• Title of article

    Possible origin of improved high temperature performance of hydrothermally aged Cu/beta zeolite catalysts

  • Author/Authors

    Charles H.F. Peden، نويسنده , , Ja Hun Kwak، نويسنده , , Sarah D. Burton، نويسنده , , Russell G. Tonkyn، نويسنده , , Do Heui Kim، نويسنده , , Jong-Hwan Lee، نويسنده , , Hung-Wen Jen، نويسنده , , Giovanni Cavataio، نويسنده , , Yisun Cheng، نويسنده , , Christine K. Lambert، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2012
  • Pages
    7
  • From page
    245
  • To page
    251
  • Abstract
    The hydrothermal stability of Cu/beta NH3 SCR catalysts are explored here. In particular, this paper focuses on the interesting ability of this catalyst to maintain and even enhance high-temperature performance for the “standard” SCR reaction after modest (900 °C, 2 h) hydrothermal aging. Characterization of the fresh and aged catalysts was performed with an aim to identify possible catalytic phases responsible for the enhanced high temperature performance. XRD, TEM and 27Al NMR all showed that the hydrothermal aging conditions used here resulted in almost complete loss of the beta zeolite structure between 1 and 2 h aging. While the 27Al NMR spectra of 2 and 10 h hydrothermally aged catalysts showed significant loss of a peak associated with tetrahedrally coordinated Al species, no new spectral features were evident. Two model catalysts, suggested by these characterization data as possible mimics of the catalytic phase formed during hydrothermal aging of Cu/beta, were prepared and tested for their performance in the “standard” SCR and NH3 oxidation reactions. The similarity in their reactivity compared to the 2 h hydrothermally aged Cu/beta catalyst suggests possible routes for preparing multi-component catalysts that may have wider temperature windows for optimum performance than those provided by current Cu/zeolite catalysts.
  • Keywords
    NH3–SCR , Selective Catalytic Reduction , Cu-zeolites , deactivation , Hydrothermal aging
  • Journal title
    CATALYSIS TODAY
  • Serial Year
    2012
  • Journal title
    CATALYSIS TODAY
  • Record number

    1238490