期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 38, 期 6, 页码 1700-1707出版社
AMER CHEMICAL SOC
DOI: 10.1021/es0345625
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Combined batch sorption and in situ X-ray absorption spectroscopy provide direct assessment of the mechanisms for Pb(II) sorption at the calcite-water interface under low-temperature conditions. At low metal concentration, 1 muM initial Pb, X-ray absorption fine structure data indicate the formation of Pb mononuclear inner-sphere complexes at the surface. A first-shell Pb-O bond length of 2.34 Angstrom is consistent with nearest oxygen neighbors in 3- or 4-fold coordination with a distorted trigonal pyramidal or square pyramidal geometry with a stereochemically active electron lone pair. For high initial Pb concentrations, 20 and 60 muM Pb, precipitation of hydrocerussite and cerussite secondary phases dominates Pb partitioning. At 5 and 10 muM initial Pb, the sorption mechanism is dual in nature with persistence of the mononuclear adsorption complex combined with precipitation of a cerussite phase occurring prior to saturation of theoretically available surface sites. The formation of inner-sphere complexes implies strong metal interactions with the surface-the mechanistic reason for the affinity of Pb for calcite as observed in macroscopic studies. The geometry of the adsorbed complex can influence Pb coprecipitation, as a change to octahedral coordination is required for incorporation into calcite. The results provide the basis for predictions of Pb sequestration by calcite in natural systems.
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