Impact of Radiation Attenuation and Temperature Evolution on Polymerization of Dimethacrylate- based Resins with a Photobleaching Photoinitiator.

VERÓNICA MUCCI; WAYNE D. COOK; CLAUDIA VALLO

POLYMER ENGINEERING AND SCIENCE

Wiley

Año: 2009 vol. 49 p. 2225 - 2233

0032-3888

Abstract The photopolymerization process of a dimethacrylate copolymer system based on bis-GMA/TEGDMA monomers activated by the camphorquinone (CQ)/amine photoinitiator system, was experimentally studied under nonisothermal conditions in 1 and 2 mm thick samples by measuring double bond conversion, temperature rise and radiation attenuation through the sample during polymerization. The temperature evolution during polymerization was also predicted by solving the energy balance coupled with the kinetic expressions for the reaction rate. Radiation attenuation as a function of depth by the photobleachable CQ results in spatial and temporal variation in the local rates of the kinetic steps involved. General relationships for spatiotemporal variations in concentration of a photobleaching initiator, in systems where attenuation and initiator consumption are taken into account, were used to compute local polymerization rates. The effects of radiation attenuation, photobleaching of the photoinitiator and variation of cure temperature at different depths into the resin, all compete to determine the double bond consumption. The increased radiation attenuation in the 2 mm thick sample was accompanied by a higher cure temperature compared with the 1 mm thick sample, and as a result, the global monomer conversion (averaged over the sample thickness) in the 1 and 2 mm thick samples was the same. Results obtained in this research highlight the inherent interlinking of thermal and radiation attenuation effects in bulk photopolymerizing systems.