2005
Identification of current nature by elimination voltammetry with linear scan
TRNKOVÁ, LibušeZákladní údaje
Originální název
Identification of current nature by elimination voltammetry with linear scan
Název česky
Identifikace při eleminační voltametrii s lineárním skenem
Autoři
TRNKOVÁ, Libuše (203 Česká republika, garant)
Vydání
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 0022-0728
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10405 Electrochemistry
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.223
Kód RIV
RIV/00216224:14310/05:00014626
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000231276000029
Klíčová slova anglicky
elimination voltammetry with linear scan; linear scan voltammetry; current elimination coefficient beta(EVLS); scan rate coefficient x; current nature; rate-determining step; reduction of Cd(II) and Pb(II); hanging mercury drop electrode; azidothymidine; electroanalysis
Štítky
Změněno: 31. 1. 2006 14:27, prof. RNDr. Libuše Trnková, CSc.
V originále
This paper is devoted to the detailed description of mathematical procedures used in the elimination voltammetry with linear scan (EVLS), and their applications to the identification of current nature. It has been shown that the EVLS, based on an elimination function generated from total currents measured at different scan rates, is widely applicable in electrochemistry. The current nature can be identified from the different course of selected elimination functions, i.e., the dependence of the current elimination coefficient beta(EVLS) on the scan rate coefficient x (see Fig. 1). This approach has been tested by studying the reduction processes of azidothymidine (AZT), Pb(II), and Cd(II) on a hanging mercury drop electrode (HMDE). In addition the calculation of elimination function conserving the diffusion current (I-d) and eliminating kinetic and charging currents (I-k, I-c) for an adsorbed electroactive substance has been presented. This elimination providing the peak-counterpeak signal which could be observed also at monitoring of Pb(II) reduction on HMDE after adsorption. The fact that EVLS can be generally applied to different ratios of scan rates has been demonstrated for the case of reversible reduction of Cd(II) in KCl solutions. Advantages and disadvantages of EVLS have been discussed.
Česky
Tato práce popisuje
Návaznosti
MSM0021622412, záměr |
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