Submicron hybrid particles were prepared by direct polymerization of three monomers of styrene, methyl methacrylate (MMA), and vinyl acetate (VAC) onto the hydrophilic surface of 230 nm silica submicron particles without any coupling agent in a semi-continuous emulsifier-free emulsion polymerization at a monomer starved condition. The polymerization was initiated by potassium persulfate with constant monomer feed at 0.01, 0.02, or 0.04 mL/min, after adding 230 nm silica seed particles. The particle growth was investigated with a laser particle size analyzer and SEM, and the particle surfaces by Fourier transform infrared spectroscopy (FT-IR). It was founded that the growth of the hybrid particles depended on the hydrophobic characteristics of the polymers. When monomer was the most hydrophobic styrene, polystyrene (PS) shells split off from the hydrophilic surface of the unmodified silica particle whenever the shells reached a limit of ~20 nm. However, both polymethyl methacrylate (PMMA) and polyvinyl acetate (PVAC) shells grew constantly on the hydrophilic surface of silica particles. In the process of the whole reaction, the SiO2/PMMA and SiO2/PVAC hybrid particles kept almost monodisperse.