Compensating for electrode polarization in dielectric spectroscopy studies of colloidal suspensions

Compensating for electrode polarization in dielectric spectroscopy studies of colloidal suspensions: Theoretical assessment of existing methods

Chassagne, C. (TU Delft Environmental Fluid Mechanics)
Dubois, Emmanuelle (Universite Pierre et Marie Curie (UPMC))
Jiménez, María L. (Universidad de Granada)
Ploeg, J.C. (Universiteit Leiden)
van Turnhout, J. (TU Delft ChemE/Algemeen)

2016

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.

Colloidal suspension
Complex conductivity and permittivity
Electrode polarization
OA-Fund TU Delft

http://resolver.tudelft.nl/uuid:2c8e785e-438a-4597-890d-8d97af079eb6

https://doi.org/10.3389/fchem.2016.00030

2296-2646

Frontiers in Chemistry, 4 (JUL)

Institutional Repository

journal article

© 2016 C. Chassagne, Emmanuelle Dubois, María L. Jiménez, J.C. Ploeg, J. van Turnhout