Colloid chemistry of clay minerals: the coagulation of montmorillonite dispersions

The transition between stable colloidal dispersions and coagulated or flocculated systems is a decisive process in practical applications of million of tons of bentonites (containing the clay mineral montmorillonite). Dispersion into the colloidal state requires the transformation of the original bentonite into the sodium form, for instance by soda activation. Therefore, we review here the coagulation of sodium montmorillonite dispersions by inorganic and organic cations and the influence of compounds of practical interest such as phosphates, cationic and anionic surfactants, alcohols, betaine-like molecules and polymers like polyphosphates, tannates, polyethylene oxides with cationic and anionic end groups, and carboxy methylcellulose. Typical properties of the sodium montmorillonite dispersions are the very low critical coagulation concentrations, the specific adsorption of counterions on the clay mineral surface, and the dependence of the cK values on the montmorillonite content in the dispersion. In most cases coagulation occurs between the negative edges and the negative face. The phosphates Na2HPO4, NaH2PO4 and Na4P2O7 increase the edge charge density and change the type of coagulation from edge (−)/face (−) to face (−)/face (−) with distinctly higher cK values. Polyanions like polyphosphate and tannate stabilize in the same way. Carboxy methylcellulose causes steric stabilization. Montmorillonite particles with adsorbed betaine-like molecules provide an example of lyosphere stabilization. [Copyright &y& Elsevier]