IP Library › Granted Patent US 10,072,111
Granted Patent B2
US 10,072,111 · App. 15/876,532 · Granted Sep 11, 2018

Spheroidal catalyst for olefin polymerization

Inventors: Qinyan Wang (Calgary, CA); Tyler Craig (Vancouver, CA); Savina Udara Suduweli Kondage (Endeavour Hills, AU); Bradley Wade Funk (Calgary, CA)
Assignee: NOVA Chemicals (International) S.A.
C08F210/16C08F4/022C08F4/649C08F4/6592C08F4/65912C08F4/65916C08F2420/04
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Quick Facts
Patent No.
US 10,072,111
App. No.
15/876,532
Granted
Sep 11, 2018
Kind
B2
Abstract

A solid, spheroidal polymerization catalyst having a particle size distribution characterized by a Dm*/Dn of less than 3.0, the catalyst comprising a phosphinimine catalyst, a cocatalyst and a magnesium chloride support. A process for the polymerization of ethylene with one or more alpha olefin catalyzed by a solid, spheroidal polymerization catalyst having a particle size distribution characterized by a Dm*/Dn of less than 3.0, the catalyst comprising a phosphinimine catalyst, a cocatalyst and a magnesium chloride support.

Claims (11)

1. A method of making a spheroidal olefin polymerization catalyst having a particle size distribution characterized by a Dm*/Dn of less than 3.0, wherein said method comprises:

i) combining a dialkylmagnesium compound with a non-protic ether,

ii) combining the product of step i) with a source of chloride anion,

iii) treating the product of step ii) to substantially remove to provide a MgCl 2 support containing less than about 2.5 wt. % of the non-protic ether,

iv) combining the product of step iii) with a phosphinimine catalyst and a cocatalyst.

2. The method of claim 1 wherein treating the product of step ii) to remove the non-protic ether comprises heating the product of step ii).

3. The method of claim 1 wherein treating the product of step ii) to remove the non-protic ether comprises adding an alkylaluminumchloride compound.

4. The method of claim 1 wherein the phosphinimine catalyst has the formula: (L)(PI)MX 2 , where M is Ti, Zr or Hf; PI is a phosphinimine ligand having the formula R 3 P═N—, where R is independently selected from the group consisting of hydrogen, halogen, and C 1 -C 20 hydrocarbyl; L is a ligand selected from the group consisting of cyclopentadienyl, substituted cyclopentadienyl, indenyl, substituted indenyl, fluorenyl, and substituted fluorenyl; and X is an activatable ligand.

5. The method of claim 1 wherein the phosphinimine catalyst has the formula: (L)((t-Bu) 3 P═N)TiX 2 , where L is a cyclopentadienyl ligand, a substituted cyclopentadienyl ligand, an indenyl ligand, or a substituted indenyl ligand; and X is an activatable ligand.

6. The method of claim 1 wherein the phosphinimine catalyst has the formula: (L)((t-Bu) 3 P═N)TiX 2 , where L is a substituted cyclopentadienyl ligand, or a substituted indenyl ligand; and X is an activatable ligand.

7. The method of claim 1 wherein the cocatalyst is selected from the group consisting of ionic activators, alkylaluminoxanes and mixtures thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2018
From: WANG, QINYAN; FUNK, BRADLEY WADE; CRAIG, TYLER; KONDAGE, SAVINI UDARA SUDUWELI
To: NOVA CHEMICALS (INTERNATIONAL) S.A.
Reel/Frame 044688/0116 →
Priority Claims (1)
CA 2874344 · Dec 15, 2014 · national
Continuity (2)
Division 14967704 · Dec 14, 2015
Related Publication 20180155476A1 · Jun 7, 2018