Hesterberg D, Chou J W, Hutchison K J, Sayers D E
Department of Soil Science, Box 7619, and Department of Physics, Box 7518, North Carolina State University, Raleigh, North Carolina 27695, USA.
Environ Sci Technol. 2001 Jul 1;35(13):2741-5. doi: 10.1021/es001960o.
Organic matter is an important sorbent of heavy metals in soils and sediments. The heterogeneity of organic matter, including the presence of various reactive O-, N-, and S-bearing ligands, makes it difficult to precisely characterize the nature of metal-ligand binding sites. The objective of this research was to characterize the extent and nature of Hg(II) bonding with reduced organic S in soil organic matter. Sulfur-rich humic acid (0.7 +/- 0.1 mol of S kg-1) was extracted from samples of surface soil from a marine wetland. Synchrotron X-ray absorption near-edge structure (XANES) analysis at the S K edge indicated that 70 +/- 3 mol % of the organic S was in a reduced oxidation state. Aqueous solutions containing 2 mmol of Hg kg-1, 0.1 M NaNO3, and humic acid added at various S/Hg molar ratios at pH 5.60 +/- 0.02 were characterized using extended X-ray absorption fine structure (EXAFS) spectroscopy at the Hg LIII edge. Spectral fitting showed that as the total S/Hg ratio increased from 0.6 to 5.6 (reduced S/Hg of 0.4-4.0), the fraction of Hg-S bonding relative to Hg-O (or Hg-N) bonding increased from 0.4 to 0.9. Results demonstrated preferential bonding of Hg(II) to reduced organic S sites and indicated that multiple sulfur ligands were coordinated with Hg2+ ions at high S/Hg ratios, which corresponded to low levels of complexed Hg(II).
有机质是土壤和沉积物中重金属的重要吸附剂。有机质的异质性,包括各种含反应性O、N和S的配体的存在,使得精确表征金属-配体结合位点的性质变得困难。本研究的目的是表征土壤有机质中Hg(II)与还原态有机硫结合的程度和性质。从滨海湿地表层土壤样品中提取了富硫腐殖酸(0.7±0.1摩尔硫/千克)。在S K边进行的同步加速器X射线吸收近边结构(XANES)分析表明,70±3摩尔%的有机硫处于还原氧化态。使用Hg LIII边的扩展X射线吸收精细结构(EXAFS)光谱对含有2毫摩尔Hg/千克、0.1 M NaNO3以及以不同S/Hg摩尔比添加腐殖酸的水溶液在pH 5.60±0.02条件下进行了表征。光谱拟合表明,随着总S/Hg比从0.6增加到5.6(还原态S/Hg为0.4 - 4.0),Hg - S键相对于Hg - O(或Hg - N)键的比例从0.4增加到0.9。结果表明Hg(II)优先与还原态有机硫位点结合,并表明在高S/Hg比时多个硫配体与Hg2+离子配位,这对应于低水平的络合Hg(II)。