Production of levoglucosenone and 5-hydroxymethylfurfural from cellulose in polar aprotic solvent-water mixtures

被引:135
作者
He, Jiayue [1 ]
Liu, Mingjie [1 ]
Huang, Kefeng [1 ]
Walker, Theodore W. [1 ]
Maravelias, Christos T. [1 ]
Dumesic, James A. [1 ]
Huber, George W. [1 ]
机构
[1] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
关键词
CATALYTIC FAST PYROLYSIS; IONIC LIQUID; GAMMA-VALEROLACTONE; SULFURIC-ACID; DEHYDRATION; CONVERSION; FRUCTOSE; BIOMASS; TRANSFORMATION; SUGARS;
D O I
10.1039/c7gc01688c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We demonstrate a process to produce levoglucosenone (LGO) and 5-hydroxymethylfurfural (HMF) from cellulose in up to 65% carbon yield using sulfuric acid as catalyst and a solvent consisting of a mixture of tetrahydrofuran (THF) with water. In pure THF, LGO is the major product of cellulose dehydration, passing through levoglucosan as an intermediate. Increasing the water content (up to 5 wt%) results in HMF as the major product. HMF is formed both by glucose dehydration and direct dehydration of LGA. The maximum combined yield of LGO and HMF (similar to 65 carbon%) is achieved in the presence of 1-2.5 wt% H2O, such that comparable amounts of these two co-products are formed. THF gave the highest total yields of LGO and HMF among the solvents investigated in this study (i.e., THF, diglyme, tetraglyme, gamma-valerolactone (GVL), cyclopentyl methyl ether (CPME), 1,4-dioxane, and dimethyl sulfoxide (DMSO)). Furthermore, the rate of LGO and HMF degradation in THF was lower than in the other solvents. LGO/HMF yields increased with increased strength of the acid catalyst (H2SO4 > H3PO4 > HCOOH), and HMF was produced more selectively than LGO in the presence of hydrochloric acid. Techno-economic analysis for LGO and HMF production from cellulose shows that the lowest LGO/HMF production costs are less than $3.00 per kg and occur at a cellulose loading and water content of 2-3% and 1.5-2.5% respectively.
引用
收藏
页码:3642 / 3653
页数:12
相关论文
共 67 条
[1]   Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass [J].
Alonso, David Martin ;
Wettstein, Stephanie G. ;
Dumesic, James A. .
GREEN CHEMISTRY, 2013, 15 (03) :584-595
[2]  
[Anonymous], 2009, APPL CATAL A, DOI DOI 10.1016/J.APCATA.2009.04.002
[3]   High yield conversion of cellulosic biomass into 5-hydroxymethylfurfural and a study of the reaction kinetics of cellulose to HMF conversion in a biphasic system [J].
Atanda, Luqman ;
Konarova, Muxina ;
Ma, Qing ;
Mukundan, Swathi ;
Shrotri, Abhijit ;
Beltramini, Jorge .
CATALYSIS SCIENCE & TECHNOLOGY, 2016, 6 (16) :6257-6266
[4]   Direct Production of 5-Hydroxymethylfurfural via Catalytic Conversion of Simple and Complex Sugars over Phosphated TiO2 [J].
Atanda, Luqman ;
Shrotri, Abhijit ;
Mukundan, Swathi ;
Ma, Qing ;
Konarova, Muxina ;
Beltramini, Jorge .
CHEMSUSCHEM, 2015, 8 (17) :2907-2916
[5]   Dehydration of fructose to 5-hydroxymethylfurfural in sub- and supercritical acetone [J].
Bicker, M ;
Hirth, J ;
Vogel, H .
GREEN CHEMISTRY, 2003, 5 (02) :280-284
[6]   Simple Chemical Transformation of Lignocellulosic Biomass into Furans for Fuels and Chemicals [J].
Binder, Joseph B. ;
Raines, Ronald T. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (05) :1979-1985
[7]  
Cai CM, 2014, GREEN CHEM, V16, P3819, DOI [10.1039/c4gc00747f, 10.1039/C4GC00747F]
[8]   THF co-solvent enhances hydrocarbon fuel precursor yields from lignocellulosic biomass [J].
Cai, Charles M. ;
Zhang, Taiying ;
Kumar, Rajeev ;
Wyman, Charles E. .
GREEN CHEMISTRY, 2013, 15 (11) :3140-3145
[9]   Dehydration of cellulose to levoglucosenone using polar aprotic solvents [J].
Cao, Fei ;
Schwartz, Thomas J. ;
McClelland, Daniel J. ;
Krishna, Siddarth H. ;
Dumesic, James A. ;
Huber, George W. .
ENERGY & ENVIRONMENTAL SCIENCE, 2015, 8 (06) :1808-1815
[10]   Production of 5-hydroxymethylfurfural and furfural by dehydration of biomass-derived mono- and poly-saccharides [J].
Chheda, Juben N. ;
Roman-Leshkov, Yuriy ;
Dumesic, James A. .
GREEN CHEMISTRY, 2007, 9 (04) :342-350