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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 673-679 
    ISSN: 0887-6266
    Keywords: scanning force microscopy ; hectorite ; polystyrene ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Many important layered silicate-polymer nanocomposite materials may be synthesized using an in-situ polymerization process. Using this technique, organic monomers are intercalated into the interlayer regions of the hosts, where subsequent polymerization may then occur. In this paper, we report on the in-situ polymerization of styrene in Cu(II)-exchanged hectorite thin films. Scanning force microscopy (SFM) images of the polymer surface reveal that the surface polystyrene is generally aggregated into groups of elongated strands. SFM imaging of the interclay regions, in conjunction with X-ray diffraction (XRD) and electron spin resonance (ESR) data, indicates that approximately 20-30% of these regions contain polystyrene, with minimal reduction in the majority of Cu2+ sites observed. XRD data shows little or no intercalation of the monomer into the true intergallery regions. Instead, the polymer likely forms in intercrystallite or planar defect regions. In addition, two distinct phases of polymeric material are found within these defect regions, a highly polymerized polystyrene in addition to a polystyrene form exhibiting greater material stiffness. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 673-679, 1998
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2551-2562 
    ISSN: 0887-6266
    Keywords: polytetrafluoroethylene ; virgin powder ; two-stage draw ; morphology ; tensile properties ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polytetrafluoroethylene (PTFE) virgin powder was ultradrawn uniaxially by a two-stage draw. A film, compression molded from powder below the melting temperature (Tm), was initially solid-state coextruded to an extrudate draw ratio (EDR) of 6-20 at an established optimum extrusion temperature of 325°C, near the Tm of 335°C. These extrudates from first draw were found to exhibit the highest ductility at 45-100°C for the second-stage tensile draw, depending on the initial EDR and draw rate. The maximum achievable total draw ratio (DRt, max) was 36-48. Such high ductility of PTFE, far below the Tg (125°C) and Tm, is in sharp contrast to other crystalline polymers that generally exhibit the highest ductility above their Tg and near Tm. The unusual draw characteristics of PTFE was ascribed to the existence of the reversible crystal/crystal transitions around room temperature and the low intermolecular force of this polymer, which leads to a rapid decrease in tensile strength with temperature. The structure and tensile properties of drawn products were sensitive to the initial EDR, although this had no significant influence on DRt,max. The most efficient and highest draw was achieved by the second-stage tensile draw of an extrudate with the highest EDR 20 at 100°C, as evaluated by the morphological and tensile properties as a function of DRt. The efficiency of draw for the cold tensile draw at 100°C was a little lower than that for solid-state coextrusion near the Tm. However, significantly higher tensile modulus and strength along the fiber axis at 24°C of 60 ± 2 GPa and 380 ± 20 MPa, respectively, were achieved by the two-stage draw, because the DRt,max was remarkably higher for this technique than for solid-state coextrusion (DRt,max = 48 vs. 25). The increase in the crystallite size along the fiber axis (D0015), determined by X-ray diffraction, is found to be a useful measure for the development of the morphological continuity along the fiber axis of drawn products.© 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2551-2562, 1998
    Additional Material: 13 Ill.
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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. 629-640 
    ISSN: 0887-6266
    Keywords: poly(acrylonitrile) ; two-stage draw ; morphology and tensile properties ; effect of molecular weight ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ultradrawing of atactic poly(acrylonitrile) (PAN) was investigated for a Mv series, ranging 8.0 × 104-2.3 × 106. Samples for the draw were prepared from 0.5-30 wt % solutions of PAN in N,N′-dimethylformamide. The solutions were converted to a gel by quenching from 100 to 0°C. The dried gel films were initially drawn uniaxially by solid-state coextrusion (first-stage draw) to an extrusion draw ratio (EDR) of 16, followed by further tensile draw at 100-250°C (second-stage draw). The maximum total draw ratio (DRt,max) and tensile properties achieved by two-stage draw increased remarkably with sample Mv. Other factors affecting ductility were the solution concentration from which gel was made and the second-stage draw temperature. The effects of these variables became more prominent with increasing Mv. The temperature for optimum second-stage draw increased with sample Mv. Both the initial gel and the drawn products showed no small-angle X-ray long period scattering maximum, suggesting the absence of a chain-folded lamellae structure, which had been found in our previous study on the drawing of nascent PAN powder. The chain orientation function (fc) and sample density (ρs) increased rapidly with DRt in the lower range (DRt 〈 30) and approached constant values of fc = 0.980-0.996 and ρs = 1.177-1.181 g/cm3, respectively, at higher DRt 〉 30-100. The tensile modulus also showed a similar increase with DRt. The tensile strength increased linearly with DRt, reaching a maximum, and decreased slightly at yet higher DRt. The highest modulus of 28.5 GPa and strength of 1.6 GPa were achieved with the highest Mv of 2.3 × 106. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 629-640, 1998
    Additional Material: 13 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1419-1422 
    ISSN: 0887-6266
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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