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Electrocatalytic oxidation of sulfite by acetylferrocene at glassy carbon electrode
Author(s) -
Gao ZuoNing,
Ma JinFu,
Liu WanYi
Publication year - 2005
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.975
Subject(s) - sulfite , chemistry , chronoamperometry , cyclic voltammetry , glassy carbon , electrochemistry , inorganic chemistry , electrocatalyst , catalysis , substrate (aquarium) , catalytic oxidation , electrode , organic chemistry , oceanography , geology
The electrochemical oxidation of sulfite catalyzed by acetylferrocene (AFc) at a glassy carbon electrode (GCE) in 0.2 M NaClO 4 aqueous solution has been studied by cyclic voltammetry. Although sulfite itself showed a sluggish electrochemical response at the GCE, the response could be enhanced greatly by using AFc as a mediator, which enables a sensitive determination of the substrate (sulfite). The reaction rate constant for catalytic oxidation was evaluated as (7.02 ± 0.05) × 10 4 M −1 s −1 by chronoamperometry. Experimental conditions that maximize the current efficiency of the electrocatalytic oxidation, such as the pH and both the catalyst (AFc) and substrate (sulfite) concentrations, were also investigated. The electrochemical kinetics of electrocatalytic oxidation of sulfite by AFc has been studied by cyclic voltammetry. In the presence of 5 × 10 −4 M AFc, the oxidation current is proportional to the sulfite concentration and the calibration plot was linear over the concentration range 2 × 10 −4 –2.4 × 10 −3 M . This result can be applied in the determination of real samples. Copyright © 2005 John Wiley & Sons, Ltd.