IP Library Granted Patent US 7,125,940
Granted Patent B2
US 7,125,940 · App. 10/741,535 · Granted Oct 24, 2006

Conjugated diene polymers and copolymer blocks and process for preparing same

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Quick Facts
Patent No.
US 7,125,940
App. No.
10/741,535
Granted
Oct 24, 2006
Kind
B2
Abstract

Disclosed is a process for preparing polymers and copolymer blocks of conjugated dienes with varying amounts of branching comprising the use of a microstructure control agent and a microstructure control agent deactivant. The polymerization can be started with or without a microstructure control agent. At some point in the polymerization prior to the completion of the addition of the conjugated diene to the polymer, the microstructure control agent can be deactivated, either partially or completely, resulting in a polymer or copolymer block having a region of less branching adjacent to a region of more branching. Preferred microstructure control agent deactivants are metal alkyls such as triethyl aluminum.

Claims (39)

1. A process for preparing a conjugated diene polymer or copolymer block having a varying amount of branching comprising combining:

(a) an anionic polymerization site;

(b) a conjugated diene monomer; and

(c) a microstructure control agent;

under reaction conditions sufficient to form a living polymer admixture and, at a point in the process prior to the completion of the polymerization of the conjugated diene monomer, combining the living polymer admixture with a microstructure control agent deactivant to mitigate or eliminate the effect of the microstructure control agent, wherein the microstructure control agent deactivant is an aluminum alkyl compound having from 1 to 20 carbon atoms per alkyl substituent and mixtures thereof.

2. The process of claim 1 wherein the conjugated diene monomer is selected from the group consisting of 1,3-butadiene, isoprene, piperylene, methylpentadiene, 1,3-cyclohexadiene, 1,3-cylcohepatdiene, 1,3-cyclooctadiene phenylbutadiene, 3,4-dimethyl-1,3-hexadiene, 4,5-diethyl-1,3-octadiene, and mixtures thereof.

3. The process of claim 2 wherein the conjugated diene monomer is 1,3-butadiene.

4. The process of claim 1 wherein the process is a process for preparing a conjugated diene copolymer block and the anionic polymerization site is a living polymer.

5. The process of claim 4 additionally comprising a step of preparing the anionic polymerization site by admixing a monomer different from the conjugated diene monomer with an initiator.

6. The process of claim 5 wherein the monomer different from the conjugated diene monomer is styrene.

7. The process of claim 1 wherein the microstructure control agent is a Lewis Base.

8. The process of claim 7 wherein the Lewis Base is selected from the group consisting of:

diethyl ether;

1,2-diethoxy-ethane;

1,2-diethoxy-propane;

o-dimethoxy-benzene;

1-t-butoxy-2-n-butoxy-ethane;

n-C 4 H 9 OCH 2 CH 2 O-n-C 4 H 9 ;

n-C 4 H 9 OCH 2 CH 2 OCH 2 OCH 3 ;

n-C4H 9 OCH 2 CH 2 OCHCH 3 OCH 2 CH 3 ;

n-C 4 H 9 OCH 2 CH 2 O-t-C 4 H 9 ;

n-C 4 H 9 OCH 2 CH 2 OCHCH 3 —O-i-C 4 H 9 ; and

mixtures thereof.

9. The process of claim 1 wherein the aluminum, alkyl having from 1 to 20 carbon atoms per alkyl substituent is selected from the group consisting of:

triethylaluminum,

trimethylaluminum,

tri-n-propylaluminum,

tri-n-butylaluminum,

triisobutylaluminum,

tri-n-hexylaluminum,

trioctylaluminum, and

mixtures thereof.

10. The process of claim 9 wherein the microstructure control agent deactivant is triethylaluminum.

11. The process of claim 1 wherein the microstructure control agent deactivant is added to the living polymer at a ratio of microstructure control agent deactivant to microstructure control agent of from about 0.1:1 to about 2:1.

12. The process of claim 11 wherein the microstructure control agent deactivant is added to the living polymer at a ratio of microstructure control agent deactivant to microstructure control agent of from about 0.5:1 to about 1.1:1.

13. The process of claim 12 wherein the microstructure control agent deactivant is added to the living polymer at a ratio of microstructure control agent deactivant to microstructure control agent of about 1:1.

14. The process of claim 1 wherein the microstructure control agent deactivant is added at a point in the process where from about 25 percent to about 75 percent of the conjugated diene monomer has been polymerized and incorporated into the living polymer.

15. The process of claim 14 wherein the microstructure control agent deactivant is added at a point in the process where about 50 percent of the conjugated diene monomer has been added and incorporated into the living polymer.

16. The process of claim 6 further comprising using a coupling agent to form a coupled block copolymer.

Assignments (13)
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jul 24, 2024
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: KRATON CHEMICAL, LLC; KRATON CORPORATION
Reel/Frame 068671/0836 →
CORRECTIVE ASSIGNMENT TO CORRECT THE PATENT NO. 8837224 TO PATENT NO. 7737224 PREVIOUSLY RECORDED AT REEL: 037448 FRAME: 0453. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 11, 2022
From: KRATON POLYMERS U.S. LLC; ARIZONA CHEMICAL COMPANY, LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 060344/0919 →
SECURITY INTEREST Recorded Mar 18, 2022
From: KRATON CHEMICAL, LLC; KRATON POLYMERS LLC; KRATON POLYMERS U.S. LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 059525/0804 →
SECURITY INTEREST Recorded Mar 18, 2022
From: KRATON CHEMICAL, LLC; KRATON POLYMERS LLC; KRATON POLYMERS U.S. LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 059864/0455 →
RELEASE OF SECURITY INTEREST Recorded Mar 16, 2022
From: BANK OF AMERICA, N.A.
To: KRATON POLYMERS U.S. LLC; KRATON CHEMICAL, LLC F/K/A ARIZONA CHEMICAL COMPANY, LLC; KRATON POLYMERS LLC; KRATON CORPORATION; KRATON CHEMICAL B.V.
Reel/Frame 059910/0017 →
RELEASE OF SECURITY INTEREST Recorded Mar 15, 2022
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: KRATON POLYMERS U.S. LLC
Reel/Frame 059366/0611 →
SECURITY INTEREST Recorded Apr 16, 2020
From: KRATON POLYMERS U.S. LLC; KRATON CHEMICAL, LLC F/K/A ARIZONA CHEMICAL COMPANY, LLC; KRATON POLYMERS LLC; KRATON CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 053020/0101 →
PATENT SECURITY AGREEMENT Recorded Jan 7, 2016
From: KRATON POLYMERS U.S. LLC
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 037457/0843 →
CORRECTIVE ASSIGNMENT TO CORRECT THE PATENT NUMBER 8837224 TO PATENT NUMBER 7737224 PREVIOUSLY RECORDED AT REEL: 037448 FRAME: 0453. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST. Recorded Jan 6, 2016
From: KRATON POLYMERS U.S. LLC; ARIZONA CHEMICAL COMPANY, LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 037448/0453 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT PATENT NUMBER 7720798 AND REPLACE WITH PATENT NUMBER 7220798 PREVIOUSLY RECORDED ON REEL 025845 FRAME 0795. ASSIGNOR(S) HEREBY CONFIRMS THE RELEASE BY SECURED PARTY. Recorded Dec 16, 2015
From: USB AG, STAMFORD BRANCH
To: KRATON POLYMERS U.S. LLC
Reel/Frame 037312/0070 →
RELEASE OF SECURITY INTEREST Recorded Feb 24, 2011
From: UBS AG, STAMFORD BRANCH
To: KRATON POLYMERS U.S. LLC
Reel/Frame 025845/0795 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2006
From: WILLIS, CARL L.
To: KRATON POLYMERS U.S. LLC
Reel/Frame 018195/0066 →
SUPPLEMENT TO PATENT SECURITY AGREEMENT Recorded May 18, 2006
From: KRATON POLYMERS U.S. LLC
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 017892/0158 →