Block copolymers, their manufacture and their use

Patent metadata

Field	Value
Publication number	US-9364825-B2
Application number	US-201514734123-A
Country	US
Kind code	B2
Filing date	Jun 9, 2015
Priority date	Jan 14, 2013
Publication date	Jun 14, 2016
Grant date	Jun 14, 2016

Abstract

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

First claim

What is claimed is:

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 high service 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 10° C. to 100° C.;

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

2. A process according to claim 1 , wherein the A block is a glassy block.

3. A process according to claim 2 , wherein the high service temperature is represented by the glass transition temperature (Tg).

4. 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.

5. The process of claim 1 , wherein the block copolymer is coupled, and the coupling agent is a divinylaromatic compound.

6. The process of claim 5 , wherein the coupling agent is divinylbenzene and n is an integer from 2-3.

7. The process of claim 1 , 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.

8. 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.

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

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

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

12. The process of claim 11 , wherein the quaternary amine has a halide counter ion.

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

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

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

16. 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.

17. The process of claim 16 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.

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

19. The process of claim 16 wherein the Z and the two R moieties form an alkoxy amine.

20. The process of claim 16 , wherein the Z and the two R moieties form morpholine, and the block copolymer is self-coupled and contains no coupling agent residue.

Assignees

• Kraton Polymers Us Llc

Inventors

• Willis Carl L
• Van Der Huizen Adrie A

Classifications

• Y02E60/521

  Cross-Sectional Technologies · mapped topic

• B01D71/82

  characterised by the presence of specified groups, e.g. introduced by chemical after-treatment · CPC title

• Y02P70/56

  Cross-Sectional Technologies · mapped topic

• B01D71/80

  Block polymers · CPC title

• B01D61/44

  Ion-selective electrodialysis · CPC title