The adsorption of heavy metal cations on two TiO2 (anatase) samples wa
s investigated. The first sample (T1) was synthesized by hydrolysis of
TiCl4, whereas the second (T2) was a commercial product. The adsorpti
on kinetics, pH curves, adsorption isotherms and adsorption capacities
were studied. Sample T1 possesses a significant capacity towards sorp
tion of heavy metal cations (approximately 5000 mu g g(-1)), which is
much higher than the adsorption capacity of the commercial sample T2 a
nd, in most instances, higher than the capacity of silica. Quantitativ
e and fast sorption of various heavy metal ions in trace concentration
s on T1 occurs, but in different pH ranges for each element. At pH 8 q
uantitative sorption was detected for Bi, Cd, Co, Cr, Cu, Fe, Ge, In,
Mn, Ni, Pb, Sb, Sn, Te, T1, V and Zn. All of the elements can be elute
d with HNO3 and EDTA and this procedure does not adversely affect the
titania for subsequent sorptions. On the basis of the results obtained
, optimum conditions for the joint and quantitative solid-phase extrac
tion of the most common heavy metal ions are proposed. A column system
for preconcentration was developed. The conditions for the quantitati
ve and reproducible elution and of subsequent AAS were established. A
method for the determination of trace elements in different waters is
proposed. It is characterized by high precision, reproducibility and c
oncentration factor.