Determination of methylmercury in marine sediment samples: Method validation and occurrence data

被引:30
|
作者
Carrasco, Luis [1 ]
Vassileva, Emilia [1 ]
机构
[1] IAEA, Dept Nucl Sci & Applicat, Environm Labs, MC-98000 Monaco, Monaco
关键词
Methylmercury; Gas chromatography-pyrolysis-atomic fluorescence spectrometry; Marine sediments; Sample preparation; Validation; Traceability; Uncertainty; ATOMIC-FLUORESCENCE SPECTROMETRY; PERFORMANCE LIQUID-CHROMATOGRAPHY; CAPILLARY GAS-CHROMATOGRAPHY; SOLID-PHASE MICROEXTRACTION; PLASMA-MASS SPECTROMETRY; ENVIRONMENTAL-SAMPLES; MERCURY METHYLATION; ASSISTED EXTRACTION; ORGANIC MERCURY; FISH-TISSUES;
D O I
10.1016/j.aca.2014.10.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The determination of methylmercury (MeHg) in sediment samples is a difficult task due to the extremely low MeHg/THg (total mercury) ratio and species interconversion. Here, we present the method validation of a cost-effective fit-for-purpose analytical procedure for the measurement of MeHg in sediments, which is based on aqueous phase ethylation, followed by purge and trap and hyphenated gas chromatography-pyrolysis-atomic fluorescence spectrometry (GC-Py-AFS) separation and detection. Four different extraction techniques, namely acid and alkaline leaching followed by solvent extraction and evaporation, microwave-assisted extraction with 2-mercaptoethanol, and acid leaching, solvent extraction and back extraction into sodium thiosulfate, were examined regarding their potential to selectively extract MeHg from estuarine sediment IAEA-405 certified reference material (CRM). The procedure based on acid leaching with HNO3/CuSO4, solvent extraction and back extraction into Na2S2O3 yielded the highest extraction recovery, i.e., 94 +/- 3% and offered the possibility to perform the extraction of a large number of samples in a short time, by eliminating the evaporation step. The artifact formation of MeHg was evaluated by high performance liquid chromatography coupled to inductively coupled plasma mass spectrometry (HPLC-ICP-MS), using isotopically enriched (MeHg)-Hg-201 and Hg-202 and it was found to be nonexistent. A full validation approach in line with ISO 17025 and Eurachem guidelines was followed. With this in mind, blanks, selectivity, working range (1-800 pg), linearity (0.9995), recovery (94-96%), repeatability (3%), intermediate precision (4%), limit of detection (0.45 pg) and limit of quantification (0.85 pg) were systematically assessed with CRM IAEA-405. The uncertainty budget was calculated and the major contribution to the combined uncertainty (16.24%, k = 2) was found to arise from the uncertainty associated with recovery (74.1%). Demonstration of traceability of measurement results is also presented. The validated measurement procedure was applied to the determination of MeHg incurred in sediments from a highly polluted and scarcely studied area in the Caribbean region. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:167 / 178
页数:12
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