Self-Organized Anisotropic Wrinkling of Molecularly Aligned Liquid Crystalline Polymer

Langmuir ◽  
2012 ◽  
Vol 28 (7) ◽  
pp. 3576-3582 ◽  
Author(s):  
Seock Hwan Kang ◽  
Jun-Hee Na ◽  
Sung Nam Moon ◽  
Woo Il Lee ◽  
Pil J. Yoo ◽  
...  
2018 ◽  
Vol 33 (23) ◽  
pp. 4092-4100 ◽  
Author(s):  
Jaehyun Sim ◽  
Sihwa Oh ◽  
Se-Um Kim ◽  
Kyuyoung Heo ◽  
Seung-Chul Park ◽  
...  

Abstract


1999 ◽  
Vol 559 ◽  
Author(s):  
M. Han ◽  
S. Morino ◽  
K. Ichimura

ABSTRACTPhoto-induced reorientational behavior of films of a liquid crystalline polymer with azobenzene side chains was studied by means of UV-Vis absorption spectroscopy and Fourier transform infrared transmission and reflection-absorption spectroscopy. The incident directions of light for photoisomerization played a critical role in the photocontrol of out-of-plane (three-dimensional) orientation of the azobenzenes in films. Tilted directions of the azobenzene residues were evaluated by using polarized UV-Vis absorption spectra. Photoreoriented states of azobenzene chromophores including photodichroism and tilted alignment were enhanced by successive annealing of photoirradiated films at temperatures close to the glass transition temperature of the polymer.


Soft Matter ◽  
2015 ◽  
Vol 11 (24) ◽  
pp. 4788-4792 ◽  
Author(s):  
Jun-Hee Na ◽  
Se-Um Kim ◽  
Youngjoo Sohn ◽  
Sin-Doo Lee

Self-organized wrinkling patterns were produced from a solution of reactive mesogens (RMs) in geometrical confinement. The symmetry of the geometrical constraints primarily governs the periodic wrinkling patterns of the RM in the wetting region through the relaxation of the curvature elasticity.


2021 ◽  
Author(s):  
Tengfei Miao ◽  
Xiaoxiao Cheng ◽  
Haotian Ma ◽  
Wei Zhang ◽  
Xiulin Zhu

A flexible chiral storage based on an achiral polymer system can be successfully achieved by chiral doping and covalent cross-linking.


Author(s):  
Wendy Putnam ◽  
Christopher Viney

Liquid crystalline polymers (solutions or melts) can be spun into fibers and films that have a higher axial strength and stiffness than conventionally processed polymers. These superior properties are due to the spontaneous molecular extension and alignment that is characteristic of liquid crystalline phases. Much of the effort in processing conventional polymers goes into extending and aligning the chains, while, in liquid crystalline polymer processing, the primary microstructural rearrangement involves converting local molecular alignment into global molecular alignment. Unfortunately, the global alignment introduced by processing relaxes quickly upon cessation of shear, and the molecular orientation develops a periodic misalignment relative to the shear direction. The axial strength and stiffness are reduced by this relaxation.Clearly there is a need to solidify the liquid crystalline state (i.e. remove heat or solvent) before significant relaxation occurs. Several researchers have observed this relaxation, mainly in solutions of hydroxypropyl cellulose (HPC) because they are lyotropic under ambient conditions.


1995 ◽  
Vol 60 (11) ◽  
pp. 1869-1874 ◽  
Author(s):  
Anatoly E. Nesterov ◽  
Yuri S. Lipatov ◽  
Vitaly V. Horichko

The phase separation in the blends of poly(methyl methacrylate) and liquid-crystalline polymer (copolymer of ethylene terephthalate and p-hydroxybenzoic acid) has been studied by the light scattering method and the cloud point curves have been obtained. Simultaneously some morphological features of the blends have been observed. It was found that the initial blends are in the state of forced compatibility and that thermally induced phase separation occurs by the mechanism of spinodal decomposition but presumably in the non-linear regime.


Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1134
Author(s):  
Bo Seok Song ◽  
Jun Young Lee ◽  
Sun Hwa Jang ◽  
Wan-Gyu Hahm

High-speed melt spinning of thermotropic liquid crystalline polymer (TLCP) resin composed of 4-hydroxybenzoic acid (HBA) and 2-hydroxy-6-napthoic acid (HNA) monomers in a molar ratio of 73/27 was conducted to investigate the characteristic structure development of the fibers under industrial spinning conditions, and the obtained as-spun TLCP fibers were analyzed in detail. The tensile strength and modulus of the fibers increased with shear rate in nozzle hole, draft in spin-line and spinning temperature and exhibited the high values of approximately 1.1 and 63 GPa, respectively, comparable to those of industrial as-spun TLCP fibers, at a shear rate of 70,000 s−1 and a draft of 25. X-ray diffraction demonstrated that the mechanical properties of the fibers increased with the crystalline orientation factor (fc) and the fractions of highly oriented crystalline and non-crystalline anisotropic phases. The results of structure analysis indicated that a characteristic skin–core structure developed at high drafts (i.e., spinning velocity) and low spinning temperatures, which contributed to weakening the mechanical properties of the TLCP fibers. It is supposed that this heterogeneous structure in the cross-section of the fibers was induced by differences in the cooling rates of the skin and core of the fiber in the spin-line.


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