Kahe Hadi, Chamsaz Mahmoud
Department of Chemistry, Faculty of sciences, Ferdowsi University of Mashhad, Mashhad, Iran.
Environ Monit Assess. 2016 Nov;188(11):601. doi: 10.1007/s10661-016-5613-8. Epub 2016 Oct 3.
A simple and reliable supramolecule-aggregated liquid solid microextraction method is described for preconcentration and determination of trace amounts of bismuth in water as well as human blood serum and hair samples. Catanionic microstructures of cetyltrimethylammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) surfactants, dissolved in deionized water/propanol, are used as a green solvent to extract bismuth (III)-diethyldithiocarbamate complexes by dispersive microextraction methodology. The extracted solid phase is easily removed and dissolved in 50 μL propanol for subsequent measurement by electrothermal atomic absorption spectrometry (ET-AAS). The procedure benefits the merits of supramolecule aggregates' properties and dispersive microextraction technique using water as the main component of disperser solvent, leading to direct interaction with analyte. Phase separation behavior of extraction solvent and different parameters influencing the extraction efficiency of bismuth ion such as salt concentration, pH, centrifugation time, amount of chelating agent, SDS:CTAB mole ratio, and solvent amounts were thoroughly optimized. Under the optimal experimental conditions, the calibration curve was linear in the range of 0.3-6 μg L Bi (III) with a limit of detection (LOD) of 0.16 μg L (S/N = 3). The relative standard deviations (RSD) of determination were obtained to be 5.1 and 6.2 % for 1 and 3 μg L of Bi (III), respectively. The developed method was successfully applied as a sensitive and accurate technique for determination of bismuth ion in human blood serum, hair samples, and a certified reference material.
本文描述了一种简单可靠的超分子聚集液固微萃取方法,用于预富集和测定水中以及人血清和头发样品中的痕量铋。将溶解在去离子水/丙醇中的十六烷基三甲基溴化铵(CTAB)和十二烷基硫酸钠(SDS)表面活性剂的阴-阳离子微结构用作绿色溶剂,通过分散微萃取方法萃取铋(III)-二乙基二硫代氨基甲酸盐络合物。萃取后的固相易于分离,并溶解在50μL丙醇中,随后用电热原子吸收光谱法(ET-AAS)进行测量。该方法兼具超分子聚集体特性和以水为主要分散剂溶剂的分散微萃取技术的优点,可直接与分析物相互作用。对萃取溶剂的相分离行为以及影响铋离子萃取效率的不同参数,如盐浓度、pH值、离心时间、螯合剂用量、SDS:CTAB摩尔比和溶剂量等进行了全面优化。在最佳实验条件下,校准曲线在0.3 - 6μg L Bi(III)范围内呈线性,检测限(LOD)为0.16μg L(S/N = 3)。对于1μg L和3μg L的Bi(III),测定的相对标准偏差(RSD)分别为5.1%和6.2%。所建立的方法成功应用于测定人血清、头发样品和一种有证标准物质中的铋离子,是一种灵敏且准确的技术。