Rochelle salt

chemical compound
Also known as: sodium potassium tartrate tetrahydrate
Also called:
Sodium Potassium Tartrate Tetrahydrate

Rochelle salt, a crystalline solid having a large piezoelectric effect (electric charge induced on its surfaces by mechanical deformation due to pressure, twisting, or bending), making it useful in sensitive acoustical and vibrational devices. Like other piezoelectric materials, Rochelle salt crystals (KNaC4H4O6·4H2O) become strained when subjected to electric fields. They decompose at moderately high temperatures (55° C [131° F]) and require protection against moisture. Piezoelectric deformation is directly proportional to the applied electric field and reverses as the polarity of the applied field is reversed. These basic properties are put to use in electromechanical transducers such as ultrasonic generators, microphones, and phonograph pickups and in electromechanical resonators. See also tartaric acid.

Related Topics:
dielectric

ferroelectricity, property of certain nonconducting crystals, or dielectrics, that exhibit spontaneous electric polarization (separation of the centre of positive and negative electric charge, making one side of the crystal positive and the opposite side negative) that can be reversed in direction by the application of an appropriate electric field. Ferroelectricity is named by analogy with ferromagnetism, which occurs in such materials as iron. Iron atoms, being tiny magnets, spontaneously align themselves in clusters called ferromagnetic domains, which in turn can be oriented predominantly in a given direction by the application of an external magnetic field.

Ferroelectric materials—for example, barium titanate (BaTiO3) and Rochelle salt—are composed of crystals in which the structural units are tiny electric dipoles; that is, in each unit the centres of positive charge and of negative charge are slightly separated. In some crystals these electric dipoles spontaneously line up in clusters called domains, and in ferroelectric crystals the domains can be oriented predominantly in one direction by a strong external electric field. Reversing the external field reverses the predominant orientation of the ferroelectric domains, though the switching to a new direction lags somewhat behind the change in the external electric field. This lag of electric polarization behind the applied electric field is ferroelectric hysteresis, named by analogy with ferromagnetic hysteresis.

Ferroelectricity ceases in a given material above a characteristic temperature, called its Curie temperature, because the heat agitates the dipoles sufficiently to overcome the forces that spontaneously align them.

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