4.8 Article

Key roles of formyl insertion mechanism and C-O scission of oxygenates on cobalt carbide in syngas Conversion: A detailed reaction network analysis

期刊

JOURNAL OF CATALYSIS
卷 413, 期 -, 页码 455-466

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2022.07.005

关键词

Syngas conversion; Cobalt carbide; Fischer-Tropsch synthesis; Mechanism; Density functional theory

资金

  1. National Natural Science Foundation of China [21978211]
  2. Natural Science Foundation of Tianjin [21JCZDJC00520]
  3. Natural Science Foundation of Ningbo [2021 J008]
  4. Tianjin University [2021XT-0008]

向作者/读者索取更多资源

This study investigates the catalytic behavior of cobalt carbide nanoprisms in the Fischer-Tropsch to olefins (FTO) process. The results show that C-O scission and CHO insertion play important roles in ethylene formation and carbon chain growth, while the selectivity towards oxygenates is suppressed.
Direct conversion of syngas to olefins and oxygenates provides nonpetroleum routes for producing value-added chemicals. Cobalt carbides (Co2C) exhibit great potential in both Fischer-Tropsch to olefins (FTO) process and higher alcohols synthesis (HAS). Among which, the morphology-specific Co2C nanoprisms have shown remarkable performance in producing lower olefins, with limited selectivity towards oxygenates. However, the underlying mechanisms for product formation on Co2C nanoprisms remain elusive, especially why olefins are abundant but oxygenates are rare is unclear. In this work, through detailed reaction network analysis and microkinetic modeling, based on first principles simulations, we demonstrate the important roles of C-O scission and CHO insertion in Co2C nanoprisms catalyzed FTO process, revealing its unique catalysis behavior. A previously neglected CHO insertion mechanism followed by hydrogenation and C-O scission opens a new pathway for ethylene formation and carbon chain growth. And oxygenate intermediates are proved unstable on Co2C(020) facet, leading to suppressed oxygenate selectivity. (C) 2022 Elsevier Inc. All rights reserved.

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