Methods for improving production in gas phase polymerization
US-12152095-B2 · Nov 26, 2024 · US
US12215181B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12215181-B2 |
| Application number | US-202017599095-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 24, 2020 |
| Priority date | Mar 28, 2019 |
| Publication date | Feb 4, 2025 |
| Grant date | Feb 4, 2025 |
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Embodiments include activators having a structure according to formula (I).
Opening claim text (preview).
The invention claimed is: 1. An activator having a structure according to formula (I): where: M is a metal in a +3 oxidation state, the metal being selected from boron, aluminum, gallium, scandium, yttrium, or a lanthanide; [Cat] + is + N(H)R N 3 , wherein each R N is independently (C 1 -C 20 ) alkyl; or + C(C 6 H 4 R C ) 3 , wherein each R C is independently chosen from (C 1 -C 30 ) alkyl; or [HN(R S )(R N ) 2 ] + , where R N is (C 1 -C 20 ) alkyl and R S is chosen from (C 1 -C 30 ) alkyl, (C 6 -C 20 ) aryl, (C 5 -C 20 ) heteroaryl, or —H; R 1 , R 2 , R 3 , R 4 R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are independently chosen from (C 1 -C 40 ) alkyl, (C 6 -C 40 ) aryl, —H, —NR C 2 , —OR C , —SR C , or halogen, wherein each R C is independently a (C 1 -C 30 ) hydrocarbyl or —H, provided at least one of R 1-4 , and one of R 5-8 , and one of R 9-12 , and one of R 13-16 is a fluorine-substituted (C 1 -C 40 ) alkyl, a fluorine-substituted (C 6 -C 40 ) aryl, or —F; and R 17 and R 18 are (C 1 -C 40 ) alkyl, (C 1 -C 40 ) heteroalkyl, a fluorine-substituted (C 1 -C 40 ) alkyl, or a fluorine-substituted (C 6 -C 40 ) aryl. 2. The activator of claim 1 , wherein R 1 , R 2 , R 3 , R 4 R 5 , R 6 , R 7 , R 8 , R 9 , R 10 R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are independently (C 1 -C 10 ) alkyl, —F, or —H, provided at least one of R 1-4 , and one of R 5-8 , and one of R 9-12 , and one of R 13-16 is a fluorine-substituted (C 1 -C 10 ) alkyl or —F. 3. The activator of claim 1 , wherein R 17 and R 18 are (C 1 -C 10 ) alkyl. 4. The activator of claim 1 , wherein [Cat] + is a protonated tertiary amine. 5. The activator of claim 1 , wherein [Cat] + is + N(H)R N 3 , wherein each R N is independently (C 1 -C 20 ) alkyl. 6. The activator of claim 1 , wherein: at least one of R 1 , R 2 , R 3 , and R 4 is —F or fluoroalkyl; at least one of R 5 , R 6 , R 7 , and R 8 is —F or fluoroalkyl; at least one of R 9 , R 10 , R 11 , and R 12 is —F or fluoroalkyl; and at least one of R 13 , R 14 , R 15 , and R 16 is —F or fluoroalkyl. 7. The activator of claim 1 , wherein: at least two of R 1 , R 2 , R 3 , and R 4 are —F or fluoroalkyl; at least two of R 5 , R 6 , R 7 , and R 8 are —F or fluoroalkyl; at least two of R 9 , R 10 , R 11 , and R 12 are —F or fluoroalkyl; and at least two of R 13 , R 14 , R 15 , and R 16 are —F or fluoroalkyl. 8. The activator of claim 1 , wherein: at least three of R 1 , R 2 , R 3 , and R 4 are —F or fluoroalkyl; at least three of R 5 , R 6 , R 7 , and R 8 are —F or fluoroalkyl; at least three of R 9 , R 10 , R 11 , and R 12 are —F or fluoroalkyl; and at least three of R 13 , R 14 , R 15 , and R 16 are —F or fluoroalkyl. 9. The activator of claim 1 , wherein: at least four of R 1 , R 2 , R 3 , and R 4 are —F or fluoroalkyl; at least four of R 5 , R 6 , R 7 , and R 8 are —F or fluoroalkyl; at least four of R 9 , R 10 , R 11 , and R 12 are —F or fluoroalkyl; and at least four of R 13 , R 14 , R 15 , and R 16 are —F or fluoroalkyl. 10. A catalyst system comprising an activator of claim 1 and a procatalyst, wherein the procatalyst is rendered catalytically active by contacting the procatalyst with the activator. 11. A process for polymerizing olefins, the process comprising contacting ethylene and optionally a (C 3 -C 40 )α-olefin in the presences of a catalysts system according to claim 10 .
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