A mechanistic insight into glucose conversion in subcritical water: Complex reaction network and the effects of acid-base catalysis

被引:24
|
作者
Yan, Zhifeng [1 ]
Lian, Jie [1 ]
Feng, Yu [1 ]
Li, Miaoting [1 ,2 ]
Long, Feng [1 ]
Cheng, Ruoqian [1 ]
Shi, Sheng [1 ]
Guo, Hong [1 ]
Lu, Jianjun [1 ,3 ]
机构
[1] Taiyuan Univ Technol, Coll Text Engn, Taiyuan 030024, Shanxi, Peoples R China
[2] Taiyuan Univ Technol, Coll Mat Sci & Engn, Taiyuan 030024, Shanxi, Peoples R China
[3] Taiyuan Univ Technol, Key Lab Coal Sci & Technol, Minist Educ & Shanxi Prov, Taiyuan 030024, Shanxi, Peoples R China
基金
山西省青年科学基金; 中国国家自然科学基金;
关键词
Glucose; Reaction mechanism; Subcritical water; Dispersion-corrected density functional theory; Acid-base bifunctional catalysis; SYNCHRONOUS-TRANSIT; SUPERCRITICAL WATER; REACTION PATHWAYS; FRUCTOSE; ISOMERIZATION; DECOMPOSITION; CELLULOSE; BIOMASS; HYDROLYSIS; KINETICS;
D O I
10.1016/j.fuel.2020.119969
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Based on the concept of system thinking and system design, a systematically mechanistic network of glucose conversion toward fructose, 5-hydroxymethyl furfural, 1,6-anhydroglucose, 1,2,4-Benzenetriol, levulinic acid, furfural, erythrose, glyceraldehyde, dihydroxyacetone, pyruvaldehyde, lactic acid, glycolaldehyde in subcritical water were performed by employing dispersion-corrected density functional theory. Fukui functions results predict the most highest reactivity of O(5) of glucose to suffer protonation in subcritical water, which may readily lead to the formation of 1,6-anhydroglucose or fructose with the comparable apparent activation energies (29.441 vs 29.305 kcal/mol). Further dehydration of monosaccharide to 5-HMF is more favorable via cyclic pathway for fructose in comparison to the acyclic pathway for glucose. The formation of levulinic acid has an apparent activation energy of 33.321 kcal/mol but the rate is limited by the numerous steps. The consumption of 5-HMF to 1,2,4-Benzenetriol exhibits a high activation energy of 76.682 kcal/mol. Retro-aldol condensation of C4 compounds prefer to give C2 rather than C3 compounds. The thermodynamic results involving the generation of C2, C3 and C4 compounds by retro-aldol condensation of open-chain C6 intermediates agree with the experimental product distribution and reactivity over temperature at the initial stage of glucose or fructose subcritical hydrolysis. Furthermore, the assistance of H+ may be responsible for the isomerization and retro-aldol condensation in glucose conversion. This comprehensive reaction network provides a fundamental understanding and deeper insight into glucose conversion, which reasonably explains experimental activity and selectivity reported for glucose and fructose conversion in subcritical water.
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页数:9
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