Kinetic theory and simulations of active polar liquid crystalline polymers

Soft Matter ◽  
2013 ◽  
Vol 9 (21) ◽  
pp. 5207 ◽  
Author(s):  
M. Gregory Forest ◽  
Qi Wang ◽  
Ruhai Zhou
2021 ◽  
Author(s):  
Shuqi Dai ◽  
Jinxing Li ◽  
Junichi Kougo ◽  
Huanyu Lei ◽  
Satoshi Aya ◽  
...  

2004 ◽  
Vol 126 (2) ◽  
pp. 180-188 ◽  
Author(s):  
Qi Wang ◽  
M. Gregory Forest ◽  
Ruhai Zhou

The kinetic theory developed in [1] for solutions of nonhomogeneous nematic liquid crystalline polymers (LCPs) of spheroidal molecular configurations is extended to account for the translational diffusion and the related spatial density variation. The new theory augments the effect of the density variation to the intermolecular potential, Smoluchowski equation and the elastic stress. It accounts for the molecular aspect ratio as well as the finite range molecular interaction so that it is applicable to liquid crystals ranging from rodlike liquid crystals at large aspect ratios to discotic ones at small aspect ratios. It also exhibits enhanced shape effects in the viscous stress and warrants a positive entropy production, thereby, the second law of thermodynamics. Moment averaged, approximate, mesoscopic theories for complex flow simulations are obtained via closure approximations. In the limit of weak distortional elasticity, weak translational diffusion, and weak flows, the theory yields the torque balance equation of the well-known Ericksen-Leslie theory.


Author(s):  
Linda C. Sawyer

Recent liquid crystalline polymer (LCP) research has sought to define structure-property relationships of these complex new materials. The two major types of LCPs, thermotropic and lyotropic LCPs, both exhibit effects of process history on the microstructure frozen into the solid state. The high mechanical anisotropy of the molecules favors formation of complex structures. Microscopy has been used to develop an understanding of these microstructures and to describe them in a fundamental structural model. Preparation methods used include microtomy, etching, fracture and sonication for study by optical and electron microscopy techniques, which have been described for polymers. The model accounts for the macrostructures and microstructures observed in highly oriented fibers and films.Rod-like liquid crystalline polymers produce oriented materials because they have extended chain structures in the solid state. These polymers have found application as high modulus fibers and films with unique properties due to the formation of ordered solutions (lyotropic) or melts (thermotropic) which transform easily into highly oriented, extended chain structures in the solid state.


Author(s):  
Christine M. Dannels ◽  
Christopher Viney

Processing polymers from the liquid crystalline state offers several advantages compared to processing from conventional fluids. These include: better axial strength and stiffness in fibers, better planar orientation in films, lower viscosity during processing, low solidification shrinkage of injection moldings (thermotropic processing), and low thermal expansion coefficients. However, the compressive strength of the solid is disappointing. Previous efforts to improve this property have focussed on synthesizing stiffer molecules. The effect of microstructural scale has been overlooked, even though its relevance to the mechanical and physical properties of more traditional materials is well established. By analogy with the behavior of metals and ceramics, one would expect a fine microstructure (i..e. a high density of orientational defects) to be desirable.Also, because much microstructural detail in liquid crystalline polymers occurs on a scale close to the wavelength of light, light is scattered on passing through these materials.


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