TY - JOUR
T1 - Synthesis gas production in methane conversion using the Pd|yttria-stabilized zirconia|Ag electrochemical membrane system
AU - Hamakawa, Satoshi
AU - Koizumi, Masaki
AU - Sato, Koichi
AU - Nakamura, Junji
AU - Uchijima, Toshio
AU - Murata, Kazuhisa
AU - Hayakawa, Takashi
AU - Takehira, Katsuomi
PY - 1998
Y1 - 1998
N2 - The electrochemical membrane reactor of YSZ (yttria-stabilized zirconia) solid electrolyte coated with Pd and Ag as anode and cathode, respectively, has been applied to the partial oxidation of methane to synthesis gas (CO + H2). The Pd|YSZ|Ag catalytic system has shown a remarkable activity for CO production at 773 K, and the selectivity to CO was quite high (96.3%) under oxygen pumping condition at 5 mA. The H2 production strongly depend on the oxidation state of the Pd anode surface. Namely, the H2 treatment of the Pd anode at 773 K for 1 h drastically reduced the ate of H2 production, while air treatment enhanced the H2 production rate. From the results of the partial oxidation of CH4 with molecular oxygen, it is considered that the reaction site of the electrochemical oxidation of CH4 to synthesis gas was the Pd-YSZ-gas-phase boundary (triple-phase boundary). In addition, it is found that the oxygen Species pumped electrochemically over the Pd surface demonstrated similar activity to adsorbed oxygen over Pd, PdOad, for the selective oxidation of CH4 to CO, when the Pd supported on YSZ was used as a fixed-bed catalyst for CH4 oxidation with the adsorbed oxygen. The difference with respect to the H2 formation between the electrochemical membrane system and the fixed-bed catalyst reactor results from differences in the average particle size of Pd and the way of the oxygen supply to the Pd surface.
AB - The electrochemical membrane reactor of YSZ (yttria-stabilized zirconia) solid electrolyte coated with Pd and Ag as anode and cathode, respectively, has been applied to the partial oxidation of methane to synthesis gas (CO + H2). The Pd|YSZ|Ag catalytic system has shown a remarkable activity for CO production at 773 K, and the selectivity to CO was quite high (96.3%) under oxygen pumping condition at 5 mA. The H2 production strongly depend on the oxidation state of the Pd anode surface. Namely, the H2 treatment of the Pd anode at 773 K for 1 h drastically reduced the ate of H2 production, while air treatment enhanced the H2 production rate. From the results of the partial oxidation of CH4 with molecular oxygen, it is considered that the reaction site of the electrochemical oxidation of CH4 to synthesis gas was the Pd-YSZ-gas-phase boundary (triple-phase boundary). In addition, it is found that the oxygen Species pumped electrochemically over the Pd surface demonstrated similar activity to adsorbed oxygen over Pd, PdOad, for the selective oxidation of CH4 to CO, when the Pd supported on YSZ was used as a fixed-bed catalyst for CH4 oxidation with the adsorbed oxygen. The difference with respect to the H2 formation between the electrochemical membrane system and the fixed-bed catalyst reactor results from differences in the average particle size of Pd and the way of the oxygen supply to the Pd surface.
UR - http://www.scopus.com/inward/record.url?scp=0000254049&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0000254049&partnerID=8YFLogxK
U2 - 10.1023/a:1019012629300
DO - 10.1023/a:1019012629300
M3 - Article
AN - SCOPUS:0000254049
VL - 52
SP - 191
EP - 197
JO - Catalysis Letters
JF - Catalysis Letters
SN - 1011-372X
IS - 3-4
ER -