The hydrophobic and hydrophilic components of the surface of talc materials
in aqueous solution were determined using ionic surfactants and their pola
r headgroup adsorption isotherms. The hydrophilic and hydrophobic surface a
reas are inferred from the amount of probe molecule adsorbed and the struct
ure of the adsorbed layer. Natural dispersion of talc shows at 298 K a pH o
f 9.4 and the electrophoretic measurements indicate that the particles are
negatively charged. The hydrophilic surface area is estimated from the adso
rption of benzyltrimethylammonium ions (BTMA(+)) through electrostatic inte
ractions as supported by the increase of divalent ions in the bulk phase an
d the decrease in the exothermic displacement enthalpy. It was also observe
d from the adsorption isotherm of benzene sulfonate anions that the density
of positive surface sites is very low and is thus neglected. The adsorptio
n of an anionic surfactant essentially occurs through dispersive interactio
ns between the nonpolar organic tail of the molecule and the hydrophobic su
rface. Furthermore, some assumptions on the structure of dodecyl sulfate su
rfactant aggregates at the interface allow the hydrophobic part of the talc
particles to be estimated. The cationic surfactant adsorption has been inv
estigated and found to corroborate the hydrophilic and hydrophobic area val
ues first obtained. (C) 2001 Academic Press.