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ZnO-ZrO2 coupling nitrogen-doped carbon nanotube bifunctional catalyst for co-production of diesel fuel and low carbon alcohol from syngas
被引:0
|作者:
Zao, Huijie
[1
]
Liu, Jing
[1
]
Yan, Beibei
[2
]
Yao, Jingang
[1
]
Liu, Saisai
[1
]
Chen, Guanyi
[2
]
机构:
[1] Shandong Univ Technol, Sch Agr Engn & Food Sci, Zibo 255000, Peoples R China
[2] Tianjin Univ, Sch Environm Sci & Engn, Tianjin 300072, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Syngas to liquid fuel;
ZnZrO2/NCNT;
Bifunctional catalyst;
Fischer-Tropsch synthesis;
Selectivity control;
OXYGEN REDUCTION REACTION;
FISCHER-TROPSCH SYNTHESIS;
SELECTIVE CONVERSION;
METHANOL SYNTHESIS;
CATHODE CATALYST;
PARTICLE-SIZE;
LOWER OLEFINS;
SYNTHESIS GAS;
LIQUID FUELS;
PERFORMANCE;
D O I:
10.1016/j.ijhydene.2024.03.193
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Catalytic syngas conversion to liquid fuel is pivotal for biomass utilization, enhancing energy security, reducing carbon emissions and curbing reliance on petroleum imports. Herein, bifunctional catalysts comprising zinc-zirconium dioxide (ZnZrO2) dispersed on nitrogen-doped multi-walled carbon nanotubes (NCNT) (ZnZrO2/NCNT) were successfully designed, enabling the simultaneous production of both diesel fuels (C-9-C-16 hydrocarbon) and methanol through direct syngas conversion. Operating at 450 degrees C, 4.5 MPa, a gas hourly space velocity (GHSV) of 4800 mL h(-1)center dot g(cat)(-1), the ZnZrO2/NCNT catalyst, featuring 2.6% nitrogen doping, exhibited exceptional performance, achieving a 50.3% selectivity for C-9-C-16 hydrocarbons and a 26.4% selectivity for methanol, while maintaining a 52.5% single-pass CO conversion rate. The C9+ selectivity significantly surpasses the bottleneck predicted by the ASF distribution theory (C9+ selectivity <36%). This starkly contrasts that of ZnO/NCNT (1.7% C-9-C-16 and 6.3% methanol) and ZrO2/NCNT (32.5% C-9-C-16 and 25.4% methanol) catalysts. Moreover, the ZnZrO2/NCNT catalyst still retained C9+ 51.5% selectivity and 25% methanol selectivity after 100 h of continuous operation. The synergistic effects resulting from the amalgamation of highly active nanostructured units with a well-encapsulation structure efficiently hinder active component migration during catalysis. This significantly enhances both the catalyst's activity and stability. Furthermore, nitrogen introduction serves as a key electron donor to ZnZrO2, thereby catalyzing the activation of CO dissociation. This activation step emerges as a pivotal factor crucial for enhancing selectivity in liquid fuel production.
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页码:460 / 471
页数:12
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