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dc.contributor.authorBeni, V.
dc.contributor.authorCollins, G.
dc.contributor.authorArrigan, Damien
dc.date.accessioned2017-01-30T14:22:39Z
dc.date.available2017-01-30T14:22:39Z
dc.date.created2011-11-18T01:21:25Z
dc.date.issued2011
dc.identifier.citationBeni, Valerio and Collins, Gillian and Arrigan, Damien. 2011. Investigation into the voltammetric behaviour and detection of selenium(IV) at metal electrodes in diverse electrolyte media. Analytica Chimica Acta. 699 (2): pp. 127-133.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/38538
dc.identifier.doi10.1016/j.aca.2011.05.027
dc.description.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 of 5-15 μM and 0.1-10 μM, respectively, with 60 s preconcentration. The sensitivities were 6.4 μA μM-1 cm-2 and 100 μA μM-1 cm-2 at the disc and the microband array, respectively. The detection limit at the microband electrode array was 25 nM, illustrating the potentiality of such microelectrodes for the development of mercury-free analytical methods for the trace detection of selenium(IV).

dc.publisherElsevier BV
dc.subjectMicroelectrode array
dc.subjectGold electrode
dc.subjectSelenium
dc.subjectAnodic stripping voltammetry
dc.titleInvestigation into the voltammetric behaviour and detection of selenium(IV) at metal electrodes in diverse electrolyte media
dc.typeJournal Article
dcterms.source.volume699
dcterms.source.startPage127
dcterms.source.endPage133
dcterms.source.issn00032670
dcterms.source.titleAnalytica Chimica Acta
curtin.note

NOTICE: This is the author's version of a work that was accepted for publication in Analytica Chimica Acta. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Analytica Chimica Acta, 699, 2, 2011. DOI: 10.1016/j.aca.2011.05.027

curtin.departmentNanochemistry Research Institute (Research Institute)
curtin.accessStatusOpen access


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