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Electrochemical synthesis and characterization of a new selective chelating agent for Ni(II) and its environmental analytical application

机译:新型镍(II)选择性螯合剂的电化学合成,表征及其环境分析应用

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This investigation involved electrochemical synthesis of a new Ni(II) selective chelating agent by electropolymerization of 4-nitrophenol in acetate medium. The prepared polymer was characterized by FT-IR, ~1H-NMR, CHNO elemental analysis, GPC, and UV-Vis spectrometry and a suitable chemical structure was suggested. This new ligand was successfully applied in cloud point extraction (CPE) of Ni(II) before flame atomic absorption spectrometry (FAAS) measurements. The pH and the concentration of the phosphate buffer, chelating agent, surfactant and salt were optimized. In the presence of foreign ions, no significant interferences were observed. Under optimum conditions, the limits of detection (LOD) and quantification (LOQ) were 0.76 and 2.53 ng mL~(-1), respectively. The mean, preconcentration factor, standard error and RSQ for five replicates of 10 ng mL~(-1) Ni(II) were calculated to be 9.78 ng mL~(-1), 29.3, 2.2% and 3.36%, respectively. The method presented good sensitivity and selectivity and was applied for the determination of trace amounts of Ni(II) in various water and wastewater samples. The results obtained by the proposed method were in good agreement with the results of inductively coupled plasma-optical emission spectrometry (ICP-OES).
机译:这项研究涉及在乙酸盐介质中通过4-硝基苯酚的电聚合电化学合成新的Ni(II)选择性螯合剂。通过FT-IR,〜1H-NMR,CHNO元素分析,GPC和UV-Vis光谱对制备的聚合物进行表征,并提出了合适的化学结构。在火焰原子吸收光谱法(FAAS)测量之前,这种新的配体已成功应用于Ni(II)的浊点萃取(CPE)。优化了pH值和磷酸盐缓冲液,螯合剂,表面活性剂和盐的浓度。在存在外来离子的情况下,未观察到明显的干扰。在最佳条件下,检出限(LOD)和定量限(LOQ)分别为0.76和2.53 ng mL〜(-1)。五次重复测定10 ng mL〜(-1)Ni(II)的平均值,预浓系数,标准误和RSQ分别为9.78 ng mL〜(-1),29.3、2.2%和3.36%。该方法具有良好的灵敏度和选择性,可用于各种水和废水样品中痕量镍(II)的测定。所提出的方法获得的结果与电感耦合等离子体发射光谱法(ICP-OES)的结果非常吻合。

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