Surfactants containing pH-switchable,
carboxylic acid moieties
are utilized in a variety of environmental, industrial, and biological
applications that require controlled stability of hydrophobic droplets
in water. For nanoemulsions, kinetically stable oil droplets in water,
surface adsorption of the anionic form of the carboxylic acid surfactant
stabilizes the droplet, whereas a dominant surface presence of the
neutral form leads to destabilization. Through the use of dynamic
light scattering, ζ-potential, and vibrational sum frequency
scattering spectroscopy (VSFSS), we investigate this mechanism and
the relative surface population of the neutral and charged species
as pH is adjusted. We find that the relative population of the two
surfactant species at the droplet surface is distinctly different
than their bulk equilibrium concentrations. The ζ-potential
measurements show that the surface concentration of the charged surfactant
stays nearly constant throughout the stabilizing pH range. In contrast,
VSFSS shows that the neutral carboxylic acid form increasingly adsorbs
to the surface with increased acidity. The spectral features of the
headgroup vibrational modes confirm this behavior and go further to
reveal additional molecular details of their adsorption. A significant
hydrogen-bonding interaction occurs between the headgroups that, along
with hydrophobic chain–chain interactions, assists in drawing
more carboxylic acid surfactant to the interface. The charged surfactant
provides the stabilizing force for these droplets, while the neutral
surfactant introduces complexity to the interfacial structure as the
pH is lowered. The results are significantly different than what has
been found for the planar oil/water studies where stabilization of
the interface is not a factor.