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HYDROTREATING CATALYTIC FUNCTIONALITIES OF SBA-16 SUPPORTED Mo, CoMo, AND NiMo CATALYSTS

机译:SBA-16支持的MO,COMO和NIMO催化剂的加氢处理催化功能

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High surface area SBA-16 was used as a support for Mo, CoMo, and NiMo formulation. The supports and catalysts were characterized by BET surface area, XRD, Temperature Programmed Reduction and Low Temperature Oxygen Chemisorption. Surface area and XRD analysis indicate that the dispersion remains more or less constant up to 8wt% Mo and beyond this loading larger MoO3 crystallites are observed. The oxygen chemisorption studies indicated that the anion vacancy concentration increases upto 8wt%Mo and then start decreasing. The TPR studies on oxide precursors indicated a two-peak pattern at lower loading and one peak pattern at higher loading due to presence of two types of reducible species. At lower loading metal to support interaction is very high and gives octahedral and tetrahedral species. At higher Mo loadings octahedral species are formed due to optimum metal support interaction. Promoters Co/or Ni seem to facilitate the reduction of molybdenum species at lower temperature. Finally, a comparison of activities of Co (Ni) Mo catalysts supported over SBA-16 and γ-Al2O3 indicate the superior activity of the former catalyst for both HDS and HYD reactions due to high dispersion of metal species as shown by O2 uptake. This higher activity is attributable to cubic mesopore connectivity resulting in better catalyst dispersion, higher reducibility of Mo, and faster diffusion of reactants and products in case of SBA-16 supported catalysts.
机译:使用高表面积SBA-16作为MO,COMO和NIMO制剂的载体。通过BET表面积,XRD,温度编程减小和低温氧化学吸附,表征载体和催化剂。表面积和XRD分析表明,分散体仍然持续至多8wt%的钼,并且超过该负载较大的moO3微晶。氧化学吸附研究表明,阴离子空位浓度增加了8wt%的Mo,然后开始减少。 TPR对氧化物前体的研究表明,由于存在两种类型的可还原物种,在较低负载下的较低负载下的双峰模式和一个峰值图案。在较低的装载金属以支持相互作用非常高,并提供八面体和四面体物种。在较高的Mo载荷,由于最佳金属支持相互作用,形成八面体物种。促进剂CO /或Ni似乎有助于在较低温度下减少钼物种。最后,支持过SBA-16和γ-Al 2 O 3的CO(Ni)Mo催化剂的活性的比较表明,由于金属物种的高分散,如O 2摄取所示,HDS和HYD反应的前一种催化剂的优异活性。该较高的活性可归因于立方中孔连通性,导致催化剂分散体更好,Mo的更高的还原性,以及在SBA-16负载型催化剂的情况下更快地扩散反应物和产品。

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