Lake pigment explained

A lake pigment is a pigment made by precipitating a dye with an inert binder, or mordant, usually a metallic salt. Unlike vermilion, ultramarine, and other pigments made from ground minerals, lake pigments are organic.[1] Manufacturers and suppliers to artists and industry frequently omit the lake designation in the name. Many lake pigments are fugitive because the dyes involved are not lightfast. Red lakes were particularly important in Renaissance and Baroque paintings; they were often used as translucent glazes to portray the colors of rich fabrics and draperies.[2]

Etymology

The term lake is derived from the term lac, the secretions of the Indian wood insect Kerria lacca (formerly Laccifer lacca or Coccus lacca).[3] [4] It has the same root as the word lacquer, and comes originally from the Hindi word, through the Arabic word and the Persian word .[5]

Chemistry

Many lake pigments are azo dyes. They characteristically have sulfonate and sometimes carboxylate substituents, which confer negative charge to the chromophore (colored species).

The metallic salts or binders used are typically colourless or almost so. The organic component of the dye determines the color of the resulting precipitate. In ancient times chalk, white clay, and crushed bones were used as sources of the calcium salts. Today metallic salts are typically chromium or cobalt, and the resulting lake pigment is diluted with an inert material such as alumina.

History and art

Lake pigments have a long history in decoration and the arts. Some have been produced for thousands of years and traded over long distances.

The red lakes were particularly important in the history of art; because they were translucent, they were often used in layers of glazes over a more opaque red (sometimes the mineral-based pigment vermilion, or sometimes a red lake mixed with lead white or vermilion) to create a deep, rich red color. They are common in paintings by Venetian artists of the 16th century, including Titian, to depict fine draperies and fabrics.

Indigo and rose madder are now produced more cheaply from synthetic sources, although some use of natural products persists, especially among artisans. The food and cosmetics industries have shown renewed interest in cochineal as a source of natural red dye.[8]

Notes and References

  1. K. Hunger. W. Herbst "Pigments, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2012.
  2. David Bomford and Ashok Roy, A Closer Look - Colour, National Gallery Company, p. 41.
  3. News: [//stainsfile.info/StainsFile/theory/mordant.htm Stain Theory – How mordants work ]. Llewellyn . Bryan D. . May 2005 . dead. https://web.archive.org/web/20070814015208/http://stainsfile.info/StainsFile/theory/mordant.htm . August 14, 2007 .
  4. "lake, n.6". OED Online. December 2011. Oxford University Press. 25 January 2012.
  5. Webster's New World Dictionary of American English, Third College Edition, 1988.
  6. Book: A Perfect Red: Empire, Espionage, and the Quest for the Color of Desire . Amy Butler Greenfield . 2005 . . 0-06-052275-5 . registration .
  7. Allevi, P. . 1991 . The 1st Total Synthesis of Carminic Acid . Journal of the Chemical Society, Chemical Communications . 18 . 18 . 1319–1320. etal . 10.1039/c39910001319.
  8. Miller . Brittney J. . Cochineal, a red dye from bugs, moves to the lab . Knowable Magazine . 25 March 2022 . 10.1146/knowable-032522-1 . free . 28 March 2022.