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Updated: Jun 14, 2026

Electrochemically and Bioelectrochemically Induced Ammonium Recovery
Published on: January 22, 2015
Treatment of nitrate contaminated water using an electrochemical method
Miao Li1, Chuanping Feng, Zhenya Zhang
1School of Water Resources and Environment, China University of Geosciences (Beijing), Beijing, China.
Abstract:
Treatment of nitrate contaminated water which is unsuitable for biological removal using an electrochemical method with Fe as a cathode and Ti/IrO(2)-Pt as an anode in an undivided cell was studied. In the absence and presence of 0.50 g/L NaCl, the nitrate-N decreased from 100.0 to 7.2 and 12.9 mg/L in 180 min, respectively, and no ammonia and nitrite by-products were detected in the presence of NaCl. The nitrate reduction rate increased with increasing current density, with the nitrate reduction rate constant k(1) increasing from 0.008 min(-1) (10 mA/cm(2)) to 0.016 min(-1) (60 mA/cm(2)) but decreasing slightly with increasing NaCl concentration. High temperature favoured nitrate reduction and the reaction followed first order kinetics. The combination of the Fe cathode and Ti/IrO(2)-Pt anode was suitable for nitrate reduction between initial pH values 3.0 and 11.0. e.g. k(1)=0.010 min(-1) (initial pH 3.0) and k(1)=0.013 min(-1) (initial pH 11.0). Moreover, the surface of all used cathodes appeared rougher than unused electrodes, which may have increased the nitrate reduction rate (4-6%).
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