过硫酸盐
氮气
氨
钙
化学
氧化钙
无机化学
过硫酸铵
氧化物
环境化学
有机化学
催化作用
聚合
聚合物
作者
Hanling Jiang,Xiaogang Wang,Aijuan Zhou,Y. Q. Liu
出处
期刊:ACS ES&T engineering
[American Chemical Society]
日期:2024-02-23
卷期号:4 (5): 1092-1101
标识
DOI:10.1021/acsestengg.3c00566
摘要
Advanced oxidation processes (AOPs) for removing ammonia nitrogen (NH4+-N) are of increasing interest in wastewater treatment. In this paper, the UV-activated persulfate (PS) process with CaO was applied to oxidize NH4+-N to nitrogen gas (N2). Nearly all of the NH4+-N (30 mg N/L) could be removed within 15 min, and the N2 selectivity was achieved at 95.0%. The addition of CaO made NH4+-N exist in the form of NH3, and HO• was the critical reactive species for NH4+-N oxidation. NO, N2H4, and NO2– were identified as oxidation intermediates and could be further removed. The reaction between N2H4 and NO2– with the assistance of UV/CaO promoted N2 generation during NH4+-N oxidation. The increased dosages of CaO (0.2 to 4.0 g/L) and PS (0.6 to 2.4 g/L) could enhance the NH4+-N oxidation, while the presence of CO32– (100 mM) significantly retarded the removal of NH4+-N. As high removal of NH4+-N (100%) and high N2 selectivity (>79.5%) could be achieved in lake water and secondary wastewater, the proposed UV/PS/CaO process could be potentially applied for the oxidation of NH4+-N in practical water treatment.
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