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Modelling lead(II) sorption to ferrihydrite and soil organic matter

机译:模拟铅(II)对水铁矿和土壤有机质的吸附

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摘要

Lead(II) adsorption to soil organic matter and iron (hydr)oxides is strong, and may control the geochemical behaviour of this metal. Here, we report the adsorption of Pb(2+) (i) to 2-line ferrihydrite, and (ii) to a mor layer. The results showed that ferrihydrite has heterogeneous Pb(2+) binding. Use of a surface complexation model indicated that similar to 1% of the surface sites adsorbed Pb(2+) more strongly than the remaining 99 %. Although only one surface complexation reaction was used (a bidentate complex of the composition (equivalent to FeOH)(2)Pb(+)), three classes of sites with different affinity for Pb(2+) were needed to simulate Pb(2+) binding correctly over all Pb/Fe ratios analysed. For the mor layer, Pb(2+) sorption was much stronger than current models for organic complexation suggest. The results could be described by the Stockholm Humic Model when the binding heterogeneity was increased, and when it was assumed that 0.2% of the binding sites were specific for Pb. Use of revised model parameters for nine Vietnamese soils suggest that lead(II) binding was more correctly simulated than before. Thus, underestimation of lead(II) sorption to both (hydr) oxide surfaces and organic matter may explain the failure of previous geochemical modelling attempts for lead(II).
机译:铅对土壤有机质和铁(氢)氧化物的吸附很强,并且可以控制这种金属的地球化学行为。在这里,我们报告Pb(2+)(i)到2线水铁矿,和(ii)到mor层的吸附。结果表明,水铁矿具有异质Pb(2+)绑定。使用表面络合模型表明,相似的1%的表面位点比其余的99%吸附Pb(2+)的强度更大。尽管仅使用了一种表面络合反应(该成分的双齿络合物(相当于FeOH)(2)Pb(+)),但需要三类对Pb(2+)具有不同亲和力的位点来模拟Pb(2+ )在所有分析的Pb / Fe比值上正确结合。对于mor层,Pb(2+)的吸附作用远强于目前的有机络合模型。当结合异质性增加时,以及假设0.2%的结合位点对Pb具有特异性时,结果可以由Stockholm Humic模型描述。对九种越南土壤使用修订后的模型参数表明,与以前相比,铅(II)结合的模拟更正确。因此,低估了铅(II)在(水)氧化物表面和有机物上的吸附量,这可能解释了先前对铅(II)进行地球化学建模尝试的失败。

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