TECHNICAL PAPERS
Apr 3, 2009

Electrolytic Oxidation of Polynuclear Aromatic Hydrocarbons from Creosote Solution Using TI/IRO2 and TI/SNO2 Circular Mesh Electrodes

Publication: Journal of Environmental Engineering
Volume 135, Issue 10

Abstract

The electrooxidation of polynuclear aromatic hydrocarbons (PAHs) in solution was investigated. Most of the PAHs compounds are toxic and hardly biodegradable, so that a chemical or physicochemical treatment is required. In this paper, we reported treatment of synthetic creosote oily effluent (COE) containing several PAHs by using Ti/IrO2 and Ti/SnO2 circular or cylindrical mesh anode electrodes. COE was prepared with distilled water and a commercial creosote solution in the presence of an amphoteric surfactant (CAS). In addition to anode material, different operating parameters were investigated such as current density, reaction time, recycling flow rate, and oxygen injection flow rate. The first series of experiments carried out in the recirculating batch reactor showed that circular Ti/SnO2 electrode was found to be more effective in removing PAHs than circular or cylindrical Ti/IrO2 electrodes. Current density and retention time played important roles for PAHs degradation efficiency, whereas circulation flow rate and oxygen injection slightly influenced the removal efficiency. Finally, the best and simplest operating conditions (82–84% of PAHs removal) determined for PAHs degradation in COE were obtained at a current density of 15mA/cm2 through 90 min of treatment with a recycling rate of 3.6 L/min but without O2 injection in the close loop. Likewise, in the recirculating batch tests, PAHs decomposition exhibited behaviors of the fist-order reaction with a rate coefficient (k) of 0.015min1 . The energy consumption was 7.5kWh/m3 . The second series of experiment using successively batch and continuous treatment of COE shows that the percentage of PAHs degradation could be maintained above 80% up to 18 h of treatment, thereafter, removal efficiency decreased owing to the formation of organic substances on the electrodes surface.

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Acknowledgments

Sincere thanks are extended to the Canada Research Chairs and to the National Sciences, Engineering Research Council of Canada, and Filter Innovations Inc. for their financial contribution (Grant No. STPGP 320053-05) to this study.UNSPECIFIED

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Go to Journal of Environmental Engineering
Journal of Environmental Engineering
Volume 135Issue 10October 2009
Pages: 1051 - 1062

History

Received: Jul 24, 2008
Accepted: Feb 10, 2009
Published online: Apr 3, 2009
Published in print: Oct 2009

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Lan-Huong Tran [email protected]
Ph.D. Student, Institut National de la Recherche Scientifique (Centre Eau, Terre et Environnement), Université du Québec, 490 rue de la Couronne, PQ G1K 9A9, Canada. E-mail: [email protected]
Patrick Drogui [email protected]
Professor, Institut National de la Recherche Scientifique (Centre Eau, Terre et Environnement), Université du Québec, 490 rue de la Couronne, PQ G1K 9A9, Canada. E-mail: [email protected]
Guy Mercier [email protected]
Professor, Institut National de la Recherche Scientifique (Centre Eau, Terre et Environnement), Université du Québec, 490 rue de la Couronne, PQ G1K 9A9, Canada. E-mail: [email protected]
Jean-François Blais [email protected]
Professor, Institut National de la Recherche Scientifique (Centre Eau, Terre et Environnement), Université du Québec, 490 rue de la Couronne, PQ G1K 9A9, Canada (corresponding author). E-mail: [email protected]

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