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Chemische Industrie Uithoorn (Cindu, later ''Cindu Chemicals'') was a chemical company in Uithoorn, Netherlands, specialising in processing coal tar. The company was founded in 1922 as ''Teerbedrijf Uithoorn'' (''TEBU''), and operated under a number of company names. It was acquired by Koppers in 2010 and renamed ''Koppers Netherlands''. A subsidiary producing polymers from tar derived chemicals was formed in 1960 as ''Neville Cindu Chemie'' (later ''Nevcin Polymers'') and operated from the same site in Uithoorn. A reactor at the factory exploded in 1992, causing three deaths and several injuries. Cindu ceased operations in 2014. History Industrial chemical activity in Uithoorn dates to at least 1863; the ''Koninklijke Chemische Fabriek'' produced primarily sulphuric acid at the site. The company was acquired by rival sulphuric acid producer Ketjen en Co.Ketjen, founded by Gerhard Tileman Ketjen; one of the predecessor companies of AKZO. who concentrated their manufacturing cap ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Uithoorn
Uithoorn () is a municipality and a town in the Netherlands, in the province of North Holland. Population centres The municipality of Uithoorn includes the town of Uithoorn and the village of De Kwakel. ''Map of the municipality of Uithoorn, June 2015'' History The name ''De Uithoorn'' (or ''De Uythoorn'') was used at the end of the Middle Ages for the location of the lower courts of the deanery of Saint John. The village formed around its courthouse. People depended on agriculture and animal husbandry. Agriculture became increasingly more difficult due to the steady soil subsidence. From c. 1600 on, peat extraction became important and resulted in the formation of large ponds, which in turn would be made into polders later on. During the Franco-Dutch War in the rampjaar, "disaster year" of 1672, Uithoorn was on the front lines and fortifications were built. During the Batavian Republic period, the neighbouring village of Thamen was merged with Uithoorn. Its economy was lim ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Creosote
Creosote is a category of carbonaceous chemicals formed by the distillation of various tars and pyrolysis of plant-derived material, such as wood, or fossil fuel. They are typically used as preservatives or antiseptics. Some creosote types were used historically as a treatment for components of seagoing and outdoor wood structures to prevent rot (e.g., bridgework and railroad ties, see image). Samples may be found commonly inside chimney flues, where the coal or wood burns under variable conditions, producing soot and tarry smoke. Creosotes are the principal chemicals responsible for the stability, scent, and flavor characteristic of smoked meat; the name is derived . The two main kinds recognized in industry are coal-tar creosote and wood-tar creosote. The coal-tar variety, having stronger and more toxic properties, has chiefly been used as a preservative for wood; coal-tar creosote was also formerly used as an escharotic, to burn malignant skin tissue, and in dentistry ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Indene
Indene is an aromatic, polycyclic hydrocarbon with chemical formula . It is composed of a benzene ring fused with a cyclopentene ring. This flammable liquid is colorless although samples often are pale yellow. The principal industrial use of indene is in the production of indene/ coumarone thermoplastic resins. Substituted indenes and their closely related indane derivatives are important structural motifs found in many natural products and biologically active molecules, such as sulindac. Isolation Indene occurs naturally in coal-tar fractions boiling around 175–185 °C. It can be obtained by heating this fraction with sodium to precipitate solid "sodio-indene". This step exploits indene's weak acidity evidenced by its deprotonation by sodium to give the indenyl derivative. The sodio-indene is converted back to indene by steam distillation. Reactivity Indene readily polymerises. Oxidation of indene with acid dichromate yields homophthalic acid (''o''-carboxylpheny ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Vinyltoluene
4-Vinyltoluene is an organic compound with the formula CH3C6H4CH=CH2. It is derivative of styrene and is used as a comonomer in the production of specialized polystyrenes. It is produced by the dehydrogenation of 4-ethyltoluene. It is also sometimes used in the production of styrene-free Polyester resin Polyester resins are synthetic resins formed by the reaction of dibasic organic acids and polyhydric alcohols. Maleic anhydride is a commonly used raw material with diacid functionality in unsaturated polyester resins. Unsaturated polyester r .... References {{Hydrocarbons Monomers Vinylbenzenes C3-Benzenes ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Styrene
Styrene is an organic compound with the chemical formula C6H5CH=CH2. Its structure consists of a vinyl group as substituent on benzene. Styrene is a colorless, oily liquid, although aged samples can appear yellowish. The compound evaporates easily and has a sweet smell, although high concentrations have a less pleasant odor. Styrene is the precursor to polystyrene and several copolymers, and is typically made from benzene for this purpose. Approximately 25 million tonnes of styrene were produced in 2010, increasing to around 35 million tonnes by 2018. Natural occurrence Styrene is named after storax balsam (often commercially sold as ''styrax''), the resin of Liquidambar trees of the Altingiaceae plant family. Styrene occurs naturally in small quantities in some plants and foods (cinnamon, coffee beans, balsam tree (other), balsam trees and peanuts) and is also found in coal tar. History In 1839, the German apothecary Eduard Simon isolated a volatile liquid from t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dicyclopentadiene
Dicyclopentadiene, abbreviated DCPD, is a chemical compound with formula . At room temperature, it is a white brittle wax, although lower purity samples can be straw coloured liquids. The pure material smells somewhat of soy wax or camphor, with less pure samples possessing a stronger acrid odor. Its energy density is 10,975 Wh/l. Dicyclopentadiene is a co-produced in large quantities in the steam cracking of naphtha and gas oils to ethylene. The major use is in resins, particularly, unsaturated polyester resins. It is also used in inks, adhesives, and paints. The top seven suppliers worldwide together had an annual capacity in 2001 of 179 kilotonnes (395 million pounds). DCPD was discovered in 1885 as a hydrocarbon among the products of pyrolysis of phenol by Henry Roscoe, who didn't identify the structure (that was made during the following decade) but accurately assumed that it was a dimer of some hydrocarbon. History and structure For many years the structure of dicy ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopentadiene
Cyclopentadiene is an organic compound with the chemical formula, formula C5H6. It is often abbreviated CpH because the cyclopentadienyl anion is abbreviated Cp−. This colorless liquid has a strong and unpleasant odor. At room temperature, this cyclic diene dimer (chemistry), dimerizes over the course of hours to give dicyclopentadiene via a Diels–Alder reaction. This dimer can be retro-Diels–Alder reaction, restored by heating to give the monomer. The compound is mainly used for the production of cyclopentene and its derivatives. It is popularly used as a precursor to the cyclopentadienyl anion (Cp−), an important ligand in cyclopentadienyl complexes in organometallic chemistry. Production and reactions Cyclopentadiene production is usually not distinguished from dicyclopentadiene since they interconvert. They are obtained from coal tar (about 10–20 g/tonne, t) and by steam Cracking (chemistry), cracking of Petroleum naphtha, naphtha (about 14 kg/t) ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Piperylene
Piperylene or 1,3-pentadiene is an organic compound with the formula . It is a volatile, flammable hydrocarbon. It is one of the five positional isomers of pentadiene. Reactions and occurrence Piperylene is a typical diene. It forms a sulfolene upon treatment with sulfur dioxide. Piperylene is the product of the decarboxylation of sorbic acid, a common anti-mold agent. Piperylene is obtained as a byproduct of ethylene production from crude oil, combustion of biomass, waste incineration and exhaust gases. It is used as a monomer in the manufacturing of plastics, adhesives and resins. at Shell Chemicals. Retrieved 2009-05-19. See also * |
Isoprene
Isoprene, or 2-methyl-1,3-butadiene, is a common volatile organic compound with the formula CH2=C(CH3)−CH=CH2. In its pure form it is a colorless volatile liquid. It is produced by many plants and animals (including humans) and its polymers are the main component of natural rubber. History and etymology Charles Greville Williams, C. G. Williams named the compound in 1860 after obtaining it from the pyrolysis of natural rubber. He correctly deduced the mass shares of carbon and hydrogen (but arrived at an incorrect formula C10H8 because the modern atomic weight of carbon was not adopted until the Karlsruhe Congress held later that year). He did not specify the reasons for the name, but it is hypothesized that it came from "propylene" with which isoprene shares some physical and chemical properties. The first one to observe recombination of isoprene into rubber-like substance was in 1879, and William A. Tilden identified its structure five years later. Natural occurrences Is ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Naphtha
Naphtha (, recorded as less common or nonstandard in all dictionaries: ) is a flammable liquid hydrocarbon mixture. Generally, it is a fraction of crude oil, but it can also be produced from natural-gas condensates, petroleum distillates, and the fractional distillation of coal tar and peat. In some industries and regions, the name ''naphtha'' refers to crude oil or refined petroleum products such as kerosene or diesel fuel. Naphtha is also known as Shellite in Australia. Etymology The word ''naphtha'' comes from Latin through Ancient Greek (), derived from Middle Persian ''naft'' ("wet", "naphtha"), the latter meaning of which was an assimilation from the Akkadian 𒉌𒆳𒊏 (see Semitic relatives such as Arabic petroleum" Syriac ''naftā'', and Hebrew , meaning petroleum). Antiquity The book of II Maccabees (2nd cent. BC) tells how a "thick water" was put on a sacrifice at the time of Nehemiah and when the sun shone it caught fire. It adds that "those aro ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Fluid Catalytic Cracking
Fluid catalytic cracking (FCC) is the conversion process used in petroleum refineries to convert the high-boiling point, high-molecular weight hydrocarbon fractions of petroleum (crude oils) into gasoline, alkene gases, and other petroleum products. The cracking of petroleum hydrocarbons was originally done by thermal cracking, now virtually replaced by catalytic cracking, which yields greater volumes of high octane rating gasoline; and produces by-product gases, with more carbon-carbon double bonds (i.e. alkenes), that are of greater economic value than the gases produced by thermal cracking. The feedstock to the FCC conversion process usually is heavy gas oil (HGO), which is that portion of the petroleum (crude oil) that has an initial boiling-point temperature of or higher, at atmospheric pressure, and that has an average molecular weight that ranges from about 200 to 600 or higher; heavy gas oil also is known as "heavy vacuum gas oil" (HVGO). In the fluid catalytic cracking ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
