Phosphine-imino-quinoline and related ligands for use in ethylene oligomerization processes
US-2024360052-A1 · Oct 31, 2024 · US
US9499455B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9499455-B2 |
| Application number | US-201514790734-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 2, 2015 |
| Priority date | Jul 4, 2014 |
| Publication date | Nov 22, 2016 |
| Grant date | Nov 22, 2016 |
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The invention concerns a process for the selective dimerization of ethylene to 1-butene employing a catalytic composition comprising at least one alkoxy or aryloxy titanium compound, at least one additive selected from ether type compounds and at least one aluminium compound.
Opening claim text (preview).
The invention claimed is: 1. A process for the selective dimerization of ethylene to 1-butene, said process comprising selectively dimerizing ethylene in the presence of a catalytic composition comprising at least one alkoxy or aryloxy titanium compound, at least one ether compound, and at least one aluminum compound, in which the molar ratio between the ether compound and the alkoxy or aryloxy titanium compound is more than 10 and the molar ratio between the aluminum compound and the alkoxy or aryloxy titanium compound is more than 4. 2. The process according to claim 1 , in which the molar ratio between the ether compound and the alkoxy or aryloxy titanium compound of the catalytic composition is in the range of 11 to 19. 3. The process according to claim 1 , in which the molar ratio between the aluminum compound and the alkoxy or aryloxy titanium compound of the catalytic composition is in the range of 5 to 15. 4. The process according to claim 1 , in which the alkoxy titanium compound is of the formula [Ti(OR) 4 ], in which R is a linear or branched alkyl radical containing 2 to 30 carbon atoms. 5. The process according to claim 1 , in which the aryloxy titanium compound is of the formula [Ti(OR′) 4 ], in which R′ is an aryl radical which is unsubstituted or is substituted with alkyl, aryl or aralkyl groups containing 2 to 30 carbon atoms. 6. The process according to claim 1 , in which the aluminum compound is selected from hydrocarbylaluminum compounds, tris(hydrocarbyl)aluminum compounds, chlorine-containing or bromine-containing hydrocarbylaluminum compounds, and aluminoxanes. 7. The process according to claim 6 , in which the aluminum compound is selected from dichloroethylaluminum, ethylaluminum sesquichloride, chlorodiethylaluminum, chlorodiisobutylaluminum, triethylaluminum, tripropylaluminum, and triisobutylaluminum. 8. The process according to claim 1 , wherein the titanium compound is [Ti(O n Bu) 4 ], the ether compound is tetrahydrofuran and is in a molar ratio with respect to the titanium compound which is more than 10, and the aluminum compound is triethylaluminum in a molar ratio with respect to the titanium compound which is more than 4. 9. The process according to claim 1 , in which the tetrahydrofuran is selected from diethyl ether, diisopropylether, 2-methoxy-2-methylpropane, 2-methoxy-2-methylbutane, 2,5-dihydrofuran, tetrahydrofuran, 2-methoxytetrahydrofuran, 2-methyltetrahydrofuran, 3-methyltetrahydrofuran, 2,3-dihydropyran, tetrahydropyran, 1,3-dioxolane, 1,3-dioxane, 1,4-dioxane, dimethoxyethane, di(2-methoxyethyl)ether, and benzofuran, used alone or in mixture. 10. The process according to claim 1 , in which the catalytic composition is used as a mixture with a solvent selected from aliphatic hydrocarbons, cycloaliphatic hydrocarbons, unsaturated hydrocarbons containing 4 to 20 carbon atoms, and chlorine-containing hydrocarbon, alone or in mixture. 11. The process according to claim 1 , wherein the dimerization reaction is performed under a total pressure of 0.5 to 20 MPa and at a temperature of 20° C. to 180° C. 12. The process according to claim 1 , carried out in a batch mode. 13. The process according to claim 1 , in which a selected volume of the catalytic composition is introduced into a reactor provided with stirring, heating and cooling means, the reactor is then pressurized using ethylene, and the temperature is adjusted. 14. The process for the selective dimerization of ethylene to 1-butene according to claim 1 , wherein a solution containing the titanium compound and the ether compound and a solution containing the aluminum compound are introduced separately into a reactor maintained under a constant pressure of ethylene in a manner so as to produce the catalytic composition. 15. The process for the selective dimerization of ethylene to 1-butene according to claim 1 , wherein a solution containing the titanium compound and the ether compound and a solution containing the aluminum compound are introduced into a first reactor/mixer in a manner so as to produce the catalytic composition, said composition then being continuously introduced into a reactor maintained under a constant pressure of ethylene. 16. A process for the preparation of a catalytic composition comprising at least one alkoxy or aryloxy titanium compound, at least one ether compound, and at least one aluminum compound, said process comprising; adding the aluminum compound to a solution containing the ether compound and the alkoxy or aryloxy titanium compound present in a molar ratio of more than 10, and the molar ratio of the aluminum compound to the titanium compound is more than 4. 17. The process according to claim 1 , carried out in a continuous implementational mode. 18. The process according to claim 2 , in which the molar ratio between the aluminum compound and the alkoxy or aryloxy titanium compound of the catalytic composition is in the range of 5 to 15. 19. The process according to claim 1 , wherein the alkoxy and aryloxy groups of said at least one alkoxy or aryloxy titanium compound are selected from tetraethoxy, tetraisopropoxy, tetra-n-butoxy, tetra-2-ethyl-hexyloxy, phenoxy, 2-methylphenoxy, 2,6-dimethylphenoxy, 2,4,6-trimethylphenoxy, 4-methylphenoxy, 2-phenylphenoxy, 2,6-diphenylphenoxy, 2,4,6-triphenylphenoxy, 4-phenylphenoxy, 2-tert-butyl-6-phenylphenoxy, 2,4-di-tert-butyl-6-phenylphenoxy, 2,6-diisopropylphenoxy, 2,6-di-tert-butylphenoxy, 4-methyl-2,6-di-tert-butylphenoxy, 2,6-dichloro-4-tert-butylphenoxy and 2,6-dibromo-4-tert-butylphenoxy, binaphthoxy, and 1,8-naphtalene-dioxy. 20. The process according to claim 1 , in which the catalytic composition is used as a mixture with a solvent selected from hexane, cyclohexane, heptane, butane or isobutane, a monoolefin containing 4 to 20 carbon atoms, a diolefin containing 4 to 20 carbon atoms, benzene, toluene, ortho-xylene, mesitylene, ethylbenzene, chlorobenzene and dichloromethane, alone or in mixture. 21. The process according to claim 1 , wherein the dimerization reaction is performed under a total pressure of 0.5 to 10 MPa and at a temperature of 40° C. to 140° C.
of aluminium or boron · CPC title
containing metal-to-carbon bond; Metal hydrides · CPC title
containing organic compounds or metal hydrides · CPC title
Addition reactions to C=C or C-C triple bonds · CPC title
Titanium · CPC title
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