Adsorption Of Ethylenediamine (EDA) On Montmorillonite Saturated with Different Cations—V. Ammonium- and Triethylammonium-Montmorillonite: Ion-Exchange, Protonation and Hydrogen-Bonding

P. Cloos, R. D. Laura and C. Badot
Laboratoire de Physico-Chimie Minérale, Place Croix du Sud 1, B-1348 Louvain-la-Neuve, Belgium

Abstract: On NH4- as well as on (C2H5)3NH-montmorillonite EDA was adsorbed in protonated form. The extent of protonation depended on the relative basicities and concentrations of the interacting compounds. In the systems exposed to EDA vapor a proton transfer process took place. A similar mechanism, involving probably a water molecule which remained associated with the EDAH+ ion, occurred on air-drying (C2H5)3NH-montmorillonite treated with aqueous EDA, whereas no adsorption was observed when the suspension was washed. On the contrary EDA added, in quantities not exceeding the CEC, to a suspension of NH4-montmorillonite was adsorbed almost exclusively as EDAH22+ ion. This is explained in terms of ion-exchange between NH4+ and EDAH+ present in aqueous medium and protonation of the second amine function through the dissociation of water molecules near the clay surface.

Hydrogen-bonding between protonated and neutral EDA was observed when the extent of adsorption was higher than the extent of protonation.

Clays and Clay Minerals; December 1975 v. 23; no. 6; p. 417-423; DOI: 10.1346/CCMN.1975.0230601
© 1975, The Clay Minerals Society
Clay Minerals Society (www.clays.org)