Electrolyte-Dependent Aggregation of Colloidal Particles near Electrodes in Oscillatory Electric Fields
| Autor: | Kelley Heatley, William D. Ristenpart, N. H. Talken, Taylor J. Woehl, Cari S. Dutcher |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Potassium hydroxide
Potassium Analytical chemistry chemistry.chemical_element Surfaces and Interfaces Electrolyte Condensed Matter Physics chemistry.chemical_compound Particle aggregation chemistry Chemical physics Electric field Electrode Electrochemistry Zeta potential Particle General Materials Science Spectroscopy |
| Zdroj: | Langmuir. 30:4887-4894 |
| ISSN: | 1520-5827 0743-7463 |
| DOI: | 10.1021/la4048243 |
| Popis: | Colloidal particles adjacent to electrodes have been observed to exhibit drastically different aggregation behavior depending on the identity of the suspending electrolyte. For example, particles suspended in potassium chloride aggregate laterally near the electrode upon application of a low-frequency (∼100 Hz) oscillatory electric field, but the same particles suspended in potassium hydroxide are instead observed to separate. Previous work has interpreted the particle aggregation or separation in terms of various types of electrically induced fluid flow around the particle, but the details remain poorly understood. Here we present experimental evidence that the aggregation rate is highly correlated to both the particle zeta potential and the electric field amplitude, both of which depend on the electrolyte type. Measurement of the aggregation rate in 26 unique electrolyte-particle combinations demonstrates that the aggregation rate decreases with increasing zeta potential magnitude (i.e., particles with a large zeta potential tended to separate regardless of sign). Likewise, direct measurements of the oscillatory electric field in different electrolytes revealed that the aggregation rate was negatively correlated with solution conductivity and thus positively correlated with the field strength. We tested the experimentally measured aggregation rates against a previously developed point dipole model and found that the model fails to capture the observed electrolyte dependence. The results point to the need for more detailed modeling to capture the effect of electrolyte on the zeta potential and solution conductivity to predict fluid flow around colloids near electrodes. |
| Databáze: | OpenAIRE |
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