ADSORPTION OF NO AND NH3 ON VANADIA TITANIA CATALYSTS - ESR AND XPS STUDIES OF ADSORPTION

被引:62
作者
ODRIOZOLA, JA
SORIA, J
SOMORJAI, GA
HEINEMANN, H
DELABANDA, JFG
GRANADOS, ML
CONESA, JC
机构
[1] UNIV CALIF BERKELEY LAWRENCE BERKELEY LAB,CTR ADV MAT,1 CYCLOTRON RD,BERKELEY,CA 94720
[2] UNIV CALIF BERKELEY LAWRENCE BERKELEY LAB,DIV CHEM SCI,BERKELEY,CA 94720
[3] CSIC,INST CATALISIS & PETR QUIM,MADRID 6,SPAIN
[4] UNIV CALIF BERKELEY,DEPT CHEM,BERKELEY,CA 94720
关键词
D O I
10.1021/j100154a047
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 adsorption of NO and NH3 on V2O5/TiO2 catalysts has been studied by ESR and XPS at temperatures and pressures close to those used for industrial tail gas cleanup from power plants and HNO3 plants, using NO reduction with ammonia. The paper extends and confirms earlier studies on pure V2O5 and TiO2 samples. The reduction of the vanadia sites by adsorbed NH3 occurs over the whole range of temperatures studied while NO adsorption is observed on the titania support. Reduction of NO to N2 occurs on the reduced vanadia sites, which are reoxidized in the process. The reduced vanadia sites, however, are blocked by chemisorbed NH3, preventing the reduction of NO which causes a drop in the NO molar conversion. The presence of oxygen (or water) in the reaction mixture plays a major role in the selectivity of the vanadium oxide catalyst since it interacts with NH3 at the reduced vanadia sites, resulting in the elimination of the NH3 poisoning of the reduced surface sites at temperatures above 550 K.
引用
收藏
页码:240 / 246
页数:7
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