Proton binding at clay surfaces in water Marcelo J. Avena a, * , Marcelo M. Mariscal b , Carlos P. De Pauli b a Departamento de Quı ´mica, Universidad Nacional del Sur, Av. Alem 1253, (8000) Bahı ´a Blanca, Provincia de Buenos Aires, Argentina b INFIQC, Departamento de Fisicoquı ´mica, Facultad de Ciencias Quı ´micas, Universidad Nacional de Co ´rdoba, Ciudad Universitaria, 5000 Co ´rdoba, Argentina Received 15 April 2002; received in revised form 7 March 2003; accepted 10 July 2003 Abstract This article discusses the points that have more impact in the protonation – deprotonation behavior of a phyllosilicate clay surface in aqueous media. Some concepts that are currently used to explain the behavior of the oxide – water interface are now applied to the clay – water interface, and a rather new interpretation of the role of structural charges on the affinity of edge groups for protons is also given. Proton binding at a phyllosilicate clay surface takes place at oxygen-containing groups. As in the case of oxygen-containing molecules, the groups behave as monoprotic entities and undergo only one protonation – deprotonation step in a normal pH range. The protonation behavior depends on the intrinsic affinity of surface groups and long-range electrostatics. The MUSIC model confirms that the proton affinity of siloxane and gibbsite-like groups located at the basal surfaces (001 planes) of 2:1 or 1:1 clays is very low. On the contrary, the proton affinity of surface groups at the broken edges is adequate to undergo protonation – deprotonation reactions in a normal pH range. The reactivity of edge groups is also affected by the presence of structural charges within the clay layer. These charges produce an electric field that modifies not only the reactivity of the basal surfaces but also that of the edge surfaces. When the edge surface has a zero net charge, the electrical potential is negative due to the presence of the mentioned negative charges. Evidences for this are obtained from proton adsorption curves performed at different supporting electrolyte concentration. D 2003 Elsevier B.V. All rights reserved. Keywords: Proton adsorption; Edge surface; Structural charge; Surface potential 1. Introduction Ion binding and ion exchange in clays have been intensively investigated topics. Proton binding, for instance, is particularly important because it can directly affect the electrical charge of the clay surface and thus indirectly affect the attachment of other substances and the stability of clay dis- persions. Through these processes, proton binding has great influence on soil fertility, soil aggregation and chemical speciation in the environment. Protonation of a clay surface can take place by ion exchange or by direct binding of H + to oxygen- containing surface groups. Both processes can be understood in terms of conventional acid – base and electrostatic theories, and only the second process 0169-1317/$ - see front matter D 2003 Elsevier B.V. All rights reserved. doi:10.1016/j.clay.2003.07.003 * Corresponding author. E-mail address: mavena@uns.edu.ar (M.J. Avena). www.elsevier.com/locate/clay Applied Clay Science 24 (2003) 3 – 9