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在基于铂/壳聚糖生物传感平台上灵敏的同时伏安法测定除草剂敌草隆和异丙隆。

Sensitive simultaneous voltammetric determination of the herbicides diuron and isoproturon at a platinum/chitosan bio-based sensing platform.

机构信息

ampere - Laboratório de Plataformas Eletroquímicas - Universidade Federal de Santa Catarina, Departamento de Química, CEP 88040-900, Florianópolis, SC, Brazil.

Universidade Federal de Santa Catarina, Departamento de Física, 88040-900, Florianópolis, SC, Brazil.

出版信息

Ecotoxicol Environ Saf. 2020 Dec 15;206:111181. doi: 10.1016/j.ecoenv.2020.111181. Epub 2020 Aug 26.

Abstract

Phenylurea herbicides are persistent contaminants, which leads their transport to the surface and ground waters, affecting human and aquatic organisms. Different analytical methods have been reported for the detection of phenylureas; however, several of them are expensive, time-consuming, and require complex pretreatment steps. Here, we show a simple method for the simultaneous electrochemical determination of two phenylurea herbicides by differential pulse adsorptive stripping voltammetry (DPAdSV) using a modified platinum/chitosan electrode. The one-step synthesized platinum/chitosan PtNPs/CS was successfully characterized by TEM, XRPD, and FT-IR, and applied through the sensing platform designated as PtNPs/CS/GCE. This bio-based modified electrode is proposed for the first time for the individual and/or simultaneous electrochemical detection of the phenylurea herbicides diuron and isoproturon compounds extensively used worldwide that present a very similar chemical structure. Electrochemical and interfacial characteristics of the modified electrode were evaluated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). It was found that the oxidation mechanism of diuron and isoproturon occurs in two different pathways, with a peak-to-peak definition of ca. 0.15 V. Under differential pulse adsorptive stripping voltammetry (DPAdSV) optimized conditions, the limit of detection (LOD) was estimated as 7 μg L for isoproturon and 20 μg L for diuron (E = +0.8 V; t = 100 s). The proposed method was successfully applied to the determination of both analytes in river water samples, at three different levels, with a recovery range of 90-110%. The employment of the bio-based sensing platform PtNPs/CS/GCE allows a novel and easy analytical method to the multi-component phenylurea herbicides detection.

摘要

苯脲类除草剂是持久性污染物,会迁移到地表水和地下水,影响人类和水生生物。已经报道了多种用于检测苯脲类除草剂的分析方法;然而,其中一些方法昂贵、耗时且需要复杂的预处理步骤。在这里,我们展示了一种使用修饰后的铂/壳聚糖电极通过差分脉冲吸附溶出伏安法(DPAdSV)同时电化学测定两种苯脲除草剂的简单方法。一步合成的铂/壳聚糖 PtNPs/CS 通过 TEM、XRPD 和 FT-IR 成功进行了表征,并应用于指定为 PtNPs/CS/GCE 的传感平台。这种基于生物的修饰电极首次被提议用于个体和/或同时电化学检测在全球范围内广泛使用的具有非常相似化学结构的苯脲除草剂敌草隆和异丙隆化合物。通过循环伏安法(CV)和电化学阻抗谱(EIS)评估了修饰电极的电化学和界面特性。发现敌草隆和异丙隆的氧化机制发生在两条不同的途径中,峰-峰定义约为 0.15 V。在差分脉冲吸附溶出伏安法(DPAdSV)优化条件下,对异丙隆的检测限(LOD)估计为 7μg L,对敌草隆的检测限(LOD)估计为 20μg L(E=+0.8 V;t=100 s)。该方法成功应用于河水样品中两种分析物的测定,在三个不同水平下,回收率范围为 90-110%。生物传感平台 PtNPs/CS/GCE 的应用允许对多组分苯脲类除草剂进行新颖且易于分析的方法检测。

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