Reverse osmosis membrane and method of producing the same
US-2024307831-A1 · Sep 19, 2024 · US
US10137418B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10137418-B2 |
| Application number | US-201414650127-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 3, 2014 |
| Priority date | Jan 14, 2013 |
| Publication date | Nov 27, 2018 |
| Grant date | Nov 27, 2018 |
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A method for making a composite polyamide membrane comprising a porous support and a thin film polyamide layer, wherein the method includes: i) applying a polar solution comprising a polyfunctional amine monomer, and a non-polar solution comprising a polyfunctional acyl halide monomer to a surface of a porous support and interfacially polymerizing the monomers to form a thin film polyamide layer, wherein the non-polar solution further comprises at least 50 vol % of a C 5 to C 20 aliphatic hydrocarbon and from 2 to 25 vol % of benzene or benzene substituted with one or more C 1 to C 6 alkyl groups; and ii) applying an aqueous solution of nitrous acid to the thin film polyamide layer.
Opening claim text (preview).
The invention claimed is: 1. A method for making a composite polyamide membrane comprising a porous support and a thin film polyamide layer, wherein the method comprises: i) applying a polar solution comprising 2.5 to 6 wt % m-phenylene amine and a non-polar solution comprising 0.05 to 0.3 wt % trimesoyl chloride to a surface of a porous support and interfacially polymerizing the monomers to form a thin film polyamide layer, wherein the non-polar solution comprises: a) 50 to 90 vol % of C5 to C20 aliphatic hydrocarbon selected from a paraffin or isoparaffin, or combination thereof, b) 3 to 15 vol % mesitylene, and c) 0.02 to 0.08 wt % 1-carboxy-3,5-dichloroformyl benzene (mhTMC); and ii) applying an aqueous solution of nitrous acid to the thin film polyamide layer. 2. The method of claim 1 wherein the thin film polyamide layer has a dissociated carboxylic acid content of at least 0.18 moles/kg at pH 9.5 as measured by RBS prior to the step of applying the aqueous solution of nitrous acid. 3. The method of claim 1 wherein the thin film polyamide layer has a dissociated carboxylic acid content of at least 0.45 moles/kg at pH 9.5 prior to the step of applying the aqueous solution of nitrous acid. 4. The method of claim 1 wherein the thin film polyamide layer has an isoelectric point (IEP) of less than or equal to 4.3 prior to the step of applying the aqueous solution of nitrous acid.
characterised by the presence of specified groups, e.g. introduced by chemical after-treatment · CPC title
Organic membrane manufacture · CPC title
in-situ membrane formation · CPC title
Introduction of specific chemical groups · CPC title
In situ manufacturing by polymerisation, polycondensation, cross-linking or chemical reaction · CPC title
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