4.7 Article

Direct electrochemical determination of carbaryl using a multi-walled carbon nanotube/cobalt phthalocyanine modified electrode

期刊

TALANTA
卷 79, 期 5, 页码 1406-1411

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2009.06.013

关键词

Carbon nanotubes; Cobalt phthalocyanine; Carbaryl; Electrochemical impedance spectroscopy; Square-wave voltammetry; Environmental monitoring

资金

  1. CNPq [201494/2008-6]
  2. Fundacao para a Ciencia e Tecnologia (FCT), Portugal [PTDC/QUI/65255/2006, PTDC/QUI/65732/2006]
  3. European Community Fund FEDER
  4. CEMUC(R) (Research Unit 285)
  5. Fundação para a Ciência e a Tecnologia [PTDC/QUI/65732/2006, PTDC/QUI/65255/2006] Funding Source: FCT

向作者/读者索取更多资源

The electrochemical detection of carbaryl at low potentials, in order to avoid matrix interferences, is an important challenge. This study describes the development, electrochemical characterization and utilization of a glassy carbon (CC) electrode modified with multi-wall carbon nanotubes (MWCNT) plus cobalt phthalocyanine (CoPc) for the quantitative determination of carbaryl in natural waters. The surface morphology was examined by scanning electron microscopy, enhanced sensitivity was observed with respect to bare glassy carbon and electrocatalytic effects reduced the oxidation potential to +0.80V vs. SCE in acetate buffer solution at pH 4.0. Electrochemical impedance spectroscopy was used to estimate the rate constant of the oxidation process and square-wave voltammetry to investigate the effect of electrolyte pH. Square-wave voltammetry in acetate buffer solution at pH 4.0. allowed the development of a method to determine carbaryl, without any previous step of extraction, clean-up, or derivatization, in the range of 0.33-6.61 mu mol L-1, with a detection limit of 5.46 +/- 0.02 nmol L-1 (1.09 +/- 0.02 mu g L-1) in water. Natural water samples spiked with carbaryl and without any purification step were successfully analyzed by the standard addition method using the GC/MWCNT/CoPc him electrode. (C) 2009 Elsevier B.V. All rights reserved.

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