Dependence of the broad frequency dielectric spectra of colloidal polystyrene particle suspensions on the difference between the counterion and co-ion diffusion coefficients

JOURNAL OF COLLOID AND INTERFACE SCIENCE

卷:298

Article

Tirado, Monica ; Grosse, Constantino

关键词: dielectric dispersion;    diffusion coefficients;    colloidal suspensions;    polystyrene particles;    counterions;    co-ions;    dielectric spectroscopy;    permittivity;    conductivity;   

DOI  :  10.1016/j.jcis.2006.01.027

来源: Elsevier

【 摘 要 】

Dielectric properties Of four suspensions of spherical polystyrene particles were measured at 25 degrees C over a broad frequency range extending from 100 Hz to 10 MHZ, using a HP 4192 A Impedance Analyzer. The instrument was coupled to a cell with parallel platinum black electrodes and variable spacing. and the quadrupole calibration method was used. The aqueous electrolyte solutions were prepared using equal concentrations of NaCl. KCI. NaAc. or KAc, so that the calculated Debye screening length and Zeta potential remained constant, while the conductivity changed. The polystyrene particles used (Interfacial Dynamics Corp., surfactant-free white sulfate latex) have a diameter of I micron and a surface charge density that is independent of the pH. The dielectric spectra were described using the Nettelblad-Niklasson expression combined with a Debye type high-frequency term and analyzed using the Shilov-Dukhin theory and numerical results. The theoretical prediction that the low-frequency dispersion parameters are determined by the co-ion diffusion Coefficient was experimentally confirmed. This also allowed to justify ail alternative definition of the characteristic time of the low-frequency dispersion. On the contrary, the prediction that the high-frequency dispersion parameters are determined by the diffusion coefficient of counterions could not be confirmed, possibly due to experimental problems. However, the zeta-potential values deduced from high-frequency data were compatible with values deduced from electrophoretic mobility measurements. (c) 2006 Elsevier Inc. All rights reserved.

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