Catalytic Conversion of Fructose, Glucose, and Sucrose to 5-(Hydroxymethyl)furfural and Levulinic and Formic Acids in γ-Valerolactone As a Green Solvent

被引:281
作者
Qi, Long [1 ]
Mui, Yiu Fung [1 ]
Lo, See Wing [1 ]
Lui, Matthew Y. [1 ]
Akien, Geoffrey R. [1 ]
Horvath, Istvan T. [1 ]
机构
[1] City Univ Hong Kong, Dept Biol & Chem, Kowloon, Hong Kong, Peoples R China
关键词
carbohydrates; 5-(hydroxymethyl)furfural; levulinic acid; formic acid; gamma-valerolactone; sulfuric acid; isotopic labeling; BIOMASS; CELLULOSE; DEHYDRATION; EFFICIENT; LIQUID; HYDROGENATION; DECOMPOSITION; 1,4-PENTANEDIOL; TRANSFORMATION; LEVOGLUCOSAN;
D O I
10.1021/cs401160y
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
The conversion of fructose, glucose, and sucrose to 5-(hydroxymethyl)furfural (HMF) and levulinic acid (LA)/formic acid (FA) was investigated in detail using sulfuric acid as the catalyst and gamma-valerolactone (GVL) as a green solvent. The H2SO4/GVL/H2O system can be tuned to produce either HMF or LA/FA by changing the acid concentration and thus allowing selective switching between the products. Although the best yields of HMF were around 75%, the LA/FA yields ranged from 50% to 70%, depending on the structure of the carbohydrates and the reaction parameters, including temperature, acid, and carbohydrate concentrations. While the conversion of fructose is much faster than glucose, sucrose behaves like a 1:1 mixture of fructose and glucose, indicating facile hydrolysis of the glycosidic bond in sucrose. The mechanism of the conversion of glucose to HMF or LA/FA in GVL involves three intermediates: 1,6-anhydro-beta-D-glucofuranose, 1,6-anhydro-beta-D-glucopyranose, and levoglucosenone.
引用
收藏
页码:1470 / 1477
页数:8
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