Electrocatalytic Reduction of Nitrate in Water with a Palladium-Modified Copper Electrode
A highly active electrocatalytic electrode for nitrate reduction was prepared by the electro-deposition of palladium onto a copper electrode. The capacity of nitrate reduction by a palladium-modified copper electrode has been studied using cyclic voltammetry (CV). The existence of a reduction peak at −0.605 V versus saturated calomel electrode in 0.1-M sodium nitrate + 0.1-M perchloric acid solution (pH = 0.86) can be found in the CV measurement. The influence of solution properties, such as pH, nitrate concentration, and other anions in solution, on nitrate reduction was determined in detail. Results showed that nitrate reduction was suppressed in alkaline solution, while it was beneficial to nitrate reduction in acid or neutral solution. At low nitrate concentrations (0.01 to 0.5 M), nitrate reduction current increased with increasing nitrate concentration, but was hindered by sulfate. At high nitrate concentrations (1 to 5 M), no significant difference on nitrate reduction was observed. Compared with other different electrodes prepared in our work (copper, titanium, and palladium-modified titanium electrodes), the palladium-modified copper electrode showed the highest electrocatalytic capacity and stability in the nitrate-reduction process.
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Document Type: Research Article
Publication date: 2006-07-01
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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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