“…In a study of Pb 2+ and Zn 2+ retention by kaolinite at metal concentrations of 100 AM, it was shown that the adsorption data were fitted closely by a constant-capacitance surface complexation model, one involving electrostatic attraction between transition metal ions and the permanent, negatively charged sites on the silanol faces of kaolinite, while the other is an inner-sphere complex at the variable-charge surface hydroxyl groups situated at the crystal edges and on the aluminol faces (Ikhsan et al, 1999). Our previous studies on the adsorption of other divalent ions (Co 2+ and Ba 2+ ) by kaolinite using ToF-SIMS depth profiling have shown that the fixation of these ions is associated with a decrease in the initial amount of exchangeable cations of the kaolinite, but that the decrease did not quantitatively agree with the amount of adsorbed Co 2+ or Ba 2+ kaolinite (Shahwan et al, 2004). In summary, when discussing the adsorption mechanism by kaolinite, in addition to the exchange of exchangeable metal cations, protons of the OH 2 + and OH groups at the edges should also be taken into consideration.…”