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  • 1
    ISSN: 1435-1528
    Keywords: Vectra B950 ; thermotropic LCP ; rheology ; structure ; orientation ; transients ; dynamic moduli
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The structure changes in the start-up flow of the thermotropic liquid crystalline polymer Vectra 8950 are probed by performing transient experiments after various flow histories. The shear and normal stress growth curves of a squeezed sample and of a randomly oriented sample show a pronounced overshoot at low strains, whereas the stress growth curve of a sample pre-sheared until steady state shows a gradual increase. This first peak is associated with the re-orientation of the director into the shearing plane. All stress transients show a second broad maximum at large strains that results from the generation of a steady defect network. The effect of varying the relaxation period after pre-shearing is reflected in the appearance of two peaks in the subsequent stress growth curves. One of these peaks shifts linearly with re laxation period and the other is more or less fixed in position. The orientation of the molecules during steady shear flow is on average in the flow direction. Intermediate orientation levels may exist in the transient depending on the amount of strain. The material is able to maintain the flow-induced orientation distribution for a long time after cessation of flow. This is reflected in a similar fashion in the initial magnitudes of the stresses and the dynamic moduli after various preshear strains. Moreover, the dynamic moduli decrease with time after cessation of steady shear flow, indicating that the orientation increases during relaxation.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1528
    Keywords: Key words Vectra B950 ; thermotropic LCP ; rheology ; structure ; orientation ; transients ; dynamic moduli
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The structure changes in the start-up flow of the thermotropic liquid crystalline polymer Vectra B950 are probed by performing transient experiments after various flow histories. The shear and normal stress growth curves of a squeezed sample and of a randomly oriented sample show a pronounced overshoot at low strains, whereas the stress growth curve of a sample pre-sheared until steady state shows a gradual increase. This first peak is associated with the re-orientation of the director into the shearing plane. All stress transients show a second broad maximum at large strains that results from the generation of a steady defect network. The effect of varying the relaxation period after pre-shearing is reflected in the appearance of two peaks in the subsequent stress growth curves. One of these peaks shifts linearly with relaxation period and the other is more or less fixed in position. The orientation of the molecules during steady shear flow is on average in the flow direction. Intermediate orientation levels may exist in the transient depending on the amount of strain. The material is able to maintain the flow-induced orientation distribution for a long time after cessation of flow. This is reflected in a similar fashion in the initial magnitudes of the stresses and the dynamic moduli after various preshear strains. Moreover, the dynamic moduli decrease with time after cessation of steady shear flow, indicating that the orientation increases during relaxation.
    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 36 (1998), S. 1795-1804 
    ISSN: 0887-6266
    Keywords: poly(ether-ester) ; rheology ; multiblock copolymer ; microphase separation transition ; crystallinity ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A microphase separation transition (MST) of a thermoplastic elastomer based on soft segments of poly(tetra methylene oxide) and hard crystalline segments of poly(tetra methylene terephthalate) has been studied by means of rheological measurements, differential scanning calorimetry (DSC), and wide-angle X-ray scattering (WAXS), showing that the MST is entirely caused by melting/crystallization, and that no separate segmental mixing/demixing transition is involved. DSC and WAXS measurements show that melting starts at 190°C, leading to crystal reorganization effects up to above 200°C, and that a gradual decrease in crystallinity occurs from below 210°C up to 224°C, above which temperature no crystals are left. Rheological measurements reveal a wide MST (207-224°C) upon heating, which coincides perfectly with the melting range. From this coincidence together with the Maxwell fluid behavior directly following the MST, it is concluded that melting leads to a one-phase liquid, and that no separate segmental mixing transition occurs. Similar results are obtained upon cooling, indicating that crystallization is the driving force for phase separation and that no separate segmental demixing step precedes crystallization. The wide MST implies a large processing window over which the rheological properties change from highly elastic, with a distinct yield stress, to normal pseudoplastic, enabling application in preparation of structured blends. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1795-1804, 1998
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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