A chemically modified electrode composed of copper microparticles dispersed into a polyaniline (PANI) film was investigated as an amperometric sensor of scarcely electroactive compounds possessing -OH and -NH2 groups. Glassy carbon was used as an electrode material and modified firstly by a PANI film, then allowed to stand in contact with a solution of copper ions, and finally, the electroreduction was done at -0.3 V. The electrochemical behaviour of the resulting modified electrode in alkaline medium was examined by cyclic voltammetry and flow-injection amperometry. Using some representative compounds, the effect of copper loading and pH on the electrode response was investigated. Constant-potential amperometric detection was applied in conjunction with anion-exchange chromatographic (AEC) separations of amino acids and carbohydrates. At an applied potential of 0.55 V vs. Ag/AgCl, the detection limits (S/N=3) for all analytes investigated ranged 5-15 pmol, and the linear dynamic range was three-four orders of magnitude above the detection limits. The resulting modified electrode was found to retain 95% of its initial response in flowing streams for 3 h of operating time.

Copper dispersed into polyaniline films as an amperometric sensor in alkaline solutions of amino acids and polyhydric compounds / I.G. Casella, T.R.I. Cataldi, A. Guerrieri, E. Desimoni. - In: ANALYTICA CHIMICA ACTA. - ISSN 0003-2670. - 335:3(1996), pp. 217-225. [10.1016/S0003-2670(96)00351-0]

Copper dispersed into polyaniline films as an amperometric sensor in alkaline solutions of amino acids and polyhydric compounds

E. Desimoni
Ultimo
1996

Abstract

A chemically modified electrode composed of copper microparticles dispersed into a polyaniline (PANI) film was investigated as an amperometric sensor of scarcely electroactive compounds possessing -OH and -NH2 groups. Glassy carbon was used as an electrode material and modified firstly by a PANI film, then allowed to stand in contact with a solution of copper ions, and finally, the electroreduction was done at -0.3 V. The electrochemical behaviour of the resulting modified electrode in alkaline medium was examined by cyclic voltammetry and flow-injection amperometry. Using some representative compounds, the effect of copper loading and pH on the electrode response was investigated. Constant-potential amperometric detection was applied in conjunction with anion-exchange chromatographic (AEC) separations of amino acids and carbohydrates. At an applied potential of 0.55 V vs. Ag/AgCl, the detection limits (S/N=3) for all analytes investigated ranged 5-15 pmol, and the linear dynamic range was three-four orders of magnitude above the detection limits. The resulting modified electrode was found to retain 95% of its initial response in flowing streams for 3 h of operating time.
Liquid chromatography ; Copper electrocatalyst ; Polyaniline ; Amino acids ; Carbohydrates
Settore CHIM/01 - Chimica Analitica
1996
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/176108
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