Anion-specific effects on the interaction forces between Al2O3 surfaces and dispersibility of Al2O3 colloids in electrolyte solutions
The agglomerates of the Al2O3 colloids in electrolyte solutions reflected the jump-in observed in the force curve of the colloid probe method. [Display omitted] ► Interaction force between Al2O3 in electrolyte solutions by the colloidal probe method was investigated. ► Force curve measurement condit...
Gespeichert in:
Veröffentlicht in: | Colloids and surfaces. A, Physicochemical and engineering aspects Physicochemical and engineering aspects, 2012-02, Vol.396, p.233-237 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The agglomerates of the Al2O3 colloids in electrolyte solutions reflected the jump-in observed in the force curve of the colloid probe method. [Display omitted]
► Interaction force between Al2O3 in electrolyte solutions by the colloidal probe method was investigated. ► Force curve measurement conditions were determined from the zeta potential results. ► Repulsive forces were observed at a short separation distance. ► The order of the repulsive force strength corresponded to the Hofmeister series and reflected the force curve results. ► Agglomerates of the Al2O3 colloids were observed in the 0.1mol/L Br− solution.
The interaction between an Al2O3 colloid and c-sapphire surface (0001) was investigated in an aqueous solution containing citrate ion, Cl−, NO3− or Br− using the colloidal probe method. The force curve measured in electrolyte solutions at pH=4 showed a good agreement with the force curve predicted by the Derjaguin–Landau–Vervey–Overbeek theory at a long separation distance. The repulsive forces were observed at a shorter separation distance. The order of the strength of the repulsive force was citrate ion>Cl−>NO3−>Br−, corresponding to the Hofmeister series. All the force curves measured in aqueous solutions at pH=10 were the same. This is caused by the cation (K+) selectively affecting surface interaction because the Al2O3 surface charged to negative at this pH. A particle size distribution measurement of the Al2O3 colloids in the 0.001–0.1mol/L Cl− and Br− aqueous solution was carried out. The agglomerates of the Al2O3 colloids were observed in 0.1mol/L Br− solutions. However, Al2O3 colloids were well dispersed in the other aqueous solutions, which are reflected by the force curve results. Jump-in was observed only in the force curve measured in the 0.1mol/L Br− solutions and not in any other solutions. |
---|---|
ISSN: | 0927-7757 1873-4359 |
DOI: | 10.1016/j.colsurfa.2011.12.072 |