Perovskite-type oxide ACo0.8Bi0.2O2.87 (A=La0.8Ba0.2): a catalyst for low-temperature CO oxidation

被引:0
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作者
H.X. Dai
H. He
W. Li
Z.Z. Gao
C.T. Au
机构
[1] Hong Kong Baptist University,Department of Chemistry
[2] Beijing University of Chemical Technology,Department of Applied Chemistry, Faculty of Science
[3] Beijing Polytechnic University,College of Environmental and Energy Engineering
来源
Catalysis Letters | 2001年 / 73卷
关键词
perovskite-type oxide catalyst; La; Ba; Co; Bi; O; low-temperature CO oxidation; O/; O isotopic exchange; lattice oxygen mobility; oxidative nonstoichiometry;
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摘要
Perovskite-type oxide ACo0.8Bi0.2O2.87 (A=La0.8Ba0.2) has been investigated as a catalyst for the oxidation of carbon monoxide. X-ray diffraction results revealed that the catalyst is single-phase and cubic in structure. The results of chemical analysis indicated that in ACo0.8Bi0.2O2.87, bismuth is pentavalent whereas cobalt is trivalent as well as bivalent; in La0.8Ba0.2CoO2.94, cobalt ions exist as Co3+ and Co4+. The substitution of Bi for Co enhanced the catalytic activity of the perovskite-type oxide significantly. Over the Bi-incorporated catalyst, at equal space velocities and with the rise in CO/O2 molar ratio, the temperature for 100% CO conversion shifted to a higher range; at a typical space velocity of 30000 h−1 and a CO/O2 molar ratio of 0.67/1.00, 100% CO conversion was observed at 250 °C. Over ACo0.8Bi0.2O2.87, at equal CO/O2 molar ratio, the temperature for 100% CO conversion decreased with a drop in space velocity; the lowest being 190 °C at a space velocity of 5000 h−1. The result of O2-TPD study illustrated that the presence of Bi ions caused the lattice oxygen of La0.8Ba0.2CoO3−δ to desorb at a lower temperature. The results of TPR, 18O/16O isotopic exchange, and CO-pulsing investigations demonstrated that the lattice oxygen of the Bi-doped catalyst is highly mobile.
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页码:149 / 156
页数:7
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