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Valorizing tail gas for superior hydrocarbon output in CO2-based Fischer-Tropsch synthesis
  • Chen, Jingyu ;
  • Zhang, Leiyu ;
  • Park, Hae Gu ;
  • Min, Ji Eun ;
  • Min, Hyung Ki ;
  • Kim, Jeong Rang ;
  • Zhang, Chundong ;
  • Jun, Ki Won ;
  • Kim, Seok Ki
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Publication Year
2025-01-01
Publisher
Elsevier B.V.
Citation
Chemical Engineering Journal, Vol.503
Keyword
AromaticsCO2 hydrogenationFischer-Tropsch synthesisLiquid fuelTandem reactor
Mesh Keyword
AromaticCO2 hydrogenationEfficient processFischer TropschHigh selectivityProduct flexibilityTail gasTandem reactorTropsch synthesisTwo-stage reactions
All Science Classification Codes (ASJC)
Chemistry (all)Environmental ChemistryChemical Engineering (all)Industrial and Manufacturing Engineering
Abstract
CO2 conversion to liquid fuels requires efficient processes that offer both high selectivity and product flexibility. Here, we demonstrate a two-stage reaction system that combines CO2 hydrogenation over KFeZn catalyst with hydrocarbon oligomerization using HZSM-5 zeolite. The system's product distribution can be precisely controlled through reaction conditions in the secondary reactor. Operating at 300 °C and 1 bar produces aromatic-rich liquid hydrocarbons with 31.7 % selectivity, while at 250 °C, the process yields gasoline-range products at 10 bar or jet fuel-range hydrocarbons at 20 bar. The system maintains stability for 120 h with approximately 72 % C5+ selectivity under optimal conditions (250 °C, 20 bar). The zeolite catalyst shows effective regeneration capability, and the produced hydrocarbons feature extensive branching, suggesting improved octane ratings. Model gas experiments demonstrate that temperature significantly influences hydrocarbon reactivity, with the tandem setup particularly promoting hetero-oligomerization of 1-butene. Process analysis reveals enhanced energy efficiency and economic viability compared to single-reactor systems, while maintaining the advantage of tunable product composition.
ISSN
1385-8947
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/34653
DOI
https://doi.org/10.1016/j.cej.2024.158531
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Type
Article
Funding
This study was supported by the Korea Institute of Energy Technology Evaluation and Planning (No. 20224C10300010) and the Technology Innovation Program (No. RS-2024-00432109) of the Ministry of Trade, Industry & Energy (MOTIE) of Korea. Additional support was provided by the \\u201CCarbon Upcycling Project for Platform Chemicals\\u201D (No. 2022M3J3A1045999, 2022M3J3A1039377) through the National Research Foundation (NRF) funded by the Ministry of Science and ICT, and the Project (KK2412-10) of the Korea Research Institute of Chemical Technology. S.K.K. also acknowledges support from the Global Learning & Academic Research Institution for Master's\\u00B7PhD Students, and Postdocs (G-LAMP) Program of the NRF grant funded by the Ministry of Education (No. RS-2023-00285390).
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Department of Chemical Engineering
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