The effect of pH and hardness metal ions on the competitive interaction between trace metal ions and inorganic and organic complexing agents found in natural waters

The effect of pH and hardness metal ions on the interactions between trace metals and both inorganic and organic complexing agents has been studied under conditions simulating natural aquatic conditions, by employing anodic stripping voltammetric titration techniques. The complexation of Bi(III), Cd(II), Cu(II), Pb(II), and Tl(I) with the hydroxo- and carbonato-ligands found in a carbonate medium has been observed to generally increase with increasing pH. Both labile and nonlabile interactions have been observed. Nonlabile interactions are predominant at low pH and labile interactions generally increase with increasing pH. Neither calcium nor magnesium affects these interactions. The complexation of humic acids with trace metals in a carbonate medium was found to be more intense than metal ion-inorganic complexation. Both labile and nonlabile complexation was found; however, no generalizations can be made concerning the type and extent of complexation because of the individual nature of the interactions of each trace metal. Calcium was found to be more effective than magnesium in inhibiting trace metal-organic complexation. The effect of calcium is to inhibit labile complexation and is most pronounced with the cadmium-humic acid system.