Partial oxidation of methane to syngas using NiO-supported catalysts

被引:26
|
作者
Drago, RS
Jurczyk, K
Kob, N [1 ]
Bhattacharyya, A
Masin, J
机构
[1] DuPont, Sabine River Lab, Orange, TX 77630 USA
[2] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[3] Amoco Chem Co, Naperville, IL 60566 USA
关键词
methane; nickel oxide; synthesis gas;
D O I
10.1023/A:1019005605676
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
Claims for the partial oxidation of methane to CO and H-2 have been clouded by the possibility of the indirect reaction sequence occurring at hot spots in the catalyst bed. In this report, we claim that the direct reaction occurs on NiO/silica at 500 degrees C with methane conversions as high as 80% and selectivities for H-2 Of 80% and CO of 70%. Arguments are presented to show that the amount of diluent gas employed prevents formation of local hot spots with temperatures high enough for the indirect reaction to occur. Consequently, this study constitutes one of the most convincing reports for the conversion of CH4 to syngas by the partial oxidation of methane. The catalyst deactivates in 10 h. Surface studies show coke formation and aggregation of NiO contribute to the loss of activity.
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页码:177 / 181
页数:5
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