GB734264A - Polymerisation of olefins - Google Patents
Polymerisation of olefinsInfo
- 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
Links
- 150000001336 alkenes Chemical class 0.000 title abstract 3
- 229910015900 BF3 Inorganic materials 0.000 abstract 10
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 10
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 8
- 239000000499 gel Substances 0.000 abstract 8
- 239000003054 catalyst Substances 0.000 abstract 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract 4
- JLDSOYXADOWAKB-UHFFFAOYSA-N aluminium nitrate Chemical compound [Al+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O JLDSOYXADOWAKB-UHFFFAOYSA-N 0.000 abstract 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 4
- 239000000395 magnesium oxide Substances 0.000 abstract 4
- 239000000377 silicon dioxide Substances 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- 230000002378 acidificating effect Effects 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 238000005336 cracking Methods 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- 230000000379 polymerizing effect Effects 0.000 abstract 2
- 235000019353 potassium silicate Nutrition 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000000741 silica gel Substances 0.000 abstract 2
- 229910002027 silica gel Inorganic materials 0.000 abstract 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 abstract 2
- 239000002002 slurry Substances 0.000 abstract 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 1
- 230000000630 rising effect Effects 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
-
- 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
- C07C2521/12—Silica and alumina
-
- 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
- C07C2521/14—Silica and magnesia
-
- 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
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.
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)
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 |
-
1951
- 1951-12-31 GB GB30454/51A patent/GB734264A/en not_active Expired
Cited By (3)
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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