Mathematical models describing kinetics of adsorption and competitive
adsorption of polymers into porous media have been developed. The mode
ls predict the constant of adsorption equilibrium, the rate constants
of adsorption, of desorption, and of substitution of small polymer cha
ins by large ones, and the maximum amount of polymer that can be adsor
bed on a unit area of the surface. Using experimental adsorption data
of monodisperse polystyrenes and porous silica, we show that there is
good agreement between the kinetic models and the experimental data.