The adsorption characteristics of a variety of divalent and trivalent
metal-EDTA complexes onto goethite (alpha-FeOOH) were examined in aque
ous solution. Uncomplexed EDTA is adsorbed as a binuclear complex at l
ow pH and as a mononuclear complex at high pH. Adsorption is ligand-li
ke with a high extent of adsorption at low pH. The process can be desc
ribed by formation of inner-sphere complexes by the surface complexati
on model with constant capacitance. The EDTA complexes of the divalent
metals Ca, Zn, Ni, Cu, Co(II), and Pb, which are quinquedentate in so
lution (free donor atoms bound to the metal ion), all showed the same
ligand-like adsorption behavior. Their adsorption as a function of pH
and concentration can be described by the formation of one type of ter
nary surface complex and can be fitted with the same equilibrium const
ant. Pd(II)EDTA, which is bidentate or quadridentate in solution, is a
dsorbed more strongly, but also in a ligand-like manner. The EDTA comp
lexes of the trivalent metals LaEDTA and BiEDTA are adsorbed very stro
ngly over the whole pH range. The sexidentate complex of Co(III) is we
akly adsorbed at low pH outer-spherically, i.e., by electrostatic inte
raction only. Fe(III)EDTA is weakly adsorbed over the whole pH range w
ith a predominant nonspecific surface complex at low pH and a specific
complex at high pH. (C) 1996 Academic Press, Inc.