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The role of Ni sites located in mesopores in the selectivity of anisole hydrodeoxygenation

机译:NI位点位于中孔中的NI位点在弧醇和氧化的选择性中的作用

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A highly dispersed Ni catalyst with an increased number of Ni sites selectively distributed in the mesopores of HBEA has been developed and applied in anisole hydrodeoxygenation (HDO) in a continuous-flow reactor under a high WHSV (2.8 min−1). The developed catalyst (Ni/BEA-OR-PH) displayed a significantly higher cyclohexane formation rate compared to the catalysts prepared by incipient wetness impregnation (Ni/BEA-IWI) and deposition–precipitation (Ni/BEA-DP) methods, which was attributed to its higher number of accessible active metal sites in mesopores. While the Ni/BEA-DP as well as Ni/BEA-OR-PH exhibited a high dispersion, a higher concentration of Ni species was located in micropores and distributed as charge-compensating cations, leading to a low concentration of high-temperature desorbed H per surface Ni, which facilitates the hydrogenolysis activity but restricts the hydrogenation of aromatics. Therefore, a high yield of BTX (benzene, toluene and xylene isomers) products was detected over Ni/BEA-DP.
机译:在HBEA的中孔中选择性分布的Ni位点数量增加的高度分散的NI催化剂已在高WHSV下的连续流动反应器中开发并应用于Anisole Hyddoxygygation(HDO)(2.8 min-1)。与通过初期湿度浸渍(NI/BEA-IWI)和沉积 - 预应(NI/BEAD-DP)制备的催化剂相比,开发的催化剂(Ni/Bea-or-PH)显示出明显更高的环己烷形成速率,这是它的催化剂。归因于其中孔中较高的可访问活性金属位点。虽然Ni/BEAD-DP以及Ni/Bea-or-PH表现出较高的分散体,但较高浓度的Ni物种位于Micropores中,并作为电荷补偿阳离子分布,导致高浓度的高温吸引力。 h每表Ni,促进氢解活性,但限制了芳香族剂的氢化。因此,在Ni/BEAD-DP上检测到BTX(苯,甲苯和二甲苯)产物的高收率。

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