IP Library Granted Patent US 12,338,301
Granted Patent B2
US 12,338,301 · App. 17/771,835 · Granted Jun 24, 2025

Bimodal catalyst systems

Inventors: Andrew J. Young (Houston, TX); Roger L. Kuhlman (Lake Jackson, TX); Angela I. Padilla-Acevedo (Lake Jackson, TX); John F. Szul (Hurricane, WV)
Assignee: Dow Global Technologies LLC
C08F210/02C08F4/02C08F4/64193C08F4/6592C08F4/76C08F2420/04C08F2500/05
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Quick Facts
Patent No.
US 12,338,301
App. No.
17/771,835
Granted
Jun 24, 2025
Kind
B2
Abstract

Embodiments provide bimodal polymerization catalyst systems comprising metallocene olefin polymerization catalysts and biphenylphenol polymerization catalysts made from biphenylphenol polymerization precatalysts of Formula I.

Claims (41)

1. A bimodal polymerization catalyst system comprising:

a metallocene olefin polymerization catalyst; and

a biphenylphenol polymerization catalyst made from a biphenylphenol polymerization precatalyst of Formula I:

wherein each of R 7 and R 8 is independently a C 1 to C 20 alkyl, aryl or aralkyl, halogen, or a hydrogen;

wherein each of R 5 and R 10 is independently a C 1 to C 20 alkyl, aryl, aralkyl, halogen, an alkyl-or aryl-substituted silyl, or a hydrogen;

wherein each of R 2 and R 13 is independently a C 1 to C 20 alkyl, aryl or aralkylor a hydrogen;

wherein each of R 15 and R 16 is independently a 2,7-disubstituted carbazol-9-yl;

wherein L is a saturated C 2 -C 3 alkyl that forms a 2-carbon bridge or 3-carbon bridge between the two oxygen atoms to which L is bonded;

wherein each X is independently halogen, a hydrogen, a (C 1 -C 20 )alkyl, a (C 7 -C 20 )aralkyl, a (C 1 -C 6 )alkyl-substituted (C 6 -C 12 )aryl, a (C 1 -C 6 )alkyl-substituted benzyl, or —CH 2 Si (R c ) 3 , where R c is C 1 -C 12 hydrocarbon;

wherein each of R 1 , R 3 , R 4 , R 6 , R 9 , R 11 , R 12 , and R 14 is independently a hydrogen; and

wherein M is a heteroatom selected from a group consisting of Zr and Hf.

2. The bimodal polymerization catalyst system of claim 1 , wherein each of R 7 and R 8 is a C 1 alkyl.

3. The bimodal polymerization catalyst system of claim 1 , wherein each of R 5 and R 10 is a di-alkyl or tri-alkyl substituted silyl.

4. The bimodal polymerization catalyst system of claim 1 , wherein each R 2 and R 13 is a 1,1,3,3-tetramethylbutyl.

5. The bimodal polymerization catalyst system of claim 1 , wherein each of R 15 and R 16 is a 2,7-di-t-butylcarbazol-9-yl.

6. The bimodal polymerization catalyst system of claim 1 , wherein L is a saturated C 3 alkyl.

7. The bimodal polymerization catalyst system of claim 1 , wherein each X is a C 1 alkyl.

8. The bimodal polymerization catalyst system of claim 1 , wherein M is Zr.

9. The bimodal polymerization catalyst system of claim 1 , wherein M is Hf.

10. The bimodal polymerization catalyst system of claim 1 , wherein the metallocene olefin polymerization catalyst is made from a metallocene precatalyst selected from the group consisting of:

(pentamethylcyclopentadienyl)(propylcyclopentadienyl)MX 2 ,

(tetramethylcyclopentadienyl)(propylcyclopentadienyl)MX 2 ,

(tetramethylcyclopentadienyl)(butylcyclopentadienyl)MX 2 ,

(methylcyclopentadienyl)(1,3-dimethyl-tetrahydroindenyl)MX 2 ,

(cyclopentadienyl)(1,3-dimethyl-tetrahydroindenyl)MX 2 ,

(cyclopentadienyl)(4,7-dimethylindenyl)MX 2 ,

(cyclopentadienyl)(1,5-dimethylindenyl)MX 2 ,

(cyclopentadienyl)(1,4-dimethylindenyl)MX 2 ,

Me 2 Si(indenyl) 2 MX 2 ,

Me 2 Si(tetrahydroindenyl) 2 MX 2 ,

(n-propyl cyclopentadienyl) 2 MX 2 ,

(n-butyl cyclopentadienyl) 2 MX 2 ,

(1-methyl, 3-butyl cyclopentadienyl) 2 MX 2 ,

HN(CH 2 CH 2 N(2,4,6-Me 3 phenyl)) 2 MX 2 ,

HN(CH 2 CH 2 N(2,3,4,5,6-Mesphenyl)) 2 MX 2 ,

(butyl cyclopentadienyl) 2 MX 2 ,

(propyl cyclopentadienyl) 2 MX 2 , and mixtures thereof,

wherein M is Zr or Hf, and X is selected from F, Cl, Br, I, Me, benzyl, CH 2 SiMe 3 , or C 1 to C 5 alkyls or alkenyls.

11. The bimodal polymerization catalyst system of claim 1 , further comprising a silica support, which supports: (a) the metallocene olefin polymerization catalyst but not the biphenylphenol polymerization catalyst made from biphenylphenol polymerization precatalyst of Formula I, (b) the biphenylphenol polymerization catalyst made from the biphenylphenol polymerization precatalyst of Formula I, but not the metallocene olefin polymerization catalyst, or (c) a combination the metallocene olefin polymerization catalyst and the biphenylphenol polymerization catalyst made from a biphenylphenol polymerization precatalyst of Formula I.

12. A method of making the bimodal polymerization catalyst system of claim 1 , the method comprising making the biphenylphenol polymerization catalyst by contacting, under activating conditions, the biphenylphenol polymerization precatalyst of Formula I with an activator.

13. The method of claim 12 , wherein the activator is spray-dried on a silica support and the method comprises making the biphenylphenol polymerization catalyst by contacting, under activating conditions, the biphenylphenol polymerization precatalyst of Formula I with supported spray-dried activator.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 19, 2024
From: SZUL, JOHN F.
To: UNION CARBIDE CORPORATION
Reel/Frame 068997/0063 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 19, 2024
From: UNION CARBIDE CORPORATION
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 068997/0092 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 19, 2024
From: YOUNG, ANDREW J.; KUHLMAN, ROGER L.; PADILLA-ACEVEDO, ANGELA I.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 068635/0325 →
Continuity (2)
Provisional Application 62930450 · Nov 4, 2019
Related Publication 20220411546A1 · Dec 29, 2022
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