4.7 Article

Mesoporous chitosan/silica hybrid material applied for development of electrochemical sensor for paracetamol in presence of dopamine

Journal

MICROPOROUS AND MESOPOROUS MATERIALS
Volume 217, Issue -, Pages 109-118

Publisher

ELSEVIER
DOI: 10.1016/j.micromeso.2015.06.010

Keywords

Mesoporous material; Carbon-paste electrode; Acetaminophen

Funding

  1. CNPq [process 477599/2013-3]
  2. CAPES
  3. FAPERGS

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A mesoporous and thermally stable chitosan/silica bioinorganic hybrid material prepared with 0.5, 1.0, 2.0 and 4.0% w/w chitosan/silica was obtained by sol gel method. The use of HF as catalyst resulted in samples with specific surface area between 400 and 472 m(2) g(-1) and mesopore diameters between 5 and 9 nm. These pore size distributions allowed the immobilization of the electroactive species, copper (II) tetrasulfonic phthalocyanine, on the surface of the hybrid material samples. The material was applied in the preparation of carbon paste electrodes that showed a satisfactory electrocatalytic activity for the redox reactions of paracetamol (p-acetylaminophenol). The electrode prepared with 1% w/w chitosan/silica showed a higher response current and cyclic voltammetry (CV) studies indicated that the paracetamol oxidation-reduction process on the electrode surface is controlled by diffusion. CV and differential pulse voltammetry (DPV) studies using this electrode, at different concentrations of paracetamol, presented a linear response in a wide range (39.8-458 mu mol L-1 for CV and 19.9-385 mu mol L-1 for DPV). It showed a low detection limit and high sensitivity. This electrode was also tested for paracetamol oxidation in the presence of dopamine (3,4-dihydroxyphenethylamine) presenting excellent selectivity, sensitivity (146 mu A L mmol(-1)), reproducibility and low detection limit (0.513 mu mol L-1). These results indicated the new material presents textural characteristics to make electrodes that can be applied as sensor for paracetamol determination, alone or in the simultaneous determination of both, paracetamol and dopamine. (C) 2015 Elsevier Inc. All rights reserved.

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