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Structural evolution of Pt/ceria-zirconia TWC catalysts during the oxidation of carbon monoxide

机译:一氧化碳氧化过程中Pt /二氧化铈-氧化锆TWC催化剂的结构演变

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摘要

The structural evolution of two Pt/ceria-zirconia catalysts, characterized by different amounts of supported Pt, was monitored by in situ X-ray diffraction during the anaerobic oxidation of CO at different temperatures. In a first phase, oxygen coming from the surface layers of the ceria-zirconia mixed oxide is consumed and no structural variation of the support is observed. After this induction time, bulk reduction of Pt/ceria-zirconia takes place as a step-like process, while the CO2 production continues at a nearly constant rate. This behavior is totally different from that of the metal-free support in similar reaction conditions, that show a gradual bulk reduction. In repeated oxidation-reduction cycles, it was observed that the induction time in Pt/ceria-zirconia is a function of the thermal history, of the amount of supported Pt and of the structural evolution of the samples. (C) 2003 Elsevier Inc. All rights reserved.
机译:通过在不同温度下CO厌氧氧化过程中的原位X射线衍射监测了两种以不同负载量的Pt为特征的Pt /二氧化铈-氧化锆催化剂的结构演变。在第一阶段中,消耗了来自二氧化铈-氧化锆混合氧化物的表面层的氧气,并且未观察到载体的结构变化。在该诱导时间之后,Pt /二氧化铈-氧化锆的大量还原是一个逐步的过程,而二氧化碳的产生几乎以恒定的速率继续进行。该行为与在类似反应条件下无金属载体的行为完全不同,后者显示出逐渐减少的体积。在重复的氧化还原循环中,观察到Pt /二氧化铈-氧化锆中的诱导时间是热历史,负载的Pt量和样品结构演变的函数。 (C)2003 Elsevier Inc.保留所有权利。

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