Method for manufacturing sulfone polymer membrane
US-2015352502-A1 · Dec 10, 2015 · US
US9745432B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9745432-B2 |
| Application number | US-201414908381-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 30, 2014 |
| Priority date | Jul 31, 2013 |
| Publication date | Aug 29, 2017 |
| Grant date | Aug 29, 2017 |
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The present invention relates to the preparation of novel anion exchange membranes from bicomponent or tricomponent copolymers containing both quaternizable and cross-linkable moieties. The bicomponent copolymers consisted with polyacrylonitrile and poly(2-dimethylaminoethyl) methacrylate and the tricomponent copolymers consisted with polyacryloniterle and poly2-dimethylaminoethyl) methacrylate and polyn-butyl acrylate. Quaternization of dimethyl amino groups of copolymer by methyl iodide followed by cross-linking of acrylonitrile groups of copolymer by hydrazine hydrate resulted anion exchange membrane with desired properties such as high ion exchange capacity (1.30-1.50 meqg −1 ), high transport number (0.92-0.93) for direct use in electrodyalysis unit. The tricomponent anion exchange membrane containing 32 wt % PDMA, 17 wt % PnBA, and 51 wt % PAN exhibited improved performance mainly in terms of low power consumption and high current efficiency during desalination of water.
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We claim: 1. A process for the preparation of anion exchange membranes (AEM) comprising quaternized, cross linked copolymers, wherein said copolymers are poly(2-dimethylaminoethyl)methacrylate (PDMA) in the range of 7 to 42 wt % and polyacrylonitrile (PAN) in the range of 30 to 93 wt % and, optionally, poly-n-butyl acrylate (PnBA) in the range of 17 to 50 wt % if present, the process comprising the steps of: i. providing a copolymer synthesized by free radical polymerization; ii. treating the copolymer as provided in step (i) with an alkyl halide in the ratio ranging between 1 to 1.5 wt % in presence of dimethylformamide (DMF), followed by stirring at a temperature in the range of 30 to 50° C. for a period in the range of 12 to 24 hr to obtain quaternized copolymer; iii. treating the quaternized copolymer as obtained in step (ii) with a diamine in presence of DMF at a temperature in the range of 70 to 80° C. for a period in the range of 40 to 50 minute, followed by drying at a temperature in the range of 70 to 80° C. for a period in the range of 3-4 h to obtain the anion exchange membranes, wherein the copolymer of step (i) is selected from polyacrylonitrile (PAN)-co-poly(2-dimethylaminoethyl)methacrylate (PDMA) (PAN-co-PDMA) or polyacrylonitrile (PAN)-co-poly(2-dimethylaminoethyl)methacrylate (PDMA)-co-poly-n-butylacrylate (PnBA) (PAN-co-PDMA-co-PnBA), and wherein the diamine is selected from hydrazine hydrate, or ethylenediamine individually or in combination thereof. 2. The process as claimed in claim 1 , wherein copolymer (PAN-co-PDMA) is prepared by free radical copolymerization of a mixture of acrylonitrile in the range of 72-70 wt % and dimethylaminoethyl methacrylate in the range of 28-30 wt % monomers. 3. The process as claimed in claim 1 , wherein copolymer (PAN-co-PDMA-co-PNBA) is prepared by free radical copolymerization of mixture of acrylonitrile in the range of 49-55 wt %, dimethylaminoethyl methacrylate in the range of 28-33 wt % and n-butyl acrylate in the range of 17-18 wt % monomers. 4. The process as claimed in claim 1 , wherein the alkyl halide is selected from methyl iodide and methyl bromide. 5. The process as claimed in claim 1 , wherein the alkyl halide concentration is 4 to 10 mol % of poly(2-dimethylaminoethyl)methacrylate unit present in the respective copolymers for quaternization reaction. 6. The process as claimed in claim 1 , wherein the diamine concentration is in the range of 15 to 40 wt % to PAN unit present in the copolymer for the cross-linking reaction.
Homopolymers or copolymers of acrylonitrile (C08J2355/02 takes precedence) · CPC title
Seawater, e.g. for desalination · CPC title
Membrane materials having positively charged functional groups · CPC title
based on macromolecular compounds obtained by reactions other than those involving carbon-to-carbon bonds, e.g. obtained by polycondensation · CPC title
electrodialysis · CPC title
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