IP Library Granted Patent US 8,778,826
Granted Patent B2
US 8,778,826 · App. 12/651,032 · Granted Jul 15, 2014

Enhanced procatalyst composition and process

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Quick Facts
Patent No.
US 8,778,826
App. No.
12/651,032
Granted
Jul 15, 2014
Kind
B2
Abstract

Disclosed herein are processes for preparing procatalyst compositions and polymers, i.e., propylene-based polymers, produced therefrom. The present procatalyst compositions improve catalyst selectivity and also increase the bulk density of the formant polymer.

Claims (13)

1. A process comprising: halogenating a procatalyst precursor in the presence of a substituted phenylene aromatic diester at a temperature from about 90° C. to less than or equal to 100° C., wherein the substituted phenylene aromatic diester is 5-tert-butyl-3-methyl-1,2-phenylene dibenzoate, to form a procatalyst composition with ethyl benzoate from 0 wt% to less than 2.3 wt %.

2. The process of claim 1 comprising contacting, under polymerization conditions, the procatalyst composition, a cocatalyst, and optionally an external electron donor with propylene and optionally one or more olefins; and forming a propylene-based polymer having less than 2.5 wt % xylene solubles.

3. A process comprising:

first halogenating a procatalyst precursor in the presence of a substituted phenylene aromatic diester at a temperature less than 115° C. to form a procatalyst intermediate, wherein the substituted phenylene aromatic diester is selected from the group consisting of 5-tert-butyl-3-methyl-1,2-phenylene dibenzoate and 4-tert-butyl-1,2phenylene dibenzoate;

second halogenating the procatalyst intermediate at a temperature greater than or equal to 115° C.;

to form a procatalyst composition with a bulk density index from about 0.28 to about 0.5.

4. The process of claim 3 comprising preparing particles of the procatalyst precursor, the particles having a D50 from about 10 μm to about 25μm.

5. The process of claim 3 comprising first halogenating the procatalyst precursor at a temperature from 90° C. to less than or equal to 100° C. and second halogenating the procatalyst intermediate at a second temperature greater than or equal to 115° C.

6. The process of claim 3 comprising second halogenating the procatalyst intermediate in the presence of a substituted phenylene aromatic diester.

7. The process of claim 3 comprising third halogenating the procatalyst intermediate at a third temperature greater than or equal to 115° C.

8. The process of claim 3 comprising contacting, under polymerization conditions, the procatalyst composition, a cocatalyst, and an external electron donor with propylene and optionally one or more olefins; and forming particles of a propylenebased polymer having a bulk density from about 0.28 g/cc to about 0.5 g/cc as measured in accordance with ASTM D 1895B.

9. The process of claim 3 wherein the substituted phenylene aromatic diester is5-tert-butyl-3-methyl-1,2-phenylene dibenzoate.

10. The process of claim 3 wherein the substituted phenylene aromatic diester is 4-tert-butyl-1,2-phenylene dibenzoate.

Assignments (13)
NOTES SECURITY INTEREST Recorded Jan 29, 2026
From: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 074532/0229 →
SECURITY AGREEMENT (NOTES) Recorded Aug 19, 2025
From: W. R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 072520/0653 →
SECURITY INTEREST Recorded Feb 17, 2023
From: W.R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 062792/0510 →
NOTES SECURITY AGREEMENT Recorded Sep 23, 2021
From: W. R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 057594/0156 →
RELEASE OF SECURITY INTEREST Recorded Sep 23, 2021
From: GOLDMAN SACHS BANK USA
To: W. R. GRACE & CO.-CONN.
Reel/Frame 057594/0026 →
TERM LOAN SECURITY AGREEMENT Recorded Sep 23, 2021
From: W. R. GRACE & CO.-CONN.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 057594/0104 →
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 →
CHANGE OF NAME Recorded Mar 21, 2011
From: DOW GLOBAL TECHNOLOGIES INC.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 025990/0927 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 18, 2010
From: GONZALEZ, KELLY; WILLIAMS, CLARK C.; CHEN, LINFENG
To: DOW GLOBAL TECHNOLOGIES INC.
Reel/Frame 024100/0630 →