A mineral-filled in situ composite was prepared by a colloidal approach by first suspending kaolin filler particles in aqueous caprolactam, and then polymerizing caprolactam in situ at high pressure and temperature. The purpose of this colloidal in situ polymerization is to improve particle dispersion and to enhance interaction of the filler to the polymer matrix. X-ray diffraction studies of the in situ kaolin/Nylon-6 composites revealed that the x-ray peak corresponding to the alpha-crystal form of Nylon-6 diminished with increasing kaolin loading, while the gamma-crystal structure became more pronounced. The degree of crystallinity of Nylon-6 remained fairly unchanged with the kaolin loading level in the in situ composites. Calorimetric and dynamic mechanical studies exhibited that the glass transition temperature of the resulting composite increased significantly with increase in kaolin concentration, suggesting strong filler-matrix interaction at the kaolin/Nylon-6 interface. Scanning electron microscopic (SEM) results showed uniform filler dispersion in the in situ composites relative to the conventional melt-mixed composites. Modulus and tensile strength of these in situ composites were found to be distinctively higher than that of the conventional melt-mixed kaolin/Nylon-6 composites. However, as typical for composite materials, drawability and fracture toughness decreased with increasing kaolin loading.