4.8 Article

Electrocatalytic reduction of nitrate in water

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WATER RESEARCH
卷 37, 期 10, 页码 2512-2519

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0043-1354(03)00008-3

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drinking water; chemical denitrification; rural communities; water quality; agriculture industry

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Nitrate (NO3-) contamination of groundwater is a common problem throughout intensive agricultural areas (nonpoint source pollution). Current processes (e.g., ion exchange, membrane separation) for NO3- removal have various disadvantages. The objective of this study was to evaluate an electrocatalytic reduction process to selectively remove NO3- from groundwater associated with small agricultural communities. A commercially available ELAT (E-Tek Inc., Natick, MA) carbon cloth with a 30% surface coated Rh (rhodium) (1 mug cm(-1)) was tested at an applied potential of -1.5 V versus standard calomel electrode (SCE) with a Pt auxiliary electrode. Electrocatalytic reduction process (electrolysis) of NO3- was tested with cyclic voltammetry (CV) in samples containing NO3- and 0.1 M NaClO4-. Nitrate and NO2- concentrations in test solutions and groundwater samples were analyzed by ion chromatography (IC). The presence of Rh on the carbon cloth surface resulted in current increase of 36% over uncoated carbon cloths. The electrocatalysis experiments using Rh coated carbon cloth resulted in reduction of NO3- and NO2- on a timescale of minutes. Nitrite is produced as a product, but is rapidly consumed upon further electrolysis. Field groundwater samples subjected to electrocatalysis experiments, without the addition of NaClO4- electrolyte, also exhibited removal of NO3- on a timescale of minutes. Overall, results suggest that at an applied potential of -1.5 V with respect to SCE, Rh coated carbon cloth can reduce NO3- concentrations in field groundwater samples from 73 to 39 mg/L (16.58 to 8.82 mg/L as N) on a timescale range of 40-60 min. The electrocatalytic reduction process described in this study may prove useful for removing NO3- and NO2- from groundwater associated with nonpoint source pollution. (C) 2003 Elsevier Science Ltd. All rights reserved.

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