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On the selectivity of cobalt-based Fischer-Tropsch catalysts: Evidence for a common precursor for methane and long-chain hydrocarbons

机译:关于钴基费-托催化剂的选择性:甲烷和长链烃的常见前体的证据

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A total of 36 cobalt-based supported catalysts were investigated in the Fischer-Tropsch reaction at industrially relevant process conditions: 483 K, 20 bar, molar H_2/CO ratio = 2.1, pellet size: 53-90 μm. The effect of adding water vapour to the feed was investigated for 20 of the catalysts, and a H_2/CO ratio of 1.0 was used for a few catalysts. The catalysts differed in support material, Co loading, promoters, Cl content, Co particle size (larger than ~6 nm), morphology, degree of reduction and preparation technique and showed a large variation in selectivity. For each set of process conditions, a linear relationship seems to exist between the selectivity to methane (and other light products) and C_(5+) indicating a common precursor, i.e. a common monomer pool, for all hydrocarbon products. A high selectivity to C_(5+) is mainly an effect of a high intrinsic chain-growth probability and unlikely to be a result of an enhanced α-olefin readsorption. The universal effect of external water addition on the hydrocarbon selectivities is limited to a decrease in the methane selectivity. A small proportion of the catalysts developed "pure methanation" sites upon exposure to high partial pressures of water.
机译:在工业相关工艺条件下,在费-托反应中研究了总共36种钴基负载型催化剂:483 K,20 bar,H_2 / CO摩尔比= 2.1,颗粒尺寸:53-90μm。对于20种催化剂,研究了向进料中添加水蒸气的效果,并且对于几种催化剂,H 2 / CO比为1.0。催化剂在载体材料,Co含量,助催化剂,Cl含量,Co粒径(大于〜6 nm),形貌,还原度和制备工艺等方面有所不同,且选择性差异较大。对于每一组工艺条件,对于甲烷(和其他轻质产物)的选择性和C_(5+)之间似乎存在线性关系,表明所有烃产物的共同前体,即共同单体池。对C_(5+)的高选择性主要是高固有链增长概率的结果,并且不太可能是增强的α-烯烃再吸收的结果。外加水对烃选择性的普遍影响仅限于甲烷选择性的降低。一小部分催化剂在暴露于高水分压时会形成“纯甲烷化”位点。

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