Effect of Electro-Fenton Application on Azo Dyes Biodegradability

被引:18
作者
Elias, B. [2 ]
Guihard, L. [2 ]
Nicolas, S. [2 ]
Fourcade, F. [1 ,3 ]
Amrane, A. [1 ,3 ]
机构
[1] Univ Rennes 1, CNRS, UMR 6226, F-35708 Rennes 7, France
[2] Univ Rennes 1, Dept Chim, IUT Rennes, F-35014 Rennes, France
[3] Univ Europeenne Bretagne, Rennes, France
关键词
electro-Fenton; Azo dyes; removal; biodegradability; toxicity; METHYL-RED-DYE; PHOTOCATALYTIC DEGRADATION; WASTE-WATER; AQUEOUS-MEDIUM; PHOTO-FENTON; ORANGE-II; MINERALIZATION; REMOVAL; DECOLORIZATION; REAGENT;
D O I
10.1002/ep.10457
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The aim of this study was to examine the feasibility of combining an electro-Fenton pre-treatment and a biological treatment to remove azo dyes from aqueous effluents. The electro-Fenton reaction was performed in a two-compartment system involving a reference (saturated calomel electrode), a platinum anode and a graphite felt cathode. For the three considered dyes, high discoloration (in the range 77.1-97.8%) and low mineralization (in the range 7.7-18.8%) after 4-h reaction were in favor of the hybrid process, which was confirmed during subsequent experiments with methyl red sodium salt (MRSS) as a model dye. When potential-controlled electrolysis at -0.5 V/SCE was performed with a carbon-felt cathode surface of 378 cm(2) and a catalytic amount of ferric iron of 1 mmol L-1, less than 1-h reaction was needed for an almost total discoloration (90.5%); while mineralization and oxidation remained low even after 48-h reaction, 11.1 and 57.2%, respectively. High discoloration level concomitantly to low mineralization and oxidation for MRSS removal which were in favor of a hybrid process, confirmed by the decrease of the COD on DOC ratio (45.1%) and the increase of the average oxidation state AOS (2.1). Final BOD5 on COD ratio of 0.24 and an absence of toxicity of the treated solution (EC50 = 165%) also showed the positive impact of an electro-Fenton pretreatment. (C) 2010 American Institute of Chemical Engineers Environ Prog, 30: 160-167, 2011
引用
收藏
页码:160 / 167
页数:8
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