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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 81 (1977), S. 2185-2191 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 86 (1982), S. 5128-5133 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 69 (1965), S. 3712-3718 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1411-1412 
    ISSN: 0449-2978
    Keywords: Physics ; 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
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1797-1801 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The current theoretical treatment of diffusion of gases in glassy polymers is based on the “dual sorption” model, but also includes certain other important assumptions, at least some of which cannot be fully justified a priori. They require experimental validation, which, however, is not possible by the procedures used or proposed so far. Methods suitable for this purpose are discussed here.
    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 26 (1988), S. 1009-1020 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The present paper is concerned with a detailed examination of the formalism and the physical basis of the dual mode mobility model used for the theoretical description of gaseous transport in glassy polymers in the light of recent theoretical and experimental work. It is shown that there are no really major differences among the original formulation of the model and later variants. A major modification becomes necessary, however, if the Langmuir sorption mode is assumed to exist in the form of patches or domains extensive enough to constitute a macroscopically recognizable phase rather than in the commonly accepted from of scattered individual adsorption sites. It is shown that the proper treatment of this case reduces to the familiar dual mode mobility formalism only under certain conditions. The interpretation of the experimental results thus far available is considered in some detail, and the usefulness of each of the aforesaid approaches in this respect is discussed.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 717-725 
    ISSN: 0887-6266
    Keywords: controlled release of active agents from swellable polymer matrices ; networks, controlled release of active agents by liquid leachants from ; swellable polymer matrices, model for leaching of solutes from ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical model, which takes proper account of the simultaneous uptake of a liquid leachant by a polymer matrix and the consequent release of a bioactive or other solute incorporated therein, is presented and the kinetics of release predicted under various conditions is investigated. This model is shown to be both more rigorous and much more widely applicable than previous attempts to approach the above problem. Furthermore, it can be easily modified or extended, in accordance with the information available about any particular system. It is, therefore, expected that the model introduced here will prove useful as a basis for the design of monolithic controlled-release devices of this type or for the evaluation of the leachability of low-level and medium-level radioactive wastes “immobilized” in polymeric matrices.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2347-2356 
    ISSN: 0887-6266
    Keywords: sorption equilibria ; cellulose acetate ; disperse dye systems ; dyeing ; dye diffusion ; kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A detailed investigation of the sorption of 4-aminoazobenzene by cellulose acetate films from aqueous solution is reported. Sorption isotherms at 75 and 60°C were linear up to saturation, in agreement with previous findings that have led to the conclusion that cellulose acetate-disperse dye systems are thermodynamically ideal. Thermodynamic analysis of these data also gave results consistent with such previous findings. The isotherms for 45 and 25°C, on the other hand, exhibited increasing curvature, in line with similar recent findings for a variety of hydrophobic polymer-disperse dye systems, and consistent with the presence of some strong absorption sites. However, the situation appears to be more complex than envisaged by simple dual-mode sorption theory. Early time desorption kinetic data were found to be consistent with Fick's law, with no indication of any significant dependence of the diffusion coefficient D on concentration (in the medium- to high-concentration range) or on film thickness. On the other hand, D was affected significantly by the history of film formation, the method of introducing the dye or heat treatment of the film. The origin of these effects was traced by DSC to definite microstructural differences. Late time kinetic data deviated significantly from the theoretical predictions based on the corresponding early time data, indicating a progressive slowdown of the desorption process. The deviations in question were generally more marked at higher temperature or film thickness, or when dyeing had been effected from the vapor phase, and were attributed to slow release of strongly adsorbed dye molecules. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 2125-2136 
    ISSN: 0887-6266
    Keywords: Non-Fickian vapor sorption ; cellulosic polymers ; cellulose acetate ; viscoelastic properties ; swelling kinetics ; mechanical properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Longitudinal swelling kinetics of cellulose acetate films sorbing acetone vapor at 30°C were studied under various conditions and correlated with the corresponding sorption kinetic measurements reported in Part I. The results were analyzed in the light of (1) previous theoretical studies of simple viscoelastic polymer-penetrant model systems and (2) mechanical stress-strain data on the cellulose acetate-acetone system, which are also reported here. The conclusions drawn from this analysis confirm and/or amplify (particularly as regards the effect of longitudinal differential swelling stresses) our previous interpretations based on sorption kinetic analysis, concerning the physical nature and causes of various features of the non-Fickian kinetic behavior of cellulosic polymer-micromolecular penetrant systems. History-dependent long-term aging effects were also observed and investigated. © 1995 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 993-1005 
    ISSN: 0887-6266
    Keywords: non-Fickian ; anomalous transport ; sorption kinetics ; vapor sorption ; cellulose polymers ; cellulose acetate ; viscoelastic properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Various aspects of the kinetics of sorption of acetone vapor by cellulose acetate films at 30°C have been studied in detail, the principal aim being to understand more thoroughly the physical nature and causes of non-Fickian behavior in this and other similar polymer-micromolecular penetrant systems. Particular attention was given to the changes in sorption (including absorption, desorption, and resorption) kinetics caused by (a) systematic variation of the vapor pressure of acetone in different ways and (b) changes in membrane thickness. It has been shown that both viscous volume swelling relaxation and longitudinal differential swelling stress effects must be invoked, in order to explain fully the observed behavior. Detailed analysis of two-stage sorption kinetics indicated (1) reasonable agreement between estimates of the diffusion coefficient reported by different authors, as long as a consistent analysis of the first stage is used, although the significance of the values given is open to some doubt, because the said first stage is found not to be free of non-Fickian features; and (2) reasonable conformity of the second stage to a first-order volume relaxation process (except a long times), with a relaxation frequency strongly dependent on the width of the concentration interval covered by the sorption experiment (and hence on the applied “osmotic stress”). The close similarity of second-stage sorption to nonlinear viscoelastic creep behavior, previously found in the cellulose-water system was confirmed and is taken further here, by demonstrating semiquantitative agreement between the corresponding “elastic swelling” and mechanical bulk moduli. ©1995 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
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