Catalytic wet air oxidation of an aqueous solution, bisphenol A (BPA), was carried out at 160°C and at 20 bar of air in a batch reactor. Silver catalysts (2.5 wt%) prepared by wet impregnation and complexation on commercial CeO 2 in addition to Ce 0.85 Zr 0.15 O 2 and Ce 0.2 Zr 0.8 O 2 sol-gel mixed oxides were synthesized and used as catalysts in the reaction. Characterizations of the catalysts were performed by using FESEM, XRD, BET, XPS and ICP-OES techniques. Residual BPA concentration was analyzed by using an UV-Vis technique and organic compound content was measured via the total organic carbon method. Commercial CeO 2 showed a smaller specific surface area and a larger crystallite size than laboratory prepared Ce-Zr mixed oxides. The highest BPA removal (76 %) was achieved after 3 h with CeO 2 , Ce 0.85 Zr 0.15 O 2 and Ag/Ce 0.85 Zr 0.15 O 2 catalysts revealing that the addition of silver had no effect on the catalytic activity of the pure supports. However, the loading of active metal to the supports by complexation decreased the adsorption of the BPA during the heating period and hence the Ag/Ce 0.85 Zr 0.15 O 2 prepared via complexation was the most active catalyst with only 1 % adsorption of BPA. Moreover, the activity of the catalysts was not related to the surface area of the samples. According to the ICP-OES analysis of the terminal water samples, leaching of the silver was occurred during oxidation experiments explaining the behavior of Ag catalysts in the reaction.