Characterisation of thermally modified hard- and softwoods by 13C CPMAS NMR

被引：392

作者：

Wikberg, H ^{[1
]}

Maunu, SL ^{[1
]}

机构：

[1] Univ Helsinki, Dept Chem, Polymer Chem Lab, FIN-00014 Helsinki, Finland

来源：

CARBOHYDRATE POLYMERS | 2004年 / 58卷 / 04期

基金：

芬兰科学院;

关键词：

C-13 CPMAS NMR; thermal modification; softwood; hardwood; crystallinity of cellulose; lignin content;

D O I：

10.1016/j.carbpol.2004.08.008

中图分类号：

O69 [应用化学];

学科分类号：

081704 ;

摘要：

The changes induced by thermal modification in the chemical structure of spruce [Picea abies (L.) Karst.], birch (Betula pendula), aspen (Populus tremula) and oak (Quercus robur) were studied by C-13 CPMAS NMR spectroscopy. Spruce, birch and aspen were thermally modified at similar to195 C and oak at similar to160 degreesC, under steam, according to an industrial-scale heat treatment process. In both hard- and softwood samples, C-13 CPMAS NMR measurements revealed a degradation of less ordered carbohydrates (i.e. hemicelluloses and amorphous cellulose) in the thermally modified wood, which resulted in an increase in the cellulose crystallinity. Furthermore, thermal modification induced changes in the lignin structure by a cleavage of the beta-O-4 linkages. In the softwood lignin, a decrease also occurred in the methoxyl group content leading to a more condensed lignin structure. (C) 2004 Elsevier Ltd. All rights reserved.

引用

页码：461 / 466

页数：6

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