Optimized spacing of active sites in Ni-Mo catalysts enhances ethanol production in syngas conversion

被引:1
|
作者
Ren, Yangbin [1 ,2 ]
Weng, Yujing [1 ,2 ]
Meng, Shihang [1 ,2 ]
Huang, Chao [1 ,2 ]
Sun, Qi [1 ,2 ]
Zhang, Yulong [1 ,2 ]
Fan, Maohong [3 ,4 ]
机构
[1] Henan Polytech Univ, Coll Chem & Chem Engn, Henan Key Lab Coal Green Convers, Jiaozuo 454000, Henan, Peoples R China
[2] Henan Polytech Univ, Coll Chem & Chem Engn, Int Joint Lab Coal Clean Utilizat, Jiaozuo 454000, Henan, Peoples R China
[3] Univ Wyoming, Coll Engn & Phys Sci, Laramie, WY 82071 USA
[4] Univ Wyoming, Sch Energy Resources, Laramie, WY 82071 USA
基金
中国国家自然科学基金;
关键词
Syngas; Ethanol; Molybdenum carbide (Mo2C); Carbon dots (CDs); C2+OH; Nickel (Ni); Active site distance; HIGHER ALCOHOLS; EFFICIENT CATALYSTS; CO HYDROGENATION; XPS; NANOPARTICLES; REACTIVITY; SUPPORT; PHASE; CH4;
D O I
10.1016/j.apcatb.2024.124750
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
The direct conversion of syngas to ethanol is highly attractive but remains challenging due to low CO conversion and poor EtOH/ROH. We investigated the conversion of syngas over a KNiMo2C catalyst modified with carbon dots (CDs) derived from Ligustrum lucidum leaves. On the Ni0.54Mo-A catalyst, a CO conversion of 43.4 % was achieved, with oxygenates selectivity and EtOH/ROH, reaching 48.2 % and 63.7 %, the space-time yield of ethanol was 132.5 mg/g(cat)/h. Comprehensive characterization revealed that CDs regulate the distance between Ni-Mo active sites, preventing excessive proximity and maintaining an optimal separation. This adjustment significantly enhances EtOH/ROH by modulating the probability of carbon chain growth. A potential new reaction pathway for directly converting syngas to ethanol is proposed, The C-C coupling of CHx* with *COOH or *CO2 is identified as a key step in carbon chain growth. This work provides a new catalytic pathway for the syngas to ethanol industry.
引用
收藏
页数:11
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