Kinetic study of selective CO oxidation in H2-rich gas on a Ru/γ-Al2O3 catalyst

被引:88
|
作者
Han, YF [1 ]
Kahlich, MJ [1 ]
Kinne, M [1 ]
Behm, RJ [1 ]
机构
[1] Univ Ulm, Abt Oberflachenchem & Katalyse, D-89069 Ulm, Germany
关键词
D O I
10.1039/b103780n
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 preferential oxidation (PROX) of CO on Ru/gamma-Al2O3 in simulated reformer gas (1.0 kPa CO, 75 kPa H-2, rest N-2) was investigated over a wide range of CO partial pressures (0.02-1.5 kPa) and O-2 excess (p(O2) : p(CO) = 0.5-5.0). Integral flow measurements in a microreactor at lambda = 2 show that similar to150degreesC is the optimum temperature for the PROX of CO, combining sufficiently high rates with a high selectivity (S approximate to 50%). Ru/gamma-Al2O3 shows a significantly higher activity and selectivity under these conditions than the conventionally used Pt/gamma-Al2O3 catalyst. Differential flow experiments allow the quantitative determination of CO and O-2 oxidation rates at 150degreesC, with reaction orders of alpha = -0.48 for CO and alpha = 0.85 for O-2. In the low temperature regime, 135-200degreesC, the apparent activation energy, E-a*, is 95+/-5 kJ mol(-1). Our findings are consistent with a Langmuir-Hinshelwood reaction mechanism in the low-rate branch, where both CO oxidation and H-2 oxidation are limited by the presence of a CO adlayer. The saturation of the reaction rate at high oxygen excess (lambda greater than or equal to 6) as well as previous data support a model where the reaction proceeds on oxygen loaded/surface oxide covered Ru particles. The minimum amount of catalyst and oxygen excess for complete removal (< 50 ppm) of CO from methanol reformate in the second stage of a double stage reactor (p(CO) <= 0.2 kPa) was calculated in reaction simulations, which were based on a plug-flow reactor model and use the kinetic parameters determined in this study. Including contributions from CO and CO2 methanation and from the reverse water gas shift reaction (RWGS) the Ru/gamma-Al2O3 catalyst shows a much better performance than Pt/gamma-Al2O3, both because of its much lower minimum noble metal mass, lower by a factor of 20, and the much better behavior under dynamic load conditions, where only the Ru catalyst remains below the critical CO level of 50 ppm for load variations to 10% and 1%, respectively.
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页码:389 / 397
页数:9
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