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Concentration cell

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Galvanic cell
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Inbattery technology, aconcentration cell is a limited form of agalvanic cell that has two equivalenthalf-cells of the same composition differing only inconcentrations. One can calculate the potential developed by such a cell using theNernst equation.[1] A concentration cell produces a smallvoltage as it attempts to reachchemical equilibrium, which occurs when the concentration of reactant in both half-cells are equal. Because an order of magnitude concentration difference produces less than 60 millivolts at room temperature, concentration cells are not typically used forenergy storage.

A concentration cell generates electricity from the reduction in thethermodynamic free energy of the electrochemical system as the difference in the chemical concentrations in the two half-cells is reduced. The same reaction occurs in the half-cells but in opposite directions, increasing the lower and decreasing the higher concentration. The energy is generated from thermal energy that the cell absorbs as heat, as the electricity flows. This generation of electricity from ambientthermal energy, without atemperature gradient, is possible because the convergence of the chemical concentrations in the two half-cells increases entropy, and this increase more than compensates for the entropy decrease when heat is converted into electrical energy.

Concentration cell methods ofchemical analysis compare a solution of known concentration with an unknown, determining the concentration of the unknown via the Nernst Equation or comparison tables against a group of standards.

The standard reduction and oxidation potentials for a concentration cell is 0V at standard conditions (1M solutions, 298K, 1 atm). This is because a concentration cell is designed to have identical electrodes immersed in solutions with different concentrations of the same ions, and at standard conditions, the electrode potentials of the half-cells are the same. Therefore, there is no net potential difference.

Concentration cellcorrosion occurs when two or more areas of ametal surface are in contact with different concentrations of the same solution. There are two general types of concentration cells.

Concentration cells can be electrode concentration cells or electrolyte concentration cells.

Electrolyte Concentration cell - In this particular electrochemical cell, the electrodes within both half-cells consist of identical substances, while the electrolyte comprises a solution of the same substance, albeit with varying concentrations.

Electrode Concentration cell - In this particular electrochemical cell, two electrodes composed of the same substance but with differing concentrations are immersed in a common solution.

Metal ion concentration cells

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In the presence ofwater, a high concentration of metalions will exist under thefaying surfaces and a low concentration of metal ions will exist adjacent to thecrevice created by the faying surfaces. Anelectrical potential will exist between the two points. The area of the metal in contact with the lower concentration of metal ions will becathodic and will be protected, and the area of metal in contact with the higher metal ion concentration will beanodic and corroded.[citation needed]

Oxygen concentration cells

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Water in contact with the metal surface will normally contain dissolvedoxygen. An oxygen cell can develop at any point where the oxygen in the air is not allowed to diffuse uniformly into the solution, thereby creating a difference in oxygen concentration between two points. Corrosion will occur at the area of low-oxygen concentration, which are anodic.

Active-passive cells

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If a metal is protected against corrosion by a tightly adhering passive film (usually anoxide) andsalt deposits on the surface in the presence of water, the active metal beneath the film will be exposed to corrosive attack in areas where the passive film is broken. An electrical potential will develop between the large area of the passive film (cathode) and the small area of the exposed active metal (anode). Rapid pitting of the active metal will result.

See also

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References

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  1. ^Almost any textbook onphysical chemistry, e.g. by I. N. Levine or P. W. Atkins, and also manygeneral chemistry texts.
Types
Primary cell
(non-rechargeable)
Secondary cell
(rechargeable)
Other cell
Cell parts
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