Determination of sulfide ligands and association with natural organic matter |
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Authors: | James R. Kramer Russell A. Bell D. Scott Smith |
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Affiliation: | 1. School of Geography and Earth Sciences, McMaster University, Hamilton, Ont., Canada L8S4K1;2. Department of Chemistry, McMaster University, Hamilton, Ont., Canada L8S4K1;3. Department of Chemistry, Wilfrid Laurier University, Waterloo, Ont., Canada N2L 3C5 |
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Abstract: | ![]() Group B metals, such as Hg, Cu, Ag, Pb and Cd bind strongly to reduced inorganic and organic S(II−) ligands. These S(II−) ligands, stable in oxic waters for significant periods of time, occur at the <1–100 s nM concentrations. It is hypothesized that S(II−) ligands are stabilized as Cu–S molecules associated with organic matter by multi-ligand binding or in nano-pore encapsulations in organic matter. S(II−) ligands are estimated by two methods: purge/trap analysis as Cr-reducible sulfide (CRS), and strong ligand (SLT) from a competitive ligand titration with Ag(I). The CRS/SLT ratio is nearly one for selected samples. CRS correlates reasonably well (r2 ∼ 0.5) with organic C with a slope of 14.6 nM per mg C. The conditional binding constant of Ag–SL is 11.3 for effluent associated with waste-water and decreases for river waters from about 12–8.8 as the strong sites are occupied with Ag(I). |
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