A two-stage analysis of the mechanism of metal ion binding by a heterogeneo
us adsorbent was developed. In the first stage, a continuous proton affinit
y distribution was calculated from potentiometric titration data using the
CONTIN method with a Langmuir kernel. Electrostatic effects were accounted
for using a diffuse layer model. In the second stage, the parameters obtain
ed from the continuous distribution function (i.e. the number of different
types of surface sites, site densities and their protonation constants) wer
e utilized in a discrete distribution to represent the adsorbent in surface
complexation and double layer models using the GRFIT speciation code. This
information on the surface groups was applied to metal ion potentiometric
titration experiments to calculate the surface complexation equilibrium con
stants of the metal ions and hence elucidate the mechanism of ion binding t
o these sites. The proposed method was applied successfully to the adsorpti
on of Sr and Cu ions on carbon-composite adsorbents, KAU-mod and SCN-mod. T
he continuous distribution method (CONTIN) revealed three types of surface
sites within these carbon-composite adsorbents with pK values ranging betwe
en 3.5-4.1, 5.3-6.3 and 7.7-8.2. The analysis of the metal ion adsorption d
ata using the GRFIT speciation code showed that only the first two surface
sites were capable of forming surface complexes with the Sr ions, and that
only the first site governed the adsorption of the Cu ions. (C) 2001 Elsevi
er Science Ltd. All rights reserved.