Transient behavior and reaction mechanism of CO catalytic ignition over a CuO-CeO 2 mixed oxide
Kang,Running1,2; Ma,Pandong1,3; He,Junyao1; Li,Huixin1; Bin,Feng1,2,4; Wei,Xiaolin1,2,4; Dou,Baojuan3; Hui,Kwun Nam5; Hui,Kwan San6
Source PublicationProceedings of the Combustion Institute
AbstractThis study focuses on the variation in activity-controlling factors during CO catalytic ignition over a CuO-CeO catalyst. The activity for CO combustion follows the decreasing order of CuO-CeO > CuO > CeO . Except for inactive CeO , increasing temperature induces CO ignition to achieve self-sustained combustion over CuO and CuO-CeO . However, CuO provides enough copper sites to adsorb CO, and abundant active lattice oxygen, thus obtaining a higher hot zone temperature (208.3 °C) than that of CuO-CeO (197.3 °C). Catalytic ignition triggers a kinetic transition from the low-rate steady-state regime to a high-rate steady-state regime. During the induction process, Raman, X-ray photoelectron spectroscopy (XPS), CO temperature-programmed desorption (CO-TPD) and infrared (IR) spectroscopy results suggested that CO is preferentially adsorbed on oxygen vacancies (Cu -[O ]-Ce ) to yield Cu -[C =O]-Ce complexes. Because of the selfpoisoning of CO, the adsorbed CO and traces of adsorbed oxygen react at a relative rate, which is entirely governed by the kinetics on the CO-covered surface and the heat transport until the pre-ignition regime. Nonetheless, the Cu -[C =O]-Ce complex is a major contributor to CO ignition. The step-response runs and kinetic models testified that after ignition, a kinetic phase transition occurs from a CO-covered surface to an active lattice oxygen-covered surface. During CO self-sustained combustion, the rapid gas diffusivity and mass transfer is beneficial for handling the low coverage of CO. The active lattice oxygen of CuO takes part in CO oxidation.
KeywordCarbon monoxide Catalytic ignition Copper-cerium oxide Reaction mechanism Transient behavior
URLView the original
Fulltext Access
Citation statistics
Cited Times [WOS]:2   [WOS Record]     [Related Records in WOS]
Document TypeJournal article
CollectionUniversity of Macau
Corresponding AuthorBin,Feng
Affiliation1.State Key Laboratory of High-Temperature Gas Dynamics, Institute of Mechanics, Chinese Academy of Sciences, Beijing 100190, PR China
2.School of Engineering Science, University of Chinese Academy of Sciences, 100049 Beijing, PR China
3.Tianjin University of Science & Technology, Tianjin 300457, PR China
4.Dalian National Laboratory for Clean Energy, Dalian 116023, PR China
5.Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau, PR China
6.Engineering, Faculty of Science, University of East Anglia, Norwich Research Park, NR4 7TJ, United Kingdom
Recommended Citation
GB/T 7714
Kang,Running,Ma,Pandong,He,Junyao,et al. Transient behavior and reaction mechanism of CO catalytic ignition over a CuO-CeO 2 mixed oxide[J]. Proceedings of the Combustion Institute,2020.
APA Kang,Running,Ma,Pandong,He,Junyao,Li,Huixin,Bin,Feng,Wei,Xiaolin,Dou,Baojuan,Hui,Kwun Nam,&Hui,Kwan San.(2020).Transient behavior and reaction mechanism of CO catalytic ignition over a CuO-CeO 2 mixed oxide.Proceedings of the Combustion Institute.
MLA Kang,Running,et al."Transient behavior and reaction mechanism of CO catalytic ignition over a CuO-CeO 2 mixed oxide".Proceedings of the Combustion Institute (2020).
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Kang,Running]'s Articles
[Ma,Pandong]'s Articles
[He,Junyao]'s Articles
Baidu academic
Similar articles in Baidu academic
[Kang,Running]'s Articles
[Ma,Pandong]'s Articles
[He,Junyao]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Kang,Running]'s Articles
[Ma,Pandong]'s Articles
[He,Junyao]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.