Oxygenate reaction pathways on transition metal surfaces

被引:378
作者
Mavrikakis, M [1 ]
Barteau, MA [1 ]
机构
[1] Univ Delaware, Dept Chem Engn, Ctr Catalyt Sci & Technol, Newark, DE 19716 USA
关键词
D O I
10.1016/S1381-1169(97)00261-6
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 importance of various oxygenates as fuels and as chemical intermediates and products continues to grow. Alcohols and aldehydes have also been the subjects of numerous surface reactivity studies. We review here the decomposition mechanisms of oxygenates on transition metal surfaces focusing primarily on metals of Groups VIII and IB. Common pathways as well as deviations from these serve to illustrate the patterns of oxygenate reactions. Several major divisions in the preferred pathways can be rationalized in terms of the affinities of metals for making metal-oxygen and metal-hydrogen bonds. Other important factors determining oxygenate reactivities include surface crystallographic structure and the detailed molecular structure of the oxygenate. Differences in product distribution between metals are frequent, even in cases where many of the reaction steps are common, primarily because of the plethora of elementary reaction steps usually involved in oxygenate decomposition on transition metal surfaces. As a result, differences late in the reaction sequence can obscure important similarities in the overall reaction network. Spectroscopic identification of common surface reaction intermediates including alkoxides, acyls, and oxametallacycles, has become increasingly important in revealing the underlying similarities in seemingly diverse oxygenate reaction pathways on transition metal surfaces. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:135 / 147
页数:13
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