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    Magnetic core–shell CuFe2O4@C3N4 hybrids for visible light photocatalysis of Orange II

    Access Status
    Fulltext not available
    Authors
    Yao, Y.
    Lu, F.
    Zhu, Y.
    Wei, F.
    Liu, X.
    Lian, C.
    Wang, Shaobin
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Yao, Y. and Lu, F. and Zhu, Y. and Wei, F. and Liu, X. and Lian, C. and Wang, S. 2015. Magnetic core–shell CuFe2O4@C3N4 hybrids for visible light photocatalysis of Orange II. Journal of Hazardous Materials. 297: pp. 224-233.
    Source Title
    Journal of Hazardous Materials
    DOI
    10.1016/j.jhazmat.2015.04.046
    ISSN
    0304-3894
    School
    Department of Chemical Engineering
    URI
    http://hdl.handle.net/20.500.11937/47950
    Collection
    • Curtin Research Publications
    Abstract

    Novel CuFe2O4@C3N4 core–shell photocatalysts were fabricated through a self-assembly method and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, transmission electron microscopy and Uv–vis diffuse reflection spectroscopy. The photocatalytic performances of the CuFe2O4@C3N4 catalysts were evaluated in photo Fenton-like discoloration of Orange II dye using H2O2 as an oxidant under visible-light irradiation (λ > 420 nm). It was found the CuFe2O4@C3N4 hybrid (mass ratio of CuFe2O4/g-C3N4 at 2:1) exhibits a superior activity as compared with single component of CuFe2O4 or g-C3N4 and the mixture of g-C3N4 and CuFe2O4, due to the elevation of the separation efficiency of photoinduced electron–hole pairs, resulted from the heterojunction between the interfaces of g-C3N4 and CuFe2O4. The quenching tests of different scavengers displayed that View the MathML sourceO2•−, radical dotOH and h+ are responsible for the Orange II decolorization. In addition, the effects of initial concentration of the dye contaminant (0.014–0.140 mM), different anions (Cl−, View the MathML sourceSO42−, View the MathML sourceNO3−, CH3COO− and View the MathML sourceHCO3−) and temperature (15–65 °C) in photoreaction were also investigated. The CuFe2O4@C3N4 sample exhibited stable performance without obvious loss of catalytic activity after five successive runs, showing a promising application for the photo-oxidative degradation of environmental contaminants.

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