Suppr超能文献

研究不同电解质介质中金属电极上硒(IV)的伏安行为和检测。

Investigation into the voltammetric behaviour and detection of selenium(IV) at metal electrodes in diverse electrolyte media.

机构信息

Tyndall National Institute, University College, Cork, Ireland.

出版信息

Anal Chim Acta. 2011 Aug 12;699(2):127-33. doi: 10.1016/j.aca.2011.05.027. Epub 2011 May 24.

Abstract

The voltammetric behaviour of selenium(IV) was studied at platinum and gold electrodes in sulphuric acid, perchloric acid and potassium chloride media as a basis for its voltammetric detection. The best voltammetric behaviour was recorded at gold electrodes with perchloric acid as the supporting electrolyte. The concomitant presence of metals, such as copper or lead, and of model biomolecules, such as bovine serum albumin, in the solution resulted in a deterioration of the electrochemical response for selenium(IV). Quantitative detection of selenium(IV) by square wave anodic stripping voltammetry at both a millimetre-sized gold disc electrode and a microband electrode array revealed linear responses to selenium concentration in the ranges 5-15 μM and 0.1-10 μM, respectively, with 60s preconcentration. The sensitivities were 6.4 μA μM(-1) cm(-2) and 100 μA μM(-1) cm(-2) at the disc and the microband array, respectively. The detection limit at the microband electrode array was 25 nM, illustrating the potentiality of such microelectrodes for the development of mercury-free analytical methods for the trace detection of selenium(IV).

摘要

硒(IV)在硫酸、高氯酸和氯化钾介质中的伏安行为在铂和金电极上进行了研究,作为其伏安检测的基础。在高氯酸作为支持电解质的情况下,金电极上记录到最佳的伏安行为。在溶液中同时存在金属(如铜或铅)和模型生物分子(如牛血清白蛋白)会导致硒(IV)的电化学响应恶化。通过在毫米大小的金圆盘电极和微带电极阵列上进行方波阳极溶出伏安法对硒(IV)进行定量检测,分别在 5-15 μM 和 0.1-10 μM 的范围内对硒浓度表现出线性响应,预浓缩时间为 60s。在圆盘和微带阵列上的灵敏度分别为 6.4 μA μM(-1) cm(-2)和 100 μA μM(-1) cm(-2)。在微带电极阵列上的检测限为 25 nM,这表明这种微电极在开发无汞分析方法用于痕量硒(IV)检测方面具有潜力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验