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Structural and catalytic properties of model supported nickel catalysts

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100055a033· OSTI ID:5042389
; ;  [1]
  1. Texas A M Univ., College Station, TX (United States)

The surface structure and catalytic properties of model silica-supported nickel catalysts have been investigated with infrared reflection-absorption spectroscopy (IRAS) and reaction kinetics of ethane hydrogenolysis and carbon monoxide methanation. Nickel particles in the range 15-80 [angstrom] were vacuum deposited onto silica thin films using established preparation procedures. Specific rates and activation energies for ethane hydrogenolysis and carbon monoxide methanation over the model catalysts are remarkably similar to the corresponding values for both traditional silica-supported nickel catalysts and nickel single crystals. The turnover frequency for CO methanation is independent of particle size for the dimensions studied. The ethane hydrolysis rate, however, increases with particle size to a maximum at approximately 25 [angstrom] and then decreases. This reactivity trend is found to parallel a change in the percentage of bridging CO on the nickel particles as determined by IRAS. 40 refs., 8 figs.

OSTI ID:
5042389
Journal Information:
Journal of Physical Chemistry; (United States), Journal Name: Journal of Physical Chemistry; (United States) Vol. 98:4; ISSN JPCHAX; ISSN 0022-3654
Country of Publication:
United States
Language:
English

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