Use of electrochemical impedance spectroscopy to determine double-layer capacitance in doped nonpolar liquids
[Display omitted] •Fluid conductivity, permittivity and double-layer capacitance can be inferred.•About 17ppm of the surfactant molecules are charged.•Only the largest micelles are charged. Electrochemical impedance spectroscopy in a thin cell (10μm) was used to infer conductivity, permittivity and...
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Veröffentlicht in: | Journal of colloid and interface science 2015-07, Vol.449, p.2-12 |
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Format: | Artikel |
Sprache: | eng |
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•Fluid conductivity, permittivity and double-layer capacitance can be inferred.•About 17ppm of the surfactant molecules are charged.•Only the largest micelles are charged.
Electrochemical impedance spectroscopy in a thin cell (10μm) was used to infer conductivity, permittivity and the differential double-layer capacitance of solutions of dodecane doped with OLOA 11000 [poly(isobutylene) succinimide] for concentrations of dopant between 0.1% and 10% by weight. All spectra (frequencies between 1Hz and 100kHz) were well fit by an equivalent circuit having four elements including a constant-phase element representing the double-layer capacitance. Using Gouy–Chapman theory for small zeta potentials and assuming univalent charge carriers, the double-layer capacitances were converted into charge carrier concentration which was found to be directly proportional to the weight percent of dopant with a 1wt% solution having 87 carriers/μm3 (the concentration of either positive or negative charges). This is only 17ppm of the total monomer concentration calculated from the average molecule weight of the dopant. Dividing the measured conductivities by the charge carrier concentration, we inferred the mobility and hydrodynamic diameters for the charged micelles. The hydrodynamic diameters of carriers were significantly larger than the average diameter of all micelles measured independently by dynamic light scattering. This suggests that only large micelles become charged. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2014.08.052 |