GB883579A - Improved hydrocarbon conversion process - Google Patents

Improved hydrocarbon conversion process

Info

Publication number
GB883579A
GB883579A GB26544/59A GB2654459A GB883579A GB 883579 A GB883579 A GB 883579A GB 26544/59 A GB26544/59 A GB 26544/59A GB 2654459 A GB2654459 A GB 2654459A GB 883579 A GB883579 A GB 883579A
Authority
GB
United Kingdom
Prior art keywords
coke
product
conduit
hydrocarbon
gas
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
GB26544/59A
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 GB883579A publication Critical patent/GB883579A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • 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
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/24Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by heating with electrical means

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Combustion & Propulsion (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

<PICT:0883579/III/1> <PICT:0883579/III/2> Carbon is deposited from a gaseous or vaporous hydrocarbon on to resistance-heated carbon-containing particles, e.g. coal or coke, in a moving or fluidised bed of the particles. The hydrocarbon may be methane or naphtha. The methane may be in the form of natural gas or refinery tail gas which has been scrubbed to remove hydrogen sulphide and carbon dioxide. Direct or alternating current may be used. The hydrocarbon is preferably passed in counter-current to a moving bed of coke particles, a portion of the coke product, e.g. 75-80%, being recycled. In the decomposition of methane, 35-70 lb., preferably 42-56 lb., of coke per 1000 cu. ft. of product hydrogen may be recycled. The bed may move upwards or downwards. In the former case a screw or piston feeder may be employed. The reaction temperature may be 1800 DEG -3000 DEG F., preferably 1900 DEG -2500 DEG F. The voltage drop may be 0,1-1000 volts, preferably 3-10 volts, per inch. The moving bed may have a density of 40-75 lb. per cu. ft. The pressure in the reaction chamber may be 65 p.s.i.g. 30 K.W.H. per 1000 cu. ft. of methane may be consumed. The contact time may be 0,5-20 sec., preferably 2-5 sec. The coke particles may have a diameter of 0,05-10 inch, preferably 0,18-0,4 inch. A portion of the circulating coke may be subjected to size reduction or may be replaced by fresh coke. Reduction may be effected by the use of jets of hydrogen or methane in the reaction chamber or by impact against a target in a separate vessel. A portion of the hot product hydrogen may be recycled and mixed with the feed hydrocarbon. A liquid hydrocarbon may thereby be vaporised. Heat may be transferred from product gas to feed hydrocarbon by the circulation of metallic or ceramic beads, sand, or graphite. The product may have a resistivity of 0,030-0,036 ohms per inch and a particle density of 110 lbs. per cu. ft. As shown in Fig. 1, a hydrocarbon feed is admitted to a reaction chamber 10 from a conduit 19 and optionally from a conduit 20, "grinding" gas, e.g. hydrogen or methane, may be admitted from a conduit 23, and product gas is withdrawn from a conduit 21. Coke is passed from a pressurised bucket lift 16 via a storage hopper 26 to the top of the reaction chamber 10, is electrically heated therein by means of a plurality of anodes 14 and cathodes 15, a portion of the product coke is withdrawn through conduit 24 and the remainder is recycled to bucket lift 16 via conduit 25, in which it is cooled by means of a water spray 27. Fresh coke may be added or recycled coke may be withdrawn via conduit 18. In a fluidised bed process the coke particles may have a size of 20-100 mesh and the bed may have a density of 40-60 lbs. per cu. ft. As shown in Fig. 3 a fluidised bed of coke particles is maintained in a reaction chamber 100 by the addition of feed hydrocarbon through line 114 and optionally through 116 and fluidising gas, which may be methane, hydrogen or an inert gas, through line 112. A portion of the product coke is removed through conduit 115 while the remainder is reduced in size by means of the fluidising gas. Feed hydrocarbon is pre-heated in chamber 102 by passage in countercurrent to granular solid which has been heated in chamber 101 by passage in countercurrent to the product gas. The cooled solid is recycled to chamber 101 via lift 103. Fine coke particles are removed from the product gas after passing through chamber 101 in a cyclone separator 108.
GB26544/59A 1958-09-02 1959-08-04 Improved hydrocarbon conversion process Expired GB883579A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US883579XA 1958-09-02 1958-09-02

Publications (1)

Publication Number Publication Date
GB883579A true GB883579A (en) 1961-11-29

Family

ID=22210910

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26544/59A Expired GB883579A (en) 1958-09-02 1959-08-04 Improved hydrocarbon conversion process

Country Status (1)

Country Link
GB (1) GB883579A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3945066A1 (en) * 2020-07-28 2022-02-02 Total Se Process to conduct a steam cracking reaction in a fluidized bed reactor
WO2022023351A1 (en) * 2020-07-28 2022-02-03 Totalenergies Se Process to conduct an endothermic steam reforming reaction in a fluidized bed reactor
WO2022023365A1 (en) * 2020-07-28 2022-02-03 Totalenergies Se Process to conduct an endothermic thio-reforming reaction of hydrocarbons in an installation comprising electrified fluidized bed reactor
WO2022023361A1 (en) * 2020-07-28 2022-02-03 Totalenergies Se Process for recovery of hydrogen halides from halo-hydrocarbons in an installation comprising electrified fluidized bed reactor

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3945066A1 (en) * 2020-07-28 2022-02-02 Total Se Process to conduct a steam cracking reaction in a fluidized bed reactor
WO2022023351A1 (en) * 2020-07-28 2022-02-03 Totalenergies Se Process to conduct an endothermic steam reforming reaction in a fluidized bed reactor
WO2022023365A1 (en) * 2020-07-28 2022-02-03 Totalenergies Se Process to conduct an endothermic thio-reforming reaction of hydrocarbons in an installation comprising electrified fluidized bed reactor
WO2022023361A1 (en) * 2020-07-28 2022-02-03 Totalenergies Se Process for recovery of hydrogen halides from halo-hydrocarbons in an installation comprising electrified fluidized bed reactor
WO2022023346A1 (en) * 2020-07-28 2022-02-03 Totalenergies Se Process to conduct a steam cracking reaction in a fluidized bed reactor
CN116194205A (en) * 2020-07-28 2023-05-30 道达尔能源一技术 Method for carrying out steam cracking reactions in a fluid bed reactor
CN116194205B (en) * 2020-07-28 2024-01-30 道达尔能源一技术 Method for carrying out steam cracking reactions in a fluid bed reactor
US11964868B2 (en) 2020-07-28 2024-04-23 Totalenergies Onetech Process to conduct an endothermic steam reforming reaction in a fluidized bed reactor

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