Zhu Can, Zhang Mingwei, Huang Chao, Han Yizhuo, Fang Kegong
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, Shanxi, People's Republic of China.
University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China.
ACS Appl Mater Interfaces. 2020 Dec 30;12(52):57950-57962. doi: 10.1021/acsami.0c19039. Epub 2020 Dec 18.
Light olefins (C-C) are important basic raw materials in chemical industries. Direct production of light olefins from syngas using zeolite encapsulation catalysts shows great potential due to their regulation of product distribution in the Fischer-Tropsch process. Herein, we report a series of silicalite-1 zeolite-encapsulated FeMnK catalysts with distinct nanostructures, including FeMnK@S-1, FeMnK@Hol-S-1, and FeMnK@HM-S-1. It was found that the FeMnK@HM-S-1 catalyst (encapsulation of FeMnK oxide in hollow mesoporous silicalite-1 crystal) had an enhanced C-C selectivity of 49% at a CO conversion of 12%. Our results revealed that superior light olefins selectivity of the FeMnK@HM-S-1 catalyst was achieved by the synergic effect between the inherent silicalite-1 micropores and the hollow mesoporous structure, which is responsible for restricting heavy hydrocarbon (C) formation, maximizing C-C hydrocarbons selectivity, quickly removing the primary light olefin products, and increasing the O/P ratio. We demonstrated that the enhanced CO adsorption and the declined H adsorption (lower [H*]/[C*] ratio) over the FeMnK@HM-S-1 catalyst could also facilitate the olefin synthesis. This work provides guidance for reasonable designing of F-T catalysts to tailor product selectivity.
轻质烯烃(C-C)是化学工业中重要的基础原料。使用沸石封装催化剂由合成气直接生产轻质烯烃,因其在费托合成过程中对产物分布的调控作用而展现出巨大潜力。在此,我们报道了一系列具有独特纳米结构的硅沸石-1封装的FeMnK催化剂,包括FeMnK@S-1、FeMnK@Hol-S-1和FeMnK@HM-S-1。研究发现,FeMnK@HM-S-1催化剂(FeMnK氧化物封装在中空介孔硅沸石-1晶体中)在CO转化率为12%时,C-C选择性提高至49%。我们的研究结果表明,FeMnK@HM-S-1催化剂优异的轻质烯烃选择性是由硅沸石-1固有微孔与中空介孔结构之间的协同效应实现的,该协同效应可限制重质烃(C)的生成、最大化C-C烃选择性、快速移除初级轻质烯烃产物并提高O/P比。我们证明,FeMnK@HM-S-1催化剂上增强的CO吸附和降低的H吸附(较低的[H*]/[C*]比)也有助于烯烃合成。这项工作为合理设计费托催化剂以调整产物选择性提供了指导。