GB671334A - Improvements in or relating to the solvent extraction of hydrocarbon or fatty oils - Google Patents

Improvements in or relating to the solvent extraction of hydrocarbon or fatty oils

Info

Publication number
GB671334A
GB671334A GB24670/48A GB2467048A GB671334A GB 671334 A GB671334 A GB 671334A GB 24670/48 A GB24670/48 A GB 24670/48A GB 2467048 A GB2467048 A GB 2467048A GB 671334 A GB671334 A GB 671334A
Authority
GB
United Kingdom
Prior art keywords
solvent
water
oil
rich
recycled
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
GB24670/48A
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
Publication of GB671334A publication Critical patent/GB671334A/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
    • C10G21/00Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents

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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

In a process of fractionating hydrocarbon or fatty oils, the oil is subjected to solvent extraction to give extract and raffinate phases, and at least one of these phases is separately distilled in the presence of a substantial amount of recycled water in a primary distillation zone. The liquid residue from this distillation consists of an oil fraction substantially free of solvent while the distillate consists of solvent containing small amounts of oil and water. This distillate is allowed to settle in a primary settling zone and forms a plurality of layers comprising a water-rich layer containing small amounts of solvent and oil and a solvent-rich layer containing small amounts of oil and water. A portion of the water-rich layer is recycled to the primary distillation zone and forms the recycled water referred to above. The remainder of the water-rich layer and the solvent-rich layer are subjected to further treatment, including separate fractional distillation, to recover solvent and residual oil, the recovered solvent being recycled to the extraction zone. The solvent employed is an organic liquid partially miscible with water and so chosen that the oil to be fractionated contains at least a small proportion of constituents having true boiling points in the range of the solvent boiling temperature or below. In the fractionation of kerosine, low-boiling gas oil or fatty oil (whether of animal or vegetable origin), a suitable solvent is furfural, but other solvents mentioned are other furan derivatives, other aldehydes such as benzaldehyde, ketones and nitrobenzene. Gas oils which may be fractionated include those derived from thermal or catalytic cracking but the process is particularly applicable to the preparation of diesel fuel from a gas oil obtained by catalytic cracking of petroleum oil. According to one form of the invention, the extract and raffinate phases are separately subjected to fractional distillation which may be azeotropic in character. The resulting distillates are separately subjected to settling in the presence of water with the formation of oil-rich, water-rich and solvent-rich layers, and liquid streams are continuously withdrawn from these separate layers for further treatment. The oil-rich liquids derived from both the extract and raffinate phases are preferably recycled at least in part to the raffinate phase fractionating zone, although they may be recycled to the extract phase fractionating zone. The water-rich liquid is recycled in part to the fractionating zone from which it is derived, while the remainder is passed to a secondary fractionating zone for recovery of solvent and elimination of water. The solvent-rich liquids are passed to a tertiary fractionating zone to dry the solvent. Provision may be made for recycling a portion of the solvent-rich liquid directly to the extraction zone to which is also returned the dried solvent. The portion recycled to the extraction zone preferably should come from the settling zone for the extract phase. The proportions of solvent-rich liquid recycled and passed to the tertiary fractionating zone are correlated to control the water or oil content of the solvent in the extraction zone. This water content is maintained not in excess of that required to saturate the solvent, but the extraction may be carried out with substantially dry solvent. If necessary, water may be introduced into the system at a point in advance of the extraction tower. The secondary and tertiary fractionating operations are operated so as to produce distillates which, upon settling in the presence of each other, separate into secondary oil-rich, water-rich and solvent-rich layers. The oil-rich layer is continuously withdrawn and, for the most part, recycled to the primary extract phase fractionating zone. The portion not recycled is treated to remove residual solvent. The secondary solvent-rich phase is advantageously passed to the tertiary fractionating zone wherein water and some oil is stripped from the solvent, the resulting recovered dry solvent being recycled for reuse. The secondary water-rich liquid is recycled as reflux to both the secondary and tertiary fractionating zones.
GB24670/48A 1947-10-07 1948-09-21 Improvements in or relating to the solvent extraction of hydrocarbon or fatty oils Expired GB671334A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US671334XA 1947-10-07 1947-10-07

Publications (1)

Publication Number Publication Date
GB671334A true GB671334A (en) 1952-04-30

Family

ID=22073927

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24670/48A Expired GB671334A (en) 1947-10-07 1948-09-21 Improvements in or relating to the solvent extraction of hydrocarbon or fatty oils

Country Status (1)

Country Link
GB (1) GB671334A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0043267A1 (en) * 1980-06-30 1982-01-06 Union Carbide Corporation Method of separating aromatic and nonaromatic hydrocarbons in mixed hydrocarbon feeds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0043267A1 (en) * 1980-06-30 1982-01-06 Union Carbide Corporation Method of separating aromatic and nonaromatic hydrocarbons in mixed hydrocarbon feeds

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