Cellulose lignocellulose

Holzfaser, /. wood fiber, ligneous fiber wood pulp = Holzfaserstoff. -papier, n. wood-pulp paper, -stoff, m. lignin cellulose lignocellulose. 

Lignin is one of the most important natural polymers. Combinations of lignin and cellulose (lignocelluloses) make up as much as 95% of the earth s land-produced biomass (and about one quarter of that is lignin). It strengthens trees and plants and protects them from the weather, insects, and... 

Fibers for commercial and domestic use are broadly classified as natural or synthetic. The natural fibers are vegetable, animal, or mineral ia origin. Vegetable fibers, as the name implies, are derived from plants. The principal chemical component ia plants is cellulose, and therefore they are also referred to as ceUulosic fibers. The fibers are usually bound by a natural phenoHc polymer, lignin, which also is frequentiy present ia the cell wall of the fiber thus vegetable fibers are also often referred to as lignocellulosic fibers, except for cotton which does not contain lignin. 

Lu and Pizzi [83] showed that lignocellulosic substrates have a distinct influence on the hardening behavior of PF-resins, whereby the activation energy of the hardening process is much lower than for the resin alone [84]. The reason is a catalytic activation of the PF-condensation by carbohydrates like crystalline and amorphous cellulose and hemicellulose. Covalent bonding between the PF-resin and the wood, especially lignin, does not play any role [84]. 

Such basic data are here presented from isothermal measurements on 5 by 90 cm lignocellulosic and cellulosic strips up to 13 mm thick. A suitable labyrinth air flow calorimeter operating at temperatures up to 250°C was built for these fairly large size samples. (7)... 

The heat release data presented with their diffences between various cellulosic and lignocellulosic material in a general way thus are in no disagreement with data in the literature. They can hopefully contribute to a better understanding of the oxidative pyrolysis. 

Up to about 70 C, plant tissues are thermally stable, as they must be in nature to avoid damage from prolonged direct exposure to the sun. Pyrolysis, the chemical decomposition by heat, starts in dry lignocellulosics around 100 C, in moist ones below 80 C. It accelerates as temperature rises, peaking in many organic materials between 275 and 300 C, at which point cellulose disintegrates. 

Thermodynamically controlled self-assembly of an equilibrated ensemble of POMs with [AlVWnO40]6 as the main component could act as a catalyst for the selective delignification of wood (lignocellulose) fibers (Figure 13.2) [55], Equilibration reactions typical of POMs kept the pH of the system near 7 during the catalysis that avoided acid or base degradation of cellulose. 

Lignocellulose is the fibrous material that forms the cell wall of a plants architecture . It consists of three major components (Fig. 2.1) cellulose, hemicellulose and lignin [3, 14-16]. It contrasts with the green parts of the plants and the seeds, which are rich in proteins, starch and/or oil. 

Various solvents are being investigated to dissolve lignocellulosic materials. Some approaches focus on the selective depolymerization and extraction of lignin and hemicellulose as pre-treatment to produce clean cellulose fibers for subsequent fermentation or for pulping. Other approaches attempt to dissolve the whole lignocellulose with or without depolymerization. The liquefaction processes that are carried out at high temperature (>300 °C), and produce a complex oil mixture, are discussed above with the pyrolysis processes. 

Lignocellulose biomass is a mixture of phenolic lignin and carbohydrates -cellulose and hemi-cellulose. It grows abundantly on earth and is largely available as agricultural and forestry residues. Lignocellulose can be converted via four major routes pyrolysis, gasification, hydrolysis and fermentation. 

Both in the USA and the EU, the introduction of renewable fuels standards is likely to increase considerably the consumption of bioethanol. Lignocelluloses from agricultural and forest industry residues and/or the carbohydrate fraction of municipal solid waste (MSW) will be the future source of biomass, but starch-rich sources such as corn grain (the major raw material for ethanol in USA) and sugar cane (in Brazil) are currently used. Although land devoted to fuel could reduce land available for food production, this is at present not a serious problem, but could become progressively more important with increasing use of bioethanol. For this reason, it is important to utilize other crops that could be cultivated in unused land (an important social factor to preserve rural populations) and, especially, start to use cellulose-based feedstocks and waste materials as raw material. 

Further research is also needed in this area. Particularly, (a) to create a new generation of cheap enzymes for hydrolysis of cellulose and lignocellulose to fermentable sugars (able to complete the biomass hydrolysis during fermentation) (b) to develop improved biocatalysts that allow us to simplify the process and reduce energy input and (c) to improve separation and recovery. 

Biocatalytic conversion of lignocellulose into bioethanol, which requires upgrading of existing processes of fermenting sugars by using enzymatic-enhanced pretreatment of (hemi)cellulose. New, improved biocatalysts are needed for this route. 

A hydrolysis step is involved in the pulp industry in order to concentrate the cellulose from wood. This uses large-scale processes whereby a liquid fraction, the lignocellulose, is formed as a by-product in the process, and contains high levels of phenolic components and their derivatives. These compounds also constitute an environmental problem due to their possible introduction into rivers, lakes, and/or seas. Chlorophenols from the cellulose bleaching process have traditionally attracted most of the interest in the analysis of industrial waste because of their high toxicity. 

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