GB897238A - Improvements relating to the removal of aromatics and sulphur from hydrocarbon feedstocks - Google Patents

Improvements relating to the removal of aromatics and sulphur from hydrocarbon feedstocks

Info

Publication number
GB897238A
GB897238A GB72960A GB72960A GB897238A GB 897238 A GB897238 A GB 897238A GB 72960 A GB72960 A GB 72960A GB 72960 A GB72960 A GB 72960A GB 897238 A GB897238 A GB 897238A
Authority
GB
United Kingdom
Prior art keywords
tungsten
catalyst
cobalt
hydrogen
molybdenum
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
GB72960A
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.)
DAVID LYCETT KNIGHTS
BP PLC
Original Assignee
DAVID LYCETT KNIGHTS
BP PLC
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 DAVID LYCETT KNIGHTS, BP PLC filed Critical DAVID LYCETT KNIGHTS
Priority to GB72960A priority Critical patent/GB897238A/en
Priority to FR849012A priority patent/FR1281534A/en
Priority to DE1961B0060773 priority patent/DE1238144B/en
Publication of GB897238A publication Critical patent/GB897238A/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
    • C10G65/00Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/04Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps
    • C10G65/08Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps at least one step being a hydrogenation of the aromatic hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/22Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
    • C07C5/2206Catalytic processes not covered by C07C5/23 - C07C5/31
    • C07C5/226Catalytic processes not covered by C07C5/23 - C07C5/31 with metals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/148Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
    • C07C7/163Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/02Boron or aluminium; Oxides or hydroxides thereof
    • C07C2521/04Alumina
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • C07C2523/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06Halogens; Compounds thereof
    • C07C2527/125Compounds comprising a halogen and scandium, yttrium, aluminium, gallium, indium or thallium
    • C07C2527/126Aluminium chloride

Landscapes

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

Abstract

Aromatics and sulphur are removed from feed-stocks boiling in the gasoline range (i.e. up to 400 DEG F.) and consisting of C4 or higher hydrocarbons containing aromatic hydrocarbons and sulphur compounds, by contacting the feedstock in the presence of hydrogen with a bed containing two catalysts, one consisting essentially of tungsten nickel sulphide and the other consisting essentially of cobalt and molybdenum oxides, either as such or in combined form, on a refractory oxide support, e.g. alumina. The reaction zone is maintained at a temperature of 400-900 DEG F. and a pressure of 50-1,200 psig. Preferably the catalysts are in separate portions of the bed, and are so arranged that the feedstock contacts the tungsten nickel sulphide catalyst first. The cobalt molybdenum catalyst preferably contains 1 to 10% of cobalt oxide, 5 to 40% of molybdenum oxide, and may also contain 0,1 to 6% of fluorine. The ratio of tungsten to nickel in the tungsten-nickel sulphide catalyst is preferably 3:1 to 10:1. The hydrogen sulphide may be removed from the product by stripping with an inert gas.ALSO:Prior to isomerisation, aromatics and sulphur compounds are removed from feedstocks boiling in the gasoline range (i.e. up to 400 DEG F) and consisting of C4 or higher hydrocarbons containing aromatic hydrocarbons and sulphur compounds, by contacting the feedstock in the presence of hydrogen with a bed containing two catalysts, one consisting essentially of tungsten nickel sulphide and the other consisting essentially of cobalt and molybdenum oxides, either as such or in combined form, on a refractory oxide support, e.g. alumina. The reaction zone is maintained at a temperature of 400 DEG F.-900 DEG F. and a pressure of 50-1200 p.s.i.g. Preferably the catalysts are in separate portions of the bed, and are so arranged that the feedstock contacts the tungsten nickel sulphide catalyst first. The cobalt molybdenum catalyst preferably contains 1%-10% of cobalt oxide, 5%-40% of molybdenum oxide, and may also contain 0.1%-6% of fluorine. The ratio of tungsten to nickel in the tungsten-nickel sulphide catalyst is preferably 3 : 1 to 10 : 1. The hydrogen sulphide may be removed from the product by stripping with an inert gas. The so treated desulphurised and dearomaticised feedstock is subjected to isomerisation by contacting it in the presence of hydrogen with a catalyst consisting essentially of an aluminium halide, for example the chloride or bromide, and a hydrogenating metal, which may be selected from Group VI(a) and VIII of the Periodic Table, preferably the platinum group, on a refractory oxide support, preferably alumina which may have been prepared from an alcoholate. The isomerisation is preferably carried out at 50 DEG F.-400 DEG F. and 0-2000 p.s.i.g., and may be effected either in the liquid or the vapour phase.
GB72960A 1960-01-08 1960-01-08 Improvements relating to the removal of aromatics and sulphur from hydrocarbon feedstocks Expired GB897238A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB72960A GB897238A (en) 1960-01-08 1960-01-08 Improvements relating to the removal of aromatics and sulphur from hydrocarbon feedstocks
FR849012A FR1281534A (en) 1960-01-08 1961-01-06 Process for removing aromatics and sulfur from raw materials containing hydrocarbons in c4 or above of the gasoline boiling range
DE1961B0060773 DE1238144B (en) 1960-01-08 1961-01-09 Process for the pretreatment of gasoline hydrocarbons for isomerization

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB72960A GB897238A (en) 1960-01-08 1960-01-08 Improvements relating to the removal of aromatics and sulphur from hydrocarbon feedstocks

Publications (1)

Publication Number Publication Date
GB897238A true GB897238A (en) 1962-05-23

Family

ID=9709512

Family Applications (1)

Application Number Title Priority Date Filing Date
GB72960A Expired GB897238A (en) 1960-01-08 1960-01-08 Improvements relating to the removal of aromatics and sulphur from hydrocarbon feedstocks

Country Status (3)

Country Link
DE (1) DE1238144B (en)
FR (1) FR1281534A (en)
GB (1) GB897238A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0504510A1 (en) * 1989-12-29 1992-09-23 Uop Combination process for hydrogenation and isomerization of benzene and paraffin-containing feedstocks

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5068025A (en) * 1990-06-27 1991-11-26 Shell Oil Company Aromatics saturation process for diesel boiling-range hydrocarbons

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE842991C (en) * 1944-01-11 1952-07-03 Basf Ag Process for improving the knock resistance of petrol
DE1018867B (en) * 1951-05-16 1957-11-07 Houdry Process Corp Process for the manufacture of catalysts
NL87006C (en) * 1952-05-15
US2769753A (en) * 1953-06-03 1956-11-06 Pure Oil Co Combination process for catalytic hydrodesulfurization and reforming of high sulfur hydrocarbon mixtures
BE545557A (en) * 1955-02-25 1900-01-01
US2900425A (en) * 1956-08-10 1959-08-18 Universal Oil Prod Co Isomerization process
US2863826A (en) * 1956-08-27 1958-12-09 Exxon Research Engineering Co Catalytic conversion of paraffins
AT200158B (en) * 1957-03-04 1958-10-25 Houdry Process Corp Process for the preparation of granulated catalysts suitable for isomerization and dehydrogenation.

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0504510A1 (en) * 1989-12-29 1992-09-23 Uop Combination process for hydrogenation and isomerization of benzene and paraffin-containing feedstocks

Also Published As

Publication number Publication date
FR1281534A (en) 1962-01-12
DE1238144B (en) 1967-04-06

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