GB734498A - Polymerisation of olefins - Google Patents
Polymerisation of olefinsInfo
- 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
Links
- 150000001336 alkenes Chemical class 0.000 title abstract 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 12
- 229910015900 BF3 Inorganic materials 0.000 abstract 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 10
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 6
- 150000002894 organic compounds Chemical class 0.000 abstract 6
- 239000003054 catalyst Substances 0.000 abstract 5
- 150000001721 carbon Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 239000007789 gas Substances 0.000 abstract 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 abstract 4
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical class CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000002250 absorbent Substances 0.000 abstract 2
- 230000002745 absorbent Effects 0.000 abstract 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 239000004927 clay Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- -1 fuller's earth Substances 0.000 abstract 2
- 150000002311 glutaric acids Chemical class 0.000 abstract 2
- 150000001261 hydroxy acids Chemical class 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 235000014655 lactic acid Nutrition 0.000 abstract 2
- 239000004310 lactic acid Substances 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000000155 melt Substances 0.000 abstract 2
- 150000003047 pimelic acids Chemical class 0.000 abstract 2
- 229920001515 polyalkylene glycol Polymers 0.000 abstract 2
- 230000000379 polymerizing effect Effects 0.000 abstract 2
- 150000007519 polyprotic acids Polymers 0.000 abstract 2
- 239000008262 pumice Substances 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 239000000377 silicon dioxide Substances 0.000 abstract 2
- 150000005846 sugar alcohols Polymers 0.000 abstract 2
- WXUAQHNMJWJLTG-VKHMYHEASA-N (S)-methylsuccinic acid Chemical compound OC(=O)[C@@H](C)CC(O)=O WXUAQHNMJWJLTG-VKHMYHEASA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 235000013844 butane Nutrition 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 235000013772 propylene glycol Nutrition 0.000 abstract 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation 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
- C07C2/06—Preparation 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
- C07C2/08—Catalytic processes
- C07C2/14—Catalytic processes with inorganic acids; with salts or anhydrides of acids
- C07C2/20—Acids of halogen; Salts thereof ; Complexes thereof with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- C07C2521/08—Silica
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/16—Clays or other mineral silicates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/18—Carbon
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/06—Halogens; Compounds thereof
- C07C2527/08—Halides
- C07C2527/12—Fluorides
- C07C2527/1213—Boron fluoride
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts 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.
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)
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 |
-
1951
- 1951-12-31 GB GB3045351A patent/GB734498A/en not_active Expired
Cited By (9)
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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