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  • Polymer and Materials Science  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 15 (1994), S. 31-36 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the present work, a comparative study of the dynamic mechanical and dielectric properties of two related polymers, poly(pentachlorophenyl methacrylate) (PPCPM) and poly(phenyl methacrylate) (PPhM), was carried out. In both polymers a similar relaxational behaviour was observed. Dielectric relaxation measurements give an improved resolution as compared with that obtained from dynamic mechanical techniques for a given process. The polymers show a secondary loss peak at approximately room temperature and a prominent peak overlapped with the conductivity electrode polarization contributions at temperatures above the glass transition temperature, studied by dielectric relaxation measurements. The activation energy associated with the relaxation process at low temperature is about 77 kJ · mol-1 (which is similar to that observed in poly(alkyl methacrylates)) whose origin is attributed to the hindered partial rotation of the carboxymethyl group. An improved method of separating dipolar contributions from the non-dipolar ones was used to characterize the high temperature relaxation process and to obtain information from the diffusion coefficient of the conducting species.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0959-8103
    Keywords: chlorinated polyethylene-polypropylene copolymers ; dynamic dielectric properties ; Fuoss-Kirkwood and Havriliak-Negami empirical equations ; 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: Dielectric relaxation measurements were carried out on eight chlorinated polyethylene-polypropylene (PEPP) copolymers in the range of temperatures covering the main dielectric absorption. Chlorination of PEPP is expected to change the dynamic dielectric properties gradually with increasing amount of chlorine in the polymer chains. Thus, in the present study, increasing degrees of chlorination give a clear shift of the glass transition temperature towards higher values, except in the range between 40 and 51% chlorine, where an anomalous behaviour was observed. The same tendency is also observed in the relaxation strength (Δ∊). The value of Δ∊ has been estimated by using a nonlinear squares regression program (LEVM6) to calculate the parameters of the Havriliak-Negami empirical equation. It appears reasonable to assume that the anomalous behaviour observed can be attributed to a compensation of the dipolar moments of chlorine groups in the macromolecules.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 196 (1995), S. 3789-3796 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of thermal treatment and subsequent chemical structural modifications on the viscoelastic and dielectric properties of PMCPI (poly(monocyclopentyl itaconate)) was studied. The low temperature relaxation (γ-relaxation) is unaffected by the thermal history or chemical modifications. The intermediate relaxation (β-relaxation) is shifted by about 40°C to higher temperature after thermal treatment. The α-relaxation (related to the glass transition temperature Tg) suffers more striking changes when moving to higher temperatures.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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