The classic hydrodynamic wetting theory leads to a linear relationship between spreading speed and the capillary force, being determined only by the surface tension of the liquid and its viscosity. Both equilibrium and dynamic processes of wetting are important in adhesion phenomena. The theory appears to be in good agreement with the results generated from experiments conducted on the spreading of poly(dimethylsiloxane) (PDMS) on soda-lime glass substrate and fails to account for the behavior of other liquids. In this study, the spreading kinetics of four different liquids (hexadecane, undecane. glycerol and water) was determined on three different solids, namely, soda-lime glass, poly(methyl methacrylate) (PMMA) and polystyrene (PS). Droplets from the same liquid allowed to spread under identical conditions on three different substrates produce distinctly different behaviors. The results show that the equilibrium contact angles are qualitatively ranked in accordance with the critical surface tension of wetting (gamma(c)) of the respective solid, i.e., high-gamma(c) solids caused the low surface tension liquids to assume the least equilibrium spreading (largest contact angle). On the other end, low-gamma(c) solids with the lowest surface tension liquid produce the most wetting (smallest contact angle). The results suggest that equilibrium spreading could be explained on the basis of the axiom 'like wets like'; in other words, polar surfaces tend to be wetted by polar liquids and vice versa.