287 modified "2023-10-02" @default.
- W3136995287 title "A new insight into catalytic ozonation of ammonia by MgO/Co3O4 composite: The effects, reaction kinetics and mechanism" @default.
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- W3136995287 doi "https://doi.org/10.1016/j.cej.2021.129461" @default.
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