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  • 1995-1999  (3)
  • 1965-1969
  • numerical simulation  (2)
  • ester interchange  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2307-2316 
    ISSN: 0887-6266
    Keywords: ester interchange ; small-angle neutron scattering ; poly(ethylene terephthalate) ; creep ; stress relaxation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Reported are a pair of studies exploring the possible role of transesterification during the deformation of poly(ethylene terephthalate) (PET) near its glass transition temperature. SANS experiments on PET-D/PET-H blends were carried out on films drawn according to the method of Petermann and Gohil at 70 and 90°C. In order to avoid effects of orientation on the SANS pattern, the measurements were made on liquid solutions made from the drawn material. The results show a decrease in the D-sequence length upon deformation, while the molecular weight of the chain is unchanged. This result indicates that bond exchange has taken place. Based upon the SANS results, an approximate activation energy in the 8-24 kcal/mol range is reported for bond interchange. To test the hypothesis that transesterification may play a role in the mechanical behavior of PET near Tg, creep measurements were carried out over a temperature range on either side of Tg. Activation energies obtained from time-temperature superposition shift factors showed a dual behavior: above Tg the activation energy matches those for diffusive processes in PET; below Tg the activation energy coincides with activation energies reported for exchange reactions in this material. The role of annealing prior to deformation is also reported, and it is shown that the activation energy increases rapidly with increasing annealing temperature. © 1996 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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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. 873-888 
    ISSN: 0887-6266
    Keywords: crystallization ; polymer blends ; pattern formation ; numerical simulation ; syndiotactic polystyrene ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The development of texture which exists in polymer spherulites grown from single phase melts containing an appreciable amount of noncrystallizable material was investigated. This texture generally consists of lamellar bundles separated by amorphous regions, both of which are typically 0.1-1 μm thick. A space-time finite element model previously developed by us was used to simulate the growth of a group of polymer lamellae. The model determines the impurity concentration field in the melt surrounding the growing lamellae and tracks the growth of each lamella. Important variables are the initial melt concentration of noncrystallizable material, the mass diffusion coefficient of noncrystallizable species, lamellar thickness, long period, and the rate of molecular attachment at the growth front. Under certain conditions, bundles did indeed develop during the simulations. These results were used to predict bundle thicknesses. The predictions of bundle texture were compared to actual textures observed in blends of syndiotactic and atactic polystyrene. It was found both experimentally and numerically that bundle thickness was a strong function of crystallization temperature and a relatively weak function of both the initial composition of noncrystallizable species and the degree of crystallinity of the lamellar stack. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 873-888, 1998
    Additional Material: 25 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 40 (1997), S. 2679-2692 
    ISSN: 0029-5981
    Keywords: space-time finite elements ; phase transformation ; crystal growth ; polymer blend ; numerical simulation ; Engineering ; Numerical Methods and Modeling
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: We present a space-time finite element formulation to study the cooperative growth of adjacent needle-like crystals in a two-dimensional, binary melt. It is assumed that the system is isothermal and that the compositions of the melt and the crystals are different. The growth rate of the crystals is taken to be a function of the melt composition in front of the growing crystals, and the composition of the melt as a function of space and time is determined by the diffusion equation. The positions of the growth fronts of each crystal are tracked. Good agreement is found between the numerical solution of an approximated one-dimensional problem and an analytical solution. Numerical results of the simulation of the growth of isolated and adjacent crystals are presented. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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