期刊
JOURNAL OF CATALYSIS
卷 235, 期 1, 页码 79-91出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2005.07.010
关键词
Pt; thoria; ceria; water-gas shift; formic acid; methanol; steam reforming
Implied in the proposed water-gas shift (WGS) mechanisms for Pt/ceria and P/thoria catalysts is the presumption that reduced defect centers are formed on the surface. This X-ray absorption near-edge spectroscopy study provides direct results indicating that Pt facilitates reduction in the surface shell of thoria. Mechanistic arguments from in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) are provided suggesting that the active sites for WGS, water-assisted formic acid decomposition, and methanol steam reforming are associated with oxygen-deficient centers. In all cases, a high H2O/reactant (i.e., carbon monoxide, formic acid, or methanol) ratio was used. For WGS, CO reacted with type II bridging OH groups at reduced centers to generate surface formate intermediates, the decomposition of which is suggested to be the rate-limiting step by the observation of a normal kinetic isotope effect (NKIE) associated with the formate coverage as monitored by DRIFTS under steady-state conditions using CO + H2O and CO + D2O feeds. The same NKIE was observed in steady-state reaction tests. Formic acid dissociated on the surface of thoria to yield the same surface formate species as observed when CO adsorbs. An identical NKIE associated with formate decomposition was observed when switching from a feed containing HCOOH + H2O and DCOOH + H2O, establishing two important commonalities: (1) similarity in the mechanistic pathway and (2) importance of the role of type II bridging OH groups at reduced centers in the catalysis. Methanol steam reforming likely proceeded through a mechanism involving adsorption at reduced centers to generate type 11 methoxy species, with subsequent conversion to formate, unidentate carbonate, and finally CO2. The higher NKIE when switching between H-labeled and D-labeled feeds suggests that conversion of methoxy species to formate may be the rate-limiting step. The methanol steam reforming reaction was selective to CO2 at low conversion, but CO selectivity increased at higher conversions, suggesting competition with the secondary reaction of reverse WGS at higher temperature. Pt/thoria was more selective at higher conversion for CO2 than a similarly loaded Pt/ceria catalyst. These results suggest that from a mechanistic standpoint, the two materials are virtually analogs of one another. (c) 2005 Elsevier Inc. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据