Concentration cell

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A concentration cell is a limited form of a galvanic cell that has two equivalent half-cells of the same composition differing only in concentrations. One can calculate the potential developed by such a cell using the Nernst Equation.^[1] A concentration cell produces a small voltage as it attempts to reach chemical 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 for energy storage.

A concentration cell generates electricity from the reduction in the thermodynamic 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 ambient thermal energy, without a temperature 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 of chemical 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.

Concentration cell corrosion occurs when two or more areas of a metal surface are in contact with different concentrations of the same solution. There are three general types of concentration cells.

Contents

  [hide] 

• 1Metal ion concentration cells
• 2Oxygen concentration cells
• 3Active-passive cells
• 4See also
• 5References

Metal ion concentration cells[edit]

In the presence of water, a high concentration of metal ions will exist under faying surfaces and a low concentration of metal ions will exist adjacent to the crevice created by the faying surfaces. An electrical potential will exist between the two points. The area of the metal in contact with the high concentration of metal ions will be cathodic and will be protected, and the area of metal in contact with the low metal ion concentration will be anodic and corroded.^{[citation needed]}

Oxygen concentration cells[edit]

Water in contact with the metal surface will normally contain dissolved oxygen. 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[edit]

If a metal is protected against corrosion by a tightly adhering passive film (usually an oxide) and salt 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[edit]

• Liquid junction potential
• Electrochemical potential
• Membrane potential
• Thermogalvanic cell
• Activity coefficient

References[edit]

1. Jump up^ Almost any textbook on physical chemistry, e.g. by I. N. Levine or P. W. Atkins, and also many general chemistry texts.

•  This article incorporates public domain material from the National Aeronautics and Space Administration document "Concentration Cell Corrosion".

[hide] v t e Galvanic cells
Types	Voltaic pile Battery  Flow battery Trough battery   Concentration cell Fuel cell Thermogalvanic cell
Primary cell (non-rechargable)	Alkaline Aluminium–air Bunsen Chromic acid Clark Daniell Dry Edison-Lalande Grove Leclanché Lithium Mercury Nickel oxyhydroxide Silicon–air Silver oxide Weston Zamboni Zinc–air Zinc–carbon
Secondary cell (rechargeable)	Automotive Lead–acid  gel / VRLA   Lithium–air Lithium–ion  Lithium polymer Lithium iron phosphate Lithium titanate Lithium–sulfur Dual carbon battery   Molten salt Nanopore Nanowire Nickel–cadmium Nickel–hydrogen Nickel–iron Nickel–lithium Nickel–metal hydride Nickel–zinc Polysulfide bromide Potassium-ion Rechargeable alkaline Sodium-ion Sodium–sulfur Vanadium redox Zinc–bromine Zinc–cerium
Cell parts	Anode Binder Catalyst Cathode Electrode Electrolyte Half-cell Ions Salt bridge Semipermeable membrane

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