Cellulose molecular structure

Fig. 26.3. The molecular structure of a cell wall. It is a fibre-reinforced composite (cellulose fibres in o matrix of hemicellulose and lignin).

The purpose of this study is only intended to illustrate and evaluate the decision tree approach for CSP prediction using as attributes the 166 molecular keys publicly available in ISIS. This assay was carried out a CHIRBASE file of 3000 molecular structures corresponding to a list of samples resolved with an a value superior to 1.8. For each solute, we have picked in CHIRBASE the traded CSP providing the highest enantioselectivity. This procedure leads to a total selection of 18 CSPs commercially available under the following names Chiralpak AD [28], Chiral-AGP [40], Chiralpak AS [28], Resolvosil BSA-7 [41], Chiral-CBH [40], CTA-I (microcrystalline cellulose triacetate) [42], Chirobiotic T [43], Crownpak CR(-i-) [28], Cyclobond I [43], DNB-Leucine covalent [29], DNB-Phenylglycine covalent [29], Chiralcel OB [28], Chiralcel OD [28], Chiralcel OJ [28], Chiralpak OT(-i-) [28], Ultron-ES-OVM [44], Whelk-0 1 [29], (/ ,/ )-(3-Gem 1 [29]. 

Nitrocellulose, of the resins used in these end uses and in car refinishing, is the nitrate ester of cellulose. The structure is linear and a wide range of (high) molecular weights is available as well as various degrees of nitration ... 

The molecular structure of cellulose, unlike that of starch, allows for strong hydrogen bonding between polymer chains. This results in the formation of strong water-resistant fibers such as those found in cotton, which is 98% cellulose. Cotton actually has a tensile strength greater than that of steel. The major industrial source of cellulose is wood ( 50% cellulose). 

These are defined as anionic dyes with substantivity for cellulosic fibres applied from an aqueous dyebath containing an electrolyte. The forces that operate between a direct dye and cellulose include hydrogen bonding, dipolar forces and non-specific hydrophobic interaction, depending on the chemical structure and polarity of the dye. Apparently multiple attachments are important, since linearity and coplanarity of molecular structure seem to be desirable features (section 3.2.1). The sorption process is reversible and numerous attempts have been made to minimise desorption by suitable aftertreatments (section 10.9.5). The two most significant non-textile outlets for direct dyes are the batchwise dyeing of leather and the continuous coloration of paper. 

Figure 2.3 The molecular structure of /3-D-glucopyranose (a), cellobiose (b) and the glucopyranose backbone of cellulose (c), and (d) a schematic of the linear arrangement of the glucopyranose units.

As Guo and Gray (114) point out, the relationship between the handedness of the supramolecular helicoidal structure and the molecular structure 01 cellulose derivatives and solvents is not at all understood" at the present time. 

Chitosan Chitosan has a molecular structure similar to cellulose. This material is produced from chitin, which is widely found in the exoskeleton of shellfish and crustaceans. Chitin is the second most abundant natural biopolymer after cellulose. Chitosan is a good adsorbent for all heavy metals. It has been estimated that chitosan can be produced from shellfish and crustaceans at a market price of 15.43 /kg. 

Plant structural material is the polysaccharide cellulose, which is a linear p (1 —> 4) linked polymer. Some structural polysaccharides incorporate nitrogen into their molecular structure an example is chitin, the material which comprises the hard exoskeletons of insects and crustaceans. Chitin is a cellulose derivative wherein the OH at C-2 is replaced by an acetylated amino group (—NHCOCH3). Microbial polysaccharides, of which the capsular or extracellular (exopolysaccharides) are probably the most important class, show more diversity both in monomer units and the nature of their linkages. 

The linear, but highly branched, molecular structure of the galactomannans is the reason for some specific properties which are quite different from those of the unbranched cellulose-like and water-insoluble mannans and glucomannans. Galactomannans are hydrated in cold water and give stable solutions even in acidic formulas. The interactions of galactomannans with other polysaccharides are the base of a variety of industrial applications. 

The primary sources of information concerning the molecular structure of cellulose have been x-ray and electron diffractometric studies, conformational analyses, and vibrational spectroscopy. The work up to 1971 was very ably reviewed by Jones (10), and by T0nnesen and Ellefsen (II, 12). They generally concluded that although much evidence can be interpreted in terms of cellulose chains possessing a two-fold axis of symmetry, in both Celluloses I and II, none of the structures proposed... 

The CBH I (D) is identical in composition and activity to the CBH I (D) previously described (2) from T. reesei QM 9123. The close correspondence of their amino acid contents (Table VI), the nearly identical content of neutral carbohydrate 6.8% by weight for the CBH I (D) produced in the presence of sophorose and 6.7% for T. reesei QM 9123 CBH I (D) grown on cellulose (2), and identical electrophoretic properties clearly argue for a common molecular structure for these CBH s I (D). The CBH II is clearly different from all other CBH s in electrophoretic mobility (Figure 12) and amino acid composition (41), but is devoid of endoglucanase activity and produces predominantly cellobiose (>90% by weight of soluble products) from cellulose. It has a sedimentation coefficient of 3.71 in comparison to CBH I (D), for which a value of 3.66 was obtained. 

This is an important class of dyes for the dyeing of paper. Direct dyes are also called substantive dyes [4,5] because they tend to have a high affinity to cellulose fibers due to their linear molecular structure and a system of conjugated double bonds and usually also exhibit good wetfastness properties with the addition of a fixative. 

The material behavior of polymers is totally controlled by their molecular structure. In fact, this is true for all polymers synthetically generated polymers as well as polymers found in nature (bio-polymers), such as natural rubber, ivory, amber, protein-based polymers or cellulose-based materials. To understand the basic aspects of material behavior and its relation to the molecular structure of polymers, in this chapter we attempt to introduce the fundamental concepts in a compact and simple way. 

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