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Catalytic properties of Ru nanoparticles embedded on ordered mesoporous carbon with different pore size in Fischer-Tropsch synthesis

机译:用不同孔径嵌入有序介孔碳的Ru纳米粒子催化性能,不同孔径在Fischer-Tropsch合成中

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摘要

A series of 3 wt% Ru embedded on ordered mesoporous carbon (OMC) catalysts with different pore sizes were prepared by autoreduction between ruthenium precursors and carbon sources at 1123 K. Ru nanoparticles were embedded on the carbon walls of OMC. Characterization technologies including power X-ray diffraction (XRD), nitrogen adsorption-desorption, transmission electron microscopy (TEM), and hydrogen temperature-programmed reduction (H2-TPR) were used to scrutinize the catalysts. The catalyst activity for Fischer-Tropsch synthesis (FTS) was measured in a fixed bed reactor. It was revealed that 3 wt% Ru-OMC catalysts exhibited highly ordered mesoporous structure and large surface area. Compared with the catalysts with smaller pores, the catalysts with larger pores were inclined to form larger Ru particles. These 3 wt% Ru-OMC catalysts with different pore sizes were more stable than 3 wt% Ru/AC catalyst during the FTS reactions because Ru particles were embedded on the carbon walls, suppressing particles aggregation, movement and oxidation. The catalytic activity and C5+ selectivity were found to increase with the increasing pore size, however, CH4 selectivity showed the opposite trend. These changes may be explained in terms of the special environment of the active Ru sites and the diffusion of products in the pores of the catalysts, suggesting that the activity and hydrocarbon selectivity are more dependent on the pore size of OMC than on the Ru particle size.udud
机译:通过在1123KK的钌前体和碳源之间自动化制备具有不同孔径的有订购的介孔碳(OMC)催化剂的3wt%ru嵌入不同孔径的催化剂.ru纳米颗粒嵌入OMC的碳壁上。包括功率X射线衍射(XRD),氮吸附 - 解吸,透射电子显微镜(TEM)和氢气温度编程(H2-TPR)的特征技术用于仔细筛选催化剂。在固定床反应器中测量Fischer-Tropsch合成(FTS)的催化剂活性。揭示了3wt%的Ru-OMC催化剂表现出高度有序的介孔结构和大表面积。与具有较小孔的催化剂相比,具有较大孔的催化剂倾斜以形成较大的Ru颗粒。在FTS反应期间,具有不同孔径的3wt%Ru-OMC催化剂的孔尺寸比3wt%Ru / Ac催化剂更稳定,因为Ru颗粒嵌入碳壁上,抑制颗粒聚集,运动和氧化。发现催化活性和C5 +选择性随着孔径的增加而增加,然而,CH 4选择性显示相反的趋势。这些变化可以根据活性Ru部位的特殊环境和产物的扩散在催化剂的孔中,表明活性和烃选择性更依赖于OMC的孔径而不是RU粒度。 ud ud

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