Skip to main content
Log in

CO Oxidation Behavior of Copper and Copper Oxides

  • Published:
Catalysis Letters Aims and scope Submit manuscript

Abstract

Carbon monoxide oxidation activities over Cu, Cu2O, and CuO were studied to seek insight into the role of the copper species in the oxidation reaction. The activity of copper oxide species can be elucidated in terms of species transformation and change in the number of surface lattice oxygen ions. The propensity of Cu2O toward valence variations and thus its ability to seize or release surface lattice oxygen more readily enables Cu2O to exhibit higher activities than the other two copper species. The non-stoichiometric metastable copper oxide species formed during reduction are very active in the course of CO oxidation because of its excellent ability to transport surface lattice oxygen. Consequently, the metastable cluster of CuO is more active than CuO, and the activity will be significantly enhanced when non-stoichiometric copper oxides are formed. In addition, the light-off behaviors were observed over both Cu and Cu2O powders. CO oxidation over metallic Cu powders was lighted-off because of a synergistic effect of temperature rises due to heat generation from Cu oxidation as well as CO oxidation over the partially oxidized copper species.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. J. T. Kummer, Prog. Energy Combust. Sci. 6 (1980) 177.

    Google Scholar 

  2. T. J. Huang and T.-C. Yu, Appl. Catal. 71 (1991) 275.

    Google Scholar 

  3. M. O'Keefie and W. J. Moore, J. Chem. Phys. 36 (1962) 3009.

    Google Scholar 

  4. G. G. Jernigan and G. A. Somorjai, J. Catal. 147 (1994) 567.

    Google Scholar 

  5. V. A. Sadykov and S. F. Tikhov, J. Catal. 165 (1997) 279.

    Google Scholar 

  6. K. Nagase, Y. Zheng, Y. Kodama and J. Kakuta, J. Catal. 187 (1999) 123.

    Google Scholar 

  7. E. D. Pierron, J. A. Rashkin and J. F. Roth, J. Catal. 9 (1967) 38.

    Google Scholar 

  8. F. Severino and J. Laine, Ind. Eng. Chem. Prod. Res. Dev. 22 (1983) 396.

    Google Scholar 

  9. K. I. Choi and M. A. Vannice, J. Catal. 131 (1991) 22.

    Google Scholar 

  10. C. A. Leon y Leon and M. A. Vannice, Appl. Catal. 69 (1991) 269.

    Google Scholar 

  11. M. Lo Jacono, A. Cimino and M. Inversi, J. Catal. 76 (1982) 320.

    Google Scholar 

  12. A. Yanase and H. Komiyama, Surf. Sci. 248 (1991) 11.

    Google Scholar 

  13. G. K. Boreskov, in: Catalysis: Science and Technology, Vol. 3, eds. J. R. Anderson and M. Boudart (Springer-Verlag, Berlin, 1982) p. 40.

    Google Scholar 

  14. A. Bielanski and J. Haber, Oxygen in Catalysis (Dekker, New York, 1991) p. 244.

    Google Scholar 

  15. G. I. Golodets, Heterogeneous Catalytic Reactions Involving Molecular Oxygen (Elsevier, Amsterdam, 1983) p. 280.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ta-Jen Huang.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Huang, TJ., Tsai, DH. CO Oxidation Behavior of Copper and Copper Oxides. Catalysis Letters 87, 173–178 (2003). https://doi.org/10.1023/A:1023495223738

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1023495223738

Navigation