Institute for Analytical and Bioanalytical Chemistry, University of Ulm , Albert-Einstein-Allee 11, 89081 Ulm, Germany.
Geochemistry and Hydrogeology, University of Bremen , Klagenfurter Straße, 28359 Bremen, Germany.
Anal Chem. 2015 Nov 3;87(21):11122-9. doi: 10.1021/acs.analchem.5b03303. Epub 2015 Oct 26.
We propose a novel analytical method for mercury (Hg) trace determination based on direct Hg preconcentration from aqueous solution onto a gold nanoparticle-decorated silica monolith (AuNP@SiO2). Detection of Hg is performed after thermal desorption by means of atomic fluorescence spectrometry. This new methodology benefits from reagent-free, time- and cost-saving procedure, due to most efficient solid-phase adsorbent and results in high sensitive quantification. The excellent analytical performance of the whole procedure is demonstrated by a limit of detection as low as 1.31 ng L(-1) for only one-min accumulation duration. A good reproducibility with standard deviations ≤5.4% is given. The feasibility of the approach in natural waters was confirmed by a recovery experiment in spiked seawater with a recovery rate of 101%. Moreover, the presented method was validated through reference analysis of a submarine groundwater discharge sample by cold vapor-atomic fluorescence spectrometry resulting in a very good agreement of the found values. Hence the novel method is a very promising new tool for low-level Hg monitoring in natural waters providing easy-handling on-site preconcentration, reagent-free stabilization as well as reagent-free, highly sensitive detection.
我们提出了一种基于直接从水溶液中预富集汞(Hg)到金纳米颗粒修饰的硅胶整体柱(AuNP@SiO2)上的新型痕量 Hg 分析方法。Hg 的检测是通过原子荧光光谱法在热解吸后进行的。由于采用了最有效的固相吸附剂,这种新方法具有无试剂、省时和节省成本的特点,且结果具有高灵敏度的定量分析。由于仅需 1 分钟的积累时间,检测限低至 1.31ng L(-1),整个过程表现出了极好的分析性能。该方法具有标准偏差≤5.4%的良好重现性。通过在加标海水中进行的回收实验,证明了该方法在天然水中的可行性,回收率为 101%。此外,通过冷蒸气-原子荧光光谱法对海底地下水排放样品进行了参考分析,验证了该方法,发现所得值非常吻合。因此,该新方法是一种非常有前景的天然水中低水平 Hg 监测的新工具,提供了易于操作的现场预浓缩、无试剂稳定以及无试剂、高灵敏度的检测。