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Ionics

, Volume 25, Issue 7, pp 3259–3268 | Cite as

The role silica pore structure plays in the performance of modified carbon paste electrodes

  • Luana V. de Souza
  • Danielle S. da Rosa
  • Oleg S. Tkachenko
  • Adriano de Araujo Gomes
  • Tania M. H. Costa
  • Leliz T. Arenas
  • Edilson V. BenvenuttiEmail author
Original Paper
  • 84 Downloads

Abstract

Four silica materials was prepared by using different synthesis procedures, with the goal of obtaining matrices with different designed textures, microporous, mesoporous, and ordered pore structured materials, as MCM-41 and SBA-15. These silica materials were used to prepare bare carbon paste electrode, without addition of other components, as nanostructured or electroactive species. In this way, it was possible to study the influence of the textural characteristics, such as surface area, pore volume, pore size, and pore shape on the electrode performance, in a detailed and individual form. The electrodes were studied by using [Fe(CN)6]3−/4− and sulfamethoxazole as probes, in diffusional processes, employing cyclic voltammetry and differential pulse voltammetry. It was observed that surface area and pore volume contribute expressively to the electroactive area. The worst results were attained for microporous materials (0.34 cm2), while the higher electroactive area values were obtained for materials with ordered pore structure, 2.01 cm2 for MCM-41 and 2.58 cm2 for SBA-15, by using [Fe(CN)6]3−/4− as probe. Regarding sulfamethoxazole as probe, the MCM-41 modified carbon paste electrode presented the best performance. The obtained sensitivity was 24.34 nA L μmol−1 and the detection limit found was 3.10 μmol L−1. These results are satisfactory considering the electrodes are constituted just by bare silica, easy to prepare, without addition of other components.

Keywords

Texture Silica materials Porosity Electrochemical Carbon paste electrode 

Notes

Acknowledgments

The authors thank CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico), FAPERGS (Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul), and CAPES (Coordenação de Aperfeiçoamento Pessoal de Nível Superior) for financial support and grants. The authors also thank CNANO (Centro de Nanociência e Nanotecnologia) and CMM (Centro de Microscopia e Microanálise) of UFRGS (Universidade Federal do Rio Grande do Sul).

Supplementary material

11581_2019_2882_MOESM1_ESM.doc (195 kb)
ESM 1 (DOC 195 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  • Luana V. de Souza
    • 1
  • Danielle S. da Rosa
    • 1
  • Oleg S. Tkachenko
    • 1
    • 2
  • Adriano de Araujo Gomes
    • 1
  • Tania M. H. Costa
    • 1
  • Leliz T. Arenas
    • 1
  • Edilson V. Benvenutti
    • 1
    Email author
  1. 1.Institute of ChemistryUFRGSPorto AlegreBrazil
  2. 2.Materials Chemistry DepartmentV. N. Karazin Kharkiv National UniversityKharkivUkraine

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