IP Library Granted Patent US 8,552,114
Granted Patent B2
US 8,552,114 · App. 13/690,533 · Granted Oct 8, 2013

Miktopolymer compositions

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Quick Facts
Patent No.
US 8,552,114
App. No.
13/690,533
Granted
Oct 8, 2013
Kind
B2
Abstract

The present invention provides a block copolymer composition and method of making the same having the structures (A 2 -B) n -X-(A 1 ) or (A 2 -B 2 ) n -X-(B 1 A 1 ), where A 1 and A 2 are each a polymer block of a monoalkenyl arene and B, B 1 , and B 2 are each a polymer block of one or more conjugated dienes or a hydrogenated diene polymer, n is an integer from 2 to 30 and X is the residue of a coupling agent.

Claims (17)

1. An elastomeric polymer composition comprising miktopolymers of the structure (A 2 -B 2 ) n -X-(B 1 -A 1 ), where

a. A 1 and A 2 are each a polymer block of a monoalkenyl arene and B 1 and B 2 are polymer blocks of one or more conjugated dienes or hydrogenated polymer blocks of one or more conjugated dienes;

b. n is an integer from 2 to 30; and

c. X is the residue of a coupling agent;

and wherein:

i. τ is an asymmetry parameter of monoalkenyl arene associated with the A 1 and A 2 blocks according to the formula τ=NA 1 /(NA 1 +NA 2 ) where NA 1 is the number of monomer units in the A 1 monoalkenyl arene block and NA 2 is the number of monomer units in an A 2 monoalkenyl arene block;

ii. f is the volume fraction of monoalkenyl arene in said miktopolymer;

iii. τ has a value of 0.7 to 0.95;

iv. f has a value greater than or equal to 0.5;

v. block A 1 has a peak molecular weight of between 10,000 and 300,000, and the ratio of the peak molecular weight of A 1 to A 2 is greater than or equal to 2; and

vi. B 2 has a peak molecular weight of between 20,000 and 150,000 and B 1 has a peak molecular weight of between 200 and 5,000.

2. The composition according to claim 1 , wherein said mono alkenyl arene for the A l and A 2 blocks is styrene and said conjugated diene for the B 2 block is selected from the group consisting of isoprene, 1,3-butadiene and mixtures thereof and the conjugated diene for the B 1 block is 1,3-butadiene.

3. The composition according to claim 2 wherein at least 90% of the unsaturated bonds in the B 1 and B 2 blocks of the polymer are hydrogenated and the conjugated diene for the B 2 block is 1,3-butadiene and wherein about 20 to about 80 mol percent of the condensed butadiene units in the B 1 and B 2 blocks have 1,2-configuration.

4. The composition according to claim 2 wherein the monoalkenyl arene content ranges from about 40 to about 75 weight percent for the total block copolymer.

5. The composition according to claim 4 wherein said block A l has a peak molecular weight of between 10,000 and 300,0006, said A 2 block has a peak molecular weight of between 5,000 and 30,000, said block B 2 has a peak molecular weight of between 20,000 and 100,000 and said block B 1 has a peak molecular weight of between 200 and 3,000.

6. The composition according to claim 1 , wherein n is an integer from 4 to 10.

7. A composition according to claim 1 , wherein the composition is catalytically hydrogenated and at least about 90 percent of the conjugated diene double bonds have been reduced and between 0 to about 10 percent of the arene double bonds have been reduced.

Assignments (10)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2012
From: HANDLIN, JR., DALE LEE; PASMAN, PETER; FREDRICKSON, GLENN H.; WILLIS, CARL L.; BENING, ROBERT C.
To: KRATON POLYMERS US LLC
Reel/Frame 029384/0859 →