Cellulose liquid crystalline polymers

Fig. 7. Comparison of experimental phase boundary concentrations between the isotropic and biphasic regions for various liquid-crystalline polymer solutions with the scaled particle theory for wormlike hard spherocylinders. ( ) schizophyllan water [65] (A) poly y-benzyl L-glutamate) (PBLG)-dimethylformamide (DMF) [66-69] (A) PBLG-m-cresoI [70] ( ) PBLG-dioxane [71] (O) PBLG-methylene chloride [71] (o) po y(n-hexyl isocyanate) (PHICH°Iuene at 10,25,30,40 °C [64] (O) PHIC-dichloromethane (DCM) at 20 °C [64] (5) a po y(yne)-platinum polymer (PYPt)-tuchIoroethane (TCE) [33] ( ) (hydroxypropyl)-cellulose (HPC)-water [34] ( ) HPC-dimethylacetamide (DMAc) [34] (N) (acetoxypropyl) cellulose (APC)-dibutylphthalate (DBP) [35] ( ) cellulose triacetate (CTA)-trifluoroacetic acid [72]...

The cellulosic polymers (12) form a type of main chain liquid crystalline polymers of special Interest for the following reasons ... 

Bhadani, S.N. Gray, D.G. Cellulose-based liquid-crystalline polymers esters of (hydroxypropyl) cellulose. Molec. Crystals Liquid Crystals 1983, 99 (1-4), 29-38. 

Harrison, P. Navard, P. Cidade, M.T. Investigation of the band texture occurring in acetoxy-propyl cellulose thermotropic liquid crystalline polymer using rheo-optical, rheological, and light scattering techniques. Rheol. Acta 1999, 38 (6), 594-605. 

High resolution solid-state NMR spectroscopy is also a very powerful method for characterizing the solid structure and the local motion of different solid polymers. We recently characterized the crystalline-noncrystalline structure for different crystalline and liquid crystalline polymers, such as polyolefins [7-12], polyesters [13-15], polyether [16], polyurethanes [17, 18] and polysaccharides, including cellulose [19-29], amylose [30, 31] and dextran [32]. On the basis of these analytical methods, we also investigated the intra- and intermolecular hydrogen bonds of PVA in both crystalline and noncrystalline regions as well as in the frozen solution state. In this chapter. 

A typical example of a thermotropic liquid crystalline polymers is the polyesters and the mesogen substituted polysiloxane. The aromatic amide, the super strength fiber known commercially as Kevlar belongs to the lyotropic liquid crystalline polymers. The other important lyotropic liquid crystalline polymers are poly(7-benzyl-L-glutamate), abbreviated as PBLG, cellulose derivatives, the tobacco mosaic virus, etc. 

To form cholesteric liquid crystalline polymers, one either polymerizes cholesteric monomers or mixes low molecular mass cholesteric liquid crystals with polymers. In the latter case, two components may be mixed homogeneously or in such a way that the polymers act as a matrix while the small molecular mass cholesteric liquid crystals are in droplets, known as the polymer-dispersed liquid crystals (PDLC) (Doane et al., 1988) or the nematic curvilinear aligned phase (NCAP) (Fergason, 1985). In addition, there are many polymers in nature exhibiting the cholesteric phase such as PBLG, cellulose, DNA, etc. 

Other important lyotropic cholesteric liquid crystalline polymer are the cellulose esters. Cellulose is a natural polymer. Their chemical formula is shown in Figure 6.24. 

Many cellulose derivatives form lyotropic liquid crystals in suitable solvents and several thermotropic cellulose derivatives have been reported (1-3) Cellulosic liquid crystalline systems reported prior to early 1982 have been tabulated (1). Since then, some new substituted cellulosic derivatives which form thermotropic cholesteric phases have been prepared (4), and much effort has been devoted to investigating the previously-reported systems. Anisotropic solutions of cellulose acetate and triacetate in tri-fluoroacetic acid have attracted the attention of several groups. Chiroptical properties (5,6), refractive index (7), phase boundaries (8), nuclear magnetic resonance spectra (9,10) and differential scanning calorimetry (11,12) have been reported for this system. However, trifluoroacetic acid causes degradation of cellulosic polymers this calls into question some of the physical measurements on these mesophases, because time is required for the mesophase solutions to achieve their equilibrium order. Mixtures of trifluoroacetic acid with chlorinated solvents have been employed to minimize this problem (13), and anisotropic solutions of cellulose acetate and triacetate in other solvents have been examined (14,15). The mesophase formed by (hydroxypropyl)cellulose (HPC) in water (16) is stable and easy to handle, and has thus attracted further attention (10,11,17-19), as has the thermotropic mesophase of HPC (20). Detailed studies of mesophase formation and chain rigidity for HPC in dimethyl acetamide (21) and for the benzoic acid ester of HPC in acetone and benzene (22) have been published. Anisotropic solutions of methylol cellulose in dimethyl sulfoxide (23) and of cellulose in dimethyl acetamide/ LiCl (24) were reported. Cellulose tricarbanilate in methyl ethyl ketone forms a liquid crystalline solution (25) with optical properties which are quite distinct from those of previously reported cholesteric cellulosic mesophases (26). 

Biodegradable liquid crystalline polymers derived from cellu-losics have been described (21,22). Such polymers include also the butyric acid ester of hydroxyethyl cellulose, the butyl ether of hy-droxypropyl cellulose, and cellulose butyl ether (20). This type of liquid crystalline polymer can be derived from waste paper. The butyric acid ester is prepared as follows (20) ... 

White JL, Dong L, Han P, Laun HM (2004) Rheological properties and associated structural characteristics of some aromatic polycondensates including liquid-crystalline polyesters and cellulose derivatives. Int Union Pure Appl Chem 76(ll) 2027-2049 Wiberg G, Hillborg H, Gedde UW (1998) Assessment of development and relaxation of orientation in a sheared thermotropic liquid crystalline copolyester. Polym Eng Sci 38 1278-1285 Wilson TS, Baird DG (1992) Transient elongational flow behavior of thermotropic liquid crystalline polymers. J Non-Newt Fluid 44 85-112... 

Self assembled Liquid Crystalline Polymer Nanocomposites constitute another important class of materials having multiple utility. Cellulose nanoparticles (CNCs) constitute one such promising class of material which has the ability to... 

One of the best examples of a man-made fiber spun from a lyotropic liquid crystalline polymer is poly (p-phenylene terephthalamide) (PPTA, Kevlar ), which was commercialized by DuPont in 1972. The Kevlar fibers possess impressive mechanical properties. Some polysaccharides are able to form lyotropic liquid crystalline states. High performance fibers from liquid crystalline spinning of cellulose mesophases have gained much interest, and a considerable amoimt of work has been done on spinning cellulose, with some of the products commercialized. This will be further discussed below. 

Liquid crystal display technology, 15 113 Liquid crystalline cellulose, 5 384-386 cellulose esters, 5 418 Liquid crystalline conducting polymers (LCCPs), 7 523-524 Liquid crystalline compounds, 15 118 central linkages found in, 15 103 Liquid crystalline materials, 15 81-120 applications of, 15 113-117 availability and safety of, 15 118 in biological systems, 15 111-113 blue phases of, 15 96 bond orientational order of, 15 85 columnar phase of, 15 96 lyotropic liquid crystals, 15 98-101 orientational distribution function and order parameter of, 15 82-85 polymer liquid crystals, 15 107-111 polymorphism in, 15 101-102 positional distribution function and order parameter of, 15 85 structure-property relations in,... 

Gray, D.G., Liquid crystalline cellulose derivatives, J. Appl. Polymer Sci. Applied Polymer Symposium, 37 179-192 (1983). 

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