Two types of polystyrene latices, one with surface carboxylic groups a
nd the other covered with a polymer shell containing carboxylic and su
lphonic groups, were analyzed in terms of their metal ion binding prop
erties. In-situ voltammetric experiments were carried out for zinc(II)
, cadmium(II) and lead(II) to characterize the thermodynamics and kine
tics of their association with the surface groups in the latex particl
es. The kinetics were investigated experimentally through the time-sca
le dependencies, and set against theoretical predictions [De Jong, H.
G. and Van Leeuwen, H. P., J. Electroanal. Chem., 1987, 234, 17; De Jo
ng, H. G. and Van Leeuwen, H. P., J. Electroanal. Chem., 1987, 235, 1]
on the basis of rigorous lability criteria and elementary complex for
mation rate constants. The core-shell latices appear to form relativel
y weak and labile complexes. In the case of highly charged latices, th
e metal/carboxylate surface complexes are stronger and lose lability a
t a high degree of dissociation. (C) 1998 Elsevier Science Ltd. All ri
ghts reserved.