Facile selective hydrogenation of bio-based furfural to furfuryl alcohol via a ZIF-67-derived Co-based catalyst

被引:0
|
作者
Yang, Zheng [1 ,2 ,3 ]
Cong, Xing-Shun [3 ]
Teng, Dao-Guang [4 ]
Wei, Xian-Yong [2 ]
Li, Zhi-Xin [2 ]
Xie, Heng-Shen [1 ]
机构
[1] Jiangsu Vocat Inst Architectural Technol, Sch Architectural Intelligence, Xuzhou 221116, Jiangsu, Peoples R China
[2] China Univ Min & Technol, Minist Educ, Key Lab Coal Proc & Efficient Utilizat, Xuzhou 221116, Jiangsu, Peoples R China
[3] Zaozhuang Univ, Coll Chem Engn, Zaozhuang 277160, Peoples R China
[4] Zhengzhou Univ, Sch Chem Engn, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Furfural; Furfuryl alcohol; Co@C-N; Catalytic hydrogenation;
D O I
暂无
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A stable, low-cost, and reusable Co nanoparticles catalyst imbedded in nitrogen-doped carbon matrix (Co@C-N) for selective catalytic hydrogenation (CHG) of furfural (FF) to furfuryl alcohol (FA) has been exploited. The catalyst is directly derived from 2-methylimidazole modified ZIF-67 MOFs (MOFs = metal-organic frameworks) by thermolysis. The Co@C-N catalytic system features 100% FF conversion and 85.6% FA selectivity under 2 MPa initial hydrogen pressure at 145 degrees C in ethanol solvent after 2 h. Co@C-N is also appropriate for scale-up catalytic hydrogenation of FF and is versatile for aromatic aldehydes as well as other aldehyde compounds, giving their corresponding alcohols in good to excellent selectivities. After the reaction, the Co@C-N could be facile recovery with an external magnetic field and reused for 6 reaction cycles without obvious deactivation of its catalytic properties. This protocal may form the basis for developing a new class of carbon matrix nanocatalyst with potential applications in sustainable catalysis fields.
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页数:10
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