共 52 条
Highly active and stable Co/La0.7Sr0.3AlO3-δ catalyst for steam reforming of toluene
被引:26
作者:
Takise, Kent
[1
]
Higo, Takuma
[1
]
Mukai, Daiki
[1
]
Ogo, Shuhei
[1
]
Sugiura, Yukihiro
[1
,2
]
Sekine, Yasushi
[1
]
机构:
[1] Waseda Univ, Dept Appl Chem, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
[2] JX Nippon Oil & Energy Corp, Cent Tech Res Lab, 8 Chidoricho, Yokohama, Kanagawa, Japan
来源:
关键词:
Perovskite oxide;
Steam reforming of toluene;
Co catalyst;
Hydrogen production;
Surficial adsorption property;
Stable catalytic activity;
HYDROTALCITE-LIKE PRECURSORS;
NI-BASED CATALYSTS;
BIOMASS TAR;
HYDROGEN-PRODUCTION;
MODEL-COMPOUND;
NICKEL-CATALYSTS;
FE;
CO;
RH;
ETHANOL;
D O I:
10.1016/j.cattod.2015.08.059
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
We investigated steam reforming of toluene as a model compound of aromatic hydrocarbons included in biomass tar over Co supported Co/La0.7Sr0.3AlO3-delta (LSAO), perovskite oxide. Ni-supported LSAO catalyst has shown high activity and coke resistance from the redox property of lattice oxygen in/on the LSAO support. Co is known as an active metal for this reaction, so Co/LSAO catalyst was investigated in this work. Co/LSAO catalyst, which showed high steady-state activity and stability, was characterized using (H2O)-O-18 isotopic transient response tests, STEM, FT-IR, Arrhenius plot and partial pressure dependence to elucidate high and stable catalytic activity. In situ FT-IR measurements revealed that reaction intermediates on Co/LSAO desorbed at 873 K or lower temperatures. Although redox property of lattice oxygen did not change at around 848 K based on isotopic transient tests, the Arrhenius plots indicate that the rate-determining step changed at around 848 K because of reaction intermediate decomposition desorption. Fast reaction and desorption of absorbed intermediates on Co/LSAO enable catalytic stability during toluene steam reforming. (C) 2015 Elsevier B.V. All rights reserved.
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页码:111 / 117
页数:7
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