pH-dependent degradation of acid orange II by zero-valent iron in presence of oxygen

被引:74
作者
He, Chun [1 ,2 ]
Yang, Jiannan [1 ]
Zhu, Linfei [1 ,4 ]
Zhang, Qiong [1 ]
Liao, Weichen [1 ]
Liu, Shangkun [1 ]
Liao, Yu [1 ]
Abou Asi, Mudar [1 ]
Shu, Dong [3 ]
机构
[1] Sun Yat Sen Univ, Sch Environm Sci & Engn, Guangzhou 510275, Guangdong, Peoples R China
[2] Guangdong Prov Key Lab Environm Pollut Control &, Guangzhou 510275, Guangdong, Peoples R China
[3] S China Normal Univ, Sch Chem & Environm, Key Lab Technol Electrochem Energy Storage & Powe, Guangzhou 510006, Guangdong, Peoples R China
[4] Florida Inst Technol, Dept Chem, Melbourne, FL 32901 USA
基金
中国国家自然科学基金;
关键词
Zero-valent iron (ZVI); Acid orange II; ZVI/O-2; system; pH-dependent; DYE WASTE-WATER; ZEROVALENT IRON; PHOTOCATALYTIC ACTIVITY; AQUEOUS-SOLUTION; AZO DYES; OXIDATION; FENTON; DECOLORIZATION; IRRADIATION; REDUCTION;
D O I
10.1016/j.seppur.2013.04.028
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this study, zero-valent iron (ZVI)-mediated advanced oxidation was applied to degrade the acid orange II (AOII) in the presence of oxygen. The effect of pH value, ZVI dosage, O-2 concentration and added Fe2+ ions on the degradation efficiency was investigated. It was found that the increases of acidity in aqueous solution, ZVI dosage and O-2 concentration were favorable to the oxidation reaction of AOII in ZVI-mediated advanced oxidation processes. The lower pH value in aqueous medium was favorable for AOII degradation in ZVI/O-2 system. The AM degradation efficiency and COD removal efficiency system could achieve more than 95% and 65% within 3 h in the ZVI/O-2 at initial pH 3.0, respectively. The AOII degradation in ZVI/O-2 system followed the first-order reaction kinetics at pH range of 3.0-7.0, while AOII degradation followed the zero-order reaction kinetics at pH range of 9.0-11.0. The measurements of H2O2 and Fe2+ in ZVI/O-2 system, and the characterization for used ZVI particles demonstrated the role of Fenton reaction in the ZVI/O-2 system, which occurred favorably at low pH to generate H2O2 and Fe2+, followed by a likely species OH to degrade AOIL The involvement of OH in oxidizing AOII was examined by determining the degradation rates using OH scavenger. Moreover, the coexistence ions had no significantly influence the oxidation process, indicating the true application process. Finally, organic compounds as intermediates of the degradation process were identified by LC/MS. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 68
页数:10
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