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树脂吸附特性在铋微电极伏安法测定Se(IV)水样制备中的应用

Use of Adsorption Properties of Resin for Water Sample Preparation in Voltammetric Determination of Se(IV) Using Bismuth Microelectrode.

作者信息

Grabarczyk Malgorzata, Fialek Marzena, Wardak Cecylia

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. 2024 Nov 21;29(23):5501. doi: 10.3390/molecules29235501.

DOI:10.3390/molecules29235501
PMID:39683660
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11643792/
Abstract

This paper proposes a simple, environmentally friendly, and efficient procedure for preparing natural water samples for the voltammetric determination of trace amounts of Se(IV). The method is based on premixing a sample with Amberlite XAD-7 resin at 50 °C. The composition of the 10 mL solution consists of the sample to be analysed, 0.1 mol L of acetate buffer at pH = 4.0, and 0.5 g of Amberlite XAD-7. After 2 min of stirring, a voltammetric measurement is carried out using a fixed bismuth microelectrode using the following potentials: -2.5 V for 2 s and -0.55 V for 30 s. The voltammetry is recorded by varying the potential from -400 mV to -1000 mV. An undisturbed Se(IV) signal is obtained in the presence of 10 mg L of Triton X-100, 5 mg L of SDS, 10 mg L of CTAB, 5 mg L of Rhamnolipid, 5 mg L of HA, 10 mg L of FA, and 2 mg L of NOM. The validity of the developed procedure is checked by analysing the certified reference materials SPS-SW1 (surface water) and TM-25.5 (Lake Ontario water) additionally enriched with surfactants and humic substances.

摘要

本文提出了一种简单、环保且高效的用于伏安法测定痕量硒(IV)的天然水样制备方法。该方法基于在50°C下将样品与Amberlite XAD - 7树脂预混合。10 mL溶液的组成包括待分析的样品、pH = 4.0的0.1 mol/L醋酸盐缓冲液和0.5 g Amberlite XAD - 7。搅拌2分钟后,使用固定铋微电极在以下电位下进行伏安测量:-2.5 V持续2 s,-0.55 V持续30 s。通过将电位从-400 mV变化到-1000 mV来记录伏安图。在存在10 mg/L Triton X - 100、5 mg/L SDS、10 mg/L CTAB、5 mg/L鼠李糖脂、5 mg/L腐殖酸、10 mg/L富里酸和2 mg/L天然有机物的情况下获得了不受干扰的硒(IV)信号。通过分析额外添加了表面活性剂和腐殖物质的有证标准物质SPS - SW1(地表水)和TM - 25.5(安大略湖水)来检验所开发方法的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/f96b879c108b/molecules-29-05501-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/68c4690a55be/molecules-29-05501-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/bea5c9d84013/molecules-29-05501-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/1be7ab9ee827/molecules-29-05501-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/3bc7e438d61d/molecules-29-05501-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/f96b879c108b/molecules-29-05501-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/68c4690a55be/molecules-29-05501-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/bea5c9d84013/molecules-29-05501-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/1be7ab9ee827/molecules-29-05501-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/3bc7e438d61d/molecules-29-05501-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/11643792/f96b879c108b/molecules-29-05501-g005a.jpg

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