Surfactantadsorption and aggregate structure at silicananoparticles: Effects of particle size and surface modification

Abstract

The influence of particle size and a surface modifier on the self-assembly of the nonionic surfactant C₁₂E₅ at silica nanoparticles was studied by adsorption measurements and small-angle neutron scattering (SANS). Silica nanoparticles of diameter 13 to 43 nm were synthesized involving the basic amino acid lysine. A strong decrease of the limiting adsorption of C₁₂E₅ with decreasing particle diameter was found. To unveil the role of lysine as a surface modifier for the observed size dependence of surfactant adsorption, the morphology of the surfactant aggregates assembled on pure siliceous nanoparticles (Ludox-TMA, 27 nm) and their evolution with increasing lysine concentration at a fixed surfactant-to-silica ratio was studied by SANS. In the absence of lysine, the surfactant forms surface micelles at silica particles. As the concentration of lysine is increased, a gradual transition from the surface micelles to detached wormlike micelles in the bulk solution is observed. The changes in surfactant aggregate morphology cause pronounced changes of the system properties, as is demonstrated by turbidity measurements as a function of temperature. These findings are discussed in terms of particle surface curvature and surfactant binding strength, which present new insight into the delicate balance between the two properties.