• Title of article

    Raney copper catalysts for the water-gas shift reaction II. Initial catalyst optimisation Original Research Article

  • Author/Authors

    J.R. Mellor، نويسنده , , N.J. Coville، نويسنده , , A.C. Sofianos، نويسنده , , R.G. Copperthwaite، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 1997
  • Pages
    11
  • From page
    185
  • To page
    195
  • Abstract
    The initial Raney copper WGS activity based on catalyst volume has been shown to be comparable to industrial and coprecipitated alternatives under varying reaction conditions. The presence of zinc oxide in the Raney copper structure was shown to be necessary for resisting catalyst deactivation due to copper crystallite sintering. Over long operating times, greater stability was maintained by increasing the Raney catalyst zinc content by leaching precursor Cusingle bondZnsingle bondAl alloys with zinc contents of up to a nominal 40 wt% for 1 h. Achieving a high catalyst zinc concentration by leaching alloys with a higher zinc content proved to be more beneficial than by increasing the catalyst zinc concentration by the zinc impregnation process. The addition of concentrated zincate to the caustic solution slowed the leach rate, promoting an increase in copper crystallite size with a corresponding decrease in copper surface area and WGS activity. Leaching precursor alloys with higher zinc contents was effective for increasing the rim zinc content of the Raney catalyst without inhibiting the leach rate and the development of large copper surface areas. A statistically significant correlation was observed between the WGS activity of Raney copper catalysts and their active metal surface areas, demonstrating that the WGS reaction is a structure insensitive reaction over Raney copper.
  • Keywords
    Water-gas shift reaction , Raney catalyst , Copper catalyst , Synthesis , Sintering
  • Journal title
    Applied Catalysis A:General
  • Serial Year
    1997
  • Journal title
    Applied Catalysis A:General
  • Record number

    1149110