The emulsion polymerization of diisopropyl fumarate initiated with a redox
initiator and an anionic emulsifier was investigated. The study:includes co
nversion and particle number determinations as a function of time, temperat
ure and the concentrations of initiator, emulsifier and monomer. The reacti
on is characterized by a limiting conversion following a linear increase of
the conversion with time from the beginning on. The reaction rate is very
much higher than those obtained in bulk or in solution polymerization.
Taking into account the results and the response of the system to an additi
on of styrene and toluene, a mechanism of radical occlusion together with a
diffusion-controlled propagation in the polymer matrix is proposed. The ve
ry high apparent activation energies for the propagation and limiting conve
rsion suggest a complex behavior.