GB1204863A - Dimerization process - Google Patents
Dimerization processInfo
- Publication number
- GB1204863A GB1204863A GB5497767A GB5497767A GB1204863A GB 1204863 A GB1204863 A GB 1204863A GB 5497767 A GB5497767 A GB 5497767A GB 5497767 A GB5497767 A GB 5497767A GB 1204863 A GB1204863 A GB 1204863A
- Authority
- GB
- United Kingdom
- Prior art keywords
- propylene
- ethylene
- nix
- pentene
- dimers
- 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
- 238000006471 dimerization reaction Methods 0.000 title abstract 3
- 238000000034 method Methods 0.000 title 1
- -1 acyclic olefin Chemical class 0.000 abstract 5
- 239000000539 dimer Substances 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- 239000005977 Ethylene Substances 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- 150000001336 alkenes Chemical class 0.000 abstract 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 abstract 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 abstract 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 abstract 1
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 abstract 1
- QYYQTLLGVAPKPN-UHFFFAOYSA-N 1-ethylcyclopentene Chemical compound CCC1=CCCC1 QYYQTLLGVAPKPN-UHFFFAOYSA-N 0.000 abstract 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 150000001399 aluminium compounds Chemical class 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 abstract 1
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 abstract 1
- 239000004913 cyclooctene Substances 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 1
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 abstract 1
- 150000003254 radicals Chemical class 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
- C07C2/26—Catalytic processes with hydrides or organic compounds
- C07C2/36—Catalytic processes with hydrides or organic compounds as phosphines, arsines, stilbines or bismuthines
-
- 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
- C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- C07C2531/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- C07C2531/22—Organic complexes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- C07C2531/24—Phosphines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US59897566A | 1966-12-05 | 1966-12-05 | |
| US67400467A | 1967-10-09 | 1967-10-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1204863A true GB1204863A (en) | 1970-09-09 |
Family
ID=27083204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5497767A Expired GB1204863A (en) | 1966-12-05 | 1967-12-04 | Dimerization process |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS4939643B1 (enrdf_load_stackoverflow) |
| BE (1) | BE707477A (enrdf_load_stackoverflow) |
| CA (1) | CA1004235A (enrdf_load_stackoverflow) |
| DE (1) | DE1667228A1 (enrdf_load_stackoverflow) |
| ES (1) | ES347915A1 (enrdf_load_stackoverflow) |
| FR (1) | FR1577248A (enrdf_load_stackoverflow) |
| GB (1) | GB1204863A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009070858A1 (en) * | 2007-12-05 | 2009-06-11 | Braskem S. A. | Integrated process for the production of ethylene-butylene copolymer, an ethylene-butylene copolymer and the use of ethylene and 1-butylene, as comonomer, sourced from renewable natural raw materials |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2709884C3 (de) * | 1977-03-07 | 1981-07-23 | Institut Neftechimiceskogo Sinteza Imeni A.V. Topcieva Akademii Nauk Sssr, Moskva | Verfahren zur Dimerisation oder Codimerisierung von Olefinen |
| DE2709883C3 (de) * | 1977-03-07 | 1981-07-16 | Institut Neftechimiceskogo Sinteza Imeni A.V. Topcieva Akademii Nauk Sssr, Moskva | Verfahren zum Dimerisieren bzw. Codimerisieren von Olefinen |
| DE2709885C3 (de) * | 1977-03-07 | 1981-06-19 | Institut neftechimičeskogo sinteza imeni A.V. Topčieva Akademii Nauk SSSR, Moskva | Verfahren zur Dimerisation von Olefinen |
| JPS61187504U (enrdf_load_stackoverflow) * | 1985-05-16 | 1986-11-22 | ||
| JPS6346101A (ja) * | 1986-04-09 | 1988-02-27 | アキレス株式会社 | 静電気帯電防止靴 |
| FR2995893B1 (fr) * | 2012-09-21 | 2014-09-05 | Axens | Procede de production de butadiene-1,3 mettant en oeuvre la dimerisation de l'ethylene et la deshydrogenation des butenes obtenus |
-
1967
- 1967-10-02 CA CA001,463A patent/CA1004235A/en not_active Expired
- 1967-12-04 GB GB5497767A patent/GB1204863A/en not_active Expired
- 1967-12-04 ES ES347915A patent/ES347915A1/es not_active Expired
- 1967-12-04 BE BE707477D patent/BE707477A/xx unknown
- 1967-12-05 JP JP7813867A patent/JPS4939643B1/ja active Pending
- 1967-12-05 DE DE19671667228 patent/DE1667228A1/de active Pending
- 1967-12-05 FR FR1577248D patent/FR1577248A/fr not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009070858A1 (en) * | 2007-12-05 | 2009-06-11 | Braskem S. A. | Integrated process for the production of ethylene-butylene copolymer, an ethylene-butylene copolymer and the use of ethylene and 1-butylene, as comonomer, sourced from renewable natural raw materials |
| US8222354B2 (en) | 2007-12-05 | 2012-07-17 | Braskem S.A. | Integrated process for the production of ethylene-butylene copolymer, an ethylene-butylene copolymer and the use of ethylene and 1-butylene, as comonomer, sourced from renewable natural raw materials |
Also Published As
| Publication number | Publication date |
|---|---|
| BE707477A (enrdf_load_stackoverflow) | 1968-06-04 |
| ES347915A1 (es) | 1969-06-01 |
| CA1004235A (en) | 1977-01-25 |
| JPS4939643B1 (enrdf_load_stackoverflow) | 1974-10-28 |
| FR1577248A (enrdf_load_stackoverflow) | 1969-08-08 |
| DE1667228A1 (de) | 1972-03-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |