• Title of article

    Photo-catalytic degradation of toxic dye amaranth on TiO2/UV in aqueous suspensions

  • Author/Authors

    Gupta، نويسنده , , Vinod K. and Jain، نويسنده , , Rajeev and Mittal، نويسنده , , Alok and Saleh، نويسنده , , Tawfik A. and Nayak، نويسنده , , Arunima and Agarwal، نويسنده , , Shilpi and Sikarwar، نويسنده , , Shalini، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2012
  • Pages
    6
  • From page
    12
  • To page
    17
  • Abstract
    The photo-catalytic degradation of an azo dye − Amaranth (AM) – has been investigated in TiO2/UV aqueous suspensions. The results obtained from the experiments during H2O2/TiO2 addition show that the highest decolorization rate is provided by the combination of (UV + TiO2 + H2O2). The decolorization efficiencies were 17%, 26%, 38% and 64% in the runs UV, UV + H2O2, UV + TiO2 and (UV + TiO2 + H2O2) after approximately 100 min illumination periods, respectively. The observed dye degradation rates followed pseudo-first order kinetics with respect to the substrate concentration under the experimental conditions used. Different experimental conditions, such as temperature, pH and presence of electron acceptor were investigated. The temperature effect was investigated at the range of 293–313 K and it was observed that decolorization rate increased by the increase in temperature. Chemical oxygen demand and dye absorbance of the photodegraded dye solution substantially decreased. Effect of pH was also investigated and it was observed that the lower the pH the higher the degradation. In addition, an enhancement in the photodegradation rate was observed by the addition of hydrogen peroxide as an electron acceptor. The adsorption trends of Amaranth at various initial concentrations followed the Langmuir isotherm trend. This work adds to the global discussion on the role of the advanced oxidation processes in water treatment.
  • Keywords
    Pollution , TiO2 , Photo-catalytic degradation , Amaranth dye , COD
  • Journal title
    Materials Science and Engineering C
  • Serial Year
    2012
  • Journal title
    Materials Science and Engineering C
  • Record number

    2101595