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Effect of Calcination Temperature on Cu-Modified Ni Catalysts Supported on Mesocellular Silica for Methane Decomposition

[Image: see text] Catalytic methane decomposition has been considered suitable for the green and sustainable production of high-purity H(2) to help reduce greenhouse gas emissions. This research developed a copper-modified nickel-supported mesocellular silica NiCu/MS(x) catalyst synthesized at diffe...

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Detalles Bibliográficos
Autores principales: Phichairatanaphong, Orrakanya, Poo-Arporn, Yingyot, Chareonpanich, Metta, Donphai, Waleeporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089693/
https://www.ncbi.nlm.nih.gov/pubmed/35573207
http://dx.doi.org/10.1021/acsomega.2c01016
Descripción
Sumario:[Image: see text] Catalytic methane decomposition has been considered suitable for the green and sustainable production of high-purity H(2) to help reduce greenhouse gas emissions. This research developed a copper-modified nickel-supported mesocellular silica NiCu/MS(x) catalyst synthesized at different calcination temperatures to improve the activity and stability in the CH(4) decomposition reaction at 600 °C. Ni and Cu metals were loaded on a mesocellular silica (MS) support using a co-impregnation method and calcined at different temperatures (500, 600, 700, and 800 °C). The NiCu/MS(600) catalyst not only had the highest H(2) yield (32.78%), which was 1.47–3.87 times higher than those of the other NiCu/MS(x) catalysts, but also showed better stability during the reaction. Calcination at 600 °C helps improve the active nickel dispersion, the reducibility of the NiCu catalyst, and the interaction of the NiCu–MS support, leading to the formation of fishbone and platelet carbon nanofibers via a tip-growth mechanism, resulting in the NiCu metals remaining active during the reaction.