Strong chemical interaction between PdO and SnO2 and the influence on catalytic combustion of methane
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作者:
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Takeguchi, T
Takeoh, O
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon, Nishikyo Ku, Kyoto 6158510, Japan
Takeoh, O
Aoyama, S
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon, Nishikyo Ku, Kyoto 6158510, Japan
Aoyama, S
Ueda, J
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon, Nishikyo Ku, Kyoto 6158510, Japan
Ueda, J
Kikuchi, R
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon, Nishikyo Ku, Kyoto 6158510, Japan
Kikuchi, R
Eguchi, K
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon, Nishikyo Ku, Kyoto 6158510, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon, Nishikyo Ku, Kyoto 6158510, Japan
Eguchi, K
[1
]
机构:
[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon, Nishikyo Ku, Kyoto 6158510, Japan
[2] Hokkaido Univ, Catalysis Res Ctr, Kita Ku, Sapporo, Hokkaido 0600811, Japan
methane combustion;
PdO/SnO2;
CO adsorption;
support effect;
mixed oxides;
D O I:
10.1016/S0926-860X(03)00418-6
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Several palladium-tin oxide (PdO-SnO2) catalysts were prepared by the impregnation (PdO/SnO2) and co-precipitation (PdO-SnO2) methods. Among the catalysts tested, the SnO2-supported 11 wt.% PdO catalyst prepared by the impregnation method showed the highest conversion at low temperatures. The reduction and adsorption properties of PdO/SnO2 were quite different from those of PdO/Al2O3 and PdO/ZrO2. X-ray diffraction (XRD) of these catalysts revealed that 10 nm PdO particles were supported on SnO2 for the impregnated catalysts, while the co-precipitated catalysts were composed of uniform PdO-SnO2 mixed oxide particles. Even at room temperature, the PdO particles in PdO/SnO2 were easily reduced to metallic Pd and absorbed H-2 with the H-2/Pd weight ratio of 0.3%. In both PdO/SnO2 and PdO-SnO2 samples, adsorption of CO was significantly suppressed because of the interaction between Pd and SnO2; the metal surface area was difficult to estimate by the CO pulse technique. (C) 2003 Elsevier B.V. All rights reserved.
机构:
Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
Kikuchi, R
Maeda, S
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机构:Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
Maeda, S
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Sasaki, K
Wennerström, S
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机构:Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
Wennerström, S
Eguchi, K
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机构:Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
机构:
Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
Kikuchi, R
Maeda, S
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机构:Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
Maeda, S
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Sasaki, K
Wennerström, S
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机构:Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
Wennerström, S
Eguchi, K
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机构:Kyoto Univ, Dept Energy & Hydrocarbon Chem, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan