Web Release Date: August 29,
Mercury(II) Sorption to Two Florida Everglades Peats: Evidence for Strong and Weak Binding and Competition by Dissolved Organic Matter Released from the Peat



and
Department of Civil, Environmental, and Architectural Engineering, University of Colorado, Boulder, Colorado 80309-0428, U.S. Geological Survey, Water Resources Division, 3215 Marine Street, Boulder, Colorado 80303, and Department of Geological Sciences, University of Colorado, Boulder, Colorado 80309
Received for review November 2, 2001
Revised manuscript received June 12, 2002
Accepted June 13, 2002
Abstract:
The binding of mercury(II) to two peats from Florida Everglades sites with different rates of mercury methylation was measured at pH 6.0 and 0.01 M ionic strength. The mercury(II) sorption isotherms, measured over a total mercury(II) range of 10-7.4 to 10-3.7 M, showed the competition for mercury(II) between the peat and dissolved organic matter released from the peat and the existence of strong and weak binding sites for mercury(II). Binding was portrayed by a model accounting for strong and weak sites on both the peat and the released DOM. The conditional binding constants (for which the ligand concentration was set as the concentration of reduced sulfur in the organic matter as measured by X-ray absorption near-edge structure spectroscopy) determined for the strong sites on the two peats were similar (Kpeat,s = 1021.8±0.1 and 1022.0±0.1 M-1), but less than those determined for the DOM strong sites (Kdom,s = 1022.8±0.1 and 1023.2±0.1 M-1), resulting in mercury(II) binding by the DOM at low mercury(II) concentrations. The magnitude of the strong site binding constant is indicative of mercury(II) interaction with organic thiol functional groups. The conditional binding constants determined for the weak peat sites (Kpeat,w = 1011.5±0.1 and 1011.8±0.1 M-1) and weak DOM sites (Kdom,w = 108.7±3.0 and 107.3±4.5 M-1) were indicative of mercury(II) interaction with carboxyl and phenol functional groups.
Download the full text: PDF | HTML