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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Il nuovo cimento della Società Italiana di Fisica 16 (1994), S. 1401-1410 
    ISSN: 0392-6737
    Keywords: Mechanical properties of liquids ; Conference proceedings
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Summary Both linear and non-linear viscoelasticity experiments have been performed in semi-dilute micellar aqueous solutions of ethanediyl-α,ω-bis (dodecylmethylammonium bromide) as a function of solution chloride (NaCl) concentration. The results suggest that both linear and non-linear properties are affected by the electrostatic interactions. In particular, the plateau modulusG′∞ and the ratioσ m/G′∞, whereσ m represents the plateau value in a stress-shear rate experiment, are enhanced as the electrostatic interactions are screened by addition of salt. The zero-shear viscosity is lowered upon addition of NaCl, due likely to an exchange of the Cl− ions with the Br− counterions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 6 (1977), S. 733-746 
    ISSN: 1572-8927
    Keywords: 1-1 Electrolytes ; DMSO ; density ; ultrasonic vibration potential ; ionic partial molal volumes ; solvation ; electrostriction ; steric hindrance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The partial molal volumes of Li+, Na+, K+, Rb+, Cs+, Cl−, Br−, I−, and NO 3 - in DMSO at 25°C have been determined from ultrasonic vibration potential data and density data for solutions of uni-univalent electrolytes. Hepler's semiemprirical equation has been used to split ionic partial molal volumes into geometric and electrostrictive contributions. The results obtained in this work confirm the conclusion of our previous studies, namely, that the contribution of electrostriction is essentially determined by the properties of that layer of atoms, 0.3 to 0.4 nm thick, in contact with the ion and by the degree of steric hindrance of the poles of the dipole of the solvent molecule. On the other hand, the geometric contribution depends on the size of the solvent molecule and also on the arrangement of the solvent molecules about the ions. It is shown that the geometric contribution to the partial molal volume of ions is largely increased when ions cannot come close enough to the poles of the solvent-molecule dipole, owing to steric hindrance.
    Type of Medium: Electronic Resource
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