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Conversion of carbohydrates and lignocellulosic biomass into 5-hydroxymethylfurfural using AlCl3·6H2O catalyst in a biphasic solvent system

机译:在两相溶剂体系中使用AlCl3·6H2O催化剂将碳水化合物和木质纤维素生物质转化为5-羟甲基糠醛

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摘要

A1C13·6H2O in a biphasic medium of water/tetrahydrofuran (THF) is effective for the synthesis of 5-hydroxymethylfurfural (HMF) from glucose-based carbohydrates. For glucose, an HMF yield of 61% was achieved in 10 min at 160 °C under microwave heating. The reaction time profile revealed the intermediacy of fructose en route to HMF with a dehydration rate constant that is approximately 4 times that of glucose isomerization to fructose. Addition of NaCl did not increase HMF yields significantly but it diminished lactic acid formation. Disaccharides (maltose and cellobiose) and starch gave good yields of HMF. However, cellulose required a higher temperature (180 °C) and longer reaction time (30 min) to give a modest yield of 37%. Several lignocellulosic biomass variants (corn stover, pine wood, grass, and poplar) were investigated with the A1C13·6H2O biphasic system. The yields of HMF were modest (20-35%) but high concurrent yields of furfural were observed (51-66%). The described AlCl3·6H2O-NaCl-H2O/THF biphasic medium has potential because it is economic, nontoxic, and it exhibits fast kinetics (10 min) under microwave heating.
机译:水/四氢呋喃(THF)的双相介质中的AlCl3·6H2O可有效地从葡萄糖基碳水化合物合成5-羟甲基糠醛(HMF)。对于葡萄糖,在微波加热下,在160°C下,在10分钟内HMF的收率达到61%。反应时间曲线揭示了果糖在进入HMF途中的中间速率,脱水速率常数约为葡萄糖异构化为果糖的脱水速率常数的4倍。 NaCl的添加不会显着增加HMF的产量,但会减少乳酸的形成。二糖(麦芽糖和纤维二糖)和淀粉可产生高产率的HMF。但是,纤维素需要更高的温度(180°C)和更长的反应时间(30分钟)才能获得37%的适度收率。使用A1C13·6H2O双相系统研究了几种木质纤维素生物质变体(玉米秸秆,松木,草和杨树)。 HMF的产量适中(20-35%),但观察到的糠醛并发产量很高(51-66%)。所描述的AlCl3·6H2O-NaCl-H2O / THF双相介质具有潜力,因为它经济,无毒,并且在微波加热下具有快速动力学(10分钟)。

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