Poly(3-methylthiophene)/palladium sub-micro-modified sensor electrode. Part II: Voltammetric and EIS studies, and analysis of catecholamine neurotransmitters, ascorbic acid and acetaminophen

被引:88
作者
Atta, Nada F. [1 ]
El-Kady, Maher F. [1 ]
机构
[1] Cairo Univ, Dept Chem, Fac Sci, Giza 12613, Egypt
关键词
Poly(3-methylthiophene); Pd nanoparticles; Electrochemical impedance spectroscopy; Catecholamine neurotransmitters; Ascorbic acid; Acetaminophen (paracetamol); CONDUCTING POLYMER ELECTRODES; GLASSY-CARBON ELECTRODE; ELECTROCHEMICAL DETERMINATION; ELECTROCATALYTIC OXIDATION; DIFFUSION-COEFFICIENTS; GOLD NANOPARTICLES; POLYANILINE FILM; DOPAMINE; NANOTUBES; IONS;
D O I
10.1016/j.talanta.2009.04.040
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Promising voltammetric sensors based on the modification of Pt and poly(3-methylthiophene) (PMT) electrodes with Pd nanoparticles were achieved for the determination of catecholamine neurotransmitters, ascorbic acid and acetaminophen. Electrochemistry of the indicated compounds was studied at these electrodes and interesting electrocatalytic effects were found. Furthermore, simple, easily prepared one electrochemical step Pd-modified Pt electrode (Pt/Pd) is reported for the first time. Cyclic voltammetry (CV) and chronocoulometry (CC) were used for the determination of the apparent diffusion coefficients in different electrolytes at these electrodes and the values are in the range from 10(-4) to 10(-5) cm(2) s(-1). Furthermore, it was found that the method of polymer formation had a substantial effect on the synergism between the polymer film and the loaded metal particles towards the oxidation of dopamine (DA) in different supporting electrolytes. This was confirmed by the CV, CC and EIS (electrochemical impedance spectroscopy) as well as SEM (Scanning Electron Microscopy) results. Pt and PMT electrodes modified with Pd nanoparticles showed excellent results for the simultaneous determination of tertiary and quaternary mixtures of the studied compounds. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:639 / 647
页数:9
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