Complexation of Cu2+ and Pb2+ by peat and humic acid

Berlin

1997

S. 685-696

7 Abb., 3 Tab., 42 Lit. Ang.

Artikel aus einer ZeitschriftUnselbständiges Werk

200163181

The binding of metal to humic substances is problematical. The approaches for studying metal binding to organic matter are briefly reviewed. Ion-selective electrodes (Cu2+ and Pb2+) were used to measure metal complexation by a whole peat and an extracted humic acid (HA) fraction. Scatchard plots and calculation of incremental formation constants were used to obtain values for the binding constants for the metals onto both peat and HA. Both the peat and the humic acid had a larger maximum binding capacity for Pb2+ than for Cu2+ (e.g. at pH = 5 HA gave 0·188 mmol Cu2+ g−1 and 0·564 mmol Pb2+ g−1: peat gave 0·111 mmol Cu2+ g−1 and 0·391 mmol Pb2+ g−1). Overall, the humic acid had a larger metal binding capacity, suggesting that extraction caused conformational or chemical changes. The binding constants (K1) for Cu2+ increased with increasing pH in both peat and humic acid, and were larger in the peat at any given pH (e.g. at pH = 5 HA gave log K1= 2·63, and peat gave log K1= 4·47 for Cu2+). The values for Pb2+ showed little change with pH or between peat and humic acid (e.g. at pH = 5 HA gave log K1= 3·03 and peat gave log K1= 3·00 for Pb2+). In the peat, Cu2+ may be more able to bind in a 2:1 stoichiometric arrangement, resulting in greater stability but smaller binding capacity, whereas Pb2+ binds predominantly in a 1:1 arrangement, with more metal being bound less strongly. Whole peat is considered to be more appropriate than an extracted humic acid fraction for the study of heavy metal binding in organic soils, as this is the material with which metals introduced into an organic soil would interact under natural conditions.