• DocumentCode
    2341796
  • Title

    Study on Photocatalytic Mechanism of Fe3+ -TiO2 -Zeolite for Oilfield Wastewater Treatment

  • Author

    Liu, Jingming ; Li, Hongyang ; Zhang, Wei ; Zhu, Zhirong ; Ma, Ji

  • Author_Institution
    Dept. of Chem., Tongji Univ., Shanghai, China
  • Volume
    2
  • fYear
    2010
  • fDate
    18-20 Dec. 2010
  • Firstpage
    526
  • Lastpage
    529
  • Abstract
    The composite photo catalyst of Fe3+-TiO2-zeolite is prepared in a bench scale, which is immobilized into a zeolite matrix by means of sol-gel technique. The oilfield wastewater in Huabei oilfield was chosen as the model pollutant to evaluate photo catalytic activity under the ultraviolet light and sunlight irradiation respectively, the possible mechanism of photo catalytic oxidation was deduced. The results indicated that under conditions of the calcined temperature of 500°C, the composite photo catalyst was got by loading nano-TiO2 of 43% and doping Fe3+ ions concentration of 6.04 × 1016 ions/cm3. COD concentration degraded could follow the first order kinetics and could meet the second national discharge standard of China. Meanwhile, the mechanism of doped Fe3+ in complex photo catalysts can capture the electrons in the conduction band, reduce the recombined rate of electrons with cavities, and improve the efficiency of light quantum.
  • Keywords
    catalysis; mining industry; oxidation; photochemistry; radiation effects; sol-gel processing; wastewater treatment; zeolites; COD concentration; Fe3-TiO2; Huabei oilfield; complex photo catalysts; conduction band; light quantum; oilfield wastewater treatment; photo catalytic oxidation; photocatalytic mechanism; sol-gel technique; sunlight irradiation; ultraviolet light; zeolite; COD removal; nano-TiO2; oilfield wastewater; photocatalyst; zeolite;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Digital Manufacturing and Automation (ICDMA), 2010 International Conference on
  • Conference_Location
    ChangSha
  • Print_ISBN
    978-0-7695-4286-7
  • Type

    conf

  • DOI
    10.1109/ICDMA.2010.403
  • Filename
    5701461