Electrocatalytic Sulphite Detection at a Liquid-Liquid-Solid Three-Phase Boundary Electrode Sensors
|Najoua Katif , Tony D. James , Ewan K. Galbraith , Frank Marken|
University of Bath, Department of Chemistry, Claverton Down, Bath BA2-7AY, United Kingdom
Electrochemically driven ion transfer processes from aqueous to organic media are readily observed at electrodes modified with an immobilised water immiscible redox liquid . The transfer of ions occurs at a potential determined by the aqueous concentration and aqueous hydration energy.
In this study anion transfer processes are investigated at a 4-(3-phenylpropyl)pyridine | aqueous electrolyte interface and employing the ferrocenylmethyl-dodecyl-dimethylammonium bromide redox system. Facile and reversible anion transfer is observed and in the case of sulphite anions a two-phase electrocatalytic process leading to sulphate is observed. The new method combines anion selectivity and sensitivity due to catalytic currents.
 The electrochemical ion-transfer reactivity of porphyrinato metal complexes in 4- (3-phenylpropyl)pyridine vertical bar water systems. M.J. Bonné, C. Reynolds, S. Yates, G. Shul, J. Niedziolka, M. Opallo, F. Marken, New J. Chem. 30 (2006) 327.
Presentation: Short communication at SMCBS'2007 International Workshop, by Najoua Katif
See On-line Journal of SMCBS'2007 International Workshop
Submitted: 2007-08-28 18:51 Revised: 2009-06-07 00:44
|© 1998-2021 pielaszek research, all rights reserved||Powered by the Conference Engine|