Electrochemical characterization of the paste carbon modified electrode with KSr2Ni0.75Nb4.25O15-delta solid in catalytic oxidation of the dipyrone


Autoria(s): Dadamos, Tony R. L.; Freitas, Bruno H.; Genova, Diego H. M.; Espirito-Santo, Rafael D.; Perez Gonzalez, Eduardo R.; Lanfredi, Silvania; Teixeira, Marcos F. S.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

05/07/2012

Resumo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Processo FAPESP: 08/00910-9

Processo FAPESP: 06/51987-6

The electrochemical behavior of a carbon paste electrode modified (CPEM) with nickel-doped potassium strontium niobate (KSr2Ni0.75Nb4.25O15-delta) of tetragonal tungsten bronze (TTB)-type structure was investigated as a new sensor for dipyrone. The optimum conditions were found in an electrode composition (in mass) of 20% KSr2Ni0.75Nb4.25O15-delta, 65% graphite and 15% mineral oil in 0.5 mol L-1 KCl solution at pH 6.0. The electrode exhibits reversible electrochemical behavior in a wide potential range (0.1-0.7 V vs. SCE), high conductivity, and stability/durability electrode in 0.50 mol L-1 KCl solution. The estimated surface concentration was found to equal 1.08 x 10(-9) mol cm(-2). The oxidation of dipyrone was performed at carbon paste electrode unmodified at +0.54 V vs. SCE and carbon paste electrode modified with KSr2Ni0.75Nb4.25O15-delta at +0.45 V vs. SCE. This result shows that the nickel-doped potassium strontium niobate on electrode surface promotes the oxidation of dipyrone. The reaction can be brought about electrochemically, where the niobium(IV) is first oxidation to a niobium(IV) oxide at the electrode surface. The niobium(IV) then undergoes a catalytic reduction by the dipyrone in solution back to the niobium(III), which can then be electrochemically re-oxidized to produce an enhancement of the anodic current. The identification of the oxidation product of dipyrone was made by mass spectrometry for elucidation of response mechanism of the sensor. Anodic peak current (I-pa) vs. dipyrone concentration for amperometric method at the modified electrode was linear in the 3.5 x 10(-5) and 3.1 x 10(-4) mol L-1 concentration range and the detection limit was 5.1 x 10(-6) mol L-1 dipyrone. At higher concentrations (>3.1 x 10(-4) mol L-1), deviation from linearity occurs. Under this condition, an electrocatalytic reaction takes place and proceeds through a mechanism similar to the Michaelis-Menten model. (C) 2012 Elsevier B.V. All rights reserved.

Formato

267-273

Identificador

http://dx.doi.org/10.1016/j.snb.2012.04.080

Sensors and Actuators B-chemical. Lausanne: Elsevier B.V. Sa, v. 169, p. 267-273, 2012.

0925-4005

http://hdl.handle.net/11449/6895

10.1016/j.snb.2012.04.080

WOS:000305719600038

Idioma(s)

eng

Publicador

Elsevier B.V. Sa

Relação

Sensors and Actuators B: Chemical

Direitos

closedAccess

Palavras-Chave #Tetragonal tungsten bronze (TTB)-type structure #Dipyrone oxidation #Amperometric measurements #X-ray diffraction #MS spectrum
Tipo

info:eu-repo/semantics/article