The miniemulsion polymerizations (MiEPs) of butyl acrylate (BA) initiated by UV-light have been studied. The oil-soluble dibenzoyl peroxide was used as a photoinitiator. Furthermore, the effect of sodium montmorillonite on kinetics and BA miniemulsion stabilized by anionic sodium dodecylsulfate (SDS) and anionic cetyltrimethylammonium bromide (CTAB) was studied. The polymerization rate vs. conversion curve of the photoinduced MiEP of BA was described by two and four nonstationary rate intervals. Two rate intervals with one rate maximum was observed with CTAB and four nonstationary rate intervals with two rate maxima appeared with SDS. Variation of the rate of polymerization with conversion was discussed in terms of types of initiating radicals and the gel effect.Keywords: photoinduced miniemulsion polymerization; clays; kinetics; composite nanoparticles Introduction For the past 20 years, there has been increased attention paid to the synthesis of nanocomposites based on either intercalated or exfoliated clay dispersed into various matrix polymers [1][2][3][4][5].There are also some studies on the formation of composite nanoparticles by the dispersion polymerization of monomers with clays as was reviewed by Capek [6]. As an alternative to the procedures described above, the preparation of nanocomposites using UV-curing technology has only recently been reported as summarized below.There are also several studies. Monomer polarity, monomer functionality, and the functional groups on the organoclay surfaces significantly impact both the degree of clay exfoliation and photopolymerization kinetics. The addition of polymerizable organoclays increases photopolymerization rate in sufficiently exfoliated clay systems, whereas the rate decreases with lower degrees of clay exfoliation. With clay exfoliation, the effective surface area is increased, resulting in immobilization of a greater number of the propagating radicals and decreased termination [7].A photoinitiator intercalated into montmorillonite had high photoinitiation efficiency, even only 1/100 (w/w) modified clay could initiate the radical polymerization with the 87% acrylate conversion on UV-light exposure. The d spacing could be enlarged to 13.9 nm after photopolymerization with organoclay loading. This approach provided a novel pathway for using the highly exfoliated clay-polymer composites for designing intercalating agents capable of introducing different functional groups [8,9].The functionalization of the sodium montmorillonite (MMTNa) surface with glycidylpropyl-triethoxysylane allows to obtain a new modified clay mineral which can be dispersed