CP MAS 13C NMR Spectroscopy in Determination of Species-Specific Differences in Wood Composition

被引:1
作者
Kostryukov, S. G. [1 ]
Petrov, P. S. [1 ]
Masterova, Yu. Yu. [1 ]
Idris, T. D. [1 ]
Hamdamov, S. S. [1 ]
Yunusov, I. A. [1 ]
Kostryukov, N. S. [2 ]
机构
[1] Ogarev Natl Res Mordovian State Univ, Saransk 430005, Russia
[2] St Petersburg State Univ Ind Technol & Design, St Petersburg 191186, Russia
关键词
solid-state C-13 NMR spectroscopy; CP MAS; wood; cellulose; hemicellulose; lignin; syringil; guaiacyl; SOLID-STATE NMR;
D O I
10.1134/S1068162022070111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In recent years, solid-state C-13 NMR spectroscopy using the techniques of cross-polarization (CP) and magic angle spinning (MAS) has been used to analyze plant materials, including wood. The composition, structure, and behavior of wood components determine the properties of wood materials in various conditions and are therefore important to know. In this work, differences in wood composition were studied for several tree species of central Russia (birch, aspen, spruce, and larch) by CP MAS C-13 NMR spectroscopy. Peaks of CP MAS C-13 NMR spectra were assigned to the main components of the wood. Cellulose was shown to occur in amorphous and crystalline forms; the presence of lignin was unambiguously confirmed by signals from aromatic carbon atoms; and hemicellulose was detected by signals from carbon atoms of the methyl groups of acetylxylose and L-rhamnose. Integral intensities were used to estimate the total proportion of cellulose and hemicellulose in relation to lignin. The lignin content in wood was observed to be maximal in the coniferous species (spruce and larch) and minimal in the deciduous species (aspen and birch).
引用
收藏
页码:1441 / 1447
页数:7
相关论文
共 23 条
[11]  
Kamide K., 2005, CELLULOSE CELLULOSE
[12]  
Katoh E, 2017, ENCYCLOPEDIA OF SPECTROSCOPY AND SPECTROMETRY, 3RD EDITION, VOL 2: G-M, P75, DOI 10.1016/B978-0-12-803224-4.00283-1
[13]  
Kostryukov S.G., 2017, KHIM RASTIT SYRYA, P31, DOI [10.14258/jcprm.2017041860, 10.14258/J*cprm.2017041860, DOI 10.14258/J*CPRM.2017041860, DOI 10.14258/JCPRM.2017041860]
[14]  
Lenz R. W., 1994, J Polym Sci Pol Chem, V32, DOI [10.1002/pola.1994.080321221, DOI 10.1002/POLA.1994.080321221]
[15]   Characterization and properties of organo-montmorillonite modified lignocellulosic fibers and their interaction mechanisms [J].
Liu, Ru ;
Chen, Yu ;
Cao, Jinzhen .
RSC ADVANCES, 2015, 5 (94) :76708-76717
[16]   DETERMINATION OF THE AROMATIC LIGNIN CONTENT IN OAK WOOD BY QUANTITATIVE SOLID-STATE C-13-NMR [J].
LOVE, GD ;
SNAPE, CE ;
JARVIS, MC .
BIOPOLYMERS, 1992, 32 (09) :1187-1192
[17]   Advanced solid-state NMR spectroscopy of natural organic matter [J].
Mao, Jingdong ;
Cao, Xiaoyan ;
Olk, Dan C. ;
Chu, Wenying ;
Schmidt-Rohr, Klaus .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2017, 100 :17-51
[18]   Inputs of solid-state NMR to evaluate and compare thermal reactivity of pine and beech woods under torrefaction conditions and modified atmosphere [J].
Melkior, T. ;
Barthomeuf, C. ;
Bardet, M. .
FUEL, 2017, 187 :250-260
[19]   Characterization of Fungal-Degraded Lime Wood by X-ray Diffraction and Cross-Polarization Magic-Angle-Spinning 13C-Nuclear Magnetic Resonance Spectroscopy [J].
Popescu, Carmen-Mihaela ;
Larsson, Per Tomas ;
Tibirna, Carmen Mihaela ;
Vasile, Cornelia .
APPLIED SPECTROSCOPY, 2010, 64 (09) :1054-1060
[20]   Solid state NMR and IR characterization of wood polymer structure in relation to tree provenance [J].
Santoni, Ilaria ;
Callone, Emanuela ;
Sandak, Anna ;
Sandak, Jakub ;
Dire, Sandra .
CARBOHYDRATE POLYMERS, 2015, 117 :710-721