A disposable chronocoulometric sensor for heavy metal ions using a diaminoterthiophene-modified electrode doped with graphene oxide

被引:49
作者
Choi, Seung-Min
Kim, Dong-Min
Jung, Ok-Sang
Shim, Yoon-Bo [1 ]
机构
[1] Pusan Natl Univ, Dept Chem, Busan 609735, South Korea
基金
新加坡国家研究基金会;
关键词
Heavy metal ions; Chronocoulometric sensor; Square wave anodic stripping voltammetry; Diaminoterthiophene; Graphene oxide; Chemically modified electrode; ANODIC-STRIPPING VOLTAMMETRY; CARBON-PASTE; WATER; LEAD; CADMIUM(II); FABRICATION; MERCURY; SILICA; COPPER;
D O I
10.1016/j.aca.2015.08.037
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The rapid simultaneous determination of cadmium, lead, copper, and mercury ions is performed by employing a disposable sensor modified with graphene oxide (GO) doped diaminoterthiophene (GO/DTT) for chronocoulometry (CC). The performances of CC with and without pre-deposition in two opposite potential step directions were compared with square wave anodic stripping voltammetry (SWASV) under various conditions. The surface of the GO/DTT modified screen print carbon electrode (SPCE) was characterized by SEM, EDXS, and electrochemical impedance spectroscopy (EIS). Experimental variables that affect the response signal such as the pH, deposition time, type of supporting electrolyte, concentration of DTT, content ratio of GO to DTT, and Nafion content were optimized. Interference effects due to other heavy metal ions were also investigated. The dynamic ranges of SWASV and CC were between 1 ng mL(-1) and 2.5 mu g mL(-1) and between 1 ng mL(-1) and 10 mu g mL(-1), respectively. The detection limits for Cd2+, Pb2+, Cu2+, Hg2+ ions were 1.9 +/- 0.4 ng mL(-1), 2.8 +/- 0.6 ng mL(-1), 0.8 +/- 0.2 ng mL(-1), and 2.6 +/- 0.9 ng mL(-1) for the CC stripping method; 2.6 +/- 0.2 ng mL(-1), 0.5 +/- 0.1 ng mL(-1), 1.8 +/- 0.3 ng mL(-1), and 3.2 +/- 0.3 ng mL(-1) for the CC deposition method; and 7.1 +/- 0.9, 1.9 +/- 0.3, 0.4 +/- 0.1, and 0.7 +/- 0.1 ng mL(-1) for SWASV. The reliability of the method for point-of-analysis was evaluated by analyzing a urine standard reference material and some water samples. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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