4.7 Article

Thermal and electrochemical studies of Fe(III) organophilic montmorillonite

Journal

JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
Volume 131, Issue 1, Pages 713-723

Publisher

SPRINGER
DOI: 10.1007/s10973-017-6327-z

Keywords

Organic montmorillonite; Electrochemistry; Determination of Fe(III) ions; Pt-modified electrode; TG-DTA; XRD

Funding

  1. CAPES
  2. Espaco Magistral Laboratorio de Aanlises, Servico de Apoio Empresarial Ltda.

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This study aimed at investigating the thermal and electrochemical behavior of montmorillonite clay-8-hydroxyquinoline (8-HQ) film in the absence and presence of aqueous Fe(III) ions. The solid film characterization by means of UV spectroscopy, thermal (TG/DTG and TG-DTA, simultaneous) studies, SEM and optical images, and XRD suggested the formation of the ternary complex type: {Pt/[> Si-O](n)[Fe(III)(OH2)(3)(8-HQ)(k)]}(3-n-k), with thermal stability up to 300 A degrees C. The electrochemical study was carried out on a platinum electrode modified by mechanical deposition of a thin solid film of the binary composite (SWy-1:8-HQ) from an aqueous suspension. The mechanical stability of the film was followed by performing 80 cyclic voltammograms. The electrochemical behavior of the modified electrode was investigated using cyclic voltammetry (CV) at different ferric ions concentration (C (Fe(III))), followed by a study of the effect of the scan rate (v) with a fixed C (Fe(III)) ions. In the CVs, two independent pairs of current peaks, A/D and C/B, were observed. For Fe(III) ions in solution, log i (p) versus log v relationship shows a process controlled first by adsorption (pair of peaks A/D) and then by diffusion control (pair of peaks C/B). The current function i (p)/v (1/2) versus v and i (p) (a) /i (p) (c) versus v allowed a suggestion of two homogeneous coupled chemical reactions associated with CE and EC mechanisms, respectively, both with fast reversible chemical reactions. The first investigation of a modified electrode showed good sensitivity (S = 25.1 mu A/mu mol L-1) to low concentrations of ferric ions and detection limit [LOD = (2.4 +/- 0.01) mu mol L-1] and high sensitivity to traces of O-2, showing that this system has great analytical potentials.

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