IP Library › Granted Patent US 9,315,592
Granted Patent B2
US 9,315,592 · App. 13/854,453 · Granted Apr 19, 2016

Process for producing procatalyst composition with alkoxyalkyl ester internal electron donor and product

Inventors: Linfeng Chen (Missouri City, TX); Tak W. Leung (Houston, TX); Kelly Gonzalez (Katy, TX); Tao Tao (Houston, TX)
Assignee: W. R. Grace & Co.-Conn.
C08F4/6498C08F10/00C08F110/06
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Quick Facts
Patent No.
US 9,315,592
App. No.
13/854,453
Granted
Apr 19, 2016
Kind
B2
Abstract

Disclosed herein are processes for preparing procatalyst compositions with an internal electron donor containing greater than 4.5 wt % of a compounded alkoxyalkyl ester. Also disclosed are catalyst compositions containing the procatalyst composition and polymers, i.e., propylene-based polymers, produced therefrom. The present procatalyst compositions improve catalyst selectivity, catalyst activity, procatalyst morphology and polymer particle morphology, and improve hydrogen response during olefin polymerization.

Claims (74)

1. A process comprising:

first contacting a procatalyst precursor with an alkoxyalkyl ester and a halogenating agent to form a procatalyst intermediate, the first contacting comprising

reacting the halogenating agent with the procatalyst precursor, and

adding the alkoxyalkyl ester from greater than 0 minutes to about 30 minutes after the reacting, thereby forming the procatalyst intermediate;

second contacting the procatalyst intermediate with an alkoxyalkyl ester that is the same or different than the alkoxyalkyl ester in the first contacting, and a halogenating agent; and

forming a procatalyst composition comprising a combination of a magnesium moiety, a titanium moiety, and the alkoxyalkyl ester, wherein the alkoxyalkyl ester is present in the amount of greater than 4.5 wt %.

2. The process of claim 1 wherein the first contacting occurs in a reaction mixture having a temperature from 30° C. to 150° C.

3. The process of claim 1 comprising third contacting the procatalyst intermediate with an alkoxyalkyl ester and a halogenating agent; and

forming a procatalyst composition comprising greater than 5.0 wt % alkoxyalkyl ester.

4. The process of claim 1 wherein the first contacting comprises contacting the procatalyst precursor with an alkoxyalkyl ester having the structure (I)

wherein R, R 1 and R 2 are the same or different, each of R and R 1 is selected from the group consisting of a C 1 -C 20 primary alkyl group, a substituted C 1 -C 20 primary alkyl group, and a C 2 -C 20 alkene group; and

R 2 is selected from the group consisting of hydrogen, a C 1 -C 20 primary alkyl group, a substituted C 1 -C 20 primary alkyl group, and a C 2 -C 20 alkene group.

5. The process of claim 1 comprising forming a procatalyst composition comprising particles having a particle size distribution (PSD) span of less than 2.0.

6. The process of claim 1 comprising adding the alkoxyalkyl ester from greater than 0 minutes to about 5 minutes after the reacting.

7. The process of claim 1 comprising forming a procatalyst composition comprising from 0.01 wt % to 0.7 wt % ethoxide.

8. The process of claim 1 comprising forming particles of the procatalyst composition having a D50 from 10 microns to 50 microns.

9. The process of claim 1 wherein the first contacting comprises contacting a mixed magnesium/titaniuim compound with the alkoxyalkyl ester and the halogenating agent.

10. The process of claim 1 comprising forming particles of the procatalyst composition and eliminating agglomeration of the particles.

11. The process of claim 1 wherein the second contacting comprises contacting the procatalyst intermediate with an alkyoxyalkyl ester that is the same as the alkoxyalkyl ester in the first contacting.

12. A process comprising:

first halogenating a procatalyst precursor to form a reaction mixture;

heating the reaction mixture to a temperature from 30° C. to 150° C.;

first adding first and second alkoxyalkyl esters to the reaction mixture from greater than 0 minutes to 30 minutes after the heating to form a procatalyst intermediate;

second halogenating the procatalyst intermediate;

second adding an alkoxyalkyl ester to the procatalyst intermediate; and

forming particles of a procatalyst composition, the particles having a particle size distribution span of less than 2.0, and wherein the procatalyst composition comprises a combination of a magnesium moiety, a titanium moiety, and the alkoxyalkyl ester, wherein the alkoxyalkyl ester is present in the amount of greater than 5.0 wt %.

13. The process of claim 12 comprising second heating the procatalysts intermediate to a temperature from 30° C. to 150° C. before the second adding.

14. the process of claim 12 comprising first adding the alkoxyalkyl esters to the reaction mixture from greater than 0 minutes to about 5 minutes after the heating to form a procatalyst intermediate.

15. A process comprising:

first contacting a procatalyst precursor with an aromatic alkoxyalkyl ester and a halogenating agent to form a procatalyst intermediate, the aromatic alkoxyalkyl ester having the structure (III)

wherein R 1 and R 2 are the same or different, R 1 is selected from the group consisting of a C 1 -C 20 primary alkyl group, a substituted C 1 -C 20 primary alkyl group, and a C 2 -C 20 alkene group;

R 2 is selected from the group consisting of hydrogen, a C 1 -C 20 primary alkyl group, a substituted C 1 -C 20 primary alkyl group, and a C 2 -C 20 alkene group;

R 3 , R 4 , R 5 are the same or different, each of R 3 , R 4 , R 5 is selected from the group consisting of a heteroatom, a C 1 -C 20 hydrocarbyl group, a substituted C 1 -C 20 hydrocarbyl group, and a C 1 -C 20 hydrocarbyloxy group;

second contacting the procatalyst intermediate with an alkoxyalkyl ester that is the same or different than the alkoxyalkyl ester in the first contacting, and a halogenating agent; and

forming a procatalyst composition comprising a combination of a magnesium moiety, a titanium moiety and greater than 10 wt % of the aromatic alkoxyalkyl ester.

16. The process of claim 15 wherein the first contacting comprises adding a first aromatic alkoxyalkyl ester of structure (III) and a second alkoxyalkyl ester to the reaction mixture.

17. The process of claim 15 wherein the second contacting comprises adding a first aromatic alkoxyalkyl ester of structure (III) and a second alkoxyalkyl ester to the procatalyst intermediate.

18. The process of claim 15 , further comprising a third contacting of the procatalyst intermediate with an alkoxyalkyl ester and a halogenating agent.

19. A process comprising:

first halogenating a procatalyst precursor to form a reaction mixture;

heating the reaction mixture to a temperature from 30° C. to 150° C.;

first adding an aromatic alkoxyalkyl ester to the reaction mixture from greater than 0 minutes to 30 minutes after the heating to form a procatalyst intermediate, the aromatic alkoyxyalkyl ester having the structure (III)

wherein R 1 and R 2 are the same or different, R 1 is selected from the group consisting of a C 1 -C 20 primary alkyl group, a substituted C 1 -C 20 primary alkyl group, and a C 2 -C 20 alkene group;

R 2 is selected from the group consisting of hydrogen, a C 1 -C 20 primary alkyl group, a substituted C 1 -C 20 primary alkyl group, and a C 2 -C 20 alkene group;

R 3 , R 4 , R 5 are the same or different, each of R 3 , R 4 , R 5 is selected from the group consisting of a heteroatom, a C 1 -C 20 hydrocarbyl group, a substituted C 1 -C 20 hydrocarbyl group, and a C 1 -C 20 hydrocarbyloxy group;

second halogenating the procatalyst intermediate;

second adding an alkoxyalkyl ester to the procatalyst intermediate; and

forming particles of a procatalyst composition, the particles having a particle size distribution span of less than 2.0.

20. The process of claim 19 comprising forming a procatalyst composition comprising a combination of a magnesium moiety, a titanium moiety and greater than 10 wt % of the aromatic alkoxyalkyl ester.

21. A process comprising:

first contacting in a reaction mixture a procatalyst precursor with a first and a second alkoxyalkyl ester and a halogenating agent to form a procatalyst intermediate, the first contacting comprising

reacting the halogenating agent with the procatalyst precursor, and

adding the first and second alkoxyalkyl esters from greater than 0 minutes to about 30 minutes after the reacting;

second contacting the procatalyst intermediate with an alkoxyalkyl ester that is the same or different than the first and second alkoxyalkyl esters in the first contacting, and a halogenating agent; and

forming a procatalyst composition comprising a combination of a magnesium moiety, a titanium moiety and greater than 4.5 wt % of the first and second alkoxyalkyl esters.

22. A process comprising:

first contacting a procatalyst precursor with an alkoxyalkyl ester and a halogenating agent to form a procatalyst intermediate, the first contacting comprising

reacting the halogenating agent with the procatalyst precursor, and

adding the alkoxyalkyl ester from greater than 0 minutes to about 30 minutes after the reacting;

second contacting the procatalyst intermediate with an alkoxyalkyl ester that is the same or different than the alkoxyalkyl ester in the first contacting, and a halogenating agent, wherein the second contacting comprises adding a first alkoxyalkyl ester and a second alkoxyalkyl ester to the procatalyst intermediate; and

forming a procatalyst composition comprising a combination of a magnesium moiety, a titanium moiety and the alkoxyalkyl ester.

23. A process comprising:

first contacting a procatalyst precursor with an alkoxyalkyl ester which is 2-methoxy-1-methylethyl benzoate and a halogenating agent to form a procatalyst intermediate, the first contacting comprising

reacting the halogenating agent with the procatalyst precursor, and

adding the alkoxyalkyl ester from greater than 0 minutes to about 30 minutes after the reacting;

second contacting the procatalyst intermediate with an alkoxyalkyl ester that is the same or different than the alkoxyalkyl ester in the first contacting, and a halogenating agent; and

forming a procatalyst composition comprising a combination of a magnesium moiety, a titanium moiety and the alkoxyalkyl ester.

24. A process comprising:

first contacting a procatalyst precursor with an alkoxyalkyl ester which is 2-methoxyethyl benzoate and a halogenating agent to form a procatalyst intermediate, the first contacting comprising

reacting the halogenating agent with the procatalyst precursor, and

adding the alkoxyalkyl ester from greater than 0 minutes to about 30 minutes after the reacting;

second contacting the procatalyst intermediate with an alkoxyalkyl ester that is the same or different than the alkoxyalkyl ester in the first contacting, and a halogenating agent; and

forming a procatalyst composition comprising a combination of a magnesium moiety, a titanium moiety and the alkoxyalkyl ester.

25. The process of claim 1 , wherein the first contacting step further comprises contacting the procatalyst precursor with a first and second alkoxyalkyl ester.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Sep 23, 2021
From: GOLDMAN SACHS BANK USA
To: W. R. GRACE & CO.-CONN.
Reel/Frame 057594/0026 →
SECURITY INTEREST Recorded Apr 3, 2018
From: W. R. GRACE & CO.-CONN.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 045828/0683 →
RELEASE OF SECURITY AGREEMENT RECORDED AT REEL/FRAME NO.: 032159/0384 Recorded Apr 3, 2018
From: GOLDMAN SACHS BANK USA, AS THE COLLATERAL AGENT
To: W.R. GRACE & CO.-CONN.
Reel/Frame 045832/0887 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME TO "W. R. GRACE & CO. - CONN." PREVIOUSLY RECORDED ON REEL 032554 FRAME 0730. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNEE NAME WAS PREVIOUSLY INCORRECTLY LISTED IN THE RECORDATION COVER SHEET DATED 3/28/2014 AS "W. R. GRACE & CO. CONN.". Recorded Apr 2, 2014
From: DOW GLOBAL TECHNOLOGIES LLC; UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY LLC
To: W. R. GRACE & CO. - CONN.
Reel/Frame 032589/0554 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2014
From: DOW GLOBAL TECHNOLOGIES LLC; UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY LLC
To: W. R. GRACE & CO. CONN.
Reel/Frame 032554/0730 →
SECURITY AGREEMENT Recorded Feb 4, 2014
From: W.R. GRACE & CO.-CONN.
To: GOLDMAN SACHS BANK USA, AS THE COLLATERAL AGENT
Reel/Frame 032159/0384 →
Continuity (2)
Continuation 12974548 · Dec 21, 2010
Related Publication 20130225398A1 · Aug 29, 2013