Suppr超能文献

利用固体铋微电极通过环境水样中吸附溶出伏安法测定钒。

The Use of a Solid Bismuth Microelectrode for Vanadium Quantification by Adsorptive Stripping Voltammetry in Environmental Water Samples.

机构信息

Department of Analytical Chemistry, Institute of Chemical Sciences, Faculty of Chemistry, Maria Curie-Sklodowska University, 20-031 Lublin, Poland.

出版信息

Molecules. 2022 Mar 27;27(7):2168. doi: 10.3390/molecules27072168.

Abstract

This paper presents for the first time the use of an environmentally friendly solid bismuth microelectrode for the voltammetric quantification of V(V) in natural water samples. These studies were designed to replace the film bismuth electrode that had been introduced to eliminate the conventional sensors based on highly toxic mercury. In the proposed procedure, V(V) is preconcentrated at the solid bismuth microelectrode surface via the formation of electroactive complexes with cupferron from a solution of 0.1-mol L acetate buffer, pH = 4.6 at a potential of -0.4 V. The linearity of the calibration graph is in the V(V) concentration range from 8 × 10 to 1 × 10 mol L with a preconcentration time of 1 min. The limit of detection (calculated as 3 σ) is 2.5 × 10 mol L for a preconcentration time of 1 min. It was also demonstrated that significant improvement in analytical parameters was achieved as a result of the activation of the solid electrode surface at a potential of -2.5 V for 2 s. The developed procedure is highly selective for the presence of foreign ions and organic compounds in tested samples. The accuracy of the recommended procedure was checked using SPS-WW1 waste water-certified reference materials of a complex composition, in which the concentration of V(V) determined by the proposed method was 95.1 ± 1.6 ng mL. Moreover, in keeping with the outlined procedure, river, tap and rain water samples were analyzed without any pretreatment, and recovery values from 96% to 106% were obtained.

摘要

本文首次提出了使用环保型固态铋微电极来测定天然水样中 V(V)的伏安定量法。这些研究旨在替代膜铋电极,以消除基于剧毒汞的传统传感器。在提出的程序中,V(V)通过与铜试剂在 0.1mol L 醋酸盐缓冲液(pH = 4.6)中的形成电活性配合物,在-0.4 V 的电位下在固态铋微电极表面预浓缩。在 1 分钟的预浓缩时间内,校准曲线的线性范围为 8×10 到 1×10 mol L,V(V)浓度范围为 8×10 到 1×10 mol L。检测限(计算为 3σ)为 2.5×10 mol L,预浓缩时间为 1 分钟。还证明,通过在-2.5 V 的电位下对固态电极表面进行 2 秒的激活,可以显著改善分析参数。该方法对测试样品中存在的外来离子和有机化合物具有高度选择性。用具有复杂组成的 SPS-WW1 废水认证参考物质检查了推荐方法的准确性,用该方法确定的 V(V)浓度为 95.1±1.6 ng mL。此外,按照概述的程序,无需进行任何预处理即可分析河水、自来水和雨水样品,回收率在 96%到 106%之间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f5b/9000851/d674be4456ff/molecules-27-02168-g001.jpg

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