TECHNICAL PAPERS
Jan 16, 2004

Catalytic Wet Oxidation of Ammonia Solution: Activity of the Copper–Lanthanum–Cerium Composite Catalyst

Publication: Journal of Environmental Engineering
Volume 130, Issue 2

Abstract

Aqueous solutions that contained 400–1,000 mg/L of ammonia were oxidized in a trickle-bed reactor in this study of copper–lanthanum–cerium composite catalysts, which were prepared by the co-precipitation of copper nitrate, lanthanum nitrate and cerium nitrate at various molar concentrations. Results revealed that the conversion of ammonia by wet oxidation in the presence of copper–lanthanum–cerium composite catalysts was a function of the molar ratio of the copper–lanthanum–cerium catalyst. The ammonia solutions were barely removed by wet oxidation in the absence of any catalyst, while around 95% of the ammonia was reduced during the wet oxidation over the copper–lanthanum–cerium (7:2:1, molar/molar/molar) catalyst at 503 K and an oxygen partial pressure of 4.0 MPa. The kinetics of ammonia oxidation over a catalyst could be explained by a zero-order rate expression. Furthermore, the effect of the initial concentration and reaction temperature on the removal of ammonia from the effluent streams was also investigated at a liquid hourly space velocity of under 9h-1 in wet catalytic processes.

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Information & Authors

Information

Published In

Go to Journal of Environmental Engineering
Journal of Environmental Engineering
Volume 130Issue 2February 2004
Pages: 193 - 200

History

Received: Apr 9, 2002
Accepted: Mar 24, 2003
Published online: Jan 16, 2004
Published in print: Feb 2004

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Authors

Affiliations

Chang-Mao Hung
Graduate Student, Institute of Environmental Engineering, National Sun Yat-Sen Univ., Kaohsiung, Taiwan 804, Republic of China.
Jie-Chung Lou
Professor, Institute of Environmental Engineering, National Sun Yat-Sen Univ., Kaohsiung, Taiwan 804, Republic of China (corresponding author).
Chia-Hua Lin
Graduate Student, Institute of Environmental Engineering, National Sun Yat-Sen Univ., Kaohsiung, Taiwan 804, Republic of China.

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