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氧化还原电位对荷兰代尔夫特受污染运河沉积物中重金属结合形态的影响。

Effect of redox potential on heavy metal binding forms in polluted canal sediments in Delft (The Netherlands).

作者信息

Kelderman P, Osman A A

机构信息

UNESCO-IHE Institute for Water Education, PO Box 3015, 2601 DA Delft, The Netherlands.

出版信息

Water Res. 2007 Oct;41(18):4251-61. doi: 10.1016/j.watres.2007.05.058. Epub 2007 Jun 6.

Abstract

Heavy metal binding forms for Cu, Zn and Pb were determined at four representative sediment sites in the canals of Delft (The Netherlands), using selective chemical extraction methods. Small differences (on average <5%) were found between duplicate extraction experiments. The dominant Cu binding form was always related to sulphide and organics in the sediment. Zn was mainly bound to iron+manganese (hydr)oxides, whereas Pb was rather evenly distributed over the different labile and non-labile binding fractions. A gradual (over about 1 month) increase in redox potentials of the anaerobic sediments led to a 7-37% sediment release of the above heavy metals; this could mainly be ascribed to oxidation of the heavy metal-sulphide bindings. Part of the released heavy metals was re-adsorbed by the labile binding phases ("exchangeable" and "carbonate bound"). Contrary to expectations, we found a decrease rather than an increase in the Fe+Mn (hydr)oxide binding forms. This can probably be ascribed to non-equilibrium reactions in the time span of the experiments, as well as side reactions such as complexation with humic acids and hindered precipitation reactions due to organic matter coatings.

摘要

采用选择性化学萃取方法,在荷兰代尔夫特运河的四个代表性沉积物位点测定了铜、锌和铅的重金属结合形态。重复萃取实验之间的差异很小(平均<5%)。沉积物中铜的主要结合形态总是与硫化物和有机物有关。锌主要与铁+锰(氢)氧化物结合,而铅在不同的不稳定和非不稳定结合组分中分布较为均匀。厌氧沉积物的氧化还原电位在大约1个月的时间内逐渐升高,导致上述重金属从沉积物中释放7%-37%;这主要归因于重金属-硫化物结合物的氧化。部分释放的重金属被不稳定结合相(“可交换”和“碳酸盐结合”)重新吸附。与预期相反,我们发现铁+锰(氢)氧化物结合形态减少而非增加。这可能归因于实验时间范围内的非平衡反应,以及诸如与腐殖酸络合和由于有机物涂层导致的沉淀反应受阻等副反应。

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