GB734264A - Polymerisation of olefins - Google Patents

Polymerisation of olefins

Info

Publication number
GB734264A
GB734264A GB30454/51A GB3045451A GB734264A GB 734264 A GB734264 A GB 734264A GB 30454/51 A GB30454/51 A GB 30454/51A GB 3045451 A GB3045451 A GB 3045451A GB 734264 A GB734264 A GB 734264A
Authority
GB
United Kingdom
Prior art keywords
silica
gel
magnesia
alumina
per cent
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
GB30454/51A
Inventor
Hans Bohlbro
Knud Rushede
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
Priority to GB30454/51A priority Critical patent/GB734264A/en
Publication of GB734264A publication Critical patent/GB734264A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08Catalytic processes
    • C07C2/14Catalytic processes with inorganic acids; with salts or anhydrides of acids
    • C07C2/20Acids of halogen; Salts thereof ; Complexes thereof with organic compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/06Halogens; Compounds thereof
    • 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
    • C07C2521/12Silica and alumina
    • 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
    • C07C2521/14Silica and magnesia
    • 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
    • C07C2527/08Halides
    • C07C2527/12Fluorides
    • C07C2527/1213Boron fluoride

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Catalysts (AREA)

Abstract

Products of gasoline boiling range are obtained by polymerizing normally gaseous olefins in the vapour phase at 0-200 DEG , preferably 20-30 DEG C., in the presence of boron fluoride chemisorbed on a binary or ternary gel which is itself active as a catalyst for cracking hydrocarbon oils. Such gels include silica-alumina, magnesia, zirconia or titania, and silica-alumina-magnesia. The major component of the gel is preferably acidic. Thus, 60-90 per cent may be silica. A silica sol may be formed by acidifying water-glass solution, this being allowed to set to a gel, impregnated with a salt of the second metal, e.g. aluminium nitrate, precipitated with ammonia, washed, and heated to activate. Alternatively, the wet silica gel is mixed with a slurry of magnesia, dried, and activated. Particles of 2-10 mm. may be used and boron fluoride adsorbed equivalent, for example, to 5-40 per cent by weight. The feed gas such as cracked refinery gas is passed through a bed of the catalyst at atmospheric or higher pressure, e.g. up to 10 atmos. Make-up BF3 may be added, e.g. in the feed, or a guard bed used to adsorb volatilized BF3, the direction of flow being later reversed. In an example, a C4 feed is passed at 133 vols/vol. catalyst/hour over a commercial silica-alumina pre-dried at 200 DEG C. for 3 days and on which 20 per cent BF3 is adsorbed, the temperature being 20 DEG C. initially and rising to 100 DEG C. Specification 536,813 is referred to.ALSO:Catalysts for polymerizing normally gaseous olefins comprise boron fluoride chemisorbed on a binary or ternary gel which is itself active as a catalyst for cracking hydrocarbon oils. Such gels include silica-alumina, magnesia, zirconia or titania, and silica - alumina - magnesia. The major component of the gel is preferably acidic. Thus, 60-90 per cent may be silica. A silica sol may be formed by acidifying water glass solution, this being allowed to set to a gel, impregnated with a salt of the second metal, e.g. aluminium nitrate, precipitated with ammonia, washed, and heated to activate. Alternatively, the wet silica gel is mixed with a slurry of magnesia, dried, and activated. Particles of 2-10 mm. may be used and boron fluoride adsorbed equivalent, for example, to 5-40 per cent by weight. The feed gas such as cracked refinery gas is passed through a bed of the catalyst at atmospheric or higher pressure, e.g. up to 10 atmos. Make-up BF3 may be added, e.g. in the feed, or a guard bed used to adsorb volatilized BF3, the direction of flow being later reversed. In an example, a C4 feed is passed over a commercial silica-alumina pre-dried at 200 DEG C. for 3 days and on which 20 per cent BF3 is adsorbed. Specification 536,813, [Group IV], is referred to.
GB30454/51A 1951-12-31 1951-12-31 Polymerisation of olefins Expired GB734264A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB30454/51A GB734264A (en) 1951-12-31 1951-12-31 Polymerisation of olefins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB30454/51A GB734264A (en) 1951-12-31 1951-12-31 Polymerisation of olefins

Publications (1)

Publication Number Publication Date
GB734264A true GB734264A (en) 1955-07-27

Family

ID=10307945

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30454/51A Expired GB734264A (en) 1951-12-31 1951-12-31 Polymerisation of olefins

Country Status (1)

Country Link
GB (1) GB734264A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1118181B (en) * 1960-06-18 1961-11-30 Gelsenberg Benzin Ag Process for the alkylation of isobutane with ethylene over solid catalysts containing boron trifluoride
US4490571A (en) * 1983-10-05 1984-12-25 Uop Inc. Oligomerization of olefins
GB2207614B (en) * 1987-07-29 1992-01-08 Nikki Chem Co Ltd Method for preparation of dialkylnaphthalenes and catalyst for the same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1118181B (en) * 1960-06-18 1961-11-30 Gelsenberg Benzin Ag Process for the alkylation of isobutane with ethylene over solid catalysts containing boron trifluoride
US4490571A (en) * 1983-10-05 1984-12-25 Uop Inc. Oligomerization of olefins
GB2207614B (en) * 1987-07-29 1992-01-08 Nikki Chem Co Ltd Method for preparation of dialkylnaphthalenes and catalyst for the same

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