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  • Polymer and Materials Science  (8)
  • 1995-1999  (8)
  • 1930-1934
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 785-790 
    ISSN: 0887-6266
    Keywords: nylon ; nylon 13,13 ; cast film ; thin films ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Substrate-free thin film of Nylon 13,13 has been prepared continuously by casting the polymer on a water surface from m-cresol solution. The uniform thickness of film is ca. 500 A, as measured with a Profilometer. Film morphology and properties have been characterized by transmission electronic microscopy (TEM), x-ray photoelectron spectroscopy, wide-angle x-ray scattering, differential scanning calorimetry and by contact angle measurements. Results show that there is no preferential accumulation of the amide group toward the water surface. A spherulite structure exists in this film with a crystallinity of 26% by DSC. Fibers were drawn from the films which had a tensile modulus of 5 GPa, stiffer than reported for this nylon as prepared by other means. Other members of the nylon series, such as Nylon 6, Nylon 12, have also been prepared in films by the same casting method under modified conditions. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 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. 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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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2271-2289 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Steady shear viscosity, dynamic viscosity, dynamic modulus, and normal force were measured via rotational rheometry for concentrated solutions of racemic mixtures of poly(benzyl-glutamate) and poly(benzyl-D-glutamate) in m-cresol. A transition from the isotropic state to liquid-crystalline order with increase in concentration was indicated by optical anisotropy and maxima in all four material functions. This occurred at a critical concentration higher than the Flory prediction. Over a well-defined range of concentrations and shear stresses, some of the liquid-crystalline solutions exhibited negative first normal-stress differences that were not due to inertial effects.
    Additional Material: 18 Ill.
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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 16 (1995), S. 813-819 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel molecular model, the latent entanglement, is proposed to explain the relationships between ductilities of polyethylene reactor powders and different conditions of synthesis. According to Hoffman's variable cluster model, irregularities in the crystallite fold surface increase as the synthesis temperature is decreased. The concept of latent entanglement stems from the potentiality of these defects to convert into active entanglements when the involved chain segments are drawn out of the crystals.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 2167-2173 
    ISSN: 0887-6266
    Keywords: scanning force microscopy ; electric conductivity ; polyaniline ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The technique of scanning force microscopy was used to study the nanometer-scale structure of NMP cast films of polyaniline. Noncontact mode images provide direct evidence that polyaniline prepared in this form is a granular conductor. The films were found to consist of micrograins whose size and density were determined by the pH of the acid solution used to protonate the films. At pH 7, the polyaniline films exhibited a mostly disordered structure, with small 2-10 nm particles visible. Protonation at pH 5 to pH 3 resulted in partial agglomeration of the primary particles into larger bundles, with sizes up to 75 nm. Treatment in solution pHs of 2 or less resulted in films consisting of close-packed bundles of dimension 20-30 nm. The conductivity of the films exhibited a sharp rise beginning with protonation at pH 2 or less. Effective medium theory (EMT), was used to model the macroscopic conductivity of these films based on the SPM measured microscopic film structure. Using the size and size distribution of polymer micrograins or bundles in a modified EMT, we are able to obtain predicted conductivities that are close to the measured values for these films. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 8
    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.
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