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高效液相色谱/电感耦合等离子体质谱法测定水中砷的形态-方法验证和不确定度评估。

Arsenic speciation in water by high-performance liquid chromatography/inductively coupled plasma mass spectrometry-method validation and uncertainty estimation.

机构信息

Department of Trace Element Analysis by Spectroscopy Methods, Faculty of Chemistry, Adam Mickiewicz University in Poznań, 89b Umultowska Street, 61-614, Poznań, Poland.

出版信息

Rapid Commun Mass Spectrom. 2014 Jan 30;28(2):159-68. doi: 10.1002/rcm.6774.

DOI:10.1002/rcm.6774
PMID:24338963
Abstract

RATIONALE

In order to obtain reliable analytical results for the separation and determination of arsenic species by high-performance liquid chromatography/inductively coupled plasma mass spectrometry (HPLC/ICP-MS), the analytical procedure must be fully validated and the measurement uncertainty of the analytical result should be estimated.

METHODS

The total arsenic concentration of the samples was determined by ICP-MS. Separation of the arsenic species, AsB, As(III), DMA, MMA and As(V), was accomplished by liquid chromatography, which was hyphenated to inductively coupled plasma mass spectrometry, used for detection purposes. Automated handling of these systems was achieved with Chromera software.

RESULTS

The separation capability between the analytical signals of arsenic species, AsB-As(III), As(III)-DMA, DMA-MMA and MMA-As(V), was 1.3, 1.1, 5.1 and 4.6, respectively. The limit of detection (LOD) values ranged from 0.070 µg L(-1) for DMA to 0.13 µg L(-1) for MMA. The expanded uncertainty U [%] values for coverage factor k = 2 estimated for AsB, As(III), DMA, MMA and As(V) were 12 %, 13 %, 5.6 %, 9.6 % and 8.6 %, respectively.

CONCLUSIONS

This study reports, for the first time, building the uncertainty budgets for five arsenic species and estimation of the expanded uncertainty (for k = 2). The qualitative and quantitative parameters determined in the validation process indicate that the presented analytical procedure can be applied for the determination of AsB, As(III), DMA, MMA and As(V) in water.

摘要

原理

为了通过高效液相色谱/电感耦合等离子体质谱法(HPLC/ICP-MS)获得砷形态分离和测定的可靠分析结果,必须对分析程序进行全面验证,并估算分析结果的测量不确定度。

方法

采用电感耦合等离子体质谱法(ICP-MS)测定样品的总砷浓度。采用液相色谱法对砷形态 AsB、As(III)、DMA、MMA 和 As(V)进行分离,该液相色谱法与电感耦合等离子体质谱法联用进行检测。采用 Chromera 软件实现这些系统的自动处理。

结果

砷形态分析信号之间的分离能力分别为 AsB-As(III)为 1.3,As(III)-DMA 为 1.1,DMA-MMA 为 5.1,MMA-As(V)为 4.6。检测限(LOD)值范围为 0.070µg/L(DMA)至 0.13µg/L(MMA)。对于覆盖因子 k=2,AsB、As(III)、DMA、MMA 和 As(V)的扩展不确定度 U [%]值分别为 12%、13%、5.6%、9.6%和 8.6%。

结论

本研究首次报告了构建五个砷形态的不确定度预算并估算扩展不确定度(k=2)。验证过程中确定的定性和定量参数表明,所提出的分析程序可用于测定水中的 AsB、As(III)、DMA、MMA 和 As(V)。

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