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一种新策略,用于对卡拉胶水凝胶修饰碳糊电极,以实现对天然水中砷的灵敏和选择性测定。

A new strategy for the modification of a carbon paste electrode with carrageenan hydrogel for a sensitive and selective determination of arsenic in natural waters.

机构信息

Pontificia Universidad Católica de Chile, Chemistry Faculty, Vicuña Mackenna 4860, Santiago 7820436, Chile.

Pontificia Universidad Católica de Chile, Biological Sciences Faculty, Avda, Libertador Bernardo OHiggins 340, Santiago 8331150, Chile.

出版信息

Talanta. 2018 Sep 1;187:259-264. doi: 10.1016/j.talanta.2018.05.028. Epub 2018 May 8.

Abstract

An adsorptive stripping voltammetric method for the determination of As(III) and As in water samples using a carrageenan modified carbon paste electrode is presented for the first time (CAR-CPE). The modified electrode was prepared in different ways: by adding CAR in solid form or as a hydrogel together with graphite and paraffin, as well as adsorbing CAR by applying a potential on an unmodified carbon paste electrode. The best results were obtained when CAR was incorporated as hydrogel (HCAR-CPE). The selection of the ratio amounts for electrode preparation was carried out applying a multivariate experimental design. Variables like amount of graphite (U), HCAR (U) and paraffin (U) were optimized using a (2+2K+C) model. The results showed that the amount of HCAR was the most significant factor, and the adequate U:U:U ratio to prepare the electrode was: 493 mg of graphite, 214 μL of paraffin and 134 μL of carrageenan as gel. The optimum parameters for the determination of As(III) were pH = 3.25 (0.01 mol L HPO/HPO solution); E = -0.50 V and t = 30 s. The electrode presents good linear behavior concentration range from 0.50 to 6.70 μg L, with a limit of detection of 0.22 μg L. The relative standard deviation was 5.0% at the 1.5 μg L As(III) level (n = 16). The method was validated by quantifying As(III) in spiked tap water from laboratory (RE: 3.0%), and it was applied for the determination of As in water samples from the Loa River (North of Chile) prior reduction of As(V) with NaSO solution, obtaining 814.00 ± 0.03 μg L. The results of the proposed method were compared with those obtained by adsorptive stripping voltammetry with HMDE and by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) techniques.

摘要

本文首次提出了一种利用卡拉胶修饰碳糊电极(CAR-CPE)测定水样中 As(III)和 As 的吸附溶出伏安法。以不同方式制备修饰电极:以固态形式或水凝胶形式加入 CAR 与石墨和石蜡一起,以及在未修饰的碳糊电极上施加电位吸附 CAR。当 CAR 作为水凝胶(HCAR-CPE)加入时,获得了最佳结果。通过应用多元实验设计进行了电极制备的比例选择。通过(2+2K+C)模型优化了诸如石墨(U)、HCAR(U)和石蜡(U)等变量的量。结果表明,HCAR 的量是最重要的因素,制备电极的适当 U:U:U 比为:石墨 493mg、石蜡 214μL 和卡拉胶凝胶 134μL。测定 As(III)的最佳参数为 pH = 3.25(0.01 mol L HPO/HPO 溶液);E = -0.50 V 和 t = 30 s。该电极在 0.50 至 6.70 μg L 的浓度范围内呈现出良好的线性行为,检测限为 0.22 μg L。在 1.5 μg L As(III)水平时,相对标准偏差为 5.0%(n = 16)。通过定量测定实验室自来水(RE:3.0%)中的 As(III)对方法进行了验证,并将其应用于测定智利北部 Loa 河水样中的 As,先用 NaSO 溶液还原 As(V),得到 814.00 ± 0.03 μg L。该方法的结果与 HMDE 吸附溶出伏安法和电感耦合等离子体质谱法(ICP-MS)的结果进行了比较。

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