Selective catalytic reduction of nitric oxide by methane in the presence of oxygen over CaO catalyst

被引:21
|
作者
Fliatoura, KD
Verykios, XE
Costa, CN
Efstathiou, AM
机构
[1] Univ Cyprus, Dept Nat Sci, Nicosia, Cyprus
[2] Univ Patras, Dept Chem Engn, GR-26500 Patras, Greece
关键词
nitric oxide reduction by CH4; NO reduction by hydrocarbon; nitrogen oxides; methane; calcium oxide; nitric oxide reduction kinetics;
D O I
10.1006/jcat.1999.2414
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 selective catalytic reduction of nitric oxide by methane in the presence of oxygen was studied over CaO catalyst in the temperature range 550-850 degrees C. The nitric oxide conversion-versus-temperature profile was found to depend on oxygen feed concentration, while the selectivity to N-2 formation was found to be 100% and independent of oxygen feed concentration in the range 1-10 mol%. The kinetic study has shown that the reaction order with respect to NO and CH4 is 1.0 and 0.5, respectively. On the other hand, the reaction order with respect to O-2 was found to be slightly positive for O-2 feed concentrations up to 1 mol% and slightly negative at higher concentrations. The apparent activation energy of the reaction in the presence of oxygen was found to be 14.6 kcal/mol. The addition of 2.5 mol% CO2 and 5 mol% H2O in the feed stream had a considerable inhibiting effect on NO conversion in the range 550-650 degrees C, while a small inhibiting effect of CO2 and a positive effect of H2O were observed in the range 700-850 degrees C. Temperature-programmed desorption (TPD) of NO revealed the presence of two well-resolved NO peaks in the temperature range 250-650 degrees C, a behavior also observed during a temperature-programmed oxidation experiment under O-2/He flow. However, during temperature-programmed surface reaction under CH4/He flow the NO desorption spectrum showed a significant shift of the stronger adsorbed NO species toward lower temperatures. Preadsorbed CO2 on the CaO surface was found to largely affect the chemisorption of NO and its desorption kinetics during TPD. The amount of deposited carbon-containing species on the catalyst surface during reaction was determined with transient titration experiments and it was found to be small. (C) 1999 Academic Press.
引用
收藏
页码:323 / 335
页数:13
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