Abstract
The voltammetric behaviour of selenium(IV) was studied at platinum and gold electrodes in sulphuric acid, perchloric acid and potassium chloride media as a basis for its voltammetric detection. The best voltammetric behaviour was recorded at gold electrodes with perchloric acid as the supporting electrolyte. The concomitant presence of metals, such as copper or lead, and of model biomolecules, such as bovine serum albumin, in the solution resulted in a deterioration of the electrochemical response for selenium(IV). Quantitative detection of selenium(IV) by square wave anodic stripping voltammetry at both a millimetre-sized gold disc electrode and a microband electrode array revealed linear responses to selenium concentration in the ranges 5-15μM and 0.1-10μM, respectively, with 60s preconcentration. The sensitivities were 6.4μAμM-1cm-2 and 100μAμM-1cm-2 at the disc and the microband array, respectively. The detection limit at the microband electrode array was 25nM, illustrating the potentiality of such microelectrodes for the development of mercury-free analytical methods for the trace detection of selenium(IV).
| Original language | English |
|---|---|
| Pages (from-to) | 127-133 |
| Number of pages | 7 |
| Journal | Analytica Chimica Acta |
| Volume | 699 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 12 Aug 2011 |
Keywords
- Anodic stripping voltammetry
- Gold electrode
- Microelectrode array
- Selenium
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