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用于环境水样中汞(II)顶空微萃取和比色测定的单滴金纳米粒子

Single-drop gold nanoparticles for headspace microextraction and colorimetric assay of mercury (II) in environmental waters.

作者信息

Tolessa Tesfaye, Tan Zhi-Qiang, Yin Yong-Guang, Liu Jing-Fu

机构信息

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China.

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085, China.

出版信息

Talanta. 2018 Jan 1;176:77-84. doi: 10.1016/j.talanta.2017.07.097. Epub 2017 Aug 3.

Abstract

A novel headspace colorimetric nanosensor strategy for specific detection of Hg(II) was developed based upon analyte induced etching and amalgamation of gold nanoparticles (AuNPs). The Hg(II) was first selectively reduced to its volatile form, Hg(0), by stannous chloride (SnCl) through chemical cold vapor generation (CVG) reaction. Then, the Hg(0) was headspace extracted into 37μL thioglycolic acid functionalized AuNP aqueous suspension containing 10% methanol as extractant and simultaneously reacted with AuNPs through the strong metallophilic Hg-Au interaction, resulting in a red-to-blue color change. Parameters influencing the chromogenic and chemical vapor generation reactions were optimized. The limit of detections were determined as 5nM through inspection by naked-eye and 1nM based on measurements by UV-Vis spectrometer, which are below the safe limit of Hg(II) in drinking water set by the US Environmental Protection Agency, showing excellent potential for monitoring ultralow levels of Hg(II) in environmental water samples. The assay was not interfered by the presence of other common metal ions even at 1000-fold excess over Hg(II) concentration. The outstanding selectivity results from the combined effect of selective reduction of Hg(II) by SnCl, efficient separation of sample matrix through headspace extraction, and amalgamation process that occurs specifically between Hg and AuNPs. The method was successfully applied to the visual detection of Hg(II) in environmental water samples at a 10nM spiking level, with recoveries in the range of 86.8-99.8%. More importantly, compared to classical colorimetric assays for detection of Hg(II), this method is featured with simplicity, quite high sensitivity and excellent selectivity. The method is also superior to most colorimetric methods for detection of Hg(II) in terms of its applicability to matrix-rich real samples including wastewater.

摘要

基于分析物诱导的金纳米颗粒(AuNPs)蚀刻和汞齐化,开发了一种用于特异性检测Hg(II)的新型顶空比色纳米传感器策略。Hg(II)首先通过化学冷蒸气发生(CVG)反应,被氯化亚锡(SnCl)选择性还原为挥发性形式Hg(0)。然后,Hg(0)被顶空萃取到37μL含有10%甲醇作为萃取剂的巯基乙酸功能化AuNP水悬浮液中,并同时通过强亲金属Hg-Au相互作用与AuNPs反应,导致颜色从红色变为蓝色。优化了影响显色和化学蒸气发生反应的参数。通过肉眼观察确定检测限为5nM,基于紫外可见光谱仪测量为1nM,低于美国环境保护局设定的饮用水中Hg(II)的安全限值,显示出监测环境水样中超低水平Hg(II)的优异潜力。即使其他常见金属离子的浓度比Hg(II)高1000倍,该测定也不受其存在的干扰。出色的选择性源于SnCl对Hg(II)的选择性还原、通过顶空萃取对样品基质的有效分离以及Hg与AuNPs之间特异性发生的汞齐化过程的综合作用。该方法成功应用于环境水样中10nM加标水平Hg(II)的目视检测,回收率在86.8-99.8%范围内。更重要的是,与用于检测Hg(II)的经典比色测定相比,该方法具有简单、灵敏度相当高和选择性优异的特点。该方法在适用于包括废水在内的富含基质的实际样品方面也优于大多数用于检测Hg(II)的比色方法。

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