IP Library Granted Patent US 9,061,254
Granted Patent B2
US 9,061,254 · App. 14/333,203 · Granted Jun 23, 2015

Block copolymers, their manufacture and their use

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Quick Facts
Patent No.
US 9,061,254
App. No.
14/333,203
Granted
Jun 23, 2015
Kind
B2
Abstract

A functionalized block copolymer polymerized using vinylbenzylamino derivative monomers for use in such applications as anionic exchange membranes.

Claims (37)

1. A process for preparing an amino-functionalized block copolymer comprising:

in an inert hydrocarbon solvent and in the presence of an initiator,

(a) polymerizing a hard end block A, the block A having a melting temperature of at least about 20° C.;

(b) polymerizing a soft interior block B, the B block having a T g of at most 20° C.;

(c) polymerizing a block D from a plurality of p-vinylbenzylamino derivative monomers, the p-vinylbenzylamino derivative monomers capable of being polymerized at a temperature range of from 20° C. to 60° C.;

thereby forming a block polymer or a living block polymer comprising the blocks A, B and D.

2. The process of claim 1 comprising:

further polymerizing one or more additional blocks A, B or D to form a block polymer having the configuration A-B-D-B-A or A-D-B-D-A, or

coupling the block polymer formed by steps (a) through (c) with a coupling agent to form a block polymer having the configuration (A-B-D) n X or (A-D-B) n X wherein X is the residue of the coupling agent and n is an integer from 2-30.

3. The process of claim 2 , wherein the block copolymer is coupled, and the coupling agent is a divinylaromatic compound.

4. The process of claim 3 , wherein the coupling agent is divinylbenzene and n is an integer from 2-3.

5. The process of claim 2 , wherein each block A is independently selected from the group consisting of polymerized (i) ethylene monomers; (ii) propylene monomers, (iii) styrene and alpha-alkyl styrene monomers having a phenyl ring which is optionally substituted by one or more alkyl groups, (iv) (meth)acrylate ester monomers, (v) conjugated diene monomers which are subsequently hydrogenation, and (vi) mixtures of monomers selected from (i) to (v),

and

wherein each block B is independently selected from the group consisting of polymerized (i) ethylene monomers, (ii) C 3 -C 8 alpha-olefin monomers, (iii) isobutylene monomers, (iv) conjugated diene monomers, (v) (meth)acrylate ester monomers, (vi) a silicon polymer, and (vii) mixtures of monomers selected from (i) to (v), wherein segments containing polymerized conjugated diene monomers are optionally hydrogenated.

6. The process of claim 5 wherein the A block is formed from substituted or unsubstituted styrene and alpha-alkyl styrene monomers, and the B block is formed from conjugated diene.

7. The process of claim 1 , wherein the amino functionality in the block D is a tertiary amine.

8. The process of claim 1 , wherein the p-vinylbenzylamino derivative monomers are selected from the group consisting of p-vinylbenzylpiperidine, p-vinylbenzylmorphiline, p-vinylbenzyldimethylamine, p-vinylbenzylpyrrolidine, p-vinylbenzyl-bis-(2-methoxyethyl)amine, p- and vinylbenzylpiperazine, and mixtures thereof.

9. The process of claim 1 , wherein the amine functionality in the polymerized block D is a quaternary amine.

10. The process of claim 9 , wherein the quaternary amine has a halide counter ion.

11. The process of claim 1 , wherein the block polymer is provided in an anionic exchange membrane.

12. The process of claim 1 , wherein the amine is a saturated or unsaturated cyclic, or aromatic amine.

13. The process of claim 1 , wherein prior to step (c), the p-vinylbenzylamine monomers are formed by reacting a p-vinylbenzylhalide with an amine.

14. The process of claim 1 wherein block D comprises on average at least one amino functionalized polymer unit of formula (I)

wherein

Z is nitrogen;

R 1 is hydrogen or alkyl;

R 2 is hydrogen;

R each independently, is hydrogen or is alkyl optionally substituted by a moiety -(A 1 -NR a ) x R b or -(A 1 -OR a ) x R b ; or

two R groups, together with the Z to which they are bonded, form a ring optionally substituted with hetero members selected from nitrogen or oxygen;

x is 1, 2 or 3;

A 1 is straight chain alkylene optionally substituted by one or more methyl and/or ethyl groups; and

R a and R b , each independently, is hydrogen or alkyl;

or a corresponding onium salt.

15. The process of claim 14 wherein the Z and the two R moieties form a ring selected from the group consisting of pyrrolidine, piperidine, piperazine, 1-azabicyclo[2,2,2]nonane, 1,4-diazabicyclo[2,2,2]octane (DABCO), morpholine, pyrrole, pyrazole, imidazole, pyridine, pyridazine, pyrimidine, pyrazine, indole, isoindole, indazole, purine, carbazole, phenoxazine, and azepine.

16. The process of claim 14 wherein when rings formed by the Z and the two R moieties have multiple nitrogen functionalities the Z and each nitrogen functionality is quaternized.

17. The process of claim 14 wherein the Z and the two R moieties form an alkoxy amine.

18. The process of claim 14 , wherein the Z and the two R moieties form morpholine, and the block copolymer is self-coupled and contains no coupling agent residue.

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 Jul 31, 2014
From: WILLIS, CARL L.; VAN DER HUIZEN, ADRIE A.
To: KRATON POLYMERS U.S. LLC
Reel/Frame 033435/0384 →