催化作用
化学
选择性催化还原
氨
傅里叶变换红外光谱
氮氧化物
无机化学
氧化还原
硝酸
反应机理
原位
红外光谱学
催化循环
光谱学
动力学
光化学
物理化学
化学工程
有机化学
工程类
物理
燃烧
量子力学
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1994-08-26
卷期号:265 (5176): 1217-1219
被引量:662
标识
DOI:10.1126/science.265.5176.1217
摘要
The selective catalytic reduction reaction of nitric oxide by ammonia over vanadia-titania catalysts is one of the methods of removing NO x pollution. In the present study, it has been possible to identify the reaction mechanism and the nature of the active sites in these catalysts by combining transient or steady-state in situ (Fourier transform infrared spectroscopy) experiments directly with on-line activity studies. The results suggest a catalytic cycle that consists of both acid and redox reactions and involves both surface V—OH (Brønsted acid sites) and V=O species. A fundamental microkinetic model is proposed, which accounts for the observed industrial kinetics performance.
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