Issue 2, 1999

EPR analysis of La1-xMxMnO3+y (M=Ce, Eu, Sr) perovskitic catalysts for methane oxidation

Abstract

A series of catalysts has been analysed before and after their use for methane flameless oxidation with air. In most cases, a g2, linearly temperature-broadened, Lorentzian-shaped EPR line was observed at T>Tmin, where Tmin is the temperature corresponding to the narrowest EPR line, ranging between 244 and 392 K, depending on the nature and concentration of the doping ion. This trend of the EPR linewidth is discussed and attributed to bottlenecked spin relaxation taking place from the Mn4+ ions to the lattice via the Mn3+ ions. With all the samples, Tmin increased after catalytic use. This has been attributed to a change of the Curie temperature, Tc, due to an increase of the conduction bandwidth, accompanying the chemical reduction from Mn4+ to Mn3+ during the catalytic process. Therefore, the presence of more Mn4+ is expected to improve the catalyst activity. In fact, lower light-off temperatures were obtained for increasing concentration of Sr or Eu, which forces Mn3+ to Mn4+, in contrast to the case of Ce4+ as dopant.

Article information

Article type
Paper

Phys. Chem. Chem. Phys., 1999,1, 355-360

EPR analysis of La1-xMxMnO3+y (M=Ce, Eu, Sr) perovskitic catalysts for methane oxidation

C. Oliva, L. Forni, P. Pasqualin, A. D'Ambrosio and A. V. Vishniakov, Phys. Chem. Chem. Phys., 1999, 1, 355 DOI: 10.1039/A807702I

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.

Social activity

Spotlight

Advertisements