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Optimized Ultrasound-Assisted Emulsification-Microextraction Followed by ICP-OES for Simultaneous Determination of Ytterbium and Holmium in Natural Water

机译:优化的超声辅助乳化-微萃取-ICP-OES法同时测定天然水中的and和Hol

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摘要

In this study, the optimized ultrasound-assisted emulsification-microextraction followed by inductively coupled plasma-optical emission spectrometry was applied to simultaneous extraction and determination of holmium (Ho3+) and ytterbium (Yb3+) in water samples. 1-(2-Pyridylazo)-2-naphthol was used as chelating agent to form extractable complexes. Volume of extraction solvent, concentration of chelating agent, pH, ultrasonic time, temperature, and concentration of salt were considered as the variables of the method. To evaluate the results, extraction recovery was selected as the response. Significance of the variables was investigated by using a half-fraction factorial design (2f−1) and the optimization was performed by applying a central composite design. The calibration graphs were linear in the range of 4–200 µg L−1 for Ho3+ and 3–500 µg L−1 for Yb3+ with determination coefficients (R2) of 0.988 and 0.997 for Ho3+ and Yb3+, respectively. Limit of detection was 0.364 µg L−1 for Ho3+ and 0.252 µg L−1 for Yb3+. The relative standard deviations (C = 200 µg L−1, n = 6) were in the range of 4.2–4.5%. The method was successfully applied to the analysis of real water samples with the recoveries in the range of 80–95%.
机译:在这项研究中,优化的超声辅助乳化-微萃取,然后进行电感耦合等离子体发射光谱法用于同时萃取和测定水中的water(Ho3 +)和(Yb3 +)。 1-(2-吡啶基偶氮)-2-萘酚用作螯合剂以形成可萃取的复合物。萃取溶剂的体积,螯合剂的浓度,pH,超声时间,温度和盐浓度被认为是该方法的变量。为了评估结果,选择提取回收率作为响应。通过半分数阶乘设计(2f-1)研究了变量的意义,并通过应用中央复合设计进行了优化。校准曲线在Ho3 +的4–200μg L-1和Yb3 +的3–500μg L-1范围内是线性的,其Ho3 +和Yb3 +的测定系数(R2)分别为0.988和0.997。 Ho3 +的检出限为0.364μggL-1,Yb3 +的检出限为0.252μggL-1。相对标准偏差(C = 200 µg L-1,n = 6)在4.2–4.5%的范围内。该方法已成功应用于实际水样的分析,回收率在80–95%之间。

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