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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 113-125 
    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: An attempt was made to evaluate the apparent elastic constant of a two-phase system G from those of the components of the system. The modulus G is expressed as follows: \documentclass{article}\pagestyle{empty}\begin{document}$ G = G_1 \frac{{\left( {7 - 5v_1 } \right)G_1 + \left( {8 - 10v_1 } \right)G_2 - \left( {7 - 5v_1 } \right)\left( {G_1 - G_2 } \right)v}}{{\left( {7 - 5v_1 } \right)G_1 + \left( {8 - 10v_1 } \right)G_2 + \left( {8 - 10v_1 } \right)\left( {G_1 - G_2 } \right)v}} $\end{document} where G1 and G2 are the shear moduli of the suspending medium and the suspended particles, respectively, v1 is the Poisson ratio of the medium, and v is the volume fraction of the particles. The results for modulus were extended to dynamic viscoelasticity by the corresponding principle. Experimental verifications with dynamic viscoelasticity data were conducted for the system of styrene-acrylonitrile copolymer interpolymerized with polybutadiene particles. For shear viscosity comparisons with experiment were made for the system linear polyethylene-polybutene-1.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2099-2103 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1585-1597 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to study the dielectric behavior of polyoxymethylene prepared by radiation-induced solid-state polymerization, large crystals of tetraoxymethylene (2 cm in diameter) were prepared by Bridgman's method and polymerized by γ-rays. The x-ray diffraction pattern of the polymer did not reveal the existence of a so-called amorphous region. In dielectric measurements, only one dielectric absorption was observed in the low-temperature region, while in the high-temperature region ε″ did not change up to about 120°C, where thermal decomposition started. When the specimen was stabilized by acetylating the endgroups in the solid state, ε″ did not change up to about 150°C. This dielectric absorption showed a significant anisotropy for the direction of an applied field. The dielectric absorption was much larger when the electric field was perpendicular to the fiber axis than when the field was parallel. The dielectric absorption was larger in a specimen which was estimated to be more imperfect according to DSC analysis. This leads to the conclusion that the dielectric absorption is attributable to defect regions. On the other hand, the dielectric absorption became larger with increasing numbers of terminal OH groups, and hence it is attributable to the response of the terminal OH groups. Moreover, the dielectric absorption was depressed by the acetylation of the OH groups in the solid state. It is, therefore, concluded that the dielectric absorption observed in polyoxymethylene prepared by solid-state polymerization of tetraoxymethylene is due to the response of terminal OH groups localized in defect regions. Polyoxymethylene crystallized from the melt gives an asymmetric low-temperature absorption. This asymmetry can be ascribed to the superposition of two relaxation processes. When its absorption curve is compared with that of the solid-state polymerized polymer, the low-temperature component can be assigned to crystal defects and the high temperature one to amorphous regions.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 585-594 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric measurements on poly(vinylidene fluoride) at higher temperatures result in anomalously large values of ε′ and ε″ at lower frequencies. When a static field is applied, a drastic decrease of ε′ and ε″ occurs. The effects of a static field can be summarized as follows: (1) the field effect upon ε′and ε″ is more significant at lower frequencies; (2) with increasing field strength, the rate of decrease of ε′and ε″ with time becomes greater and the ultimate values are smaller; (3) when the field is removed, ε′and ε″ recover but the ultimate recovery is incomplete; (4) the field effect depends strongly on temperature. Such behavior seems to be attributable to the displacement of ionic impurities and to their electrolysis. These results provided a method to remove the contribution of ionic impurities to ε′and ε″ and to measure the relaxation process due only to dipoles of a polymer. The application of this method revealed the dielectric high temperature absorption which had been masked by the ionic conduction in poly(vinyl fluoride).
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1177-1188 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An explicit mechanism is described for the anomalous increase in dielectric constant and dielectric loss at low frequencies and high temperatures for poly(vinylidene fluoride) containing ionic impurities. Relations are proposed for the ionic contributions, εi″ and εi″, to the dielectric constant and dielectric loss: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {\varepsilon _i ^\prime = (2v_0 q^2 /\pi ^{1/2} lkT){\rm }(D_0 /f)^{3/2} e^{ - (3Ed/2 + W/2\varepsilon 0)/kT} } \\ \\ {\varepsilon _i ^\prime = (2v_0 q^2 /kT){\rm }(D_0 f){\rm }e^{ - (Ed + W/2\varepsilon 0)/kT} } \\ \end{array} $$\end{document} where v0 and D0 are the concentration and the diffusion coefficient of the mobile ions at infinite temperature, q is the charge of an ion (in cgs electrostatic units), l is the distance between electrodes, k is the Boltzmann constant, T is the absolute temperature, Ed is the apparent activation energy for diffusion of the ions, and W is the dissociation energy of the ionic impurities. From the slopes of curves of log εT′ versus 1/T and log ε″T versus 1/T for poly(vinylidene fluoride), energies Ed = 34 kcal/mole and W = 342 kcal/mole were obtained.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 10 (1972), S. 2155-2166 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A diffusion equation for the distribution of ionic impurities in a polymer under a dc field has been solved analytically for the conditions that neither injection nor absorption of impurity ions takes place at either electrode and that the ions do not interact. By using the solution of the diffusion equation, an ionic contribution to the complex dielectric constant is calculated. The most important results are as follows. (1) At high temperatures and low frequencies, the dielectric loss factor of the polymer decreases exponentially with the time elapsed after the application of the dc bias. (2) The dielectric constant is not greatly affected by the bias. (3) The ionic contribution to the loss factor in the absence of the dc bias is represented as ∊i″ = 4πνDq2/ωkT, where ν is the density of mobile ions, D the diffusion coefficient, q the charge of an ion, ω the angular frequency, k the Boltzmann constant, and T the absolute temperature. (4) A method is presented for distinguishing between the apparent activation energy for diffusion and that for generation of mobile ions.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 10 (1972), S. 2093-2096 
    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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