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用同位素稀释质谱法测定意大利南部潜在污染土壤中的六价铬。

Hexavalent chromium quantification by isotope dilution mass spectrometry in potentially contaminated soils from south Italy.

机构信息

Department of Agricultural Sciences, University of Naples Federico II, Via Università 100, 80055, Portici, Naples, Italy.

Department of Agricultural Sciences, University of Naples Federico II, Via Università 100, 80055, Portici, Naples, Italy; CIRAM - Interdepartmental Center for Environmental Research, University of Naples Federico II, Via Mezzocannone 16, 80134, Naples, Italy.

出版信息

Chemosphere. 2019 Oct;233:92-100. doi: 10.1016/j.chemosphere.2019.05.212. Epub 2019 May 25.

DOI:10.1016/j.chemosphere.2019.05.212
PMID:31170588
Abstract

Due to carcinogenicity of hexavalent chromium [Cr(VI)], its accurate quantification in Cr-contaminated soils is of paramount importance. The aim of this work was to quantify Cr(VI) by species-specific IDMS in soil samples from two Italian case studies: A) farmland potentially contaminated by pseudo-total Cr and Zn and heavy hydrocarbons due to past illegal burial of tannery wastes; B) Solofrana valley where volcanic soils are potentially contaminated by pseudo-total Cr and Cu due to tannery activities. Hexavalent Cr extraction from soils was performed by focused microwaves (5 min at 80 °C) using 50 mM EDTA, followed by the separation of Cr species by IC and detection by ICP-MS. The Cr(VI) extracted from 20 soil samples of case study A ranged from 0.15 to 11.18 μg g, with 70% of samples exceeding the Cr(VI) screening value set by Italian Parliament for residential/urban soil to assess their potential contamination. Higher levels of Cr(VI) (22.0-107.1 μg g) were extracted from other 7 Cr-most-enriched soil samples, which required a pre-treatment with n-hexane to remove part of organic compounds from each sample, since these reducing agents made the quantification of Cr(VI) by IDMS more challenging because they caused an almost complete reduction of Cr(VI) used for IDMS quantification. Hexavalent Cr extracted from soil samples of case study B ranged from 0.70 to 5.79 μg g, with 42% of samples exceeding the value set by Italian legislation. In both case studies, the Cr(VI) extracted from soil was significantly correlated to the pseudo-total Cr content.

摘要

由于六价铬[Cr(VI)]的致癌性,准确量化污染土壤中的 Cr(VI)含量至关重要。本工作旨在通过特定物种的 IDMS 量化意大利两个案例研究中土壤样品中的 Cr(VI):A)农田由于过去非法掩埋制革废物而受到总 Cr 和 Zn 以及重质碳氢化合物的潜在污染;B)索罗弗兰纳山谷,由于制革活动,火山土壤可能受到总 Cr 和 Cu 的潜在污染。使用 50 mM EDTA 通过聚焦微波(80°C 下 5 分钟)从土壤中提取六价 Cr,然后通过 IC 分离 Cr 物种并用 ICP-MS 检测。从案例研究 A 的 20 个土壤样品中提取的 Cr(VI)范围为 0.15 至 11.18μg/g,其中 70%的样品超过了意大利议会为评估住宅/城市土壤潜在污染而设定的 Cr(VI)筛选值。从其他 7 个 Cr 含量较高的土壤样品中提取了更高水平的 Cr(VI)(22.0-107.1μg/g),这些样品需要先用正己烷预处理,以去除每个样品中部分有机化合物,因为这些还原剂使 IDMS 定量 Cr(VI)更具挑战性,因为它们几乎完全还原了用于 IDMS 定量的 Cr(VI)。从案例研究 B 的土壤样品中提取的 Cr(VI)范围为 0.70 至 5.79μg/g,其中 42%的样品超过了意大利法规设定的值。在这两个案例研究中,从土壤中提取的 Cr(VI)与总 Cr 含量呈显著相关。

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