IP Library Granted Patent US 8,067,328
Granted Patent B2
US 8,067,328 · App. 11/660,050 · Granted Nov 29, 2011

Polymerisation and oligomerisation catalysts

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Quick Facts
Patent No.
US 8,067,328
App. No.
11/660,050
Granted
Nov 29, 2011
Kind
B2
Abstract

A polymerization catalyst composition comprising (1) a transition metal compound of Formula (A), Z being 5-membered heterocyclic containing at least one carbon, at least one nitrogen and at least one of nitrogen, sulphur and oxygen, the others being nitrogen or carbon; M is a Group 3 to 11 metal or a lanthamide metal; E 1 and E 2 are divalent groups of aliphatic, alicyclic, aromatic or alkyl substituted aromatic hydrocarbon, or heterocyclic; D 1 and D 2 are donor atoms or groups; X is an anionic group, L is a neutral donor group; n=m=zero or 1; y and z are zero or integer such that X and L satisfy valency/oxidation state of M, (2) a catalyst-activating support which is a solid particulate substance, insoluble in hydrocarbons, comprising at least magnesium and aluminum atoms and hydrocarbyloxy groups containing 1 to 20 carbon atoms, the molar ration of Mg/Al being in the range 1.0 to 300 and the molar ratio of hydrocarbyloxy groups to aluminum atoms being in the range 0.5 to 2.0, and optionally, (3) an additional activator selected from aluminum alkyl and boron compounds.

Claims (30)

1. A polymerisation catalyst composition comprising

(1) a transition metal compound having the following Formula A,

wherein Z comprises a five-membered heterocyclic group, the five membered heterocyclic group containing at least one carbon atom, at least one nitrogen atom and at least one other hetero atom selected from nitrogen, sulphur and oxygen, the remaining atoms in said ring being selected from nitrogen and carbon; M is a metal from Group 3 to 11 of the Periodic Table or a lanthanide metal; E 1 and E 2 are divalent groups independently selected from (i) aliphatic hydrocarbon, (ii) alicyclic hydrocarbon, (iii) aromatic hydrocarbon, (iv) alkyl substituted aromatic hydrocarbon, (v) heterocyclic groups and (vi) heterosubstituted derivatives of said groups (i) to (v); D 1 and D 2 are donor atoms or groups; E 1 and E 2 are not linked other than through the donor atom or group D 1 ; X is an anionic group, L is a neutral donor group; n=m=1; y and z are independently zero or integers such that the number of X and L groups satisfy the valency and oxidation state of the metal M,

(2) a catalyst-activating support which is a solid particulate substance, insoluble in hydrocarbons, comprising at least magnesium and aluminium atoms and hydrocarbyloxy groups containing 1 to 20 carbons atoms, the molar ratio of Mg/Al being in the range 1.0 to 300 and the molar ratio of hydrocarbyloxy groups to aluminium atoms being in the range 0.05 to 2.0, and

(3) an additional activator selected from aluminium alkyl activators and boron compound activators.

2. A polymerisation catalyst as claimed in claim 1 wherein the average particle size of the support material is in the range 3 to 80 micrometers (μm).

3. A polymerisation catalyst as claimed in claim 1 wherein at least one of the atoms present in the ring of the five-membered heterocyclic group Z is bonded directly to E 1 and a second atom in the ring is bonded directly to M.

4. A polymerisation catalyst as claimed in claim 1 wherein the atom in the five-membered ring bonded directly to E 1 is adjacent to a second atom in said ring, said second atom being bonded directly to M.

5. A polymerisation catalyst as claimed in claim 1 wherein Z is an imidazole-containing group.

6. A polymerisation catalyst as claimed in claim 1 wherein D 2 and Z are identical imidazole containing groups.

7. A polymerisation catalyst as claimed in claim 5 or 6 wherein the imidazole-containing group Z is selected from the group consisting of formula I, II and III

R 1 to R 11 being independently hydrogen or a monovalent (i) aliphatic hydrocarbon, (ii) alicyclic hydrocarbon, (iii) aromatic hydrocarbon, (iv) alkyl substituted aromatic hydrocarbon, (v) heterocyclic groups, (vi) heterosubstituted derivatives of said groups (i) to (v), and (vii) hydrocarbyl-substituted heteroatom groups and the free valence bond b being bonded to E.

8. A polymerisation catalyst as claimed in claim 7 wherein the bond between Z and M in Formula A is provided by a bond connected from M to one of the nitrogen atoms of the group depicted in Formula I, II or III.

9. A polymerisation catalyst as claimed in claim 1 wherein M is selected from Sc, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W, and Mn.

10. A polymerisation catalyst as claimed in claim 1 wherein the anionic group X is selected from chloride, bromide, methyl, benzyl, phenyl, acetate, acetylacetonate; diethyl amide, methoxide, ethoxide, phenoxide and hydroxyl.

11. A polymerisation catalyst as claimed in claim 1 wherein X is a non-coordinating or weakly-coordinating anion.

12. A polymerisation catalyst as claimed in claim 11 wherein X is tetrafluoroborate, a fluorinated aryl borate or a triflate.

13. A polymerisation catalyst as claimed in claim 1 wherein the neutral donor group L is selected from diethyl ether, THF, diethyl amine, trimethylamine, pyridine, trimethyl phosphine, triphenyl phosphine, water; an olefin and a neutral, conjugated or nonconjugated diene.

14. A polymerisation catalyst as claimed in claim 1 wherein the activator (3) for the catalyst is selected from organoaluminium compounds, organoboron compounds and mixtures thereof.

15. A polymerisation catalyst as claimed in claim 14 wherein the organoaluminium compound is selected from trimethylaluminium, triethylaluminium, tributylaluminium, tri-n-octylaluminium, ethylaluminium dichloride, diethylaluminium chloride, tris(pentafluorophenyl)aluminium and an alumoxane.

16. A polymerisation catalyst as claimed in claim 14 wherein the organoboron compound is selected from dimethylphenylammoniumtetra(phenyl)borate, trityltetra(phenyl)borate, triphenylboron, dimethylphenylammonium tetra(pentafluorophenyl)borate, sodium tetrakis[(bis-3,5-trifluoromethyl)phenyl]borate, H + (OEt 2 )[(bis-3,5-trifluoromethyl)phenyl]borate, trityltetra(pentafluorophenyl)borate and tris(pentafluorophenyl) boron.

17. A polymerisation catalyst as claimed in claim 1 wherein the catalyst contains a halogen compound catalyst promoter.

18. A polymerisation catalyst as claimed in claim 17 wherein the promoter is selected from carbon tetrachloride, hexachloroethylene, benzylbromide, benzylchloride, 2,3-dichloropropylene, 1,3-dichloropropylene, ethyl trichloroacetate, chloroform and n-butylchloride.

19. A polymerisation catalyst comprising a catalyst as claimed in claim 1 together with one or more other catalysts for polymerising 1-olefins.

20. A polymerisation catalyst as claimed in claim 19 wherein the one or more other catalysts are selected from Ziegler-Natta catalyst systems, metallocene-based catalysts, non metallocene transition metal or lanthanide based catalysts and heat activated supported chromium oxide catalysts.

21. A process for the polymerisation and copolymerisation of 1-olefins, cycloolefins or dienes, comprising contacting the monomer under polymerisation conditions with the polymerisation catalyst claimed in claim 1 .

22. A process for making homopolymer comprising contacting the catalyst claimed in claim 1 with a monomer selected from ethylene, propylene, butene, hexene, styrene or conjugated or non-conjugated dienes.

23. A process for making copolymer comprising contacting the catalyst claimed in claim 1 with at least one monomer selected from ethylene, propylene, 1-butene, 1-hexene, 4-methylpentene-1,1-octene, norbornene, substituted norbornenes, dienes, ethylidene norbornene, methyl methacrylate, methyl acrylate, butyl acrylate, acrylonitrile, vinyl acetate, vinyl chloride, and styrene.

24. A process for making copolymer comprising contacting the catalyst claimed in claim 1 with ethylene and one or more of propylene, butene, hexene-1 and 4-methylpentene-1.

25. A process for making copolymer comprising contacting the catalyst claimed in claim 23 wherein the diene is butadiene.

Assignments (11)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2014
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: INEOS SALES (UK) LIMITED
Reel/Frame 032388/0553 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 13, 2014
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 032264/0400 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT SUPPLEMENT Recorded Feb 13, 2014
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 032264/0470 →
SECURITY AGREEMENT Recorded Jun 26, 2012
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 028444/0639 →
SECURITY INTEREST Recorded Feb 23, 2012
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 027748/0039 →
SECURITY INTEREST Recorded Nov 28, 2011
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 027286/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2011
From: INEOS EUROPE LIMITED
To: INEOS COMMERCIAL SERVICES UK LIMITED
Reel/Frame 027060/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2007
From: GIBSON, VERNON CHARLES; TOMOV, ATANAS KOSTADINOV; JACOBSEN, GRANT BERENT
To: INNOVENE EUROPE LIMITED
Reel/Frame 018939/0341 →
CHANGE OF REGISTERED ADDRESS Recorded Feb 12, 2007
From: INEOS EUROPE LIMITED
To: INEOS EUROPE LIMITED
Reel/Frame 018948/0471 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2007
From: INNOVENE EUROPE LIMITED
To: INEOS EUROPE LIMITED
Reel/Frame 018949/0113 →
CHANGE OF REGISTERED ADDRESS Recorded Feb 12, 2007
From: INEOS EUROPE LIMITED
To: INEOS EUROPE LIMITED
Reel/Frame 019096/0214 →