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The impact of increased oxygen conditions on metal - contaminated sediments part I: Effects on redox status, sediment geochemistry and metal bioavailability

机译:氧气条件增加对金属污染的沉积物的影响第一部分:对氧化还原状态,沉积物地球化学和金属生物利用度的影响

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摘要

In order to evaluate the effect of improved oxygen concentrations in overlying surface water on the redox status, sediment geochemistry and metal bioavailability in metal-polluted sediments a 54 days lab experiment with two different experimental treatments was conducted (90% and 40% O_2). Changes in redox potential (Eh) in the sediment were monitored over time. At 6 different time points (after 0, 2, 5, 12, 32 and 54 days) and at 4 sediment depths (0-1, 1-4, 4-8 and 8-15 cm), acid volatile sulfides (AVS), simultaneously extracted metals (SEM) and total organic carbon (TOC) were measured and metal release to overlying surface water was determined. Labile metal species in both water and sediment were measured using Diffusive Gradients in Thin films (DGT). Our results showed that elevated oxygen levels in overlying surface water led to an Eh increase in the sediment of the 90% O_2 treatment from 0 to ±200 mV while AVS concentrations in the upper sediment layer decreased by 70%. Following AVS oxidation metal availability in the pore water was highly elevated after 54 days. However, Cu remained strongly bound to the sediment during the whole experiment. Only a limited metal release to the overlying surface water was noticed, which was due to the fact that SEM_tot concentrations in the sediment did not yet exceeded AVS levels ([SEM_tot - AVS]/f_oc = 0) after 54 days. Additionally, adsorption on Fe and Mn hydroxides and particulate organic carbon also slowed down any potential metal release. Our results indicated that increasing oxygen concentrations due to general water quality improvements can enhance the mobility of trace metals which may result in the leaching of sediment-bound metals to overlying surface water, even in undisturbed watercourses.
机译:为了评估上覆地表水中改善的氧浓度对金属污染沉积物中氧化还原状态,沉积物地球化学和金属生物利用度的影响,进行了一项为期54天的实验室实验,采用两种不同的实验处理方法(90%和40%O_2)。随时间监测沉积物中氧化还原电势(Eh)的变化。在6个不同的时间点(0、2、5、12、32和54天后)和4个沉积深度(0-1、1-4、4-8和8-15 cm),酸挥发性硫化物(AVS) ,同时测量了提取的金属(SEM)和总有机碳(TOC),并确定了金属向上层地表水中的释放。使用薄膜中的扩散梯度(DGT)测量了水和沉积物中的不稳定金属种类。我们的研究结果表明,上覆地表水中氧气含量的升高导致90%O_2处理的沉积物中Eh从0增加到±200 mV,而上沉积层中的AVS浓度降低了70%。经过AVS氧化后,54天后,孔隙水中的金属利用率大大提高。但是,在整个实验过程中,Cu仍然牢固地与沉积物结合。仅观察到有限的金属释放到上层地表水中,这是由于在54天后沉积物中的SEM_tot浓度尚未超过AVS水平([SEM_tot-AVS] / f_oc = 0)。另外,在铁和锰的氢氧化物和颗粒有机碳上的吸附也减慢了任何潜在的金属释放。我们的结果表明,由于总体水质的改善而增加了氧气浓度,可以提高痕量金属的迁移率,甚至在不受干扰的水道中,也可能导致与沉积物结合的金属向上层地表水浸出。

著录项

  • 来源
    《Water Research》 |2012年第7期|p.2205-2214|共10页
  • 作者单位

    Department of Biology, Ecophysiology, Biochemistry and Toxicology Group, University of Antwerp, Groenenborgerlaan 171, 2020 Antwerpen, Belgium;

    Department of Biology, Ecosystem Management Research Group, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium;

    Department of Biology, Ecosystem Management Research Group, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium;

    Department of Biology, Ecophysiology, Biochemistry and Toxicology Group, University of Antwerp, Groenenborgerlaan 171, 2020 Antwerpen, Belgium;

    Department of Biology, Ecophysiology, Biochemistry and Toxicology Group, University of Antwerp, Groenenborgerlaan 171, 2020 Antwerpen, Belgium;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    acid volatile sulfides (AVS); redox potential (EH); sediment geochemistry; diffusive gradients in thin; films (DGT); metal pollution;

    机译:酸性挥发性硫化物(AVS);氧化还原电位(EH);沉积物地球化学稀薄的扩散梯度;电影(DGT);金属污染;
  • 入库时间 2022-08-17 13:46:17

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