Method of preparing metallocene catalyst for polyolefin preparation

Patent metadata

Field	Value
Publication number	US-11077434-B2
Application number	US-201715774448-A
Country	US
Kind code	B2
Filing date	Jul 7, 2017
Priority date	Jul 7, 2016
Publication date	Aug 3, 2021
Grant date	Aug 3, 2021

Abstract

A method of preparing a high-purity metallocene catalyst capable of providing various selectivities and high activities for polyolefin copolymers, wherein a metallocene compound is formed by reacting a ligand compound with a zirconium compound, and then lithium chloride as a reaction by-product included in the metallocene compound is prepared in a form of a complex compound and effectively removed in a subsequent step of extracting the catalyst, thereby effectively preparing the high-purity metallocene catalyst, is provided.

First claim

The invention claimed is:

1. A method of preparing a metallocene catalyst, the method comprising the steps of:
A) forming a metallocene compound by reacting a ligand compound represented by the following Chemical Formula 1 with a zirconium compound comprising chloride in the presence of an alkyl lithium;
B) adding a first solvent to the reaction products from step A) including the metallocene compound to form a lithium chloride—the first solvent complex; and
C) adding a second solvent to the reaction products from step B) to precipitate the lithium chloride—the first solvent complex, followed by filtration:

wherein R 1 is a C 6-20 aryl substituted with a C 1-20 alkyl;
R 2 , R 3 , and R 4 are each independently hydrogen, a halogen, a C 1-20 alkyl, a C 2-20 alkenyl, a C 1-20 alkylsilyl, a C 1-20 silylalkyl, a C 1-20 alkoxysilyl, a C 1-20 ether, a C 1-20 silylether, a C 1-20 alkoxy, a C 6-20 aryl, a C 7-20 alkylaryl, or a C 7-20 arylalkyl;
A is carbon, silicon, or germanium;
R 5 is a C 1-20 alkyl substituted with a C 1-20 alkoxy; and
R 6 is hydrogen, a C 1-20 alkyl, or a C 2-20 alkenyl,
wherein the first solvent is one or more selected from the group consisting of 1,4-dioxane and 1,3-dioxolane, and
wherein the second solvent is one or more selected from the group consisting of dichloromethane, chloroform, carbon tetrachloride, benzene, and toluene.

2. The method according to claim 1 , wherein the zirconium compound is bis(N,N′-diphenyl-1,3-propanediamido)dichlorozirconium bis(tetrahydrofuran).

3. The method according to claim 1 , wherein R 1 is a phenyl substituted with a t-butyl.

4. The method according to claim 1 , wherein R 1 is 4-(t-butyl)-phenyl.

5. The method according to claim 1 , wherein R 2 , R 3 , and R 4 are hydrogen.

6. The method according to claim 1 , wherein A is silicon.

7. The method according to claim 1 , wherein R 5 is 3-(t-butoxy)-propyl, and R 6 is methyl.

8. The method according to claim 1 , wherein the first solvent is added and stirred for 1 h or more.

9. The method according to claim 1 , wherein the first solvent is removed before step C) by vacuum distillation under conditions of a pressure of 0.5 mbar to 2.0 mbar and a temperature of 30° C. to 45° C.

10. The method according to claim 1 , wherein the second solvent is added and filtration is performed, and then the second solvent is removed from the obtained filtrate, followed by recrystallization using one or more solvents selected from the group consisting of dichloromethane and hexane.

Assignees

• Lg Chemical Ltd

Inventors

• Park Hee Kwang
• Lee Hye Kyung
• Kim Byung Seok
• Cheong Jae Youp
• Jeon Sang Jin

Classifications

• C08F2420/10

  Heteroatom-substituted bridge, i.e. Cp or analog where the bridge linking the two Cps or analogs is substituted by at least one group that contains a heteroatom · CPC title

• C08F110/06 Primary

  Propene · CPC title

• C08F4/65908

  in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+ · CPC title

• C08F4/65916

  supported on a carrier, e.g. silica, MgCl2, polymer · CPC title

• C08F4/65912

  in combination with an organoaluminium compound · CPC title