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  • Physics  (470)
  • 1980-1984
  • 1975-1979  (470)
  • 1970-1974
  • 1975  (470)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 431-436 
    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.
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  • 2
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Partial molar excess free enthalpies (or excess chemical potentials) at infinite dilution were obtained over a large temperature range by gas chromatography. Data on n-alkenes in Apiezon M are interpreted by the Prigogine-Patterson theory; data on normal and branched alkanes in squalane and polydimethylsiloxane (PDMS) are discussed in terms of the Prigogine-Patterson theory and the solution theory of Flory, Orwoll, and Vrij. For the alkane-PDMS systems heats of dilution and partial excess heat capacity data are given.The aim of this work is to get some insight in the applicability of these solution theories to mixtures of fluids, the properties of which may slightly violate the basic assumptions of these theories. It is shown that orientational order in and a large cross-sectional chain diameter of the polymer solvent do not affect their applicability to the partical molar excess free enthalpies of apolar mixtures, whereas large dissimilarities between the force fields around the segments of the mixture components and/or dissimilar chain flexibilities detract from the applicability of these theories (alkanes in PDMS).Special attention has been paid to the effects of dissimilar size and shape of the segments of the mixture compounds on the magnitude of the interchange interaction parameter. It is shown that the multiple-connected segment model after Lichtenthaler et al. does not warrant a reliable combinatorial contribution. Comparison of the interaction parameters obtained for n-alkanes in n-alkanes, Apiezon, squalane, and polyisobutylene and for branched alkanes in squalane reveals that the magnitude of this parameter is affected by small end-effects due to the relative weakness of methyl-methylene interactions.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 437-441 
    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.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 579-597 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical properties of crosslinked SBR containing varying amounts of a glass bead filler have been studied. It is shown that the stress-strain response at a given test rate and temperature can be rationalized provided dewetting around the glass bead filler is taken into account. Direct measurements of the volume dilatation as a function of both strain and filler content have been obtained. This information in conjunction with the model proposed herein has been used to satisfactorily reproduce the stress-strain curves to strains up to about 200%. It is also shown that at the break point complete dewetting has occurred so that the rupture properties of the filled are the same as that of the unfilled gum. This was found to be true for all temperatures and rates studied.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 599-605 
    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.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 663-666 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 675-682 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the preceding paper, general equations were established for the motions of chains confined to a tetrahedral lattice. In the present paper, bond orientation correlation and autocorrelation functions are explicitly calculated for the case where only three-bond elementary motions are considered. Effects due to the chain end are analyzed and the relaxation time distribution function is established. The expressions obtained reflect the influence of the chain structure. Finally, to characterize the dynamic behavior of chains in orientation relaxation experiments, the notion of an independent kinetic segment is proposed.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 683-702 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The elastic free energy for a tetrafunctional network is here expressed as \documentclass{article}\pagestyle{empty}\begin{document}$$ G_{{\rm el}} = C_1 \left( {\lambda _1 ^2 + \lambda _2 ^2 + \lambda _3 ^2 - 3} \right) + C_2 \left[ {\left( {\lambda _1 \lambda _2 \lambda _3 } \right)^m \left( {\lambda _1 ^{ - 2} + \lambda _2 ^{ - 2} + \lambda _3 ^{ - 2} } \right) - 3} \right] - \left( {{{C_1 } \mathord{\left/ {\vphantom {{C_1 } {C_2 }}} \right. \kern-\nulldelimiterspace} {C_2 }}} \right){\rm }\ln {\rm }\left( {\lambda _1 \lambda _2 \lambda _3 } \right) $$\end{document} where λ1, etc., are the principal extension ratios relative to the state of reference (wherein 〈r2〉 = 〈r2〉0), and C1, C2, and m are arbitrary parameters. The free energy of a swollen system is taken to be the sum G = Gmix + Gel of Gel and the free energy of mixing \documentclass{article}\pagestyle{empty}\begin{document}$ G_{{\rm mix}} = RT\left[ {n_1 \ln v_1 + n_2 \ln v_2 + \bar \chi n_1 v_2 } \right] $\end{document}. Stress-strain relations and the chemical potential μ1 are derived from G as functions of the elasticity parameters C1, C2, and m, and of the thermodynamic interaction parameter χ or of \documentclass{article}\pagestyle{empty}\begin{document}$\chi = \bar \chi + n_1 v_2^{ - 1} \partial \bar \chi /\partial n_1 $\end{document}. The dilation of the semi-open system subject to deformation when exposed to diluent at fixed activity is derived as the sum of the dilation at fixed composition and the dilation due to absorption of diluent. Experiments are reported on the dependence of the equilibrium retractive force on elongation for cross-linked polydimethylsiloxanes (PDMS) exposed to benzene or hexamethyldisiloxane vapor at regulated activities. Volume fractions of samples covered the range v2 = 1.00 to v2 ≈ 0.30. With the choice of m = ½ the elastic behavior of a given polymer is well represented by one combination of values for C1 and C2 at all dilutions by either diluent. The dependence of the Mooney-Rivlin (C2) term on volume is thus established, at least for PDMS, and the scope of the semi-empirical free energy expression and its consequents is greatly enlarged. Values of χ deduced from the equilibrium swelling of the unstrained networks exposed to benzene at various activities are in excellent agreement with those obtained previously from vapor pressures and osmotic pressures on linear PDMS. The results of Allen, Kirkham, Padget, and Price on the elastic behavior of natural rubber are discussed, with particular reference to the coefficients of dilation with elongation which they determined at fixed composition. The present results lend strong support to the principle of additivity of the free energies attributable to the network and to the bulk liquid system, respectively. This principle is fundamental to the analysis of rubber elasticity.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 775-786 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relaxation modulus G(t) and the stress decay after cessation of steady shear flow were measured on concentrated solutions of polystyrenes in diethyl phthalate. Ranges of concentration c and molecular weight M of the polymer were from 0.112 to 0.329 g/ml and from 1.23 × 106 to 7.62 × 106, respectively. The relaxation spectrum H(τ) as calculated from G(t) for the solution of very high M was found to be composed of two parts. One, at relatively short times, was a broad distribution (plateau zone) with height proportional to c2. The second, at the long-time end, was very sensitive to concentration and gave rise to a maximum in H(τ) for very high concentrations. The behavior of H(τ) at long times was examined quantitatively by evaluating the longest relaxation time τ10 and the corresponding relaxation strength G10 from G(t) and from the stress decay function, on the assumption of a discrete distribution of relaxation times at long times. The longest relaxation time was approximately proportional to M3.5, even at relatively low concentrations where the zero-shear viscosity was not proportional to M3.5. The strengths of relaxation modes with the longest few relaxation times are proportional to the third power of concentration.
    Additional Material: 12 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 825-834 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: EPR and matrix ENDOR spectra have been examined for polyenyl radicals in γ-irradiated PVF, PVF2, PVC, and PMMA polymers. Proton matrix ENDOR is observed for all four polymers, and fluorine matrix ENDOR for PVF and PVF2. By line shape analysis of the ENDOR spectra obtained under comparable conditions, delocalization diameters for the unpaired electron of the polyenyl radical in each polymer are obtained. These diameters indicate extensive delocalization over 5-7 carbon double bonds for the polyenyl radicals investigated. It is suggested that these conjugated and crosslinked radiation products account for the observed nondevelopment of electron beam resist PMMA material at high radiation charge densities.
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