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Nitrate reduction by zero-valent iron under different pH regimes

Authors
Choe, SHLiljestrand, HMKhim, 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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공과대학 (건축사회환경공학부)
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