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  • Physics  (87)
  • 1995-1999  (35)
  • 1965-1969  (52)
  • 1940-1944
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 1203-1221 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper deals with some new methods for synthesis of the polymeric semiconductors by conjugated reactions and also with electrophysical properties of the polymers. Elimination of hydrogen halides from α,β-dihalo derivatives by bases (calcium oxide or tertiary amines) yields polymers with conjugated bonds. The reaction proceeds at 200-300°C. under atmospheric or elevated pressures, acetylenes being the intermediates. α,β-Dihalo compounds with calcium carbide above 150°C. produce polyacetylenic copolymers by elimination of two moles of hydrogen halide, also by generating acetylene from calcium carbide. The identical reaction (elimination of water) was observed between carbonyl compounds and calcium carbide. Elimination of water from monoand bifunctional phenols in the presence of zinc chloride under pressure above 200°C. yields polyphenylenes and polyhydroxyphenylenes, dehydrobenzene (benzyne) and hydroxybenzyne being intermediates. The polyhydroxyphenylenes prepared have a degree of polymerization from 4-5 to several thousand and are of interest as intermediates for thermostable resins, inhibitors etc. Linear polycyanamide and polycyanic acid were first prepared by polycondensation of urea with ammonium bicarbonate in the presence of zinc chloride. Analogous polymers were obtained from the ring-opening polymerization of melamine and cyanuric acid. The polymers show good semiconductor and ion-exchange properties. Polycondensation of ketones with ammonium bicarbonate also gave conjugated polymers. Thus, organometallic polymers were prepared from acetyl- and diacetyl ferrocene. We have also studied electrophysical, magnetic, and catalytic properties of the conjugated polymers prepared by the new methods. The electrical conductivity of the best specimens ranged from 10-3 to 10-6 ohm-1 cm.-1; the number of electrons unpaired was 1018-1019 spins/g.
    Additional Material: 1 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 639-653 
    ISSN: 0887-6266
    Keywords: plasticized ethyl cellulose ; sorption and diffusion coefficient of oxygen ; degree of substitution ; plasticizer content ; cohesive energy density ; unoccupied volume and partition of ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Plasticized films cast from ethyl cellulose were examined to evaluate the effect of the degree of substitution, DS, and the plasticizer content on the sorption and diffusion of oxygen. Sorption and permeation measurements were performed over a temperature range of 25-65°C on three different types of ethyl cellulose in the DS range 1.7-2.5 that had been plasticized with organic esters of comparatively low molecular weight. Sorption coefficients were determined by the pressure decay method, and permeability coefficients were measured independently according to ASTM D-1434-66. The diffusion coefficients were calculated assuming Fickian transport, and were compared to the values directly obtained from the evaluation of the sorption kinetics. The permeability coefficient indicates that there is a significant improvement of the barrier properties of the materials when the DS is reduced and when the plasticizer content is at the absolute minimum required. It was found that the variation in the magnitude of the permeability coefficient is related to the value of the diffusion coefficient, which is governed by the chemical composition of the mixtures. In contrast, the solubility of oxygen was determined by the physical state of the polymer matrix and increased rapidly at temperatures significantly below the glass transition temperature. Using an ergodic model, the diffusion coefficients obtained were related to the size distribution of microvoids in the materials and relative values for the diffusion coefficient were computed as a function of DS and temperature. The model calculates the concentration (number per volume) of voids that are large enough to be occupied by a penetrant molecule. It was assumed that the unoccupied volume fraction as a function of the cohesive energy density follows a Boltzmann distribution. The cohesive energy density and the unoccupied volume fraction of the polymer-plasticizer mixtures were calculated by fitting the Simha-Somcynsky equation of state to pressure-volume-temperature data. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 639-653, 1997
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 2147-2157 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The equations characterizing the temperature dependence of the mobility of molecules in the glass transition region are compared and analysed. A relationship between the parameters of the relaxation theory of the glass transition and the concept of free volume is established. The Williams-Landel-Ferry equation is treated in terms of the relaxation theory of glass transition.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1083-1091 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements have been made of the anisotropy of viscoelastic behavior in cold-drawn low-density and high-density polyethylene sheets. In the low-density polymer the β transition was shown to be highly anisotropic, maximum losses corresponding to shear on planes containing the axis of drawing and on planes perpendicular to this axis. In high-density polyethylene the α transition shows anisotropy.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 747-748 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 5 (1967), S. 1119-1144 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Experimental data obtained from stress-strain curves of five different textile fibers, at a series of different, constant strain rates covering a range of 61/2 decades have been used to study two methods of nonlinear viscoelastic analysis proposed elsewhere. According to the first of these, time and strain effects are factorizable so that stress σ, strain ε and time t are related by the equation σf1(ε)/ε = f(t),. This is shown to be unsatisfactory with the present materials, but an empirical modification to σf1(ε)/ε = f2(ε) + f(t) is satisfactory. According to the second, general nonlinear viscoelastic behavior can be described by an equation which reduces to the form σ/ε = F1(t) + εF2(t) + ε2F3(t) + when applied to extension at a constant strain rate. This series is shown to be strongly divergent except at fairly small stains. In fact, if it is truncated after about three terms, which are as many as can be estimated with any significance in the present experiments, it is applicable only to strains of about 3-4% and less. Numerical techniques which enable standard statistical procedures to be used have been devised to perform the above analyses and are described in detail.
    Additional Material: 19 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 2067-2070 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1785-1809 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Infrared spectroscopic studies have been made of mixed crystals of linear polyethylene and perdeuteropolyethylene. On the basis of normal vibration analyses by Tasumi and Krimm it had been shown that the study of crystal splittings of internal chain modes in such mixed crystals could provide information on the geometry of chain folding. The present results, which include a study of n-paraffin (C36) mixed crystals, confirm these predictions. They show that (110) folding predominates in dilute solution grown crystals, and that this is transformed to (200) folding in melt-crystallized polymer. Folding with adjacent re-entry is favored, a random re-entry model being clearly eliminated.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 5 (1967), S. 1055-1059 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method of evaluating osmotic coefficients of polyelectrolyte solutions is suggested for systems in which a two-phase equilibrium is maintained between the polymer solution and a polymer precipitate so that the “polymer” terms Cpdμp in the Gibbs-Duhem relationship may be neglected. The method is applied to a polybase system, and the osmotic coefficients calculated from the experimental data are discussed in terms of the theory of Alexandrowicz. The results are found to be in line with the above theory but the characteristic parameter φp, the fraction of free counterions, is about twice as large as values previously observed in polyacids.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 5 (1967), S. 1323-1325 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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