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1,3-Butadiene
1,3-Butadiene () is the organic compound with the formula (CH2=CH)2. It is a colorless gas that is easily condensed to a liquid. It is important industrially as a precursor to synthetic rubber. The molecule can be viewed as the union of two vinyl groups. It is the simplest conjugated diene. Although butadiene breaks down quickly in the atmosphere, it is nevertheless found in ambient air in urban and suburban areas as a consequence of its constant emission from motor vehicles. The name butadiene can also refer to the isomer, 1,2-butadiene, which is a cumulated diene with structure H2C=C=CH−CH3. This allene has no industrial significance. History In 1863, the French chemist E. Caventou isolated butadiene from the pyrolysis of amyl alcohol. This hydrocarbon was identified as butadiene in 1886, after Henry Edward Armstrong isolated it from among the pyrolysis products of petroleum. In 1910, the Russian chemist Sergei Lebedev polymerized butadiene and obtained a material wit ...
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Conjugated Diene
In organic chemistry a diene ( ) (diolefin ( ) or alkadiene) is a covalent compound that contains two double bonds, usually among carbon atoms. They thus contain two alk''ene'' units, with the standard prefix ''di'' of systematic nomenclature. As a subunit of more complex molecules, dienes occur in naturally occurring and synthetic chemicals and are used in organic synthesis. Conjugated dienes are widely used as monomers in the polymer industry. Polyunsaturated fats are of interest to nutrition. Classes Dienes can be divided into three classes, depending on the relative location of the double bonds: #Cumulated dienes have the double bonds sharing a common atom. The result is more specifically called an allene. #Conjugated dienes have conjugated double bonds separated by one single bond. Conjugated dienes are more stable than other dienes because of resonance. #Unconjugated dienes have the double bonds separated by two or more single bonds. They are usually less stable than ...
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Diene
In organic chemistry a diene ( ) (diolefin ( ) or alkadiene) is a covalent compound that contains two double bonds, usually among carbon atoms. They thus contain two alk''ene'' units, with the standard prefix ''di'' of systematic nomenclature. As a subunit of more complex molecules, dienes occur in naturally occurring and synthetic chemicals and are used in organic synthesis. Conjugated dienes are widely used as monomers in the polymer industry. Polyunsaturated fats are of interest to nutrition. Classes Dienes can be divided into three classes, depending on the relative location of the double bonds: #Cumulated dienes have the double bonds sharing a common atom. The result is more specifically called an allene. #Conjugated dienes have conjugated double bonds separated by one single bond. Conjugated dienes are more stable than other dienes because of resonance. #Unconjugated dienes have the double bonds separated by two or more single bonds. They are usually less stable tha ...
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Synthetic Rubber
A synthetic rubber is an artificial elastomer. They are polymers synthesized from petroleum byproducts. About 32-million metric tons of rubbers are produced annually in the United States, and of that amount two thirds are synthetic. Synthetic rubber, just like natural rubber, has many uses in the automotive industry for tires, door and window profiles, Seal (mechanical), seals such as O-rings and gaskets, hoses, Belt (mechanical), belts, Rubber mat, matting, and flooring. They offer a different range of physical and chemical properties, so can improve the reliability of a given product or application. Synthetic rubbers are superior to natural rubbers in two major respects, thermal stability and resistance to oils and related compounds. They are more resistant to oxidizing agents, such as oxygen and ozone which can reduce the life of products like tires. History of synthetic rubber The expanded use of bicycles, and particularly their pneumatic tires, starting in the 1890s, create ...
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Exhaust Gas
Exhaust gas or flue gas is emitted as a result of the combustion of fuels such as natural gas, gasoline (petrol), diesel fuel, fuel oil, biodiesel blends, or coal. According to the type of engine, it is discharged into the atmosphere through an exhaust pipe, flue gas stack, or propelling nozzle. It often disperses downwind in a pattern called an ''exhaust plume''. It is a major component of motor vehicle emissions (and from stationary internal combustion engines), which can also include crankcase blow-by and evaporation of unused gasoline. Motor vehicle emissions contribute to air pollution and are a major ingredient in the creation of smog in some large cities. A 2013 study by the Massachusetts Institute of Technology (MIT) indicates that 53,000 early deaths occur per year in the United States alone because of vehicle emissions. According to another study from the same university, traffic fumes alone cause the death of 5,000 people every year just in the United Kingdom. Comp ...
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Walter Bock
Walter Bock (20 January 1895 – 25 October 1948)Death record Nr. 3271/Köln I for Ludwig Walter Robert Bock of Oct. 26, 1948, Landesarchiv NRW, Duisburg was a German chemist who developed styrene-butadiene copolymer by emulsion polymerization as a synthetic rubber (SBR). Early life Walter Bock was born on January 10, 1895 in the small village of Wenzen (now part of Einbeck) in the Duchy of Brunswick. He was the fourth of nine children. His father, Wilhelm Bock, was the sole teacher in Wenzen. From 1905 to 1914 Bock attended high school in Brunswick. Immediately after graduation he joined the army and served as an officer in World War I. He commanded an infantry company until he was wounded in July 1918. In October 1918 he began studying chemistry. After receiving his Ph.D. from the University of Göttingen in October 1921, Bock found employment as chemist at the Köln Rottweil AG in Premnitz. In the fall of 1924 Bock joined the Dr. Zellner laboratories in Berlin, where he to ...
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Eduard Tschunker
Eduard Model Accessories is a Czech manufacturer of plastic models and finescale model accessories. Formed in 1989 in the city of Most, Eduard began in a rented cellar as a manufacturer of photoetched brass model components. Following the success of their early products, the company branched off into plastic models in 1993. As of 2006, Eduard's product line contained some 30 plastic kits and more than 800 individual photoetch detail sets. To the plastic modeller community at large, Eduard has become a household word in the field of photoetched parts, and their products are available worldwide. Eduard aircraft kits range from World War I to the present day. Some notable ones include: most of the famous World War I fighters are: Fokker D.VII, Pfalz D.III, Albatros D.III and the Sopwith Pup, while World War II had the: Yakovlev Yak-3, Hawker Hurricane, Spitfire and the Messerschmitt Bf 109 The Messerschmitt Bf 109 is a German World War II fighter aircraft that was, along wit ...
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British Empire
The British Empire was composed of the dominions, colonies, protectorates, mandates, and other territories ruled or administered by the United Kingdom and its predecessor states. It began with the overseas possessions and trading posts established by England between the late 16th and early 18th centuries. At its height it was the largest empire in history and, for over a century, was the foremost global power. By 1913, the British Empire held sway over 412 million people, of the world population at the time, and by 1920, it covered , of the Earth's total land area. As a result, its constitutional, legal, linguistic, and cultural legacy is widespread. At the peak of its power, it was described as "the empire on which the sun never sets", as the Sun was always shining on at least one of its territories. During the Age of Discovery in the 15th and 16th centuries, Portugal and Spain pioneered European exploration of the globe, and in the process established large overse ...
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Sergei Vasilyevich Lebedev
Sergei Vasilievich Lebedev (russian: Сергей Васильевич Лебедев; 13 July 1874 – 2 May 1934) was a Russian/Soviet chemist and the inventor of polybutadiene synthetic rubber, the first commercially viable and mass-produced type of synthetic rubber. Biography Lebedev was born in 1874 in Lublin and went to school in Warsaw. In 1900, he graduated from St. Petersburg University and found work at the Petersburg Margarine Factory. Starting in 1902, Lebedev moved from university to university in Russia, starting at the Saint-Petersburg Institute for Railroad Engineering. In 1904, he returned to St. Petersburg University to work under Alexey Favorsky (Stalin Prize, 1941, for contributions to the manufacture of synthetic rubber). In 1905, he married his second wife, the artist Anna Ostroumova-Lebedeva. In 1915, Lebedev was appointed Professor at the Women's Pedagogical Institute in St. Petersburg. After 1916, he was a Professor of the Saint Petersburg ...
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Henry Edward Armstrong
Henry Edward Armstrong FRS FRSE (Hon) (6 May 1848 – 13 July 1937) was a British chemist. Although Armstrong was active in many areas of scientific research, such as the chemistry of naphthalene derivatives, he is remembered today largely for his ideas and work on the teaching of science. Armstrong's acid is named for him. Life and work Armstrong was born the son of Richard Armstrong, a commission agent and importer, and Mary Ann Biddle. He lived most of his life in Lewisham, a suburb of London. After finishing school in 1864 at age 16, he spent a winter in Gibraltar, with a relative, for health reasons. In the spring of 1865, Armstrong returned to England and entered the Royal College of Chemistry in London, now the department of chemistry at Imperial College. Chemical training in those days was not lengthy, and at the age of 18 he was selected by Edward Frankland to assist in devising methods of determining organic impurities in sewage. Armstrong pursued further studies ...
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Amyl Alcohol
An amyl alcohol is any of eight alcohols with the formula C5H12O. A mixture of pentyl, amyl alcohols (also called amyl alcohol) can be obtained from fusel alcohol. Amyl alcohol is used as a solvent and in esterification, by which is produced amyl acetate and other important products. The name ''amyl alcohol'' without further specification applies to the normal (straight-chain) form, 1-Pentanol, 1-pentanol. These are the 8 alcohols that are structural isomers with molecular formula C5H12O: : Three of these alcohols, 2-methyl-1-butanol, 2-pentanol, and 3-methyl-2-butanol (methyl isopropyl carbinol), are therefore optical isomerism, optically active. The most important amyl alcohol is isoamyl alcohol, the chief one generated by fermentation in the production of alcoholic beverages and a constituent of fusel oil. The other amyl alcohols may be obtained synthetically. References

{{DEFAULTSORT:Amyl Alcohol Alkanols GABAA receptor positive allosteric modulators ...
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Pyrolysis
The pyrolysis (or devolatilization) process is the thermal decomposition of materials at elevated temperatures, often in an inert atmosphere. It involves a change of chemical composition. The word is coined from the Greek-derived elements ''pyro'' "fire", "heat", "fever" and '' lysis'' "separating". Pyrolysis is most commonly used in the treatment of organic materials. It is one of the processes involved in charring wood.''Burning of wood''
, InnoFireWood's website. Accessed on 2010-02-06.
In general, pyrolysis of organic substances produces volatile products and leaves , a carbon-rich solid residue. Extreme pyrolysis, which leaves mostly

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Allene
In organic chemistry, allenes are organic compounds in which one carbon atom has double bonds with each of its two adjacent carbon centres (). Allenes are classified as diene#Classes, cumulated dienes. The parent compound of this class is propadiene, which is itself also called ''allene''. Compounds with an allene-type structure but with more than three carbon atoms are members of a larger class of compounds called cumulenes with bonding. History For many years, allenes were viewed as curiosities but thought to be synthetically useless and difficult to prepare and to work with.The Chemistry of the Allenes (vol. 1−3); Landor, S. R., Ed.; cademic Press: London, 1982. Reportedly, the first synthesis of an allene, glutinic acid, was performed in an attempt to prove the non-existence of this class of compounds. The situation began to change in the 1950s, and more than 300 papers on allenes have been published in 2012 alone. These compounds are not just interesting intermediates ...
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