Spontaneous
emulsification of 3-(trimethoxysilyl) propyl methacrylate
(TPM) can produce complex and active colloids, nanoparticles, or monodisperse
Pickering emulsions. Despite the applicability of TPM in particle
synthesis, the nucleation and growth mechanisms of TPM emulsions are
still poorly understood. We investigate droplet formation and growth
of TPM in aqueous solutions under quiescent conditions. Our results
show that in the absence of stirring the mechanisms of diffusion and
stranding likely drive the spontaneous emulsification of TPM through
the formation of co-soluble species during hydrolysis. In addition,
turbidity and dynamic light scattering experiments show that the pH
modulates the growth mechanism. At pH 10.1, the droplets grow via
Ostwald ripening, while at pH 11.5, the droplets grow via monomer
addition. Adding surfactants [Tween, sodium dodecyl sulfate (SDS),
or cetyltrimethylammonium bromide] leads to <100 nm droplets that
are kinetically stable. The growth of Tween droplets occurs through
addition of TPM species while the number density of droplets is kept
constant. In addition, in the presence of the ionic surfactant SDS,
electrostatic repulsion between the solubilized TPM species and SDS
leads to a significant increase in the number density of droplets
as well as additional nucleation events. Finally, imaging of the solubilization
of TPM in capillaries shows that in the absence of a surfactant, TPM
hydrolysis is likely the rate-limiting step for emulsification, whereas
the presence of silica particles in the aqueous phase likely acts
as a catalyst of TPM hydrolysis. Our experiments highlight the importance
of diffusion and solubilization of TPM species in the aqueous phase
in the nucleation and growth of droplets.