Compensating for Electrode Polarization in Dielectric Spectroscopy Stuides of Colloidal Suspensions: Theoretical Assessment of Existing Methods

被引:43
作者
Chassagne, Claire [1 ]
Dubois, Emmanuelle [2 ]
Jimenez, Maria L. [3 ]
van der Ploeg, J. P. M. [4 ]
van Turnhout, Jan [5 ]
机构
[1] Delft Univ Technol, Environm Fluid Mech, Fac Civil Engn & Geosci, Delft, Netherlands
[2] Univ Paris 06, Sorbonne Univ, CNRS, Lab PHENIX, Paris, France
[3] Univ Granada, Dept Fis Aplicada, Granada, Spain
[4] Leiden Univ, Leiden Inst Chem, Leiden, Netherlands
[5] Delft Univ Technol, Dept Chem Engn, Delft, Netherlands
关键词
colloidal suspension; complex conductivity and permittivity; electrode polarization; FREQUENCY-DEPENDENT POLARIZATION; GENERAL PLANAR ELECTRODES; ARBITRARY MAGNITUDE; ZETA POTENTIALS; DOUBLE-LAYER; PERMITTIVITY; CONDUCTIVITY; IMPEDANCE; SPECTRA; RANGE;
D O I
10.3389/fchem.2016.00030
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dielectric spectroscopy can be used to determine the dipole moment of colloidal particles from which important interfacial electrokinetic properties, for instance their zeta potential, can be deduced. Unfortunately, dielectric spectroscopy measurements are hampered by electrode polarization (EP). In this article, we review several procedures to compensate for this effect. First EP in electrolyte solutions is described: the complex conductivity is derived as function of frequency, for two cell geometries (planar and cylindrical) with blocking electrodes. The corresponding equivalent circuit for the electrolyte solution is given for each geometry. This equivalent circuit model is extended to suspensions. The complex conductivity of a suspension, in the presence of EP, is then calculated from the impedance. Different methods for compensating for EP are critically assessed, with the help of the theoretical findings. Their limit of validity is given in terms of characteristic frequencies. We can identify with one of these frequencies the frequency range within which data uncorrected for EP may be used to assess the dipole moment of colloidal particles. In order to extract this dipole moment from the measured data, two methods are reviewed: one is based on the use of existing models for the complex conductivity of suspensions, the other is the logarithmic derivative method. An extension to multiple relaxations of the logarithmic derivative method is proposed.
引用
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页数:19
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