Depolymerization of oak wood lignin under mild conditions using the acidic ionic liquid 1-H-3-methylimidazolium chloride as both solvent and catalyst

被引:96
作者
Cox, Blair J. [1 ]
Ekerdt, John G. [1 ]
机构
[1] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
关键词
Lignin; Ionic liquid; Biomass; Pretreatment; MODEL-COMPOUND; CHEMISTRY; FUTURE;
D O I
10.1016/j.biortech.2012.05.012
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Oak wood lignin, which was separated from the wood using dissolution in the ionic liquid 1-methyl-3-ethylimidazolium acetate and subsequent precipitation, was successfully depolymerized in the acidic ionic liquid 1-H-3-methylimidazolium chloride under mild conditions (110-150 degrees C). Based on gel permeation chromatography results, an increase in temperature from 110 to 150 degrees C increased the rate of reaction, but did not significantly change the final size of the lignin fragments. Nuclear magnetic resonance and infrared spectroscopy were utilized to demonstrate that the depolymerization proceeded via a hydrolysis reaction that cleaved the alkyl-aryl ether linkages. Coupling of the lignin fragments was also shown to occur in the reaction mixture. These hydrolysis results are consistent with the literature on acid catalyzed depolymerization of lignin in conventional solvents and with recent model compound studies involving guaiacylglycerol-beta-guaiacyl ether and veratrylglycerol-beta-guaiacyl ether done in acidic ionic liquids. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:584 / 588
页数:5
相关论文
共 19 条
[1]   LIGNIN CHEMISTRY - PAST, PRESENT AND FUTURE [J].
ADLER, E .
WOOD SCIENCE AND TECHNOLOGY, 1977, 11 (03) :169-218
[2]  
[Anonymous], 2005, BIOMASS FEEDSTOCK BI
[3]  
[Anonymous], 2012, RENEWABLE ENERGY SOU
[4]   Review of current and future softwood kraft lignin process chemistry [J].
Chakar, FS ;
Ragauskas, AJ .
INDUSTRIAL CROPS AND PRODUCTS, 2004, 20 (02) :131-141
[5]   Catalytic degradation of lignin model compounds in acidic imidazolium based ionic liquids: Hammett acidity and anion effects [J].
Cox, Blair J. ;
Jia, Songyan ;
Zhang, Z. Conrad ;
Ekerdt, John G. .
POLYMER DEGRADATION AND STABILITY, 2011, 96 (04) :426-431
[6]   Regulation of genes in Streptomyces bacteria required for catabolism of lignin-derived aromatic compounds [J].
Davis, Jennifer R. ;
Sello, Jason K. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2010, 86 (03) :921-929
[7]   Historical developments in hydroprocessing bio-oils [J].
Elliott, Douglas C. .
ENERGY & FUELS, 2007, 21 (03) :1792-1815
[8]   Lignin depolymerisation in supercritical carbon dioxide/acetone/water fluid for the production of aromatic chemicals [J].
Gosselink, Richard J. A. ;
Teunissen, Wouter ;
van Dam, Jan E. G. ;
de Jong, Ed ;
Gellerstedt, Goran ;
Scott, Elinor L. ;
Sanders, Johan P. M. .
BIORESOURCE TECHNOLOGY, 2012, 106 :173-177
[9]   Advances in C-O Bond Transformations in Lignin-Derived Compounds for Biofuels Production [J].
Hicks, Jason C. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2011, 2 (18) :2280-2287
[10]  
Holladay J.E., 2007, DOE Rep. PNNL