GB817126A - Isomerization process and preparation of feed stream therefor - Google Patents

Isomerization process and preparation of feed stream therefor

Info

Publication number
GB817126A
GB817126A GB39179/57A GB3917957A GB817126A GB 817126 A GB817126 A GB 817126A GB 39179/57 A GB39179/57 A GB 39179/57A GB 3917957 A GB3917957 A GB 3917957A GB 817126 A GB817126 A GB 817126A
Authority
GB
United Kingdom
Prior art keywords
adsorbent
per cent
isoparaffins
vol
feed
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
GB39179/57A
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.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering 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 Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of GB817126A publication Critical patent/GB817126A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G61/00Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen
    • C10G61/02Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen plural serial stages only
    • C10G61/06Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen plural serial stages only the refining step being a sorption process

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

In a combination hydrocarbon separation and isomerization process a light naphtha boiling within the range 60-180 DEG F. containing aromatic and normal paraffinic hydrocarbons is passed through a contacting zone containing an adsorbent which selectively adsorbs aromatic hydrocarbons, at least a portion of the aromatic free naphtha is subjected to isomerization to form high octane isoparaffins and at least a portion of such isoparaffins is used to desorb aromatic hydrocarbons from the adsorbent to give a stream of a mixture of isoparaffinic and aromatic hydrocarbons. The naphtha feed is preferably depentonised. The adsorbent used may be a suitable char but is preferably a molecular sieve having 6-15 pore openings. The feed is preferably vaporized and conditions of 180-400 DEG F. and 0-100 p.s.i.g. are used with flow rates of 0.05-5 vol./vol./hr. over fixed, moving or fluidized beds of adsorbent. The raffinate may then be fractionated to remove naphthenes and highly branched isoparaffins, only straight chain paraffins or paraffins with single branches passing to the isomerization. This is preferably a liquid phase process over a Friedel-Crafts catalyst such as aluminium chloride supported on "Porocel." Olefines should not be present in amounts more than 0.2 per cent, but 0.2-0.5 volume per cent of benzene may be present and 5-20 volume per cent of naphthenes. Temperatures of 100-275 DEG F., pressures of 100-450 p.s.i.g. and flow rates of 0.3-3 vol./vol./hr. are used. Hydrogen chloride may be present in the feed as an activator in amounts of 0.1-6.0 weight per cent and 0.1-3 mol. per cent of hydrogen may be added. The isomerisate is then fed to the fractionator before the isomeriser to remove highly branched isoparaffins and recycle other materials. This fractionator may be placed after the isomeriser if the feed contains little isoparaffins and in another alternative is placed before the contacting zone. The highly branched product is passed through the adsorbent in the vapour phase at 140-500 DEG F. Extraneous desorbents may be used in conjunction with the isomerisate such as heavier paraffins and naphthenes or purge gases.
GB39179/57A 1957-01-07 1957-12-17 Isomerization process and preparation of feed stream therefor Expired GB817126A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US817126XA 1957-01-07 1957-01-07

Publications (1)

Publication Number Publication Date
GB817126A true GB817126A (en) 1959-07-22

Family

ID=22165904

Family Applications (1)

Application Number Title Priority Date Filing Date
GB39179/57A Expired GB817126A (en) 1957-01-07 1957-12-17 Isomerization process and preparation of feed stream therefor

Country Status (1)

Country Link
GB (1) GB817126A (en)

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