A highly active catalyst for CO oxidation has been obtained by mutual precipitation from dilute solutions of CuSO4, KMnO4, MnSO4 and Na2CO3 calcinated in a vacuum at 280 °C. Having obtained the catalyst in this way, it was tested, together with three other commercial catalysts of different origins, using various physicochemical methods. Differential thermal analysis has shown that only two different general CO-oxidation mechanisms exist.
V. Dondur, S. Lampa and D. Vučelić, J. Chem. Soc., Faraday Trans. 1, 1983, 79, 1633 DOI: 10.1039/F19837901633
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...