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・ 1-Naphthaleneacetic acid
・ 1-Naphthol
・ 1-Naphthyl isothiocyanate
・ 1-Naphthylamine
・ 1-Nitropropane
・ 1-Nitropyrene
・ 1-Nonacosanol
・ 1-Nonanol
・ 1-Nonyl-4-phenol
・ 1-Nonylnaphthalene
・ 1-NP
・ 1-Octacosanol
・ 1-Octanol
・ 1-Octen-3-ol
・ 1-Octen-3-yl acetate
1-Octene
・ 1-OQA+19
・ 1-Page
・ 1-Pentanol
・ 1-Pentyne
・ 1-Phenylethylamine
・ 1-phosphatidylinositol 4-kinase
・ 1-phosphatidylinositol-3-phosphate 5-kinase
・ 1-phosphatidylinositol-4-phosphate 5-kinase
・ 1-phosphatidylinositol-5-phosphate 4-kinase
・ 1-phosphofructokinase
・ 1-planar graph
・ 1-Propanol
・ 1-Pyrroline dehydrogenase
・ 1-pyrroline-4-hydroxy-2-carboxylate deaminase


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1-Octene : ウィキペディア英語版
1-Octene

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1-Octene is an organic compound with a formula CH2CHC6H13. The alkene is classified as a higher olefin and alpha-olefin, meaning that the double bond is located at the alpha (primary) position, endowing this compound with higher reactivity and thus useful chemical properties. 1-Octene is one of the important linear alpha olefins in industry. It is a colourless liquid.
==Synthesis==
In industry, 1-octene is commonly manufactured by two main routes: oligomerization of ethylene and by Fischer-Tropsch synthesis followed by purification. Another route to 1-octene that has been used commercially on a small scale is dehydration of alcohols. Prior to the 1970s, 1-octene was also manufactured by thermal cracking of waxes, whereas linear internal octenes were also manufactured by chlorination/dehydrochlorination of linear paraffins.
There are five commercial processes that oligomerize ethylene to 1-octene. Four of these processes produce 1-octene as a part of a wide distribution of alpha-olefins. In typical circumstances, 1-hexene content of the entire distribution of alpha-olefins ranges from about 25% of the distribution in the Ethyl (Innovene) process to about 8% of distribution in some modes of the Gulf (CP Chemicals) and Idemitsu processes.
The only commercial process to isolate 1-octene from a wide mixture of C8 hydrocarbons is practiced by Sasol, a South African oil and gas and petrochemical company. For commercial purposes, Sasol employs Fischer-Tropsch synthesis to make fuels from synthesis gas derived from coal and recovers 1-octene from these fuel streams, where the initial 1-octene concentration in a narrow distillation cut may be 60%, with the remainder being vinylidenes, linear and branched internal olefins, linear and branched paraffins, alcohols, aldehydes, carboxylic acids, and aromatic compounds.
In recent years, two on-purpose 1-octene technologies have been commercialised: a butadiene telomerisation plant (Dow, Tarragona), and a 1-heptene to 1-octene plant based on a Fischer-Tropsch-derived C7 olefin stream (Sasol, Secunda). Sasol is currently in the engineering phase of a new 1-octene technology based on selective tetramerisation of ethylene.〔 〕

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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