The effect of prepolymer molecular weight on the solid-state polymerization (SSP) of poly(bisphenol A carbonate) was investigated using nitrogen (N-2) as a sweep fluid. Prepolymers with different number-average molecular weights, 3800 and 2400 g/mol, were synthesized using melt transesterification. SSP of the two prepolymers then was carried out at reaction temperatures in the range 120-190 degrees C, with a prepolymer particle size in the range 20-45 mu m and a N2 flow rate of 1600 mL/min. The glass transition temperature (T-g), number-average molecular weight (M-n), and percent crystallinity were measured at various times during each SSR The phenyl-to-phenolic end-group ratio of the prepolymers and the solid-state synthesized polymers was determined using 125.76 MHz C-13 and 500.13 MHz H-1 nuclear magnetic resonance (NMR) spectroscopy. At each reaction temperature, SSP of the higher-molecular-weight prepolymer (M-n = 3800 g/mol) always resulted in higher-molecular-weight polymers, compared with the polymers synthesized using the lower molecular weight prepolymer (M-n = 2400 g/mol). Both the crystallinity and the lamellar thickness of the polymers synthesized from the lower-molecular-weight prepolymer were significantly higher than for those synthesized from the higher-molecular-weight prepolymer. Higher crystallinity and lamellar thickness may lower the reaction rate by reducing chain-end mobility, effectively reducing the rate constant for the reaction of end groups. (C) 2008 Wiley Periodicals, Inc.