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首页> 外文期刊>Journal of Chromatographic Science >Separation and Sensitive Detection of Lanthanides by Capillary Electrophoresis and Contactless Conductivity Detection
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Separation and Sensitive Detection of Lanthanides by Capillary Electrophoresis and Contactless Conductivity Detection

机译:用毛细管电泳分离和敏感检测镧系元素和非接触式电导检测

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A rapid and sensitive capillary zone electrophoresis method for the simultaneous separation and determination of lanthanide ions, combined with capacitively coupled contactless conductivity detection (C~4D), is reported. The influence of experimental parameters on separation was investigated. The optimal separation conditions were obtained when 4.5mM 2-hydroxyisobutyric acid and 1mM acetic acid (HAc) at pH 4.5 were used as buffer solution. Under these conditions, complete separation of all 14 lanthanide ions was achieved in 6 min. With the use of the C~4D detector, the sensitive detection of non-UV active lanthanide ions was achieved without the need of a UV active ligand or a visualization agent. The sensitivities were further enhanced with a sample stacking procedure. The limits of detection were to be found between 2.77 and 8.26 nmol/L and the limits of quantification were between 9.29 and 27.5 nmol/L for 14 lanthanide ions.
机译:报道了一种快速敏感的毛细管区电泳方法,用于同时分离和测定镧系元素,与电容耦合的非接触式导电检测(C〜4D)相结合。 研究了实验参数对分离的影响。 当使用45mM 2-羟基异丁酸和1mM乙酸(HAC)以缓冲溶液时,获得最佳分离条件。 在这些条件下,在6分钟内实现了所有14个镧系元素离子的完全分离。 通过使用C〜4D检测器,实现了非UV活性镧系元素离子的敏感性检测,而不需要UV活性配体或可视化剂。 通过样品堆叠程序进一步增强了敏感性。 在2.77和8.26之间发现检测限率为2.77和8.26 nmol / L,量化限制为14镧离子的9.29和27.5 nmol / l。

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