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Quantitative and Qualitative Examination of Particle-particle Interactions Using Colloidal Probe Nanoscopy
Published on: July 18, 2014
Predicting aggregation rates of colloidal particles from direct force measurements
F Javier Montes Ruiz-Cabello1, Gregor Trefalt, Zita Csendes
1Department of Inorganic and Analytical Chemistry, University of Geneva , Sciences II, Quai Ernest-Ansermet 30, 1205 Geneva, Switzerland.
The Journal of Physical Chemistry. B
|September 11, 2013
Summary
Direct force measurements reveal key interactions driving colloidal particle aggregation. Atomic force microscopy (AFM) identified non-DLVO forces at short distances, crucial for predicting aggregation rates.
Area of Science:
- Colloid and Surface Science
- Physical Chemistry
- Materials Science
Background:
- Colloidal suspensions are ubiquitous in nature and industry.
- Understanding interparticle forces is crucial for controlling suspension behavior, such as aggregation.
- The Derjaguin, Landau, Verwey, and Overbeek (DLVO) theory is a cornerstone for describing colloidal interactions.
Purpose of the Study:
- To directly measure forces between charged colloidal latex particles.
- To investigate the influence of cation valency on interparticle forces.
- To assess the predictive power of force measurements for colloidal aggregation rates.
Main Methods:
- Utilized the multiparticle colloidal probe technique with atomic force microscopy (AFM).
- Performed direct force measurements in aqueous solutions with varying inorganic monovalent and multivalent cations.
- Measured aggregation rates independently using light scattering.
Main Results:
- DLVO theory accurately described force profiles down to a few nanometers for monovalent and divalent cations.
- A significant non-DLVO attraction was observed at shorter distances.
- Highly charged cations induced a longer-ranged non-DLVO attraction, attributed to surface charge heterogeneities.
- Force measurements successfully predicted observed aggregation rates.
Conclusions:
- Direct force measurements effectively capture the primary interactions governing aggregation in colloidal suspensions.
- Non-DLVO forces play a critical role in colloidal interactions, especially at short distances and with multivalent cations.
- Surface charge heterogeneities can significantly influence interparticle forces and aggregation behavior.

