Dehydration of sugars to 5-hydroxymethylfurfural and non-stoichiometric formic and levulinic acids over mesoporous Ta and Ta-W oxide solid acid catalysts

被引:25
作者
Guo, Bin [1 ]
He, Lulu [1 ]
Tang, Gangfeng [1 ]
Zhang, Li [1 ]
Ye, Lin [1 ]
Yue, Bin [1 ]
Tsang, Shik Chi Edman [2 ]
He, Heyong [1 ]
机构
[1] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai 200433, Peoples R China
[2] Univ Oxford, Dept Chem, Wolfson Catalysis Ctr, Oxford OX1 3QR, England
基金
中国国家自然科学基金;
关键词
Glucose; Fructose; HMF Solid acid; Tantalum oxide; Ta-W oxide; STATE P-31 NMR; FRUCTOSE DEHYDRATION; GLUCOSE DEHYDRATION; TUNGSTATED ZIRCONIA; BIPHASIC SYSTEM; CONVERSION; LEWIS; SITES; PHOSPHATE; WATER;
D O I
10.1016/S1872-2067(19)63519-9
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of mesoporous Ta and Ta-W oxides have been prepared and employed as solid acid catalysts for the dehydration of fructose and glucose to 5-hydroxymethylfurfural (HMF). Solid state P-31 MAS NMR spectroscopic results using trimethylphosphine (TMP) as a probe molecule show that the acid strength and the ratio of Bronsted to Lewis acid sites increase gradually with the addition of tungsten in tantalum oxide. It is found that high sugar conversion and HMF selectivity are achieved over catalyst with relatively high ratios of Bronsted to Lewis acid sites. Unexpected stoichiometric excess of formic acid relative to levulinic acid can be observed mainly because of direct decomposition of fructose over Lewis acid sites. The addition of 2-butanol leads to the increase of sugars conversion and the HMF selectivity, especially for the catalyst with high ratio of Bronsted to Lewis acid sites. Among them, Ta7W3 oxide catalyst shows 54% HMF selectivity and good reusability with the addition of 2-butanol by extracting HMF from aqueous phase and removing humins deposed on the surface of the catalyst. (C) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1248 / 1260
页数:13
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