Co0-Coδ+ active pairs tailored by Ga-Al-O spinel for CO2-to-ethanol synthesis

被引:35
作者
An, Kang [1 ]
Zhang, Siran [1 ]
Wang, Hong [2 ]
Li, Ningyan [1 ]
Zhang, Ziyang [1 ]
Liu, Yuan [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn, Dept Catalysis Sci & Technol, Tianjin 300350, Peoples R China
[2] Inner Mongolia Univ Technol, Chem Engn Coll, Hohhot 010051, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; hydrogenation; Ethanol Synthesis; Co Nanoparticles; Gallium; Interaction; CO2; HYDROGENATION; ETHANOL SYNTHESIS; HIGHER ALCOHOLS; SELECTIVE HYDROGENATION; CARBON-DIOXIDE; CATALYSTS; COBALT; MORPHOLOGY; METHANOL; SUPPORT;
D O I
10.1016/j.cej.2022.134606
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Direct hydrogenation of CO2 into ethanol has been considered as an up-and-coming way to achieve CO2 utili-zation. Ethanol can be generated by reverse water gas shift as well as CO hydrogenation over Co-based catalysts, where the regulation of Co-0 -Co delta+ is critical. Herein, we designed a supported Co-based catalyst doped with gallium, which was derived from Co-Al-O spinel precursor to facilitate synergistic catalyzing for CO2-to-ethanol transformation. The selectivity of ethanol reached 20.1 % in a continuous flow fixed micro-reactor over reduced CoGa1.Al-0(1).O-0(4)/SiO2 catalyst at 270 degrees C and 3.0 MPa. Results of characterization show that the existence of the strong interaction between Ga oxide and cobalt induced the configuration of Co-0 -Co delta+ active pairs, which promotes the process of ethanol synthesis by coupling the dissociation (CHx*)/non-dissociation (CO*) of the intermediates. The strategy by tuning the interaction between cobalt and gallium and/or aluminum oxide brings an avenue to tailor Co-0 -Co delta+ active pairs for the hydrogenation of CO and CO2.
引用
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页数:11
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