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Electrochemically and Bioelectrochemically Induced Ammonium Recovery
Published on: January 22, 2015
Electrochemical Shortcut Denitrification Coupled with Chemical Diazotization for Low-Carbon Nitrate Wastewater
Weixing Zhang1, Furong Guo2, Weiting Gong2
1Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Applied & Environmental Chemistry, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, 430079, P. R. China.
Abstract:
Efficient treatment of nitrate (NO3 -) 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 NO3 - 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 (NO3 --to-NO2 - conversion) with chemical diazotization (ESD-CD), where NO3 - is first electrochemically reduced to NO2 - by an oxide-derived Cu foam electrode, which then reacts with sulfamate (NH2SO3 -) via chemical diazotization to rapidly generate N2. For 5000 mg-N L-1 simulated NO3 - wastewater, the ESD-CD achieved 98.8% NO3 - removal efficiency, 99.9% N2 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 NO3 - wastewater (3085.2 mg-N L-1) with over 96.6% NO3 - removal efficiency and 99.2% N2 selectivity, and also reduced operational costs by 64.4% and 74.9%, and CO2 emissions by 79.5% and 93.3% in comparison with biological denitrification and multiple-effect evaporation, underscoring the promising potential of coupling selective electrochemical NO3 - reduction with chemical diazotization for sustainable treatment of high-concentration NO3 - wastewater.
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