Methane partial oxidation on Pt/CeO2-ZrO2 in the absence of gaseous oxygen

被引:105
|
作者
Pantu, P
Kim, K
Gavalas, GR [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[2] Yeungnam Univ, Sch Chem Engn & Technol, Kyongsan 712749, South Korea
关键词
cerium oxide; methane partial oxidation; redox oxide; synthesis gas;
D O I
10.1016/S0926-860X(99)00429-9
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 methane to synthesis gas over platinum or ruthenium supported on Ce1-xZrxO2 (x=0, 0.2 and 0.5) was studied at 550-700 degrees C in the absence of gaseous oxygen. The reaction was carried out in a packed-bed reactor under continuous or pulsed flows of methane. Oxidation utilized oxide oxygen and was initially very fast but slowed down as the oxide support became progressively reduced. Addition of ZrO2 into CeO2 considerably increased the rate of methane oxidation and enhanced the reducibility of CeO2 but decreased the selectivity to carbon monoxide and hydrogen, Specifically it was found that significant production of carbon dioxide and water occurred on the freshly oxidized solid until a certain degree of reduction was reached beyond which the selectivity to carbon monoxide and hydrogen rose to over 90%. This critical degree of reduction was 10%, 40% and 65% for the solid compositions x=0, 0.2 and 0.5, respectively. Additional experiments carried out using carbon monoxide pulses showed that carbon monoxide oxidation declines sharply and becomes negligible beyond this degree of reduction while oxidation of methane continues much further. Comparison of the two metals showed that platinum is more active but the reaction rate did not change much in the range of platinum loadings of 0.25-1 wt.%. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:203 / 214
页数:12
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