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  • 1
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 427-431 
    ISSN: 0887-6258
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 2181-2192 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: 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.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 38 (1989), S. 2131-2147 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Permeability coefficients, P̄, for NH3 AND H2S in 11 different types of silicone membranes were measured in the temperature range from 10.0 to 55.0°C and at pressures up to 115 psig (∼ 7.8 atm). The values of P̄ for NH3 and H2S in different silicone polymers decrease considerably as the bulkiness of the functional groups in the side and backbone chains of these polymers increases. the substitution of Si—O bonds with stifer Si—C bonds in the backbone chains also results in a considerable decrease in gas permeability. the values of P̄ for NH3 and H2S increse exponentially with incresing δp, the pressure difference across the membrancs. The temperature dependence of NH3 and H2S varies greatly: P̄ can increase, decrease, or pass through a minimum with increasing temperature, depending on the nature of the silicone polymer. The temperature dependence of P̄ is also affected in some cases by Δp. The permeability behavior of silicone polymers to NH3 and H2S is compared with that to other penetrant gases, and the factors which might affect this behavior are discussed.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 1889-1901 
    ISSN: 0001-1541
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: 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.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 31 (1985), S. 1167-1177 
    ISSN: 0001-1541
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: 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.
    Zusätzliches Material: 13 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 27 (1989), S. 1209-1220 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Zusätzliches Material: 7 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 27 (1989), S. 205-222 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The effects of plasticization on the transport of gases and vapors in and through glassy polymers are examined from the viewpoint of the “dual-mode” sorption model with partial immobilization. The analysis assumes the existence of two penetrant populations with different mobilities in the Henry's law and Langmuir domains of the glassy polymers. These mobilities are characterized by their mutual diffusion coefficients DD and DH. The plasticization of the polymer by penetrant gases is reflected in the concentration dependence of DD and DH. Expressions for the effective (apparent) diffusion and permeability coefficients are derived assuming that DD and DH are exponential functions of the penetrant concentration in the polymers. The results of this study are compared with a similar analysis which assumed the existence of a single mobile penetrant population. The present analysis provides information on the effects of plasticization on the penetrant transport in the Henry's law and Langmuir domains separately. The effects of antiplasticization or clustering of penetrant molecules on the effective diffusion and permeability coefficients are also examined.
    Zusätzliches Material: 11 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 24 (1986), S. 2149-2166 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Zusätzliches Material: 8 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 25 (1987), S. 1263-1298 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Zusätzliches Material: 30 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 405-429 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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