Search results
1000 BC – 300 AD. The first known use of rubber was by the Olmec, the first major civilisation in Mexico. They used natural latex from the Hevea tree to make rubber used to make balls for a Mesoamerican ballgame.
- Partnership
(European Tyre and Rubber Manufacturers Association) on a...
- EU Legislation
ERCA cooperates with European institutions and a broad range...
- Safety & Sustainability
Rubber products are used in a range of applications where...
- About Erca
History of Rubber; How is rubber made? Where are Rubber...
- Cookies Policy
What are Rubber Chemicals? History of Rubber; How is rubber...
- Partnership
The Rubber Industry. In 1889, John Dunlop of England produced the first commercially successful tire for bicycles and would later create the first automobile tire in 1906. As the auto industry began taking off after 1910s, rubber continued to be a hot commodity.
- Overview
- The rise of synthetic rubber
The origins of the elastomers forming the base of synthetic rubber can be traced to the first half of the 19th century, when attempts were made to elucidate the composition and structure of natural rubber with the eventual goal of reproducing the material. In 1838 the German F.C. Himly obtained a volatile distillate from the substance, and in 1860 the Englishman C. Greville Williams broke down rubber by distillation into three parts—oil, tar, and “spirit”—this last part being the more volatile fraction and the main constituent, which Williams named isoprene. The Frenchman Georges Bouchardat, with the aid of hydrogen chloride gas and prolonged distillation, converted isoprene to a rubberlike substance in 1875, and in 1882 another Briton, W.A. Tilden, produced isoprene by the destructive distillation of turpentine. Tilden also assigned isoprene the structural formula CH2=C(CH3)―CH=CH2.
The efforts outlined above were attempts to replicate natural rubber. It was only when the search for chemical equivalents to natural rubber was abandoned and comparable physical properties were emphasized that synthetic rubber came into being. The choice fell upon butadiene (CH2=CH―CH=CH2), a compound similar to isoprene, as the basis for a synthetic product. Several significant contributions came from Russia. In 1901 Ivan Kondakov discovered that dimethyl butadiene, when heated with potash, produced a rubberlike substance, and in 1910 S.V. Lebedev polymerized butadiene, which he obtained from ethyl alcohol. During World War I, Germany, under the stimulus of the blockade imposed by the Allies, began production of “methyl rubber” by using Kondakov’s process. This was an inferior substitute by present-day standards, and after the war German manufacturers returned to the cheaper and more satisfactory natural product. Research and experiments continued, however, and in 1926 the German G. Ebert succeeded in producing a sodium-polymerized rubber from butadiene. During the following decade this material evolved into various types of “buna” rubber (so called from the initial syllables of the two materials used to make them: butadiene and natrium [sodium]).
In the Soviet Union, production of polybutadiene by using Lebedev’s process was begun in 1932–33, using potatoes and limestone as raw materials. By 1940 the Soviet Union had the largest synthetic rubber industry in the world, producing more than 50,000 tons per year. In Germany, meanwhile, the first synthetic elastomer that could be used to replace natural rubber and make satisfactory tires was developed at I.G. Farben by Walter Bock and Eduard Tschunkur, who synthesized a rubbery copolymer of styrene and butadiene in 1929, using an emulsion process. The Germans referred to this rubber as Buna S; the British called it SBR, or styrene-butadiene rubber. Because styrene and butadiene can be made from petroleum, grain alcohol, or coal, SBR was in great demand during World War II. Immense amounts were made—as much as 100,000 tons per year in Germany and the Soviet Union. About 800,000 tons of SBR were produced per year in the United States, where it received the wartime designation GR-S (government rubber-styrene). During the war German chemical engineers perfected low-temperature, or “cold,” polymerization of SBR, producing a more uniform product.
Other important synthetic elastomers were discovered in the decades before World War II, though none was suitable for making tires. Among these were polysulfides, synthesized in the United States by Joseph Patrick in 1926 and commercialized after 1930 as oil-resistant thiokol rubbers; polychloroprene, discovered by Arnold Collins in 1931 and commercialized by the DuPont Company in 1932 as Duprene (later neoprene), a high-strength oil-resistant rubber; nitrile rubber (NBR), an oil-resistant copolymer of acrylonitrile and butadiene synthesized by Erich Konrad and Tschunkur in 1930 and known as Buna N in Germany; and butyl rubber (IIR), a copolymer of isoprene and isobutylene discovered in 1937 by the Americans R.M. Thomas and W.J. Sparks at Standard Oil Company (New Jersey).
After World War II, increasing sophistication in synthetic chemistry led to many new polymers and elastomers. In 1953–54 two chemists, Karl Ziegler of Germany and Giulio Natta of Italy, developed a family of organometallic catalysts that were able to control precisely the placing and arrangement of units along the polymer chain and thus produce regular (stereospecific) structures. With the use of such catalysts, isoprene was polymerized in such a manner that each unit in the chain was linked to its predecessor in a cis configuration, virtually identical to the structure of natural rubber. In this way virtually 100 percent cis-polyisoprene, “synthetic natural rubber,” was made. In 1961 the same type of catalyst with butadiene as the monomer was used to produce cis-1,4-polybutadiene, a rubber that was found to have excellent abrasion resistance, especially in tires subjected to severe service conditions.
Several other advances characterized the postwar years. For example, block copolymers, in which a long sequence of one chemical unit is followed in the same molecule by a long sequence of another, were made, using many different units and sequence lengths. New oil-resistant and heat-resistant elastomers were introduced, including the styrene-acrylonitrile copolymers, the polysulfides, and chlorinated and chlorosulfonated polyethylene. Control has been achieved, to some degree, over the wide range of molecular length found in most polymers, so narrow or broad distributions can be produced in many cases, with quite different viscous properties. In addition, polymers have been synthesized with branched molecules, either with many small branches along the main chain or with several long “arms” radiating from a central point, giving different flow properties and more facile cross-linking.
The origins of the elastomers forming the base of synthetic rubber can be traced to the first half of the 19th century, when attempts were made to elucidate the composition and structure of natural rubber with the eventual goal of reproducing the material. In 1838 the German F.C. Himly obtained a volatile distillate from the substance, and in 1860 the Englishman C. Greville Williams broke down rubber by distillation into three parts—oil, tar, and “spirit”—this last part being the more volatile fraction and the main constituent, which Williams named isoprene. The Frenchman Georges Bouchardat, with the aid of hydrogen chloride gas and prolonged distillation, converted isoprene to a rubberlike substance in 1875, and in 1882 another Briton, W.A. Tilden, produced isoprene by the destructive distillation of turpentine. Tilden also assigned isoprene the structural formula CH2=C(CH3)―CH=CH2.
The efforts outlined above were attempts to replicate natural rubber. It was only when the search for chemical equivalents to natural rubber was abandoned and comparable physical properties were emphasized that synthetic rubber came into being. The choice fell upon butadiene (CH2=CH―CH=CH2), a compound similar to isoprene, as the basis for a synthetic product. Several significant contributions came from Russia. In 1901 Ivan Kondakov discovered that dimethyl butadiene, when heated with potash, produced a rubberlike substance, and in 1910 S.V. Lebedev polymerized butadiene, which he obtained from ethyl alcohol. During World War I, Germany, under the stimulus of the blockade imposed by the Allies, began production of “methyl rubber” by using Kondakov’s process. This was an inferior substitute by present-day standards, and after the war German manufacturers returned to the cheaper and more satisfactory natural product. Research and experiments continued, however, and in 1926 the German G. Ebert succeeded in producing a sodium-polymerized rubber from butadiene. During the following decade this material evolved into various types of “buna” rubber (so called from the initial syllables of the two materials used to make them: butadiene and natrium [sodium]).
In the Soviet Union, production of polybutadiene by using Lebedev’s process was begun in 1932–33, using potatoes and limestone as raw materials. By 1940 the Soviet Union had the largest synthetic rubber industry in the world, producing more than 50,000 tons per year. In Germany, meanwhile, the first synthetic elastomer that could be used to replace natural rubber and make satisfactory tires was developed at I.G. Farben by Walter Bock and Eduard Tschunkur, who synthesized a rubbery copolymer of styrene and butadiene in 1929, using an emulsion process. The Germans referred to this rubber as Buna S; the British called it SBR, or styrene-butadiene rubber. Because styrene and butadiene can be made from petroleum, grain alcohol, or coal, SBR was in great demand during World War II. Immense amounts were made—as much as 100,000 tons per year in Germany and the Soviet Union. About 800,000 tons of SBR were produced per year in the United States, where it received the wartime designation GR-S (government rubber-styrene). During the war German chemical engineers perfected low-temperature, or “cold,” polymerization of SBR, producing a more uniform product.
Other important synthetic elastomers were discovered in the decades before World War II, though none was suitable for making tires. Among these were polysulfides, synthesized in the United States by Joseph Patrick in 1926 and commercialized after 1930 as oil-resistant thiokol rubbers; polychloroprene, discovered by Arnold Collins in 1931 and commercialized by the DuPont Company in 1932 as Duprene (later neoprene), a high-strength oil-resistant rubber; nitrile rubber (NBR), an oil-resistant copolymer of acrylonitrile and butadiene synthesized by Erich Konrad and Tschunkur in 1930 and known as Buna N in Germany; and butyl rubber (IIR), a copolymer of isoprene and isobutylene discovered in 1937 by the Americans R.M. Thomas and W.J. Sparks at Standard Oil Company (New Jersey).
After World War II, increasing sophistication in synthetic chemistry led to many new polymers and elastomers. In 1953–54 two chemists, Karl Ziegler of Germany and Giulio Natta of Italy, developed a family of organometallic catalysts that were able to control precisely the placing and arrangement of units along the polymer chain and thus produce regular (stereospecific) structures. With the use of such catalysts, isoprene was polymerized in such a manner that each unit in the chain was linked to its predecessor in a cis configuration, virtually identical to the structure of natural rubber. In this way virtually 100 percent cis-polyisoprene, “synthetic natural rubber,” was made. In 1961 the same type of catalyst with butadiene as the monomer was used to produce cis-1,4-polybutadiene, a rubber that was found to have excellent abrasion resistance, especially in tires subjected to severe service conditions.
Several other advances characterized the postwar years. For example, block copolymers, in which a long sequence of one chemical unit is followed in the same molecule by a long sequence of another, were made, using many different units and sequence lengths. New oil-resistant and heat-resistant elastomers were introduced, including the styrene-acrylonitrile copolymers, the polysulfides, and chlorinated and chlorosulfonated polyethylene. Control has been achieved, to some degree, over the wide range of molecular length found in most polymers, so narrow or broad distributions can be produced in many cases, with quite different viscous properties. In addition, polymers have been synthesized with branched molecules, either with many small branches along the main chain or with several long “arms” radiating from a central point, giving different flow properties and more facile cross-linking.
- Alan N. Gent
In 1876, Henry Wickham gathered thousands of seeds of this plant from Brazil, and they were germinated in Kew Gardens, England. The seedlings were then sent to Colombo, Indonesia, Singapore, and British Malaya. Malaya later became the biggest producer of rubber.
A Brief History of Rubber. Based on Wade Davis, One River 1996. Rubber is one of the most important products to come out of the rainforest. Though Indigenous rainforest dwellers of South America have been using rubber for generations, it was not until 1839 that rubber had its first practical application in the industrial world.
Joseph Priestley is credited with the discovery c.1770 of its use as an eraser, thus the name rubber. The first rubber factory in the world was established near Paris in 1803, the first in England by Thomas Hancock in 1820.
People also ask
When was rubber first used?
When did rubber become a hot commodity?
Where did rubber come from?
Where did synthetic rubber come from?
When did the rubber boom start?
How was rubber discovered?
Apr 30, 2018 · Written by a social and cultural historian at the University of Akron (the city that was long called the “rubber capital of the world”), this short book examines the history of rubber, mainly in th...
