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.
引用
收藏
页码:460 / 471
页数:12
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