Optimisation of mercury film deposition on glassy carbon electrodes: evaluation of the combined effects of pH, thiocyanate ion and deposition potential [An article from: Analytica Chimica Acta] Buy on Amazon

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Optimisation of mercury film deposition on glassy carbon electrodes: evaluation of the combined effects of pH, thiocyanate ion and deposition potential [An article from: Analytica Chimica Acta]

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PublisherElsevier
ISBN / ASINB000RR02XQ
ISBN-13978B000RR02X0
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States  🇺🇸

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This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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The combined effects of pH, thiocyanate ion and deposition potential in the characteristics of thin mercury film electrodes plated on glassy carbon surfaces are evaluated. Charges of deposited mercury are used as an experimental parameter for the estimation of the effectiveness of the mercury deposition procedure. The sensitivity of the anodic stripping voltammetry (ASV) method for the determination of lead at in situ and at ex situ formed thin mercury films are also examined. It was concluded that, in acidic solutions (pH 2.5-5.7) and fairly negative deposition potentials, e.g. -1.3 to -1.5V, thiocyanate ion promotes the formation of the mercury film, in respect both to the amount of deposited mercury and to the mercury deposition rate. Also, the mercury coatings produced in thiocyanate solutions are more homogeneous, as depicted by microscopic examinations. In the presence of thiocyanate there is no obvious advantage of using high concentrations of mercury and/or high deposition times for the in situ and ex situ preparation of the mercury film electrodes. The optimised thin mercury film electrode ex situ prepared in a 5.0mM thiocyanate solution of pH 3.4 was successfully applied to the ASV determination of lead and copper in acidified seawater (pH 2). The limit of detection (3@s) was 6x10^-^1^1M for lead and 2x10^-^1^0M for copper for a deposition time of 5min. Relative standard deviations (R.S.D.s) of
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