Hostname: page-component-7bb8b95d7b-l4ctd Total loading time: 0 Render date: 2024-09-17T19:45:40.288Z Has data issue: false hasContentIssue false

Chemical Products from Lignocellulosics*

Published online by Cambridge University Press:  29 November 2013

Get access

Extract

Lignocellulosics represent that mass of organic matter produced by land-growing plants in the form of trees, shrubs, and agricultural crops. Lignocellulosics are renewable, and they sustain living conditions on our planet by recycling carbon dioxide to oxygen. Lignocellulosics serve the planet as a carbon sink. Chlorophyll is the essential catalyst and sunlight the necessary energy source that drive this carbon dioxide reduction to an organic mass that varies little from the carbon-to-oxygen ratio of carbon monoxide.

There is, however, no distinct “lignocellulose” molecule. Instead, nature has found it necessary to formulate a multiphase material consisting of cellulose, hemicelluloses, and lignin. The composition of this multiphase material can be likened to a fiber-reinforced organic glass where cellulose serves as lightweight fiber, lignin serves as a continuous (glassy) matrix, and hemicelluloses serve as coupling agents. The overall composition suggests that there is 35–45% cellulose, 25–35% hemicelluloses, 20–25% lignin, and various minor constituents.

In chemical terms, cellulose is a linear homopolysaccharide with a high degree of crystallinity. It consists of 1,4-β-linked D-glucopyranose units connected in syndiotactic fashion (on alternating sides of the main chain). Cellulose molecules in nature occur with molecular weights exceeding 2 million. Hemicelluloses, by contrast, are branched heterosaccharides of lesser molecular weight. They rarely exceed 20,000 daltons. Hemicelluloses are either rich in glucomannan chains (softwoods), or they consist primarily of branched xylans (hardwoods and annual crops). The chemical composition of hemicelluloses is extraordinarily similar to cellulose (i.e., polyanhydro-pyranoside), but their morphological structure is vastly different.

Type
Reprocessing Paper and Wood-Based Materials
Copyright
Copyright © Materials Research Society 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

*

This article is based, in part, on a paper given at the International Workshop on Environmentally Compatible Materials and Recycling Technology, Tsukuba, Japan, November 15–17, 1993.

References

1.Vincent, J.F.V., Structural Biomaterials (John Wiley & Sons, New York, 1982).CrossRefGoogle Scholar
2.Walsh, D.J., Higgins, J.S., and Maconnachie, A., eds., “Polymer Blends and Mixtures,” NATO ASI Series E: Applied Science, No. 89 (Martinus Nijhoff Publishers, 1985).Google Scholar
3.Malm, C.J. and Hiatt, G.D., in Cellulose and Cellulose Derivatives, edited by Ott, E., Spurlin, H.M., and Grafflin, M.W. (Interscience Publ., New York, London, 1954) p. 763.Google Scholar
4.Timell, T.E., Carbohydr. Chem. 19 (1964) p. 247.Google Scholar
5.Sjostrom, E., Tappi 60(9) (1977) p. 151.Google Scholar
6.Kaar, W.E., Jain, R.K., Sealey, J.E., and Glasser, W.G., manuscript in preparation.Google Scholar
7.Glasser, W.G. and Kelley, S.S., “Lignin,” in Encyclopedia of Polymer Science and Engineering, Vol. 8 (John Wiley & Sons, 1987), p. 795.Google Scholar
8.Glasser, W.G., Barnett, C.A., Muller, P.C., and Sarkanen, K.V., J. Agric. Food Chem. 31 (5) (1983) p. 921.CrossRefGoogle Scholar
9.Johnson, D.C., in Cellulose Chemistry and Its Applications, edited by Nevell, T.P. and Zeronian, S.H. (Ellis Horwood Ltd., Chichester, United Kingdom, 1985) p. 181.Google Scholar
10.Samaranayake, G. and Glasser, W.G., Carbohydr. Polym. 22 (1993) p. 17.CrossRefGoogle Scholar
11.Glasser, W.G., Samaranayake, G., Dumay, M., and Davé, V., manuscript in preparation.Google Scholar
12.Glasser, W.G., Ravindran, G., Samaranayake, G., and Jain, R.K., manuscript in preparation.Google Scholar
13.de Oliveira, W. and Glasser, W.G., J. Appl. Polym. Sci., in press.Google Scholar
14.Glasser, W.G. and Jain, R.K., Holzforschung 47 (3) (1993) p. 225.CrossRefGoogle Scholar
15.Jain, R.K. and Glasser, W.G., Holzforschung 47 (4) (1993), p. 325.CrossRefGoogle Scholar
16.Glasser, W.G., Knudsen, J.S., and Chang, C-S., J. Wood Chem. Tech. 8 (2) (1988) p. 221.CrossRefGoogle Scholar