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Efficient hierarchically structured composites containing cobalt catalyst for clean synthetic fuel production from Fischer–Tropsch synthesis

机译:含钴催化剂的高效分层结构复合材料,用于费托合成生产清洁合成燃料

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We report a straightforward preparation method to synthesize hierarchical composite consisting of TiO_2-coated multi-walled carbon nanotubes (CNTs) decorating a macroscopic host structure of α-Al_2O_3. The obtained composite possesses moderate specific surface area and very open porous structure, as well as moderate interaction with active sites, which significantly improve the cobalt nanoparticles dispersion and the mass diffusion during the reaction. The Co/TiO_2/CNT-α-Al_2O_3 (CoTiCNTA) catalyst is then used in the Fischer–Tropsch synthesis (FTS) process. This hierarchical catalyst achieves a FTS rate to C_(5+) of 0.80 g_(C5+) gcat~(-1) h~(-1) along with a long-chain hydrocarbons (C_(5+)) selectivity of 85%, which can be pointed out as the most outstanding noble promoter-free catalyst for the FTS process. The as-synthesized catalyst also exhibits an extremely high stability as a function of time on stream which is also one of the prerequisites for the development of future FTS catalysts, especially for the Biomass-to-Liquids process where trace amount of impurities and/or moisture could have an impact on the catalyst stability. The present work also introduces a new investigation methodology based on the use of zero field ~(59)Co NMR, which allows one to map in a precise manner the cobalt active phase distribution and to correlate it with the FTS performance. It is expected that such technique would be extremely helpful for the understanding of the catalyst structure–performance relationship and for future optimization in the FTS process as well as in other fields of investigation where cobalt particles are involved.
机译:我们报告了一种简单的制备方法来合成由TiO_2涂层的多壁碳纳米管(CNT)组成的多层复合材料,该多层复合材料装饰了α-Al_2O_3的宏观主体结构。所获得的复合物具有适度的比表面积和非常开放的多孔结构,以及与活性位点的适度相互作用,这显着改善了反应期间钴纳米颗粒的分散和质量扩散。然后,将Co / TiO_2 /CNT-α-Al_2O_3(CoTiCNTA)催化剂用于费托合成(FTS)过程。该分级催化剂的C_(5+)的FTS速率达到0.80 g_(C5 +)gcat〜(-1)h〜(-1),同时长链烃(C_(5+))的选择性为85%,可以指出,它是FTS工艺中最杰出的无贵金属助催化剂。合成后的催化剂还具有极高的稳定性,这是生产时间的函数,这也是开发未来FTS催化剂的先决条件之一,特别是对于其中痕量杂质和/或痕量杂质的生物质制液工艺而言水分可能会影响催化剂的稳定性。本工作还介绍了一种基于零场〜(59)Co NMR的新研究方法,该方法可精确绘制钴活性相分布并将其与FTS性能相关。预计这种技术将对理解催化剂的结构与性能之间的关系以及对FTS工艺以及涉及钴颗粒的其他研究领域的未来优化非常有帮助。

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