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采用化学萃取法分析氯碱厂高污染土壤中的汞形态。

Mercury speciation in highly contaminated soils from chlor-alkali plants using chemical extractions.

作者信息

Neculita Carmen-Mihaela, Zagury Gérald J, Deschênes Louise

机构信息

Department of Civil, Geological and Mining Engineering, Ecole Polytechnique de Montréal, P.O. Box 6079, Station Centre-ville, Montreal, QC, Canada H3C 3A7.

出版信息

J Environ Qual. 2005 Jan-Feb;34(1):255-62.

Abstract

A four-step novel sequential extraction procedure (SEP) was developed to assess Hg fractionation and mobility in three highly contaminated soils from chlor-alkali plants (CAPs). The SEP was validated using a certified reference material (CRM) and pure Hg compounds. Total, volatile, and methyl Hg concentrations were also determined using single extractions. Mercury was separated into four fractions defined as water-soluble (F1), exchangeable (F2) (0.5 M NH4Ac-EDTA and 1 M CaCl2 were tested), organic (F3) (successive extractions with 0.2 M NaOH and CH3COOH 4% [v/v]), and residual (F4) (HNO3 + H2SO4 + HClO4). The soil characterization revealed extremely contaminated (295 +/- 18 to 11 500 +/- 500 mg Hg kg(-1)) coarse-grained sandy soils having an alkaline pH (7.9-9.1), high chloride concentrations (5-35 mg kg(-1)), and very low organic carbon content (0.00-18.2 g kg(-1)). Methyl Hg concentrations were low (0.2-19.3 microg kg(-1)) in all soils. Sequential extractions indicated that the majority of the Hg was associated with the residual fraction (F4). In Soils 1 and 3, however, high percentages (88-98%) of the total Hg were present as volatile Hg. Therefore, in these two soils, a high proportion of volatile Hg was present in the residual fraction. The nonresidual fraction (F1 + F2 + F3) was most abundant in Soil 1 (14-42%), suggesting a higher availability of Hg in this soil. The developed and validated SEP was reproducible and efficient for highly contaminated samples. Recovery ranged between 93 and 98% for the CRM and 70 and 130% for the CAP-contaminated soils.

摘要

开发了一种新颖的四步连续提取程序(SEP),以评估来自氯碱厂(CAPs)的三种高度污染土壤中汞的形态和迁移性。该SEP使用认证参考物质(CRM)和纯汞化合物进行了验证。还使用单次提取法测定了总汞、挥发性汞和甲基汞的浓度。汞被分为四个部分,分别定义为水溶性(F1)、可交换性(F2)(测试了0.5 M NH4Ac-EDTA和1 M CaCl2)、有机态(F3)(用0.2 M NaOH和4% [v/v] CH3COOH连续提取)和残渣态(F4)(HNO3 + H2SO4 + HClO4)。土壤特征显示,这些土壤为粗粒砂土,污染极其严重(295±18至11500±500 mg Hg kg(-1)),pH呈碱性(7.9 - 9.1),氯化物浓度高(5 - 35 mg kg(-1)),有机碳含量极低(0.00 - 18.2 g kg(-1))。所有土壤中的甲基汞浓度都很低(0.2 - 19.3 μg kg(-1))。连续提取表明,大部分汞与残渣态部分(F4)相关。然而,在土壤1和土壤3中,总汞的高比例(88 - 98%)以挥发性汞的形式存在。因此,在这两种土壤中,残渣态部分存在高比例的挥发性汞。非残渣态部分(F1 + F2 + F3)在土壤1中最为丰富(14 - 42%),表明该土壤中汞的有效性更高。所开发和验证的SEP对于高度污染的样品具有可重复性和高效性。CRM的回收率在93%至98%之间,CAP污染土壤的回收率在70%至130%之间。

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