Interfacial Tension of a Liquid Crystalline Polymer in an Isotropic Polymer Matrix

2005 ◽  
Vol 38 (17) ◽  
pp. 7343-7351 ◽  
Author(s):  
Jian Wu ◽  
Patrick T. Mather
Keyword(s):  
Interfacial Tension ◽  
Polymer Matrix ◽  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Crystalline Polymer

scholarly journals Tilted Orientation of Photochromic Dyes with Guest-Host Effect of Liquid Crystalline Polymer Matrix for Electrical UV Sensing

Sensors ◽  
2015 ◽  
Vol 16 (1) ◽  
pp. 38 ◽  
Author(s):  
Amid Ranjkesh ◽  
Min-Kyu Park ◽  
Do Park ◽  
Ji-Sub Park ◽  
Jun-Chan Choi ◽  
...  
Keyword(s):  
Polymer Matrix ◽  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Crystalline Polymer ◽  
Host Effect

scholarly journals Photo-Responsivity Improvement of Photo-Mobile Polymers Actuators Based on a Novel LCs/Azobenzene Copolymer and ZnO Nanoparticles Network

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3320
Author(s):  
Domenico Sagnelli ◽  
Marcella Calabrese ◽  
Olga Kaczmarczyk ◽  
Massimo Rippa ◽  
Ambra Vestri ◽  
...  
Keyword(s):  
Optical Properties ◽  
Polymer Matrix ◽  
Zno Nanoparticles ◽  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Polymer Network ◽  
Crystalline Polymer ◽  
Photochromic Properties ◽  
Novel Applications ◽  
Incoming Light

The efficiency of photomobile polymers (PMP) in the conversion of light into mechanical work plays a fundamental role in achieving cutting-edge innovation in the development of novel applications ranging from energy harvesting to sensor approaches. Because of their photochromic properties, azobenzene monomers have been shown to be an efficient material for the preparation of PMPs with appropriate photoresponsivity. Upon integration of the azobenzene molecules as moieties into a polymer, they act as an engine, allowing fast movements of up to 50 Hz. In this work we show a promising approach for integrating ZnO nanoparticles into a liquid crystalline polymer network. The addition of such nanoparticles allows the trapping of incoming light, which acts as diffusive points in the polymer matrix. We characterized the achieved nanocomposite material in terms of thermomechanical and optical properties and finally demonstrated that the doped PMP was better performing that the undoped PMP film.

Observing the relaxation of molecular orientation in sheared liquid crystalline polymer solutions

1990 ◽  
Vol 48 (4) ◽  
pp. 1092-1093
Author(s):  
Wendy Putnam ◽  
Christopher Viney
Keyword(s):  
Molecular Orientation ◽  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Crystalline Polymer ◽  
Polymer Processing ◽  
Molecular Alignment ◽  
Global Alignment ◽  
Shear Direction ◽  
Axial Strength ◽  
Strength And Stiffness

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.

Phase Separation in Liquid-Crystalline Copolymer/Poly(methyl methacrylate) Blends

1995 ◽  
Vol 60 (11) ◽  
pp. 1869-1874 ◽  
Author(s):  
Anatoly E. Nesterov ◽  
Yuri S. Lipatov ◽  
Vitaly V. Horichko
Keyword(s):  
Phase Separation ◽  
Methyl Methacrylate ◽  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Ethylene Terephthalate ◽  
Crystalline Polymer ◽  
Scattering Method ◽  
Thermally Induced ◽  
Poly Methyl Methacrylate ◽  
Copolymer Poly

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.

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