Catalyst for polymerization of olefins and process thereof

Patent metadata

Field	Value
Publication number	US-9676876-B2
Application number	US-201314417099-A
Country	US
Kind code	B2
Filing date	Sep 24, 2013
Priority date	Sep 24, 2012
Publication date	Jun 13, 2017
Grant date	Jun 13, 2017

Abstract

The present invention provides a process for preparation of a solid titanium catalyst component for use as pro-catalyst for a Ziegler-Natta catalyst system. The solid titanium catalyst component comprises a combination of 15 to 20 wt % of a magnesium moiety, 1.0 to 6.0 wt % of a titanium moiety and 5.0 to 20 wt % of an internal donor, said solid titanium catalyst component has an average particle size in the range of 1 to 100 μm, characterized by a three point particle size distribution of D10 in the range of 1 to 10 μm; D50 in the range of to 25 μm and D90 in the range of 15 to 50 μm. The present invention also provides a 15 Ziegler-Natta catalyst system comprising the solid titanium catalyst component and the method of polymerizing and/or copolymerizing olefins by using the Ziegler-Natta catalyst system.

First claim

We claim:

1. A process for preparation of a solid titanium catalyst component for use as pro-catalyst for a Ziegler-Natta catalyst system, said process consisting essentially of:
(a) contacting a dialkyl magnesium compound represented by R′R″Mg with a magnesium solubilizing compound to form a reaction mixture, wherein each of R′ and R″ is a hydrocarbon group having C 1 -C 20 carbon atoms, and wherein contacting the dialkyl magnesium compound with the magnesium solubilizing compound results in formation of first reaction mixture comprising magnesium alkoxide in the reaction mixture;
(b) adding a titanium compound represented by Ti(OR′″) p X 4-p , where X is a halogen atom; R′″ is a hydrocarbon group and p is an integer having value less than or equal to 4 to convert the magnesium alkoxide in the reaction mixture to form second reaction mixture;
(c) adding at least one internal electron donor either after step (a) or after step (b) to obtain a catalyst component; and
(d) activating the catalyst component using a solution comprising a titanium compound and an inert solvent and recovering a solid titanium catalyst component.

2. The process as claimed in claim 1 , wherein the magnesium solubilizing compound is liquid alcohol represented by ROH, wherein R is a hydrocarbon group having C 1 -C 20 carbon atoms; and wherein:
a. liquid alcohol is selected from the group consisting of aliphatic alcohol, alicyclic alcohol, aromatic alcohol, aliphatic alcohol containing an alkoxy group and mixture thereof.

3. The process as claimed in claim 1 , comprising:
(a) contacting a dialkyl magnesium compound represented by R′R″Mg with a magnesium solubilizing liquid alcohol represented by ROH to form a first reaction mixture comprising magnesium alkoxide, wherein contacting the dialkyl magnesium compound with the liquid alcohol results in the following reaction:
R′R″Mg+2ROH→Mg(OR) 2 +R′H+R″H

wherein each of R, R′ and R″ is a hydrocarbon group having C 1 -C 20 carbon atoms;

(b) adding a titanium compound represented by Ti(OR′″) p X 4-p , where X is a halogen atom; R′″ is a hydrocarbon group and p is an integer having value less than or equal to 4 to the first reaction mixture to obtain a second reaction mixture comprising magnesium dihalide;
(c) adding at least one internal electron donor to the second mixture to obtain a catalyst component; and
(d) activating the catalyst component using a solution comprising a titanium compound and an inert solvent and recovering a solid titanium catalyst component.

4. The process as claimed in claim 3 , wherein step (a) comprises:
i. contacting dialkyl magnesium compound with liquid alcohol at a temperature maintained in the range of 2 to 8° C. to obtain a third reaction mixture; and
ii. gradually increasing the temperature of the third reaction mixture to a value in the range of 50 to 70° C. and maintaining the temperature for a time period of 15 to 45 minutes to form the first reaction mixture comprising magnesium alkoxide.

5. The process as claimed in claim 3 , wherein step (b) comprises:
i. diluting the first reaction mixture with an inert solvent & cooling the same to a temperature in the range of −35 to −10° C.;
ii. dissolving the titanium compound in a solvent to obtain a solution and cooling the solution; and
iii. gradually mixing the solution thus obtained above in step (ii) with the diluted reaction mixture of step (i) at a temperature in the range of −35 to −10° C. to obtain the second reaction mixture.

6. The process as claimed in claim 3 , wherein step (c) comprises:
i. gradually increasing the temperature of second reaction mixture to a value in the range of 25 to 50° C.;
ii. adding a source of internal electron donor;
iii. gradually increasing the temperature to a value in the range of 100 to 130° C. and maintaining the temperature for a time period of 10 to 20 minutes to form the catalyst component; and
iv. recovering the catalyst component thus formed.

7. The process as claimed in claim 3 , wherein step (d) comprises:
i. treating the catalyst component with a solution comprising the titanium compound and an inert solvent and maintaining the same a temperature value in the range of 100 to 120° C. for 10 to 20 minutes; and
ii. optionally repeating the aforesaid step for a predetermined number of times.

8. The process as claimed in claim 1 , comprising
A. contacting a dialkyl magnesium compound represented by R′R″Mg with a liquid alcohol represented by ROH to form a first reaction mixture comprising magnesium alkoxide, wherein the contacting of the dialkyl magnesium compound with a liquid alcohol results in the following reaction:
R′R″Mg+2ROH→Mg(OR) 2 +R′H+R″H

wherein each of R, R′ and R″ is a hydrocarbon group;

B. adding at least one internal electron donor to the first reaction mixture to obtain a second reaction mixture;
C. adding a titanium compound represented by Ti(OR′″) p X 4-p , where X is a halogen atom; R′″ is a hydrocarbon group and p is an integer having value less than or equal to 4 to the second reaction mixture of step (b) to obtain a catalyst component; and
D. activating the catalyst component using a solution comprising a titanium compound and an inert solvent and recovering a solid titanium catalyst component.

9. The process as claimed in claim 8 , wherein step (A) comprises:
i. contacting dialkyl magnesium compound with liquid alcohol at a temperature is maintained in the range of 2 to 8° C. to obtain a third reaction mixture; and
ii. gradually increasing the temperature of the third reaction mixture to a value in the range of 50 to 70° C. and maintaining the temperature for a time period of 15 to 45 minutes to form the first reaction mixture comprising magnesium alkoxide.

10. The process as claimed in claim 8 , wherein step (B) comprises:
i. diluting the first reaction mixture with an inert solvent & cooling the same to a temperature in the range of −35 to −10° C.;
ii. adding a source of internal electron donor to the first reaction mixture to obtain the second reaction mixture.

11. The process as claimed in claim 8 , wherein step (C) comprises:
i. dissolving the titanium compound in a solvent to obtain a solution and cooling the solution; and
ii. gradually mixing the solution of step (i) with the second reaction mixture at a temperature in the range of −35 to −10° C. to obtain the catalyst component.

12. The process as claimed in claim 8 , wherein step (D) comprises:
i. treating the catalyst component with a solution comprising the titanium compound and an inert solvent and maintaining the same a temperature value in the range of 100 to 120° C. for 10 to 20 minutes; and
ii. optionally repeating step (i) for a predetermined number of times.

13. The process as claimed in claim 1 , wherein the dialkyl magnesium compound is selected from the group consisting of dialkylmagnesium such as dimethylmagnesium, diethylmagnesium, diisopropylmagnesium, dibutylmagnesium, dihexylmagnesium, dioctylmagnesium, ethylbutylmagnesium and butyloctylmagnesium.

14. The process as claimed in claim 2 , wherein the liquid alcohol is selected from the group consisting of aliphatic alcohol, alicyclic alcohol, aromatic alcohol, aliphatic alcohol containing an alkoxy group and mixture thereof; wherein:
the aliphatic alcohol is selected from the group consisting of methanol, ethanol, propanol, butanol, 2-methylpentanol, 2-ethylbutanol, n-heptanol, n-octanol, 2-ethylhexanol, decanol and dodecanol,
alicyclic alcohols is selected from the group consisting of cyclohexanol and methylcyclohexanol;
aromatic alcohol is selected from the group consisting of benzy

Assignees

• Indian Oil Corp Ltd

Inventors

• Singh Gurmeet
• Kumar Naresh
• Kaur Sukhdeep
• Kapur Gurpreet Singh
• Kant Shashi
• Basu Biswajit
• Malhotra Ravinder Kumar
• Nenseth Svein
• Lindroos Jarmo

Classifications

• C08F10/06 Primary

  Propene · CPC title

• C08F210/06

  Propene · CPC title

• C08F2500/03

  Narrow molecular weight distribution, i.e. Mw/Mn < 3 · CPC title

• C08F4/651

  Pretreating with non-metals or metal-free compounds · CPC title

• C08F2500/18

  Bulk density · CPC title