High-performance anion exchange membranes and methods of making same

Patent metadata

Field	Value
Publication number	US-10626029-B2
Application number	US-201715805746-A
Country	US
Kind code	B2
Filing date	Nov 7, 2017
Priority date	Oct 4, 2012
Publication date	Apr 21, 2020
Grant date	Apr 21, 2020

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-cm2 and an apparent permselectivity of at least about 95%. The anion exchange membranes may be produced by a unique, two step process.

First claim

The invention claimed is:

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.

Assignees

• Evoqua Water Tech Llc
• Lin Jenny

Inventors

• Lin Juchui Ray

Classifications

• C08J5/2287

  After-treatment · CPC title

• C08J2323/06

  Polyethene · CPC title

• H01M8/103

  having nitrogen, e.g. sulfonated polybenzimidazoles [S-PBI], polybenzimidazoles with phosphoric acid, sulfonated polyamides [S-PA] or sulfonated polyphosphazenes [S-PPh] · CPC title

• B01J47/12

  characterised by the use of ion-exchange material in the form of ribbons, filaments, fibres or sheets, e.g. membranes (electrodialysis or electro-osmosis B01D61/42) · CPC title

• C02F1/4693 Primary

  electrodialysis · CPC title