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  • Polymer and Materials Science  (14)
  • 1980-1984  (14)
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Keywords
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Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 1755-1774 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The permeabilities and diffusivities of methane, ethane, propane, n-butane, and isobutane in commercially available poly(tetrafluoroethylene) (TFE) and poly(fluoroethylene-propylene) (FEP) Teflon have been measured in a Pasternak-type permeation cell. Experiments were carried out at upstream hydrocarbon partial pressures up to 50 torr (1000-60,000 ppm gas phase concentration) and temperatures from 40 to 195°C with films of 0.0508 and 0.127 mm thickness using nitrogen as carrier gas on the upstream and downstream sides of the membrane. The transient and steady-state permeation data are described well by a combination of Henry's law and Fick's law with a concentration-independent diffusion coefficient. Linear Arrhenius plots of both permeabilities and diffusivities were obtained. Linear correlations were found both between the activation energy for diffusion and the square of the gas molecule diameter, and between the logarithm of solubility at 90°C and the penetrant boiling point. Separation factors for binary mixtures of hydrocarbons were measured for TFE at 140°C and found to be similar to those predicted by individual permeabilities in most cases. Measurements with mixed gases were not made for FEP Teflon, but selectivities of FEP are expected to be similarly well described by the ratios of the pure gas permeabilities at the low partial pressures studied. The effect of annealing FEP Teflon for 24 hr at 200°C was found to produce an average of 20-30% reduction in solubility as well as a 9% increase in the activation energy for diffusion compared to as-received films. These effects are believed to be due to increased crystallinity in the sample upon annealing.
    Additional Material: 11 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2805-2809 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 209-218 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Permeabilities and diffusivities of methyl chloride and benzene vapors at low activities in FEP Teflon membranes were measured in a continuous-flow permeation cell, at temperatures ranging from 47°C to 150°C. In all cases investigated, the permeabilities and diffusivities were independent of the penetrant partial pressure, and the permeation process was well described by a Henry's law sorption-Fickian diffusion model. The activation energies for permeation and diffusion and the sorption enthalpy were respectively 34.8 kJ/mol, 50.1 kJ/mol, and -15.3 kJ/mol for methyl chloride and 49.5 kJ/mol, 69.1 kJ/mol, and -19.6 kJ/mol for benzene. The diffusional activation energies for these two substances and other low molecular weight hydrocarbons correlate reasonably well with the Lennard-Jones collision diameters of the penetrant molecules. The solubilities correlate approximately with the penetrant boiling points, but the highly polar nature of methyl chloride and the aromaticity of benzene lead to deviations between the solubilities of these substances and those of nonpolar aliphatics with the same tendency to condense from the vapor phase.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 2179-2186 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Equilibrium sorption isotherms for water vapor in commercial polyacrylonitrile film are presented. The data are discussed in terms of hte dual-mode sorption model at low vapor activities with cluster formation occuring at higher activities. The film samples were treated by a two-stage extraction process to remove a tenaciously held solvent present from the manufacturing process. Extraction of the residual had a minor effect on the equilibrium sorption of water in the film. The temperature dependence of the various sorption parameters is presented and discussed in detailed.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 159-170 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Carbon dioxide sorption isotherms in poly(methyl methacrylate) (PMMA) and poly(ethyl methacrylate) (PEMA) are reported for pressures up to 20 atm. Temperatures between 35 and 80°C were studied for PMMA and temperatures between 30 and 55°C were studied for PEMA. Typical dual mode sorption isotherms concave to the pressure axis were observed in all cases. The measured Langmuir sorption capacities of both polymers extrapolated to zero at the glass transition (Tg) consistent with the behavior of other glassy polymer/gas systems. Sorption enthalpies for CO2 in the Henry's law mode for PMMA and PEMA are in the same range (-2 to -4 kcal/mole) as has been reported for a variety of other glassy polymers such as poly(ethylene terephthalate), polycarbonate, and polyacrylonitrile. Some of the data suggest that postcasting treatment of the PEMA films left a small amount of residual solvent in the film. the presence of the trace residual solvent during quenching from the rubbery to the glassy state after annealing appears to cause a dilation of the Langmuir capacity and an alteration in the apparent Langmuir affinity constant of the PEMA film. These results suggest the possibility of tailoring physical properties of glassy polymers such as sorptivity, permeability, impact strength, and craze resistance by doping small amounts of selected residuals into polymers prior to quenching to the glassy state from the rubbery state.
    Additional Material: 10 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 1163-1175 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Sorption of pure anhydrous ammonia and pure sulfur dioxide in Kapton polymide has been measured at 30 and 35°C at subatmospheric pressures using a McBain quartz spring balance. The sulfur dioxide sorption and desorption was well described by the Fickian transport model; however, the ammonia sorption exhibited significant deviations from Fickian behavior. A substantial fraction of the initially sorbed ammonia remained in the film after extended periods under vacuum at 35°C. Infrared analysis of the treated film revealed the presence of new carbonyl and nitrogen-hydrogen stretching peaks characteristic of primary and secondary amides. These observations suggest that the ammonia reacts chemically with some of the imide linkages. Based on infrared analysis of the ammonia-exposed Kapton, heating the sample under vacuum at 120°C caused re-formation of most of the orginally disturbed imide structures, with attendant evolution of ammonia as a condensation product.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 1095-1110 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The kinetics and equilibria of benzene sorption in poly(ethylene terephthalate) were measured at 40°C, 50°C, and 60°C, with benzene activities ranging from 0.02 to 0.3. At most experimental conditions, diffusion was found to be Fickian; however, evidence of non-Fickian transport was found at the highest activity levels. Values of the diffusion coefficient of benzene range from 10-14 cm2/s at 40°C to 10-12 cm2/s at 60°C in the limit of low concentrations. Nonlinear isotherms observed for benzene sorption were successfully interpreted in terms of the dual mode model for sorption in glassy polymers, whereby the sorbed penetrant exists as two populations: one sorbed according to Henry's law and the other following a Langmuir isotherm. Non-Fickian transport data were correlated with a model that superimposes diffusion of both the Henry's law and Langmuir populations (the “partial immobilization” model) upon first-order relaxation of the polymer matrix.
    Additional Material: 12 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 1513-1530 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model is discussed which explains reported complex effects of feed composition and pressure on component permeabilities in high-pressure gas separators based on glassy polymer membranes. A special form of Fick's law which accounts for the fact that penetrants in glassy polymers sorb into and diffuse through two different molecular environments provides the basis for the analysis of gas mixture permeation. Potential deviations from the theory are discussed in terms of separable solubility-and mobility-related effects.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 753-763 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Permeability data are reported for carbon dioxide in Lexan polycarbonate at 35°C. Measurements were made for both pure carbon dioxide and for a mixed feed consisting of carbon dioxide with a 117.8-torr (0.155-atm) Partial pressure of isopentane. The effects of varying upstream CO2 driving pressure from 1 up to 20 atm were studied. The permeability to CO2 is reduced significantly in the presence of isopentane; however, the fractional depression of the CO2 permeability due to the isopentane at low driving pressures is much more significant than at high CO2 driving pressures. The well-known pressure dependence of carbon dioxide permeabilities in glassy polymers, therefore, is largely diminished by introducing isopentane to the pure carbon dioxide feed. These observations are consistent with a model for transport in glassy polymers which explains the observed trends in terms of competition between the two penetrants for microvoid sorption sites existing in the non-equilibrium glassy polymer. Exclusion of carbon dioxide from microvoid sorption sites by the more condensable isopentane preempts transport through the microvoid regions, resulting in the observed depression of the CO2 permeability.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1485-1495 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics and equilibria of SO2 sorption in Kapton polyimide film have been measured at 25°C for pressures up to 58 cm Hg using a quartz spring balance. The observed equilibria are described well by the dual-mode model for sorption of penetrants in glassy polymers. Observed hysteresis in sorption-desorption cycling indicates that the diffusivity of SO2 increases markedly with increasing local penetrant concentration in the polymer. The concentration dependence of the effective average diffusion coefficient is described well by an expression from dual-mode theory. The Langmuir component of the sorption population has an extremely low mobility compared to that of the Henry's law component; in fact, the so-called “total immobilization” limiting case, which assigns a zero diffusion coefficient to this component, appears to be satisfactory under the conditions studied. These results, coupled with published results for other penetrants, suggest that the degree of immobilization of the Langmuir population depends to a great extent on the condensability and/or the molecular size of the penetrant. Predictions of the SO2 diffusion time lag and permeability in Kapton as functions of the upstream SO2 pressure are presented and discussed in terms of the dual-mode theory.
    Additional Material: 6 Ill.
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