Activated carbon catalyzed persulfate oxidation of Azo dye acid orange 7 at ambient temperature

被引:461
作者
Yang, Shiying [1 ,2 ]
Yang, Xin [1 ]
Shao, Xueting [1 ]
Niu, Rui [1 ]
Wang, Leilei [1 ]
机构
[1] Ocean Univ China, Coll Environm Sci & Engn, Qingdao 266100, Peoples R China
[2] Minist Educ, Key Lab Marine Environm & Ecol, Qingdao 266100, Peoples R China
关键词
Persulfate oxidation; Activated carbon; Acid orange 7; Radical mechanism; Recovery; WET PEROXIDE OXIDATION; BUTYL ETHER MTBE; HYDROGEN-PEROXIDE; AQUEOUS-SOLUTION; RATE CONSTANTS; ORGANIC CONTAMINANTS; FENTONS REAGENT; DEGRADATION; ADSORPTION; WATER;
D O I
10.1016/j.jhazmat.2010.11.057
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Persulfate (PS) oxidative degradation of azo dye acid orange 7 (AO7) in an aqueous solution was studied in the presence of suspended granular activated carbon (GAC) at ambient temperature (e.g., 25 degrees C). It was observed that there existed a remarkable synergistic effect in the GAC/PS combined system. Higher PS concentration and GAC dosage resulted in higher AO7 degrading rates. Near-neutral was the optimal initial pH. Adsorption had an adverse effect on AO7 degradation. AO7 had not only a good decolorization, but a good mineralization. The decomposition of PS followed a first-order kinetics behavior both in the presence and in the absence of AO7. Radical mechanism was studied and three radical scavengers (methanol (MA), tert-butanol (TBA), phenol) were used to determine the kind of major active species taking part in the degradation of AO7 and the location of degradation reaction. It was assumed that the degradation of AO7 did not occur in the liquid phase, but in the porous bulk and boundary layer on the external surface of GAC. SO(4)(-center dot) or HO(center dot), generated on or near the surface of GAC, played a major role in the AO7 degradation. Finally, the recovery performance of GAC was studied through the GAC reuse experiments. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:659 / 666
页数:8
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