IP Library Granted Patent US 7,893,003
Granted Patent B2
US 7,893,003 · App. 12/390,785 · Granted Feb 22, 2011

Catalyst composition with mixed selectivity control agent and method

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Quick Facts
Patent No.
US 7,893,003
App. No.
12/390,785
Granted
Feb 22, 2011
Kind
B2
Abstract

The present disclosure provides a Ziegler-Natta catalyst composition comprising a procatalyst, a cocatalyst and a mixed external electron donor comprising a first selectivity control agent, a second selectivity control agent, and an activity limiting agent. A polymerization process incorporating the present catalyst composition produces a high-stiffness propylene-based polymer with a melt flow rate greater than about 50 g/10 min. The polymerization process occurs in a single reactor, utilizing standard hydrogen concentration with no visbreaking.

Claims (18)

1. A catalyst composition comprising:

a Ziegler-Natta procatalyst composition comprising titanium, magnesium and an internal electron donor;

a cocatalyst; and

a mixed external electron donor (M-EED) comprising an activity limiting agent (ALA), a first selectivity control agent (SCA1) comprising an alkoxysilane, a second selectivity control agent (SCA2) selected from the group consisting of an alkoxysilane, a diether, and a dialkoxybenzene, a SCA1:SCA2 mole ratio from 0.1-1.0:1, a mole ratio of total-SCA to ALA less than 1.0, and the catalyst composition is a self-limiting catalyst composition.

2. The catalyst composition of claim 1 wherein the procatalyst composition comprises an internal electron donor comprising a bidentate composition.

3. The catalyst composition of claim 1 wherein the SCA1 comprises a member selected from the group consisting of a dimethoxysilane, a dimethoxysilane having at least one secondary alkyl group, a dimethoxysilane having a secondary amino group directly bonded to the silicon atom, and combinations thereof.

4. The catalyst composition of claim 1 wherein SCA2 is selected from the group consisting of a diethoxysilane, a triethoxysilane, a tetraethoxysilane, a trimethoxysilane, a diether, a dialkoxybenzene, a dimethoxysilane containing two linear alkyl groups, a dimethoxysilane containing two alkenyl groups, and combinations thereof.

5. The catalyst composition of claim 1 wherein the ALA is selected from the group consisting of an aromatic ester or a derivative thereof, an aliphatic ester or a derivative thereof, a diether, a poly(alkylene glycol) ester, and combinations thereof.

6. The catalyst composition of claim 1 comprising an aluminum-containing cocatalyst and a mole ratio of A1to M-EED less than about 6.0.

7. The catalyst composition of claim 1 wherein SCA1 comprises dicyclopentyldimethoxysilane.

8. The catalyst composition of claim 1 wherein SCA2 is selected from the group consisting of methylcyclohexyldiethoxysilane, di-isobutyldiethoxysilane, n-propyltriethoxysilane, tetraethoxysilane, di-n-butyl-dimethoxysilane, benzyltriethoxysilane, but-3-enyltriethoxysilane, 1-(triethoxysilyl)-2-pentene, (triethoxysilyl)cyclohexane, and combinations thereof.

9. The catalyst composition of claim 1 wherein the ALA comprises isopropyl myristate.

10. The catalyst composition of claim 1 wherein SCA1 comprises dicyclopentyldimethoxysilane and SCA2 is selected from the group consisting of methylcyclohexyldimethoxysilane, di-n-butyl-dimethoxysilane, n-propyltriethoxysilane, benzyltriethoxysilane, and (triethoxysilyl)cyclohexane.

11. The catalyst composition of claim 1 wherein SCA1 comprises dicyclopentyldimethoxysilane and SCA2 comprises 1-ethoxy-2-n -pentoxybenzene.

12. The catalyst composition of claim 1 wherein the ALA comprises a C 1-4 alkyl ester of aliphatic C 8-20 monocarboxylic acid.

13. The catalyst composition of claim 1 wherein the procatalyst composition comprises a phthalate.

14. The catalyst composition of claim 1 wherein SCA1 is selected from the group consisting of dicyclopentyldimethoxysilane and diisopropyldimethoxysilane and SCA2 is selected from the group consisting of vinyltriethoxysilane, dimethyldimethoxysilane, ethyltriethoxysilane, n-propyltriethoxysilane, and tetraethoxysilane.

15. The catalyst composition of claim 1 wherein the M-EED comprises from 5 mol % to 10 mol % total SCA and from 95 mol % to 90 mol % ALA.

Assignments (16)
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 INTEREST Recorded Aug 19, 2025
From: W. R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 072519/0265 →
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 Aug 19, 2025
From: W. R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 072519/0240 →
SECURITY INTEREST Recorded Apr 2, 2023
From: W. R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 063199/0472 →
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 025992/0443 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2009
From: UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY LLC
To: DOW GLOBAL TECHNOLOGIES INC.
Reel/Frame 022593/0575 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2009
From: CHEN, LINFENG
To: UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY LLC
Reel/Frame 022601/0679 →