Method of making reaction induced phase separation membranes and uses thereof

Patent metadata

Field	Value
Publication number	US-10960359-B2
Application number	US-201715424558-A
Country	US
Kind code	B2
Filing date	Feb 3, 2017
Priority date	Feb 5, 2016
Publication date	Mar 30, 2021
Grant date	Mar 30, 2021

Abstract

Provided herein are methods of making asymmetric membranes comprising a first layer and a second layer. The methods include preparing a polymeric solution comprising one or more polymers, casting the polymeric solution to form a polymeric film, contacting the polymeric film with a solvent comprising a crosslinker under conditions to form a first layer on the top of the film, wherein the first layer is dense and solvent resistant, and contacting the polymeric film having the dense, solvent-resistant first layer with a non-solvent solution under conditions that form a porous second layer on the bottom of the film.

First claim

What is claimed is:

1. An asymmetric membrane having a first layer and a second layer, produced by the process comprising the steps of:
(a) preparing a polymeric solution comprising one or more polymers, said preparing step includes a condensation reaction of monomers in a first solvent;
(b) casting the polymeric solution to form a polymeric film;
(c) contacting the polymeric film with a second solvent comprising a crosslinker under conditions to form a first layer on a top side of the polymeric film, wherein the crosslinker includes one or more functional groups that are incorporated into the first layer, the first layer is a dense, solvent-resistant first layer including crosslinked polymeric chains, said contacting step includes immersing the polymeric film for an immersion time of more than 0.1 seconds in the second solvent comprising the crosslinker, and said solvent-resistant first layer floats on a remaining part of the polymeric film; and
(d) contacting the polymeric film having the dense, solvent-resistant first layer with a non-solvent solution under conditions that form, by precipitation of the remaining part of the polymeric film, a porous second layer on the bottom of the polymeric film, the second layer including uncrosslinked polymeric chains and not the one or more functional groups.

2. The product produced by the process of claim 1 wherein the polymeric film is 10 microns to 500 microns in thickness.

3. The product produced by the process of claim 1 wherein said immersion time in step (c) does not extend more than 300 seconds.

4. The product produced by the process of claim 1 wherein the non-solvent solution is water.

5. The product produced by the process of claim 1 wherein the polymeric solution of step (a) further comprises the first solvent and wherein the second solvent of step (c) is the same as the first solvent.

6. The product produced by the process of claim 1 wherein the crosslinker is a bifunctional alkyl halide, a multifunctional alkyl halide, a bifunctional isocyanate, a multifunctional isocyanate a bifunctional acyl chloride, a multifunctional acyl chloride, or any combination thereof.

7. The product produced by the process of claim 1 wherein the crosslinker comprises the formula XRY, where X is the same as Y, and wherein X or Y is I, Br, Cl, F, CN, COCl, C6H4SO3H, or an epoxy group, and wherein R is an aliphatic or aromatic moiety.

8. The product produced by the process of claim 1 wherein the crosslinker comprises the formula X—R—Y, where X is different than Y, and wherein X or Y is I, Br, Cl, F, CN, COCl, C6H4SO3H, or an epoxy group, and wherein R is an aliphatic or aromatic moiety.

9. The product produced by the process of claim 1 wherein the crosslinker is 1,4-dibromo-p-xylene (DBX), 2,3,6,7,14,15-hexakis (bromomethyl)-9,10-dihydro-9,10-[1′,2′] benzenoanthracene (Tr-X), or combinations thereof.

10. The product produced by the process of claim 1 wherein the one or more of the functional groups crosslink within one minute or less in the presence of the solvent comprising the crosslinker to form the dense first layer.

11. The product produced by the process of claim 1 wherein the one or more polymers comprise polythiosemicarbazide polymer (PTSC), polybenzimidazole polymer (FBI), or combinations thereof.

12. The product produced by the process of claim 1 wherein the solvent is dimethyl sulfoxide (DMSO), Dimethylacetamide (DMAc), Dimethylformamide (DMF), Tetrahydrofuran (THF), N-methyl-2-pyrrolidone (NMP), or combinations thereof.

13. The product produced by the process of claim 1 wherein the polymeric solution comprises 5-35% (weight/weight) of the polymer.

14. The product produced by the process of claim 1 wherein the crosslinker comprises 0.1-10% (weight/weight) of the solvent comprising the crosslinker.

15. The product produced by the process of claim 1 wherein the solvent comprises DMSO.

16. The product produced by the process of claim 1 wherein the contacting with the non-solvent solution comprises 30 minutes to 24 hours.

17. The product produced by the process of claim 1 wherein the dense first layer is 10 nm to 10 μm in thickness.

18. A method of making a multi-layer asymmetric membrane comprising the steps of:
(a) preparing a polymeric solution comprising one or more polymers, said preparing step includes a condensation reaction of monomers in a first solvent;
(b) casting the polymeric solution to form a polymeric film;
(c) contacting the polymeric film with a second solvent comprising a crosslinker under conditions to form a first layer on a top side of the polymeric film, wherein the crosslinker includes one or more functional groups that are incorporated into the first layer, the first layer is a dense, solvent-resistant first layer including crosslinked polymeric chains, said contacting step includes immersing the polymeric film for an immersion time of more than 0.1 seconds in the second solvent comprising the crosslinker and said solvent-resistant first layer floats on a remaining part of the polymeric film; and
(d) contacting the polymeric film, having the dense, solvent-resistant first layer, with a non-solvent solution under conditions that form, by precipitation of the remaining part of the polymeric film, a porous second layer on the bottom of the polymeric film, the second layer including uncrosslinked polymeric chains and not the one or more functional groups.

19. The method of claim 18 , wherein the polymeric film is 10 microns to 500 microns in thickness.

20. The method of claim 18 , wherein said immersion time in step (c) does not extend more than 300 seconds.

21. The method of claim 18 , wherein the non-solvent solution is water.

22. The method of claim 18 , wherein the polymeric solution of step (a) further comprises the first solvent and wherein the second solvent of step (c) is the same as the first solvent.

23. The method of claim 18 , wherein the crosslinker is a bifunctional alkyl halide, a multifunctional alkyl halide, a bifunctional isocyanate, a multifunctional isocyanate a bifunctional acyl chloride, a multifunctional acyl chloride, or any combination thereof.

24. The method of claim 18 , wherein the crosslinker comprises the formula X—R—Y, where X is the same as Y, and wherein X or Y is I, Br, Cl, F, CN, COCl, C6H4SO3H, or an epoxy group, and wherein R is an aliphatic or aromatic moiety.

25. The method of claim 18 , wherein the crosslinker comprises the formula X—R—Y, where X is different than Y, and wherein X or Y is I, Br, Cl, F, CN, COCl, C6H4SO3H, or an epoxy group, and wherein R is an aliphatic or aromatic moiety.

26. The method of claim 18 , wherein the crosslinker is 1,4-dibromo-p-xylene (DBX), 2,3,6,7,14,15-hexakis (bromomethyl)-9,10-dihydro-9,10-[1′,2′] benzenoanthracene (Tr-X), or combinations thereof.

27. The method of claim 18 , wherein the one or more of the functional groups crosslink within one minute or less in the presence of the solvent comprising the crosslinker to form the dense first layer.

28. The method of claim 18 , wherein the one or more polymers comprise polythiosemicarbazide polymer (PTSC), polybenzimidazole polymer (FBI), or combinations thereof.

29. The method of claim 18 , wherein the solvent is dimethyl sulfoxide (DMSO), Dimethylacetamide (DMAc), Dimethylformamide (DMF), Tetrahydrofuran (THF), N-methyl-2-pyrrolidone (NMP), or co

Assignees

• Univ King Abdullah Sci & Tech

Inventors

• Peinemann Klaus-Viktor
• Aburabie Jamaliah Hani
• Villalobos Vazquez De La Parra Luis Francisco

Classifications

• B01D69/1216

  Three or more layers · CPC title

• B01D69/1214

  Chemically bonded layers, e.g. cross-linking · CPC title

• B01D67/0013 Primary

  Casting processes · CPC title

• B01D2323/30

  Cross-linking · CPC title

• B01D67/0006

  by chemical reactions (in-situ polymerisation, polycondensation, cross-linking or reaction for manufacturing composite membranes B01D69/125) · CPC title