GB602376A - Improvements in the distillation of mixtures of coal and hydrocarbon oil - Google Patents

Improvements in the distillation of mixtures of coal and hydrocarbon oil

Info

Publication number
GB602376A
GB602376A GB24577/45A GB2457745A GB602376A GB 602376 A GB602376 A GB 602376A GB 24577/45 A GB24577/45 A GB 24577/45A GB 2457745 A GB2457745 A GB 2457745A GB 602376 A GB602376 A GB 602376A
Authority
GB
United Kingdom
Prior art keywords
line
coal
separated
zone
distillation
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
GB24577/45A
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 GB602376A publication Critical patent/GB602376A/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
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/04Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B55/00Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material
    • C10B55/02Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material with solid materials
    • 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
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/02Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by distillation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

<PICT:0602376/III/1> Finely divided coal, peat or lignite is mixed with an acylic hydrocarbon oil having an upper boiling point between 700 DEG and 800 DEG F. to form a suspension containing at least 50 per cent of coal. The suspension is continuously passed through a distillation zone maintained at an elevated temperature not exceeding 800 DEG F. The distillate and coked residue are separated, and at least a part of the latter is reacted with steam to produce water-gas which is used to make a synthetic hydrocarbon oil. A fraction of this synthetic oil with an upper boiling point between 700 DEG and 800 DEG F. is separated and utilized in the mixing zone. The distillate from the distillation zone is preferably cracked or reformed, and gasoline fractionated from the product. Motor fuels may also be separated from the synthetic oil. Ground coal from line 1 is mixed in line 2 with paraffinic oil boiling in the range 300 DEG -800 DEG F. which has been made in later stages of the continuous process and is supplied through line 17. Hot ash and coke are then introduced through lines 5 and 6 respectively, and the mixture passes into distillation zone 4 where a temperature of about 700 DEG to 800 DEG F. is maintained. The "hindred settling" technique is employed in zone 4, the particle size of the coal and the vapour velocity being adjusted so that the coal remains in the zone from 3 to 30 minutes. The distillation products are separated in separator 8 from whence the vapours are passed to cracking plant 11 and fractionating column 12. Gasoline is withdrawn through line 13; 8.0 barrels being obtained from 1 ton of coal. The bottom fraction may be supplied to the mixing line 2 through lines 16 and 17. The coked residue from separator 8 is introduced into line 19 through which flows steam and oxygen and, if desired, the gases from column 12. The mixture is conveyed to generator 21 where water gas is produced at a temperature in the range 1600 DEG -2500 DEG F., unconverted coke being withdrawn through line 6 to supply heat for the main distillation step. The water gas is separated from ash in separator 23, and passed to plant 25 where liquid hydrocarbons are synthesized. These are fractionated in column 27; light motor fuel being withdrawn through line 28, diesel fuel through line 29, and a fraction having an end boiling point of about 700 DEG to 800 DEG through line 30 and/or line 31; the latter fraction is supplied to mixing line 2 through line 17. The overhead gases from column 27 are either recycled to the synthesis plant or passed through line 38 into steam feed line 19.ALSO:Liquid hydrocarbons are produced from water gas at atmospheric pressure, or pressures up to 150 lbs./sq. inch (gauge) using a catalyst containing metallic cobalt, iron, nickel or copper, promoted with an oxide of chromium, zinc, aluminium, magnesium or the rare earth metals, and carried on kieselguhr, pumice, or hydrated silica and alumina gel. Optimum gas composition ranges from 0.5 to 2.5 volumes of hydrogen per volume of carbon monoxide. The reaction temperature is between 350 DEG and 430 DEG F. with catalysts containing cobalt and magnesia, and between 550 DEG and 650 DEG F. with those containing iron. Fluid catalyst technique may be employed.
GB24577/45A 1945-02-22 1945-09-21 Improvements in the distillation of mixtures of coal and hydrocarbon oil Expired GB602376A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US602376XA 1945-02-22 1945-02-22

Publications (1)

Publication Number Publication Date
GB602376A true GB602376A (en) 1948-05-26

Family

ID=22028231

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24577/45A Expired GB602376A (en) 1945-02-22 1945-09-21 Improvements in the distillation of mixtures of coal and hydrocarbon oil

Country Status (1)

Country Link
GB (1) GB602376A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0165305A1 (en) * 1983-12-12 1985-12-27 David L Baker Chemical reformer.

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0165305A1 (en) * 1983-12-12 1985-12-27 David L Baker Chemical reformer.
EP0165305A4 (en) * 1983-12-12 1988-01-26 David L Baker Chemical reformer.

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