Catalytic behavior toward oxidative steam reforming of dimethyl ether over CuFe2O4-Al2O3 composite catalysts

被引:28
|
作者
Faungnawakij, Kajornsak [1 ]
Viriya-empikul, Nawin [1 ]
机构
[1] Natl Sci & Technol Dev Agcy, Natl Nanotechnol Ctr NANOTEC, Pathum Thani 12120, Thailand
关键词
Oxidative steam reforming; Dimethyl ether; Hydrogen; Copper iron spinet; Alumina; Nanocomposite; TEMPERATURE FUEL-CELLS; SOLID-ACID CATALYSTS; GAS SHIFT REACTION; HYDROGEN-PRODUCTION; OXIDE CATALYST; CO OXIDATION; METHANOL; METAL; DME; CU;
D O I
10.1016/j.apcata.2010.04.011
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
Oxidative steam reforming of dimethyl ether (DME OSR) for hydrogen production was studied over CuFe2O4-Al2O3 composite catalysts. The catalytic behaviors of the catalysts were investigated in terms of DME conversion, H-2 production rate, and selectivity to CO2, CO, and CH4 as well as the catalyst temperature and gaseous concentration profiles along the catalyst bed. The catalysts exhibited good reforming activity and low CO formation (<2.5 vol.%) with trace amounts of other byproducts in the temperature range of 275-375 degrees C, steam/DME of 2.5, and O-2/DME of 0-1. The increase in O-2/DME resulted in improved DME conversion, but lower selectivity to H2. The catalyst was essentially stable in DME OSR in the 200 h stability test in the temperature range of 317-335 degrees C, while H-2 concentration was stably obtained at ca. 62 vol.%. Oxygen was rapidly consumed in the beginning zone of the catalyst bed where the exothermic partial oxidation of DME along with CO oxidation would preferentially occur. The majority of reactions in the remaining zone was endothermic steam reforming of DME together with water gas shift reaction. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 27
页数:7
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