Continuous upgrading of methanol and ethanol to isobutanol by heterogeneous catalysis over Cu-CeO2/AC catalyst and the combination

被引:0
|
作者
Li, Xing [1 ]
Li, Xiaonian [1 ]
机构
[1] Zhejiang Univ Technol, Ind Catalysis Inst, State Key Lab Breeding Base Green Chem Synth Techn, Hangzhou 310032, Peoples R China
来源
MOLECULAR CATALYSIS | 2024年 / 569卷
基金
中国国家自然科学基金;
关键词
Cu-CeO 2 /AC catalyst; Methanol; Ethanol; Isobutanol; Catalytic upgrading; SELECTIVE SYNTHESIS; HYDROGEN-PRODUCTION; NI; CU; PD; BUTANOL; CO; BIOBUTANOL; REDUCTION; OXIDATION;
D O I
10.1016/j.mcat.2024.114641
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
Isobutanol has the highest octane value among several types of butanols and is the most ideal fuel substitute. Developing an efficient continuous production system for synthesis of isobutanol from methanol and ethanol is the key to industrialization. The existing heterogeneous catalysts were all applied to batch reactor systems. The first heterogeneous catalyst, activated carbon supported Cu-CeO2 (Cu-CeO2/AC), with excellent performance for the continuous synthesis system of isobutanol from methanol and ethanol was revealed in this paper. Through XRD, TEM, H2-TPR, CO2-TPD, and FT-IR, it was demonstrated that CeO2 not only enhanced the stability of Cu nanoparticles, but also provided a large number of hydroxyl aldehyde condensation active sites. Cu provided dehydrogenation active sites. The synergy of Cu active sites and CeO2 active sites completed the Guerbet reaction cycle. 3Cu-CeO2/AC exhibited a high ethanol conversion rate (81.6 %) and isobutanol selectivity (54.0 %). Finally, based on the analysis of reaction thermodynamics and dynamics, a catalyst combination mode of dehydrogenation + aldol condensation + hydrogenation was proposed, which improved the conversion of ethanol (81 % to 85%) and selectivity of isobutanol (54% to 65%).
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页数:12
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