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Visual and colorimetric detection of mercury(II) ion using gold nanoparticles stabilized with a dithia-diaza ligand

机译:使用二硫杂二氮杂配体稳定的金纳米颗粒的目视和比色检测汞离子

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We have developed a simple method for the highly selective colorimetric detection of dissolved mercury(II) ions via direct formation of gold nanoparticles (AuNPs). The dithia-diaza ligand 2-[3-(2-amino-ethylsulfanyl)-propylsulfanyl]-ethylamine (AEPE) was used as a stabilizer to protect AuNPs from aggregation and to impart highly selective recognition of Hg(II) ion over other metal ions. A solution of Au(III) ion is directly reduced by sodium borohydride in the presence of AEPE and the detergent Triton X-100. This results in the formation of AEPE-AuNPs and a red coloration of the solution. On the other hand, in the presence of Hg(II), the solution turns blue within a few seconds after the addition of borohydride. This can be detected spectrophotometrically or even visually. The method was successfully applied to quantify Hg(II) levels in water sample, with a minimum detectable concentration as low as 35 nM.
机译:我们已经开发了一种通过直接形成金纳米颗粒(AuNPs)高度选择性比色法检测溶解的汞(II)离子的简单方法。二硫杂二氮杂配体2- [3-(2-氨基-乙基硫烷基)-丙基硫烷基]-乙胺(AEPE)被用作稳定剂,以保护AuNP避免聚集,并赋予Hg(II)离子比其他金属高度选择性的识别能力离子。在AEPE和去污剂Triton X-100的存在下,硼氢化钠直接还原Au(III)离子的溶液。这导致AEPE-AuNP的形成和溶液的红色。另一方面,在存在Hg(II)的情况下,添加硼氢化物后几秒钟内溶液变成蓝色。可以通过分光光度法或什至是视觉检测。该方法已成功应用于定量水样品中Hg(II)的水平,最低可检测浓度低至35 nM。

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