Tuning the intermolecular dative interactions in vanadium-oxo linear chain compounds: formation of a new type of liquid crystalline polymer. [Erratum to document cited in CA116(12):117814y]

1993 ◽  
Vol 115 (24) ◽  
pp. 11656-11656 ◽  
Author(s):  
Andre Serrette ◽  
Patrick J. Carroll ◽  
Timothy M. Swager
Keyword(s):  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Linear Chain ◽  
Crystalline Polymer ◽  
New Type ◽  
Chain Compounds

Synthesis and Performance of a Novel Coumarin-Containing Side-Chain Liquid Crystalline Polymer

2011 ◽  
Vol 181-182 ◽  
pp. 197-200
Author(s):  
Yu Lei Zhao ◽  
Wei Min Zhang ◽  
Ji Lei Li ◽  
Fan Fan Yu ◽  
Jia Ling Pu
Keyword(s):  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Crystalline Polymer ◽  
Liquid Crystalline Polymers ◽  
Side Chain ◽  
Polarized Optical Microscopy ◽  
Crystalline Polymers ◽  
New Type ◽  
And Performance ◽  
Thermal Stability Of

A new type of able liquid crystalline polymer with a coumarin-containing mesogenic side group that could be photo-crosslinked was synthesized in this paper. The structure of the intermediates, monomers and polymers were characterized with FTIR and 1HNMR measurement. DSC, TG, and hot stage polarized optical microscopy were employed to study the phase transition temperature, mesophase texture, and thermal stability of the liquid crystalline polymers. The results indicated that both the monomer and polymer exhibited liquid-crystalline features over a wide temperature range.

Recognition of a new type of main chain liquid-crystalline polymer: poly(1-olefin sulfones)

1993 ◽  
Vol 26 (16) ◽  
pp. 4192-4195 ◽  
Author(s):  
Narendra N. Dass ◽  
Richard W. Date ◽  
Allan H. Fawcett ◽  
John D. McLaughlin ◽  
Olumide A. Sosanwo
Keyword(s):  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Main Chain ◽  
Crystalline Polymer ◽  
New Type

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.

scholarly journals Fiber Formation and Structural Development of HBA/HNA Thermotropic Liquid Crystalline Polymer in High-Speed Melt Spinning

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1134
Author(s):  
Bo Seok Song ◽  
Jun Young Lee ◽  
Sun Hwa Jang ◽  
Wan-Gyu Hahm
Keyword(s):  
Mechanical Properties ◽  
Shear Rate ◽  
High Speed ◽  
Melt Spinning ◽  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Crystalline Polymer ◽  
Fiber Formation ◽  
Structural Development ◽  
Thermotropic Liquid Crystalline Polymer

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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