4.6 Article

Simultaneous voltammetric determination of nitrophenol isomers at ordered mesoporous carbon modified electrode

期刊

ELECTROCHIMICA ACTA
卷 106, 期 -, 页码 127-134

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2013.05.055

关键词

Ordered mesoporous carbons; Voltammetric detection; Nitrophenol isomers; Simultaneous determination

资金

  1. National Natural Science Foundation of China [21173049, 31200598, 21275152]
  2. National Science Foundation for Fostering Talents in Basic Research of National Natural Science Foundation of China [J1103303, J2012-029]
  3. Hundred-Talent-Project, Chinese Academy of Sciences [KSCX2-YW-BR-7]

向作者/读者索取更多资源

In this paper, ordered mesoporous carbons (OMCs) modified glassy carbon electrode (GCE) (OMCs/GCE) was employed to investigate the electrochemical behavior of o-nitrophenol (o-NP), m-nitrophenol (m-NP) and p-nitrophenol (p-NP) in ambient-N-2 phosphate buffer saline. Compared with bare GCE, the OMCs/GCE exhibited obvious electrocatalytic activity towards nitrophenol isomers. The electrochemical reaction mechanism of nitrophenol at the modified electrode was also studied. At OMCs/GCE, the three nitrophenol isomers could be identified and separated successfully and the simultaneous determination was realized by detecting the reduction peaks of their intermediate products (at 0.209 V vs. saturated calomel electrode for p-NP, 0.020 V for m-NP and -0.201 V for o-NP) with differential pulse voltammetry. Under the optimized experimental conditions, the linear ranges of the calibration curves were 2-90 mu M for p-NP, 1-100 mu M for m-NP and 0.5-90 mu M for o-NP with limits of detection of 0.1 mu M, 0.06 mu M and 0.08 mu M for p-NP, m-NP and o-NP, respectively (S/N = 3). Therefore, the proposed method is simple, rapid, stable, sensitive, specific, reproducible and cost-effective, which can be applicable for real samples detection. (c) 2013 Elsevier Ltd. All rights reserved.

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