首页> 外文会议>NATO Advanced Research Workshop on Soil Chemical Pollution, Risk Assessment, Remediation and Security >A Single Chemical Extraction Scheme for the Simultaneous Evaluation of the Potential Mobility of a Metalloid (As) and Metallic Elements (Cd, Cu, Ni, Pb, Zn) in Contaminated Soils and Mine Wastes
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A Single Chemical Extraction Scheme for the Simultaneous Evaluation of the Potential Mobility of a Metalloid (As) and Metallic Elements (Cd, Cu, Ni, Pb, Zn) in Contaminated Soils and Mine Wastes

机译:单一化学提取方案,用于同时评估污染的土壤和矿废物中的金属(AS)和金属元素(CD,Cu,Ni,Pb,Zn)的潜在迁移率

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The total concentration of toxic chemical elements present in contaminated soils and mine wastes does not provide reliable information about the risk they present to Man and the Environment. Realistic assessments imply determining the fraction of total pollutant load susceptible to be solubilized and thus potentially transferred to the hydrocycle and the biosphere. Chemical extraction is the most commonly used method to reach this objective. Here we investigate two of the classical methods of sequential extraction, the first developed for cationic metallic elements (Tessier et al., 1979), the second for the oxyanionic phosphorus, a chemical analogue of arsenic (Woolson et al., 1983) and we propose a single protocol capable of simultaneous giving useful information about the reactivity of both cationic and anionic pollutants (often present together in contamination due to mining and smelting activities or heavy chemical industry). If the method of Tessier et al. (1979) is used for arsenic, it underestimates its potential mobility. The method we propose does not provide direct clues about the geochemical associations of the toxic elements in the contaminated solids but it gives instead information about (a) the potentially mobile fraction of these elements and (b) their geochemical behavior in the presence of a large range of physical-chemical conditions (acidic, alkaline, oxidizing, reducing), data of interest for remediation measures.
机译:污染的土壤和矿山废物中存在的有毒化学元素的总浓度并不能提供有关他们向人类和环境所呈现的风险的可靠信息。现实评估意味着确定易溶解的总污染物载荷的分数溶解,因此可能转移到氢循环和生物圈。化学提取是达到此目标的最常用方法。在这里,我们研究了两个连续提取的经典方法,首先为阳离子金属元素开发(Tessier等,1979),第二种用于氧基磷,砷的化学类似物(Woolson等,1983)和我们提出一种能够同时提供有关阳离子和阴离子污染物的反应性的有用信息的单一方案(由于采矿和冶炼活动或重型化学工业而污染物一起呈现在一起)。如果TESSIER等人的方法。 (1979)用于砷,它低估了其潜在的流动性。我们提出的方法不提供关于污染固体中毒元素的地球化学关联的直接线索,但它给出了关于(a)这些元素的潜在移动分数和(b)其在大的地球化学行为中的信息物理化学条件范围(酸性,碱性,氧化,还原),对修复措施的兴趣数据。

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