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Title: The effect of carbon and oxygen on the surface chemistry of tungsten carbides

Miscellaneous ·
OSTI ID:6900211

Two phases of tungsten carbide, WC and {beta}W{sub 2}C, were prepared with 30 and 100 m{sup 2}/g{sup {minus}1} respectively. The {beta}W{sub 2}C was synthesized by the temperature programmed reaction (TRP) of WO{sub 3}, in NH{sub 3} followed by carburization of the product {beta}W{sub 2}N with a mixture of CH{sub 4} and H{sub 2}. The WC phase was made from WO{sub 3} with a mixture of CH{sub 4} and H{sub 2}. Under the experimental conditions chosen, CH{sub 4} also decomposed to form a carbonaceous deposit on the surface. This deposit was removed as CH{sub 4} by flowing H{sub 2} over the samples at 973 K. Following this treatment the samples are designated fresh samples. The surface of tungsten carbides was probed by the catalytic reactions of 2,2-dimethylpropane and n-hexane in H{sub 2}. Samples exposed to O{sub 2} were found to behave very differently from the fresh samples. Fresh samples catalyzed only the breaking of carbon-carbon bonds. With the samples exposed to O{sub 2}, isomerization of n-hexane to 2- and 3-methylpentane and of 2,2-dimethylpropane to isopentane was also observed, the latter reaction having been previously reported on low S{sub g} samples than had been also exposed inadvertently to O{sub 2}. The main conclusion of the work is that surface oxygen is a key component in the isomerization of hydrocarbons over tungsten carbide. The role of oxygen in the isomerization of neopentane may be the same as the currently proposed role of oxygen in the metathesis of alkenes over tungsten oxides. By contrast, for the isomerization of n-hexane, oxygen may simply provide the acidic sites available on the alumina of supported platinum in the typical bifunctional mechanism of alkane isomerization.

Research Organization:
Stanford Univ., CA (USA)
OSTI ID:
6900211
Resource Relation:
Other Information: Thesis (Ph. D.)
Country of Publication:
United States
Language:
English

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