Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

The structure and activity of silica-supported palladium-cobalt alloys. I. Alloy homogeneity, surface composition, and activity for neopentane conversion

Journal Article · · Journal of Catalysis; (United States)
; ; ;  [1];  [2];  [3]
  1. Polish Academy of Sciences, Warsaw (Poland)
  2. Hungarian Academy of Sciences, Budapest (Hungary)
  3. N.D. Zelinsky Institute of Organic Chemistry, Moscow (Russian Federation)

Chemisorption of H[sub 2] and CO, temperature-programmed reduction (TPR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and neopentane conversion show that differences in preparation method and overall metal loading lead to the formation of different Pd-Co bimetallic materials (changes in reducibility, metal particle size, and lateral homogeneity). Well-homogenized Pd-Co particles exhibit a very pronounced minimum in the plot of catalytic activity versus Pd-Co alloy composition. At the same time, a maximum exists in the isomerization selectivity vs the alloy composition. These deviations from the catalytic behavior of physical mixtures of the monometallic (Pd and Co) catalysts provide a basis for the estimation of how two metals interact with each other in a supported catalyst. Incipient wetness impregnation of silica by considerable amounts (10 wt%) of metal salts leads to the formation of catalyst precursors which are fully reduced at 380[degrees]C yielding good dispersion and lateral homogeneity. Chemisorption and in situ XRD studies are compatible with the kinetic investigations, but information on metal interaction by these methods is less clear. For high metal-loaded Pd-Co/SiO[sub 2] catalysts, comparison of H[sub 2] chemisorption and XRD data suggests surface enrichment in palladium, which is confirmed by XPS. 26 refs., 6 figs., 4 tabs.

OSTI ID:
5602045
Journal Information:
Journal of Catalysis; (United States), Journal Name: Journal of Catalysis; (United States) Vol. 142:2; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English