Nitrate reduction by zero-valent iron under different pH regimes
- Authors
- Choe, SH; Liljestrand, HM; Khim, J
- Issue Date
- 3월-2004
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Keywords
- SULFATE GREEN RUST; CHLORINATED ETHENES; CHEMICAL REDUCTION; METALLIC IRON; GROUND-WATER; KINETICS; NITRITE; DEHALOGENATION; DECHLORINATION; DEGRADATION
- Citation
- APPLIED GEOCHEMISTRY, v.19, no.3, pp.335 - 342
- Indexed
- SCIE
SCOPUS
- Journal Title
- APPLIED GEOCHEMISTRY
- Volume
- 19
- Number
- 3
- Start Page
- 335
- End Page
- 342
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/124329
- DOI
- 10.1016/j.apgeochem.2003.08.001
- ISSN
- 0883-2927
- Abstract
- Nitrate in drinking water can pose a threat to human health. A study of the reduction of NO3-, by Fe-0 is reported here. The anaerobic reduction of NO3- was carried out using Fe-0 powder in unbuffered solutions from pH 2 to greater than 10. The initial pH of the solution was adjusted to 2, 3, or 4 by addition of HCl, H2SO4, or CH3COOH, because the Fe oxidation and NO3- reduction reactions consume acidity. Under the conditions of this study, NH3/NH4+ were the only N products. The formation of green rusts divided the NO3- reduction process into two phases. Green rusts formed around a pH of 6.5 and contributed to the stabilization of pH. With H2SO4, the available Fe surface area was limited, initially by the excessive accumulation of H-2 gas at the interface, which inhibited NO3- reduction. The surface area normalized pseudo-first order reaction rates for NO3- reduction at pH > 6.5 or after the formation of green rusts are consistent with those reported for buffered solutions. (C) 2003 Elsevier Ltd. All rights reserved.
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