4.5 Article

Characterization and catalytic activity of soft-templated NiO-CeO2 mixed oxides for CO and CO2 co-methanation

Journal

FRONTIERS OF CHEMICAL SCIENCE AND ENGINEERING
Volume 15, Issue 2, Pages 251-268

Publisher

SPRINGER
DOI: 10.1007/s11705-020-1951-8

Keywords

soft template method; NiO-CeO2 catalysts; CO and CO2 co-methanation; synthetic natural gas production

Funding

  1. Universita degli Studi di Cagliari

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Nanosized NiO, CeO(2)and NiO-CeO(2)mixed oxides were prepared using the soft template method, resulting in nanocrystals of about 4 nm in size regardless of the Ni/Ce molar ratio. Defective sites were formed at the NiO-CeO(2)interface, with strong interaction between Ni species and the support, and CeO(2) showed effective adsorption of CO2. The NiCe system showed promising catalytic performance in CO(x)co-methanation reaction under various conditions and remained stable after thermal stress for up to 50 hours, indicating potential for practical applications.
Nanosized NiO, CeO(2)and NiO-CeO(2)mixed oxides with different Ni/Ce molar ratios were prepared by the soft template method. All the samples were characterized by different techniques as to their chemical composition, structure, morphology and texture. On the catalysts submitted to the same reduction pretreatment adopted for the activity tests the surface basic properties and specific metal surface area were also determined. NiO and CeO(2)nanocrystals of about 4 nm in size were obtained, regardless of the Ni/Ce molar ratio. The Raman and X-ray photoelectron spectroscopy results proved the formation of defective sites at the NiO-CeO(2)interface, where Ni species are in strong interaction with the support. The microcalorimetric and Fourier transform infrared analyses of the reduced samples highlighted that, unlike metallic nickel, CeO(2)is able to effectively adsorb CO2, forming carbonates and hydrogen carbonates. After reduction in H(2)at 400 degrees C for 1 h, the catalytic performance was studied in the CO and CO(2)co-methanation reaction. Catalytic tests were performed at atmospheric pressure and 300 degrees C, using CO/CO2/H(2)molar compositions of 1/1/7 or 1/1/5, and space velocities equal to 72000 or 450000 cm(3)center dot h(-1)center dot g(cat)(-1). Whereas CO was almost completely hydrogenated in any investigated experimental conditions, CO(2)conversion was strongly affected by both the CO/CO2/H(2)ratio and the space velocity. The faster and definitely preferred CO hydrogenation was explained in the light of the different mechanisms of CO and CO(2)methanation. On a selected sample, the influence of the reaction temperature and of a higher number of space velocity values, as well as the stability, were also studied. Provided that the Ni content is optimized, the NiCe system investigated was very promising, being highly active for the CO(x)co-methanation reaction in a wide range of operating conditions and stable (up to 50 h) also when submitted to thermal stress.

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