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E s is the reduction potential of A (if the electrolyte and the electrode are in their standard conditions, then this potential is a standard reduction potential). As E approaches E s, the current on the surface increases, and when E = E s, the concentration of A equals that of the oxidized/reduced A at the surface ([A] = [A −]). [4]
Since Δ r G o = -nFE o, the electrode potential is a representation of the Gibbs energy change for the given reduction. The sum of the Gibbs energy changes for subsequent reductions (e.g. from O 2 to H 2 O 2, then from H 2 O 2 to H 2 O) is the same as the Gibbs energy change for the overall reduction (i.e. from O 2 to H 2 O), in accordance ...
In order to flatten the steep learning curve aqion provides an introduction to fundamental water-related topics in form of a "chemical pocket calculator". Second. The program mediates between two terminological concepts: The calculations are performed in the "scientific realm" of thermodynamics (activities, speciation, log K values, ionic ...
A positive slope between two species indicates a tendency for an oxidation reaction, while a negative slope between two species indicates a tendency for reduction. For example, if the manganese in [HMnO 4 ] − has an oxidation state of +6 and nE ° = 4, and in MnO 2 the oxidation state is +4 and nE ° = 0, then the slope Δ y /Δ x is 4/2 = 2 ...
In aqueous solutions, redox potential is a measure of the tendency of the solution to either gain or lose electrons in a reaction. A solution with a higher (more positive) reduction potential than some other molecule will have a tendency to gain electrons from this molecule (i.e. to be reduced by oxidizing this other molecule) and a solution with a lower (more negative) reduction potential ...
Early voltammetric techniques had many problems, limiting their viability for everyday use in analytical chemistry. In polarography, these problems included the fact that mercury is oxidized at a potential that is more positive than +0.2 Volt, making it harder to analyze the results for the analytes in the positive region of the potential.
For oxygen (O) the oxidation number began as 0 and decreased to 2−. These changes can be viewed as two "half-reactions" that occur concurrently: Oxidation half reaction: Fe 0 → Fe 3+ + 3e −; Reduction half reaction: O 2 + 4e − → 2 O 2−; Iron (Fe) has been oxidized because the oxidation number increased.
The electrodes are immobile and sit in unstirred solutions during cyclic voltammetry. This "still" solution method gives rise to cyclic voltammetry's characteristic diffusion-controlled peaks. This method also allows a portion of the analyte to remain after reduction or oxidation so that it may display further redox activity. Stirring the ...