Hydrolysis of Cellulose by Using Catalytic Amounts of FeCl2 in Ionic Liquids

被引:66
|
作者
Tao, Furong [1 ,2 ]
Song, Huanling [1 ]
Chou, Lingjun [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
关键词
biomass; carbohydrates; hydrolysis; ionic liquids; sustainable chemistry; LIGNOCELLULOSIC BIOMASS; CHROMATOGRAPHIC DETERMINATION; CONVERSION; DISSOLUTION; BIOFUELS; ACID; FRUCTOSE; CHLORIDE; LIGNIN; SYSTEM;
D O I
10.1002/cssc.201000184
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Microcrystalline cellulose (MCC) is hydrolyzed to an appreciable extent (70 %) by using 1-(4-sulfonic acid) butyl 3-methylimid azolium hydrogen sulfate (IL-1) as effective catalyst Valuable chemicals such as 5 hydroxymethyl furfural (HMF) and furfural, are obtained in relatively high yields (15% and 7%, respectively) Interestingly the introduction of FeCl2 as catalyst into IL-1 further enhances the catalytic activity as proved by the higher, conversion of MCC (84%) and higher yields of HMF and furfural (34% and 19%, respectively) under the same experimental; conditions although small amounts of levulinic acid (LA) and total reducing sugars (TRS) were also found The hydrolysis of MCC scarcely proceeded, or showed a lower efficiency in the absence of catalyst (4%) or with Al2O3 (7%), inorganic acids (<= 65%) or several other ionic liquids (<= 24%) as catalyst Dimers of furan compounds were detected as the main by-products as analyzed by HPLC MS from the mass spectrometry analysis, the components of the gas-phase products were determined to be methane ethane, CO CO2, and H-2 A mechanism to explain the high activity of FeCl2 in the IL-1 system is proposed Recycling of the IL 1 catalyst showed an almost constant activity during five successive trials The simple and effective catalyst system may prove valuable in facilitating the energy-efficient and cost-effective conversion of biomass into biofuels and platform chemicals
引用
收藏
页码:1298 / 1303
页数:6
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