Effect of transition metals (Cu, Co and Fe) on the autothermal reforming of methane over Ni/Ce0.2Zr0.1Al0.7Oδ catalyst
被引:11
作者:
Dong, Xinfa
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S China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R ChinaS China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R China
Dong, Xinfa
[1
]
Cai, Xiulan
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S China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R ChinaS China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R China
Cai, Xiulan
[1
]
Song, Yibing
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机构:
Shantou Univ, Dept Chem, Shantou 515063, Peoples R ChinaS China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R China
Song, Yibing
[2
]
Lin, Weiming
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S China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R ChinaS China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R China
Lin, Weiming
[1
]
机构:
[1] S China Univ Technol, Sch Chem & Energy Engn, Guangzhou 510640, Peoples R China
[2] Shantou Univ, Dept Chem, Shantou 515063, Peoples R China
来源:
JOURNAL OF NATURAL GAS CHEMISTRY
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2007年
/
16卷
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01期
The transition metals (Cu, Co, and Fe) were applied to modify Ni/Ce0.2Zr0.1Al0.7O delta catalyst. The effects of transition metals on the catalytic properties of Ni/Ce0.2Zr0.1Al0.7O delta autothermal reforming of methane were investigated. The Ni-supported catalysts were characterized by XRD, TPR and XPS. Tests in autothermal reforming of methane to hydrogen showed that the addition of transition metals (Cu and Co) significantly increased the activity of catalyst under the conditions of lower reaction temperature, and Ni/Cu0.05Ce0.2Zr0.1Al0.65O delta was found to have the highest conversion of CH4 among all catalysts in the operation temperatures ranging from 923 K to 1023 K. TPR, XRD and XPS measurements indicated that the cubic phases of CexZr1-xO2 solid solution were formed in the preparation process of catalysts. Strong interaction was found to exist between NiO and CexZr1-xO2 solid solution. The addition of Cu improved the dispersion of NiO, inhibited the formation of NiAl2O4, and thus significantly promoted the activity of the catalyst Ni/Cu0.05Ce0.2Zr0.1Al0.65O delta.
机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Ayabe, S
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Omoto, H
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Omoto, H
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Utaka, T
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Utaka, T
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Kikuchi, R
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Kikuchi, R
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Sasaki, K
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Sasaki, K
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Teraoka, Y
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Teraoka, Y
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Eguchi, K
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Ayabe, S
;
Omoto, H
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Omoto, H
;
Utaka, T
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Utaka, T
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Kikuchi, R
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Kikuchi, R
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Sasaki, K
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Sasaki, K
;
Teraoka, Y
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机构:Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
Teraoka, Y
;
Eguchi, K
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan