College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China.
Anal Chim Acta. 2012 Feb 3;713:92-6. doi: 10.1016/j.aca.2011.11.022. Epub 2011 Nov 19.
A new approach to performing extraction and preconcentration employing functionalized magnetic nanoparticles for the determination of trace metals is presented. Alumina-coated iron oxide nanoparticles were synthesized and used as the solid support. The nanoparticles were functionalized with sodium dodecyl sulfate and used as adsorbents for solid phase extraction of the analyte. Extraction, elution, and detection procedures were performed sequentially in the sequential injection lab-on-valve (SI-LOV) system followed by electrothermal atomic absorption spectrometry (ETAAS). Mixtures of hydrophobic analytes were successfully extracted from solution using the synthesized magnetic adsorbents. The potential use of the established scheme was demonstrated by taking cobalt as a model analyte. Under the optimal conditions, the calibration curve showed an excellent linearity in the concentration range of 0.01-5 μg L(-1), and the relative standard deviation was 2.8% at the 0.5 μg L(-1) level (n=11). The limit of detection was 6 ng L(-1) with a sampling frequency of 18 h(-1). The present method has been successfully applied to cobalt determination in water samples and two certified reference materials.
提出了一种新的方法,使用功能化磁性纳米粒子进行萃取和预浓缩,以测定痕量金属。合成了氧化铝包覆的氧化铁纳米粒子,并将其用作固体支撑物。纳米粒子用十二烷基硫酸钠功能化,并用作分析物固相萃取的吸附剂。萃取、洗脱和检测程序在顺序注射阀上的实验室(SI-LOV)系统中顺序进行,然后进行电热原子吸收光谱法(ETAAS)分析。使用合成的磁性吸附剂可以成功地从溶液中萃取疏水性分析物的混合物。通过以钴作为模型分析物,证明了所建立方案的潜在用途。在最佳条件下,校准曲线在 0.01-5 μg L(-1)浓度范围内具有极好的线性,在 0.5 μg L(-1)水平下的相对标准偏差为 2.8%(n=11)。检测限为 6 ng L(-1),采样频率为 18 h(-1)。该方法已成功应用于水样和两种认证参考材料中钴的测定。