化学
氨
氯胺
氯
激进的
无机化学
光化学
氮气
电化学
有机化学
电极
物理化学
作者
Shuo Wang,Xiaoling Huang,Luowei Pei,Xinyi Zhu,Songming Zhu,Ying Liu,Zhangying Ye
标识
DOI:10.1016/j.jclepro.2022.135515
摘要
UV photo-electrocatalytic process has emerged as a promising approach for the abatement of ammonia nitrogen in wastewater. However, the radical chemistry for ammonia nitrogen removal in this process requires further clarification. The heterogeneous reaction pathways and mechanism of ammonia nitrogen oxidation in the UV photo-electrocatalytic process were investigated in this study. Photocurrents of the Ti/RuO2-IrO2-TiO2 electrodes with good electrocatalytic behavior were enhanced by UV radiation. Compared with the electrocatalytic process, the removal rates of ammonia nitrogen were improved by 12.4%∼20% at the Cl− concentration of 50 mM in the photo-electrocatalytic process. The ammonia nitrogen was mainly transferred into N2, meanwhile, the formation of nitrogenous by-products, active chlorine, and chloramines was inhibited in the photo-electrocatalytic process. The contribution of UV radiation was to photo-decompose the active chlorine and chloramines, generating free radicals. The removal efficiency of ammonia nitrogen reached more than 64% after the elimination of free radicals. The electro-generated HOCl was the principal species for ammonia nitrogen removal, and the synergistic effect for the acceleration of ammonia nitrogen oxidation resulted from the photo-generated chlorine radicals. This investigation provides insight into the electrochemistry, photochemistry, and radical chemistry for the heterogeneous catalytic degradation of ammonia nitrogen by UV photo-electrocatalytic process.
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