The partial oxidation of methanol using a fuel cell reactor

被引:23
|
作者
Otsuka, K [1 ]
Ina, T [1 ]
Yamanaka, I [1 ]
机构
[1] Tokyo Inst Technol, Grad Sch Sci & Engn, Dept Appl Chem, Meguro Ku, Tokyo 1528552, Japan
关键词
cell reactor; methanol; dimethoxymethane; methyl formate; partial oxidation; iridium; platinum;
D O I
10.1016/S0926-860X(03)00130-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Partial oxidation of methanol was performed with a gas-phase [CH3OH|H3PO4|O-2] cell reactor by using noble metals as electrocatalysts over the temperature range of 343-373 K. Among the noble metal electrocatalysts tested, the Ir (anode)-Pt (cathode) combination showed the best cell performance for partial oxidation of methanol into dimethoxymethane (DMM) and methyl formate (W). The cell gave a maximum current density of 34 mA cm(-2) at 373 K; one-pass conversion of methanol was 14% and the turn-over number per Ir was 6.6 h(-1). The kinetic results of the oxidation of methanol with the [CH3OH, Ir|H3PO4|Pt, O-2] cell could be explained in terms of the reaction mechanism proposed. In general, the cell performance in the oxidation of methanol for different combinations of anode-cathode electrocatalysts was strongly deteriorated with the diffusion of methanol from the anode to the cathode (cross-over). However, the cell of Ir (anode)-Pt (cathode) combination was specifically resistant to this unfavorable effect. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:219 / 229
页数:11
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