Bifunctional molybdenum oxide/acid catalysts for hydroisomerization of n-heptane
Publication date
2020-10
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Abstract
Numerus research studies focus on replacing scarce noble metals by non-noble transition metals in solid catalysts. The (de)hydrogenation function in bifunctional catalysts for hydroisomerization and hydrocracking of alkanes is usually performed by a precious metal such as Pt, or a metal sulfide such as MoS2. In this study, we investigated the possibility of replacing Pt with a non-sulfided MoOx catalyst in combination with a mesoporous solid acid for the hydroisomerization of n-heptane. MoOx particles size as well as the preparation techniques were varied in order to identify the Mo active phase for (de)hydrogenation. We demonstrated that an optimized non-precious metal MoOx catalyst can perform similarly to its Pt counterpart in the n-heptane conversion when used in combination with a mesoporous solid acid.
Keywords
Bifunctional catalysts, Hydroisomerization, Mo oxide, Solid acid, Taverne, Catalysis, Physical and Theoretical Chemistry
Citation
Harmel, J, Roberts, T, Zhang, Z, Sunley, G, de Jongh, P & de Jong, K P 2020, 'Bifunctional molybdenum oxide/acid catalysts for hydroisomerization of n-heptane', Journal of Catalysis, vol. 390, pp. 161-169. https://doi.org/10.1016/j.jcat.2020.08.004