Turpentine
Wikipedia, the free encyclopedia - Cite This SourceTurpentine (also called spirit of turpentine, oil of turpentine, wood turpentine, gum turpentine) is a fluid obtained by the distillation of resin obtained from trees, mainly pine trees. It is composed of terpenes, mainly the monoterpenes alpha-pinene and beta-pinene. It has a potent odor similar to that of nail polish remover. It is sometimes known colloquially as turps, but this more often refers to turpentine substitute (or mineral turpentine).
The word turpentine is formed (via French and Latin) from the Greek word terebinthine, the name of a species of tree, the terebinth tree, from whose sap the spirit was originally distilled.
Production
One of the earliest sources was the terebinth or turpentine tree (Pistacia terebinthus), a Mediterranean tree related to the pistachio.
Important pines for turpentine production include:
- Maritime Pine Pinus pinaster
- Aleppo Pine Pinus halepensis
- Masson's Pine Pinus massoniana
- Sumatran Pine Pinus merkusii
- Longleaf Pine Pinus palustris
- Loblolly Pine Pinus taeda
- Ponderosa Pine Pinus ponderosa
Industrial uses
The two primary uses of turpentine in industry are as a solvent and as a source of materials for organic synthesis.As a solvent, turpentine is used for thinning oil-based paints, for producing varnishes, and as a raw material for the chemical industry. Its industrial use as a solvent in industrialized nations has largely been replaced by the much cheaper turpentine substitutes distilled from crude oil.
Canada balsam, also called Canada turpentine or balsam of fir, is a turpentine which is made from the resin of the balsam fir.
Venice turpentine is produced from the Western Larch Larix occidentalis.
Turpentine is also used as a source of raw materials in the synthesis of fragrant chemical compounds. Commercially used camphor, linalool, alpha-terpineol, and geraniol are all usually produced from alpha-pinene and beta-pinene, which are two of the chief chemical components of turpentine. These pinenes are separated and purified by distillation. The mixture of diterpenes and triterpenes that is left as residue after turpentine distillation is sold as rosin.
Turpentine is also added to many cleaning and sanitary products due to its antiseptic properties and its "clean scent".
Hazards
Turpentine is an organic solvent, and thus poses many of the same hazards as do other such substances. Its vapor can burn the skin and eyes, damage the lungs and respiratory system, as well as the central nervous system when inhaled, and cause renal failure when ingested, among other things. It is highly flammable.Medicinal and other end uses
Turpentine, and petroleum distillates such as coal oil, or kerosene have has been used medicinally since ancient times, as topical and sometimes internal home remedies. Topically it has been used for abrasions and wounds, as a treatment for lice, and when mixed with animal fat it has been used as a chest rub, or inhaler for nasal and throat ailments. Many modern chest rubs such as the Vicks variety, still contain turpentine in their formulations.Though internal administration of these toxic petroleum products is no longer common today, it was once administered by masking the taste by dosing sugar cubes, molasses, or honey, or when unavailable, straight. It was touted as treatment for intestinal parasites due to its alleged antiseptic and diuretic properties, and a general cure-all.
In early 19th Century America, turpentine was sometimes burned in lamps as a cheap alternative to whale oil. It was most commonly used for outdoor lighting, due to its strong odor.
References
External links
- Chemical Database: Turpentine (EnvironmentalChemistry.com)
- IPCS INCHEM Turpentine classification, hazard, and property table
- Gum naval stores: Turpentine and rosin from pine resin
- Turpentine produced in forced labor camps "Turpentine Camps" in the 30s and 40s aka "Debt Slavery"
- Florida State Archive photographs of turpentine camps and laborers
- Timber and Turpentine Industries
See also
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Last updated on Thursday March 13, 2008 at 19:45:03 PDT (GMT -0700)
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