One-pot synthesis of 1,4-butanediol via the deep hydrogenation of maleic anhydride over Cu-xMo/SiO2 catalysts

被引:0
|
作者
Cui, Kai [1 ]
Yang, Jiaming [1 ]
Jing, Yuli [1 ]
Chen, Junwen [2 ]
Zhao, Chen [1 ]
Wu, Peng [1 ]
Li, Xiaohong [1 ]
机构
[1] East China Normal Univ, ECNU Engn Ctr Sustainable Carbon, State Key Lab Petr Mol & Proc Engn, Shanghai Key Lab Green Chem & Chem Proc,Sch Chem &, Shanghai 200062, Peoples R China
[2] Sinopec Res Inst Petr Proc Co LTD, State Key Lab Petr Mol & Proc Engn, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
LIQUID-PHASE HYDROGENATION; DIMETHYL OXALATE; SELECTIVE HYDROGENATION; ETHYLENE-GLYCOL; CHEMOSELECTIVE HYDROGENATION; GAMMA-BUTYROLACTONE; CU/SIO2; CATALYSTS; COPPER-CATALYSTS; OXIDATION; OXIDE;
D O I
10.1039/d4cy01006j
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
Sustainability issues have led to a gradual market expansion for the 1,4-butanediol (BDO) monomer of the biodegradable plastics to replace conventional plastics. Maleic anhydride (MA) can be derived from the oxidation of bio-based furfural or fructose. Although the hydrogenation of MA can produce a series of products, including succinic anhydride (SA), gamma-butyrolactone (GBL), BDO and tetrahydrofuran (THF), the one-pot deep hydrogenation of MA to BDO or THF under mild conditions has been rarely reported in the literature until now. Herein, we report the production of BDO from the one-pot deep hydrogenation of MA over a Cu-0.03Mo/SiO2 catalyst, achieving 100% MA conversion and 88.3% BDO yield. The Cu-0.03Mo/SiO2 catalyst also showed good long-term stability without obvious loss in activity or BDO selectivity during a 160 h time-on-stream test. Doping Mo to Cu/SiO2 catalysts in an optimal amount adjusted the distribution of Cu0/Cu+ species and modulated the interaction of Cu-SiO2 and surface acidity, so that the activation of hydrogen, MA and relevant intermediates can become balanced, in addition to the restriction of side-reactions. This study provides potential for the green synthesis of BDO with non-precious Cu-based catalysts.
引用
收藏
页码:7081 / 7092
页数:12
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