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  • Physics  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 14 (1976), S. 2109-2112 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 15 (1977), S. 2055-2056 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2287-2296 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dilute solution viscosity measurements of nylon-6 in molten SbCl3 reveal a polyelectrolyte effect that becomes more pronounced with increased molecular weight of the polymer sample. Intrinisic viscosities result in a relationship of [η] = 2.35 × 10-6M1.45w for nylon-6 in SbCl3 at 100°C, which indicates a high polymeric chain extension in molten SbCl3 in the limit of zero concentration. Infrared (IR) and nuclear magnetic resonance (NMR) spectra indicate that a substantial fraction of the amide groups in each polymer chain remains unaffected, whereas the rest is interacted, probably, with SbCl4-ions originating from the self-ionization of SbCl3.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2549-2565 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure of nylon 6 fibers is analyzed by x-ray diffraction. Our results suggest that only two forms of nylon 6, α and γ, along with lattice distortion and crystallite size, are sufficient to explain the whole range of crystalline structures observed in nylon 6. The γ phase is the preferred initial form in a number of nylon 6 samples. The lattice distortion of the γ form along the chain axis varies from 0.8 to 2.4%, depending on the processing conditions. Upon annealing nylon 6 fibers, the α form is produced primarily by γ-to-α conversion in high-orientation fibers, while additional α form can also crystallize from the amorphous phase in low-orientation fibers. Finally, we show that α crystallites are favored during conditioning of poorly crystallized fibers in a humid atmosphere, and therefore fibers with α as the major crystalline form are produced upon drawing these conditioned fibers. Fibers drawn without lag time contain primarily the γ phase.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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