In this study, the wet oxidation (WO) of two ammonium compounds, (NH4)(2)SO4 and [Cu(NF3)(4)]SO4, was carried out using persulfate (Na2S2O8, PS). Experiments involving the WO of ammonia were conducted in a lab-scale batch reactor at temperatures 313-343 K and a molar feed ratio of [Na-4(+)]/iSzOil = 1/5 under ambient air pressure. The results showed that in the (NH4)2SO4/PS system, ammonia was decomposed at temperatures above 323 K under alkaline conditions. The ammonia conversion increased with the increasing production of sulfate-free radicals at higher temperatures. At 343 K, after a 120-min reaction time, more than 95% of ammonia was decomposed at pH 13.5 and pH 8.0-11.0 in the (NH4)2SO4/PS and [Cu(NI13)41SO4/PS systems, respectively. Besides the major product of nitrogen gas, small quantities of NOi and NO were produced, but NO and NO2 were not produced in the two systems. The results also showed that the initial rates of ammonia decomposition and nitrogen gas production were higher in the [(NH4)(2)SO4/PS system than in the (NH4)(2)SO4/PS system. However, the N2 yield was saturated at approximately 75% in the [Cu(N1-13)4]SO4/PS system, which was lower than that after a 180-min reaction time in the (NH4)2SO41 PS system (-85%). Ammonia was more easily oxidized to N0j in the [Cu(NH3)(4)SO4/PS system (-18%) compared with the (NH4)(2)SO4/PS system (-7.5%), but no appreciable change occurred in the NO yield (-8%) in the two systems. Thus, it was proved that ammonia was effectively decomposed in the two reaction systems at temperatures lower than 343 K under ambient air pressure. (C) 2014 Elsevier B.V. All rights reserved.