A COMPREHENSIVE MONTE CARLO SIMULATION OF STYRENE ATOM TRANSFER RADICAL POLYMERIZATION

An optimized and high-performance Monte Carlo simulation is developed to take thorough account of four different cases of termination in styrene ATRP. According to the simulation results, the bimolecular termination rate constant sharply drops throughout the polymerization when either chain-length dependency of termination rate constant, gel effect, or both together is applied to the simulation. In addition, as expected, the initiator is quickly decomposed at the early stages of the polymerization. The concentration of the catalyst in lower oxidation state decreases at first and then plateaus at higher conversion; furthermore, the steady concentration of (MtY)-Y-n/L in the polymerization is the highest when the chain-length-dependent diffusion-controlled termination rate constant is employed in the simulation. The rates of deactivation and chain end degradation reactions are also smaller in this case. Therefore, the fraction of dormant chains is higher throughout the reaction and consequently the portion of dead polymers decreases. Besides, molecular weight increases linearly with conversion; however, when neither gel effect nor chain-length dependency of termination rate constant is considered, the molecular weight deviates from linearity at the end of the reaction. The peak of chain length distribution shifts toward higher molecular weight too during the reaction. Finally, the molecular weight distribution broadens at higher conversion; however, the chain length distribution of polymers produced under conditions of applying chain-length-dependent diffusion-controlled termination rate constant is narrower.