The low-frequency electrical conductivity of dielectric colloids (polystyrene and silica) and metallic (silver) ones in aqueous solutions shows a power-law behavior in time during the salt-induced cluster-cluster aggregation. We interpret this fact using current theories of heterogeneous dielectric
Estimations of the aggregation time of various colloidal systems
β Scribed by Leon G.B Bremer; Pieter Walstra; Ton van Vliet
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 546 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0927-7757
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β¦ Synopsis
Scaling approximations for the time after which macroscopic aggregation becomes visible are derived for various colloidal systems. It is shown that the aggregation rate, which is generally used as a measure of stability, is not the only factor determining the aggregation time. The total number of bonds that have to be formed before aggregation becomes visible is at least as important. The aggregation rate increases abruptly when orthokinetic aggregation or sedimentation becomes dominant or just before gelation occurs. This enables the estimation of an aggregation time without the use of an arbitrary or operational definition of visibility. This aggregation time refers to macroscopic aggregation, e.g. visible sedimentation or gelation. Complications that hinder an accurate determination of the aggregation time are listed, and their effects on the aggregation time are predicted.
The obtained scaling relations provide useful insights into the progress and results of colloidal aggregation phenomena.
π SIMILAR VOLUMES
Orthokinetic aggregation of colloids trapped at the air-liquid interface was studied by direct imaging in a couette cell. This method allowed us to follow the temporal evolution of both the cluster-mass distribution and the cluster structure at a shear rate where Brownian aggregation is suppressed.