Magnetic resonance studies of thermally modified wood

被引:286
作者
Sivonen, H
Maunu, SL
Sundholm, F
Jämsä, S
Viitaniemi, P
机构
[1] Univ Helsinki, Polymer Chem Lab, FIN-00014 Helsinki, Finland
[2] VTT Bldg Technol, Espoo 02044, Finland
关键词
thermally modified wood; C-13 CPMAS NMR spectroscopy; crystallinity index; dipolar dephasing; ESR spectroscopy; free radicals;
D O I
10.1515/HF.2002.098
中图分类号
S7 [林业];
学科分类号
0829 ; 0907 ;
摘要
Thermal modification of wood produces a wood material with many interesting properties, such as enhanced dimensional stability, lower equilibrium moisture content and increased biological durability. Changes in the chemical structure of pine (Pinus sylvestris) caused by thermal treatment were investigated by studying various components of wood using C-13 CPMAS NMR spectroscopy. Electron spin resonance (ESR) spectroscopy on the same set of samples was used to study the formation and stability of free radicals formed during the treatment. The most remarkable changes revealed by solid state NMR were the increase in relative crystallinity of cellulose and destruction and deacetylation of hemicelfuloses. Changes in the lignin fraction were mostly registered as diminishment in the methoxyl content, although the intensity of the aromatic region increased relative to the carbohydrate fraction during the treatment. Increase in the intensities of the ESR signals from thermally treated wood samples proves the formation of stable free radicals. In addition, radical formation is believed to take part in condensation reactions leading to crosslinks within the lignin and possibly between lignin and other wood components. Both of the methods used indicate that the changes are most remarkable when the treatment temperature is over 200 degreesC.
引用
收藏
页码:648 / 654
页数:7
相关论文
共 24 条
[1]   EVIDENCE FOR THE EXISTENCE OF ASSOCIATED LIGNIN CARBOHYDRATE POLYMERS AS REVEALED BY C-13 CPMAS SOLID-STATE NMR-SPECTROSCOPY [J].
GERASIMOWICZ, WV ;
HICKS, KB ;
PFEFFER, PE .
MACROMOLECULES, 1984, 17 (12) :2597-2603
[3]   A COMPARISON OF SOLUTION AND SOLID-STATE C-13 NMR-SPECTRA OF LIGNINS AND LIGNIN MODEL COMPOUNDS [J].
HAWKES, GE ;
SMITH, CZ ;
UTLEY, JHP ;
VARGAS, RR ;
VIERTLER, H .
HOLZFORSCHUNG, 1993, 47 (04) :302-312
[4]  
HEMMINGSON JA, 1985, J WOOD CHEM TECHNOL, V5, P159, DOI 10.1080/02773818508085186
[5]  
HORII F, 1985, CELL CHEM TECHNOL, V19, P513
[6]  
IVANOV MA, 1970, BUM PROM, V4, P22
[7]  
Jämsä S, 1999, SURF COAT INT, V82, P297
[8]  
Jamsa S, 2000, PIGM RESIN TECHNOL, V29, P68, DOI DOI 10.1108/03699420010317807
[9]   Interaction of lignin and polysaccharides in beech wood (Fagus sylvatica) during drying processes [J].
Košiková B. ;
Hricovíni M. ;
Cosentino C. .
Wood Science and Technology, 1999, 33 (5) :373-380
[10]   C-13 NMR DISTINCTION BETWEEN CATEGORIES OF MOLECULAR ORDER AND DISORDER IN CELLULOSE [J].
NEWMAN, RH ;
HEMMINGSON, JA .
CELLULOSE, 1995, 2 (02) :95-110