Modeling adsorption-desorption processes of Cu on edge and planar sites of montmorillonite.

The effect of the ionic strength on adsorption of Cu on calcium montmorillonite was studied at concentrations ranging from 31 to 516 microM. An adsorption model was employed in the analysis of the data. When the background electrolyte was NaClO4, the ionic exchange was suppressed at 0.5 M concentration, and Cu adsorption took place on edge sites, reaching a plateau at about 24 mmol/kg. A further increase in ionic strength did not have any effect on Cu adsorption, suggesting that the heavy metal was adsorbed by inner-sphere complexes on the edge sites of the clay. A binding coefficient for Cu2+ on the edge sites K = 2 x 10(4) M(-1) was determined, indicating very high affinity of Cu2+ for these sites. When the electrolyte used was NaCl, the amounts of Cu adsorbed were reduced. The model predicted well the adsorption data by considering the adsorption of CuCl+ species. Adsorption-desorption processes of Cu on calcium montmorillonite in media of 0.01 and 0.1 M NaCl showed hysteresis. Model calculations also predict the desorption fairly well. According to the model, the hysteresis is mainly attributed to the heterogeneity of sites for the adsorption of Cu. The hysteresis arising from the planar sites is largely due to reduced competition of ion species for adsorption and enhancement in the magnitude of the surface potential.