Voltammetry selectivity

Selectivity Selectivity in voltammetry is determined by the difference between half-wave potentials or peak potentials, with minimum differences of+0.2-0.3 V required for a linear potential scan, and +0.04-0.05 V for differential pulse voltammetry. Selectivity can be improved by adjusting solution conditions. As we have seen, the presence of a complexing ligand can substantially shift the potential at which an analyte is oxidized or reduced. Other solution parameters, such as pH, also can be used to improve selectivity. 

Typical measurement is performed using RDE or RRDE voltammetry. In the first case one can control diffusion limitation, enabling more reliable extraction of kinetic currents. In the case of RRDE voltammetry selectivity is also assessed. Alternatively, one can estimate selectivity of O2 reduction to H2O (OH ) using K-L analysis (see Section 2.2) In order to obtain proper ORR j-E curves several steps are necessary (clearmess of electrochemical cell and the electrolyte is assumed, which in some case requires the use of specifically prepared cell) ... 

When either pulse polarography or anodic stripping voltammetry can be used, the selection is often based on the analyte s expected concentration and the desired... 

Faraday s law (p. 496) galvanostat (p. 464) glass electrode (p. 477) hanging mercury drop electrode (p. 509) hydrodynamic voltammetry (p. 513) indicator electrode (p. 462) ionophore (p. 482) ion-selective electrode (p. 475) liquid-based ion-selective electrode (p. 482) liquid junction potential (p. 470) mass transport (p. 511) mediator (p. 500) membrane potential (p. 475) migration (p. 512) nonfaradaic current (p. 512)... 

The methods of investigation of metal species in natural waters must possess by well dividing ability and high sensitivity and selectivity to determination of several metal forms. The catalytic including chemiluminescent (CL) techniques and anodic stripping voltammetry (ASV) are the most useful to determination of trace metals and their forms. The methods considered ai e characterized by a low detection limits. Moreover, they allow detection of the most toxic form of metals, that is, metal free ions and labile complexes. 

Of fundamental importance in understanding the electrochemistry of ion-selective membranes and also of biomembranes is the research in the field of voltammetry at ITIES mainly pioneered by Koryta and coworkers 99 101 . Koryta also demonstrated convincingly that a treatment like corroding metal electrodes is possible 102). For the latter, the description in the form of an Evans-diagram is most appropriate Fig. 4 shows schematically some mixed potentials, which are likely to arise at cation-selective membranes if interfering ions disturb an ideal Nernstian behavior82. Here, the vertical axis describes the galvani potential differences (absolute po-... 

Anion selective electrodes, 156, 158 Anodic shipping voltammetry, 76 Antibody, 183 Antimony, 85... 

Pali), P and Stamford, JA (1994) Real-time monitoring of endogenous noradrenaline release in rat brain slices using fast cyclic voltammetry. 3. Selective detection of noradrenaline efflux in the locus coeruleus. Brain Res. 634 275-282. 

Many methods of determining individual colorants and blended compositions have been selected, critically reviewed, and published. Combined methods such as paper chromatography, TLC, HPLC, spectrophotometry, voltammetry, and more recently, CZE have been developed. Table 6.6.1 presents some of these methods. 

Under optimum conditions LPS voltammetry is an order of magnitude more sensitive than polarography (i.e., the detection limit is about 10 M). As in classical polarography, somewhat higher sensitivity and selectivity can be attained when using a differential version (i.e., when recording, as a function of potential, not the current but its derivative with respect to potential). 

Monitoring enzyme catalyzed reactions by voltammetry and amperometry is an extremely active area of bioelectrochemical interest. Whereas liquid chromatography provides selectivity, the use of enzymes to generate electroactive products provides specificity to electroanalytical techniques. In essence, enzymes are used as a derivatiz-ing agent to convert a nonelectroactive species into an electroactive species. Alternatively, electrochemistry has been used as a sensitive method to follow enzymatic reactions and to determine enzyme activity. Enzyme-linked immunoassays with electrochemical detection have been reported to provide even greater specificity and sensitivity than other enzyme linked electrochemical techniques. 

Electrochemistry voltammetry, anodic stripping (ASV), cathodic stripping (CSV), polarography, differential pulse polarography (DPP), ion selective electrode (ISE)... 

A hanging electrolyte drop has also been applied to determine ionic species in solution using differential-pulse-stripping voltammetry procedures [69]. Particular emphasis was given to assessing the selectivity and sensitivity of the method. The technique of current-scan polarography has also been applied in the study of electron-transfer [70] and coupled electron-transfer-ion-transfer [71,72] reactions at the ITIES in this configuration. 

Electrochemical methods such as potentiometry allow analyses up to p,gL quantities, or, with methods such as voltammetry, they extend into the micro-trace range. Table 8.74 compares potentiometry to other electroanalytical techniques. Potentiometry and ion-selective electrodes are described in various books [476-480],... 

Table 8.76 shows the main characteristics of voltammetry. Trace-element analysis by electrochemical methods is attractive due to the low limits of detection that can be achieved at relatively low cost. The advantage of using standard addition as a means of calibration and quantification is that matrix effects in the sample are taken into consideration. Analytical responses in voltammetry sometimes lack the predictability of techniques such as optical spectrometry, mostly because interactions at electrode/solution interfaces can be extremely complex. The role of the electrolyte and additional solutions in voltammetry are crucial. Many determinations are pH dependent, and the electrolyte can increase both the conductivity and selectivity of the solution. Voltammetry offers some advantages over atomic absorption. It allows the determination of an element under different oxidation states (e.g. Fe2+/Fe3+). 

In the stripping voltammetry, in general it is anodic SV which, owing to its extreme sensitivity and selectivity together with its cheapness, has gained so much analytical importance that for instance the Kemforschungsanlage Jiilich (F.R.G.) recently (1983) replaced their atomic absorption spectrometer with an SV system for the simultaneous determination of Cu, Cd, Pb, etc. 

Tacussel and their application by Gonon et al.148 to differential pulse voltammetry (DPV) and differential normal pulse voltammetry (DNPV) in vivo, also called the biopulse technique the microelectrodes are implanted in the living animal brain and variations in the concentrations of some molecules can be followed via the Tacussel PRG 5 and BIPAD instruments (see also the selection of commercial models in Table 3.4). 

Alemu et al. [35] developed a very sensitive and selective procedure for the determination of niclosamide based on square-wave voltammetry at a glassy carbon electrode. Cyclic voltammetry was used to investigate the electrochemical reduction of niclosamide at a glassy carbon electrode. Niclosamide was first irreversibly reduced from N02 to NHOH at —0.659 V in aqueous buffer solution of pH 8.5. Following optimization of the voltammetric parameters, pH and reproducibility, a linear calibration curve over the range 5 x 10 x to 1 x 10-6 mol/dm3 was achieved, with a detection limit of 2.05 x 10-8 mol/dm3 niclosamide. The results of the analysis suggested that the proposed method has promise for the routine determination of niclosamide in the products examined [35]. 

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