GB1474491A - Texaco dev corp alkylation process - Google Patents

Texaco dev corp alkylation process

Info

Publication number
GB1474491A
GB1474491A GB424075A GB424075A GB1474491A GB 1474491 A GB1474491 A GB 1474491A GB 424075 A GB424075 A GB 424075A GB 424075 A GB424075 A GB 424075A GB 1474491 A GB1474491 A GB 1474491A
Authority
GB
United Kingdom
Prior art keywords
zone
isobutane
fraction
impurities
phase
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
GB424075A
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.)
Texaco Development Corp
Original Assignee
Texaco Development Corp
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 Texaco Development Corp filed Critical Texaco Development Corp
Priority to GB424075A priority Critical patent/GB1474491A/en
Publication of GB1474491A publication Critical patent/GB1474491A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07C2/60Catalytic processes with halides
    • 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Landscapes

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

Abstract

1474491 Alkylating isobutane with ethylene TEXACO DEVELOPMENT CORP 31 Jan 1975 4240/75 Heading C5E In an aluminium chloride catalysed alkylation process wherein isobutane and ethylene are contacted with an aluminium chloridehydrocarbon complex catalyst and ethyl chloride in an alkylation reaction zone in the liquid phase, under alkylating conditions, and with agitation sufficient to form an emulsion of reactant hydrocarbons and catalyst, wherein ethylene charge to said process contains C 1 -C 3 range normal paraffin diluents, wherein fresh isobutane charge to said process contains C 3 - C 4 range normal paraffin diluents and impurities which are reactive with aluminium chloride; the procedure comprises: (a) reacting, in an alkylation reaction zone, an isobutane stream substantially free of normal paraffin hydrocarbons and impurities which are reactive with aluminium chloride with an ethylene stream containing C 1 -C 3 normal paraffin impurities in the presence of an aluminium chloridehydrocarbon complex catalyst and hydrogen chloride catalyst activator for production of alkylated hydrocarbons; (b) separating, in a product separation zone, the reaction effluent from said alkylation reactionzone into a hydrocarbon phase essentially free of aluminium chloride-hydrocarbon complex catalyst and a catalyst phase; (c) recycling a major portion of said catalyst phase from product separation zone to said alkylation reaction zone for said reacting step a; (d) fractionating, in a debutanizing zone, hydrocarbon phase into a C 5 and heavier alkylated hydrocarbon product fraction and a recycle hydrocarbon fraction comprising isobutane with minor amount of ethyl chloride, C 1 -C 4 normal paraffin hydrocarbons and unreacted ethylene; (e) recycling a major portion of said recycle hydrocarbon fraction to said alkylation reaction zone for reaction of said isobutane with said unreacted ethylene in step (a); (f) contacting, in a contacting zone, a minor portion of said catalyst phase from said product separation zone with said fresh isobutane charge containing C 3 -C 4 range normal paraffin diluents and impurities which are reactive with aluminium chloride for conversion of said reactive impurities into compounds soluble in said catalyst phase; (g) separating, in a separation zone, the effluent from said contacting zone into a catalyst phase containing conversion products of said reactive impurities from said fresh isobutane charge and an isobutane phase containing C 3 -C 4 normal paraffin impurities and substantially free of said reactive impurities; (h) fractionating, in a depropanizing zone, the isobutane phase from said separation zone and a minor portion of said recycle hydrocarbon fraction from said debutanizing zone into a C 1 -C 3 fraction comprising C 1 -C 3 normal paraffins and a minor portion of said unreacted ethylene and a depropanizing zone bottoms fraction comprising a major portion of isobutane and minor amounts of normal butane and ethyl chloride; (i) fractionating, in a deisobutanizing zone, said depropanizing zone bottoms fraction into a butane fraction comprising normal butane and ethyl chloride and an isobutane fraction substantially free of C 1 -C 4 normal paraffin diluents and said reactive impurities; and (j) charging said isobutane fraction from said deisobutanizing zone to said alkylation reaction zone as the isobutane stream of step (a).
GB424075A 1975-01-31 1975-01-31 Texaco dev corp alkylation process Expired GB1474491A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB424075A GB1474491A (en) 1975-01-31 1975-01-31 Texaco dev corp alkylation process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB424075A GB1474491A (en) 1975-01-31 1975-01-31 Texaco dev corp alkylation process

Publications (1)

Publication Number Publication Date
GB1474491A true GB1474491A (en) 1977-05-25

Family

ID=9773369

Family Applications (1)

Application Number Title Priority Date Filing Date
GB424075A Expired GB1474491A (en) 1975-01-31 1975-01-31 Texaco dev corp alkylation process

Country Status (1)

Country Link
GB (1) GB1474491A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0593477A4 (en) * 1990-08-20 1993-09-16 Mobil Oil Corp Isoparaffin/olefin alkylation.

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0593477A4 (en) * 1990-08-20 1993-09-16 Mobil Oil Corp Isoparaffin/olefin alkylation.
EP0593477A1 (en) * 1990-08-20 1994-04-27 Mobil Oil Corporation Isoparaffin/olefin alkylation

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee