词条 | 1-Octene |
释义 |
| Watchedfields = changed | verifiedrevid = 477208427 | Name = 1-Octene | ImageFile = octene.png | ImageSize = 220px | ImageName = 1-Octene | ImageFile1 = 1-Octene-3D-balls.png | ImageSize1 = 220px | ImageAlt1 = 1-Octene molecule | PIN = Oct-1-ene | OtherNames = Octene-1, octylene; 1-n-ctene; hexylethylene; oct-1-ene; octene |Section1={{Chembox Identifiers | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI = 46708 | ChemSpiderID = 7833 | PubChem = 8125 | InChI = 1/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3 | InChIKey = KWKAKUADMBZCLK-UHFFFAOYAN | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = KWKAKUADMBZCLK-UHFFFAOYSA-N | CASNo_Ref = {{cascite|correct|CAS}} | CASNo = 111-66-0 | SMILES = C=CCCCCCC }} |Section2={{Chembox Properties | Formula = C8H16 | MolarMass = 112.24 g/mol | Density = 0.715 g/cm3 | MeltingPtC = -101.7 | MeltingPt_ref =[1] | BoilingPtC = 121 | BoilingPt_ref = [1] }} 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. SynthesisIn 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.[2] ApplicationsThe main use of 1-octene is as a comonomer in production of polyethylene. High-density polyethylene (HDPE) and linear low-density polyethylene (LLDPE) use approximately 2–4% and 8–10% of comonomers, respectively. Another significant use of 1-octene is for production of linear aldehyde via the oxo synthesis (hydroformylation) to give the C9 aldehyde (nonanal). Oxidation of this aldehyde gives the short-chain fatty acid nonanoic acid. Hydrogenation of the same aldehyde gives the fatty alcohol 1-nonanol, which is used as a plasticizer. References1. ^1 http://webbook.nist.gov/cgi/cbook.cgi?ID=C111660&Units=SI&Mask=1EFF {{Hydrides by group}}{{DEFAULTSORT:Octene, 1-}}2. ^{{cite journal | last1 = Bollmann | first1 = Annette | last2 = Blann | first2 = Kevin | last3 = Dixon | first3 = John T. | last4 = Hess | first4 = Fiona M. | last5 = Killian | first5 = Esna | last6 = Maumela | first6 = Hulisani | last7 = McGuinness | first7 = David S. | last8 = Morgan | first8 = David H. | last9 = Neveling | first9 = Arno | last10 = Otto | first10 = Stefanus | last11 = Overett | first11 = Matthew | last12 = Slawin | first12 = Alexandra M. Z. | last13 = Wasserscheid | first13 = Peter | last14 = Kuhlmann | first14 = Sven | year = 2004 | title = Ethylene Tetramerization: A New Route to Produce 1-Octene in Exceptionally High Selectivities | url = | journal = J. Am. Chem. Soc. | volume = 126 | issue = 45| pages = 14712–14713 | doi = 10.1021/ja045602n }} 1 : Alkenes |
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