GB578085A - Improved process for the isomerization of paraffins - Google Patents

Improved process for the isomerization of paraffins

Info

Publication number
GB578085A
GB578085A GB6466/43A GB646643A GB578085A GB 578085 A GB578085 A GB 578085A GB 6466/43 A GB6466/43 A GB 6466/43A GB 646643 A GB646643 A GB 646643A GB 578085 A GB578085 A GB 578085A
Authority
GB
United Kingdom
Prior art keywords
promoter
butane
absorber
overhead
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB6466/43A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB578085A publication Critical patent/GB578085A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/22Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
    • C07C5/27Rearrangement of carbon atoms in the hydrocarbon skeleton
    • C07C5/2767Changing the number of side-chains
    • C07C5/277Catalytic processes
    • C07C5/2778Catalytic processes with inorganic acids; with salts or anhydrides of acids
    • C07C5/2786Acids of halogen; Salts thereof
    • C07C5/2789Metal halides; Complexes thereof with organic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

<PICT:0578085/IV/1> Normal paraffins of at least 4 carbon atoms are isomerized using a Friedel-Crafts' type catalyst and a gaseous halogen-containing promoter, the reacted mixture being passed through a stripping zone to remove the promoter and gaseous degradation products which are subjected to selective absorption with liquefied hydrocarbon feed under controlled conditions of temperature, pressure and throughput, so that the feed to the isomerization zone contains a desired constant quantity of the promoter. The reacted mixture is stripped and the overhead comprising, for example, hydrogen halide and degradation products such as methane, ethane and propane, passed direct to an absorber where the promoter is absorbed and the inert gases removed as overhead. The absorber may be of a bubble plate or packed tower type, the liquid hydrocarbon flowing down against the stream of promoter. A reboiler or steam jacket may be used to keep a constant temperature, the pressure being controlled by a condenser at the top of the column which normally operates under total reflux conditions. Part only of the feed may pass through the tower so that after admixture with the remainder the desired concentration of promoter is obtained. When isomerizing butane using aluminium chloride and hydrogen chloride, the absorption column is operated between about 100-200 lbs./sq. in. and at a temperature varying between about 50 DEG and 110 DEG F. to give a concentration of promoter varying between about 12 and 2 per cent. The solution of promoter in butane is then brought to a temperature of about 125-220 DEG F. for liquid phase, or 200-450 DEG F. for vapour phase operation. Liquefied butane is fed to absorber 7 by lines 2, 5 and absorbs hydrogen chloride fed by line 43 from an outside source or from the stripping tower 39. Both the solution leaving by line 8, and the overhead may be recycled to ensure equilibrium under the absorption conditions. Inert gases may be withdrawn through line 12, and the butane solution led by pipes 15, 21 to reactor 24 containing "Porocel" (Registered Trade Mark) with absorbed aluminium chloride. The reaction products pass, if desired, partly or wholly by way of cooler 30, to a surge drum 32 which also removes any catalyst, and thence to stripper 39 wherein the pressure is maintained slightly above that of the absorber and the top temperature about the same, while the bottom temperature is generally about 150-300 DEG F. and is controlled by reboiler 47. The overhead comprising hydrogen chloride and part or substantially all the propane returns to the absorber. The bottoms are treated with caustic soda in mixer 50, the butane layer being separated in settler 52 and fed to fractionator 60 giving isobutane with any propane as overhead and normal butane with some pentane which may be returned to the isomerizer through lines 68, 70 and drier 69.
GB6466/43A 1942-05-09 1943-04-22 Improved process for the isomerization of paraffins Expired GB578085A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US578085XA 1942-05-09 1942-05-09

Publications (1)

Publication Number Publication Date
GB578085A true GB578085A (en) 1946-06-14

Family

ID=22012875

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6466/43A Expired GB578085A (en) 1942-05-09 1943-04-22 Improved process for the isomerization of paraffins

Country Status (1)

Country Link
GB (1) GB578085A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103342681A (en) * 2013-05-31 2013-10-09 黄冈银河阿迪药业有限公司 Process and device for improving utilization rate of ethylene oxide of metronidazole production raw materials
EP3012311A1 (en) 2014-10-20 2016-04-27 Axens Method for isomerisation of c5/c6 hydrocarbon fractions with recycling of chlorinated compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103342681A (en) * 2013-05-31 2013-10-09 黄冈银河阿迪药业有限公司 Process and device for improving utilization rate of ethylene oxide of metronidazole production raw materials
EP3012311A1 (en) 2014-10-20 2016-04-27 Axens Method for isomerisation of c5/c6 hydrocarbon fractions with recycling of chlorinated compounds

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