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  • 11
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 18 (1955), S. 535-542 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Viscosities of polyacrylate ion in the presence of potassium bromide, sodium bromide, lithium bromide, sodium iodide, sodium hydroxide, and hydrochloride acid in aqueous solution were measured over the approximate ranges 0.0-0.6% polymer and salt up to saturation with respect to polyacrylate or to salt. The general initial effect of added electrolyte is to reduce the ratio ηsp/c and to convert the curve characteristic of polyelectrolytes into a straight line, which can be extrapolated to zero polymer concentration to given [η], the intrinsic viscosity of the polymer in the presence of excess salt. Sodium hydroxide and sodium bromide produce minima in plots of [η] against salt concentration. Sodium iodide precipitates polyacrylate at 1.5 N iodide as a translucent gel, which redissolves at 3.0 N and finally reprecipitates at 6 N. In the latter range of concentration, [η] exhibits a maximum. Both by-ions and counter-ions have specific effects on the viscosity of the polyion.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 36 (1959), S. 1-1 
    ISSN: 0022-3832
    Keywords: 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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  • 13
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The quaternization of poly-4-vinylpyridine by n-butyl bromide in tetramethylene sulfone and in propylene carbonate at 25, 50, and 75°C. begins as a simple second-order reaction with a rate constant approximately equal to that for 4-picoline. As the quaternization proceeds, the rate decreases due to the charge which is being built up on the polymer, and the quaternization of the last half of the pyridine side groups occurs at about one-tenth the initial rate. The kinetics can be summarized by the equation: \documentclass{article}\pagestyle{empty}\begin{document}$$ {{dx} \mathord{\left/ {\vphantom {{dx} {dt}}} \right. \kern-\nulldelimiterspace} {dt}} = [k_0 e^{ - \alpha t} + k_2 (1 - e^{ - \alpha t} )](A - x)(B - x) $$\end{document} where x is concentration of bromide ion at time t, A is initial concentration of butyl bromide, B is initial concentration of polymer in monomoles per liter, k0 is the initial rate constant for quaternizing isolated pyridine groups, k2 is the rate constant for quaternizing pyridine groups both of whose neighbors are already quarternized, and α is a parameter which depends on temperature, initial concentrations, and on the intrinsic rate constants. A simple graphical method is described which permits evaluation of k0, k2, and α from the data. At 25° in tetramethylene sulfone, k0 = 5.0 × 10-4 l./mole min., k2 = 5 × 10-5, and α/A = 2 × 10-4.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The osmotic pressures of two samples of poly-4-vinyl-N-n-butylpyridonium bromide (average D. P. 730 and 1900) were measured in 93% ethanol in the concentration range 0.02-0.20 g./100 cc. The osmotic pressures were higher than those of the corresponding parent polymers, due to partial dissociation of bromide ions. Because of the low dielectric constant ( ε′ = 28) of the solvent and the high concentration of positive charge in the polycations, however, a large fraction of the bromide ions (≥ 95%) were bound by electrostatic attraction to the cations and contributed neither to osmotic pressure nor to conductance. Unlike neutral polymers, the ratio (osmotic pressure over concentration) increases with dilution, due to increasing dissociation with dilution. Addition of an excess of a simple one-one electrolyte (lithium bromide) almost completely suppressed the dissociation of the polysalt and gave osmotic pressures of the same order of magnitude as those of the neutral polymers. The resulting curves were linear, with a considerably smaller slope than for the parent polymer. Combining the results on osmotic pressure with conductance data, the transference numbers of the polycations were estimated to be 0.28 and 0.52 for degrees of polymerization 730 and 1900 respectively. The conductance of lithium bromide is decreased by the addition of these polyelectrolytes, possible due to the association of an excess of anions to the polycations under the influence of their electrostatic fields.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 6 (1951), S. 305-317 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 12 (1954), S. 185-198 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 17
    ISSN: 0022-3832
    Keywords: 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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  • 18
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly-4-vinylpyridine was precipitated from a toluene solution of the monomer after addition of benzoyl Peroxide. The sample used in these experiments had a molecular weight of 77,000, (DP 730) as determined by osmotic pressure in alcohol solution, and an intrinsic viscosity of 0.36 in this solvent. The hydrochloride is water soluble and behaves like the salt of an extremely weak base with an over-all average base dissociation constant of 0.011 × 10-9, about one thousandth that of 4-ethylpyridine. The decrease in apparent base strength is ascribed to the chain structure which produces high local concentrations of pyridine groups, independent of the total concentration. By addition of butyl bromide to the polymer in nitromethane, a long chain quaternary ammonium salt is formed which is also water soluble. Its conductance is not sensitive to concentration down to about 0.003 N, after which the conductance rises sharply with further dilution. Dissociation, calculated by the classical Arrhenius method, indicates that a minimum of about 20% of the bromide ions are free, the remainder being associated by Coulomb attraction to the chainlike positive ion. As the dielectric constant of the solvent is decreased by addition of ethanol, the relative amount of free bromide ions decreases. The viscosity of the polyelectrolyte in aqueous or alcoholic solution, when plotted in the conventional way (ηsp/c versus c), approaches infinity at zero concentration instead of approaching a limiting constant linearly. A plot of $ {{\eta _{sp} } \mathord{\left/ {\vphantom {{\eta _{sp} } {\sqrt c }}} \right. \kern-\nulldelimiterspace} {\sqrt c }} $ versus $ \sqrt c $ is, however, linear; this behavior is characteristic of strong electrolytes. The coefficient of the square root term in concentration for the polymer is larger, by orders of magnitude, than that for ordinary electrolytes. The coefficient of the linear term in the square root function is about equal to the intrinsic viscosity of the parent polymer.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 6 (1951), S. 511-521 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyelectrolytes were prepared by partial quaternization of poly-2-vinylpyridine (M = 45,000) with methyl bromide and butyl bromide. Viscosities of the former salt were measured in water and methanol; of the latter in water, methanol, ethanol and nitrobenzene. A new method of calibrating viscometers is described. Shear constants of the salts in aqueous solution were determined. The viscosity data conform to the equation: \documentclass{article}\pagestyle{empty}\begin{document}$$ z = {A \mathord{\left/ {\vphantom {A {(1 + B\sqrt C )}}} \right. \kern-\nulldelimiterspace} {(1 + B\sqrt C )}} + D $$\end{document}Correlations between both structure of salt and dielectric constant of solvent, and the constants of the equation were found. Quaternary derivatives of poly-2-vinylpyridine are more rodlike than corresponding derivatives of poly-4-vinylpyridine.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 593-598 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Apparent viscosities of aqueous solutions of polyvinylbutylpyridinium bromide (DP = 2000), after correction for instrument constants, are linear in average rate of shear in the capillary viscometer. If a non-Newtonian solute in a Newtonian solvent is assumed, the rather complicated experimental viscosity-pressure curves at various concentrations may be summarized by the simple expression ηsp./C = z∞ (1 - αz∞β)where z∞ is ηsp./C extrapolated to zero rate of shear and β is the average velocity gradient.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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