TY - JOUR
T1 - Highly active and stable Co/La0.7Sr0.3AlO3-δ catalyst for steam reforming of toluene
AU - Takise, Kent
AU - Higo, Takuma
AU - Mukai, Daiki
AU - Ogo, Shuhei
AU - Sugiura, Yukihiro
AU - Sekine, Yasushi
N1 - Publisher Copyright:
© 2015 Elsevier B.V. All rights reserved.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - We investigated steam reforming of toluene as a model compound of aromatic hydrocarbons included in biomass tar over Co supported La0.7Sr0.3AlO3-δ (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 H218O 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.
AB - We investigated steam reforming of toluene as a model compound of aromatic hydrocarbons included in biomass tar over Co supported La0.7Sr0.3AlO3-δ (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 H218O 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.
KW - Co catalyst
KW - Hydrogen production
KW - Perovskite oxide
KW - Stable catalytic activity
KW - Steam reforming of toluene
KW - Surficial adsorption property
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U2 - 10.1016/j.cattod.2015.08.059
DO - 10.1016/j.cattod.2015.08.059
M3 - Article
AN - SCOPUS:84959332802
SN - 0920-5861
VL - 265
SP - 111
EP - 117
JO - Catalysis Today
JF - Catalysis Today
ER -