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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 537-551 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ion implantation of impurities into thin films of poly(p-phenylene sulfide) (PPS) is found to increase the conductivity of the material by up to 12 orders of magnitude. The increase is stable under exposure to ambient conditions, in contrast to the instability of the conductivity increases in PPS produced by chemical doping with AsF5. PPS films 0.1-0.2 μm thick are spin cast from solution onto interdigitated electrodes patterned on an oxidized silicon substrate. The room-temperature interelectrode resistance is measured as a function of implantation fluence. An estimate of film conductivity is obtained from this resistance with a simple model for the electrode and film geometry. A first experiment yielded similar conductivity increases for implantation of either arsenic or krypton. At a fluence of 1 × 1016cm-;2, which corresponds to an average impurity concentration of 2.5 × 1021cm-3, the conductivity reaches an apparently saturated value of 1.5 × 10-5 (Ω cm)-1. Infrared spectra of the films before and after implantation suggest that crosslinking may be present in the implanted films, and Auger studies show stoichiometric changes throughout the implanted layer. These results suggest that the observed conductivity changes are the result of molecular rearrangements produced by the implantation rather than the result of specific chemical doping. Specific chemical doping may, however, explain the results of a second experiment in which implantation of bromine resulted in substantially larger conductivities found to increase at an approximate linear rate from a value of 1.0 × 10-4 (Ω cm)-1 at a fluence of 1 × 1016 cm-2 to a value of 4.0 × 10-4 (Ω cm)-1 at a fluence of 3.16 × 1016 cm-2.
    Additional Material: 9 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1195-1203 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric methods have been employed to study the high-pressure behavior of a polyurethane elastomer (Solithane 113) in the vicinity of its α transition. The α-loss peak is shifted to higher temperatures and broadened somewhat with the application of hydrostatic pressure up to 6.4 kbars. The slope of Tα vs. P, or dTα/dP, obtained at low frequencies was found to be equal to dTg/dP obtained by a volumetric method. Moreover, it attained a nonzero limiting value at high pressures for each frequency tested (3 - 30,000 Hz) and the limiting value itself increased with increasing frequency from 10.5°C/kbar at 3 Hz to 18°C/kbar at 30,000 Hz. The activation enthalpy ΔH* was found to be nearly constant over the pressure range tested, but the activation volume ΔV* decreased with increasing pressure. The relation dTα/dP = T (ΔV*/ΔH*) was shown to hold for the elastomer.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1079-1090 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cellulose triacetate (CTA) forms cholesteric mesophases in trifluoroacetic acetic acid (TFA) and mixtures of TFA and CH2Cl2, 1,2-dichloroethane (1,2-DCE), and CHCl3. Cholesteric pitches and solution flow times indicate that the order of solvent powers is TFA-CH2Cl2 〉 TFA-1,2-DCE 〉 TFA 〉 TFA-CHCl3, which is the order of decreasing acidity of the solvent systems. With TFA-CH2Cl2 as solvent, the one-fourth power of the pitch varies inversely with the CTA concentration, and increases linearly with temperature. The pitch increases exponentially with time and increases faster the more acidic the solvent. In a magnetic field a cholesteric to nematic transition occurs. A minimum in solution viscosity occurs at 34% w/v of CH2Cl2 for solutions in TFA-CH2Cl2. The miscibility gap as a function of molecular weight depends on the solvent composition and is smaller the higher the acidity of the solvent. Agreement between the experimentally observed A and B points and the theoretical points is better for the Khokhlov and Semenov theory for semiflexible chains than for the original Flory theory or the Flory-Ronca modification.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 3033-3033 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 2607-2607 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    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 21 (1983), S. 1-9 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Integrated optical techniques and resonance Raman spectroscopy have been combined to investigate the intermolecular interactions at dye/polymer and dye/glass interfaces. Frequency shifts and intensity changes of bands assigned to the stretching vibrations of the bridged quinoline rings of the cyanine dye chromophore have been utilized to gain insight into the relative strength of adhesive forces at the surface. Polarized Raman measurements were made to determine the orientation of the chromophores on a poly(vinyl alcohol) surface. This was done to assess the possibility of hydrogen bond formation between the ring nitrogen atoms and the polar hydroxyl groups at the surface.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 189-195 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dilute-solution properties of six poly(tetrahydro-4H-pyranyl-2-methacrylate) (PTHPM) fractions covering the molecular weight (Mw) range 4.8 × 104 to 8.4 × 105 (Mw/Mn = 1.2-1.4) were studied in tetrahydrofuran, a good solvent, and in isobutanol, a θ solvent a t 30.5°C as determined by light scattering from the A2 vs. T plot. The unperturbed dimensions were calculated from a low-angle laser light-scattering and intrinsic-viscosity data. The results indicate that PTHPM is less extended chain than poly(cyclohexyl methacrylate) (PCyM). The higher flexibility of PTHPM parallels the lower T, (57°C) of this polymer relative to PCyM (66°C).
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 241-249 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In a search for a liquid-liquid transition in the melt of polystyrene, we have measured and analyzed a number of compression isotherms to 1800 kg/cm2 in a relevant temperature range (1.2Tg 〈 T 〈 1.4Tg). Volume data were recorded at pressure intervals of 10 kg/cm2, i.e., at pressure intervals 5-20 times smaller than used in previous work. For the analysis the data were fitted to the Tait equation. Deviations between fits and data are small, typically 0.0004 cm3/g, but nonrandom. From the absence of any systematic shifts of the nonrandom deviation patterns with temperature, we conclude that the deviations are not manifestations of a pressure-dependent liquid-liquid transition, and that there is, in fact, no evidence for the existence of such a transition in our data.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 309-317 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1563-1566 
    ISSN: 0098-1273
    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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