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Ethane hydrogenolysis and hydrogen chemisorption over niobia-promoted rhodium catalysts: A new phase by a strong rhodium-niobia interaction

Journal Article · · Journal of Catalysis; (USA)

Niobia-promoted Rh/SiO{sub 2} catalysts, containing niobia (Nb{sub 2}O{sub 5}) deposited onto Rh/SiO{sub 2} catalysts, exhibited chemical behavior characteristic of strong metal-support interaction, the Rh-Nb{sub 2}O{sub 5} interaction being as strong as that in the Rh/Nb{sub 2}O{sub 5} system. In a typical case, after the high-temperature reduction at 773 K, the H{sub 2} chemisorption ability diminished almost to zero and the catalytic activity for ethane hydrogenolysis decreased by about seven orders of magnitude, compared with the low-temperature reduction (LTR) at 373 K. The phenomenon is reversed after the oxidation in O{sub 2} at 673 K followed by LTR. The extent of Rh-Nb{sub 2}O{sub 5} interaction was sensitive to preparation variables such as the amount of Nb{sub 2}O{sub 5} deposited and preparation method. In particular, the extent of interaction was increased significantly by calcining Nb{sub 2}O{sub 5}-promoted Rh catalysts in air at high temperatures (973 K). An X-ray diffraction study suggested formation of a new phase (RbNbO{sub 4}) by the calcination treatment at 973 K. Temperature-programmed reduction results showed that the reduction peaks shifted to the higher temperature side as the degree of the Rh-Nb{sub 2}O{sub 5} interaction increased. A model for the metal-oxide interaction in the present catalyst system is discussed in terms of the formation of a surface RhNbO{sub 4} compound and the decoration of the Rh surface with a niobia species (NbO{sub x}).

OSTI ID:
6556686
Journal Information:
Journal of Catalysis; (USA), Journal Name: Journal of Catalysis; (USA) Vol. 112:2; ISSN 0021-9517; ISSN JCTLA
Country of Publication:
United States
Language:
English

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