Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Highly efficient cobalt-modified hopcalite catalysts prepared through crednerite-spinel transformation. / Svintsitskiy, D. A.; Kvasova, E. S.; Kardash, T. Yu и др.
в: Reaction Chemistry and Engineering, 17.01.2025.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Highly efficient cobalt-modified hopcalite catalysts prepared through crednerite-spinel transformation
AU - Svintsitskiy, D. A.
AU - Kvasova, E. S.
AU - Kardash, T. Yu
AU - Sokovikov, N. A.
AU - Stonkus, O. A.
AU - Boronin, A. I.
PY - 2025/1/17
Y1 - 2025/1/17
N2 - 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.
AB - 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.
KW - Bioremediation
KW - Cobalt
KW - Cobalt metallography
KW - Cobalt metallurgy
KW - Crystal lattices
KW - Manganese oxide
KW - Catalytic properties
KW - Cubic spinel structure
KW - Hopcalite catalysts
KW - Hydrothermally
KW - Low-temperature CO oxidation
KW - Manganese spinels
KW - Oxidation reactions
KW - Reaction conditions
KW - Spinel particles
KW - Spinel-type
KW - Catalytic oxidation
UR - https://www.mendeley.com/catalogue/ef32f4f1-4115-3b97-8f6d-747b5182d305/
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85216762747&origin=inward&txGid=34307dc974dfff302e3879aaaacc0e65
U2 - 10.1039/d4re00552j
DO - 10.1039/d4re00552j
M3 - Article
JO - Reaction Chemistry and Engineering
JF - Reaction Chemistry and Engineering
SN - 2058-9883
ER -
ID: 64572476