Aplicação de nanotubos de carbono no desenvolvimento de sensores amperométricos para compostos fenólicos

Detalhes bibliográficos
Ano de defesa: 2016
Autor(a) principal: Cardoso, Rafael Melo
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Uberlândia
BR
Programa de Pós-graduação em Química
Ciências Exatas e da Terra
UFU
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://repositorio.ufu.br/handle/123456789/17455
http://doi.org/10.14393/ufu.di.2016.210
Resumo: This work investigates the development of electrochemical sensors employing glassy-carbon electrodes modified with multi-walled carbon nanotubes (MWCNT). Two different diameters (110-170 nm x 5-9, μm corresponding to LD-MWCNT, and 6-9 nm x 5 μm, corresponding to SD-MWCNT), chemically treated with concentrated acids, subjected to amperometric and voltammetric analyses for the electrochemical oxidation of hydroquinone (HQ), tert-butylhydroquinone (TBHQ), catechol (CT), and pyrogallol (PY). The electrochemical response for all phenolic compounds in glassy-carbon electrode modified with nanostructured materials showed a small decrease in the overpotential of oxidation reactions (<80 mV). Furthermore, the values of ΔEpeak (distance between peak potential of the redox pair) were substantially reduced at LD-MWCNT and even more at SD-MWCNT compared to the unmodified electrode. Voltammetric tests showed a substantial increase (three fold) in oxidation current for the HQ, TBHQ, and PY on the modified electrode with SD-MWCNT. Amperometric measurements coupled to BIA system conducted in two different working potentials for each analyte also revealed the best performance of SD-MWCNT (increase up to four fold in sensitivity) for the detection of studied antioxidants, especially for the detection at lower potentials (0.5 V to HQ, TBHQ and PY and 0.6 V to CT). The analytical results obtained at lower potentials were respectively for HQ, TBHQ, CT and PY: large linear concentration ranges from 1 to 1000 μmol L-1; low limits of detection, 0.014 μmol L-1 / 0.011 μmol L-1/ 0.034 μmol L-1/ 0.013 μmol L-1; low relative standard deviation values, 0.9% / 3.5% / 1.3% / 2.8% , high theoretical analytical frequency, 1368,9 injections h-1 / 820,7 injections h-1 / 1018,7 injections h-1 / 987,9 injections h-1, employing the batch-injection analysis system. Moreover, an amperometric method for the determination of PY was developed and applied for biodiesel samples (produced from soybean, canola and cottonseed oils) spiked with the antioxidant, and recovery values of 95% were obtained.