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Assessing natural contents of hazardous metals in soils by different analytical methods and its impact on environmental legislative measures

机译:用不同分析方法评估土壤中有害金属的天然含量及其对环境立法措施的影响

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摘要

A variety of analytical techniques are commonly used to assess natural metal concentrations in soils. Although the choice of the analytical procedure may appear to be an unimportant issue, through an example from the Po Plain we document that for specific hazardous metals the arbitrary choice between separate analytical techniques may have contrasting legislative implications. Comparative analyses of 160 soil samples obtained with X-ray Fluorescence (XRF) and aqua-regia Inductive Coupled Plasma Mass Spectrometry (ICP-MS), respectively, reveal a systematic lower efficiency of chromium determination by ICP-MS (45-60% of XRF determinations), irrespective of the laboratory chosen. Maximum permissible concentrations of chromium for residential and recreational sites were invariably exceeded by sediments deriving from chromium-rich parent rocks after XRF analyses. In contrast, replicate determinations following aqua regia digestion were generally below the threshold values, defining the same soils as unpolluted. This study thus emphasises the need for strictly standardised procedures of metal determination.
机译:通常使用各种分析技术来评估土壤中的天然金属浓度。尽管分析方法的选择似乎无关紧要,但通过Po Plain的一个示例,我们记录了对于特定的有害金属,在单独的分析技术之间进行任意选择可能会产生不同的立法含义。分别通过X射线荧光(XRF)和水域感应耦合等离子体质谱(ICP-MS)获得的160个土壤样品的比较分析显示,ICP-MS测定铬的系统效率较低(45% XRF测定),与选择的实验室无关。 XRF分析后,源自富铬母岩的沉积物始终超过居民和娱乐场所的最大铬容许浓度。相反,王水消化后的重复测定通常低于阈值,定义为与未污染土壤相同的土壤。因此,这项研究强调了对金属测定必须严格标准化的程序的需要。

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