TY - JOUR
T1 - Effect of metal addition to Ru/TiO2 catalyst on selective CO methanation
AU - Tada, Shohei
AU - Kikuchi, Ryuji
AU - Takagaki, Atsushi
AU - Sugawara, Takashi
AU - Ted Oyama, S.
AU - Satokawa, Shigeo
N1 - Funding Information:
This study was supported by New Energy and Industrial Technology Development Organization (NEDO) .
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Selective CO methanation over Ru/TiO2, Ru-Ni/TiO2, Ru-Co/TiO2, Ru-Fe/TiO2, Ru-La/TiO2, Ru-K/TiO2, and Ru-Ni-La/TiO2 was investigated as a CO removal method from reformate gas for polymer electrolyte fuel cell applications, and the selectivity and activity were examined. The addition of Co and La to Ru/TiO2 improved both CO and CO2 methanation, while the addition of Ni raised only the activity for CO methanation. The addition of La increased the electron density in the Ru species, which likely enhanced the dissociation of the CO bond of CO on Ru probably due to back donation of electrons from Ru to CO. This led to high CO methanation activity over Ru-La/TiO2. The trimetallic catalyst Ru-Ni-La/TiO2 showed the highest CO methanation activity among the prepared catalysts, resulting in a wider temperature range for selective CO methanation at low temperatures compared to Ru/TiO2.
AB - Selective CO methanation over Ru/TiO2, Ru-Ni/TiO2, Ru-Co/TiO2, Ru-Fe/TiO2, Ru-La/TiO2, Ru-K/TiO2, and Ru-Ni-La/TiO2 was investigated as a CO removal method from reformate gas for polymer electrolyte fuel cell applications, and the selectivity and activity were examined. The addition of Co and La to Ru/TiO2 improved both CO and CO2 methanation, while the addition of Ni raised only the activity for CO methanation. The addition of La increased the electron density in the Ru species, which likely enhanced the dissociation of the CO bond of CO on Ru probably due to back donation of electrons from Ru to CO. This led to high CO methanation activity over Ru-La/TiO2. The trimetallic catalyst Ru-Ni-La/TiO2 showed the highest CO methanation activity among the prepared catalysts, resulting in a wider temperature range for selective CO methanation at low temperatures compared to Ru/TiO2.
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U2 - 10.1016/j.cattod.2013.09.048
DO - 10.1016/j.cattod.2013.09.048
M3 - Article
AN - SCOPUS:84901191284
SN - 0920-5861
VL - 232
SP - 16
EP - 21
JO - Catalysis Today
JF - Catalysis Today
ER -