Silica particles have been obtained by addition of Tetraethoxysilane (TEOS)
to water-in-oil (W/O) emulsions. The present paper studies the role of eth
anol, present in the system due to TEOS hydrolysis, in the emulsion propert
ies during silica particle formation. Evolution in phase behaviour was obse
rved during the reactions. Initial emulsions were stable, but soon after TE
OS addition, in presence of hydrochloric (HCl), they became unstable. Phase
behaviour changed, appearing three liquid phases if agitation was interrup
ted. It was observed that ethanol could increase the HLB temperature (T-HLB
) of the emulsion systems. It also could increase the temperature range in
which three liquid phases would coexist in equilibrium. This was related to
a reduction in the interfacial tension, which was also dependent on ethano
l concentration. The interfacial tensions decreased until a minimum was rea
ched, where three liquid phases could form. All this greatly affected emuls
ion stability. Emulsion phase separation, due to coalescence, was very fast
after critical concentrations of ethanol were reached. Therefore, the size
of silica particles were coalescence-controlled. Their size could be reduc
ed by addition of a block copolymer surfactant. This surfactant was able to
both increase stability and reduce interfacial tensions. This trend was th
e same for the different systems studied. Systems with slower coalescence e
ventually provided smaller particle size. (C) 2001 Elsevier Science B.V. Al
l rights reserved.