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Effect of carbon support on Fischer-Tropsch synthesis activity and product distribution over Co-based catalysts

机译:碳载体对费-托合成活性和钴基催化剂上产物分布的影响

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The ordered mesoporous carbon (CMK-3) was prepared using SBA-15 as template and sucrose as carbon source. Co catalysts supported on CNTs, CMK-3 and AC were prepared by incipient wetness. Their physical properties, morphologies and Fischer-Tropsch synthesis (FTS) activities were assessed. It was found that Co3O4 particles mainly dispersed inside the tubes (or pores) of Co/CNTs and Co/CMK-3 but outside the pores of Co/AC Co3O4 particle size depended closely on the support structure. After H2 reduction, the three catalysts had a similar cobalt particle size. The cobalt particle size of Co/CNTs was maintained well due to the special confinement effect of CNTs. CNTs were more stable at high temperature in H2 atmosphere than CMK-3 and AC and the reduction degree of Co/CNTs was higher than the other two catalysts. The good crystallized graphitic structure facilitated the electron transfer between the cobalt and CO molecules on Co/CNTs. So Co/CNTs had a better FTS performance than Co/CMK-3 and Co/AC catalysts. Carbon support structure influenced the C_(5+) selectivity, C_(5+) hydrocarbon distribution and CO turnover frequency. Furthermore, a positive relationship existed between C2-C4 olefin/paraffin ratio and C_(5+) selectivity. High olefin content and low space velocity benefit the heavy hydrocarbon production.
机译:以SBA-15为模板,以蔗糖为碳源,制备有序介孔碳(CMK-3)。通过初期润湿制备了负载在CNT,CMK-3和AC上的Co催化剂。评估了它们的物理性质,形态和费-托合成(FTS)活性。发现Co 3 O 4颗粒主要分散在Co / CNT和Co / CMK-3的管(或孔)内部,但在Co / AC Co 3 O 4颗粒的孔外部紧密地依赖于载体结构。还原氢气后,三种催化剂的钴粒度相似。由于碳纳米管的特殊限制作用,钴/碳纳米管的钴颗粒尺寸保持良好。 CNT在H2气氛下高温下比CMK-3和AC更稳定,并且Co / CNTs的还原度高于其他两种催化剂。良好的结晶石墨结构促进了Co / CNT上钴和CO分子之间的电子转移。因此,Co / CNTs比Co / CMK-3和Co / AC催化剂具有更好的FTS性能。碳载体结构影响了C_(5+)的选择性,C_(5+)的碳氢化合物分布和CO转换频率。此外,C 2 -C 4烯烃/链烷烃比与C_(5+)选择性之间存在正相关。高烯烃含量和低空速有利于重烃的生产。

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