Patent Application

App. No. 11/884,653

Abstract

Claims (38)

1 - 16 . (canceled)

17 . A process for the polymerisation of ethylene or the copolymerisation of ethylene and alpha-olefins in the presence of a catalyst system comprising as components

(a) a transition metal compound,

(b) a non-aluminoxane activator, and

(c) optionally a support,

said process characterised in that said catalyst system comprises a prepolymer prepared by contact of the catalyst components with ethylene or ethylene and one of more alpha-olefins at a temperature in the range 60° C. to 100° C.

18 . A process according to claim 17 wherein the prepolymer is prepared at a temperature in the range 70° C. to 90° C.

19 . A process according to claim 17 wherein the prepolymer is prepared in the gas phase.

20 . A process according to claim 17 wherein the prepolymer is prepared by contact with the catalyst components with ethylene.

21 . A process for polymerising ethylene or copolymerising ethylene and one or more alpha-olefins comprising:—

(1) in a first stage prepolymerising ethylene or ethylene and one or more alpha-olefins at a temperature in the range 60° C. to 100° C. in the presence of a catalyst system comprising (a) a transition metal compound, (b) a non-aluminoxane activator and optionally (c) a support,

(2) optionally, recovering the prepolymerised catalyst, and

(3) in a second stage polymerising ethylene or ethylene and one or more alpha-olefins at a temperature in the range 70° C. to 100° C. in the presence of said prepolymerised catalyst.

22 . A process according to claim 21 wherein the second stage is performed at a temperature in the range 80° C. to 90° C.

23 . A process according to claim 21 wherein both stages are performed in the gas phase.

24 . A process according to claim 17 wherein the alpha-olefin is chosen from 1-butene, 1-hexene or 4-methyl-1-pentene.

25 . A process according to claim 24 wherein the alpha-olefin is 1-hexene.

26 . A process according to claim 21 wherein the prepolymer is prepared in-situ.

27 . A process according to claim 17 or claim 21 wherein the transition metal compound is a metallocene.

28 . A process according to claim 27 wherein the metallocene has the formula:

wherein:—

R′ each occurrence is independently selected from hydrogen, hydrocarbyl, silyl, germyl, halo, cyano, and combinations thereof, said R′ having up to 20 nonhydrogen atoms, and optionally, two R′ groups (where R′ is not hydrogen, halo or cyano) together form a divalent derivative thereof connected to adjacent positions of the cyclopentadienyl ring to form a fused ring structure;

X is a neutral η 4 bonded diene group having up to 30 non-hydrogen atoms, which forms a π-complex with M;

Y is —O—, —S—, —NR*—, —PR*—,

M is titanium or zirconium in the +2 formal oxidation state;

Z* is SiR* 2 , CR* 2 , SiR* 2 SIR* 2 , CR* 2 CR* 2 , CR*═CR*, CR* 2 SIR* 2 , or GeR* 2 , wherein:

R* each occurrence is independently hydrogen, or a member selected from hydrocarbyl, silyl, halogenated alkyl, halogenated aryl, and combinations thereof, said

R* having up to 10 non-hydrogen atoms, and optionally, two R* groups from Z* (when R* is not hydrogen), or an R* group from Z* and an R* group from Y form a ring system.

29 . A process according to claim 17 or claim 21 wherein the non-aluminoxane activator has the formula:

(L*-H) + d (A d− )

wherein

L* is a neutral Lewis base

(L*-H) + d is a Bronsted acid

A d− is a non-coordinating compatible anion having a charge of d, and

d is an integer from 1 to 3.

30 . A process according to claim 29 wherein the non-aluminoxane activator comprises a cation and an anion wherein the anion has at least one substituent comprising a moiety having an active hydrogen.

31 . A process according to claim 17 or claim 21 wherein the support is an inorganic metal oxide.

32 . A process according to claim 31 wherein the inorganic metal oxide is silica.

Assignments (9)