• DocumentCode
    2515997
  • Title

    Photocatalytic Degradation of Crystal Violet Using Prepared Bismuth Titanate Mixed Oxide

  • Author

    Liu, Jia ; Yin, Lifeng ; Xu, Lv ; Niu, Junfeng

  • Author_Institution
    State Key Lab. of Water Environ. Simulation, Beijing Normal Univ., Beijing, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    3
  • Abstract
    A novel photocatalyst bismuth titanate mixed oxide (BTMO) was prepared by the solvent thermal synthesis method. The structure and morphology of BTMO were characterized by powder X-ray diffraction and scan electron microscope, respectively. Ultraviolet and visible diffuse reflection spectra were measured to account for the photoabsorption properties of BTMO. The tests of photocatalytic activity of BTMO were conducted by the photocatalytic degradation of crystal violet under UV irradiation. The results indicate that 0.05 g BTMO with initial concentration of crystal violet 20 mg L-1 irradiated for 1.5 h shows the highest photocatalytic activity. The photocatalyst properties of BTMO were associated with their crystal and electronic structures.
  • Keywords
    X-ray diffraction; band structure; bismuth compounds; catalysis; catalysts; crystal structure; photochemistry; photoexcitation; reflectivity; scanning electron microscopy; ultraviolet radiation effects; Bi12TiO20; Bi4Ti3O12; UV irradiation; crystal structure; crystal violet; electronic structure; photoabsorption; photocatalyst; photocatalytic degradation; powder X-ray diffraction; scanning electron microscope; solvent thermal synthesis; time 1.5 h; ultraviolet diffuse reflection spectra; visible diffuse reflection spectra; Bismuth; Morphology; Powders; Reflection; Scanning electron microscopy; Solvents; Testing; Thermal degradation; Titanium compounds; X-ray diffraction;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5163186
  • Filename
    5163186