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  • Chemistry  (13)
  • Chemical Engineering  (2)
  • 1995-1999  (2)
  • 1985-1989  (11)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 427-431 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 1889-1901 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The separation of a He—CH4 mixture containing 9.95 mol% He in permeator modules that incorporate two different types of polymer membranes was studied theoretically and experimentally. The membranes were symmetric dense capillaries of silicone rubber and asymmetric hollow fibers of cellulose triacetate. These membranes exhibit reverse selectivities for He and CH4, silicone rubber being more permeable to CH4, and cellulose triacetate more permeable to He. The simultaneous use of these two types of membranes in a permeator enhances the enrichment and recovery of He compared to the levels obtained with a single-membrane permeator utilizing either membrane alone. The experimental results were found to confirm the theoretical predictions, the agreement being better at the lower stage cuts.
    Additional Material: 11 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 31 (1985), S. 1167-1177 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Mathematical models have been developed for the separation of binary gas mixtures in permeator modules housing two different types of membranes simultaneously. The membranes are selected so as to exhibit reverse selectivities toward the components of a mixture, i.e., so that one membrane is more permeable to one of the components while the second membrane is more permeable to the other component. The mathematical models describe the membrane separation process for three kinds of flow patterns of the permeated (low pressure) and unpermeated (high pressure) gas streams in the permeator, namely, “perfect mixing,” counter-current flow, and cocurrent flow. Numerical solutions of the models indicate that the extent of separation achievable in a two-membrane permeator can be much higher than in a conventional single-membrane permeator. Also, for given product compositions, the membrane area requirements of the former permeator can be lower than those of the latter. Countercurrent flow is generally the most efficient flow pattern in a two-membrane permeator, and “perfect mixing” is the least efficient one, but the opposite is true under special operating conditions.
    Additional Material: 13 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 1209-1220 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The transport of gases in many glassy polymers can be described satisfactorily by means of a “dual-mode sorption” model. The transport behavior observed with a given gas/polymer system can be characterized by the model parameters, which are obtained from solubility measurements in conjunction with absorption/desorption or permeability measurements. The present study discusses the inverse problem, namely, the prediction of the absorption/desorption behavior of a gas in a glassy polymer from a specified set of dual-mode sorption parameters. Satisfactory agreement is obtained between reported absorption rates of sulfur dioxide in glassy polycarbonate and of water vapor in Kapton®††Trademark of E. I. du Pont de Nemours & Co. and the rates predicted by the dual-mode sorption model. This study also confirms the consistency of the model.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 2149-2166 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Permeability coefficients for Ar, SF6, CF4, and C2H2F2 (1,1-difluoroethylene) in polyethylene membranes were determined from steady-state permeation rates at temperatures from 5 to 50°C, and at applied gas pressures of up to 15 atm. The temperature and pressure dependence of the permeability coefficients was represented satisfactorily by an extension of Fujita's free volume model of diffusion of small molecules in polymers. The parameters required by this model were determined from independent absorption (diffusivity) measurements with the above gases in polyethylene rods. The present work confirms the results of previous studies with CO2, CH4 C2H4 and C3H8 in polyethylene.
    Additional Material: 8 Ill.
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  • 6
    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.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 25 (1987), S. 1263-1298 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Permeability coefficients P for He, O2, N2, CO2 CH4, C2H4, C2H6, and C3H8 in 12 different silicone polymer membranes were determined at 35.0°C and pressures up to 9 atm. Values of P for CO2, CH4, and C3H8 were also determined at 10.0 and 55.0°C. In addition, mean diffusion coefficients D and solubility coefficients S were obtained for CO2, CH4, and C3H8 in 6 silicone polymers at 10.0, 35.0, and 55.0°C. Substitution of increasingly bulkier functional groups in the side and backbone chains of silicone polymers results in a significant decrease in P for a given penetrant gas. This is due mainly to a decrease in D, whereas S decreases to a much lesser extent. Backbone substitutions appear to have a somewhat lesser effect in depressing P than equivalent side-chain substitutions. The selectivity of a silicone membrane for a gas A relative to a gas B, i.e., the permeability ratio P(A)/P(B), may increase or decrease as a result of such substitutions, but only if the substituted groups are sufficiently bulky. The selectivity of the more highly permeable silicone membranes is controlled by the ratio S(A)/S(B), whereas the selectivity of the less permeable membranes depends on both the ratios D(A)/D(B) and S(A)/S(B). The permeability as well as the selectivity of one silicone membrane toward CO2 were significantly enhanced by the substitution of a fluorine-containing side group that increased the solubility of CO2 in that polymer.
    Additional Material: 30 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 405-429 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solubility coefficients, S, and diffusion coefficients, D, have been determined for ethane and n-butane in poly(n-butyl methacrylate) (PnBMA) by the microbalance technique in the temperature range from -14 to 50°C, which encompasses the glass transition of the polymer (22-35°C). S and D for ethane were found to be independent of penetrant pressure and concentration at all temperatures studied No transition to “dual-mode” sorption behavior, as reported for a number of penetrants in glassy polymers, was observed with ethane, even at the lowest experimental temperature. Plots of log S and log D versus 1-T, the reciprocal absolute temperature, were linear for the ethane-PnBMA system and did not exhibit discontinuities in the glass transition region. The above results suggest that the same mechanism of solution and transport of ethane in PnBMA is operative both above and below the glass transition of the polymer under the experimental conditions. This behavior is attributed to the low “excess” free volume of glassy PnBMA, as indicated by the small difference between the coefficients of thermal expansion of this polymer in its rubbery and glassy states. Possible conditions for the appearance of dual-mode gas sorption are discussed. A similar study with the n-butane-PnBMA system showed that the polymer was plasticized by the penetrant below 20°C, due to the higher solubility of n-butane compared with that of ethane in PnBMA.
    Additional Material: 13 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 1887-1909 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The permeability of nine different polyimide membranes to H2, N2, O2, CH4, and CO2 has been determined at 35°C and at applied pressures of up to 9 atm. The dianhydride monomers used for the synthesis of the polymides were PMDA and 6FDA, whereas the diamine monomers were ODA, BDAF, and p-PDA. The selectivities of the 6FDA polymides toward CO2 relative to CH4 are higher than those of the PMDA polyimides at comparable CO2 permeabilities. Both types of polyimides exhibit significantly higher CO2/CH4 selectivities than more common glassy polymers, such as cellulose acetate, polysulfone, and polycarbonate. The selectivities of the PMDA and 6FDA polyimides to O2 relative to N2 are of the same magnitude and generally higher than those of common glassy polymers with similar O2 permeabilities. The polymides are more permeable to N2 than to CH4, whereas the opposite is true for many other glassy polymers. Possible factors responsible for the above behavior, such as segmental mobility, mean interchain distance, and formation of charge transfer complexes, are examined. The relevance of the study to the development of more highly gas-selective and permeable membranes for the separation of gas mixtures is also discussed.
    Additional Material: 13 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 2033-2047 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The solubility of methane, carbon dioxide, and propane in five silicone polymers was measured at 10.0, 35.0 and 55.0°C and at pressures up to 26 atm. The polymers were poly(dimethyl siloxane), poly(methyl propyl siloxane), poly(methyl octyl siloxane), poly(trifluoropropyl methyl siloxane), and poly(phenyl methyl siloxane). At a given temperature and pressure, the solubility of the penetrant gases decreases with increasing bulkiness of the polymer side chains, and with decreasing critical temperature of the penetrant. The solubility of carbon dioxide in poly(trifluoropropyl methyl siloxane) appears to be anomalously high, possibly because of specific penetrant/polymer interactions. The temperature and pressure dependence of the solubility coefficients for the penetrant/polymer systems studied are described, and different methods of correlating these coefficients are compared.
    Additional Material: 10 Ill.
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