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    A comparative study of spinel structured Mn3O4, Co3O4 and Fe3O4 nanoparticles in catalytic oxidation of phenolic contaminants in aqueous solutions

    193332_193332.pdf (877.6Kb)
    Access Status
    Open access
    Authors
    Saputra, E.
    Muhammad, S.
    Sun, Hongqi
    Ang, Ha Ming
    Tade, Moses
    Wang, Shaobin
    Date
    2013
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Saputra, Edy and Muhammad, Syaifullah and Sun, Hongqi and Ang, Ha-Ming and Tade, Moses O. and Wang, Shaobin. 2013. A comparative study of spinel structured Mn3O4, Co3O4 and Fe3O4 nanoparticles in catalytic oxidation of phenolic contaminants in aqueous solutions. Journal of Colloid and Interface Science. 407: pp. 467-473.
    Source Title
    Journal of Colloid and Interface Science
    DOI
    10.1016/j.jcis.2013.06.061
    ISSN
    0021-9797
    Remarks

    NOTICE: This is the author’s version of a work that was accepted for publication in Journal of Colloid and Interface Science. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in International Journal of Colloid and Interface Science, Vol. 407 (2013). http://doi.org/10.1016/j.jcis.2013.06.061

    URI
    http://hdl.handle.net/20.500.11937/31728
    Collection
    • Curtin Research Publications
    Abstract

    Spinel structured Mn3O4, Co3O4 and Fe3O4 nanoparticles were prepared, characterized, and tested in degradation of aqueous phenol in the presence of peroxymonosulfate. It was found that Mn3O4 and Co3O4 nanoparticles are highly effective in heterogeneous activation of peroxymonosulfate to produce sulfate radicals for phenol degradation. The activity shows an order of Mn3O4 > Co3O4 > Fe3O4. Mn3O4 could fast and completely remove phenol in about 20 min, at the conditions of 25 ppm phenol, 0.4 g/L catalyst, 2 g/L oxone®, and 25 °C. A pseudo first order model would fit to phenol degradation kinetics and activation energies on Mn3O4 and Co3O4 were obtained as 38.5 and 66.2 kJ/mol, respectively. In addition, Mn3O4 exhibited excellent catalytic stability in several runs, demonstrating that Mn3O4 is a promising catalyst alternative to toxic Co3O4 for water treatment.

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