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Partitioning of Zn, Cd, Pb, and Cu in organic-rich soil profiles in the vicinity of a zinc smelter

机译:锌冶炼厂附近富含有机质土壤剖面中锌,镉,铅和铜的分配

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A five-step sequential extraction procedure was applied to organic-rich soil samples from five soil profiles situated 1–8 km from a zinc smelter. The partitioning of Zn, Cd, Pb, and Cu into five operationally defined fractions (exchangeable, “carbonate’’-bound, reducible, oxidizable, and residual) was studied at different soil depths down to 35cm. In the surface soil (0–1 cm) a major part of Pb and Cu was extracted in the oxidizable fraction, whereas for Zn and Cd slightly more was extracted in the ‘‘carbonate”-fraction than in the other four fractions. Extracted metal proportions in the oxidizable fraction were respectively of the order of 30%, 20%, 50%, and 80% for Zn, Cd, Pb, and Cu in the surface soil for all sites, but these proportions decreased with soil depth. In the surface soil less than 20% of all the elements were extracted in the residual fraction, but the proportions associated with this fraction generally increased with soil depth. In the C-horizon, differences in extracted proportions of Pb and Cu in the residual fraction were probably due to geochemical factors, whereas for Zn the low extracted proportion at a highly contaminated site (20%) may be due to Zn migration to the C-horizon at this site. For Cd the extracted proportions in the C-horizon were lower than for the other elements, generally below 20%, presumably because Cd is weaker in terms of its adsorption to the soil than the other elements studied. Total concentrations of the metals decreased strongly with increasing distance from the smelter, but less systematic differences were observed for their distributions among fractions. Potentially bioavailable metal proportions (exchangeable + “carbonate”-bound fraction) in the surface soil were about 50%, 60%, 20%, and 10% for Zn, Cd, Pb, and Cu, respectively. In C-horizon soil the mobility sequence CdZnPb = Cu was generally observed. The present results indicate that the concentrations and chemical fractionation of Zn, Pb, and Cd in these soils represent a considerable risk to natural terrestrial food chains.
机译:五步序贯提取程序应用于距锌冶炼厂1-8 km的五个土壤剖面中富含有机物的土壤样品。在低至35cm的不同土壤深度下,研究了将Zn,Cd,Pb和Cu分为五个可操作定义的部分(可交换的,“碳酸盐结合的”,可还原的,可氧化的和残留的)。在表层土壤(0-1cm)中,大部分的Pb和Cu被提取为可氧化的馏分,而对于Zn和Cd,在“碳酸盐”馏分中的提取率要比其他四个馏分高。对于所有场所,表层土壤中的Zn,Cd,Pb和Cu的可氧化级分中提取的金属比例分别约为30%,20%,50%和80%,但这些比例随土壤深度而降低。在表层土壤中,只有不到20%的元素从残留部分中提取出来,但与该部分有关的比例通常随土壤深度的增加而增加。在C地平线中,残留部分中Pb和Cu的提取比例差异可能是由于地球化学因素造成的,而对于Zn,在高污染位点(20%)的较低提取比例可能是由于Zn向C的迁移所致。 -水平在此站点。对于Cd,在C水平仪中提取的比例要低于其他元素,通常低于20%,这大概是因为Cd在土壤中的吸附比其他研究元素要弱。金属的总浓度随与冶炼厂距离的增加而大大降低,但是在各馏分之间的分布观察到的系统差异较小。对于锌,镉,铅和铜,表层土壤中潜在的生物利用金属比例(可交换的+“碳酸盐”结合部分)分别约为50%,60%,20%和10%。在C型水平土壤中,通常观察到迁移率序列Cd> Zn> Pb = Cu。目前的结果表明,这些土壤中Zn,Pb和Cd的浓度和化学分馏代表了天然陆地食物链的巨大风险。

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