4.7 Article

A differential pulse voltammetric method for simultaneous determination of ascorbic acid, dopamine, and uric acid using poly (3-(5-chloro-2-hydroxyphenylazo)-4,5-dihydroxynaphthalene-2,7-disulfonic acid) film modified glassy carbon electrode

期刊

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
卷 633, 期 1, 页码 212-220

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2009.06.001

关键词

Dihydroxynaphthalene disulfonic acid derivative; Modified glassy carbon electrode; Electrocatalytic; Ascorbic acid; Dopamine; Uric acid; Voltammetry

资金

  1. Research Council of Isfahan University of Technology (IUT)
  2. Center of Excellence in Sensor and Green Chemistry

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A stable modified glassy carbon electrode based on the poly 3-(5-chloro-2-hydroxyphenylazo)-4,5-dihydroxynaphthalene-2,7-disulfonic acid (CDDA) film was prepared by electrochemical polymerization technique to investigate its electrochemical behavior by cyclic voltammetry. The properties of the electrodeposited films, during preparation under different conditions, and their stability were examined. The homogeneous rate constant, k(s), for the electron transfer between CDDA and glassy carbon electrode was calculated as 5.25( +/- 0.20) x 10(2) Cm s(-1). The modified electrode showed electrocatalytic activity toward ascorbic acid (AA), dopamine (DA), and uric acid (UA) oxidation in a buffer solution (pH 4.0) with a diminution of their overpotential of about 0.12, 0.35, and 0.50 V for AA, DA, and UA. respectively. An increase could also be observed in their peak currents. The modified glassy carbon electrode was applied to the electrocatalytic oxidation of DA, AA, and UA, which resolved the overlapping of the anodic peaks of DA, AA, and UA into three well-defined voltammetric peaks in differential pulse voltammetry (DPV). This modified electrode was quite effective not only for detecting DA, AA, and UA, but also for simultaneous determination of these species in a mixture. The separation of the oxidation peak potentials for ascorbic acid-dopamine and dopamine-uric acid were about 0.16 V and 0.17 V, respectively. The final DPV peaks potential of AA, DA and UA were 0.28, 0.44. and 0.61 V, respectively. The calibration curves for DA, AA, and UA were linear for a wide range of concentrations of each species including 5.0-240 mu mol L-1 AA, 5.0-280 mu mol L-1 DA, and 0.1-18.0 mu mol L-1 UA. Detection limits of 1.43 mu mol L-1 AA, 0.29 mu mol L-1 DA and 0.016 mu mol L-1 UA were observed at pH 4. Interference studies showed that the modified electrode exhibits excellent selectivity toward AA, DA, and UA. (C) 2009 Elsevier B.V. All rights reserved.

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