Article ID Journal Published Year Pages File Type
4982683 Colloids and Surfaces A: Physicochemical and Engineering Aspects 2016 7 Pages PDF
Abstract

•Non-aqueous reverse micelles are created without the addition of cosurfactant.•This is the first report where stable EG/BHDC reverse micelles are formed and characterized.•EG solubilization capacity depends on the external phase composition, and decreases as the n-heptane content increases.•The micellar size increases when n-heptane content increases.•n-heptane favors the droplet-droplet attractions.

We present results on a new system that forms non-aqueous reverse micelles (RMs) created with a cationic surfactant, benzyl-n-hexadecyldimethylammonium chloride (BHDC), encapsulating ethylene glycol (EG), in different nonpolar solvents blends of n-heptane:benzene. It is shown that a cationic surfactant forms RMs using EG as polar solvent without the addition of a co-surfactant. In particular, we analyzed the EG solubilization capacity, the droplet size values and the interface composition of EG/BHDC/n-heptane:benzene RMs, using dynamic light scattering (DLS) and the solvatochromic behavior of 1-methyl-8-oxyquinolinium betaine (QB) as molecular dye.The EG solubilization capacity depends on the external phase composition decreasing when the n-heptane content increases. Using DLS technique, we demonstrate the formation of RMs, and observe that for the same [EG]/[BHDC] ratio, the micellar size increases when n-heptane content increases.Using QB it was found that EG penetrates into the micellar interface changing dramatically the composition and the droplet-droplet interaction, in comparison when water is encapsulated.

Graphical abstractEG and BHDC can form stable non-aqueous reverse micelles in benzene:n-heptane solvent blends without the needing of co-surfactant.Download high-res image (105KB)Download full-size image

Keywords
Related Topics
Physical Sciences and Engineering Chemical Engineering Colloid and Surface Chemistry
Authors
, , , ,