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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 554-557 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dilute solution viscosity properties of fractions of two linear and one branched sample of polyvinyl acetate in benzene and of two linear and one branched fraction in several solvents were measured at 35°C. Values of total slope, b (from plots of ηsp/c vs. c), and intrinsic viscosities were obtained under the requirement that k′ + β = 0.500 ± 0.002. Empirical plots of log b vs. log [η] gave lines which were straight within the limits of accuracy of the data. For the linear fractions in benzene, Huggins' k′ was constant and the slope of the log b vs. log [η] line was 2; for the branched fractions in benzene, k′ increased with [η] and the slope of the log b vs. log [η] line was greater than 2. The log b vs. log [η] plots form the basis for a “one-point” method for determining [η]. Consideration of these data along with results reported in the literature indicates that k′ is measurably sensitive to branching only for fractions possessing a certain minimum combination of size and complexity. However, in some cases where the variations of k′ are inconclusive, use of the slope of the log b vs. log [η] line may provide a reliable indication of branching. It was found that a comparison between the branched and linear series could also be made at constant values of [η] or b. Two linear fractions in different solvents obeyed a type of Huggins relationship in which k′ did not vary with solvent and the slope of the log b vs. log [η] line was 2. For a higher molecular weight branched fraction, however, k′ varied from solvent to solvent and the slope of the log-log plot was about 1.7. These data do not support a reference point concept of “true” intrinsic viscosity based on a simple linear relationship between b and [η]. Preliminary results dealing with the effects of the shear rate indicated that the measured viscosity properties of branched fractions may be more seriously affected by changes in shear rate than those of linear fractions.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies have been made by a sorption-desorption procedure on the diffusion of water vapor at relative humidities of from 30 to 85% into the polymers, polyvinyl acetate cellulose acetate (37.9% acetyl), cellulose nitrate (12.0% N), 6-10 nylon, and polyvinyl alcohol. Diffusion of water in polyvinyl acetate obeys Fick's law at temperatures of from 30 to 50°C. and also at 22°C., which is below the second-order transition. The energy of activation for diffusion of water into polyvinyl acetate is 15 kcal. per mole and at 40°C. the diffusion coefficient is 7 × 10-6 cm.2/min. In contrast to the results with organic vapors, the diffusion coefficient for water is found to be independent of concentration of water in the polyvinyl acetate. Similar behavior is found for diffusion of water at 40° into cellulose acetate, cellulose nitrate, and 6-10 nylon. The chief difference is that for these three polymers the diffusion departs mildly from Fick's law at the later stages of some of the sorption and desorption experiments. This generally uncomplicated diffusion of water in these three polymers contrasts with the markedly anomalous diffusion found for organic vapors such as methanol and acetone into cellulose acetate and nitrate. With polyvinyl alcohol the diffusion of water is distinctly anomalous and closely resembles the non-Fickian diffusion of organic vapors in cellulose acetate and nitrate. One consequence is that the rate of sorption and desorption of water in polyvinyl alcohol is considerably slower than in the other polymers and is also concentration dependent.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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