GB734498A - Polymerisation of olefins - Google Patents

Polymerisation of olefins

Info

Publication number
GB734498A
GB734498A GB3045351A GB3045351A GB734498A GB 734498 A GB734498 A GB 734498A GB 3045351 A GB3045351 A GB 3045351A GB 3045351 A GB3045351 A GB 3045351A GB 734498 A GB734498 A GB 734498A
Authority
GB
United Kingdom
Prior art keywords
complex
boron fluoride
active
acids
organic compound
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
GB3045351A
Inventor
Hans Bohlbro
Knud Riishede
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 GB3045351A priority Critical patent/GB734498A/en
Publication of GB734498A publication Critical patent/GB734498A/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
    • 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
    • C07C2521/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • C07C2521/08Silica
    • 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
    • C07C2521/16Clays or other mineral silicates
    • 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
    • C07C2521/18Carbon
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treating Waste Gases (AREA)
  • Catalysts (AREA)

Abstract

Products of gasoline boiling range are obtained by polymerizing normally gaseous olefins in the vapour phase at 0-200, preferably 20-30 DEG C., in the presence of a complex of boron fluoride with a saturated organic compound containing at least two "active" oxygen atoms attached to different carbon atoms. "Active" oxygen atoms are those having one valency satisfied by a carbon atom and the other by an atom other than a second carbon atom. Thus, active oxygen groups are hydroxyl, carboxyl, and carbonyl. The carbon chain between the two active oxygens is desirably not more than four carbon atoms. Preferably the organic compound boils above 100 or 150 DEG C., and is liquid at normal temperatures or melts not greatly above 50, and preferably below about 60 DEG C. Examples of suitable compounds are polyhydric alcohols, polybasic acids or esters thereof, and hydroxy acids, e.g. ethylene glycol and its homologues, polyalkylene glycols, e.g. di- and tri-ethylene or propylene glycols, glycerol, glutaric and pimelic acids, methyl succinate, hydroxy-propionic and butyric acids and their homologues. The complex is generally prepared by adding boron fluoride in a molar ratio of 1-2 : 1 to the organic compound, at ordinary or slightly elevated temperature. The product is suitably adsorbed on a carrier, e.g. activated carbon or clay, fuller's earth, pumice, kieselguhr, silica or alumina gel. A preferred feed is cracked refinery gas. Pressure may be atmospheric, and is generally less than 10 atmos. The gas may be passed through a fixed bed of the catalyst on a carrier while supplementary complex or boron fluoride may be injected to maintain activity. Alternatively, a guard bed of absorbent may be provided on the outlet side of the catalyst chamber to absorb volatilized complex or boron fluoride. Direction of flow of the feed may then be reversed. In examples, a feed containing butenes, butanes, and propane is passed down through a bed of complex on activated carbon, the former containing BF3 and lactic acid or ethylene glycol, and reaction temperature being 20 DEG C., which may later be raised to 70 DEG , 90 DEG or 100 DEG C.ALSO:Catalysts for polymerizing normally gaseous olefins comprise a complex of boron fluoride with a saturated organic compound containing at least two "active" oxygen atoms attached to different carbon atoms. "Active" oxygen atoms are those having one valency satisfied by a carbon atom and the other by an atom other than a second carbon atom. Thus, active oxygen groups are hydroxyl, carboxyl, and carbonyl. The carbon chain between the two active oxygens is desirably not more than four carbon atoms. Preferably the organic compound boils above 100 DEG or 150 DEG C., and is liquid at normal temperatures or melts not greatly above 50, and preferably below about 60 DEG C. Examples of suitable compounds are polyhydric alcohols, polybasic acids or esters thereof, and hydroxy acids, e.g. ethylene glycol and its homologues, polyalkylene glycols, glycerol, glutaric and pimelic acids, methyl succinatel hydroxy-propionic and butyric acids and their homologues. The complex is generally prepared by adding boron fluoride in a molar ratio of 1-2 : 1 to the organic compound, at ordinary or slightly elevated temperature. The product is suitably adsorbed on a carrier, e.g. activated carbon or clay, fuller's earth, pumice, kieselguhr, silica or alumina gel. A preferred feed is cracked refinery gas. Pressure may be atmospheric and is generally less than 10 atoms. The gas may be passed through a fixed bed of the catalyst on a carrier while supplementary complex or boron fluoride may be injected to maintain activity. Alternatively, a guard bed of absorbent may be provided on the outlet side of the catalyst chamber to absorb volatilized complex or boron fluoride. Direction of flow of the feed may then be reversed. In examples, the complex contains BF3 and lactic acid or ethylene glycol and is supported on activated carbon.
GB3045351A 1951-12-31 1951-12-31 Polymerisation of olefins Expired GB734498A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3045351A GB734498A (en) 1951-12-31 1951-12-31 Polymerisation of olefins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3045351A GB734498A (en) 1951-12-31 1951-12-31 Polymerisation of olefins

Publications (1)

Publication Number Publication Date
GB734498A true GB734498A (en) 1955-08-03

Family

ID=10307928

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3045351A Expired GB734498A (en) 1951-12-31 1951-12-31 Polymerisation of olefins

Country Status (1)

Country Link
GB (1) GB734498A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0010372A1 (en) * 1978-10-16 1980-04-30 Allied Corporation Recyclable boron trifluoride catalyst and method of using same
US4409415A (en) * 1981-09-18 1983-10-11 Gulf Research & Development Company Olefin oligomerization using boron trifluoride and an alcohol-polyol cocatalyst
FR2548194A1 (en) * 1983-06-28 1985-01-04 Ato Chimie Process for the manufacture of difunctional alpha-omega oligoisobutylenes, and oligoisobutylenes thus obtained
GB2156377A (en) * 1984-03-26 1985-10-09 Chevron Res Co-oligomerization of olefins
US4910321A (en) * 1985-06-20 1990-03-20 University Of Akron Living catalysts, complexes and polymers therefrom
US4929683A (en) * 1986-08-25 1990-05-29 University Of Akron Living polymerization of olefin to end-functionalized polymers
US5003124A (en) * 1982-11-17 1991-03-26 Chemical Research & Licensing Company Oligomerization process
US5122572A (en) * 1985-06-20 1992-06-16 Kennedy Joseph P Living catalysts, complexes and polymers therefrom
US5190730A (en) * 1982-11-17 1993-03-02 Chemical Research & Licensing Company Reactor for exothermic reactions

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0010372A1 (en) * 1978-10-16 1980-04-30 Allied Corporation Recyclable boron trifluoride catalyst and method of using same
US4409415A (en) * 1981-09-18 1983-10-11 Gulf Research & Development Company Olefin oligomerization using boron trifluoride and an alcohol-polyol cocatalyst
US5003124A (en) * 1982-11-17 1991-03-26 Chemical Research & Licensing Company Oligomerization process
US5190730A (en) * 1982-11-17 1993-03-02 Chemical Research & Licensing Company Reactor for exothermic reactions
FR2548194A1 (en) * 1983-06-28 1985-01-04 Ato Chimie Process for the manufacture of difunctional alpha-omega oligoisobutylenes, and oligoisobutylenes thus obtained
GB2156377A (en) * 1984-03-26 1985-10-09 Chevron Res Co-oligomerization of olefins
US4910321A (en) * 1985-06-20 1990-03-20 University Of Akron Living catalysts, complexes and polymers therefrom
US5122572A (en) * 1985-06-20 1992-06-16 Kennedy Joseph P Living catalysts, complexes and polymers therefrom
US4929683A (en) * 1986-08-25 1990-05-29 University Of Akron Living polymerization of olefin to end-functionalized polymers

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