## Abstract For Abstract see ChemInform Abstract in Full Text.
Colloidal Particles at Solid–Liquid Interfaces: Mechanisms of Desorption Kinetics
✍ Scribed by Michael Weiss; Yves Lüthi; Jaro Rička; Thomas Jörg; Hans Bebie
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 200 KB
- Volume
- 206
- Category
- Article
- ISSN
- 0021-9797
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✦ Synopsis
We study the sorption of colloids on equally charged surfaces. Our focus is on the time scale from hours to weeks, where adsorption is not an irreversible process but interplays with (spontaneous) desorption. Using model calculations, we show how the desorption kinetics is influenced by readsorption, a potential barrier, a secondary potential minimum, local variation of the potential, and bond aging. In the experimental part we present results of in situ observation of the sorption kinetics of polystyrene latex particles onto a glass surface. Combining the evanescent field method with video microscopy, we were able to identify the particle arrival and departure times individually and therefrom determine the adhesion time distribution function. The nonexponentiality of this function can be explained by a gamma distribution of the potential depth at the binding sites as well as by logarithmic bond aging. Copyright 1998 Academic Press.
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sors (Cd 2/ for CdS or Zn 2/ for ZnS) into the nanoreactors Adsorption isotherms have been determined for the binding of and on the extent of Cd 2/ (or Zn 2/ ) adsorption at the silica Cd 2/ onto the surfaces of hydrophilic A200 SiO 2 and hydrophobic particle interfaces. We have determined, therefor