TY - JOUR

T1 - Synthesis of Ni2+-Modified Cerium Aluminate and Study of its Physicochemical and Catalytic Properties in the Dry Reforming of Methane Into Synthesis Gas Reaction

AU - Shutilov, A. a.

AU - Marchuk, A. s.

AU - Zenkovets, G. a.

N1 - This work was funded by the Russian Science Foundation (project No. 23-23-10054, https://rscf.ru/project/23-23-10054/) and by the Government of the Novosibirsk Region (Agreement No. 0000005406995998235120802/No. p-72).

PY - 2025/3/28

Y1 - 2025/3/28

N2 - NixCe1–xAlO3–δ catalysts (x = 0-0.5) are prepared by the solution combustion synthesis method. According to the powder XRD data, thermal treatment of the products at 700 °C in air leads mainly to the formation of the cerium aluminate phase and to small amounts of highly dispersed cerium dioxide phase. An increase in the nickel content in the sample significantly decreases the content of the cerium dioxide phase. The prepared Ni2+-modified cerium aluminate samples are precursors of catalysts for the dry reforming of methane reaction (DRM) and are characterized by high specific surface area and a developed porous structure. The study of the phase composition of these samples after their preliminary reduction (“activation”) in a hydrogen-containing gas mixture and subsequent performance in the reaction medium conditions shows that the Ni2+ ions are reduced, come out from the structure to the surface, and form metal Ni particles with a size of 5-8 nm. The influence of catalysts′ chemical composition on their properties in the DRM reaction is studied. The representative Ni0.5Ce0.5AlO3–δ catalyst shows stable performance in the DRM reaction for 30 h at T = 700 °C with a CH4 conversion of 77%, an H2 yield of 43%, and an extremely short contact time τ of 30 ms. High catalytic activity of the obtained catalysts in the DRM reaction is due to the formation of the active phase represented by highly-dispersed coking-resistant metal Ni nanoparticles on the inherently large specific surface area of the Ni2+-modified cerium aluminate.

AB - NixCe1–xAlO3–δ catalysts (x = 0-0.5) are prepared by the solution combustion synthesis method. According to the powder XRD data, thermal treatment of the products at 700 °C in air leads mainly to the formation of the cerium aluminate phase and to small amounts of highly dispersed cerium dioxide phase. An increase in the nickel content in the sample significantly decreases the content of the cerium dioxide phase. The prepared Ni2+-modified cerium aluminate samples are precursors of catalysts for the dry reforming of methane reaction (DRM) and are characterized by high specific surface area and a developed porous structure. The study of the phase composition of these samples after their preliminary reduction (“activation”) in a hydrogen-containing gas mixture and subsequent performance in the reaction medium conditions shows that the Ni2+ ions are reduced, come out from the structure to the surface, and form metal Ni particles with a size of 5-8 nm. The influence of catalysts′ chemical composition on their properties in the DRM reaction is studied. The representative Ni0.5Ce0.5AlO3–δ catalyst shows stable performance in the DRM reaction for 30 h at T = 700 °C with a CH4 conversion of 77%, an H2 yield of 43%, and an extremely short contact time τ of 30 ms. High catalytic activity of the obtained catalysts in the DRM reaction is due to the formation of the active phase represented by highly-dispersed coking-resistant metal Ni nanoparticles on the inherently large specific surface area of the Ni2+-modified cerium aluminate.

KW - coking resistance

KW - dry reforming of methane

KW - greenhouse gas utilization

KW - H2

KW - Ni2+-modified cerium aluminate

KW - solution combustion synthesis

KW - synthesis gas

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-105001316558&origin=inward&txGid=fe895781a25cd7be5c0c25f46cb0909e

U2 - 10.1134/S0022476625030126

DO - 10.1134/S0022476625030126

M3 - Article

VL - 66

SP - 554

EP - 568

JO - Journal of Structural Chemistry

JF - Journal of Structural Chemistry

SN - 0022-4766

IS - 3

ER -