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首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Ionic liquid-based ultrasound-assisted dispersive liquid-liquid microextraction combined with electrothermal atomic absorption spectrometry for a sensitive determination of cadmium in water samples
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Ionic liquid-based ultrasound-assisted dispersive liquid-liquid microextraction combined with electrothermal atomic absorption spectrometry for a sensitive determination of cadmium in water samples

机译:离子液体基超声辅助分散液-液微萃取-电热原子吸收光谱法联用测定水样中的镉

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A new method was developed for the determination of cadmium in water samples using ionic liquid-based ultrasound-assisted dispersive liquid-liquid microextraction (IL-based USA-DLLME) followed by electrothermal atomic absorption spectrometry (ETAAS). The IL-based USA-DLLME procedure is free of volatile organic solvents, and there is no need for a dispersive solvent, in contrast to conventional DLLME. The ionic liquid, l-hexyl-3-methylimidazolium hexafluorophosphate (HMIMPF6), was quickly disrupted by an ultrasonic probe for 1 min and dispersed in water samples like a cloud. At this stage, a hydrophobic cadmium-DDTC complex was formed and extracted into the fine droplets of HMIMPF6. After centrifugation, the concentration of the enriched cadmium in the sedimented phase was determined by ETAAS. Some effective parameters of the complex formation and microextraction, such as the concentration of the chelating agent, the pH, the volume of the extraction solvent, the extraction time, and the salt effect, have been optimized. Under optimal conditions, a high extraction efficiency and selectivity were reached for the extraction of 1.0 ng of cadmium in 10.0 mL of water solution employing 73 uL of HMIMPF6 as the extraction solvent. The enrichment factor of the method is 67. The detection limit was 7.4 ng L~(-1) and the characteristic mass (mo, 0.0044 absorbance) of the proposed method was 0.02 pg for cadmium (Cd). The relative standard deviation (RSD) for 11 replicates of 50 ng L~(-1) Cd was 3.3%. The method was applied to the analysis of tap, well, river, and lake water samples and the Environmental Water Reference Material GSBZ 50009-88 (200921). The recoveries of spiked samples were in the range of 87.2-106%.
机译:开发了一种新方法,该方法使用离子液体基超声辅助分散液-液微萃取(基于IL的USA-DLLME),然后进行电热原子吸收光谱法(ETAAS)测定水中的镉。与传统的DLLME相比,基于IL的USA-DLLME方法不含挥发性有机溶剂,并且不需要分散溶剂。离子液体1-己基-3-甲基咪唑六氟磷酸盐(HMIMPF6)被超声波探头快速破坏1分钟,并散布在像云一样的水样中。在此阶段,形成了疏水性镉-DDTC复合物,并将其提取到HMIMPF6的细小液滴中。离心后,通过ETAAS测定沉淀相中富集镉的浓度。优化了配合物形成和微萃取的一些有效参数,例如螯合剂的浓度,pH,萃取溶剂的体积,萃取时间和盐分作用。在最佳条件下,使用73 uL HMIMPF6作为萃取溶剂,可以在10.0 mL水溶液中萃取1.0 ng镉,具有很高的萃取效率和选择性。该方法的富集系数为67。检出限为7.4 ng L〜(-1),该方法的特征质量(mo,0.0044吸光度)为镉(Cd)0.02 pg。 50 ng L〜(-1)Cd的11次重复试验的相对标准偏差(RSD)为3.3%。该方法适用于自来水,井水,河流和湖泊水样品以及环境水参考材料GSBZ 50009-88(200921)的分析。加标样品的回收率在87.2-106%之间。

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