Abstract
The acid-base dissociation behaviour of the surface of γ-FeOOH is investigated by potentiometric acid-base titrations of the oxide suspensions in aqueous solutions. The zero point of charge (p.z.c.) of the electrical double layer of the reversible oxide solution interface is determined: in KNO 3 titrations at various ionic strenghts cross over at pH = 7.6; by coincidence with the pH of the isoelectric point, determined by microelectrophoresis, the cross over of titrations in KNO 3 is identified as the point of zero charge of the surface. Specific effects regarding monovalent anions (Cl −, ClO 4 −) are found to be absent, while SO 4 −− strongly adsorbs on the γ-FeOOH surface, thus modifying the balance of the positive and negative groups on the surface. The sequence of interaction of monovalent cations with the surface is reported: K + < Na + < Li +. Surprising and of particular interest are the strong adsorption of Na +, which has always been reported to interact only electrostatically with oxide surfaces, and the absence of specific interactions with Cl − ions.
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