Removal of Acid Orange 7 in simulated wastewater using a three-dimensional electrode reactor: Removal mechanisms and dye degradation pathway

被引:214
|
作者
Zhao, Hua-Zhang [1 ]
Sun, Yan [1 ]
Xu, Li-Na [1 ]
Ni, Jin-Ren [1 ]
机构
[1] Peking Univ, Dept Environm Engn, Coll Environm Sci & Engn, Key Lab Water & Sediment Sci,Minist Educ, Beijing 100871, Peoples R China
关键词
Electrolytic treatment; Three-dimensional electrode reactor; Acid Orange 7; Removal mechanisms; Degradation pathway; BORON-DOPED DIAMOND; INDUCED PHOTOCATALYTIC DEGRADATION; AQUEOUS TIO2 SUSPENSIONS; II AZO-DYE; ELECTROCHEMICAL DEGRADATION; ORGANIC POLLUTANTS; ANODIC-OXIDATION; ACID-ORANGE-7; DECOLORIZATION; PHENOL;
D O I
10.1016/j.chemosphere.2009.10.034
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The removal of Acid Orange 7 (AO7) in simulated wastewater was experimentally investigated using a three-dimensional electrode reactor with granular activated carbon as the particle electrode, ACF (activated carbon fiber)/Fe as the anode, and ACF/Ti as the cathode. Particular attention was paid to the reaction mechanisms and the dye degradation pathway in the system. The removal of AO7 in the system was mainly dependent on the oxidation by the produced active substances (center dot OH, etc.) and the coagulation by Fe(II) or Fe(III) dissolved from the anode. The former mechanism was predominant. A possible pathway for AO7 degradation was proposed by monitoring the temporal evolution of intermediates in the solution, with the use of some techniques including GC/MS, FTIR and HPLC. The AO7 molecule was observed to be firstly decomposed to aromatic intermediates, further degraded to ring opening products and finally mineralized to CO(2), H(2)O and inorganic salts. The intermediates increased the biodegradability of the wastewater, which was proved by the increase of the BOD/COD value after electrolysis treatment. The three-dimensional electrode method can be considered an effective alternative to dye wastewater pretreatment prior to the biological process. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:46 / 51
页数:6
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