化学
催化作用
离解(化学)
动力学
傅里叶变换红外光谱
微晶
动能
多相催化
红外光谱学
反应速率
无机化学
核化学
物理化学
化学工程
结晶学
有机化学
物理
量子力学
工程类
作者
J.R. Regalbuto,Eduardo E. Wolf
标识
DOI:10.1016/0021-9517(88)90180-7
摘要
Abstract The kinetics of the NOCO reaction and promotion mechanism of WO 3 on Pt WO 3 SiO 2 catalysts was studied by FTIR spectroscopy in an in situ recycle IR microreacto. It was found that addition of WO 3 to Pt SiO 2 increased activity toward the NOCO reaction. The kinetics displayed an inhibition behavior with increasing CO concentration, but WO 3 served to decrease CO surface coverage during the inhibited regime. However, the rate of NO dissociation over Pt was slowest for the most active (tungsta-containing) catalysts. Characterization studies showed previously that addition of WO 3 resulted in the decoration of Pt crystallites by suboxides of WO 3 . The promotional effects and kinetic results are explained in terms of the participation of PtWO x adlineation sites, which resulted from the decoration effect. Using this concept, a correlation between the increased activity and the concentration of adlineation sites successfully explained the kinetics and IR results obtained with all the catalysts used. The addition of WO 3 to Pt SiO 2 is believed to produce a small number of adlineation sites having very high NO dissociation activity.
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