ABSTRACT
The objective of this research work is to understand the effect of the surface charge density on the charge reversal phenomenon. To this end, we use experimental results and computer simulations. In particular, we measure the electrophoretic mobility of latex particles (macroions) in the presence of a multivalent electrolyte. We have focused on the electrolyte concentration range at which a reversal in the electrophoretic mobility is expected to happen. In particular, the role of the surface charge on the charge reversal process is looked into from several latexes with the same functional group but different surface charge densities. Although the mechanism responsible for the colloidal charge reversal is still a controversial issue, it is proved that ionic correlations are behind the appearance of such phenomenon (especially near the macroion surface). This conclusion can be inferred from a great variety of theoretical models. According to them, one of the factors that determine the charge reversal is the surface charge density of the macroions. However, this feature has been rarely analyzed in experiments. Our results appear therefore as a demanded survey to test the validity of the theoretical predictions. Moreover, we have also performed Monte Carlo simulations that take the ion size into account. The correlation found between experiments and simulations is fairly good. The combination of these techniques provides new insight into the colloidal charge reversal phenomena showing the effect of surface charge.
ABSTRACT
Dynamic light scattering (DLS) and fluorescence recovery after pattern photobleaching (FRAPP) were used to study the interaction of low molecular weight poly(ethylene glycol) (PEG) with micelles of two different surfactants: tetradecyldimethyl aminoxide (C(14)DMAO, zwitterionic) and pentaethylene glycol n-dodecyl monoether (C(12)E(5), non-ionic). By using an amphiphilic fluorescent probe or a fluorescent-labeled PEG molecule, FRAPP experiments allowed to follow the diffusion of the surfactant-polymer complex either by looking at the micelle diffusion or at the polymer diffusion. Experiments performed with both fluorescent probes gave the same diffusion coefficient showing that the micelles and the polymer form a complex in dilute solutions. Similar experiments showed that PEG interacts as well with pentaethylene glycol n-dodecyl monoether (C(12)E(5)).