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Solid phase speciation of arsenic by sequential extraction in standard reference materials and industrially contaminated soil samples

机译:通过在标准参考物质和工业污染土壤样品中连续萃取而对砷进行固相形态分析

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摘要

Availability, mobility, (phyto)toxicity and potential risk of contaminants is strongly affected by the manner of appearance of elements, the so-called speciation. Operational fractionation methods like sequential extractions have been applied for a long time to determine the solid phase speciation of heavy metals since direct determination of specific chemical compounds can not always be easily achieved. The three-step sequential extraction scheme recommended by the BCR and two extraction schemes based on the phosphorus-like protocol proposed by Manful (1992, Occurrence and Ecochemical Behaviours of Arsenic in a Goldsmelter Impacted Area in Ghana, PhD dissertation, at the RUG) were applied to four standard reference materials (SRM) and to a batch of samples from industrially contaminated sites, heavily contaminated with arsenic and heavy metals. The SRM 2710 (Montana soil) was found to be the most useful reference material for metal (Mn, Cu, Zn, As, Cd and Pb) fractionation using the BCR sequential extraction procedure. Two sequential extraction schemes were developed and compared for arsenic with the aim to establish a better fractionation and recovery rate than the BCR-scheme for this element in the SRM samples. The major part of arsenic was released from the heavily contaminated samples after NaOH-extraction. Inferior extraction variability and recovery in the heavily contaminated samples compared to SRMs could be mainly contributed to subsample heterogeneity.
机译:元素的出现方式(所谓的物种形成)强烈影响可用性,迁移率,(植物)毒性和污染物的潜在风险。由于无法始终轻松地直接测定特定化合物,因此很长时间以来就一直采用操作性分馏方法(例如顺序萃取)来确定重金属的固相形态。 BCR推荐的三步顺序萃取方案和Manful提出的基于磷样方案的两种萃取方案(1992年,加纳金矿冶炼厂受影响地区的砷的发生和生态化学行为,在RUG上发表的博士学位论文)是应用于四种标准参考物质(SRM)以及来自工业污染场所的一批样品,这些场所被砷和重金属严重污染。发现SRM 2710(蒙大拿州土壤)是使用BCR顺序萃取程序分离金属(锰,铜,锌,砷,镉和铅)最有用的参考材料。针对SRM样品中的这种元素,开发了两种顺序萃取方案并比较了砷的含量,目的是建立比BCR方案更好的分馏和回收率。 NaOH萃取后,大部分砷从重度污染的样品中释放出来。与SRM相比,重度污染样品中的提取变异性和回收率较低,这可能是造成子样品异质性的主要原因。

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