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Studies of the Electrochemical Degradation of Acetaminophen Using a Real‐Time Biomimetic Sensor
Author(s) -
Quintino de Oliveira Mariana Calora,
Tanaka Auro Atsushi,
de Vasconce los Lanza Marcos Roberto,
Del PilarTaboada Sotomayor Maria
Publication year - 2011
Publication title -
electroanalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 128
eISSN - 1521-4109
pISSN - 1040-0397
DOI - 10.1002/elan.201100255
Subject(s) - degradation (telecommunications) , amperometry , electrolyte , supporting electrolyte , electrochemistry , anode , reaction rate constant , volumetric flow rate , chemistry , electrochemical gas sensor , electrode , analytical chemistry (journal) , materials science , chromatography , kinetics , computer science , telecommunications , physics , quantum mechanics
Real‐time monitoring of the electrochemical degradation of acetaminophen was performed using a biomimetic sensor coupled to a flow injection analysis (FIA) system. Degradation of the drug was carried out at constant current density (24 to 180 mA cm −2 ) in an electrolyte consisting of 0.1 mol L −1 K 2 SO 4 /5.0×10 −4 mol L −1 FeSO 4 ⋅7H 2 O. Two commercial DSA anodes (DSA‐Cl 2 and DSA‐O 2 ) were compared. The degradation process was monitored on‐line using an amperometric sensor based on the biomimetic catalyst iron(III) tetrapyridinoporphyrazine (FeTPyPz), coupled to the degradation cell. The optimized FIA detection system employed the electrolyte solution as carrier, a flow rate of 1.25 mL min −1 and an injected sample volume of 75 µL. The real‐time data obtained showed, as expected, that acetaminophen degradation followed pseudo‐first order kinetics, with the DSA‐Cl 2 anode showing a higher efficiency according to the calculated apparent rate constant values. The advantage of the proposed on‐line system is that a larger number of points can be monitored in a shorter time compared to other off‐line methods, which improves the accuracy of estimates of electrochemical degradation constants.
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