Search our site:

 

 

Zeta Potential and Colloidal Behavior

  • Bulk solids have lower free energy than colloids and are stable systems whereas colloids exist in a meta-stable state - they are constantly under the influence of attractive forces
  • Repulsive forces keep them from aggregating
  • In most polar liquids these forces come from particle charge
  • Changes in the free energy may lead to state instability
  • Stability can be adjusted and measured
    • Zeta potential is a measure of dispersion stability
    • Higher zeta potential implies more stable dispersions
    • Low values can indicate colloid instability which could lead to aggregation.

  • Counterions build up near the surface
  • Due to diffusion, counterions and co-ions eventually equilibriate
  • At the shear plane, the potential difference is defined to be the zeta potential

Isoelectric Point

  • Zeta potential changes with
    • Salt concentration
    • Potential determining ion concentration
      • pH for example
    • Surfactant concentration
  • The concentration of the potential determining ion at which the zeta potential is zero is defined as the isoelectric point (IEP)
  • The isoelectric point is a very important measure and relates strongly to stability

IEP values for some common oxides

Material
pH of Isoelectric point
Silica (SiO2)
2
Anatase (TiO2)
4
Zirconia (ZrO2)
4
Stannic Oxide (SnO)
6
Hematite (Fe2O3)
8
Alumina (Al2O3)
9
Lead Oxide (PbO)
10
Magnesia (MgO)
12


Effect on Zeta Potential of Surface Modifications for TiO2

  • R960 (TiO2) has an IEP at pH ~7
  • R931 doped with silica, has an IEP at pH ~ 5
  • R900 doped with alumina, has an IEP at pH ~9
  • Surface doping shifts IEP as expected
  • Zeta potential depends on surface chemistry, not bulk chemistry