Catalysts for the formation of multimodal polymers

Patent metadata

Field	Value
Publication number	US-10087268-B2
Application number	US-201615252684-A
Country	US
Kind code	B2
Filing date	Aug 31, 2016
Priority date	Oct 22, 2015
Publication date	Oct 2, 2018
Grant date	Oct 2, 2018

Abstract

Disclosed are methods for polymerizing olefin monomers comprising contacting one or more olefin monomers with a cosupported catalyst system and an activator. Also disclosed are polymers produced using the catalyst systems and methods disclosed herein. The polymers have a multimodal molecular weight distribution and may be produced in a single reactor.

First claim

What is claimed is:

1. A supported catalyst system comprising a catalyst compound represented by Formula I and a catalyst compound represented by Formula II, wherein Formula I is:

where T is a bridging group; N is nitrogen; M* is Cr, Mo, or W, where M* is in a +3 oxidation state prior to contacting with activator; each X is, independently, selected from the group consisting of hydrocarbyl radicals having from 1 to 20 carbon atoms, hydrides, amides, alkoxides, sulfides, phosphides, halides, dienes, amines, phosphines, ethers, and a combination thereof, including that two X's may form a part of a fused ring or a ring system;
each R 1 , R 2 , R 3 , and R 4 is, independently, hydrogen, a C 1 to C 12 hydrocarbyl, a substituted C 1 to C 12 hydrocarbyl, a heteroatom, or substituted heteroatom group; and each R 5 and R 6 is, independently, a C 1 to C 12 hydrocarbyl, a substituted C 1 to C 12 hydrocarbyl, a heteroatom, or substituted heteroatom group, where the R 5 and R 6 groups may form a fused ring or multicenter fused ring system where the rings may be aromatic, partially saturated or saturated; and
Formula II is:

where M is a group 4 metal; T* is a group 14 atom; D is a substituted or unsubstituted aromatic group; R a and R b are, independently, hydrogen, halogen, or a C 1 to C 20 substituted or unsubstituted hydrocarbyl, and R a and R b can form a cyclic structure including substituted or unsubstituted aromatic, partially saturated, or saturated cyclic or fused ring system; each X 1 and X 2 is, independently, selected from the group consisting of C 1 to C 20 substituted or unsubstituted hydrocarbyl groups, hydrides, amides, amines, alkoxides, sulfides, phosphides, halides, dienes, phosphines, and ethers; and X 1 and X 2 can form a cyclic structure including aromatic, partially saturated, or saturated cyclic or fused ring system; each of R 11 , R 12 , R 13 , R 14 , and R 15 is, independently, hydrogen, halide, alkoxide or a C 1 to C 40 substituted or unsubstituted hydrocarbyl group, and any of adjacent R 12 , R 13 , R 14 , and/or R 15 groups may form a fused ring or multicenter fused ring systems, where the rings may be substituted or unsubstituted, and may be aromatic, partially unsaturated, or unsaturated; and each of R 7 , R 8 , R 9 , and R 10 is, independently, hydrogen or a C 1 to C 40 substituted or unsubstituted hydrocarbyl group; and further provided that at least two of R 7 , R 8 , R 9 , and R 10 are C 1 to C 40 substituted or unsubstituted hydrocarbyl groups.

2. The catalyst system of claim 1 , wherein M* is Cr and M is Zr.

3. The catalyst system of claim 1 , wherein R 5 and R 6 form a fused ring or multicenter fused ring system where the rings may be aromatic, partially saturated, or saturated.

4. The catalyst system of claim 1 , wherein N(R 5 )(R 6 ) is selected from the group consisting of pyrrolidine, aziridine, azetidine, piperidine, azepane, azocane, azonane, azecane, 1H-azirine, 1,2-dihydroazete, 2-pyrroline, 3-pyrroline, 1,4-dihydropyridine, azepine, azonine, indole, isoindole, indoline, isoindoline, or a substituted analog thereof.

5. The catalyst system of claim 1 , wherein each R 5 and R 6 , is, independently, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, docecyl, or an isomer thereof, or Cl, Br, F, I or Si; and each R 1 , R 2 , R 3 , R 4 , R 8 , R 9 , R 10 , and R 11 is, independently, selected from the group consisting of hydrogen, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, docecyl, or an isomer thereof, Cl, F, I, Br, and Si.

6. The catalyst system of claim 1 , wherein each X is, independently, selected from chloride, bromide, methyl, ethyl, propyl, butyl, and pentyl.

7. The catalyst system of claim 1 , wherein T is represented by the formula, (R* 2 G) g , where each G is C, Si, or Ge, g is 1 or 2, and each R* is, independently, hydrogen, halogen, C 1 to C 20 hydrocarbyl or a C 1 to C 20 substituted hydrocarbyl, and two or more R* can form a cyclic structure including aromatic, partially saturated, or saturated cyclic or fused ring system.

8. The catalyst system of claim 1 , wherein the compound represented by Formula I comprises one or more of: ethylene (cyclopentadienyl)(pyrrolidine)chromium dichloride; dimethylsilyl (cyclopentadienyl)(pyrrolidine)chromium dichloride; phenylene (cyclopentadienyl)(pyrrolidine)chromium dichloride; and diphenylsilyl (cyclopentadienyl)(pyrrolidine)chromium dichloride; and the compound represented by Formula II comprises bis(1-methyl, 3-n-butyl cyclopentadienyl)zirconium dichloride.

9. The catalyst system of claim 1 , wherein D is selected from the group consisting of substituted or unsubstituted phenyl, naphthyl, biphenyl, cyclopropenyl, tropylium, cyclooctatetraenyl, furanyl, pyridinyl, borabenzyl, thiophenyl, azolyl, oxazolyl, and imidazolyl.

10. The catalyst system of claim 1 , wherein T* is silicon or germanium.

11. The catalyst system of claim 1 , wherein each R a and R b is, independently, selected from the group consisting of halides, C 1 to C 20 substituted or unsubstituted hydrocarbyl groups, and cyclic structures where R a and R b form a heterocyclopentyl, heterocyclobutyl, or heterocyclohexyl structure with T* being the heteroatom.

12. The catalyst system of claim 1 , wherein each X 1 and X 2 is, independently, selected from the group consisting of halides and C 1 to C 20 substituted or unsubstituted hydrocarbyl groups.

13. The catalyst system of claim 1 , wherein each of R 7 , R 8 , R 9 R 10 , R 11 , R 12 , R 13 , R 14 , and R 15 is, independently, hydrogen or a C 1 to C 20 substituted or unsubstituted hydrocarbyl group.

14. The catalyst system of claim 1 , wherein each of R 7 , R 8 , R 9 , and R 10 is, independently, selected from the group consisting of methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, t-butyl, pentyl, hexyl, heptyl, octyl, decyl, and undecyl groups.

15. The catalyst system of claim 1 , wherein adjacent R 7 , R 8 , R 9 , and/or R 10 groups fuse together with the cyclopentadienyl group to form a substituted or unsubstituted fluorene.

16. The catalyst system of claim 1 , wherein each R a and R b is, independently, selected from the group consisting of chlorides, fluorides, methyl, and ethyl groups.

17. The catalyst system of claim 1 , wherein T* is silicon or germanium; each R a and R b is, independently, selected from the group consisting of halides, C 1 to C 20 substituted or unsubstituted hydrocarbyl groups, and cyclic structures where R a and R b form a heterocyclopentyl, heterocyclobutyl, or heterocyclohexyl structure with T being the heteroatom; and each R 7 , R 8 , R 9 R 10 , R 11 , R 12 , R 13 , R 14 , and R 15 is, independently, hydrogen or a C 1 to C 20 substituted or unsubstituted hydrocarbyl group.

18. The catalyst system of claim 1 , wherein the support is silica.

19. The catalyst system of claim 1 , further comprising an activator.

20. The catalyst system of claim 19 , wherein the activator comprises aluminoxane, a non-coordinating anion activator, or a compound represented by the formula:
(Z) d + (A d− )

wherein Z is (L-H), L is an neutral Lewis base; H is hydrogen; (L-H) + is a Bronsted acid; A d− is a non-coordinating anion having the charge d-;

Assignees

• Exxonmobil Chemical Patents Inc

Inventors

• Alliger Glen E
• Mccullough Laughlin G

Classifications

• C08F2500/05

  Bimodal or multimodal molecular weight distribution · CPC title

• C08F210/16 Primary

  Copolymers of ethene with alpha-alkenes, e.g. EP rubbers · CPC title

• C08F4/65927

  two cyclopentadienyl rings being mutually bridged · CPC title

• C08F2500/12

  Melt flow index or melt flow ratio · CPC title

• C08F2420/01

  Cp or analog bridged to a non-Cp X neutral donor · CPC title