Poly(n-butyl methacrylate) (PBMA) composites with calcium carbonate (CaCO 3 ) were prepared by in situ radical copolymerization of butyl methacrylate (BMA) and methacrylic acid (MA) with precipitated calcium carbonate. To compare the different rheological behaviors of the monomer mixtures with CaCO 3 and the composites, the steady and dynamic viscosities of BMA/MA/CaCO 3 and poly(BMA/MA/CaCO 3 ) were measured by means of steady and oscillatory shear flows. The viscosity of the mixture BMA/MA/CaCO 3 was found to increase evidently with the increasing of CaCO 3 %. The influence of MA% on viscosity of BMA/MA/CaCO 3 was slight. During the in situ polymerization, the viscosity of the reacting system was measured to be enhanced by a factor of about 10 4 from the monomer/ CaCO 3 mixture to composites. The dependency of zeroshear viscosity on molar mass of PBMA was also investigated. The relation between the zero-shear viscosity and molar mass is 0 ϭ 10 Ϫ15 M w 3.5 . The evolution of the viscosity with the temperature for both PBMA and its composites was obtained and time-temperature superposition was used to build master curves for the dynamic moduli. The flow activation energies were found to be 115.0, 148.6, and 178.7 kJ/mol for PBMA, composite PBMA/CaCO 3 (90/10), and PBMA/MA/CaCO 3 (89/1/10), respectively. The viscosity of the composites containing less than 10% CaCO 3 was lower than that of pure PBMA with the same molar mass.