6. The amount of the various wood components, viz cellulose, hemicelluloses, lignin, extractives and inorganics can vary widely
depending on wood species. In addition, structural differences exist between the various types of wood tissue as well as
between the individual cell wall layers. Irrespective of morphological differences, the gross composition of wood (or pulp) can
Be determined by first applying a homogenization of the material, followed by solvent extraction to remove low molecular
weight organics.
Introduction
Acid hydrolysis of the residue results in a precipitate consisting of highly condensed lignin (Klason lignin) and a solution of
monomeric sugars. The latter are separated (by GC, HPLC or CE analysis) and quantified whereas the Klason lignin is
determined gravimetrically. For the analysis of inorganics, present in the wood as carbonates, phosphates etc, combustion of
the wood sample and gravimetric determination of the ash can be used. The individual components of the ash can be
further analysed using e.g. inductively coupled plasma mass spectrometry (ICP-MS).
7.
8.
9. Periodate oxidation
Wet chemical analyses of carbohydrates and polysaccharides were developed a long time ago and are still in use
frequently although NMR methods can also be used. For the general detection of carbohydrate structures, an
oxidation of the sample with periodate is convenient since periodate reacts with vicinal dihydroxy compounds. In the
reaction, each hydroxyl group is converted to an aldehyde or, for glycerol structures, an additional formation of formic
acid
10. The separation of the individual polysaccharides present in wood and other lignocellulosic material is not trivial due to the
complex arrangement of polymers making up the cell wall with lignin acting as an incrusting material. The necessary increase
in accessibility of the polysaccharides can be obtained by a selective oxidative degradation of the lignin with sodium chlorite
under mild acid conditions
11. The further separation of the individual polysaccharide components present in wood can be done with holocellulose as the
starting material. In the complicated separation scheme (Figure 9.4), strong alkali is used to dissolve the predominant portion of
the xylan and galactoglucomannan leaving cellulose and glucomannan as a residue. The fact that sugar units like mannose having
vicinal hydroxyl groups in a cis-configuration can form soluble borate complexes and insoluble barium salts (Figure9.5) can
be used to further separate the individual hemicelluloses.
12.
13. The composition, structure and morphology of the polysaccharides present in wood and pulps are of great importance since
these to a major extent determine the properties of the resulting fibers. A simple quantification of the monomeric sugar units
present in a wood or pulp sample can be done as outlined in Figure 9.1. After the acid hydrolysis, the mixture of sugars can be
reduced with sodium borohydride to convert all reducing end-groups to the corresponding alcohol groups. Thereby, only one
product from each pair of anomeric sugar units is obtained. After a subsequent acetylation, the mixture is analysed by gas
chromatography (Figure 9.6). Other separation techniques are also frequently used such as HPLC or CE (capillary electrophoresis)
With or without derivatization.
Sugar compotition
14. An alternative method for the analysis of monomeric sugar units is based on acid hydrolysis in methanol (methanolysis). The
reaction results in a conversion of the polysaccharides to the corresponding methylglucosides with a major advantage being a
Much better preservation of the uronic acid groups. In the reaction, the latter are esterified and this promotes a more
complete hydrolysis of otherwise resistant glucosidic linkages such as those between xylose and 4-Omethyl-glucuronic acid in
xylans.
15.
16. For the isolation of lignin from kraft pulp, methods based on acid and/or enzymatic hydrolysis
of carbohydrate-carbohydrate and lignin-carbohydrate linkages are frequently employed
whereas lignin from alkaline pulping liquors can be isolated by precipitation with acid.
17. The characteristic feature of a lignin (or lignan) is the presence of aromatic methoxyl groups.
Except for the p-hydroxyphenyl units constituting part of compression wood and grass
lignins, virtually all aromatic units contain at least one methoxyl group. This can be analysed
By reacting the sample with hydriodic acid followed by gas chromatographic analysis of the
methyl iodide that is formed
18. For the direct chemical analysis of isolated lignin or of lignin present in wood or pulps,
degradation methods employing oxidation with potassium permanganate โ hydrogen peroxide
or ozone can be used. Among other methods, acid hydrolysis in the presence of ethanethiol,
thioacidolysis, is the most important. The first of these reactions is outlined in Figure 9.12. In a
four-step procedure, the lignin-containing sample is first alkylated to protect the phenolic
hydroxyl groups. Oxidation in two steps with potassium permanganate and hydrogen peroxide
converts all side-chains to aromatic carboxyl groups and these are finally esterified to provide
derivatives suitable for gas chromatographic analysis.