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首页> 外文期刊>Journal of Catalysis >alpha-alumina as catalyst support in Co Fischer-Tropsch synthesis and the effect of added water; encompassing transient effects
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alpha-alumina as catalyst support in Co Fischer-Tropsch synthesis and the effect of added water; encompassing transient effects

机译:α-氧化铝作为CoFischer-Tropsch合成中的催化剂载体和添加的水的作用; 包含瞬态效果

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Three catalyst supports containing from 84 to 100% alpha-alumina prepared by heat treatment of gamma-alumina have been impregnated with cobalt and rhenium. The catalysts were tested for Fischer-Tropsch synthesis (FTS) under dry and enhanced water vapor pressure conditions. Both activity and selectivity to higher hydrocarbons respond positive to water added or generated in situ by the reaction. A linear trend between formation of methane and C5+. products was found, but displaced to higher C5+, values compared to catalysts on gamma-alumina. Calculation of chain propagation probabilities (alpha(n)) for alpha-alumina supported catalysts discloses that the first step, characterized by alpha(1), increases the most under higher water partial pressure. Moreover, alpha(1) is significantly higher for alpha- compared to all gamma-alumina supports irrespective of pore sizes of the latter. These results are ascribed to suppression of hydrogen coverage on the cobalt surface, linked to more regular cobalt crystallites, accompanied by enhanced water assisted generation of CHx polymerization monomers. Surprisingly, the following alpha(2) probability is comparably low for alpha-alumina supports, although it increases significantly with water concentration. Linear correlations are found between each pair of parameters alpha(1), alpha(2), alpha(4)' and SC5+; giving support to a mechanistic model where all products are interlinked, including methane. Transients observed when water was added or removed from the system are ascribed to pore diffusion. Selectivities in these periods follow closely the general selectivity trends found for different process conditions. (C) 2019 Elsevier Inc. All rights reserved.
机译:含有84至100%通过通过γ-氧化铝的热处理制备的84-100%α-氧化铝的三种催化剂载体已浸渍钴和铼。在干燥和增强的水蒸气压力条件下测试催化剂的Fischer-Tropsch合成(FTS)。对更高碳氢化合物的活性和选择性既通过反应响应添加或原位生成的水。甲烷和C5 +形成之间的线性趋势。发现产品,但置换到更高的C5 +,与γ-氧化铝催化剂相比的值。用于α-氧化铝负载型催化剂的链繁殖概率(α(n))的计算公开了一种具有α(1),其特征在于α(1)的第一步骤增加了较高的水分压力。此外,与所有γ-氧化铝相比,α(1)显着高于所有γ-氧化铝,而不管后者的孔径如何。这些结果依附于钴表面上的氢覆盖物,与更常规的钴微晶相连,伴随着增强的水辅助产生CHX聚合单体。令人惊讶的是,对于α-氧化铝支持,以下α(2)概率相当低,但它随水浓度显着增加。每对参数α(1),α(2),α(4)'和SC5 +之间存在线性相关性。支持所有产品的机制模型,包括甲烷。当加入或从系统中除去水时,瞬变观察到孔隙扩散。在这些时期的选择性遵循针对不同工艺条件的一般选择性趋势紧密遵循。 (c)2019 Elsevier Inc.保留所有权利。

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