Effect of different oxygen species originating from the dissociation of O2, N2O and NO on the selectivity of the Pt-catalysed NH3 oxidation

被引:4
作者
Kondratenko, V. A.
Baerns, M.
机构
[1] Univ Rostock, Aussenstelle Berlin, Leibniz Inst Katalyse eV, D-12489 Berlin, Germany
[2] Ruhr Univ Bochum, Lehrstuhl Tech Chem, D-44801 Bochum, Germany
关键词
TAP reactor; ammonia oxidation; product distribution; reaction mechanism; transient experiments in vacuum; Pt catalyst; Pt gauze; adsorbed oxygen species;
D O I
10.1016/j.cattod.2006.08.067
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An effect of oxygen species formed from O-2, N2O and NO on the selectivity of the catalytic oxidation of ammonia was studied over a polycrystalline Pt catalyst using the temporal analysis of products (TAP) reactor. The transient experiments were performed in the temperature range between 773 and 1073 K in a sequential pulse mode with a time interval of 0.2 s between the pulses of the oxidant (O-2, N2O and NO) and NH3. In contrast to adsorbed oxygen species formed from NO, those from O-2, and N2O reacted with ammonia yielding NO. It is suggested that the difference between these oxidising agents may be related to the different active sites for dissociation of O-2, N2O and NO, where oxygen species of various Pt-O strength are formed. Weaker bound oxygen species, which are active for NO formation, originate from O-2 and N2O rather than from NO. These species may be of bi-atomic nature. (c) 2006 Elsevier B.V. All rights reserved.
引用
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页码:210 / 216
页数:7
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