• DocumentCode
    2521725
  • Title

    Study on Methane Conversion to Synthesis Gas over Nano Pt/MgO Catalysts: II. Characterization of Pt-IV Catalysts

  • Author

    Yang, Min ; Papp, Helmut

  • Author_Institution
    Coll. of Environ. & Chem. Eng., Dalian Jiaotong Univ., Dalian, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    A series nanometer Pt/MgO (Pt-IV) catalysts with different Pt loading were prepared by using impregnation method. A lot of techniques (BET, XRD, TPR, TEM , and so on) were used to characterize the physico-chemical properties of the catalysts. CO2 reforming of methane to synthesis gas was carried out to test the catalytic activity. The results show that the loading of Pt has little influence on the texture and surface property. The dispersed Pt is in metallic state and is very stable when the catalysts were calcined at higher temperature. The particle size of dispersed Pt is about 2 nm. The calcination temperature influences the structure of the support, and the agglomeration of MgO particles takes place during the higher temperature calcination. The Pt-IV catalysts have very high activity for carbon dioxide reforming of CH4 to synthesis gas, especially at high Pt loaing.
  • Keywords
    X-ray diffraction; calcination; catalysis; magnesium compounds; nanostructured materials; nanotechnology; organic compounds; platinum; transmission electron microscopy; Pt loading; Pt-MgO; TEM; XRD; agglomeration; calcination temperature; carbon dioxide; impregnation method; metallic state; methane conversion; nanocatalysts; particle size; physico-chemical property; synthesis gas; Calcination; Carbon dioxide; Chemical engineering; Chemistry; Educational institutions; Oxidation; Stability; Temperature; Testing; USA Councils;
  • 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.2009.5163485
  • Filename
    5163485