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The photoinitiation of the polymerization of methyl methacrylate by the dye neutral red in the presence of thiethylamine was studied in order to determine the mechanism that leads to the formation of the initiating radicals. An expression for the yield of free radicals was deduced from the mechanism, and the experimental values for the equilibrium and reaction constants of the ground, singlet and triplet states of the dye in the presence of the other components of the formulation, were used to calculat the behaviour of the system when varying the concentration of the co-initiator triethylamine. The observed dependence fits closely the global polymerization rates obtained directly from polymerization kinetics studied by dilatometry. The amine 4-anisidine has also been used as co-initiator. The photoinitiated polymerization of multifunctional monomers was followed by real time infrared spectroscopy (RTIR) and by photo differential scanning calorimeter (PhotoDSC). Several parameters influence this kinetic such as temperature, photoinitiator concentration, light intensity, polymerizable function concentration, and material thickness. The initiators used in this study were the dyes safranine and thioxanthone. The co-initiators used were the amines TEA, TEOHA and EDB. The swelling of films of these copolymers were determined by chloroform absorption. A good inverse relationship was found between the swelling and the polymerization rates. Copolymers of styrenesulfonate and methyl methacrylate, or hydroxyethyl methacrylate, were prepared by photoinitiation polymerization using the cationic dye Safranine in hydrotropic medium. The reactions were be carried out at Stys concentrations higher than the MHC (minimum hydrotrope concentration) where the monomer forms aggregates.

"Estudo de polimerização fotoiniciada por corantes em diferentes meios"