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Title: Characterization of supported palladium catalysts II. Pd/SiO sub 2

Journal Article · · Journal of Catalysis; (USA)
;  [1]
  1. Institute of Physical Chemistry of the Polish Academy of Sciences, Warszawa (Poland)

The isomerization of neopentane has been investigated over the 0.76 wt% Pd/SiO{sub 2} catalyst. It is found that after high temperature reduction (HTR, at 873 K) the selectivity for isomerization is much higher than that after low temperature reduction (LTR, at 573 K). A variety of experiments, including kinetic, chemisorption (O{sub 2}, H{sub 2}, and CO), temperature-programmed desorption of H{sub 2}, and X-ray diffraction, showed that this selectivity enhancement cannot be interpreted in terms of H{sub 2} retention by catalyst. Instead, the formation of Pd-Si compound(s) (most probably Pd{sub 3}Si) during HTR seems immediately responsible for the catalytic behavior of HTR Pd/SiO{sub 2} catalysts. A mechanism is proposed for the Pd-SiO{sub 2} interaction in which Pd atoms (or ions) are incorporated into the silica support (via oxygen vacancies) and a new phase of palladium silicide is formed. Regeneration by an oxygen treatment of the HTR sample does not fully restore the low isomerization selectivity typical of LTR samples. The additional selectivity is attributed to an overlayer of oxidized silicon species (after oxidation of the HTR sample) which partially cover the metal.

OSTI ID:
6352000
Journal Information:
Journal of Catalysis; (USA), Vol. 117:2; ISSN 0021-9517
Country of Publication:
United States
Language:
English

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