首页> 外文期刊>Analytical methods >Selective extraction and preconcentration of ultra-trace level of mercury ions in water and fish samples using Fe3O4-magnetite-nanoparticles functionalized by triazene compound prior to its determination by inductively coupled plasma-optical emission spectrometry
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Selective extraction and preconcentration of ultra-trace level of mercury ions in water and fish samples using Fe3O4-magnetite-nanoparticles functionalized by triazene compound prior to its determination by inductively coupled plasma-optical emission spectrometry

机译:用三氮烯化合物官能化的Fe3O4-磁铁矿-纳米粒子选择性萃取和富集水和鱼样品中的痕量汞离子,然后通过电感耦合等离子体发射光谱法测定

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In this paper, new modified magnetite nanoparticles functionalized with triazene groups were designed and synthesized for extraction/preconcentration of sub-ppb level of mercury ions in water and fish samples prior to its determination with inductively coupled plasma optical emission spectrometry (ICP-OES). In the separation process, aqueous solution of Hg2+ ions was mixed with 150 mg of Fe3O4 magnetite nanoparticles modified with 1-(p-acetyl phenyl)-3-(o-ethoxy phenyl) triazene (AET) and then external magnetic field was applied for isolation of magnetite nanoparticles containing mercury ions. Experimental conditions for effective adsorption including pH, sample volume, eluent concentration and existing co-existing ions have been studied and established. Under the optimal extraction and preconcentration conditions, the limit of detection (LOD) of 0.04 ng mL?1 and the relative standard deviation (R.S.D) of 2.09% for five replicate extractions and measurements of 10 μg of Hg2+ ion in 1000 mL water solution were achieved by ICP-OES. The sorption capacity of functionalized Fe3O4 magnetite nanoparticles under optimum conditions has been found to be 10.26 mg of mercury ion per gram at pH 7 with the preconcentration factor of 500 (2 mL of elution for a 1000 mL sample volume). Standard solutions containing Hg2+ in the concentration range of 0.2–200 ng mL?1 were examined by the proposed procedure and it was observed that calibration curve was linear in this range (R2 = 0.999). The special advantages of the proposed method are high enrichment factor, fast separation and low detection limits compared with other methods...
机译:本文设计并合成了用三氮烯基官能化的新型改性磁铁矿纳米颗粒,用于在水和鱼样品中汞离子的亚ppb级萃取/预富集,然后用电感耦合等离子体发射光谱法(ICP-OES)测定。在分离过程中,将Hg2 +离子的水溶液与150 mg的1-(对乙酰基苯基)-3-(邻乙氧基苯基)三氮烯(AET)改性的Fe3O4磁铁矿纳米颗粒混合,然后施加外部磁场分离含汞离子的磁铁矿纳米颗粒。已经研究并建立了有效吸附的实验条件,包括pH,样品量,洗脱液浓度和现有的共存离子。在最佳萃取和预浓缩条件下,五次重复萃取和在1000 mL水溶液中测量10μgHg2 +离子的检测限(LOD)为0.04 ng mL?1,相对标准偏差(RSD)为2.09%。通过ICP-OES实现。发现在最佳条件下,功能化的Fe3O4磁铁矿纳米颗粒在pH值为7时的吸附容量为10.26 mg汞离子/克,预浓系数为500(对于1000 mL样品体积,洗脱液为2 mL)。通过提议的程序检查了浓度范围为0.2–200 ng mL?1的Hg2 +的标准溶液,并且观察到在该范围内校准曲线是线性的(R2 = 0.999)。与其他方法相比,该方法的特殊优势是高富集因子,快速分离和低检测限。

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