异构化
路易斯酸
化学
催化作用
介孔材料
沸石
产量(工程)
水解
果糖
有机化学
金属
可重用性
组合化学
路易斯酸催化
介孔二氧化硅
D-葡萄糖
介孔有机硅
协同催化
乙醇
分解
作者
Guanjie Yu,Yang Liu,Chaojie Zhang,Shuwen Zhou,Yao Tang,Hengli Qian,Chao Xie,Ting Xia,Xinyu Bai,Jingrong Wang,Ziteng Hao,Fei Qu,Anna Rui,Meiting Ju,Qidong Hou
标识
DOI:10.1002/anie.202524977
摘要
Lewis acid catalyzed glucose isomerization is a vital step in biorefinery, but it's restricted by the limited catalytic toolkit and reaction equilibrium. Herein, we report that engineering Lewis acid sites in a mesoporous zeolite can greatly boost productivity. Incorporating a few of Sn species into KIT-6 zeolite with the assistance of phosphorylation delivered SnPO/KIT(x) materials with abundant Lewis acid sites and a few of Brønsted acid sites, while conserving the ordered mesoporous structure. Moreover, the Lewis acidic Sn sites have a coordination environment distinct from those in traditional zeolites and metal phosphates, as is crucial to facilitate isomerization and to control side-reactions. Rigorous experiments showed that the use of SnPO/KIT(80) catalyst in two-step isomerization process combined with adequate hydrolysis of ethyl fructoside attains a fructose yield of 71.5%, surpassing the state-of-the-art catalytic systems, along with good reusability and tolerance to high-concentration glucose. These findings highlight the great potential of precisely manipulating coordination environment of Lewis acid sites to boost catalytic performance.
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