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  • Artikel  (10)
  • Artikel: DFG Deutsche Nationallizenzen  (10)
  • diffusion  (10)
  • Wiley-Blackwell  (10)
  • American Ceramics Society
  • 1995-1999  (10)
  • 1985-1989
  • 1997  (10)
  • Physik  (10)
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  • Artikel  (10)
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  • Artikel: DFG Deutsche Nationallizenzen  (10)
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  • Wiley-Blackwell  (10)
  • American Ceramics Society
  • Springer  (3)
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  • 1995-1999  (10)
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  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1737-1746 
    ISSN: 0887-6266
    Schlagwort(e): free volume ; dual mode ; diffusion ; glassy polymer ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The development of a new model for the diffusion of gas molecules in glassy polymers is presented which utilizes concepts from free volume theory and relies on a dual-mode interpretation of sorptive dilation in glassy polymers. Three assumptions are made in the development of the model. First, the free volume available for molecular transport processes is taken as constant below the glass transition temperature. Second, two populations of gas molecules are assumed to exist - one which contributes to the maintenance of an iso-free volume state upon sorptive dilation and one which does not contribute owing to sorption into regions of unrelaxed volume. Third, the former population is assumed to be mobile while the latter is not. The resulting model predicts, at constant temperature, a diffusion coefficient that is independent of solute volume fraction. This is in contrast to the widely used dual-mode sorption model with partial immobilization for gas transport in glassy polymers which leads to a diffusion coefficient that is dependent on solute mole fraction through the molar gas concentration. The new model is used to interpret gas transport data from permeation experiments for carbon dioxide, methane, and ethylene in three polycarbonates. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1737-1746, 1997
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1261-1267 
    ISSN: 0887-6266
    Schlagwort(e): FTIR-ATR spectroscopy ; gravimetric sorption ; diffusion ; polymer ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In this study, vapor sorption FTIR-ATR (Fourier Transform Infrared Attenuated Total Reflectance) spectroscopy was combined with a conventional gravimetric sorption balance to examine diffusion in polymers. Mutual diffusion coefficients of methyl ethyl ketone in polyisobutylene were measured using both methods at various penetrant activities and temperatures in the range 40-60°C. Actual penetrant concentrations were determined from the sorption balance. The diffusion coefficients from the two techniques agree very well with each other. In addition, the diffusivity data from both techniques could be correlated successfully as a function of temperature and concentration with the Vrentas and Duda free-volume model. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1261-1267, 1997
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2435-2445 
    ISSN: 0887-6266
    Schlagwort(e): diffusion ; interphase ; composition profiles ; interdiffusion ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An experimental method to determine interphase composition profiles in amorphous polymers pairs and polymer-solvent pairs is presented. The method is based on the measurement of dynamic mechanical properties of slender composite beams, and well-established properties of amorphous polymer homogeneous blends and solutions. The method does not require tracers. A simple calibration procedure is included in the description, and some results for a polystyrene-polystyrene pair are used to illustrate the method application. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2435-2445, 1997
    Zusätzliches Material: 18 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2503-2510 
    ISSN: 0887-6266
    Schlagwort(e): rheology ; diffusion ; star-branched polymers ; polyisoprene ; terminal viscosity ; molecular weight dependence ; temperature dependence ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Recent experimental investigation of the terminal relaxation in high molecular weight polyisoprenes by dynamic mechanical measurements (C. A. Bero and C.M. Roland, Macromolecules, 29, 1562 (1996)) has found the terminal relaxation times to be more sensitive to changes in temperature for three-arm stars than for the linear polyisoprenes. Moreover, these measurements, carried out with significantly higher molecular weight samples than heretofore, show that the molecular weight dependence of the terminal relaxation times for three-arm star polyisoprenes is much weaker than the exponential dependence previously proposed (L. J. Fetters, et al., Macromolecules, 26, 647 (1993)). Tracer diffusion of labeled linear and three-arm star polyethylene-like diffusant molecules in a highly entangled linear polyethylene matrix exhibit temperature and molecular weight dependencies similar to those observed spectroscopically from bulk polymers. Both the temperature and molecular weight dependencies for the star-branched polymers are at variance with the predictions of the reptation model. It is shown here, however, that these observations can be reconciled through application of the coupling model of relaxation. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2503-2510, 1997
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 725-734 
    ISSN: 0887-6266
    Schlagwort(e): swelling ; sorption ; diffusion ; natural rubber ; interaction parameter ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The sorption and transport of four aliphatic hydrocarbons into natural rubber crosslinked by different vulcanization systems [conventional (CV), efficient (EV), peroxide (DCP) and a mixed system consisting of sulfur and peroxide (mixed)] were investigated in the temperature interval of 28-60°C. Of the four systems, natural rubber vulcanized by DCP exhibited lowest penetrant uptake. It was observed that the kinetics of liquid sorption in every case deviates from the regular Fickian trend, characteristic of sorption of liquids by rubbers. The diffusion coefficient, activation energy of sorption, enthalpy, entropy, and the rubber-solvent interaction parameter were evaluated for the four systems from the swelling data. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 725-734, 1997
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1043-1048 
    ISSN: 0887-6266
    Schlagwort(e): diffusion ; gold, silver ; polycarbonate ; glassy state ; free-volume theory ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Diffusion coefficients between 5 × 10-14 and 1 × 10-16 cm2 s-1 have been measured for diffusion of gold and silver in the glassy state of bisphenol trimethylcyclohexanen polycarbonate in the temperature range between Tg = 507 K and 420 K using the radiotracer technique in combination with ion-beam sputtering for serial sectioning. The Arrhenius plot exhibits a downward curvature, which is interpreted within an extension of the free-volume theory to the glassy state by Vrentas and Duda. The very small metal diffusivities in comparison to values for gas molecules of comparable size suggest substantial interaction energies. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35:1043-1048, 1997
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2083-2091 
    ISSN: 0887-6266
    Schlagwort(e): nuclear reaction analysis ; copolymer blends ; diffusion ; poly(arylether sulfone)s ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The interdiffusion and miscibility behavior of three different types of modified poly(arylether sulfone)s with deuterated poly(arylether sulfone) is studied by depth profiling using the nuclear reaction D(3He, α)p. The diffusion coefficients are found to be in the range of 10-15 and 10-14 cm2/s at 195°C. A random copolymer of poly(arylether sulfone) containing 4,4-bis-(4′-hydroxyphenyl)valeric acid units is only partially miscible with deuterated poly(arylether sulfone) when the comonomer content is 8.8 mol %, whereas blends with comonomer contents of 1.7 and 4.5 mol % are miscible as indicated by complete interdiffusion. The transition from miscibility to immiscibility is caused by repulsive interactions of copolymer segments and can be explained in terms of a mean-field theory of random copolymer blends. Also, poly(arylether sulfone)s grafted with 0.4 wt % maleic anhydride or having pyromellitic anhydride endgroups are miscible with deuterated poly(arylether sulfone)s. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2083-2091, 1997
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2397-2408 
    ISSN: 0887-6266
    Schlagwort(e): diffusion ; glassy polymers ; small molecules ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Small molecules in glassy polymers are considered to occupy sites with a distribution of free energies of dissolution. Then their diffusivity depends on concentration and temperature in the same way as it has been derived for hydrogen atoms in metallic glasses. For hydrogen it was shown that the tracer diffusion coefficient is proportional to the activity coefficient of the solute atoms. The latter can be evaluated from measured data of sorption of the small molecules in the polymer. Knowing this quantity, the thermodynamic factor can be calculated and the concentration dependence of the mutual diffusion coefficient is obtained in excellent agreement with published experimental results. New experimental results are presented for the diffusion coefficient of CO2 in Kapton and four polycarbonates (BPA-PC, BPZ-PC, TMBPA-PC, and TMC-PC) in the low CO2 pressure range of a few mbar up to 1 bar. The results are in agreement with the model developed for hydrogen. The reference diffusion coefficient, which is a fitting parameter of the model that is independent of the distribution of free energies is smallest for the polycarbonate BPZ-PC having a high γ-relaxation temperature. This correlation between the diffusion coefficient and the dynamics of the polymer can be found for other substituted polycarbonates as well. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2397-2408, 1997
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 569-585 
    ISSN: 0887-6266
    Schlagwort(e): phase inversion ; diffusion ; in situ dynamics ; membrane morphology ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The diffusion and gelation dynamics of nonsolvent-induced phase inversion in several polyethersulfone (PES)/solvent/nonsolvent systems are observed using a dark-ground optical technique. The observed dynamics are correlated with the resultant morphologies of the solidified gels obtained via scanning electron microscopy. In situ dynamic measurements show that rapid precipitations result in finger formation and delayed precipitations result in sponge formation. Rapid precipitations for some systems also exhibit an initial region of high, anomalous diffusion front motion which correlates well with the appearance of finger-like macrovoids in the film sublayer. Micrographs of both thin (200-300 μm) and thick (3 mm) films formed by liquid-liquid demixing clearly show that the overall morphologies scale with initial film thickness. However, as observed for the cellulose acetate (CA)/dimethylsulfoxide (DMSO)/H2O system, the possibility of crystallization can complicate the scaling analysis. A ternary diffusion model is also employed to describe the isothermal diffusion encountered during the formation of PES membranes. Binary thermodynamic and kinetic parameters needed for computations are determined from experimental data. Model results agree well with experimental observations. The model accurately predicts the transition from finger-to-sponge formation, as well as other observed trends in dynamics and morphology. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 569-585, 1997
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 948-951 
    ISSN: 0142-2421
    Schlagwort(e): SIMS ; thin film ; imaging ; diffusion ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: The diffusion of D2O into and through oxide films on Zr—Nb alloys was investigated using secondary ion mass spectrometry (SIMS) image analysis. In preparation for this, the microscopic structures of the oxide were studied in relation to the grain structures in the underlying alloy. On alloys containing low concentrations of niobium (1-2.5 wt.%), the oxide was found to exhibit more localized growth, particularly above grain boundaries in the alloy. Such oxide regions appeared to be considerably more porous to D2O ingress. By contrast, the oxide film on the Zr 20 wt.% Nb alloy was found to be the most resistant to D2O ingress; no local regions of higher porosity could be found. © 1997 John Wiley & Sons, Ltd.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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