- Research Article
- 10.17580/nfm.2025.02.05
The catalytic activity of the highly dispersed solid solution Ce0.80Zr0.10La0.05M0.05O2 – δ (where M = Nd, Sm or Gd) in the complete oxidation reaction of methane
- Dec 25, 2025
- Non-ferrous Metals
- E Yu Liberman + 3 more +3
Highly dispersed, fluorite-like solid solutions (Ce0.80Zr0.10La0.05M0.05O2 – δ), where M = Nd, Sm or Gd, were synthesized by co-precipitating metal hydroxides, followed by heat treatment. The chemical composition of the resulting materials was confirmed by inductively coupled plasma optical emission spectroscopy. X-ray phase analysis confirmed the formation of the Ce0.80Zr0.10La0.05M0.05O2 – δ solid solutions, where M = Nd, Sm or Gd, based on the cerium dioxide crystal lattice. According to transmission electron microscopy data, the average particle size is 13 ± 2 nm. The synthesised materials have a mesoporous structure with a specific surface area of 83–86 m2/g, a total pore volume of 0.101–0.104 cm3/g and a pore diameter of 3.6–3.8 nm. The catalysts exhibit high activity in the complete oxidation of methane (model mixture composition: CH4 – 1 vol.%; O2 – 8 vol.%; N2 – balance). A correlation has been established between the catalytic activity of solid solutions and the ionic radius of the rare earth dopant M. The activity of synthesised solid solutions (Ce0.80Zr0.10La0.05M0.05O2 – δ), where M = Nd, Sm or Gd, decreases in the order Gd → Sm → Nd. The highest activity is observed in the presence of the Ce0.80Zr0.10La0.05M0.05O2 – δ catalyst, which has the smallest ionic radius of the M3+ dopants studied. The temperatures at which 50% and 99% conversion are achieved in the presence of the sample are 356 °C and 477 °C, respectively. The application of Ce0.80Zr0.10La0.05M0.05O2 – δ as a carrier for the active component, palladium, shows promise. The catalytic activity of 0.3% PdO/Ce0.80Zr0.10La0.05M0.05O2 – δ exceeds that of the industrial analogue, 0.3% PdO/γ-Al2O3, demonstrating the feasibility of using the synthesized solid solution as a carrier for the active component. The authors would like to thank the Center for Collective Use at the D.I. Mendeleev Russian Chemical Technology University for conducting research on the elemental composition of the samples.The work was carried out as part of a state assignment from the Ministry of Science and Higher Education of the Russian Federation (FSSM-2023-0004 “Scientific foundations of transition metal-based catalysis systems for promising redox reactions of selective conversion of hydrocarbons and oxygen-containing organic substrates”).
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