4.2 Article

Structural characterization of Th-doped TiO2 photocatalyst and its extension of response to solar light for photocatalytic oxidation of oryzalin pesticide: a comparative study

期刊

CENTRAL EUROPEAN JOURNAL OF CHEMISTRY
卷 7, 期 1, 页码 118-129

出版社

SCIENDO
DOI: 10.2478/s11532-008-0101-9

关键词

Th-doped TiO2; Oryzalin; Photocatalysis; Mid band gaps of TiO2; Spectroscopic analysis

资金

  1. UGC-Major Research Project
  2. UGC-DRS
  3. UGC-FIST
  4. CMR Institute of Technology, Bangalore

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The degradation efficiency of Th-doped TiO2 / TiO2 photocatalysts were investigated under UV and solar light illumination. The model compound chosen for the study was Oryzalin (OZ). Doping of inner transition metal ion Th was intended to modify the electronic properties of TiO2. The Th-doped TiO2 were synthesized by incorporating 0.02, 0.04, 0.06, and 0.1 atom percentage of Th into the TiO2 lattice by solid-state reaction. The stochiometry of the prepared samples is Ti1-xThxO2, where 'x' is the percentage of Th. The samples were characterized by UV-Visible absorption, UV-Visible -Diffused reflectance spectra, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Analysis (EDX) and X-ray Diffraction (XRD). The pore size and surface area of these samples were studied by Brunauer, Emmett and Teller (BET) adsorption method. It was found that metal ion doping at various percentage compositions enables a large shift in the absorption band of the TiO2 towards visible light region. This is due to the formation of various mid band gaps at 2.84 eV, 2.804 eV, 2.66 eV, and 2.55 eV. The extent of degradation of the pesticide was followed by UV-Visible spectroscopy and GC-MS methods. Based on the spectral analysis, the probable degradation reaction mechanism for OZ is proposed. These results indicate that Th-doped TiO2 with the modified electronic properties is a good catalyst under solar light irradiation. But these particles show marginal variation in rates under UV-illumination. All the photodegradation reactions follow the first order kinetics.

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