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Structure and function of slow release organic carbon source in groundwater in-situ denitrification

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Structure and function of slow release organic carbon source in groundwater in-situ denitrification. / Zhang, D. Y.; Li, G. H.; Wang, Y. et al.
5th World Water Congress: drinking water treatment processes : selected papers of the 5th World Water Congress of the International Water Association held in Beijing, China, 10-14 September 2006. ed. / Helmut Kroiss. London: I W A PUBLISHING, 2006. p. 105-113 (WATER SCIENCE AND TECHNOLOGY: WATER SUPPLY; Vol. 6).

Research output: Contribution in Book/Report/Proceedings - With ISBN/ISSNConference contribution/Paperpeer-review

Harvard

Zhang, DY, Li, GH, Wang, Y & Zhou, GZ 2006, Structure and function of slow release organic carbon source in groundwater in-situ denitrification. in H Kroiss (ed.), 5th World Water Congress: drinking water treatment processes : selected papers of the 5th World Water Congress of the International Water Association held in Beijing, China, 10-14 September 2006. WATER SCIENCE AND TECHNOLOGY: WATER SUPPLY, vol. 6, I W A PUBLISHING, London, pp. 105-113, 5th World Water Congress of the International-Water-Association, Beijing, 10/09/06. https://doi.org/10.2166/ws.2006.785

APA

Zhang, D. Y., Li, G. H., Wang, Y., & Zhou, G. Z. (2006). Structure and function of slow release organic carbon source in groundwater in-situ denitrification. In H. Kroiss (Ed.), 5th World Water Congress: drinking water treatment processes : selected papers of the 5th World Water Congress of the International Water Association held in Beijing, China, 10-14 September 2006 (pp. 105-113). (WATER SCIENCE AND TECHNOLOGY: WATER SUPPLY; Vol. 6). I W A PUBLISHING. https://doi.org/10.2166/ws.2006.785

Vancouver

Zhang DY, Li GH, Wang Y, Zhou GZ. Structure and function of slow release organic carbon source in groundwater in-situ denitrification. In Kroiss H, editor, 5th World Water Congress: drinking water treatment processes : selected papers of the 5th World Water Congress of the International Water Association held in Beijing, China, 10-14 September 2006. London: I W A PUBLISHING. 2006. p. 105-113. (WATER SCIENCE AND TECHNOLOGY: WATER SUPPLY). doi: 10.2166/ws.2006.785

Author

Zhang, D. Y. ; Li, G. H. ; Wang, Y. et al. / Structure and function of slow release organic carbon source in groundwater in-situ denitrification. 5th World Water Congress: drinking water treatment processes : selected papers of the 5th World Water Congress of the International Water Association held in Beijing, China, 10-14 September 2006. editor / Helmut Kroiss. London : I W A PUBLISHING, 2006. pp. 105-113 (WATER SCIENCE AND TECHNOLOGY: WATER SUPPLY).

Bibtex

@inproceedings{dbcecbc82c5b409e9b38f4e60edd1b7b,
title = "Structure and function of slow release organic carbon source in groundwater in-situ denitrification",
abstract = "Many nitrate pollution cases exceed the threshold as recommended by the World Health Organization (50 mg NO3/L) and by the USA (10 mg N/L) for drinking water. In-situ denitrification was regarded as a good method to decrease nitrate contamination but is restricted by carbon absent in groundwater. Considering the disadvantages of known carbon sources, this paper provided slow-release organic carbon-source (SOC) technique to solve the problem and the results showed that SOC materials showed good performance during simulated groundwater denitrification. Structure analysis suggested that hydroxy chemical bond existed between PVA and starch in SOC and surface configuration changed with materials dissolving into water. After seven days of domestication, with 40-50 mg/L initial NO3-N, denitrification efficiency increased from 80.6% to 90.7% and the real COD consumption per N-NO3 reduction was 1.82-3.73 with 2.79 as average. Denitrification process followed the law of zero order kinetics and the parameter of denitrification dynamics, K, was from 0.1366 to 0.1873. It was suggested that SOC was a potential carbon source material (electron donor) suitable for in-situ groundwater denitrification.",
keywords = "groundwater, SOC, denitrification, in-situ",
author = "Zhang, {D. Y.} and Li, {G. H.} and Y. Wang and Zhou, {G. Z.}",
year = "2006",
doi = "10.2166/ws.2006.785",
language = "English",
isbn = "978-1-84339-587-4",
series = "WATER SCIENCE AND TECHNOLOGY: WATER SUPPLY",
publisher = "I W A PUBLISHING",
pages = "105--113",
editor = "Helmut Kroiss",
booktitle = "5th World Water Congress",
note = "5th World Water Congress of the International-Water-Association ; Conference date: 10-09-2006 Through 14-09-2006",

}

RIS

TY - GEN

T1 - Structure and function of slow release organic carbon source in groundwater in-situ denitrification

AU - Zhang, D. Y.

AU - Li, G. H.

AU - Wang, Y.

AU - Zhou, G. Z.

PY - 2006

Y1 - 2006

N2 - Many nitrate pollution cases exceed the threshold as recommended by the World Health Organization (50 mg NO3/L) and by the USA (10 mg N/L) for drinking water. In-situ denitrification was regarded as a good method to decrease nitrate contamination but is restricted by carbon absent in groundwater. Considering the disadvantages of known carbon sources, this paper provided slow-release organic carbon-source (SOC) technique to solve the problem and the results showed that SOC materials showed good performance during simulated groundwater denitrification. Structure analysis suggested that hydroxy chemical bond existed between PVA and starch in SOC and surface configuration changed with materials dissolving into water. After seven days of domestication, with 40-50 mg/L initial NO3-N, denitrification efficiency increased from 80.6% to 90.7% and the real COD consumption per N-NO3 reduction was 1.82-3.73 with 2.79 as average. Denitrification process followed the law of zero order kinetics and the parameter of denitrification dynamics, K, was from 0.1366 to 0.1873. It was suggested that SOC was a potential carbon source material (electron donor) suitable for in-situ groundwater denitrification.

AB - Many nitrate pollution cases exceed the threshold as recommended by the World Health Organization (50 mg NO3/L) and by the USA (10 mg N/L) for drinking water. In-situ denitrification was regarded as a good method to decrease nitrate contamination but is restricted by carbon absent in groundwater. Considering the disadvantages of known carbon sources, this paper provided slow-release organic carbon-source (SOC) technique to solve the problem and the results showed that SOC materials showed good performance during simulated groundwater denitrification. Structure analysis suggested that hydroxy chemical bond existed between PVA and starch in SOC and surface configuration changed with materials dissolving into water. After seven days of domestication, with 40-50 mg/L initial NO3-N, denitrification efficiency increased from 80.6% to 90.7% and the real COD consumption per N-NO3 reduction was 1.82-3.73 with 2.79 as average. Denitrification process followed the law of zero order kinetics and the parameter of denitrification dynamics, K, was from 0.1366 to 0.1873. It was suggested that SOC was a potential carbon source material (electron donor) suitable for in-situ groundwater denitrification.

KW - groundwater

KW - SOC

KW - denitrification

KW - in-situ

U2 - 10.2166/ws.2006.785

DO - 10.2166/ws.2006.785

M3 - Conference contribution/Paper

SN - 978-1-84339-587-4

T3 - WATER SCIENCE AND TECHNOLOGY: WATER SUPPLY

SP - 105

EP - 113

BT - 5th World Water Congress

A2 - Kroiss, Helmut

PB - I W A PUBLISHING

CY - London

T2 - 5th World Water Congress of the International-Water-Association

Y2 - 10 September 2006 through 14 September 2006

ER -