Process for the preparation of a branched polyolefin

Patent metadata

Field	Value
Publication number	US-10450388-B2
Application number	US-201515537926-A
Country	US
Kind code	B2
Filing date	Dec 23, 2015
Priority date	Dec 23, 2014
Publication date	Oct 22, 2019
Grant date	Oct 22, 2019

Abstract

The present invention relates to a process for the preparation of a branched polyolefin via the polymerization of an olefin monomer and an olefin monomer comprising a main group metal hydrocarbyl chain transfer agent. The invention moreover relates to polyolefins obtained by said process.

First claim

The invention claimed is:

1. A process for the preparation of a branched polyolefin, said process comprising the step of:
A) a polymerization step comprising copolymerizing at least one first type of olefin monomer and at least one second type of olefin monomer comprising a main group metal hydrocarbyl chain transfer agent functionality according to Formula 1a:
R 100 (n-2) R 101 M n+ R 102    (Formula 1a)

using a catalyst system to obtain a polyolefin having one or multiple main group metal end-functionalized branches; wherein said catalyst system comprises:
i) a metal catalyst or catalyst precursor comprising a metal from Group 3-10 of the IUPAC Periodic Table of elements;
ii) optionally a co-catalyst; and
iii) an additional chain transfer and/or chain shuttling agent comprising a main group metal hydrocarbyl or hydride;
wherein
M is a main group metal;
n is the oxidation state of M; and
R 100 , R 101 and R 102 of Formula 1a are each independently selected from the group consisting of a hydride, a C1-C18 hydrocarbyl group, or a hydrocarbyl group Q with the proviso that at least one of R 100 , R 101 and R 102 is a hydrocarbyl group Q, wherein hydrocarbyl group Q is according to Formula 1b:

(Formula 1b)

wherein
Z is bonded to M and Z is a C1-C18 hydrocarbyl group;
R 105 optionally forms a cyclic group with Z; and
R 103 and R 104 and R 105 are each independently selected from hydrogen or a hydrocarbyl group; and

B) contacting said main group metal hydrocarbyl functionalized branched growth product obtained in step A) with a quenching agent to obtain the branched polyolefin.

2. The process according to claim 1 , wherein the quenching agent in step B) is a protic reagent.

3. The process according to claim 1 ,
wherein R 100 , R 101 and R 102 are hydrocarbyl group Q or
wherein R 100 is a C2-C4 hydrocarbyl group and R 101 and R 102 is hydrocarbyl group Q or
wherein R 100 and R 101 are a C2-C4 hydrocarbyl group and R 102 is hydrocarbyl group Q.

4. The process according to any claim 1 , wherein the hydrocarbyl group Q according to Formula 1b is a linear α-olefin group or a cyclic unsaturated hydrocarbyl group.

5. The process according to claim 1 , wherein the at least one second type of olefin monomer comprising a main group metal hydrocarbyl chain transfer agent is selected from the group consisting of bis(isobutyl)(5-ethylen-yl-2-norbornene) aluminum, di(isobutyl)(7-octen-1-yl) aluminum, di(isobutyl)(5-hexen-1-yl) aluminum, di(isobutyl)(3-buten-1-yl) aluminum, tris(5-ethylen-yl-2-norbornene) aluminum, tris(7-octen-1-yl) aluminum, tris(5-hexen-1-yl) aluminum, or tris(3-buten-1-yl) aluminum, ethyl(5-ethylen-yl-2-norbornene) zinc, ethyl(7-octen-1-yl) zinc, ethyl(5-hexen-1-yl) zinc, ethyl(3-buten-1-yl) zinc, bis(5-ethylen-yl-2-norbornene) zinc, bis(7-octen-1-yl) zinc, bis(5-hexen-1-yl) zinc, and bis(3-buten-1-yl) zinc.

6. The process according to claim 1 , wherein the co-catalyst is selected from the group consisting of MAO, DMAO, MMAO, SMAO, fluorinated aryl borane and fluorinated aryl borane borate.

7. The process according to claim 1 , wherein the metal catalyst used in step A) comprises a metal selected from the group consisting of Ti, Zr, Hf, V, Cr, Fe, Co, Ni, and Pd.

8. The process according to claim 7 , wherein said metal catalyst is a Group 4 single-site catalyst, optionally a metallocene or a post-metallocene.

9. The process according to claim 8 , wherein said catalyst is a C s -, C 1 -, or C 2 -symmetric zirconium metallocene.

10. The process according to claim 1 , wherein the additional chain transfer and/or chain shuttling agent is selected from the group consisting of hydrocarbyl aluminum, hydrocarbyl magnesium, hydrocarbyl zinc, hydrocarbyl gallium, hydrocarbyl boron, hydrocarbyl calcium, aluminum hydride, magnesium hydride, zinc hydride, gallium hydride, boron hydride, calcium hydride and a combination thereof.

11. The process according to claim 1 , wherein the at least one first type of olefin monomer used in step A) is selected from the group consisting of ethylene, propylene, 1-butene, 4-methyl-1-pentene, 1-pentene, 1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene, 1-undecene, 1-dodecene, 1-tridecene, 1-tetradecene, 1-pentadecene, 1-hexadecene, 1-heptadecene, 1-octadecene, 1-cyclopentene, cyclopentene, cyclohexene, norbornene, ethylidene-norbornene, vinylidene-norbornene, and a combination thereof.

12. The process according to claim 1 , wherein the branched polyolefin has a number average molecular weight (Mn) between 500 and 1,000,000 g/mol and a polydispersity index (Ð=M w /M n ) of between 1.1 and 5.0.

13. The process according to claim 1 , wherein R 100 and R 101 are isobutyl and R 102 is hydrocarbyl group Q.

14. The process according to claim 13 , wherein the hydrocarbyl group Q according to Formula 1b is oct-7-en-1-yl or 5-alkylenebicyclo[2.2.1]hept-2-ene.

15. The process according to claim 11 , wherein the at least one second type of olefin monomer comprising a main group metal hydrocarbyl chain transfer agent is selected from the group consisting of bis(isobutyl)(5-ethylen-yl-2-norbornene) aluminum, di(isobutyl)(7-octen-1-yl) aluminum, di(isobutyl)(5-hexen-1-yl) aluminum, di(isobutyl)(3-buten-1-yl) aluminum, tris(5-ethylen-yl-2-norbornene) aluminum, tris(7-octen-1-yl) aluminum, tris(5-hexen-1-yl) aluminum, or tris(3-buten-1-yl) aluminum, ethyl(5-ethylen-yl-2-norbornene) zinc, ethyl(7-octen-1-yl) zinc, ethyl(5-hexen-1-yl) zinc, ethyl(3-buten-1-yl) zinc, bis(5-ethylen-yl-2-norbornene) zinc, bis(7-octen-1-yl) zinc, bis(5-hexen-1-yl) zinc, and bis(3-buten-1-yl) zinc.

16. The process according to claim 15 , wherein
the co-catalyst is selected from the group consisting of MAO, DMAO, MMAO, SMAO, fluorinated aryl borane and fluorinated aryl borane borate;
the metal catalyst used in step A) comprises Ti, Zr or Hf; and
the additional chain transfer and/or chain shuttling agent is selected from the group consisting of hydrocarbyl aluminum, hydrocarbyl magnesium, hydrocarbyl zinc, hydrocarbyl gallium, hydrocarbyl boron, hydrocarbyl calcium, aluminum hydride, magnesium hydride, zinc hydride, gallium hydride, boron hydride, calcium hydride, and a combination thereof.

17. The process according to claim 16 , wherein the at least one first type of olefin monomer used in step A) is selected from the group consisting of ethylene, propylene, 1-butene, 4-methyl-1-pentene, 1-pentene, 1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene, 1-undecene, 1-dodecene, 1-tridecene, 1-tetradecene, 1-pentadecene, 1-hexadecene, 1-heptadecene, 1-octadecene, 1-cyclopentene, cyclopentene, cyclohexene, norbornene, ethylidene-norbornene, vinylidene-norbornene, and a combination thereof.

18. The process of according to claim 17 , wherein the branched polyolefin has a number average molecular weight (Mn) between 500 and 1,000,000 g/mol and a polydispersity index (Ð=M w /M n ) of between 1.1 and 5.0.

19. The process according to claim 17 , wherein said catalyst is a bridged bis-indenyl zirconium dihalide.

20. The process according to claim 19 , wherein the branched polyolefin has a number average molecular weight (Mn) between 500 and 1,000,000 g/mol and a polydispersity index (Ð=M w /M n ) of between 1.1 and 5.0.

Assignees

• Sabic Global Technologies Bv

Inventors

• Duchateau Robbert R
• Bouyahyi Miloud
• Jasinska-Walc Lidia
• Zuideveld Martin Alexander

Classifications

• C08F10/00

  Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond · CPC title

• C08F4/65927

  two cyclopentadienyl rings being mutually bridged · CPC title

• C08F210/16 Primary

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

• C08F2/38 Primary

  Polymerisation using regulators, e.g. chain terminating agents {, e.g. telomerisation} · CPC title

• C08F210/14

  Monomers containing five or more carbon atoms · CPC title