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Valorizing tail gas for superior hydrocarbon output in CO2-based Fischer-Tropsch synthesis
被引:0
|作者:
Chen, Jingyu
[1
,2
]
Zhang, Leiyu
[3
]
Park, Hae-Gu
[2
]
Min, Ji-Eun
[2
]
Min, Hyung-Ki
[2
]
Kim, Jeong-Rang
[2
]
Zhang, Chundong
[3
]
Jun, Ki-Won
[2
]
Kim, Seok Ki
[4
,5
]
机构:
[1] Korea Univ Sci & Technol UST, Adv Mat & Chem Engn, Yuseong, Daejeon 34113, South Korea
[2] Carbon Resources Inst, Korea Res Inst Chem Technol KRICT, Hydrogen & C1 Gas Res Ctr, Daejeon 34114, South Korea
[3] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
[4] Ajou Univ, Dept Energy Syst Res, Suwon 16499, South Korea
[5] Ajou Univ, Dept Chem Engn, Suwon 16499, South Korea
基金:
新加坡国家研究基金会;
关键词:
CO;
2;
hydrogenation;
Tandem reactor;
Fischer-Tropsch synthesis;
Aromatics;
Liquid fuel;
CO2;
HYDROGENATION;
HETEROGENEOUS CATALYSTS;
OLEFIN OLIGOMERIZATION;
LIGHT-HYDROCARBONS;
BTEX AROMATICS;
HZSM-5;
CONVERSION;
FUELS;
TRANSFORMATION;
DEACTIVATION;
D O I:
10.1016/j.cej.2024.158531
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
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 degrees C and 1 bar produces aromatic-rich liquid hydrocarbons with 31.7 % selectivity, while at 250 degrees 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 degrees 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.
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页数:12
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