The reactions of paraquat and divalent metal ions with humic acid: Factors influencing stoichiometry 2

Abstract

Laurentide humic acid has been titrated with paraquat and with selected divalent metal ions. In some cases, the humic acid was spiked with one cation before titration with another one. Several equivalence points were determined for the binding of the divalent cations, including paraquat. Three equivalence points agreed well with values predicted from the acidic properties of the humic acid. Eight independent experiments gave nine replicate values for an equivalence point that corresponds to 79.2 mole % of the total pairs of carboxyl groups. It is postulated that this represents a large molecular weight or structural fraction of the humic acid. The remaining 20.8 mole % can either bind one divalent cation to two carboxylate anions or bind one divalent cation to one carboxylate anion, with another anion providing for charge balance. Aggregation ‐ disaggregation and dissolution ‐precipitation phenomena may determine which case prevails, and they in turn are sensitive to the chemical compositions of samples. It should be possible to develop analytical chemical methods for characterizing the stoichiometric properties of humic acid samples.