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Potentiometry passively measures the potential of a solution between two electrodes, affecting the solution very little in the process. One electrode is called the reference electrode and has a constant potential, while the other one is an indicator electrode whose potential changes with the sample's composition. Therefore, the difference in ...
Reference electrodes generally used are hydrogen electrodes, calomel electrodes, and silver chloride electrodes. The indicator electrode forms an electrochemical half-cell with the interested ions in the test solution. The reference electrode forms the other half-cell. The overall electric potential is calculated as
Type III sensors make the electrode concept even more confusing. With respect to the design of a solid state sensor, the auxiliary phase looks as part of the electrode. But it cannot be an electrode because auxiliary phase materials are not generally good electrical conductor. In spite of this confusion, type III design offers more feasibility ...
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An ion-selective electrode (ISE), also known as a specific ion electrode (SIE), is a simple membrane-based potentiometric device which measures the activity of ions in solution. [1] It is a transducer (or sensor ) that converts the change in the concentration of a specific ion dissolved in a solution into an electrical potential .
The Gran plot is based on the Nernst equation which can be written as = + {+} where E is a measured electrode potential, E 0 is a standard electrode potential, s is the slope, ideally equal to RT/nF, and {H +} is the activity of the hydrogen ion.
A redox indicator (also called an oxidation-reduction indicator) is an indicator which undergoes a definite color change at a specific electrode potential. The requirement for fast and reversible color change means that the oxidation-reduction equilibrium for an indicator redox system needs to be established very quickly. Therefore, only a few ...
Cathodic stripping voltammetry is a voltammetric method for quantitative determination of specific ionic species. [6] It is similar to the trace analysis method anodic stripping voltammetry, except that for the plating step, the potential is held at an oxidizing potential, and the oxidized species are stripped from the electrode by sweeping the potential negatively.