IP Library Granted Patent US 10,626,029
Granted Patent B2
US 10,626,029 · App. 15/805,746 · Granted Apr 21, 2020

High-performance anion exchange membranes and methods of making same

Inventor: Juchui Ray Lin (Bedford, MA)
Assignee: Evoqua Water Technologies LLC
C02F1/4693B01D61/422B01J41/14B01J47/12B05D3/067B05D3/068B05D5/00C02F1/4695C08F222/1006C08F226/06C08J5/2287H01M8/103H01M8/1058H01M8/1072C02F2101/101C02F2101/106C02F2101/108C02F2101/12C02F2101/163C02F2103/04C02F2103/08C02F2103/32C08J2323/06C08J2323/12C08J2327/06C08J2327/12C08J2327/18C08J2439/02H01M2008/1095Y02P70/56Y02W10/33Y02W10/37
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Quick Facts
Patent No.
US 10,626,029
App. No.
15/805,746
Granted
Apr 21, 2020
Kind
B2
Abstract

Anion exchange membranes may include a polymeric microporous substrate and a cross-linked anion exchange polymeric layer on the substrate. Anion exchange membranes may have a resistivity of less than about 1.5 Ohm-cm 2 and an apparent permselectivity of at least about 95%. The anion exchange membranes may be produced by a unique, two step process.

Claims (14)

1. A method of making an anion exchange membrane, comprising:

mixing a tertiary amine monomer with a quaternization agent to produce a quaternary amine monomer;

mixing a cross-linking agent and a solvent with the functional monomer to form a monomeric solution; and

casting the monomeric solution on a polymeric microporous substrate to form the anion exchange membrane.

2. The method of claim 1 , wherein the tertiary amine monomer is selected from the group consisting of 1-vinylimidazole, 2-methyl-1-vinylimidazole, 9-vinylcarbazole, N-ethyl-2-vinylcarbazole, 2-vinylpyridine, 3-vinylpyridine, 4-vinylpyridine, and mixtures thereof.

3. The method of claim 2 , wherein the quaternization agent is selected from the group consisting of benzyl chloride, benzyl bromide, benzyl iodide, p-dichlorobenzene, m-dichlorobenzene, 1,4-dichloro-2-nitrobenzene, 3-(benzyloxy)benzyl chloride, 4-(benzyloxy)benzyl chloride, 2-(trifluoromethyl)-benzyl chloride, 3-(trifluoromethyl)benzyl chloride, 4-(trifluoromethyl)benzyl chloride, 1-chlorohexane, 1-chloropentane, 1-chlorobutane, 1-chloropropane, 1,6dichlorohexane, 1,5-dichloropentane, 1,4-dichlorobutane, 1,3-dichloropropane, 1-bromohexane, 1-bromopentane, 1-bromobutane, 1-bromopropane, 1,6-dibromohexane, 1,5-dibromopentane, 1,4-dibromobutane, 1,3-dibromopropane, 1-iodohexane, 1-iodopentane, 1-iodobutane, 1-iodoopropane, 1-iodideethane, 1-iodidemethane,1,6-diiodohexane, 1,5-diiodorpentane, 1,4-diiodobutane,1,3-diiodopropane, and mixtures thereof.

4. The method of claim 3 , wherein the cross-linking agent is selected from the group consisting of vinylbenzyl chloride, m-divinylbenzene, ethyleneglycol-dimethacrylate, p-dichlorobenzene, m-dichlorobenzene, 1,4-dichloro-2-nitrobenzene, 1,6dichlorohexane, 1,5-dichloropentane, 1,4-dichlorobutane, 1,3-dichloropropane, 1,6-dibromohexane, 1,5-dibromopentane, 1,4-dibromobutane, 1,3-dibromopropane, 1,6-dibromohexane, 1,5-dibromopentane, 1,4-dibromobutane, 1,3-dibromopropane, 1,4-butanediol dimethacrylate, 1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, pentaerythritol triacrylate, divinyl benzene, (m- and p-mixture), trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, ethoxylated (n) bisphenol A di(meth)acrylate (n=1.5, 2, 4, 6, 10, 30), ethoxylated (n) trimethylolpropanetri(meth)acrylate (n=3, 6, 9, 10, 15, 20), propoxylated(n) trimethylolpropane triacrylate (n=3, 6), and mixtures thereof.

5. The method of claim 4 , wherein the solvent is selected from the group consisting of dipropyleneglycol, n-propanol, 2-propanol, 1-methyl-2-pyrrolidinone, 1-butanol, and mixtures thereof.

6. The method of claim 5 , further comprising mixing a polymerization initiator with the monomer solution.

7. The method of claim 6 , wherein the polymerization initiator is selected from the group consisting of organic peroxides, 2,2′-azobis [2, [2-imdazolin-2-yl]-propane] dihydrochloride, α, α′-azoisobutyronitrile, 2,2′-azobis[2-methylpropioaminidine] dihydrochloride, 2,2′-azobis[2, [2-imdazolin-2-yl]-propane], dimethyl 2,2′-azobis[2-methylpropionate] and benzoyl peroxide.

8. The method of claim 7 , further comprising controlling polymerization with an inhibitor.

9. The method of claim 8 , wherein the polymerization inhibitor is selected from the group consisting of 4-methoxyphenol and 4-tert-butyl catechol.

10. The method of claim 9 , wherein the polymeric microporous substrate comprises at least one polymeric material selected from the group consisting of polypropylene, high molecular weight polyethylene, ultrahigh molecular weight polyethylene, polyvinyl chloride, polyvinylidene difluoride, and polytetrafluoroethylene.

11. The method of claim 10 , wherein casting comprises applying heat at a temperature of about 0° C. to about 100° C., ultraviolet light at a wavelength of about 100 nm to about 400 nm, or ionizing radiation.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded May 26, 2023
From: JPMORGAN CHASE BANK N.A., AS COLLATERAL AGENT
To: EVOQUA WATER TECHNOLOGIES LLC; NEPTUNE BENSON, INC.
Reel/Frame 063787/0943 →
SECURITY INTEREST Recorded Apr 7, 2021
From: EVOQUA WATER TECHNOLOGIES LLC; NEPTUNE BENSON, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 055848/0689 →
Continuity (3)
Division 14433063
Provisional Application 61709475 · Oct 4, 2012
Related Publication 20180057370A1 · Mar 1, 2018
Cited By (4)
US 12,341,228 US 12,374,711 US 12,603,388 US 12,712,192