Liu Shuan, Zhu Jianwen, Wang Qi, Fang Yanfen, Huang Yingping. Degradation of organic pollutants by photo/electro-Fenton sacrificial anode system[J]. Chinese Journal of Environmental Engineering, 2010, 4(12): 2699-2704.
Citation: Liu Shuan, Zhu Jianwen, Wang Qi, Fang Yanfen, Huang Yingping. Degradation of organic pollutants by photo/electro-Fenton sacrificial anode system[J]. Chinese Journal of Environmental Engineering, 2010, 4(12): 2699-2704.

Degradation of organic pollutants by photo/electro-Fenton sacrificial anode system

  • Received Date: 09/12/2009
    Accepted Date: 24/10/2009
    Fund Project:
  • In this study, the degradation of organic pollutants (i.e. orange Ⅱ and 2,4-dichiprophenol (2,4-DCP)) was studied by sacrificial anode Fenton reaction, employing iron as anode and graphite as cathode under the irradiation of visible light (λ>450 nm) and the addition of electricity. The results showed that the optimum conditions for the degradation of orange Ⅱ were additional voltage of 3 V, pH value of 3.0, and hydrogen peroxide concentration of 5×10-5 mol/L. Under these conditions, the mineralized rate for orange Ⅱ was 78% in 10 hours, and the degradation rate for 2,4-DCP was 91.4% in 210 min.In order to investigate the degradation mechanism of the target compound, the electrochemical characteristics of the electrode were determined by in situ cyclic voltammetry, and the variations of hydrogen peroxide and hydroxyl radical during the degradation were traced by enzyme catalysis method and fluorescence spectrometry. The results showed that the degradation process mainly involved hydroxyl radical course.
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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Degradation of organic pollutants by photo/electro-Fenton sacrificial anode system

Fund Project:

Abstract: In this study, the degradation of organic pollutants (i.e. orange Ⅱ and 2,4-dichiprophenol (2,4-DCP)) was studied by sacrificial anode Fenton reaction, employing iron as anode and graphite as cathode under the irradiation of visible light (λ>450 nm) and the addition of electricity. The results showed that the optimum conditions for the degradation of orange Ⅱ were additional voltage of 3 V, pH value of 3.0, and hydrogen peroxide concentration of 5×10-5 mol/L. Under these conditions, the mineralized rate for orange Ⅱ was 78% in 10 hours, and the degradation rate for 2,4-DCP was 91.4% in 210 min.In order to investigate the degradation mechanism of the target compound, the electrochemical characteristics of the electrode were determined by in situ cyclic voltammetry, and the variations of hydrogen peroxide and hydroxyl radical during the degradation were traced by enzyme catalysis method and fluorescence spectrometry. The results showed that the degradation process mainly involved hydroxyl radical course.

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