SYNOPSISPolystyrene (PS) (l)/Poly (n-butyl acrylate (BA)/amide type functional monomer) (2) structured latex particles were prepared through emulsion polymerization varying the hydrophilicity of the functional monomer employed. The second-stage polymerization kinetics, the size and morphology of latex particles, and the location of the functional groups in the final latexes were studied, in order to relate them to the thermomechanical properties of films cast from these latexes, It has been shown that, as expected, increasing the hydrophobicity leads to a better homogeneity in the copolymer formed during the second-stage polymerization, while the more hydrophilic functional monomer partly homopolymerizes in a separate phase. However, the functionalization by all the monomers used in this work, prevents the PS seed particles to form a continuous skeleton (percolated network). Further heat treatments a t 140°C do not lead to the formation of a continuous PS phase as for pure BA/pure PS two-stage particles. In addition, some thermally induced crosslinking effects are discussed in relation with the functional monomer location within the particles. 0 1995 John Wiley & Sons, Inc. Keywords: core-shell N-methylol acrylamide N-methylol methacrylamide N-isobutoxy methyl acrylamide butyl acrylate polystyrene seed latex emulsion polymerization structured particles particle morphology functional monomers latex films phase arrangement mechanical properties film forming scanning electron microscopy annealing percolation coalescence
I NTRO DU CTlO NIn traditional emulsion polymerization, a functional monomer is such that, when used in small proportions (up to 10% based on the total monomer mixture), it provides the base polymer with a chemical group which is capable of modifying the physicochemical properties of the resulting latex (e.g., viscosity, stability), and/or of the polymer which is recovered from that latex (e.g., adhesion, softening