首页> 外文期刊>Journal of the Serbian Chemical Society >Ionic liquid-based dispersive liquid-liquid microextraction combined with high performance liquid chromatography-UV detection for simultaneous preconcentration and determination of Ni, Co, Cu and Zn in water samples
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Ionic liquid-based dispersive liquid-liquid microextraction combined with high performance liquid chromatography-UV detection for simultaneous preconcentration and determination of Ni, Co, Cu and Zn in water samples

机译:离子液体基分散液-液微萃取与高效液相色谱-紫外检测相结合,用于同时预富集和测定水中样品中的镍,钴,铜和锌

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Ionic liquid-based dispersive liquid-liquid microextraction (IL-DLLME) coupled with high performance liquid chromatography (HPLC)-UV detection was developed for simultaneous extraction and determination of nickel, cobalt, copper and zinc ions. In the proposed approach, salophen (N,N'-bis(salisyliden)-1,2-phenylenediamine) was used as a chelating agent; the ionic liquid, 1-hexeyl-3-methylimidazolium hexafluorophosphate, and acetone were selected as extracting and dispersive solvents, respectively. After extraction, phase separation was performed by centrifugation and the sedimented phase (ionic liquid) was solubilized in acetonitrile and directly injected into the HPLC for subsequent analysis. Baseline separation of metal ion complexes was achieved on a RP-C18 column using a gradient elution of the mixtures of methanol-acetonitrile-water as the mobile phase at a flow rate of 1.0 mL min-1. The influence of variables such as sample pH, concentration of the chelating agent, amount of ionic liquid (extraction solvent), disperser solvent volume, extraction time, salt effect and centrifugation speed were studied and optimized. Under the optimum conditions, the enrichment factor of 222 was obtained. The detection limits for Ni, Co, Cu and Zn were 0.8, 1.6, 1.9 and 2.8 μg L?1, respectively. The relative standard deviations (RSDs) were in the range of 3.6-5.0 % for all of the investigated metal ions. The proposed procedure was successfully applied to the determination of the studied metal ions in water samples.
机译:开发了基于离子液体的分散液-液微萃取(IL-DLLME)与高效液相色谱(HPLC)-UV检测技术,用于同时萃取和测定镍,钴,铜和锌离子的方法。在所提出的方法中,将柳氮酚(N,N′-双(水杨酰)-1,2-苯二胺)用作螯合剂。分别选择离子液体,1-己基-3-甲基咪唑六氟磷酸盐和丙酮作为萃取溶剂和分散溶剂。萃取后,通过离心进行相分离,并将沉淀的相(离子液体)溶解在乙腈中,然后直接注入HPLC中进行后续分析。在RP-C18色谱柱上以1.0 mL min-1的流速梯度洗脱甲醇-乙腈-水的混合物作为流动相,实现了金属离子络合物的基线分离。研究并优化了样品pH值,螯合剂浓度,离子液体(萃取溶剂)的量,分散剂溶剂的体积,萃取时间,盐效应和离心速度等变量的影响。在最佳条件下,富集系数为222。 Ni,Co,Cu和Zn的检出限分别为0.8、1.6、1.9和2.8μgL?1。对于所有研究的金属离子,相对标准偏差(RSD)在3.6-5.0%的范围内。所提出的方法已成功地用于测定水中样品中所研究的金属离子。

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