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Application of Modified Magnetite Nanoparticles as a New Sorbent for Separation/Preconcentration of Mercury(II) Trace Amounts and its Determination by Cold Vapor Atomic Absorption Spectrometry

机译:改性磁铁矿纳米颗粒作为分离/富集痕量汞(II)的新型吸附剂的应用及其冷蒸气原子吸收光谱法的测定

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摘要

A new, simple, fast and reliable method has been developed to separation/preconcentration of trace amounts of mercury ions using dithizone/sodium dodecyl sulfate-immobilized on alumina-coated magnetite nanoparticles (DTZ/SDS-ACMNPs) and its determination by cold vapor atomic absorption spectrometry (CVAAS). This method avoided the time-consuming column-passing process of loading large volume samples in traditional solid phase extraction (SPE) through the rapid isolation of DTZ/SDS-ACMNPs with an adscititious magnet. Under the optimal experimental conditions, the enrichment factor, detection limit, linear range and relative standard deviation (RSD) of Hg(II) ions were 250 (for 500 mL of sample solution), 0.058 µg mL–1, 0.2–80.0 µg mL–1 and 3.55 % (for 5.0 µg mL–1, n=10), respectively. The adsorbed mercury ions were quantitatively eluted by 2.0 mL of 0.4 mol L–1 HBr solution. The pre¬sented procedure was successfully applied for determination of mercury content in the different samples of water and blood.
机译:已经开发了一种新的,简单,快速和可靠的方法,用于固定/固定在氧化铝涂层磁铁矿纳米颗粒(DTZ / SDS-ACMNPs)上的双硫zone /十二烷基硫酸钠分离/预富集痕量汞离子,并通过冷蒸气原子测定吸收光谱法(CVAAS)。该方法通过用吸附磁体快速隔离DTZ / SDS-ACMNP,避免了传统固相萃取(SPE)中加载大体积样品的费时的列传递过程。在最佳实验条件下,Hg(II)离子的富集系数,检测限,线性范围和相对标准偏差(RSD)为250(对于500 mL样品溶液),0.058 µg mL–1、0.2–80.0 µg mL分别为–1和3.55%(对于5.0 µg mL–1,n = 10)。吸附的汞离子被2.0 mL的0.4 mol L–1 HBr溶液定量洗脱。所提出的程序已成功地用于测定水和血液的不同样品中的汞含量。

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