The potential of capillary electrophoresis (CE) has been demonstrated
for the analysis and characterization of humic substances (fulvic and
humic acids). Humic substances were effectively separated by capillary
gel electrophoresis (acrylamide gel CGE) and CE with cellulose deriva
tive solutions using a 50 mM tris-borate buffer (pH 8.3) with 2 mM EDT
A, or 5% polyvinylpyrrolidone (PNVP). They were detected by UV absorpt
ion at 260 nm and by emission at 490 nm (excitation at 390 nm). The us
ing these gel systems leads to the separation of humic substances into
two fractions, which comprise lower-molecular weight components as we
ll as higher ones. The addition of iron (III) chloride resulted in a d
ecrease in the peak of the lower molecular-weight components, which mo
st likely arose from an aggregation of the lower-molecular weight frac
tion due to binding bond formation through the hydrolyzed Fe(III) ion.
When sodium hypochlorite solution was added to the humic substance, s
ome peaks decreased with increasing the residual chlorine concentratio
ns. Therefore, the gel-mode CE enables one to monitor the reaction beh
avior as well as the fate of humic substances in an aquatic system in
relation to the binding of metal ions and the oxidation processes.