Heterogeneous electro-Fenton oxidation of azo dye methyl orange catalyzed by magnetic Fe3O4 nanoparticles

被引:42
|
作者
Jiang, Hao [1 ]
Sun, Yabing [1 ]
Feng, Jingwei [2 ,3 ]
Wang, Jian [1 ]
机构
[1] Nanjing Univ, State Key Lab Pollut Control & Resources Reuse, Sch Environm, Nanjing 210046, Jiangsu, Peoples R China
[2] Hefei Univ Technol, Sch Civil & Hydraul Engn, Hefei 230009, Peoples R China
[3] Hohai Univ, State Key Lab Hydrol Water Resources & Hydraul En, Nanjing 210098, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
electro-Fenton process; H2O2; iron leaching; magnetic Fe3O4 nanoparticles; methyl orange; PHOTOCATALYTIC DEGRADATION; HYDROGEN-PEROXIDE; DECOLORIZATION; REMOVAL; WATER; DFT; NBO;
D O I
10.2166/wst.2016.300
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Azo dye methyl orange (MO) degradation by heterogeneous electro-Fenton (EF) with a magnetic nano-Fe3O4 catalyst was investigated. In this study, Fe3O4 was synthesized by a coprecipitation method and characterized by X-ray diffraction and scanning electron microscopy. The influences of the main operating parameters such as current density, pH, catalyst dosage and aeration rate were studied. The results revealed that higher current density, catalyst dosage and aeration rate facilitated the degradation of MO, whereas the degradation efficiency of MO was decreased with an increase in the initial pH. After 90 min EF process, the volume of 500 mL, the initial concentration of 50 mg L-1 MO solution could be degraded by 86.6% with the addition of 1 g L-1 Fe3O4 under the current density of 10 mA cm(-2) and pH 3, compared with 69.5% for the electrolytic process alone. Meanwhile, a total organic carbon removal of 32% was obtained, up to 35.5 mg L-1 accumulated H2O2 and less than 3.5mg L-1 Fe leaching were detected. Moreover, based on the results of natural bond orbital (at B3LYP/6-311G (d, p)) and liquid chromatograph-triple quadrupole mass spectrometer analysis, nine intermediates were identified and the proposed degradation pathways were investigated.
引用
收藏
页码:1116 / 1126
页数:11
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