Magnetic Solid Phase Extraction of Au(III) using Fe3O4 Nanoparticles Prior to its Flame Atomic Absorption Spectrometric Determination

Z. M. Khoshhesab
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引用次数: 1

Abstract

A simple solid phase extraction procedure has been proposed for determination of Au(III) based on separation and preconcentration using magnetite nanoparticles (MNPs) prior to its determination by flame atomic absorption spectrometry. The influences of experimental parameters including sample pH, sorbent mass, contact time, volume and type of eluent, and interference of some ions with extraction of Au(III) ions were investigated using batch procedure. The maximum adsorption capacity of the sorbent for Au(III) was found to be 45.0 mg g-1. The sorption of Au(III) ions was quantitative in the pH range of 4.0–5.0 and quantitative desorption was achieved using 10 mL of thiourea (0.5 mol L-1)/hydrochloric acid (1 mol L-1) solution. In the initial solution, the calibration curve was linear in the range of 8.8 - 666.0 I¼g L-1 with R2 = 0.9994 (n = 8), the detection limit (3Sb, n = 8) was 6.2 I¼g L-1, relative standard deviation (R.S.D) of 20 I¼g mL-1 of Au(III) was 3.9% (n = 8), and the preconcentration factor was 30. The proposed method has been applied to the determination of Au(III) in water and wastewater samples with good recoveries in the range of 95% –103%.
Fe3O4纳米颗粒在火焰原子吸收光谱测定前的磁固相萃取金(III
在火焰原子吸收光谱法测定金(III)之前,提出了一种简单的固相萃取方法,该方法基于磁铁矿纳米颗粒(MNPs)的分离和预富集。采用间歇法考察了样品pH、吸附剂质量、接触时间、洗脱液体积和类型以及部分离子干扰对Au(III)离子提取的影响。该吸附剂对Au(III)的最大吸附量为45.0 mg g-1。Au(III)离子的定量吸附在pH为4.0 - 5.0范围内,定量解吸采用10 mL硫脲(0.5 mol L-1)/盐酸(1 mol L-1)溶液。在初始溶液中,校准曲线在8.8 ~ 666.0 μ g L-1范围内呈线性关系,R2 = 0.9994 (n = 8),检出限(3Sb, n = 8)为6.2 μ g L-1, Au(III) 20 μ g mL-1的相对标准偏差(rsd)为3.9% (n = 8),富集因子为30。该方法可用于水、废水样品中Au(III)的测定,回收率为95% ~ 103%。
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