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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 86 (1982), S. 4094-4095 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 9 (1980), S. 617-625 
    ISSN: 1572-8927
    Keywords: Electrolytic conductivity ; ion association ; mean activity coefficients ; ion-water interactions ; lithium borate ; sodium borate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The conductivities of aqueous solutions of sodium borate at 25°C and lithium borate at various temperatures are reported. The conductivity of the B(OH) 4 − ion is 35.3 ±0.2 S-cm2-mole−1 at 25°C. The electrolytes are both associated, the lithium salt being more associated than the sodium salt. The mobilities and association constants obtained from the conductivity data agree with a model recently proposed for the H2O−B(OH) 4 − interactions. A discrepancy in the reported thermodynamic behavior of NaB(OH)4 aqueous solutions has been resolved by means of the association constants obtained in the present study. Thus the usefulness of the conductivity measurements to determine excess chemical potentials of binary electrolytes in dilute solution is again shown.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-8927
    Keywords: Aprotic solvents ; association of ions ; conductance ; dissociation ; hydrochloric acid ; ionization ; ion-solvent interactions ; sulfolane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The molar conductance of solutions of HCl (concentrations from 3×10−4 to 0.033 mol-l−1) in water-sulfolane (tetramethylenesulfone) mixtures of mole fractions (X2) of sulfolane of 0.25, 0.50, 0.75, and 0.85 at 25, 30, and 40°C have been determined. The dielectric constants of the solvents varied from 45 to 60 at 25°C. The data were analyzed by the full Pitts equation, the expanded Pitts equation, and the expanded Fuoss-Hsia equations, all of which give comparable results for the limiting molar conductanceA o and for the ion-pair association constant KA for HCl. These equations were unsuccessful for the analysis of supplemental data in pure sulfolane. At 25°C, the pK for dissociation of HCl varies from 0.4 (X2=0.25) to 2.9 (X2=0.85). The extent of ion pairing is apparently strongly influenced by selective ion-solvent interactions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 341-352 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effect on ion-exchange resins of the polystyrene type of a thermal treatment has been studied by heating strong cation and strong anion resins in water at 95°C and 250°C and obtaining the IR spectra of the remaining resins as well as those of the decomposition products extracted by the water. The degradation of the resins is highly dependent on their ionic form. The —(OH-) and the —(H+) forms are more labile, losing completely their exchange capacity at 250°C, while the —(Li+) form retains considerable ion-exchange capacity. On the other hand, the hydrothermal process affects differently the backbone of the anion and the cation resins. There are similarities in the type of decomposition products found after hydrothermal treatment with those observed after radiolytic exposure of the resins. Heating the resins in water reduces the crosslinking of the polystyrene matrix.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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