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  • Physics  (56)
  • 2015-2019
  • 1975-1979  (56)
  • 1950-1954
  • 1940-1944
  • 1930-1934
  • 1925-1929
  • 1978  (56)
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  • 2015-2019
  • 1975-1979  (56)
  • 1950-1954
  • 1940-1944
  • 1930-1934
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  • 11
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 667-678 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Three of the Poisson's ratios have been measured on a low-density polyethylene (LDPE) sheet with parallel lamellas morphology over the temperature range from +20 to -60°C. The measurements were carried out using a specially constructed lateral extensometer which utilized the Hall effect to detect the very small strains involved. The Poisson's ratios show considerable temperature dependence, and at high temperature the overall deformation approximates to pure shear as previously noted. It is suggested that this relates to the onset of the c-shear relaxation.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 12
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 989-998 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Measurements of the increase in the relative permittivity for solutions of polystyrenes, poly(p-ethoxystyrene), poly(methyl methacrylate), and poly(N-vinyl carbazole) when subjected to shear gradients are reported. The influences of such factors as shear rate, concentration, viscosity, solvent permittivity, polymer dipole moment, and polymer molecular weight on the phenomenon are described. An empirical correlation for the diverse data obtained with polystyrenes and poly(p-ethoxystyrene) has been established, but this relation does not entirely match the theoretically predicted effects. We discuss the various physical processes which may have an influence on the observed phenomenon.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 13
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1135-1138 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 14
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The storage and loss shear moduli G′ and G″ of dilute solutions of two samples of sodium poly(styrene sulfonate) with molecular weights (M) of 3.28 × 105 have been measured. The Birnboim-Schrag multiple-lumped resonator technique was used in the frequency range 100-8000 Hz, and the intrinsic moduli were obtained by extrapolation to infinite dilution. Measurements were performed over the temperature range from 1.0 to 25.0°C in aqueous solvents containing from 0 to 60% by weight glycerol and from 0.001 to 0.005M added salt. The large intrinsic viscosities indicated high extension of the polymer, and the frequency dependences of G′ and G″ were matched well by hybrid relaxation spectra combining rodlike and coil-like behavior. In a solvent containing 0.001M sodium ion and no glycerol, the end-over-end rotational relaxation times for the two molecular weights corresponded to proportionality to the 1.7 power of M. With increasing molecular weight, ionic strength, and/or glycerol concentration, the polyelectrolyte appeared to become less extended, and its behavior more nearly coil-like.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 15
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 583-597 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Millar-type interpenetrating polymer networks (IPNs) are composed of two identical networks. In the present case Millar IPNs of polystyrene/polystyrene were prepared where the crosslinker levels of the two networks differed by a factor of 10. Polymer network I contained 0.4% divinylbenzene (DVB) and polymer network II contained 4% DVB, the polymers having the following weight proportions: 75/25, 50/50, and 25/75. A single polystyrene network containing 2.2% DVB was synthesized for comparison with the 50/50 Millar IPN, both containing the same average amount of crosslinker. The creep behavior of the Millar IPNs was found to be dominated by polymer network I, as were the rubbery moduli and swelling behavior in toluene. These results suggested that polymer I domains are more continuous in space and polymer II domains are less continuous. The Donatelli equation predicted polymer II domain sizes of 60 Å to 100 Å for the Millar IPNs. Electron micrographs of specimens containing 1% isoprene in polymer II offered visual evidence for the segregation of polymer II domains from polymer I, and showed that the polymer II domains were, in fact, less continuous. Polymer II domains varied from about 50 to 100 Å in size, as predicted. These results have implications for gelation processes in general.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 16
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1515-1518 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 17
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1583-1592 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: There are several reports in the literature to the effect that when isotactic polystyrene crystallizes from moderately dilute solution, lamellas (precipitate) form at high crystallization temperatures and gels at low temperatures. We report here the occurrence of a very similar phenomenon during the crystallization of ethylene-butene-1 copolymers. The observations for the latter system can be given a straightforward explanation based on the demonstrated compositional fractionation that occurs on crystallization. Low co-unit content copolymers are associated with lamellas. Gels invariably contain much higher co-unit content. A generalization of these findings is invoked to explain the previous polystyrene results. A new resonance detected by 13C NMR experiments in this polymer can be ascribed to head-head sequences.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 18
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1947-1963 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: High-pressure CO2 sorption data in semicrystalline poly(ethylene terephthalate) (PET) are presented for temperatures ranging from 25 to 115°C. The results are described by Henry's law above the glass-transition temperature of PET, while a dual-mode sorption model comprised of a Henry's law and a Langmuir isotherm applies in the glassy state. The disappearance of the Langmuir capacity of the polymer above Tg presumably results from the elimination of regions of localized lower density which are frozen into the glass upon quenching from the rubbery state. Exposure of PET to a high CO2 pressure produced a systematic variation in the apparent sorption equilibria. Correlation of the Langmuir capacity of PET with the dilatometric parameters of the polymer provides a useful framework for understanding the origin of the Langmuir sorption mode and for interpreting annealing and conditioning effects in glassy polymers.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 19
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 2031-2047 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The hydrostatic extrusion behavior of polyoxymethylene (POM) is described. Extrusions were performed at 164°C for a range of different molecular weight grades. Excellent unflawed lengths of extrudate were obtained with axial Young's moduli, measured at room temperature, reaching values as high as 24 GPa. The extrusion characteristics are discussed in terms of the very strong dependence of the flow stress of POM on strain and strain rate and pressure. In addition to measurements of Young's modulus over a wide temperature range, data for shear modulus and transvers modulus are also presented. A limited amount of other structural measurements is presented.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 20
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 2005-2014 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: High-resolution electron microscopy studies have been carried out on four glassy polymers examined in previous small-angle x-ray scattering (SAXS) investigations. The polymers include polycarbonate, poly(ethylene terephthalate), poly(vinyl chloride), and polystyrene. For all four polymers, both bright field and dark-field observations indicate the general absence of microstructural features of a size down to the resolution limit of the electron microscope. Only “pepper and salt” features on a scale ca. 5 Å are seen as characteristic of the structures. These features reflect simple interferences as the resolution limit is approached, and are seen for single crystal and oxide glasses as well as for the polymers. The present results, taken together with structural information from light scattering, SAXS, and small-angle neutron scattering, indicate that glassy polymers should be regarded as having rendom structures. The combined results are inconsistent with heterogeneous microstructures having regions of locally high order present in large volume fractions.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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