Decomposition of nitric oxide and its reduction by CO over superconducting and related cuprate catalysts |
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Authors: | Istvan Halasz Alan Brenner Mordecai Shelef K. Y. Simon Ng |
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Affiliation: | (1) Department of Chemistry, Wayne State University, 48202 Detroit, Michigan, USA;(2) Scientific Research Staff, Ford Motor Co., 48121 Dearborn, Michigan, USA;(3) Department of Chemical Engineering, Wayne State University, 48202 Detroit, Michigan, USA;(4) Present address: Chemical Research Institute of the Hungarian Academy of Sciences, Budapest, Hungary |
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Abstract: | Catalytic activities of five non-conducting and three superconducting cuprates were measured for the decomposition of NO and the reduction of NO by CO. The concentration of the reactants and the space velocities approximate the conditions of automotive catalysts. In contrast to earlier results, obtained at 20 to 30 times higher partial pressures of NO and 20 to 100 times lower space velocities, none of the catalysts, including five perovskite-like cuprates, showed significant activity for the decomposition of NO at reaction temperatures up to 700 °C. All catalysts were fairly active for the reduction of NO. At temperatures above about 400 °C on the perovskite-like cuprates YBa2Cu3O7-x and Ba2CuO3.5-x, the rates for NO reduction were higher than on CuO. All catalysts lost activity for NO reduction in the presence of oxygen (oxidizing conditions). |
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Keywords: | NO reduction NO decomposition reduction of NO by CO cuprate catalysts superconducting catalysts |
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