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在 1,10-菲啰啉存在下,吸附溶出伏安法灵敏测定食品中的痕量铜。

Highly sensitive determination of trace copper in food by adsorptive stripping voltammetry in the presence of 1,10-phenanthroline.

机构信息

Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Wattana, Bangkok 10110, Thailand.

出版信息

Talanta. 2013 Apr 15;108:1-6. doi: 10.1016/j.talanta.2013.02.031. Epub 2013 Mar 5.

Abstract

A highly sensitive, rapid, simple and selective adsorptive stripping assay for the determination of trace copper(II) is proposed. The methodology is based on the adsorptive accumulation of copper(II)-1,10-phenanthroline complexes onto a glassy carbon electrode, followed by oxidation of the adsorbed species by voltammetric scanning using square-wave voltammetry. The influences of experimental variables on the sensitivity of the proposed method, such as the effects of pH, ligand concentration, accumulation time, accumulation potential and interferences, were investigated. Under optimal conditions, the proposed method showed linearity from 0.1 ng mL(-1) to 50 ng mL(-1). The 3 S/N detection limits were 0.0185 ng mL(-1), and the relative standard deviations (n=10) were 0.09-4.71% for intra-day and 0.05-7.14% for inter-day analyses, respectively. The application of the proposed method to the direct analysis of food samples yielded results that agreed with those obtained from including inductively coupled plasma-optical emission spectrometry (ICP-OES) assays according to a paired t-test. The results are a step toward the development of an alternative and reliable analytical method for food research, which requires the direct determination of copper.

摘要

提出了一种用于痕量铜(II)测定的高灵敏度、快速、简单和选择性的吸附溶出分析方法。该方法基于铜(II)-1,10-邻菲啰啉配合物在玻碳电极上的吸附积累,然后通过方波伏安法进行电化学扫描,氧化吸附物种。研究了实验变量对所提出方法灵敏度的影响,例如 pH、配体浓度、积累时间、积累电位和干扰的影响。在最佳条件下,所提出的方法在 0.1 ng mL(-1)至 50 ng mL(-1)范围内呈现线性关系。3 S/N 的检测限为 0.0185 ng mL(-1),日内和日间分析的相对标准偏差(n=10)分别为 0.09-4.71%和 0.05-7.14%。该方法应用于食品样品的直接分析,所得结果与根据配对 t 检验与电感耦合等离子体-光学发射光谱法 (ICP-OES) 测定结果一致。这些结果为开发用于食品研究的替代和可靠的分析方法迈出了一步,该方法需要直接测定铜。

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