Microwave activation of the electro-oxidation of glucose in alkaline media
Ghanem, M. A., Compton, R. G., Coles, B. A., Canals, A., Vuorema, A., John, P. and Marken, F., 2005. Microwave activation of the electro-oxidation of glucose in alkaline media. Physical Chemistry Chemical Physics, 7 (20), pp. 3552-3559.
Related documents:This repository does not currently have the full-text of this item.
You may be able to access a copy if URLs are provided below.
The oxidation of glucose is a complex process usually requiring catalytically active electrode surfaces or enzyme modified electrodes. In this study the effect of high intensity microwave radiation on the oxidation of glucose in alkaline solution at Au, Cu, and Ni electrodes is reported. Calibration experiments with the Fe(CN)(6)(3-/4-) redox system in aqueous 0.1 M NaOH indicate that strong thermal effects occur at both 50 and 500 mu m diameter electrodes with temperatures reaching 380 K. Extreme mass transport effects with mass transport coefficients of k(mt) > 0.01 m s(-1) (or k(mt) > 1.0 cm s(-1)) are observed at 50 mu m diameter electrodes in the presence of microwaves. The electrocatalytic oxidation of glucose at 500 mu m diameter Au, Cu, or Ni electrodes immersed in 0.1 M NaOH and in the presence of microwave radiation is shown to be dominated by kinetic control. The magnitude of glucose oxidation currents at Cu electrodes is shown to depend on the thickness of a pre-formed oxide layer. At 50 mu m diameter Au, Cu, or Ni electrodes microwave enhanced current densities are generally higher, but only at Au electrodes is a significantly increased rate for the electrocatalytic oxidation of glucose to gluconolactone observed. This rate enhancement appears to be independent of temperature but microwave intensity dependent, and therefore non-thermal in nature. Voltammetric currents observed at Ni electrodes in the presence of microwaves show the best correlation with glucose concentration and are therefore analytically most useful.
|Creators||Ghanem, M. A., Compton, R. G., Coles, B. A., Canals, A., Vuorema, A., John, P. and Marken, F.|
|Departments||Faculty of Science > Chemistry|
|Additional Information||ID number: ISI:000232307900006|
Actions (login required)