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GB600471A - Improvements in or relating to the production of aviation gasoline - Google Patents

Improvements in or relating to the production of aviation gasoline

Info

Publication number
GB600471A
GB600471A GB123145A GB123145A GB600471A GB 600471 A GB600471 A GB 600471A GB 123145 A GB123145 A GB 123145A GB 123145 A GB123145 A GB 123145A GB 600471 A GB600471 A GB 600471A
Authority
GB
United Kingdom
Prior art keywords
fraction
benzene
boiling
fractionated
products
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
GB123145A
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
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB600471A publication Critical patent/GB600471A/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
    • C10G59/00Treatment of naphtha by two or more reforming processes only or by at least one reforming process and at least one process which does not substantially change the boiling range of the naphtha
    • C10G59/02Treatment of naphtha by two or more reforming processes only or by at least one reforming process and at least one process which does not substantially change the boiling range of the naphtha plural serial stages only
    • C10G59/04Treatment of naphtha by two or more reforming processes only or by at least one reforming process and at least one process which does not substantially change the boiling range of the naphtha plural serial stages only including at least one catalytic and at least one non-catalytic reforming step

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

A petroleum fraction is catalytically cracked or a naphtha catalytically reformed, an aromatic-rich fraction boiling within the range 200-500 DEG F. is separated, thermally cracked at at least 1200 DEG F. for a time from a few seconds to a fraction of a second, and an aromatic fraction of aviation gasoline boiling range is recovered from the products. The thermal cracking converts non-aromatics to lower boiling products, and higher boiling aromatics to benzene and toluene. The product may be acid treated to remove olefinic constituents and, if desired, fractionated to separate benzene and toluene or excess benzene may be alkylated to cumene. A high boiling feedstock such as gas oil or refined crude, may be catalytically cracked at about 800-1050 DEG F. using silica-alumina or other catalyst in a stationary or moving bed or as suspended powder. The products are fractionated to obtain a light fraction boiling up to about 200-225 DEG F. which may be worked up to a gasoline, and a fraction preferably of B.R. about 200-350 DEG F. which contains 50-80 per cent aromatics. This fraction, preferably with a diluent such as steam or hydrocarbon gases, for example steam equivalent to 80 mol. per cent of the mixture, is heated at 1200-1600 DEG F. and then quenched with water to 600-1000 DEG F. Hydrocarbons and water are condensed and the hydrocarbon layer fractionated to give a light fraction from which olefins and diolefins may be recovered, a heavy naphtha which may be used as a solvent or motor fuel or treated to recover naphthalene if present in the feed to the cracking step, and an intermediate aromatic fraction containing benzene, toluene and xylenes, for example a 145-350 DEG F. cut. This is freed from olefins with sulphuric acid, clay or fuller's earth and yields an aviation gasoline blending stock. The temperature in the thermal cracking stage should be at least equal to 1332-107.6 log. S + 10S-1,45, where S is the contact time in seconds. Alternatively, a naphtha, preferably a virgin naphtha of B.R. about 300-400 DEG F. containing more than 40 per cent naphthenes and cyclo-olefins, may be hydroformed at 850-1100 DEG F. using Group 6 oxides or sulphides, preferably molybdenum oxide on alumina, and the products fractionated as before, an intermediate fraction of B.R. 250-350 DEG or 450 DEG F. being thermally cracked, preferably with steam, quenched, and the desired aromatic fraction recovered.ALSO:A petroleum fraction is catalytically cracked or a naphtha catalytically reformed, an aromatic-rich fraction boiling within the range 200-500 DEG F. is separated, thermally cracked at at least 1200 DEG F. for a time from a few seconds to a fraction of a second, and an aromatic fraction of aviation gasoline boiling range is recovered from the products. The thermal cracking converts non-aromatics to lower boiling products, and higher boiling aromatics to benzene and toluene. The product may be acid treated to remove olefinic constituents and, if desired, fractionated to separate benzene and toluene or excess benzene may be alkylated to cumene. A high boiling feedstock such as gas oil or refined crude may be catalytically cracked at about 800-1050 DEG F. using silica-alumina or other catalyst in a stationary or moving bed or as suspended powder. The products are fractionated to obtain a light fraction boiling up to about 200-225 DEG F. which may be worked up to a gasoline, and a fraction preferably of B.R. about 200-350 DEG F. which contains 50-80 per cent aromatics. This fraction, preferably with a diluent such as steam or hydrocarbon gases, for example steam equivalent to 80 mol. per cent of the mixture, is heated at 1200-1600 and then quenched with water to 600-1000 DEG F. Hydrocarbons and water are condensed and the hydrocarbon layer fractionated to give a light fraction from which olefins and diolefins may be recovered, a heavy naphtha which may be used as a solvent or motor fuel or treated to recover naphthalene if present in the feed to the cracking step, and an intermediate aromatic fraction containing benzene, toluene, and xylenes, for example a 145-350 DEG F. cut. This is freed from olefins with sulphuric acid, clay or fuller's earth and yields an aviation gasoline blending stock. The temperature ( DEG F.) in the thermal cracking stage should be at least equal to 1332-107.6 log S+10S-1,45, where S is the contact time in seconds. Alternatively, a naphtha, preferably a virgin naphtha of B.R. about 300-400 DEG F. containing more than 40 per cent of naphthenes and cyclo-olefins, may be hydroformed at 850-110 DEG F. using Group 6 oxides or sulphides, preferably molybdenum oxide on alumina, and the products fractionated as before, an intermediate fraction of B.R. 250-350 DEG or 450 DEG F. being thermally cracked, preferably with steam, quenched and the desired aromatic fraction recovered. It may be fractionated to recover benzene and toluene or benzene in excess of specifications for aviation gasolene may be alkylated with propene and phosphoric acid at 400-500 DEG F. and 600 p.s.i. to yield cumene.
GB123145A 1945-01-15 Improvements in or relating to the production of aviation gasoline Expired GB600471A (en)

Publications (1)

Publication Number Publication Date
GB600471A true GB600471A (en) 1948-04-09

Family

ID=1626727

Family Applications (1)

Application Number Title Priority Date Filing Date
GB123145A Expired GB600471A (en) 1945-01-15 Improvements in or relating to the production of aviation gasoline

Country Status (1)

Country Link
GB (1) GB600471A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE969795C (en) * 1952-11-03 1958-07-17 Bataafsche Petroleum Process for the production of gasoline with an octane number in the range from 90 to 100 from directly distilled gasoline by reforming
EP1365004A1 (en) * 2002-05-23 2003-11-26 ATOFINA Research Production of olefins

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE969795C (en) * 1952-11-03 1958-07-17 Bataafsche Petroleum Process for the production of gasoline with an octane number in the range from 90 to 100 from directly distilled gasoline by reforming
EP1365004A1 (en) * 2002-05-23 2003-11-26 ATOFINA Research Production of olefins
WO2003099964A1 (en) * 2002-05-23 2003-12-04 Total Petrochemicals Research Feluy Production of olefins
EP2267101A3 (en) * 2002-05-23 2011-03-02 Total Petrochemicals Research Feluy Production of olefins
US8071833B2 (en) 2002-05-23 2011-12-06 Total Petrochemicals Research Feluy Production of olefins

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