GB575797A - Improvements relating to the isomerisation and alkylation of hydrocarbons - Google Patents

Improvements relating to the isomerisation and alkylation of hydrocarbons

Info

Publication number
GB575797A
GB575797A GB16619/42A GB1661942A GB575797A GB 575797 A GB575797 A GB 575797A GB 16619/42 A GB16619/42 A GB 16619/42A GB 1661942 A GB1661942 A GB 1661942A GB 575797 A GB575797 A GB 575797A
Authority
GB
United Kingdom
Prior art keywords
acid
per cent
butane
isobutane
isomerization
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
GB16619/42A
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 GB575797A publication Critical patent/GB575797A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C9/00Aliphatic saturated hydrocarbons
    • C07C9/14Aliphatic saturated hydrocarbons with five to fifteen carbon atoms
    • C07C9/16Branched-chain hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/54Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
    • C07C2/56Addition to acyclic hydrocarbons
    • C07C2/58Catalytic processes
    • C07C2/62Catalytic processes with acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/148Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
    • C07C7/17Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound with acids or sulfur oxides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/02Sulfur, selenium or tellurium; Compounds thereof
    • C07C2527/053Sulfates or other compounds comprising the anion (SnO3n+1)2-
    • C07C2527/054Sulfuric acid or other acids with the formula H2Sn03n+1
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06Halogens; Compounds thereof
    • C07C2527/08Halides
    • C07C2527/10Chlorides
    • C07C2527/11Hydrogen chloride
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06Halogens; Compounds thereof
    • C07C2527/125Compounds comprising a halogen and scandium, yttrium, aluminium, gallium, indium or thallium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06Halogens; Compounds thereof
    • C07C2527/125Compounds comprising a halogen and scandium, yttrium, aluminium, gallium, indium or thallium
    • C07C2527/126Aluminium chloride

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Water Supply & Treatment (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

In the catalytic isomerization of normal paraffins or hydrocarbon mixtures consisting mainly thereof, the feed, before passing to the isomerizer is freed from olefins and moisture by contacting with sulphuric acid, initially of not less than 98 per cent concentration, and not less than 96 per cent after absorbing the olefins. The process is applicable to the isomerization of butane or pentane cuts with aluminium chloride, alone or on a carrier, such as bauxite, the purification preferably being effected by liquid phase counter-current flow. The acid solution may be used for alkylating isoparaffins. A treated butane feed, after removing acid, may be isomerized in the vapour phase at 250-350 DEG F. and 100-400 lbs./sq. in. using aluminium chloride promoted with hydrogen chloride. The isoparaffins produced may be fed with the used acid and additional olefines as required to an alkylation stage. The molar ratio of isobutane to butenes is from 3 to 10 : 1, preferably 5 : 1, with a volume of acid to hydrocarbon feed of 1 : 1, a temperature of 25-80 DEG , preferably 35 DEG F., and a time of contact of 20-200, preferably 60 mins. Butane containing isobutane, butenes, moisture and other impurities is liquefied and washed in counter-current with 98 per cent or more sulphuric acid, part of which may be recycled. The purified feed passes through an acid separator and preheater to an isomerizer, if necessary after removal of isoparaffin. The product is stripped of HC1, washed, and treated to separate isobutane which is fed to an alkylation stage, n-butane being recycled. Acid containing absorbed olefins, isobutane, additional butenes and fresh acid are fed to an alkylator. The product, after acid separation, is fractionated in stages to recover alkylate, iso- and n-butanes. Comparative figures are given for the isomerization of untreated and acid-treated n-pentane containing pentenes which is given two batch treatments each for 1 hour with 5 per cent by volume of 98 per cent sulphuric acid prior to liquid phase isomerization with 100 per cent by weight of aluminium chloride and 22 per cent hydrogen chloride for 2 hours at 75 DEG F. and 200-220 lbs./sq. in. Specifications 538,307 and 553,334 are referred to.
GB16619/42A 1941-12-16 1942-11-24 Improvements relating to the isomerisation and alkylation of hydrocarbons Expired GB575797A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US575797XA 1941-12-16 1941-12-16

Publications (1)

Publication Number Publication Date
GB575797A true GB575797A (en) 1946-03-06

Family

ID=22011480

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16619/42A Expired GB575797A (en) 1941-12-16 1942-11-24 Improvements relating to the isomerisation and alkylation of hydrocarbons

Country Status (1)

Country Link
GB (1) GB575797A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10995045B2 (en) 2018-10-09 2021-05-04 Uop Llc Isomerization zone in alkylate complex

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10995045B2 (en) 2018-10-09 2021-05-04 Uop Llc Isomerization zone in alkylate complex

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