• Title of article

    Catalytic combustion over platinum group catalysts: fuel-lean versus fuel-rich operation

  • Author/Authors

    Maxim Lyubovsky، نويسنده , , Lance L. Smith، نويسنده , , Marco Castaldi، نويسنده , , Hasan Karim، نويسنده , , Brian Nentwick، نويسنده , , Shahrokh Etemad، نويسنده , , Rene LaPierre، نويسنده , , William C. Pfefferle، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2003
  • Pages
    14
  • From page
    71
  • To page
    84
  • Abstract
    Performance data are presented for methane oxidation on alumina-supported Pd, Pt, and Rh catalysts under both fuel-rich and fuel-lean conditions. Catalyst activity was measured in a micro-scale isothermal reactor at temperatures between 300 and 800 °C. Non-isothermal (near adiabatic) temperature and reaction data were obtained in a full-length (non-differential) sub-scale reactor operating at high pressure (0.9 MPa) and constant inlet temperature, simulating actual reactor operation in catalytic combustion applications. Under fuel-lean conditions, Pd catalyst was the most active, although deactivation occurred above 650 °C, with reactivation upon cooling. Rh catalyst also deactivated above 750 °C, but did not reactivate. Pt catalyst was active above 600 °C. Fuel-lean reaction products were CO2 and H2O for all three catalysts. The same catalysts tested under fuel-rich conditions demonstrated much higher activity. In addition, a ‘lightoff’ temperature was found (between 450 and 600 °C), where a stepwise increase in reaction rate was observed. Following ‘lightoff’ partial oxidation products (CO, H2) appeared in the mixture, and their concentration increased with increasing temperature. All three catalysts exhibited this behavior. High-pressure (0.9 MPa) sub-scale reactor and combustor data are shown, demonstrating the benefits of fuel-rich operation over the catalyst for ultra-low emissions combustion.
  • Keywords
    Catalytic combustion , gas turbine , Methane oxidation , Reaction Mechanism
  • Journal title
    CATALYSIS TODAY
  • Serial Year
    2003
  • Journal title
    CATALYSIS TODAY
  • Record number

    1231802