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In the application of passive cathodic protection, a galvanic anode, a piece of a more electrochemically "active" metal (more negative electrode potential), is attached to the vulnerable metal surface where it is exposed to an electrolyte. Galvanic anodes are selected because they have a more "active" voltage than the metal of the target ...
An anodic protection system includes an external power supply connected to auxiliary cathodes and controlled by a feedback signal from one or more reference electrodes. [3] Careful design and control is required when using anodic protection for several reasons, including excessive current when passivation is lost or unstable, leading to ...
The cathodic current is balanced by the anodic current. This ongoing current in both directions is called the exchange current density. When the potential is set more negative than the formal potential, the cathodic current is greater than the anodic current. Written as a reduction, cathodic current is positive.
The difference can be measured as a difference in voltage potential: the less noble metal is the one with a lower (that is, more negative) electrode potential than the nobler one, and will function as the anode (electron or anion attractor) within the electrolyte device functioning as described above (a galvanic cell).
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.
Corrosion prevention measures, including Cathodic protection, designing to prevent corrosion and coating of structures fall within the regime of corrosion engineering. However, corrosion science and engineering go hand-in-hand and they cannot be separated: it is a permanent marriage to produce new and better methods of protection from time to time.
The upper graph shows the current density as function of the overpotential η . The anodic and cathodic current densities are shown as j a and j c, respectively for α=α a =α c =0.5 and j 0 =1mAcm −2 (close to values for platinum and palladium). The lower graph shows the logarithmic plot for different values of α (Tafel plot).
Depending on whether the reaction on the electrode is a reduction or an oxidation, the working electrode is called cathodic or anodic, respectively. Common working electrodes can consist of materials ranging from noble metals such as gold or platinum , to inert carbon such as glassy carbon , boron -doped diamond [ 4 ] or pyrolytic carbon , and ...