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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1481-1495 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It has been shown that sorption equilibrium in the system polymer-mixed solvent and the total sorption as one of its manifestations can be derived from osmotic equilibrium. The equilibrium relation for the dependence of the osmotic pressure II (as the potential for total sorption) on the composition of the ternary polymer-containing phase also includes the preferential sorption ε. This complication leads to difficulties in the analysis of the dependence of II on composition: for this reason, analysis has been limited to the case of a very dilute polymer phase. If preferential sorption is neglected, the occurrence of an extremum on the curve representing the dependence of the total sorption on the composition of the mixed solvent is affected by the Flory-Huggins parameters as in the occurrence of an inversion in preferential sorption, with the exception that in the former case the difference in the molar volumes of the solvent components contributes a term smaller by a factor of two. In the general case, however, the contribution of preferential sorption to the osmotic pressure (which has always a negative sign) also plays its role. Consequently, while total sorption, at a low preferential sorption and at a large positive value of the solvent-solvent interaction parameter χ12, can exhibit a maximum, a larger preferential sorption can overcompensate the effect of the parameter χ12, so that a minimum appears. The coexistence of a minimum with a maximum on the same curve is possible in some cases with positive χ12. The latter theoretical predictions have not yet been confirmed experimentally. At a negative χ12 the extremum is always a minimum.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1467-1480 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Osmotic and sorption equilibria in the system polymer-binary solvent can be represented with advantage in coordinates (u1, v3), where v3 is the volume fraction of the polymer and u1 gives the composition (volume fraction) of the binary solvent in the polymer phase. The coexistence lines and osmotic isobars are plotted; the former are used to read the preferential sorption ε of one of the solvent components in the polymer. The newly formulated equilibrium condition for the preferential sorption is applied to the Flory-Huggins theory extended by the ternary interaction parameter χT. This is used as a starting point for analyzing the conditions under which inversion of preferential sorption takes place, i.e., the sign of ε changes. The existence of inversion and the course of the inversion line in the v3 versus u1 plot are affected in a decisive manner by the extent to which the effect of the mutual interaction of solvent components prevails over the effect of the relative difference between their molar volumes and of the difference in strength of their interaction with the polymer. The effect of the ratio of molar volumes upon the preferential sorption increases with the concentration of the polymer, so that for v3 not too far from unity the component having the smaller molecule is necessarily sorbed preferentially. If, therefore, both types of small molecules are not of the same size, the inversion vanishes for large v3 even in systems where it actually occurs if v3 is small. On the contrary, the same effect can in other cases have as its consequence an inversion at moderate values of v3, even if it does not appear as v3 approaches zero; a similar effect can also be produced by a nonzero value of the interaction parameter χT. The neighborhood of the inversion line can have a “divergent” or a “convergent” character, depending on whether the component being preferentially sorbed is that present in excess. The former case is observed with negative and the latter for the positive values of the binary solvent-solvent interaction parameter χ12. The inversion with the divergent neighborhood has not yet been confirmed experimentally, owing to the small number of systems investigated.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 151-157 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The problem of the segregation of subchains in an isolated molecule of an A-B block copolymer is closely related to that of the mutually excluded volume of two chemically differing macromolecules. Therefore, by resorting to the “segment cloud” model used by Flory and Krigbaum to calculate the excluded volume, it was possible to derive an expression for the number of contacts between the two blocks in the same molecule. From the results of the calculation it follows that only partial block segregation can be expected unless the condensation of one of the subcoils to a dense globule occurs, owing to the effect of a poor solvent quality.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 181-184 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
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  • 5
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heats of mixing of methanol with butyl isobutyrate and with oligomers of butyl methacrylate (monomer to tetramer) having a butoxyl group on one chain end have been measured. To discuss the effect of hydrogen bonding on the heat values, it is appropriate to correlate the heat per mole of binding sites with the binding site fraction. This dependence can be described by a single curve for all oligomers studied, in contrast to the results obtained in a previous paper for the same oligomers with chloroform. This fact suggests that the binding parameters for methanol are not influenced by the degree of polymerization.
    Additional Material: 2 Ill.
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  • 6
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Abhängigkeit der bevorzugten Sorption von der Zusammensetzung des Lösungsmittelgemisches im System Tetrachlormethan-Methano-Polymethylacrylat wurde gemessen. Diese Abhängigkeit wurde unter der Voralussetzung Korreliert, Daß der Parameter der ternären Wechselwirkung dem der binären Wechselwirkung der niedermolekularen Komponenten proportional ist. Die Beziehung zwischen der gemessenen und einer analogen Abhängigkeit im System Tetrachlormethan -Methanol-Polymethylmethacrylat wird diskutiert.
    Notes: The dependence of preferential sorption on the mixed solvent composition was measured for the system tetrachloromethane-methanol- poly(methyl acrylate). A correlation method was applied to the experimental data assuming the ternary interaction parameter to be proportional to the parameter of the binary interaction of the low-molecular-weight components. A comparison of the measured dependence with an analogous one for the system tetrachloromethane-methanol-poly(methyl methacrylate) is also discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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