University of Ioannina, Department of Chemistry, Ioannina 45110 Greece.
Talanta. 2011 May 15;84(3):834-9. doi: 10.1016/j.talanta.2011.02.013. Epub 2011 Feb 19.
Magnetically driven separation technology has received considerable attention in recent decade for its great potential application. In this study, we investigate the application of silica-modified magnetite nanoparticles (NPs) coated with a cationic surfactant as adsorbent for microextraction and determination of trace amounts of Cu(II), Ni(II), Co(II), Cd(II), Pb(II) and Mn(II) from environmental water samples. The synthesized silica-coated NPs in combination with cetylpyridinium bromide have the ability to adsolubilize the metal ions after complexation with 8-hydroxyquinoline. The NPs bearing the target metals are easily separated from the aqueous solution by applying an external magnetic field and the complexed metals were desorbed using acidic methanol. The desorbed analytes are introduced into the graphite furnace of an atomic absorption spectrometer. The effect of pH, complexing agent, amount of cetylpyridinium bromide, microextraction time, desorption conditions, ionic strength on extraction efficiency of the metal ions are investigated and optimized. Under the optimized conditions, the detection limits for Cu(II), Ni(II), Co(II), Cd(II), Pb(II) and Mn(II) are 4.7, 9.1, 9.5, 2.3, 7.4 and 15.3 ng L(-1), respectively and the relative standard deviations (n=6) are less than 3.6%. The accuracy of the method was evaluated by recovery measurements on the spiked samples and good recoveries (93-113%) with low RSDs were achieved.
近年来,磁性驱动分离技术因其潜在的巨大应用前景而受到广泛关注。在这项研究中,我们研究了用阳离子表面活性剂包覆的二氧化硅修饰的磁铁矿纳米粒子(NPs)作为吸附剂,用于从环境水样中微量萃取和测定 Cu(II)、Ni(II)、Co(II)、Cd(II)、Pb(II)和 Mn(II)。合成的二氧化硅包覆的 NPs 与十六烷基吡啶溴化物结合后,具有在与 8-羟基喹啉络合后吸附溶解金属离子的能力。带有目标金属的 NPs 可以通过施加外部磁场从水溶液中轻易分离出来,并用酸性甲醇将络合的金属洗脱下来。洗脱的分析物被引入原子吸收光谱仪的石墨炉中。考察并优化了 pH 值、络合剂、十六烷基吡啶溴化物用量、微萃取时间、洗脱条件、离子强度对金属离子萃取效率的影响。在优化条件下,Cu(II)、Ni(II)、Co(II)、Cd(II)、Pb(II)和 Mn(II)的检出限分别为 4.7、9.1、9.5、2.3、7.4 和 15.3 ng L(-1),相对标准偏差(n=6)小于 3.6%。通过对加标样品的回收率测量来评估方法的准确性,得到了良好的回收率(93-113%)和低 RSD。