US2002016257A1PendingUtilityA1
Catalyst system and its use in a polymerization process
Priority: Nov 18, 1999Filed: Apr 6, 2001Published: Feb 7, 2002
Est. expiryNov 18, 2019(expired)· nominal 20-yr term from priority
C08L 2205/02C08L 23/16C08F 210/16C08F 4/65916C08F 4/65912C08L 2314/06C08L 23/0815C08F 10/02
45
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Claims
Abstract
The present invention relates to a catalyst system of a Group 15 containing metal catalyst compound and a Lewis acid aluminum containing activator and to a supported catalyst system thereof and to a process for polymerizing olefin(s) utilizing them.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A process for polymerizing olefin(s) in the presence of a catalyst system comprising a Group 15 containing metal catalyst compound and a Lewis acid aluminum containing activator.
2 . The process of claim 1 wherein the Group 15 containing metal catalyst compound is a Group 15 containing bidentate or tridentate ligated metal catalyst compound.
3 . The process of claim 1 wherein the Group 15 containing metal catalyst compound is a metal atom bound to at least one substituted alkyl leaving group having 6 or greater carbon atoms and to at least two Group 15 atoms, where at least one of the at least two Group 15 atoms is bound to a Group 15 or 16 atom through a bridging group.
4 . The process of claim 3 wherein the bridging group is selected from the group consisting of a C 1 to C 20 hydrocarbon group, a heteroatom containing group, silicon, germanium, tin, lead, and phosphorus.
5 . The process of claim 4 wherein the Group 15 or 16 atom may also be bound to nothing, a hydrogen, a Group 14 atom containing group, a halogen, or a heteroatom containing group, and wherein each of the two Group 15 atoms are also bound to a cyclic group and may optionally be bound to hydrogen, a halogen, a heteroatom or a hydrocarbyl group, or a heteroatom containing group.
6 . The process of claim 1 wherein the Group 15 containing metal compound is represented by the formulae:
wherein
M is metal;
each X is a leaving group;
y is 0 or 1;
n is the oxidation state of M;
m is the formal charge of the YZL or the YZL′ ligand;
L is a Group 15 or 16 element;
L′ is a Group 15 or 16 element or Group 14 containing group;
Y is a Group 15 element;
Z is a Group 15 element;
R 1 and R 2 are independently a C 1 to C 20 hydrocarbon group, a heteroatom containing group having up to twenty carbon atoms, silicon, germanium, tin, lead, or phosphorus;
R 3 is absent or a hydrocarbon group, hydrogen, a halogen, a heteroatom containing group;
R 4 and R 5 are independently an alkyl group, an aryl group, substituted aryl group, a cyclic alkyl group, a substituted cyclic alkyl group, a cyclic arylalkyl group, a substituted cyclic arylalkyl group or multiple ring system;
R 1 and R 2 may be interconnected to each other, and/or R 4 and R 5 may be interconnected to each other;
R 6 and R 7 are independently absent, or hydrogen, an alkyl group, halogen, heteroatom or a hydrocarbyl group; and
R* is absent, or is hydrogen, a Group 14 atom containing group, a halogen, a heteroatom containing group.
7 . The process of claim 6 wherein R 4 and R 5 are represented by the formula:
wherein R 8 to R 12 are each independently hydrogen, a C 1 to C 40 alkyl group, a halide, a heteroatom, a heteroatom containing group containing up to 40 carbon atoms, preferably a C 1 to C 20 linear or branched alkyl group, preferably a methyl, ethyl, propyl or butyl group, any two R groups may form a cyclic group and/or a heterocyclic group. The cyclic groups may be aromatic.
8 . The process of claim 7 wherein R 9 , R 10 and R 12 are independently a methyl, ethyl, propyl or butyl group and X is a substituted alkyl group having greater than 6 carbon atoms.
9 . The process of claim 7 wherein R 9 , R 10 and R 12 are methyl groups, and R 8 and R 11 are hydrogen and X is a alkyl substituted with an aryl group.
10 . The process of claim 6 wherein L, Y, and Z are independently nitrogen, R 1 and R 2 are a hydrocarbon radical, R 3 is hydrogen, and R 6 and R 7 are absent.
11 . The process of claim 6 wherein L and Z are independently nitrogen, L′ is a hydrocarbyl radical, and R 6 and R 7 are absent.
12 . The process of claim 1 wherein the catalyst system is supported on a carrier.
13 . The process of claim 1 wherein the process is a continuous gas phase process.
14 . The process of claim 1 wherein the process is a continuous slurry phase process.
15 . The process of claim 1 wherein the olefin(s) is ethylene or propylene.
16 . The process of claim 1 wherein the olefins are ethylene and at least one other monomer having from 3 to 20 carbon atoms.
17 . The process of claim 1 wherein the catalysts system further comprises an activator.
18 . A supported catalyst system comprising: a Group 15 containing metal catalyst compound, an activator and a carrier.
19 . The supported catalyst system of claim 18 wherein the Group 15 containing metal catalyst compound is a Group 15 containing bidentate or tridentate ligated metal catalyst compound having a substituted hydrocarbon leaving group.
20 . The supported catalyst system of claim 18 wherein the Group 15 containing metal catalyst compound is contacted with the activator to form a reaction product that is then contacted with the carrier.Join the waitlist — get patent alerts
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