TY - JOUR
T1 - Steam reforming of aromatic hydrocarbon at low temperature in electric field
AU - Takise, Kent
AU - Sato, Ayaka
AU - Muraguchi, Keisuke
AU - Ogo, Shuhei
AU - Sekine, Yasushi
N1 - Publisher Copyright:
© 2019 Elsevier B.V.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2019/3/5
Y1 - 2019/3/5
N2 - Toluene steam reforming was conducted over Ni-supported La0.7Sr0.3AlO3-δ (LSAO) perovskite oxide at 473 K in an electric field, and high toluene conversion was achieved even at such low temperature. Steam reforming is generally done at higher temperatures because of the endothermic nature of this reaction and coke prevention, which requires the contribution of heat energy in great amounts. Reportedly, water activation is particularly difficult to achieve at lower temperatures. Results of kinetic analyses such as Arrhenius plots and partial pressure dependence have revealed that imposing an electric field promotes water activation over Ni/LSAO catalyst. According to steady state isotopic kinetic analysis (SSITKA) and temperature programmed desorption infrared (TPD-IR) measurements, such water activation was accelerated via a redox mechanism using surface lattice oxygen of LSAO. The stimulated mobile lattice oxygen oxidized the adsorbed toluene and formed coke precursor in the electric field. The electric field achieved a lowered reaction temperature for efficient hydrogen production and coke suppression with redox property of LSAO support during toluene steam reforming.
AB - Toluene steam reforming was conducted over Ni-supported La0.7Sr0.3AlO3-δ (LSAO) perovskite oxide at 473 K in an electric field, and high toluene conversion was achieved even at such low temperature. Steam reforming is generally done at higher temperatures because of the endothermic nature of this reaction and coke prevention, which requires the contribution of heat energy in great amounts. Reportedly, water activation is particularly difficult to achieve at lower temperatures. Results of kinetic analyses such as Arrhenius plots and partial pressure dependence have revealed that imposing an electric field promotes water activation over Ni/LSAO catalyst. According to steady state isotopic kinetic analysis (SSITKA) and temperature programmed desorption infrared (TPD-IR) measurements, such water activation was accelerated via a redox mechanism using surface lattice oxygen of LSAO. The stimulated mobile lattice oxygen oxidized the adsorbed toluene and formed coke precursor in the electric field. The electric field achieved a lowered reaction temperature for efficient hydrogen production and coke suppression with redox property of LSAO support during toluene steam reforming.
KW - Coke suppression
KW - Hydrogen production
KW - Ni catalyst
KW - Perovskite-type oxide
KW - Redox mechanism
KW - Toluene steam reforming
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U2 - 10.1016/j.apcata.2019.01.011
DO - 10.1016/j.apcata.2019.01.011
M3 - Article
AN - SCOPUS:85060246556
SN - 0926-860X
VL - 573
SP - 56
EP - 63
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
ER -