Highly efficient cobalt-modified hopcalite catalysts prepared through crednerite–spinel transformation

Abstract

The work presents a study and comparison of the catalytic properties of hopcalite catalysts composed of copper–manganese and copper–cobalt–manganese spinel particles in the low-temperature CO oxidation reaction. The cubic spinel structure was formed immediately under reaction conditions through the transformation of hydrothermally prepared crednerite CuMn(Co)O2 particles. Both the initial crednerite-type and the resultant spinel-type particles (Cu, Mn, Co)3O4 exhibited a lamellar morphology and a uniform distribution of elements throughout their bulk and surface. It was found that the modification of the copper–manganese oxide with cobalt resulted in increased particle dispersion and a significant distortion of the crednerite crystal lattice. As a result, this modification reduced the temperature required for the crednerite-to-spinel transformation to 250 °C, whereas the unmodified catalyst is transformed after heating to 350–400 °C only. Furthermore, it was demonstrated that during the CO oxidation at room temperature, the modified spinel particles (Cu, Mn, Co)3O4 exhibited a specific catalytic activity ∼3.5 times greater than that of the copper–manganese system. This enhancement is associated with the stabilization of a more oxidized surface state for the modified spinel particles, which may involve an increased contribution of Co3+ and Mn4+ surface species, as well as an enhancement in the overall lattice oxygen mobility.

Graphical abstract: Highly efficient cobalt-modified hopcalite catalysts prepared through crednerite–spinel transformation

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Article information

Article type
Paper
Submitted
14 Nov 2024
Accepted
17 Jan 2025
First published
17 Jan 2025

React. Chem. Eng., 2025, Advance Article

Highly efficient cobalt-modified hopcalite catalysts prepared through crednerite–spinel transformation

D. A. Svintsitskiy, E. S. Kvasova, T. Yu. Kardash, N. A. Sokovikov, O. A. Stonkus and A. I. Boronin, React. Chem. Eng., 2025, Advance Article , DOI: 10.1039/D4RE00552J

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