Liquid propylene oligomers and methods of making same
US-9732300-B2 · Aug 15, 2017 · US
US9708549B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9708549-B2 |
| Application number | US-201314132208-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 18, 2013 |
| Priority date | Dec 18, 2013 |
| Publication date | Jul 18, 2017 |
| Grant date | Jul 18, 2017 |
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The present application relates to method for oligomerizing olefin or for producing polyalphaolefin utilizing catalyst mixtures comprising aluminum halides and an organic liquid carrier. A process comprising contacting 1) a catalyst mixture comprising i) an aluminum trihalide and ii) an organic liquid carrier comprising first olefins, wherein the organic liquid carrier first olefins comprise at least 60 mole % 1,2-disubstituted olefins, trisubstituted olefins, or any combination thereof; and 2) a monomer comprising second olefins to form an oligomer product. An oligomer product produced by the process comprising contacting 1) a catalyst mixture comprising i) an aluminum trihalide and ii) an organic liquid carrier comprising first olefins, wherein the organic liquid carrier olefins comprise at least 75 mole % 1,2-disubstituted olefins, trisubstituted olefins, or any combination thereof; and 2) a monomer comprising second olefins to form an oligomer product.
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What is claimed is: 1. A process comprising: contacting 1) a catalyst mixture comprising i) an aluminum trihalide and ii) an organic liquid carrier comprising first olefins, wherein the organic liquid carrier first olefins comprise at least 60 mole % 1,2-disubstituted olefins; and 2) a monomer comprising second olefins to form an oligomer product. 2. The process of claim 1 , wherein the organic liquid carrier first olefins comprise less than 5 mole % alpha olefins. 3. The process of claim 1 , wherein the organic liquid carrier first olefins comprise less than 20 mole % tetrasubstituted olefins, vinylidenes, or any combinations thereof. 4. The process of claim 1 , wherein the organic liquid carrier first olefins comprise at least 75 mole % 1,2-disubstituted olefins, wherein the 1,2-disubstituted olefins comprise C 6 to C 24 disubstituted olefins. 5. The process of claim 1 , wherein the aluminum trihalide comprises aluminum trichloride, aluminum tribromide, or any combination thereof. 6. The process of claim 1 , wherein the catalyst mixture has an aluminum trihalide to organic liquid carrier first olefins molal concentration ranging from 0.15 mole/kg to 4.0 mole/kg. 7. The process of claim 1 , wherein the catalyst mixture further comprises a promoter. 8. The process of claim 1 , wherein the catalyst mixture, the monomer, and a promoter are contacted to form an oligomer product. 9. The process of claim 7 , wherein the promoter comprises water, an alcohol, a carboxylic acid, an ester, a ketone, an ether, a halogenated hydrocarbon, or any combination thereof. 10. The process of claim 1 , wherein the catalyst mixture further comprises a metal halide, an alkyl metal halide, an alkyl metal compound, or any combination thereof or wherein the catalyst mixture, the monomer, and a metal halide, an alkyl metal halide, an alkyl metal compound, or any combination thereof are contacted to form the oligomer product; and wherein the metal halide and the aluminum trihalide are different. 11. The process of claim 1 , wherein the aluminum trihalide and the monomer are contacted at a molar ratio ranging from 5×10 −8 :1 to 1.1×10 −2 :1. 12. The process of claim 1 , wherein the monomer comprises C 3 to C 30 olefins. 13. The process of claim 1 , wherein the monomer comprises alpha olefins. 14. The process of claim 1 , wherein the monomer comprises 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, or any combination thereof. 15. The process of claim 1 , wherein the monomer comprises at least 50 mole % normal alpha olefins. 16. The process of claim 1 , wherein the oligomer product is formed under oligomerization conditions comprising a temperature ranging from 0° C. to 200° C. 17. The process of claim 1 , wherein the oligomer product is formed under oligomerization conditions comprising a substantial absence of an organic solvent. 18. The process of claim 1 , wherein at least 50 mole % of the monomer is converted to the oligomer product. 19. The process of claim 1 , further comprising contacting a reactor effluent with a catalyst deactivating agent. 20. The process of claim 1 , further comprising separating at least a portion of the oligomer product from the monomer, to yield a separated oligomer product. 21. The process of claim 20 , further comprising hydrogenating the separated oligomer product to form a polyalphaolefin.
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