Hydrodeoxygenation of guaiacol over BEA supported bimetallic Ni-Fe catalysts with varied impregnation sequence

加氢脱氧 催化作用 氢解 化学 双金属片 愈创木酚 环己烷 金属 甲苯 选择性 无机化学 核化学 有机化学
作者
Penghui Yan,Eric M. Kennedy,Michael Stockenhuber
出处
期刊:Journal of Catalysis [Elsevier BV]
卷期号:404: 1-11 被引量:26
标识
DOI:10.1016/j.jcat.2021.08.033
摘要

BEA supported Ni-Fe catalysts, prepared by various impregnation techniques, were characterised and examined for their activity for the hydrodeoxygenation (HDO) of guaiacol and hydrogenation of toluene. The aim of the study was to explore the factors affecting the formation of Ni-Fe active species and explore the relationship between the concentration of surface Ni, Ni-Fe species and HDO activity. Catalysts prepared initially with Fe, or co-currently with Fe and Ni exhibited a higher level of HDO rate compared to catalyst that was prepared with Ni initially. When a catalyst was impregnated initially with Fe, metal-supported interaction was relatively weak, thus the formation of Ni-Fe species was promoted. In contrast, a reduced number of Ni sites was involved in the formation of Ni-Fe species when the catalyst was initially impregnated with Ni, resulting in a low HDO rate. The rate of cyclohexane formation is proportional to the concentration of surface Ni-Fe over the catalysts with similar Ni and Fe loadings but prepared by different impregnation sequences. The enhanced HDO rate is attributed to the hydrogenolysis activity of Ni-Fe species. The effect of Ni/Fe ratio on HDO activity was also investigated under differential conditions and the catalyst with a Ni/Fe mass ratio of 3.3 exhibited the highest rate of cyclohexane formation.
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