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Catalytic reduction of no over perovskite-type catalysts
Authors:Seong-Soo Hong  Gun-Dae Lee  Jong-Won Park  Dae-Won Park  Kyung-Mok Cho  Kwang-Jung Oh
Affiliation:(1) Department of Chemical Engineering, Pukyong National University, 100 Yongdang-dong, Nam-ku, 608-739 Pusan, Korea;(2) Surface & Coating, Engineering, Pukyong National University, 100 Yongdang-dong, Nam-ku, 608-739 Pusan, Korea;(3) Department of Chemical Engineering, Pukyong National University, 100 Yongdang-dong, Nam-ku, 608-739 Pusan, Korea;(4) Metallurgical Engineering, Pukyong National University, 100 Yongdang-dong, Nam-ku, 608-739 Pusan, Korea;(5) Environmental Engineering, Pusan National University, 609-735 Pusan, Korea
Abstract:In the present work, we have investigated the reduction of NO by propane over perovskite-type oxides prepared by malic acid method. The catalysts were modified to enhance the activity by substitution of metal into A or B site of perovskite oxides. In addition, the reaction conditions, such as temperature, O2 concentration, and space velocity have been varied to understand their effects on the catalytic performance. In the LaCoO3 type catalyst, the partial substitution of Ba and Sr into A site enhanced the catalytic activity in the reduction of NO. For the La0.6Ba (Sr)o.4 Co1−x FexO3 (x=0-1.0) catalyst, the partial substitution of Fe into B site enhanced the conversion of NO, but excess amount of Fe decreased the conversion of NO. The surface area and catalytic activity of perovskite catalysts prepared by malic acid method showed higher values than those of solid reaction method. The conversion of NO increased with increasing O2 concentration and contact time. The introduction of water into reactant feed decreased the catalytic activity but the deactivation was shown to be reversible over La0.6Ba0.4Co1−x ,FexO3 catalyst.
Keywords:Reduction of NO                      Perovskite-type Oxides                      Malic Acid Method                      Effect of Water                      Substitution of Ba                      Sr and Fe  TPR
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