Cationic polymers for use as anion exchange polyelectrolytes

Patent metadata

Field	Value
Publication number	US-10934374-B2
Application number	US-201916977294-A
Country	US
Kind code	B2
Filing date	Mar 11, 2019
Priority date	Mar 12, 2018
Publication date	Mar 2, 2021
Grant date	Mar 2, 2021

Abstract

Described herein are cationic polymers having a plurality of quaternary amino groups, methods of making such polymers, and uses of such polymers as ion exchange membranes in electrochemical devices.

First claim

What is claimed is:

1. A method for preparing a cationic polymer having a plurality of quaternary amino groups, the method comprising:
providing a first precursor polymer having a plurality of pendant carboxylic acid groups, the first precursor polymer comprising x repeat units of Formula (I) and y repeat units of Formula (II)

wherein
each R 1 is independently hydrogen or methyl;
each R 2 is independently hydrogen or methyl;
the variable x represents an overall mole fraction of the repeat units of Formula (I), with random or block repeat unit distribution;
the variable y represents an overall mole fraction of the repeat units of Formula (II) in the first precursor polymer, with random or block repeat unit distribution, wherein y is in a range of about 0.04 to about 0.40;

reacting the pendant carboxylic acid groups of the first precursor polymer with an amine compound having at least one primary or secondary amino group to form a second precursor polymer having pendant amide groups;
treating the second precursor polymer having pendant amide groups to form a third precursor polymer having pendant secondary and/or tertiary amino groups; and
reacting the third precursor polymer having pendant secondary and/or tertiary amino groups with an alkylating agent to form the cationic polymer having the plurality of pendant quaternary amino groups, wherein the cationic polymer having the plurality of pendant quaternary amino groups comprises x repeat units of Formula (I) and z repeat units of Formula (III)

wherein
each R 3 is independently (a) a cationic group having a plurality of quaternary amino groups; or (b) a cationic group comprising a heterocyclic ring, the heterocyclic ring having a single quaternary amino group and at least one additional heteroatom that is nitrogen or oxygen, wherein the heterocyclic ring is saturated; or (c) a cationic group having a heterocyclic ring directly attached to the polymer backbone, wherein the heterocyclic ring is not attached to the polymeric backbone through a nitrogen atom, the heterocyclic ring having a single quaternary amino group and 1 or 2 additional heteroatoms selected from nitrogen and oxygen, the heterocyclic ring optionally fused to a second ring that is carbocyclic or heterocyclic;
the variable x represents an overall mole fraction of the repeat units of Formula (I), with random or block repeat unit distribution; and
the variable z represents the overall mole fraction of the repeat units of Formula (III) in the cationic polymer, with random or block repeat unit distribution, wherein z is in a range of about 0.04 to about 0.40.

2. The method of claim 1 , wherein the precursor copolymer is a copolymer of ethylene and (meth)acrylic acid.

3. The method of claim 1 , wherein the amine compound that is reacted with the first precursor polymer has at least two amino groups and at least one of these amino groups is a primary or secondary amino group.

4. The method of claim 1 , wherein the amine compound that is reacted with the first precursor polymer is of Formula (IV)
HR 4 N—R 5 —[NR 4 —R 5 ]—NR 4 R 4    (IV)

wherein
each R 4 is independently a hydrogen or alkyl;
each R 5 is independently an alkylene; and
v is an integer in a range of 0 to 10.

5. The method of claim 1 , wherein amine compound is an alkylene diamine of formula H 2 N—CH 2 —(CH 2 ) q —CH 2 —NH 2 and the third precursor polymer has pendant groups that are *—CH 2 —NH—CH 2 —(CH 2 ) q —CH 2 —NH 2 , the method further comprising reacting the pendant groups of the third precursor polymer with an aldehyde compound of formula R 6 —(CO)—H to form a cyclic pendant group of Formula (V)

wherein
R 6 is an alkyl or aryl; and
q is 0 or 1.

6. The method of claim 1 , wherein the second precursor polymer has pendant amide groups of formula *—(CO)—NH—R 5 —NH 2 and the pendant amide groups of the second precursor are further reacted with an aldehyde of formula R 7 —(CO)—H, a dione having two R 8 groups, and an ammonium salt before the reducing step to form pendant groups of Formula (VI)

wherein
each R 7 is independently alkyl, aryl or alkylaryl; and
each R 8 is an alkyl or aryl.

7. The method of claim 1 , wherein the amine compound is imidazoline, piperazine, morpholine, 2,6-dimethylmorpholine, 2-azatricyclo[3.3.1.1]decane, and 2,6-diazatricyclo[3.3.1.1]decane.

8. The method of claim 7 , wherein the second precursor polymer has pendant groups of Formula (XV)

where R 13 is alkyl or hydrogen.

9. The method of claim 1 , wherein an o-phenylene diamine is reacted with the first precursor polymer to form the second precursor polymer and wherein treating the second precursor polymer to form the third precursor polymer comprises heating the second precursor polymer in the presence of an acid catalyst to form pendant groups of Formula (XII)

directly attached to a hydrocarbon backbone of the third precursor polymer, wherein R 20 is hydrogen, alkyl, or aryl.

10. A cationic polymer comprising x repeat units of Formula (I) and z repeat units of Formula (III)

wherein
each R 1 is independently hydrogen or methyl;
each R 2 is independently hydrogen or methyl;
each R 3 is independently (a) a cationic group having a plurality of quaternary amino groups; or (b) a cationic group comprising a heterocyclic ring, the heterocyclic ring having a single quaternary amino group and at least one additional heteroatom that is nitrogen or oxygen, wherein the heterocyclic ring is saturated; or (c) a cationic group having a heterocyclic ring directly attached to the polymer backbone, wherein the heterocyclic ring is not attached to the polymeric backbone through a nitrogen atom, the heterocyclic ring having a single quaternary amino group and 1 or 2 additional heteroatoms selected from nitrogen and oxygen, the heterocyclic ring optionally fused to a second ring that is carbocyclic or heterocyclic; and
the variable x represents an overall mole fraction of the repeat units of Formula (I), with random or block repeat unit distribution; and
the variable z represents the overall monomer mole fraction of the repeat units of Formula (III) in the cationic polymer, with random or block repeat unit distribution, wherein z is in a range of about 0.04 to about 0.40; and
the cationic group having a corresponding anionic counter ion.

11. The cationic polymer of claim 10 , wherein R 3 is a cationic group of Formula (VII))))
*—CH 2 —(NR 9 R 10 ) + —R 11 —[(NR 9 R 10 ) + —R 11 ] p —(NR 9 (R 10 ) 2 ) +    (VII)

wherein
each R 9 and R 10 is independently an alkyl;
each R 11 is independently an alkylene;
p is an integer in a range of 0 to 10; and
each cationic group has a corresponding counter ion.

12. The cationic polymer of claim 10 , where the R 3 is a cationic group is of Formula (VIII)

Assignees

• 3M Innovative Properties Co

Inventors

• Yandrasits Michael A
• Fort Eric H
• Kaplun Marina M
• Laskowski Carl A
• Quast Matthew J

Classifications

• H01M2300/0091

  in the form of mixtures · CPC title

• H01M8/1051

  Non-ion-conducting additives, e.g. stabilisers, SiO2 or ZrO2 · CPC title

• H01M2008/1095

  Fuel cells with polymeric electrolytes · CPC title

• C08J5/22 Primary

  Films, membranes or diaphragms · CPC title

• C08F2810/00

  Chemical modification of a polymer · CPC title