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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3991-4001 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Terpolymerization of tetrafluoroethylene (TFE) with propylene (P) and isobutylene (iB) by γ radiation at temperatures of -78 to 40°C, a dose rate of 5 × 104-5 × 105 rad/hr, and an iB/P molar ratio of 40/10-5/45 in the monomer mixture was carried out. Alternating copolymers of TFE and α-olefins, that is, P and iB, were formed at various monomer compositions. No crystalline structure was observed in the terpolymer obtained below an iB/P molar ratio of 15/35 in the monomer mixture but a partly crystalline order increased with the amounts of iB in terpolymer. The crystal lattice of the TFE-iB copolymer was affected by the introduction of P. The dose rate dependencies of the polymerization rate and inherent viscosity were 0.8 and -0.2, respectively. The activation energy of polymerization was 2.4 kcal/mole, and the relative reactivity ratio of iB and P for a TFE radical chain end was estimated as 4.50 by the treatment of the free propagating mechanism.
    Additional Material: 10 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 16 (1978), S. 907-914 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric properties of vinyl acetate and methyl methacrylate oligomers having chemically different end groups were compared. Dielectric measurements were carried out over the frequency range between 23 and 3 MHz and the temperature range between +50 and -50°C. The static dielectric constants of these oligomers are between 10 and 20. The relaxations were analyzed with the Havriliak-Negami equation. The dielectric properties depend on the chain end groups on the oligomers. The distribution of relaxation times of the vinyl acetate oligomers was wider than that of poly(vinyl acetate). It was concluded that two cooperative motions, that of the principal chain and that of the chain and that of the chain end group, take part in the dielectric relaxation of these short chain molecules.
    Additional Material: 6 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 17 (1979), S. 1789-1796 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric properties of low-molecular-weight propylene glycols HO—[CH(CH3)CH2O]n—H (n = 3, 4, 5) were investigated to clarify the effect of chain length on the dielectric properties. The measurement of dielectric constant and dielectric loss was carried out over the frequency range 30 Hz to 30 MHz at temperatures of -20 to -65°C. The static dielectric constants of these glycols are between 10 and 30, slightly smaller than values for the corresponding ethylene glycols of the same degree of polymerization. All of the Cole-Cole arcs, even that for pentapropylene glycol, can be represented by the empirical Davidson-Cole equation. The dielectric properties of homologous propylene glycols are compared with those for the ethylene glycols and are discussed in terms of the effects of chain length and intermolecular hydrogen bonds.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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