4.7 Article

Understanding the dipyrone oxidation allying electrochemical and computational approaches

Journal

ANALYTICA CHIMICA ACTA
Volume 1051, Issue -, Pages 49-57

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2018.11.035

Keywords

Dipyrone; Boron-doped diamond electrode; Square-wave voltammetry; Quantum-chemical mechanism

Funding

  1. CNPq-INCT [573925/2008-9, 573548/2008-0]
  2. CAPES (Funcap) [2133/2012, 23038.007973/2012-90]
  3. PRONEX/FUNCAP [PR2-0101-00030.01.00/15]
  4. CNPq [400223/2014-7, 303596/2014-7, 302801/2014-6]
  5. CNPq-PVE 2014
  6. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior - Brasil (CAPES) [001]
  7. CAPES
  8. CAPES-PNPD

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Electroanalytical methodology by boron-doped diamond electrode (BDDE) associated to the square-wave voltammetry (SWV) for the determination of hydrolyzed dipyrone (DIP) in commercial formulations, raw natural waters and in human urine was developed. Through cyclic voltammetry (CV), it was shown that the oxidation of the DIP on the BDDE was irreversible with diffusional control. Computational studies suggested that the oxidation mechanism of DIP occurred with participation of two electrons and one proton. The analytical curves were obtained for concentrations of DIP ranging from 1.0 x 10(-6) to 6.5 x 10(-5) mol L-1 (r = 0.9994). The values of detection limit (LOD) and quantification limit (LOQ) of DIP were calculated from SWV and found to be 2.6 x 10(-7) mol L-1 and 8.8 x 10(-7) mol L-1. The methodology was effectively applied to real samples with the values of calculated recoveries varying between 91.0% and 117.3% and validated by iodometric titration experiments whose values were between 93.3% and 106.9%. The proposed methodology with BDDE represents an alternative tool and it has advantageous, such as very easy handling, low cost, no need for modification, low detection limit. Furthermore, it can be used for the routine analysis of DIP in different real samples. (C) 2018 Elsevier B.V. All rights reserved.

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