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One-pot conversion of glucose to 5-hydroxymethylfurfural under aqueous conditions using acid/base bifunctional mesoporous silica catalyst
被引:15
|作者:
Modak, Arindam
[1
,2
]
Mankar, Akshay R.
[1
]
Sonde, R. R.
[1
]
Pant, Kamal K.
[1
]
机构:
[1] Indian Inst Technol Delhi, Dept Chem Engn, New Delhi 110016, India
[2] Amity Univ, Amity Inst Appl Sci AIAS, Amity Rd,Sect 125, Noida 201301, Uttar Pradesh, India
来源:
关键词:
Acid;
base bifunctional catalyst;
Microwave synthesis;
Glucose conversion;
5-Hydroxymethylfurfural;
Kinetic modeling;
HOT COMPRESSED WATER;
EFFICIENT CONVERSION;
PHOSPHATE CATALYSTS;
REACTION-MECHANISM;
LEVULINIC ACID;
BASE CATALYSTS;
CELLULOSE;
FRUCTOSE;
BIOMASS;
ISOMERIZATION;
D O I:
10.1016/j.renene.2023.05.058
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
One-pot conversion of carbohydrate-derived biomass compounds to 5-hydroxymethylfurfural (HMF) using an environmentally green solvent such as water is meritorious, yet challenging, which requires the strategic design of catalysts. We prepare an ordered bifunctional organocatalyst (MS-AB) containing 3-aminopropylacetic acid grafted within the silica nanocage that converts glucose-to-HMF, exhibiting the highest HMF yield (60 wt. %/85.7 mol%) in water and under microwave conditions. Moreover, the calculated activation energies (150-170 degrees C) for glucose isomerization to fructose, vis -`a-vis dehydration to HMF were 59.06 and 138.05 kJ mol-1, respectively which can even be comparable with the metal-catalyzed reactions. Further evidence was shown from the rate constant values, indicating fructose dehydration is faster (rate constant: k2: 1.92 x 10-2 to 1.13 x 10-1 min-1) than glucose isomerization (rate constant: k1: 2.5 to 5.3 x 10-3 min-1). Considering the advantages associated with MS-AB, the results might showcase the potential of organocatalyst for sustainable utilization of lignocellulosic biomass to platform chemicals.
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页码:97 / 110
页数:14
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