化学
动力学
氨
化学计量学
激进的
化学吸附
催化作用
氘
氮气
氢
无机化学
氨生产
动力学同位素效应
速率决定步骤
物理化学
有机化学
物理
量子力学
作者
A. Ozaki,F. R. S. Sir Hugh Taylor,M. Boudart
出处
期刊:Proceedings of the Royal Society of London
[Royal Society]
日期:1960-10-04
卷期号:258 (1292): 47-62
被引量:119
标识
DOI:10.1098/rspa.1960.0174
摘要
The reaction rate in stoichiometric mixtures of nitrogen and hydrogen or deuterium has been measured on two different doubly promoted iron catalysts, between 218 and 302 °C, ⅓ and 1 atm and over a 300-fold range of efficiencies. The kinetic data as well as the isotope effect indicate that the rate-determining step is the chemisorption of nitrogen on a surface mainly covered with NH radicals. The presence on the surface of NH radicals instead of nitrogen atoms opens new perspectives on the kinetics and mechanism of ammonia synthesis.
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