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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 4321-4324 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 27 (1989), S. 879-892 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sorption and dilation in the system poly(ethyl methacrylate) (PEMA) and carbon dioxide are reported for pressures up to 50 atm over the temperature range 15-85°C. The sorption isotherms were obtained gravimetrically. The dilation accompanying sorption was measured directly with a cathetometer. At low temperatures the sorption and dilation isotherms were concave toward the pressure axis in the low-pressure region and turned to convex with increasing pressure. As the experimental temperature approached and exceeded the glass transition temperature of 61°C, both isotherms became convex or linear over the whole range of pressure. Partial molar volumes of CO2 in PEMA were obtained from sorption and dilation data, which were described well by the extended dual-mode sorption and dilation models developed recently. The temperature dependence of the dual-mode parameters and the isothermal glass transition are discussed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 1297-1308 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sorption of N2, O2, Ar, CH4, CO2, C2H4, and C2H6 in poly (dimethyl siloxane) liquid and rubber and the dilation of the polymers due to sorption of the gases are studied at 25°C under pressures up to 50 atm. In the liquid, the sorption isotherms for low-solubility and high-solubility gases are described by Henry's law and the Flory-Huggins equation, respectively. Gas sorption in the rubber, which contains a 29 wt % silica filler, follows the dual-mode sorption model, though marked hysteresis is observed in the sorption of O2 and CH4. The dilation isotherms increase linearly or exponentially in both polymers with increasing pressure. Considering that gas molecules adsorbed into micropores of the filler particles do not participate in the dilation, partial molar volumes of the dissolved gases in the rubber are determined from data of sorption and dilation. The values are nearly equal to the partial molar volumes in the liquid (48-60 cm3/mol).
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1177-1181 
    ISSN: 0887-6266
    Keywords: plasticization of poly(ethyl methacrylate) by dissolved argon ; poly(ethyl methacrylate) plasticization by dissolved argon ; sorption of argon in poly(ethyl methacrylate) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 281-286 
    ISSN: 0887-6266
    Keywords: poly(ethylene-co-vinyl acetate), gas sorption in ; dilation of poly(ethylene-co-vinyl acetate) due to gas sorption ; partial molar volume of dissolved gases ; thermal expansivity of dissolved gas ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sorption and dilation properties of polymer-gas systems involving poly(ethylene-co-vinyl acetate) and N2, CH4, or CO2, have been investigated at pressures up to 50 atm at temperatures of 10-40°C. Sorption isotherms for low-solubility gases (i.e., CH4 and N2) can be described by Henry's law, and those for high-solubility gas (i.e., CO2) by Flory-Huggins dissolution equation. Dilation isotherms are similar in contour to the corresponding sorption isotherms. From the obtained sorption and dilation data, partial molar volumes of the gases in the polymer were determined as a function of temperature. Thermal expansivity of dissolved CO2 molecules was estimated at ca. 2.4 × 10-3°C-1 from the temperature dependence of partial molar volume. The expansivity is smaller than that of liquid CO2 and larger than those of the polymer and organic liquids. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2027-2033 
    ISSN: 0887-6266
    Keywords: Sorption ; dilation ; diffusion ; penetrant-induced isothermal glass transition ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of a penetrant-induced isothermal glass transition on sorption, dilation, and diffusion behavior was studied in a single experimental run for CO2 in cast polybenzylmethacrylate films. The dual-mode type sorption isotherms below the glass transition temperature of the polymer changed to linear ones above a certain concentration. Meanwhile, partial molar volume of CO2 determined from the dilation of the films above the concentration gave a value very close to the one reported for rubbery polymers, and diffusion coefficients became less concentration-dependent. The results were conformable to the concept of unrelaxed volume in glassy polymers. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1049-1053 
    ISSN: 0887-6266
    Keywords: thermodynamic interaction ; Flory-Huggins parameter ; rubbery polymer ; gas ; Henry's law coefficient ; partial molar volume ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Flory-Huggins interaction parameters χ for 23 gases (He, Ne, Ar, Kr, Xe, H2, N2, O2, N2O, CO2, CH4, C2H4, C2H6, C3H6, C3H8, 1,3-C4H6, four C4H8's, n-C4H10, iso-C4H10, and n-C5H12) in five rubbery polymers (1,2-polybutadiene (PB), poly(ethylene-co-vinyl acetate)) (EVAc), polyethylene (PE), polypropylene (PP), and poly(dimethyl siloxane) (PDMS) were determined from either literature data on Henry's law coefficient and partial molar volume or those on sorptive dilation for each polymer/gas system. Values of χ for the gases increased in the order of PDMS 〈 PP ≡ PB 〈 EVAc ≡ PE. Among the gases except He and H2 whose χ values are not reliable, Ne and Xe have respectively the highest and the lowest values of χ for the polyolefins. The χ values of the hydrocarbons were compared together with previously reported χ values of n-alkanes C3-C10. The dependencies of χ upon concentration and temperature were discussed on the basis of the literature data. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1049-1053, 1997
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1695-1702 
    ISSN: 0887-6266
    Keywords: sorption ; dilation ; diffusion ; conditioning effect ; glassy polymer ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sorption, dilation, and diffusion behaviors were studied for the system of polysulfone/CO2 with regard to the effects of CO2 conditioning, i.e., exposure to high-pressure CO2. Concurrent measurements of solubility, dilation, and diffusivity were performed for polysulfone films before and after the conditioning at 25 and 50 atm. While the solubility and dilation were enhanced by the conditioning, the diffusivity appeared to be depressed. Results were analyzed on the basis of the dual-mode sorption model, with the assumption that the Henry's law dissolution was not affected by the conditioning. Consistent description was achieved then by attributing the changes to increased amount of Langmuir adsorption. The conditioning effect on the diffusivity, which had not been reported before based on CO2 sorption kinetics, suggests that the permeability of glassy polymers would not always be enhanced by the conditioning, but may also be decreased. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1695-1702, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 1715-1724 
    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 CO2 in poly(vinyl benzoate) was gravimetrically measured at pressures up to 1 atm. Sorption isotherms were determined above and below the glass transition temperature Tg from 5 to 85°C. The isotherms were analyzed by the dual-mode sorption model assuming that the plasticizing effect of sorbed CO2 is negligible at this pressure range. The solubilities and Henry's law dissolution parameters were compared with those obtained by the high-pressure sorption and permeation measurements. Henry's law dissolution parameters were in good agreement with one another. However, the solubilities first determined here were smaller than those determined by the high-pressure sorption experiment at the same temperature. It was clear that the Langmuir capacity of the present specimen was smaller in spite of similar high-pressure CO2 exposure. Relaxation of the polymer was expected to be one of the reasons. This expectation was confirmed from the observation and analysis of sorption isotherms after two kinds of treatments. After annealing above Tg, the Langmuir capacity was shown to be decreased to 1/2 or even to 1/3 from the sorption isotherms below 45°C. This means that the conditioning to the high-pressure CO2 surely has a large effect on the nature of glassy polymer. Just after high-pressure CO2 exposure at 25°C, increased solubility was observed. Furthermore, the slow decrease of solubility, that is, the decrease of conditioning effect, was also followed from the continual measurements at 25°C. This result reflects not only the characteristic of sorption capacity after high-pressure CO2 exposure, but also the relaxation of polymer in glassy state.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 945-950 
    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 effect of pressure on gas permeability of a rubbery polymer, 1,2-polybutadiene, is investigated for 15 gases with various molecular sizes and solubilities in the ranges of pressure up to 110 atm at 25°C. The permeability for slightly soluble gases (He, Ne, H2, N2, O2, and Ar) decreases with increasing pressure, and that for soluble gases (CH4, Kr, CO2, N2O, C2H4, Xe, C2H6, C3H6, and C3H8) increases with increasing pressure. Logarithms of permeability coefficient versus feed-gas pressure for the slightly soluble gases, CH4 and Kr, is linear within each pressure range, whereas such plots become convex toward the pressure axis for more soluble gases, such as CO2, N2O, C2H4, Xe, C2H6, C3H6, and C3H8. By analyzing the pressure dependence of permeability using sorption data of the gases, contributions of concentration and hydrostatic pressure to the gas diffusivity are estimated. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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