IP Library Granted Patent US 12,569,802
Granted Patent B2
US 12,569,802 · App. 17/615,503 · Granted Mar 10, 2026

Guanidine-containing membranes and methods of using thereof

Inventors: W.S. Winston Ho (Columbus, OH); Yang Han (Columbus, OH)
Assignee: Ohio State Innovation Foundation
B01D53/228B01D69/02B01D69/10B01D69/12B01D69/141B01D69/142B01D71/021B01D71/441B01D71/60B01D71/68B01D2325/20
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Quick Facts
Patent No.
US 12,569,802
App. No.
17/615,503
Granted
Mar 10, 2026
Kind
B2
Abstract

Membranes, methods of making the membranes, and methods of using the membranes are described herein. The membrane can comprise a support layer; and a selective polymer layer disposed (e.g., coated) on the support layer. The selective polymer layer can comprise a polymer matrix (e.g., a hydrophilic polymer, an amine-containing polymer, or a combination thereof), and a guanidine-based mobile carrier dispersed within the polymer matrix. Optionally, the selective polymer later can further include an amine-based mobile carrier, a CO 2 -philic ether, a graphene oxide, carbon nanotubes, or a combination thereof, dispersed within the polymer matrix. The membranes can be used to separate carbon dioxide from other gases, such as hydrogen and/or nitrogen. Also provided are methods of separating gas streams using the membranes described herein.

Claims (28)

1 . A membrane comprising:

a support layer; and

a selective polymer layer disposed on the support layer, the selective polymer layer comprising a polymer matrix and a guanidine-based mobile carrier having a molecular weight of less than 1,000 Da dispersed within the polymer matrix.

2 . The membrane of claim 1 , wherein the guanidine-based mobile carrier comprises a compound defined by Formula I below

wherein

R 1 and R 2 are each independently selected from the group consisting of H, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-4 haloalkyl, C 3-10 cycloalkyl, 6-10 membered aryl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, wherein said C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-4 haloalkyl, C 3-10 cycloalkyl, 6-10 membered aryl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, are optionally substituted with 1, 2, 3, or 4 independently selected R A groups, or R 1 and R 2 , together with the N atom to which they are attached, form a 4-9 membered heterocycloalkyl group or a 5-6 membered heteroaryl group, each optionally substituted with 1, 2, or 3 independently selected R A groups;

R 3 and R 4 are each independently selected from the group consisting of H, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-4 haloalkyl, C 3-10 cycloalkyl, 6-10 membered aryl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, wherein said C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-4 haloalkyl, C 3-10 cycloalkyl, 6-10 membered aryl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, are optionally substituted with 1, 2, 3, or 4 independently selected R A groups, or R 3 and R 4 , together with the N atom to which they are attached, form a 4-9 membered heterocycloalkyl group or a 5-6 membered heteroaryl group, each optionally substituted with 1, 2, or 3 independently selected R A groups;

R 5 is selected from the group consisting of H, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-4 haloalkyl, C 3-10 cycloalkyl, 6-10 membered aryl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, wherein said C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-4 haloalkyl, C 3-10 cycloalkyl, 6-10 membered aryl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, are optionally substituted with 1, 2, 3, or 4 independently selected R A groups; and

each R A is independently selected from OH, NO 2 , CN, halo, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-4 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, cyano-C 1-3 alkyl, HO—C 1-3 alkyl, amino, C 1-6 alkylamino, di(C 1-6 alkyl)amino, thio, C 1-6 alkylthio, C 1-6 alkylsulfinyl, C 1-6 alkylsulfonyl, carbamyl, C 1-6 alkylcarbamyl, di(C 1-6 alkyl)carbamyl, carboxy, C 1-6 alkylcarbonyl, C 1-6 alkoxycarbonyl, C 1-6 alkylcarbonylamino, C 1-6 alkylsulfonylamino, aminosulfonyl, C 1-6 alkylaminosulfonyl, di(C 1-6 alkyl)aminosulfonyl, aminosulfonylamino, C 1-6 alkylaminosulfonylamino, di(C 1-6 alkyl)aminosulfonylamino, aminocarbonylamino, C 1-6 alkylaminocarbonylamino, and di(C 1-6 alkyl)aminocarbonylamino.

3 . The membrane of claim 2 , wherein R 1 , R 2 , R 3 , and R 4 are all C 1-4 alkyl.

4 . The membrane of any of claim 2 , wherein R 5 is H.

5 . The membrane of any of claim 2 , wherein R 5 is C 1-6 alkyl optionally substituted with 1, 2, 3, or 4 independently selected R A groups.

6 . The membrane of claim 5 , wherein R 5 is C 1-6 alkyl substituted with an OH group.

7 . The membrane of claim 5 , wherein R 5 is C 1-6 alkyl substituted with an amino group.

8 . The membrane of any of claim 1 , wherein the guanidine-based mobile carrier comprises one of the following

wherein n is an integer from 1 to 12, such as from 1 to 6, TMG is tetramethyguanidine, and PZC is piperazine-1-carboximidamide.

9 . The membrane of any of claim 1 , wherein the polymer matrix comprises a hydrophilic polymer, an amine-containing polymer, or a combination thereof.

10 . The membrane of claim 9 , wherein the amine-containing polymer is selected from the group consisting of polyvinylamine, polyallylamine, polyethyleneimine, poly-N-isopropylallylamine, poly-N-tert-butylallylamine, poly-N-1,2-dimethylpropylallylamine, poly-N-methylallylamine, poly-N,N-dimethylallylamine, poly-2-vinylpiperidine, poly-4-vinylpiperidine, polyaminostyrene, chitosan, copolymers, and blends thereof.

11 . The membrane of any of claim 1 , wherein the selective polymer layer further comprises an amine-containing mobile carrier.

12 . The membrane of claim 11 , wherein the amine-containing mobile carrier comprises a salt of a primary amine or a salt of a secondary amine.

13 . The membrane of any of claim 11 , wherein the amine-containing mobile carrier comprises a salt selected from the group consisting of aminoisobutyric acid-potassium salt, aminoisobutyric acid-lithium salt, aminoisobutyric acid-piperazine salt, glycine-potassium salt, glycine-lithium salt, glycine-piperazine salt, dimethylglycine-potassium salt, dimethylglycine-lithium salt, dimethylglycine-piperazine salt, piperadine-2-carboxlic acid-potassium salt, piperadine-2-carboxlic acid-lithium salt, piperadine-2-carboxlic acid-piperazine salt, piperadine-4-carboxlic acid-potassium salt, piperadine-4-carboxlic acid-lithium salt, piperadine-4-carboxlic acid-piperazine salt, piperadine-3-carboxlic acid-potassium salt, piperadine-3-carboxlic acid-lithium salt, piperadine-3-carboxlic acid-piperazine salt, and blends thereof.

14 . The membrane of any of claim 11 , wherein the amine-containing mobile carrier comprises an amino acid salt.

15 . The membrane of any of claim 14 , wherein the amino acid salt comprises a glycinate salt, a sarcosinate salt, or an aminoisobutyrate salt.

16 . The membrane of any of claim 1 , wherein the selective polymer layer further comprises a CO 2 -philic ether.

17 . The membrane of any of claim 1 , wherein the selective polymer layer further comprises a cross-linking agent.

18 . The membrane of any of claim 1 , wherein the selective polymer layer further comprises graphene oxide dispersed within the polymer matrix.

19 . The membrane of any of claim 1 , wherein the selective polymer layer further comprises carbon nanotubes dispersed within the polymer matrix.

20 . A method for separating a first gas from a feed gas stream, the method comprising contacting a membrane defined by any of claim 1 with the feed gas stream comprising the first gas under conditions effective to afford transmembrane permeation of the first gas.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 24, 2022
From: OHIO STATE UNIVERSITY
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 060173/0503 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2021
From: HO, W.S. WINSTON; HAN, YANG
To: OHIO STATE INNOVATION FOUNDATION
Reel/Frame 058247/0954 →
Continuity (2)
Provisional Application 62855368 · May 31, 2019
Related Publication 20220305436A1 · Sep 29, 2022
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