In our previous article, we established that polycarbonate (PC) can react with the diglycidyl ether of bisphenol-A (DGEBA) at 200ะC through transesterification and addition reactions, resulting in degraded PC chains with phenolic end groups and also in PC/DGEBA copolymers. However, these reactions can be minimized or eliminated at lower temperatures, below 160ะC. In this article, Fourier transform infrared analysis (FTIR) was used to study the curing kinetics of epoxies in the presence of PC. The curing agent was an aromatic amine, diaminodiphenyl methane (DDM). FTIR results showed that the presence of a small amount of PC promoted the amineepoxide reactions, probably due to the catalytic effect of the phenolic end groups in the PC chains. However, the PC did not alter the epoxy cure reaction mechanism. Two different blending processes were used to premix the PC and DGEBA, namely, solutionblending and melt-blending processes, in order to give different extents of prereactions. If a solution-blending process was used, PC tended to undergo crystallization during an early stage of cure. When a melt-blending process was used, no melting peak was observed in the thermograms of the differential scanning calorimeter (DSC) for the modified epoxies; PC chains bonded to DGEBA during prereaction at 200ะC, thus inhibiting the crystallization of PC during cure.