TY - JOUR
T1 - Carbon dioxide reforming of methane over Ni incorporated into Ce-ZrO 2 catalysts
AU - Roh, Hyun Seog
AU - Potdar, H. S.
AU - Jun, Ki Won
AU - Kim, Jae Woo
AU - Oh, Young Sam
PY - 2004/11/25
Y1 - 2004/11/25
N2 - A co-precipitation/digestion method was employed in a single step to prepare Ni-Ce-ZrO2 catalysts useful for carbon dioxide reforming of methane. The loading amount of Ni and the ratio of CeO 2 to ZrO2 were systematically varied to optimize the co-precipitated Ni-Ce-ZrO2 catalysts. The prepared catalysts were characterized by various physico-chemical characterization techniques such as XRD, BET surface area, hydrogen chemisorption, SEM, TPR and XPS. It was found that 15% Ni (w/w) co-precipitated with Ce0.8Zr0.2O2 having cubic phase gave synthesis gas with CH4 conversion more than 97% at 800 °C and such activity was maintained without significant loss during the reaction for 100 h. On the contrary, Ni-Ce-ZrO2 having tetragonal phase (Ce0.2Zr 0.8O2) or mixed phase (Ce0.8Zr 0.5O2) deactivated during the reaction due to carbon formation. The enhanced catalytic activity and stability of the co-precipitated Ni-Ce0.8Zr0.2O2 catalyst is attributed to a combination of the nano-crystalline nature of cubic Ce0.8Zr0.2O2 support and the finely dispersed nano-sized NiOx crystallites, resulting in the intimate contact between Ni and Ce0.8Zr0.2O 2 particles.
AB - A co-precipitation/digestion method was employed in a single step to prepare Ni-Ce-ZrO2 catalysts useful for carbon dioxide reforming of methane. The loading amount of Ni and the ratio of CeO 2 to ZrO2 were systematically varied to optimize the co-precipitated Ni-Ce-ZrO2 catalysts. The prepared catalysts were characterized by various physico-chemical characterization techniques such as XRD, BET surface area, hydrogen chemisorption, SEM, TPR and XPS. It was found that 15% Ni (w/w) co-precipitated with Ce0.8Zr0.2O2 having cubic phase gave synthesis gas with CH4 conversion more than 97% at 800 °C and such activity was maintained without significant loss during the reaction for 100 h. On the contrary, Ni-Ce-ZrO2 having tetragonal phase (Ce0.2Zr 0.8O2) or mixed phase (Ce0.8Zr 0.5O2) deactivated during the reaction due to carbon formation. The enhanced catalytic activity and stability of the co-precipitated Ni-Ce0.8Zr0.2O2 catalyst is attributed to a combination of the nano-crystalline nature of cubic Ce0.8Zr0.2O2 support and the finely dispersed nano-sized NiOx crystallites, resulting in the intimate contact between Ni and Ce0.8Zr0.2O 2 particles.
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U2 - 10.1016/j.apcata.2004.08.009
DO - 10.1016/j.apcata.2004.08.009
M3 - Article
AN - SCOPUS:6444242331
SN - 0926-860X
VL - 276
SP - 231
EP - 239
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
IS - 1-2
ER -