Simultaneous electrochemical sensing of thallium, lead and mercury using a novel ionic liquid/graphene modified electrode

被引:142
|
作者
Bagheri, Hasan [1 ]
Afkhami, Abbas [2 ]
Khoshsafar, Hosein [2 ]
Rezaei, Mosayeb [2 ]
Sabounchei, Seyed Javad [2 ]
Sarlakifar, Mehdi [2 ]
机构
[1] Baqiyatallah Univ Med Sci, Chem Injuries Res Ctr, Tehran, Iran
[2] Bu Ali Sina Univ, Fac Chem, Hamadan, Iran
关键词
Electrochemical sensor; Chemically modified carbon paste electrode; Heavy metals; Graphene; Simultaneous determination of heavy metals; CARBON-PASTE ELECTRODE; ANODIC-STRIPPING VOLTAMMETRY; CHEMICALLY-MODIFIED ELECTRODE; SYNTHESIZED SCHIFF-BASE; LANGMUIR-BLODGETT-FILM; GRAPHENE OXIDE; POTENTIOMETRIC SENSOR; COMPOSITE ELECTRODE; GRAPHITE ELECTRODE; BIOLOGICAL SAMPLES;
D O I
10.1016/j.aca.2015.03.004
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the present manuscript, an electrochemical sensor for the sensitive detection of Tl-+,Tl- Pb2+ and Hg2+ is described. A new composite electrode has been fabricated using graphene, 1-n-octylpyridinum hexafluorophosphate (OPFP), and [2,4-Cl2C6H3C(O)CHPPh3] (L), as a new synthetic phosphorus ylide. The physicochemical and electrochemical characterizations of fabricated sensor were investigated in details. The advantages of the proposed composite electrode are its ability in simultaneous electrochemical detection of Tl+, Pb2+ and Hg2+ with good selectivity, stability and no need for separating of the three species from complex mixtures prior to electrochemical measurements. The analytical performance of the proposed electrode was examined using square wave voltammetry. Tl-+,Tl- Pb2+ and Hg2+ can be determined in linear ranges from 1.25 x 10(9) to 2.00x10(-7) mol L-1. Low detection limits of 3.57 x 10(-10) mol L-1 for Tl+, 4.50 x 10(-10) mol L-1 for Pb2+ and 3.86 x 10(-10) mol L-1 for Hg2+ were achieved. Finally, the proposed electrochemical sensor was applied to detect trace analyte ions in various water and soil samples with satisfactory results. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:56 / 66
页数:11
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