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Fulvic Acid Reduced GO and Phthalocyanine Nanorods as Reaction Platform for Simultaneous Determination of Catechol, Hydroquinone, Phenol and p-nitrophenol.

Authors :
Yu Zhang
Qiang Xie
Zhi Xia
Guofeng Gui
Feng Deng
Source :
Journal of The Electrochemical Society; 2019, Vol. 166 Issue 14, pB1293-B1299, 7p
Publication Year :
2019

Abstract

In this paper, a novel nanocomposite fulvic acid reduced graphene oxide (FA-rGO) and Co-phthalocyanine nanorods (CoPcNRs) was prepared and used to construct an electrochemical sensor for simultaneous detection of catechol (CC), hydroquinone (HQ), phenol (PN) and p-nitrophenol (p-NP). FA as reductant used to prepare FA-rGO nanocomposite, which fabricated by hydrothermal method and freeze-drying process. The method is environmentally friendly and realizes the gentle reduction of GO. CoPcNRs were synthesized by surfactant-assisted ultrasonic method. The microstructure and morphologies of the as-prepared materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and UV-Vis spectrophotometer. The electrochemical oxidation of CC, HQ, PN and p-NP was investigated using differential pulse voltammetry (DPV). The results show that the FA-rGO/CoPcNRs modified electrode exhibits excellent electrochemical activity toward the simultaneous redox of CC, HQ, PN and p-NP. Under optimal conditions, the linear ranges of CC, HQ, PN and p-NP were 1 μM-650 μM, 2 μM-450 μM, 2 μM-160 μM, 2 μM-140 μM, with 0.3 μM, 0.65 μM, 0.65 μMand 0.65 μM, respectively. In addition, themodified electrode showed good selectivity, sensitivity and stability. The application in real samples was also evaluated, and the recoveries suggesting that FA-rGO/CoPcNRs nanocomposites could be used as an excellent potential reaction platform for the simultaneous determination of CC, HQ, PN and p-NP in environmental samples. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00134651
Volume :
166
Issue :
14
Database :
Supplemental Index
Journal :
Journal of The Electrochemical Society
Publication Type :
Academic Journal
Accession number :
139172305
Full Text :
https://doi.org/10.1149/2.0351914jes