Molecular composition of water-soluble lignins separated from different non-food biomasses

被引:24
作者
Savy, Davide [1 ]
Nebbioso, Antonio [1 ]
Mazzei, Pierluigi [1 ]
Drosos, Marios [1 ]
Piccolo, Alessandro [1 ]
机构
[1] Ctr Interdipartimentale Ric Risonanza Magnet Nucl, I-80055 Portici, Italy
关键词
Lignin; Alkaline hydrogen peroxide; Giant reed; Miscanthus; DFRC; H-1-C-13; HSQC-NMR; P-31-NMR; ARUNDO-DONAX; DFRC METHOD; HYDROGEN-PEROXIDE; WOOD CHEMISTRY; WHEAT-STRAW; P-31; NMR; DELIGNIFICATION; OXIDATION; GIGANTEUS;
D O I
10.1016/j.fuproc.2014.11.011
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Separation of water-soluble lignins from lignocellulosic biomass provides a new and still poorly exploited feed-stock to increase the sustainability of biorefineries. We applied derivatization followed by a reductive cleavage (DFRC) method, 2D-HSQC-NMR, and (PNMR)-P-31 after P-31-labeling, to investigate molecular composition in water-soluble lignins obtained by alkaline oxidation from three biomass materials for energy (miscanthus, giant reed and an industrially pre-treated giant reed). Chromatographic identification of lignin products cleaved by DFRC showed a large predominance of guaiacyl (G) units in all biomasses and a lesser abundance of syringyl (S) and p-coumaryl (P) monomers. Our S/G ratios disagree with those reported in literature by other lignin separation methods. Carboxyl functions (ferulic and pcoumaric acids) were revealed by heterocorrelated H-1-C-13 HSQC-NMR, and confirmed by P-31-NMR spectra of (31) P-labeled lignin molecules. An understanding of molecular composition of water-soluble lignins from biomass sources for energy is essential for lignin most efficient exploitation in either industrial or agricultural applications. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 181
页数:7
相关论文
共 37 条
[1]   P-31 NMR-SPECTROSCOPY IN WOOD CHEMISTRY .1. MODEL COMPOUNDS [J].
ARCHIPOV, Y ;
ARGYROPOULOS, DS ;
BOLKER, HI ;
HEITNER, C .
JOURNAL OF WOOD CHEMISTRY AND TECHNOLOGY, 1991, 11 (02) :137-157
[2]  
Argyropoulos D.S., 2010, Lignins and Lignans: Advances in Chemistry, P245
[3]   P-31 NMR IN WOOD CHEMISTRY - A REVIEW OF RECENT PROGRESS [J].
ARGYROPOULOS, DS .
RESEARCH ON CHEMICAL INTERMEDIATES, 1995, 21 (3-5) :373-395
[4]   Characterization of Miscanthus giganteus Lignin Isolated by Ethanol Organosolv Process under Reflux Condition [J].
Bauer, Stefan ;
Sorek, Hagit ;
Mitchell, Valerie D. ;
Ibanez, Ana B. ;
Wemmer, David E. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2012, 60 (33) :8203-8212
[5]  
Christou M, 2012, BIOREFINERY: FROM BIOMASS TO CHEMICALS AND FUELS, P49
[6]   Biomimetic degradation of lignin and lignin model compounds by synthetic anionic and cationic water soluble manganese and iron porphyrins [J].
Crestini, C ;
Saladino, R ;
Tagliatesta, P ;
Boschi, T .
BIOORGANIC & MEDICINAL CHEMISTRY, 1999, 7 (09) :1897-1905
[7]   Structural analysis of wheat straw lignin by quantitative P-31 and 2D NMR spectroscopy. The occurrence of ester bonds and alpha-O-4 substructures [J].
Crestini, C ;
Argyropoulos, DS .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (04) :1212-1219
[8]   THE REACTIONS OF LIGNIN WITH ALKALINE HYDROGEN-PEROXIDE .3. THE OXIDATION OF CONJUGATED CARBONYL STRUCTURES [J].
GELLERSTEDT, G ;
AGNEMO, R .
ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1980, 34 (04) :275-280
[9]  
GIERER J, 1985, WOOD SCI TECHNOL, V19, P289
[10]   THE CHEMISTRY OF DELIGNIFICATION - A GENERAL CONCEPT [J].
GIERER, J .
HOLZFORSCHUNG, 1982, 36 (01) :43-51