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Influence of Operating Conditions on Electrochemical Reduction of Nitrate in Groundwater

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The influences of current density, initial pH, cation and anion concentrations, and the coexistence of Ca2+ and HCO3 on the efficiency of electrochemical nitrate reduction by a copper cathode and Ti/IrO2 anode in an undivided cell were studied. In the presence of 5 mM of sodium chloride (NaCl), the nitrate-nitrogen concentration decreased from 3.57 to 0.69 mM in 120 minutes, and no ammonia or nitrite byproducts were detected. The nitrate reduction rate increased as the current density increased. The electrochemical method performed well at an initial pH range of 3.0 to 11.0. The rate of nitrate reduction increased as concentrations of Na+, K+, and Ca2+ increased. The anion of the supporting electrolyte decreased the rate of reduction in the order Cl > HCO3 2- = CO3 2- > SO4 2- at both 5 mM and 10 mM of anion. The coexistence of Ca2+ and HCO3 ions could inhibit nitrate reduction. The concentration of nitrate-nitrogen in polluted groundwater decreased from 2.80 to 0.31 mM after electrolysis for 120 minutes.

Keywords: Ti/IrO2; anion; cation; copper; electrohemical; nitrate reduction

Document Type: Research Article


Affiliations: 1:  School of Water Resources and Environment, China University of Geosciences (Beijing), Beijing 100083, China 2:  China Institute of Water Resources and Hydropower Research, Beijing, China

Publication date: March 1, 2013

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  • Water Environment Research® (WER®) publishes peer-reviewed research papers, research notes, state-of-the-art and critical reviews on original, fundamental and applied research in all scientific and technical areas related to water quality, pollution control, and management. An annual Literature Review provides a review of published books and articles on water quality topics from the previous year.

    Published as: Sewage Works Journal, 1928 - 1949; Sewage and Industrial Wastes, 1950 - 1959; Journal Water Pollution Control Federation, 1959 - Oct 1989; Research Journal Water Pollution Control Federation, Nov 1989 - 1991; Water Environment Research, 1992 - present.
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