Solubility liquid crystal

Film Preparation and Molecular Orientation of Soluble Liquid Crystal Polymer... 

DNAs are soluble only in aqueous solutions and their fibrous crystals can be prepared by slow evaporation from the aqueous solution. Duplex structures in the fibers have been studied by X-ray diffraction [2,3] and sohd state NMR [4-6]. Orientation of DNA strands by using hydrodynamic flow gradients in the dilute aqueous solution [7,8] and lyotropic liquid crystal... 

Solvent viscosity vs, concentration plots for cellulose dissolved in TFA-CH2CI2 (70/30, v/v) do not exhibit a maximum (1I,S1) in contrast to the typicid behavior of polymer liquid crystal solutions. This same behavior is exhibited by other cellulose-solvent systems (52,fiQ). Conio et al. (59) si gest that due to the close proximity of the cholesteric mesophase to its solubility limit, it is only observed in a metastable condition. 

Boy et al. [79] used lyotropic liquid crystals (LC) for the immobilization of HfeHNL. The solid LC phase is not used because of the high viscosity. Therefore, the LC is used in a biphasic system consisting of the LC and an organic solvent. Such biphasic liquid crystal systems consist of organic solvent, water, and surfactant, where poorly soluble substrates and products are dissolved in the organic solvent and the liquid crystal matrix, which contains the enzyme, has a protective effect on it. By optimization and by virtue of the immobilization, it is possible to establish an extractive continuous process [79]. 

Micellar properties are affected by changes in the environment, eg, temperature, solvents, electrolytes, and solubilized components. These changes indude complicated phase changes, viscosity effects, gd formation, and liquefication of liquid crystals. Of the simpler changes, high concentrations of water-soluble alcohols in aqueous solution often dissolve micelles and in nonaqueous solvents addition of water frequendy causes a sharp increase in micellar size. 

PFMB can be used to prepare aromatic polyimides that display solubility in ketone, ether, and polar aprotic solvents. This unusual solubility can be utilized in die facile preparation of thin films that display anisotropy in their structures and properties. The anisotropy in the optical properties of the films makes them promising candidates for use as compensation layers in liquid-crystal displays. Their low dielectric constants and CTEs in combination with their outstanding thennal and thermooxidative stabilities make diem candidates for dielectric layers in microelectronics applications. 

AMPHIPHILIC. Molecule having a water-soluble polar head (hydrophilic) and a water-insoluble organic tail (hydrophobic), e.g.. octyl alcohol, sodium stearate. Such molecules arc necessary for emulsion formation and for controlling the structure of liquid crystals. 

The polyamides are soluble in high sirength sulfuric acid or in mixtures of hexamelhylphosphoiamide. AMV-diinethylaeciamidc. and l.ifT. The liquid-crystal phase is optically anisotropic and the texture is nematic. The nematic texture can he transformed lo a chiral nematic texture by adding chiral species us a dopant or incorporating a chiral unit in the main chain as a copolymer. 

Although polymorphism in plastic crystals is less frequent than in liquid crystals, it does exist. Tetrakis(methylmercapto)methane, C(SCH3)4, for example, has four crystal modifications of which the three high temperature forms have a high degree of plasticity 100). Also, it has been observed that plastic crystals are frequently mutually soluble 16b), a consequence of the less restrictive crystal structures. Phase separation of these solutions occurs often on transition to the fully ordered crystal, giving rise to quite complicated phase diagrams102). 

The conditions for surfactants to be useful to form liquid crystals exist when the cross-sectional areas of the polar group and the hydrocarbon chain are similar. This means that double-chain surfactants are eminently suited, and lecithin (qv) is a natural choice. Combinations of a monochain ionic surfactant with a long-chain carboxylic acid or alcohol yield lamellar liquid crystals at low concentrations, but suffer the disadvantage of the alcohol being too soluble in the oil phase. A combination of long-chain carboxylic acid plus an amine of equal chain length suffers less from this problem because of extensive ionization of both amphiphiles. 

Phase diagrams of water, hydrocarbon, and nonionic surfactants (polyoxyethylene alkyl ethers) are presented, and their general features are related to the PIT value or HLB temperature. The pronounced solubilization changes in the isotropic liquid phases which have been observed in the HLB temperature range were limited to the association of the surfactant into micelles. The solubility of water in a liquid surfactant and the regions of liquid crystals obtained from water-surfactant interaction varied only slightly in the HLB temperature range. 

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