Self-wetting porous membranes (I)

Patent metadata

Field	Value
Publication number	US-9724649-B2
Application number	US-201514750382-A
Country	US
Kind code	B2
Filing date	Jun 25, 2015
Priority date	Jun 25, 2015
Publication date	Aug 8, 2017
Grant date	Aug 8, 2017

Abstract

Disclosed is a self-wetting porous membrane comprising an aromatic hydrophobic polymer such as polysulfone and a wetting agent comprising a copolymer of formula A-B or A-B-A, wherein A is a hydrophilic segment comprising a polymerized monomer of the formula (I): CH 2 ═C(R 1 )(R 2 ), wherein R 1 and R 2 are as described herein, and B is an aromatic hydrophobic polymeric segment, wherein segments B and A are linked through an amidoalkylthio group. Also disclosed is a method of preparing a self-wetting membrane comprising casting a solution containing an aromatic hydrophobic polymer and the wetting agent, followed by subjecting the cast solution to phase inversion. The self-wetting porous membrane finds use in hemodialysis, microfiltration, and ultrafiltration.

First claim

The invention claimed is:

1. A self-wetting porous membrane comprising an aromatic hydrophobic polymer and a wetting agent comprising a copolymer of formula A-B or A-B-A,
wherein A is a hydrophilic segment comprising a polymerized monomer or mixture of monomers, wherein the monomer is of the formula (I):
CH 2 ═C(R 1 )(R 2 )  (I),

wherein R 1 is hydrogen or alkyl, and R 2 is selected from substituted or unsubstituted heterocyclyl, substituted or unsubstituted heteroaryl, formylamino, formylaminoalkyl, aminocarbonyl, alkylcarbonyloxy, and aminocarbonylalkyl substituted with a zwitterionic group,
and B is an aromatic hydrophobic polymeric segment, wherein segments B and A are linked through an amidoalkylthio group.

2. The self-wetting porous membrane of claim 1 , wherein R 1 is hydrogen or methyl, and R 2 is selected from pyrrolidinonyl, pyridinyl, imidazolyl, N-methylimidazolyl, formylamino, formylaminomethyl, aminocarbonyl, methylcarbonyloxy, and aminocarbonylpropyl substituted with a zwitterionic group.

3. The self-wetting porous membrane of claim 1 , wherein the monomer of A is selected from 1-vinylpyrrolid-2-one, N-[3-(dimethylamino)propyl]methacrylamide, vinyl acetate, 1-vinylimidazole, 1-vinyl-3-methylimidazole, 1-vinyl-2-pyridine, 1-vinyl-4-pyridine, acrylamide, N-vinylformamide, and N-allylformamide, and 3-(methacrylamidopropyl)dimethyl(3-sulfopropyl)ammonium inner salt.

4. The self-wetting porous membrane of claim 1 , wherein the aromatic hydrophobic polymeric segment B is selected from polysulfone, polyethersulfone, polyphenyl ether, polyphenylene ether sulfone, polyphenylene oxide, polyether ether ketone, polyether ketone ketone, and polyetherimide.

5. The self-wetting porous membrane of claim 1 , wherein the aromatic hydrophobic polymeric segment B is polysulfone.

6. The self-wetting porous membrane of claim 1 , wherein the aromatic hydrophobic polymer is selected from polysulfone, polyethersulfone, polyphenyl ether, polyphenylene ether sulfone, polyphenylene oxide, polycarbonate, poly(phthalazinone ether sulfone ketone), polyether ketone, polyether ether ketone, polyether ketone ketone, polyimide, polyetherimide, and polyamide-imide.

7. The self-wetting porous membrane of claim 1 , wherein the aromatic hydrophobic polymer is polysulfone or polyethersulfone.

8. The self-wetting porous membrane of claim 1 , the copolymer is of the formula (Ia) or (Ib):
T-(A′) m1 -X—[B]—X-(A′) m2 -T  (Ia),

Y—[B]—X-(A′) m1 -T  (Ib),

wherein B is the aromatic hydrophobic polymeric segment, A′ is a polymeric segment of the hydrophilic monomer, X is —NHC(═O)(CH 2 ) p S—, wherein p is 1-3, T is an end group selected from the group consisting of 2-methylpropionitrile, benzoate, acetate, laurate, t-butyloxy and cumyloxy, m 1 and m 2 are each from about 5 to 50, and Y is a group other than amino group.

9. The self-wetting porous membrane of claim 1 , wherein the copolymer is of the formula:

wherein each of m 1 and m 2 is from about 5 to about 50 and n is from about 20 to about 200.

10. A method of preparing a self-wetting porous membrane comprising:
(i) casting a solution comprising a solvent, an aromatic hydrophobic polymer, and a copolymer of formula A-B or A-B-A, wherein A is a hydrophilic segment comprising a polymerized monomer or mixture of monomers, wherein the monomer is of the formula (I):
CH 2 ═C(R 1 )(R 2 )  (I),

wherein R 1 is hydrogen or alkyl, and R 2 is selected from substituted or unsubstituted heterocyclyl, substituted or unsubstituted heteroaryl, formylamino, formylaminoalkyl, aminocarbonyl, alkylcarbonyloxy, and aminocarbonylalkyl substituted with a zwitterionic group,
and B is an aromatic hydrophobic polymeric segment, wherein segments B and A are linked through an amidoalkylthio group, to a desired shape;
(ii) subjecting the cast solution to phase inversion to form the self-wetting porous membrane; and
(iii) optionally rinsing the self-wetting porous membrane with water.

11. The method of claim 10 , wherein R 1 is hydrogen or methyl, and R 2 is selected from pyrrolidinonyl, pyridinyl, imidazolyl, N-methylimidazolyl, formylamino, formylaminomethyl, aminocarbonyl, methylcarbonyloxy, and aminocarbonylpropyl substituted with a zwitterionic group.

12. The method of claim 10 , wherein the monomer of A is selected from 1-vinylpyrrolid-2-one, N-[3-(dimethylamino)propyl]methacrylamide, vinyl acetate, 1-vinylimidazole, 1-vinyl-3-methylimidazole, 1-vinyl-2-pyridine, 1-vinyl-4-pyridine, acrylamide, N-vinylformamide, and N-allylformamide, and 3-(methacrylamidopropyl)dimethyl(3-sulfopropyl)ammonium inner salt.

13. The method of claim 10 , wherein the aromatic hydrophobic polymeric segment B of the copolymer is selected from polysulfone, polyethersulfone, polyphenyl ether, polyphenylene ether sulfone, polyphenylene oxide, polyether ether ketone, polyphenyl sulfide, and polyetherimide.

14. The method of claim 10 , wherein the aromatic hydrophobic polymeric segment B of the copolymer is polysulfone.

15. The method of claim 10 , wherein the aromatic hydrophobic polymer is selected from polysulfone, polyethersulfone, polyphenylene ether, polyphenylene ether sulfone, polyphenylene oxide, polycarbonate, poly(phthalazinone ether sulfone ketone), polyether ketone, polyether ether ketone, polyether ketone ketone, polyimide, polyetherimide, and polyamide-imide.

16. The method of claim 10 , wherein the aromatic hydrophobic polymer is polysulfone or polyethersulfone.

17. The method of claim 10 , wherein the copolymer is of the formula (Ia) or (Ib):
T-(A′) m1 -X—[B]—X-(A′) m2 -T  (Ia),

Y—[B]—X-(A′) m1 -T  (Ib),

wherein B is the aromatic hydrophobic polymeric segment, A′ is a polymeric segment of the hydrophilic monomer, X is —NHC(═O)(CH 2 ) p S—, wherein p is 1-3, T is an end group selected from the group consisiting of 2-methylpropionitrile, benzoate, acetate, laurate, t-butyloxy and cumyloxy, m 1 and m 2 are each from about 5 to 50, and Y is a group other than amino group.

18. The method of claim 10 , wherein the copolymer is of the formula:

wherein each of m 1 and m 2 is from about 5 to about 50 and n is from about 20 to about 200.

19. A self-wetting porous membrane prepared by the method of claim 10 .

20. A method of filtering a fluid, the method comprising passing the fluid through the self-wetting porous membrane of claim 1 .

Assignees

• Pall Corp

Inventors

• Stasiak Marcin
• Ait-Haddou Hassan

Classifications

• C08F220/606

  and containing other heteroatoms · CPC title

• B01D2323/02

  Hydrophilization · CPC title

• B01D67/0002

  Organic membrane manufacture · CPC title

• C08F293/00

  Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule (on to polymers modified by introduction of unsaturated end groups C08F290/02) · CPC title

• B01D71/80

  Block polymers · CPC title