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Determination of iodide in urine by ion-pair chromatography with electrochemical detection

机译:离子对色谱-电化学检测法测定尿中的碘化物

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摘要

A variety of parameters affecting the determination of iodide in biological materials by ion-pair chromatography and electrochemical detection were examined in detail. It became apparent that the pH value, the ionpair concentration, the proportion of organic solvent and of organic bases as a component of the buffer solution, as well as the salt concentration in the eluent system could effectively influence the retention characteristics of iodide in the chromatographic system, resulting in the separation of potential interfering substances. The presence of other anions in the sample matrix has to be taken into consideration, particularly thiocyanate because of its long retention time. Investigations of the electrochemical detection mechanism revealed that the reaction hitherto assumed to be responsible for detector signal genertion (formation of AgI) is incorrect. In addition, a much more sensitive detection of iodide than that cited in the literature to date is possible if the detector potential is optimally selected and chromatography. Use of a gold electrode rather than a silver electrode also considerably enhances the reliability of the procedure.
机译:详细研究了影响通过离子对色谱法和电化学检测法测定生物材料中碘化物的各种参数。显而易见的是,pH值,离子对浓度,作为缓冲溶液成分的有机溶剂和有机碱的比例以及洗脱液系统中的盐浓度都可以有效地影响碘化物在色谱中的保留特性。系统,从而分离出潜在的干扰物质。必须考虑样品基质中其他阴离子的存在,特别是硫氰酸盐,因为其保留时间长。电化学检测机制的研究表明,迄今被认为是造成检测器信号生成(AgI形成)的原因的反应是不正确的。另外,如果最优选择检测器电位并进行色谱分析,则碘化物的检测灵敏度可能比迄今为止的文献更敏感。使用金电极而不是银电极也大大提高了程序的可靠性。

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