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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1095-1105 
    ISSN: 0887-6266
    Keywords: NMR ; dynamics ; polyethylene oxide (PEO) ; polymethyl methacrylate (PMMA) ; polymer blend ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Longitudinal relaxation of proton magnetisation was used to characterize the molecular motions of PEO chains in compatible PEO (hydrogenated)/PMMA (deuterated) blends. Both the temperature and the PEO concentration, Φ, were varied. A maximum in the spin-lattice relaxation rate was observed and its properties were analyzed as a function of Φ. For Φ ≤ 0.50, the maximum is observed below the glass transition temperature of the blend; this shows that PEO chains dispersed in a matrix of PMMA remain highly mobile on a local scale even below Tg(Φ). A frequency-temperature correspondence procedure, applied to the measurements performed at two Larmor frequencies, 32 and 60 MHz, leads to a characteristic correlation time for PEO molecular motions. Its temperature dependence obeys a WLF free volume relation above the glass transition of the blends. The PEO free volume fraction and its thermal expansion are strongly reduced by the presence of the PMMA chains. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1095-1105, 1997
    Additional Material: 9 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 22 (1984), S. 931-955 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The transition of NMR properties from a solidlike spin system response to a liquidlike one observed on molten polymers or on concentrated solutions is analyzed to characterize the slow diffusion process of long linear polyisobutylene (PIB) chains. It is first shown that the relaxation function of the transverse magnetic component of protons linked to PIB chains obeys a superposition property when the polymer concentration is varied from 0.5 to 1.0g/cm3; this is interpreted as reflecting the applicability of the viscoelastic submolecule concept to the description of NMR properties. The transition in NMR properties is then analyzed numerically, using a model of polymer chain relaxation based on a multiple-relaxation-mode process analogous to the Rouse model. The terminal relaxation time τv1 is shown to depend upon the chain molecular weight M as M3; it is found to be equal to 8.3 × 10-2 s for molecular weight M = 2.25 × 105 and concentration c = 0.47 g/cm3 in carbon disulfide at room temperature.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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