Catalytic partial oxidation of ethanol over noble metal catalysts

被引:158
|
作者
Salge, JR [1 ]
Deluga, GA [1 ]
Schmidt, LD [1 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
关键词
D O I
10.1016/j.jcat.2005.07.021
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
The catalytic partial oxidation of ethanol and ethanol-water was investigated over noble metal and metal plus ceria-coated alumina foams at catalyst contact times < 10 ms. The effects of catalyst, flow rate, and water addition on selectivity and conversion were examined. Rh-Ce catalysts were the most active and stable. Without water addition, ethanol was converted directly to H-2 with > 80% selectivity and > 95% conversion with Rh-Ce catalysts. Rh, Pt, Pd, and Rh-Ru produced less H-2, with Pt and Pd producing < 50% H-2. Pt, Pd, and Rh also produced more CH4 and C2H4 than Rh-Ce. There was a smaller dependence on flow rate for Rh-Ce catalysts than other catalysts. Variation of a factor of 2 produced small changes in H-2, and lower flow rates produced less CH4 and C2H4. Autothermal operation was achieved at as low as 10 mol% ethanol in water. Adding water to the Rh-Ce catalyzed reactor increased H-2 selectivity and reduced selectivity to CO to < 50% due to increased water-gas shift and steam reforming activity. With added water, the selectivity to H-2 exceeds 100%, because both ethanol and water contribute H-2. Also, the total selectivity of all unwanted products, mostly CH4, is < 3% at the H-2 production maximum with water addition. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 78
页数:10
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