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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 8 (1979), S. 557-571 
    ISSN: 1572-8927
    Keywords: Ion-solvent interaction ; ion pairs ; conductance in mixed solvents ; tetrabutylammonium bromide ; tetraphenylphosphonium bromide ; tetraphenylphosphonium chloride ; tetrapropylammonium bromide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Conductances at 25.00°C are reported for the following systems: tetrabutylammonium bromide in dimethyl sulfoxide-acetone mixtures (Bu4NBr in Me2SO−Me2CO); tetraphenylphosphonium bromide (Ph4PBr) in water Me2SO, Me2CO, and in the mixtures H2O−Me2SO, Me2SO−Me2CO and Me2CO−H2O; Ph4PCl in Me2SO, Me2CO, H2O−Me2SO, and Me2SO−Me2CO; and tetrapropylammonium bromide (Pr4NBr) in Me2SO and Me2CO. The data were analyzed using the Fuoss 1978 equation which is based on the coupled equilibria: (unpaired ions)⇌(solvent-separated pairs)⇌(contact pairs). The conductimetric pairing constantK A =K R(l+K s) is the product of two factors:K R, which describes the first (diffusion controlled) equilibrium andK s=exp(−E s/kT), which describes the second (system-specific) equilibrium. Ions with overlapping cospheres (of diameterR) are defined as paired: their center-to-center distancer lies in the rangea≤r≤R; contact pairs (r=a) are ions which have one ion of opposite charge as a nearest neighbor, all other nearest and next nearest neighbors being solvent molecules. The quantityE s is the difference in free energy between the states defined byr=R andr=a. For the Me2SO−Me2CO systems,E s is positive for solutions in Me2SO and decreases through zero to negative values as the fraction of the less polarizable acetone increases. For solutions in waterE s is also positive. On addition of Me2SO or Me2CO,E s initially increases, goes through a maximum, and then decreases to negative values as the fraction of the less polarizable component increases. The decrease is an electrostatic effect, common to all the systems. The initial increase inE s appears when the small water molecules surrounding solvent-separated pairs are replaced by organic molecules which have greater volumes than water.
    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 conductance in diphenyl ether at 35°C. and 60 cycles of the picrate of a 4-vinylpyridine-styrene copolymer (10:90) has been measured. The equivalent conductance, based on the nitrogen content, is of the same order as that of picoline picrate, and varies with concentration in accordance with the law of ion association.
    Additional Material: 2 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: A series of copolymers, of 4-vinylpyridine and styrene, covering the range 1.5 to 100% vinylpyridine were prepared in 20% toluene solution at 80°. Strong electrolytes were then made by the addition of n-butyl bromide in nitromethane solution. The salts with high vinylpyridine content were soluble in water, alcohols, nitromethane, and other polar solvents. Viscosities of the parent copolymers in methyl ethyl ketone were in the range 0.15-0.20; osmotic pressures gave molecular weights in the range 50,000-80,000. The polyelectrolytes in nitromethane and nitromethane-dioxane mixtures gave viscosity-concentration curves which were strongly concave upwards: at 1 mg./100 cc., the reduced viscosity of the salt of polyvinylpyridine in nitromethane was 6.0. The salts of the different copolymers did not differ much in their viscosities at concentrations above a few tenths of a gram per 100 cc., a fact which shows a high degree of ionic association; only as zero concentration is approached, can the detailed polymer structure be seen. The extent of association at a given concentration is controlled by the amount of vinylpyridine in the copolymer and by the dielectric constant of the solvent. Addition of simple one-one electrolytes, such as tetrabuty lammonium bromide, suppresses the electrostatic increase in viscosity which otherwise appears at low concentrations. The following empirical equation: \documentclass{article}\pagestyle{empty}\begin{document}$$ {{\eta _{{\rm sp}} } \mathord{\left/ {\vphantom {{\eta _{{\rm sp}} } {\rm C}}} \right. \kern-\nulldelimiterspace} {\rm C}} = {{\rm A} \mathord{\left/ {\vphantom {{\rm A} {\left( {1 + {\rm B}\sqrt {\rm C} } \right)}}} \right. \kern-\nulldelimiterspace} {\left( {1 + {\rm B}\sqrt {\rm C} } \right)}} + {\rm D} $$\end{document} was found to fit the data for the different systems studied. The constant A depends on copolymerization ratio and probably on molecular weight; it is a measure of the extent to which the polymer coil can spread out at infinite dilution as a consequence of the intramolecular Coulomb repulsion between charges attached to the chain. It is roughly several orders of magnitude larger than the intrinsic viscosity of the parent polymer. The constant B is a measure of the electrostatic forces and increases with decreasing dielectric constant of the solvent.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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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  • 5
    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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  • 6
    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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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 16 (1955), S. 201-208 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The addition of carboxylic acid to Epon 834-phthalic anhydride resins accelerates the rate of cure. The maximum thermal yield point corresponds to reaction of all the epoxide groups in the ratio of two anhydride carbonyls to one epoxide oxygen or of one acid carbonyl to one epoxide oxygen. The initial presence of some secondary alcohol groups appears to be essential for initiation of reaction as suggested by Fisch and Hofmann. Carboxylic acids react directly with epoxide groups to produce secondary alcohols which in turn react with phthalic anhydride, regenerating carboxylic acid groups. Succinic acid gives a rapid cure (although not as fast as amines) to a resin with only slightly lowered thermal yield point, while benzoic acid depresses the yield point by about 15° because it acts as a chain-stopper.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    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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  • 9
    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.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 4 (1949), S. 96-96 
    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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