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首页> 外文期刊>Water Research >Mercury speciation analyses in HgCl_2-contaminated soils and groundwater-Implications for risk assessment and remediation strategies
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Mercury speciation analyses in HgCl_2-contaminated soils and groundwater-Implications for risk assessment and remediation strategies

机译:受HgCl_2污染的土壤和地下水中的汞形态分析-对风险评估和补救策略的意义

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Since the 19th century, mercury(II)chloride (HgCl_2) has been used on wood impregnation sites to prevent wooden poles from decay, leaving behind a legacy of highly contaminated soil/aquifer systems. Little is known about species transformation and mobility of HgCl_2 in contaminated soils and groundwater. At such a site the behaviour of HgCl_2 in soils and groundwater was investigated to assist in risk assessment and remediation. The soil is low in organic carbon and contains up to 11,000 mgHg/kg. Mercury (Hg) concentrations in groundwater decrease from 230 to 0.5 μg/l within a distance of 1.3 km. Hg species transformations in soil and aqueous samples were analysed by means of solid-phase Hg pyrolysis and CV-AAS. In aqueous samples, Hg species were distinguished between ionic/ reactive Hg and complex-bound Hg. Potential mobility of Hg in soils was studied through batch experiments. Most Hg in the soil is matrix-bound HgCl_2, whereas in the aquifer secondary formation to Hg~0 could be observed. Aqueous Hg speciation in groundwater and soil solutions shows that an average of 84% of soluble Hg exists as easily reducible, inorganic Hg species (mostly HgCl_2). The proportion of complex-bound Hg increases with distance due to the transformation of inorganic HgCl_2. The frequent occurrence of Hg~0 in the aquifer suggests the formation and degassing of Hg~0, which is, in addition to dilution, an important process, lowering Hg concentrations in the groundwater. High percentage of mobile Hg (3-26%) and low seepage fluxes will result in continuous Hg release over centuries requiring long-term groundwater remediation. Results of soluble Hg speciation suggest that filtering materials should be adapted to ionic Hg species, e.g. specific resins or amalgamating metal alloys.
机译:自19世纪以来,氯化汞(HgCl_2)一直用于木材浸渍场所,以防止木杆腐烂,从而留下了高度污染的土壤/含水层系统。关于HgCl_2在受污染的土壤和地下水中的物种转化和迁移率知之甚少。在这样的场所,对HgCl_2在土壤和地下水中的行为进行了研究,以帮助进行风险评估和补救。土壤中的有机碳含量低,含量高达11,000 mgHg / kg。在1.3公里的距离内,地下水中的汞(Hg)浓度从230μg/ l降至0.5μg/ l。通过固相汞热解和CV-AAS分析了土壤和含水样品中的汞物种转化。在水性样品中,Hg种类在离子/反应性Hg和与络合物结合的Hg之间有所区别。通过分批实验研究了汞在土壤中的潜在迁移率。土壤中的大多数汞是基质结合的HgCl_2,而在含水层中可以观察到Hg〜0的次生形成。地下水和土壤溶液中的汞水溶液形态分析表明,平均有84%的可溶性汞以易还原的无机汞形式存在(主要为HgCl_2)。由于无机HgCl_2的转化,与结合物结合的Hg的比例随距离的增加而增加。 Hg〜0在含水层中的频繁发生表明Hg〜0的形成和脱气,这是除稀释外的重要过程,它降低了地下水中的Hg浓度。流动汞的百分比较高(3-26%)和渗漏通量较低,将导致数百年来需要长期修复地下水的汞不断释放。可溶性汞形态的结果表明,过滤材料应适用于离子汞物种,例如特定的树脂或金属合金。

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