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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1491-1499 
    ISSN: 0887-6266
    Keywords: side-chain liquid crystalline polymers ; orientation and relaxation ; mesophase transitions ; infrared dichroism ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The orientation relaxation behavior of a stretched side-chain liquid crystalline polymer (SCLCP) on a poly(vinyl alcohol) (PVA) film under strain was investigated through infrared dichroism at temperatures near its phase transitions. We found a reorientation of the aligned mesogens over the smectic to nematic transition of the SCLCP, changing the alignment from an initially, mechanically induced perpendicular orientation to a parallel orientation with respect to the film-stretching direction. This reorientation was found to be irreversible during subsequent nematic to smectic transition, with the parallel orientation preserved. We show that it is possible to stop the reorientation process by cooling the SCLCP back to its smectic phase just before the change in the alignment direction. Moreover, this interruption can result in a stable, zero macroscopic orientation of the mesogens in the stretched SCLCP, and a subsequent heating to the smectic-nematic transition allows the reorientation process to restart and to be completed. We discuss the possible mechanisms for this mesophase transition-induced reorientation and the factors that could influence the process. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1491-1499, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 198 (1997), S. 1035-1049 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The melting behavior of two non-oriented poly(3-alkylthiophene)s (P3ATs) containing 12 and 14 carbon atoms, respectively, in the alkyl side chain was investigated by means of differential scanning calorimetry. We show that the two P3ATs display three melting endotherms after an isothermal annealing from the melt. Two of the melting peaks arise from the ordered structures which are completed in the course of the quenching of the sample from the melt, and judging from the essentially constant melting temperatures and heats of fusion, they are not influenced by the subsequent isothermal annealing conditions. On the other hand, a much slower crystallization induced by the annealing, which occurs over a wide range of temperatures, is responsible for the appearance of a third melting endotherm which is strongly dependent on the crystallization condition. We show that this secondary crystallization is not a perfection of the existing ordered structures, rather it results in distinct crystals which melt at a temperature Tm slightly above the crystallization temperature Tc. Moreover, it is shown that the plot of Tm versus Tc parallels the line of Tm = Tc, and that the difference Tm - Tc increases linearly as the number of carbon atoms in the side chain decreases. On the basis of the calorimetric and X-ray diffraction measurements, it is suggested that the secondary crystallization originates from the alkyl side chains.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 1955-1970 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nonradiative energy transfer (NRET) method has been used to study the miscibility of polymer blends in the solid state. This can be done by labeling the polymers with fluorescence donor and acceptor chromophores. The efficiency of energy transfer, which reveals the interpenetration of the chains, is measured by following changes in the fluorescence intensity ratio of the donor and acceptor as a function of the concentration of the polymer mixture and by comparison with reference values corresponding to totally miscible and totally immiscible systems. It is shown that the reference ratio corresponding to the absence of energy transfer must be determined by using donor-labeled and acceptor-labeled polymer films, instead of making measurements in chromophore solutions in organic solvents, as has usually been done. It is also shown that fluorescence quenching is important in such studies, since it can lead to variations of the fluorescence intensity ratio by more than an order of magnitude; this factor varies with blend concentration and is particularly sensitive to the presence of halogen atoms. The NRET technique has been applied to several PVC/CPVC binary blends and to PCL/PVC/CPVC ternary blends in which PVC and CPVC were labeled by naphthalene and anthracene, respectively [PCL is poly(ε-caprolactone), PVC is poly(vinyl chloride), and CPVC is chlorinated PVC]. For binary blends, the measured intensity ratios indicate the immiscibility of PVC with CPVC, although there is nonnegligible energy transfer between the two phases. For ternary blends, the intensity ratios indicate that the addition of up to 40 wt % of PCL to the immiscible PVC/CPVC binary system leads to the formation of two coexisting PCL/PVC and PCL/CPVC phases.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 3281-3288 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermal relaxation behavior of a mechanically induced macroscopic orientation of the mesogenic groups in a side-chain liquid crystalline polyacrylate was investigated using timedependent polarized infrared spectroscopy. It was found that a complete relaxation occurred only at temperatures in the nematic to isotropic transition region, and that, more interestingly, the completely relaxed macroscopic orientation was recoverable by cooling the sample to its nematic state. This thermally induced relaxation and recovery of the macroscopic orientation was reversible upon repeated temperature changing cycles over an aging time of more than five hours. Moreover, the level of the orientation recovery was found to be sensitive to the recovery and relaxation temperatures and to the annealing duration at the relaxation temperature before cooling. A tentative interpretation is proposed for this orientation recovery.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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