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利用电感耦合等离子体质谱法对天然水中环境相关水平的镭进行定量分析:一种萃取和预浓缩方法的优化、验证及局限性

Quantification of Ra at environmental relevant levels in natural waters by ICP-MS: Optimization, validation and limitations of an extraction and preconcentration approach.

作者信息

Lagacé François, Foucher Delphine, Surette Céline, Clarisse Olivier

机构信息

Department of Chemistry and Biochemistry, Université de Moncton, 18 Avenue Antonine Maillet, Moncton, NB, Canada E1A 3E9.

Department of Chemistry and Biochemistry, Université de Moncton, 18 Avenue Antonine Maillet, Moncton, NB, Canada E1A 3E9.

出版信息

Talanta. 2017 May 15;167:658-665. doi: 10.1016/j.talanta.2017.02.031. Epub 2017 Feb 20.

DOI:10.1016/j.talanta.2017.02.031
PMID:28340775
Abstract

Radium (Ra) at environmental relevant levels in natural waters was determined by ICP-MS after an off-line pre-concentration procedure. The latter consisted of Ra selective elution from potential interfering elements (i.e. other alkaline earth cations: Ba, Sr, Ca, Mg) on a series of two different ion exchange resins (AG50W-X8 and Sr-resin). The overall analytical method was optimized according to the instrumental performance, the volume of water sample loaded on resins, and the sample salinity. Longer acquisition time (up to 150 s) was required to ensure stable measurement of Ra by ICP-MS at ultra trace level (1.0pgL). For a synthetic groundwater spiked with Ra at 10.0pgL, the analytical procedure demonstrated efficient separation of the analyte from its potential interfering elements and a complete recovery, independent of the sample volume tested from 10 up to 100mL. For synthetic seawater spiked at a level of 10.0pgL of Ra, the total load of salts on the two resins should not exceed 0.35g in order to ensure a complete separation and recovery of Ra. The method was validated on natural waters (i.e. groundwater, freshwater and seawater samples) spiked with Ra at different levels (0.0, 0.5, 1.0 and 5.0pgL). Absolute Ra detection limits were determined at 0.020pgL (0.73mBqL) and 0.12pgL (4.4mBqL) respectively for 60.0mL of freshwater sample and for 10.0mL of seawater.

摘要

通过离线预浓缩程序后,采用电感耦合等离子体质谱法(ICP-MS)测定天然水体中环境相关水平的镭(Ra)。该程序包括在一系列两种不同的离子交换树脂(AG50W-X8和锶树脂)上从潜在干扰元素(即其他碱土金属阳离子:钡、锶、钙、镁)中选择性洗脱镭。根据仪器性能、加载到树脂上的水样体积和样品盐度对整个分析方法进行了优化。为确保在超痕量水平(1.0pg/L)下通过ICP-MS稳定测量镭,需要更长的采集时间(长达150秒)。对于添加了10.0pg/L镭的合成地下水,该分析程序证明了分析物与其潜在干扰元素的有效分离和完全回收,与测试的10至100mL样品体积无关。对于添加了10.0pg/L镭的合成海水,为确保镭的完全分离和回收,两种树脂上的盐总负载不应超过0.35g。该方法在添加了不同水平(0.0、0.5、1.0和5.0pg/L)镭的天然水体(即地下水、淡水和海水样品)上进行了验证。对于60.0mL淡水样品和10.0mL海水,绝对镭检测限分别确定为0.020pg/L(0.73mBq/L)和0.12pg/L(4.4mBq/L)。

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