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Influence of synthesis conditions on NO oxidation and NOx storage performances of La0.7Sr0.3MnO3 perovskite-type catalyst in lean-burn atmospheres
Authors:Yan-Hua Dong  Hui Xian  Jiao-Long Lv  Cheng Liu  Li Guo  Ming Meng  Yi-Sheng Tan  Noritatsu Tsubaki  Xin-Gang Li
Affiliation:1. Tianjin Key Laboratory of Applied Catalysis Science & Technology, School of Chemical Engineering & Technology, Tianjin University, Tianjin 300072, PR China;2. Pei-Yang Distillation Engineering Limited Company, Tianjin 300072, PR China;3. The Synergistic Innovation Center of Chemistry and Chemical Engineering of Tianjin, Tianjin 300072, PR China;4. State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Science, Taiyuan 030001, PR China;5. Department of Applied Chemistry, School of Engineering, University of Toyama, Gofuku 3190, Toyama City, Toyama 930-8555, Japan
Abstract:Synthesis conditions of catalysts can significantly affect catalytic activities for a certain reaction. Here, a series of the La0.7Sr0.3MnO3 perovskite-type catalysts was prepared by the sol–gel method under the different synthesis conditions. The faster calefactive velocities during calcination of the xerogel precursors would produce a lot of the impurities and cause the dropped amount of the excessive oxygen in perovskite, as well as the aggregated particles and the decreased surface areas; the higher calcination temperature would sinter the perovskite phases seriously; and the initial pH value of the precursor solution would greatly affect the morphology of the catalysts including the shape and the size, which directly linked to their NOx storage capacity. Moreover, our findings revealed that the NO oxidation ability was determined by the amount of the excessive oxygen species in the perovskite. Here, the optimum synthesis conditions were achieved with the calcination temperature of 700 °C, the calefactive velocity of 2 °C min−1, and the precursor solution of pH = 8. This catalyst presented the best performances for the NO oxidization and NOx storage, i.e. the NO-to-NO2 conversion of 70.2% and the NOx storage capacity of 170.4 μmol g−1.
Keywords:Oxides  Sol&ndash  gel growth  Oxidation  X-ray diffraction topography  Electron microscopy  Differential thermal analysis
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