Sorption studies of SO42-, Cl-, Br- and NO3- ions on ferric oxide gel have shown that these ions replace surface OH groups. The particle diffusion-controlled exchanges follow mainly the Helfferich first mechanism. This situation is different from that in weak-base resins in the similar case of ionization of weakly dissociated groups by reaction with H+ co-ions. The interdiffusion coefficient D(i)BAR decreases in the order SO42- > Cl- > Br- > NO3-. It was deduced that, at least for SO42-, the complexing ability with Fe(III) at the gel/water interface is weaker than that in solution.