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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 3347-3349 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 1619-1638 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The morphology associated with the liquid-induced crystallization of poly(ethylene terephthalate) (PET) blended either with poly(tetramethylene terephthalate) (PTMT), atactic polystyrene (APS), or polycarbonate of bisphenol A (PC) was studied, along with the effects of nucleating agents and polymer molecular weight on this type of crystallization in PET. It was found that melt-mixed blends of PET and either PTMT or PC led to an apparent well-mixed, two-component material in which some copolymer formation may be in evidence judging from the material superstructure. Blending PET with APS appeared to produce distinctly phase-separated materials in which PET could be crystallized and APS dissolved out of the structure as a result of treatment of the blend with certain types of liquid. The incorporation of nucleating agents into PET was shown to measurably influence the spherulitic character of the subsequently liquid-induced crystallized polymer. Finally, it was determined that liquid-induced crystallized PET samples with number-average molecular weights of 18,000 and 30,000 had identical characteristic morphology and apparent crystallization kinetics.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1529-1544 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The diffusion of vapors and liquids which induce crystallization in initially amorphous, unoriented poly(ethylene terephthalate) (PET) films was studied. It was determined that these vapors and liquids penetrate the polymer as distinct fronts, and the kinetics of this penetration and the weight uptake kinetics both follow apparent Fickian behavior. Distinct cavitation advanced into the polymer at the penetrant front-dry polymer interface in certain PET-liquid systems, and phenomenological explanations of its existence and of the general diffusion process observed are offered. Finally, the diffusion of the highly interactive liquids dioxane and methylene chloride into cold-drawn PET was studied and shown to occur considerably more slowly than does the diffusion of these liquids into unoriented films.
    Additional Material: 15 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1545-1557 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical properties of initially amorphous, unoriented poly(ethylene terephthalate) (PET) films crystallized in acetone and dioxane at room temperature were studied under tensile testing conditions. It was found that the nature of the liquid, the morphology it induced, and its significant residual level trapped within the PET following this type of crystallization all influenced the observed mechanical behavior. Further, thermally treating PET at 70, 90, and 174°C prior to the liquid treatments appeared to inhibit the effects of the liquids on the resultant mechanical behavior. Finally, because these liquids penetrated the polymer as distinct fronts, laminate-type structures were generated in the films. It then was shown that an ideal parallel element laminate could adequately model the mechanical behavior of the films.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1559-1582 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By small-angle x-ray scattering, a systematic investigation was performed of the long spacing of poly(ethylene terephthalate) (PET) crystallized in a liquid environment. The results indicated that the measured long spacings were temperature dependent and apparently relatively insensitive to liquid type under the conditions studied. The kinetic nucleation model of polymer crystallization was found to adequately explain this dependence. The differences in the long spacings between thermal and liquid-induced crystallization were in part rationalized in terms of the suspected supercoolings involved in the respective processes. Calculation of the spherulite growth rates for liquid-induced crystallization was made on the basis of the kinetic nucleation model and the classic theory of polymer-diluent crystallization. The results were shown to agree with inferential experimental observations of these growth rates and to elucidate the physics underlying liquid-induced crystallization. Finally, use of this growth rate theory in conjunction with a previous model for overall crystallization kinetics was shown to adequately describe and predict the diffusion-limited kinetics observed experimentally for most liquid-induced crystallization situations.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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