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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
- 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
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