反硝化
化学
硝酸盐
电化学
废水
污水处理
化学需氧量
环境化学
化学工业
碳纤维
蒸发
法拉第效率
过程(计算)
氮气
联轴节(管道)
工业废水处理
化学反应
化学还原
电解
制浆造纸工业
化学过程
废物管理
环境工程
无机化学
化工产品
化学能
环境科学
作者
Weixing Zhang,Furong Guo,Weiting Gong,Di Yang,Xia Yin,Falong Jia,Wendong Wei,Yancai Yao,Lizhi Zhang
标识
DOI:10.1002/anie.202516226
摘要
Abstract Efficient treatment of nitrate (NO 3 − ) wastewater with low carbon emission is a tough challenge because traditional multiple‐effect evaporation and biological denitrification are carbon‐intensive, especially in the case of NO 3 − concentration higher than 1000 mg‐N L −1 . In this study, we demonstrate a low‐carbon and high‐energy‐efficiency denitrification strategy by coupling electrochemical shortcut denitrification (NO 3 − ‐to‐NO 2 − conversion) with chemical diazotization (ESD‐CD), where NO 3 − is first electrochemically reduced to NO 2 − by an oxide‐derived Cu foam electrode, which then reacts with sulfamate (NH 2 SO 3 − ) via chemical diazotization to rapidly generate N 2 . For 5000 mg‐N L −1 simulated NO 3 − wastewater, the ESD‐CD achieved 98.8% NO 3 − removal efficiency, 99.9% N 2 selectivity, and 95.3% Faradaic efficiency. Impressively, its energy consumption was as low as 9.97 kWh kg‐N −1 , and its denitrification rate reached an unprecedented record of 24.87 g‐N m −2 h −1 . Driven by photovoltaic cells, the ESD‐CD process maintained stable performance in treating industrial NO 3 − wastewater (3085.2 mg‐N L −1 ) with over 96.6% NO 3 − removal efficiency and 99.2% N 2 selectivity, and also reduced operational costs by 64.4% and 74.9%, and CO 2 emissions by 79.5% and 93.3% in comparison with biological denitrification and multiple‐effect evaporation, underscoring the promising potential of coupling selective electrochemical NO 3 − reduction with chemical diazotization for sustainable treatment of high‐concentration NO 3 − wastewater.
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