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Charging Poly(methyl Methacrylate) Latexes in Nonpolar Solvents: Effect of Particle Concentration
Gregory N Smith1, Silvia Ahualli2, Ángel V Delgado2
1School of Chemistry, University of Bristol , Cantock's Close, Bristol BS8 1TS, United Kingdom.
Electrophoretic mobility of charged colloids decreases with concentration due to particle interactions, not surfactant depletion. This finding is crucial for accurate electrokinetic potential determination in nonpolar solvents.
Area of Science:
- Colloid Science
- Physical Chemistry
- Materials Science
Background:
- Electrophoresis studies charged colloids in nonpolar solvents.
- Poly(methyl methacrylate) (PMMA) latexes stabilized by poly(12-hydroxystearic acid) in dodecane were used.
- Aerosol OT (AOT) surfactant acted as the charging agent.
Purpose of the Study:
- Investigate the decrease in electrophoretic mobility (μ) of PMMA latexes with increasing particle volume fraction.
- Determine the cause of decreased mobility: surfactant reservoir depletion or interparticle interactions.
- Accurately determine the electrokinetic zeta (ζ) potential.
Main Methods:
- Electrophoresis measurements were conducted at varying particle concentrations.
- Contrast-variation small-angle neutron scattering (SANS) with deuterated AOT (AOT-d34) studied surfactant incorporation.
- Electrokinetic modeling was employed to analyze interparticle interactions.
Main Results:
- Electrophoretic mobility (μ) decreased as particle concentration increased.
- SANS confirmed consistent AOT-d34 incorporation across all volume fractions, ruling out surfactant depletion.
- Solvodynamic and electrical interactions between particles were identified as the cause of mobility decrease.
Conclusions:
- Interparticle interactions, not surfactant depletion, explain the reduced electrophoretic mobility in PMMA latexes.
- These interactions are present at all accessible particle volume fractions.
- Accounting for these interactions is essential for accurate electrokinetic zeta (ζ) potential determination in charged colloidal systems.
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