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    Room-light-induced indoor air purification using an efficient Pt/N-TiO2 photocatalyst

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    Fulltext not available
    Authors
    Sun, Hongqi
    Ullah, Ruh
    Chong, Siewhui
    Ang, Ha Ming
    Tade, Moses
    Wang, Shaobin
    Date
    2011
    Type
    Journal Article
    
    Metadata
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    Citation
    Sun, Hongqi and Ullah, Ruh and Chong, Siewhui and Ang, Hua Ming and Tade, Moses O. and Wang, Shaobin. 2011. Room-light-induced indoor air purification using an efficient Pt/N-TiO2 photocatalyst. Applied Catalysis B: Environmental. 108-109: pp. 127-133.
    Source Title
    Applied Catalysis B: Environmental
    DOI
    10.1016/j.apcatb.2011.08.017
    ISSN
    09263373
    School
    Department of Chemical Engineering
    URI
    http://hdl.handle.net/20.500.11937/24604
    Collection
    • Curtin Research Publications
    Abstract

    A conceptual air purifier harvesting fluorescent room lights was tested in this study. Visible photocatalysis was applied to facilitate the degradation of volatile organic compounds (VOCs) on a highly efficient visible light photocatalyst, Pt/N-TiO2 synthesised via a sol–gel process. The as-prepared photocatalyst was characterised by many techniques, such as XRD, XPS, UV–vis DRS, N2 adsorption and SEM, etc. XPS spectra revealed that platinum was at a chemical state of 2+, while nitrogen existed as NOx species. The unique chemical compositions made the photocatalyst respond to visible light with a band gap of 2.69 eV, and present a broad absorption shoulder extended further into infrared region. The photocatalytic activities under irradiations of λ > 387, 430 and 490 nm were evaluated by photodegradation of phenol solutions. Under UV–vis light, the Pt/N-TiO2 exhibited 5.5 times higher activity than Degussa P25. Various gaseous pollutants were degraded by employing the Pt/N-TiO2 in a batch reactor. The capability of photodegradation of VOCs under room lights was also proven by the decomposition of gaseous toluene in a continuous reactor using fluorescent lamps (6 × 10 W). The mechanism of the enhanced activity in degradation of VOCs and potential application were discussed.

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