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Influence of the acid-base character of supported vanadium catalysts on their catalytic properties for the oxidative dehydrogenation of n-butane

Journal Article · · Journal of Catalysis
;  [1];  [2]
  1. Instituto de Tecnologia Quimi ca, Valencia (Spain)
  2. Universidade de Valencia, Burjasot (Spain); and others
The oxidative dehydrogenation of n-butane on supported vanadium catalysts has been studied. Al{sub 2}O{sub 3}, sepiolite, hydrotalcite (Mg/Al atomic ratio of 3.0), and MgO were used as supports. The vanadium content of supported catalysts was varied to obtain dispersed vanadium species. The strength and number of Lewis acid sites (determined by FTIR of adsorbed pyridine) decreases in the following trend: V/Al{sub 2}O{sub 3} > V/Sepiolite > V/ hydrotalcite > V/MgO. {sup 51}V NMR spectroscopy indicates that tetrahedral V{sup 5+}-species (with different distortion degree and/or environment) are the main vanadium species. Temperature-programmed reduction results show that the reducibility of catalysts, determined from the onset temperature of H{sub 2}-consumption, decreases in the order V/Al{sub 2}O{sub 3} > V/MgO (first peak) > V/Sepiolite > V/MgO (second peak) {approx} V/hydrotalcite. The catalytic activity for n-butane oxidation follows a trend similar to that observed in TPR, concluding that the catalytic activity is related to the reducibility of surface vanadium species in the catalysts. However, the selectivity to dehydrogenated products, as well as the distribution of C{sub 4}-olefins, can be tentatively related to the acid-base character of catalysts. Thus, the selectivities to 1-butene and butadiene decrease in the order V/MgO > V/Hydrotalcite > V/Sepiolite > V/Al{sub 2}O{sub 3}, while the selectivities to 2-butene and carbon oxides present the opposite trend. 48 refs., 10 figs., 4 tabs.
OSTI ID:
223999
Journal Information:
Journal of Catalysis, Journal Name: Journal of Catalysis Journal Issue: 2 Vol. 157; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English

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