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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 2181-2192 
    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: Mean permeability coefficients for CH4 and CO2 (P̄CH4 and P̄CO2) in cellulose acetate (CA, DS = 2.45) were determined at 35°C (95°F) and at pressures up to about 54 atm (800 psia). The measurements were made with pure CH4 and CO2 as well as with CH4/CO2 mixtures containing 9.7, 24.0, and 46.1 mol % CO2. In the measurements with the pure gases, P̄CH4 was found to decrease with increasing pressure, as expected from the “dual-mode” sorption model. By contrast, P̄CO2 passes through a minimum and then increases with increasing pressure, probably due to the plasticization (swelling) of CA by CO2. The values of P̄CH4 and P̄CO2 determined with the mixtures containing 9.7 and 24.0 mol % CO2 decrease with increasing total pressure; this behavior is adequately described by the extended “dual-mode” sorption model for mixtures. By contrast, the values of P̄CH4 and P̄CO2 obtained with the mixture containing 46.1 mol % CO2 pass through a minimum and then increase as the total pressure is raised, probably also due to the plasticization of CA by CO2. The CO2/CH4 selectivity (≡P̄CO2/P̄CH4) of the CA membrances decreases with increasing total pressure and, at constant pressure, decreases with increasing CO2 concentration in the feed mixture. The effects of exposing the CA membranes to high-pressure CO2 prior to the permeability measurements (“conditioning” effects) on P̄CH4 and P̄CO2 have also been studied. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 965-975 
    ISSN: 0887-6266
    Keywords: solubility ; permeation ; water vapor ; polyimide membranes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Permeability, diffusion, and solubility coefficients for H2O vapor in four different 6FDA-based polyimides were determined at temperatures between 25 and 45°C and over a wide range of relative humidities. The solubility of H2O vapor in some of the polyimides studied can be described by the “dual-mode sorption” model whereas in other polyimides it is represented by the Flory-Huggins equation, which suggests that the latter polymers are plasticized by H2O. The solubility of H2O vapor in the polyimides decreases as the temperature is raised and increases with increasing polarity of the polymer. The diffusion coefficients for H2O in the polyimides studied either increase or pass through a weak maximum with increasing H2O activity, or concentration in the polymers. The latter behavior is probably due to a clustering of H2O molecules in the polyimides at higher H2O activities or concentrations. The diffusion coefficients for H2O decrease as the chain-packing density of the polyimides increases. The permeability coefficients for H2O vapor in 6FDA-based polyimide membranes either increase slightly or are constant as the H2O activity is increased. The experimental values of the permeability coefficients are consistent with the values determined from diffusion and solubility coefficients. The permeability of the polyimides to H2O vapor appears to be controlled by the solubility of H2O in the polymers. The polyimides studied exhibit a very high selectivity for H2O vapor relative to CH4, and therefore are potentially useful membrane materials for the dehydration of natural gas. ©1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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