Composite polyamide membrane treated with dihyroxyaryl compounds and nitrous acid

US9452391B1 · US · B1

Patent metadata
FieldValue
Publication numberUS-9452391-B1
Application numberUS-201415030506-A
CountryUS
Kind codeB1
Filing dateOct 29, 2014
Priority dateDec 2, 2013
Publication dateSep 27, 2016
Grant dateSep 27, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method for making a composite polyamide membrane comprising a porous support and a polyamide layer, including the steps of: i) applying a polar solution including a polyfunctional amine monomer and a non-polar solution including a polyfunctional acyl halide monomer to a surface of a porous support and interfacially polymerizing the monomers to form a polyamide layer; ii) applying a dihydroxyaryl compound to the polyamide layer, wherein the dihydroxyaryl compound is represented by: formula wherein D, D′, D″ and D′″ are independently selected from: alkyl, alkoxy, hydrogen, halogen, hydroxyl and amine, and L is a linking group; and iii) exposing the thin film polyamide layer to nitrous acid.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for making a composite polyamide membrane comprising a porous support and a polyamide layer, wherein the method comprises: 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 polyamide layer; ii) applying a dihydroxyaryl compound to the polyamide layer, wherein the dihydroxyaryl compound is represented by  wherein D, D′, D″ and D′″ are independently selected from: alkyl, alkoxy, hydrogen, halogen, hydroxyl and amine, E and E′ are independently selected from: amide, amine, azo, ether and ester, and L′ is selected from at least one of: aliphatic and arylene, and iii) exposing the thin film polyamide layer to nitrous acid; wherein step ii) is performed before, during or after step iii). 2. The method of claim 1 wherein steps i), ii) and iii) are performed sequentially. 3. The method of claim 1 wherein D, D′, D″, and D′″ are hydrogen. 4. The method of claim 1 wherein E and E′ are independently selected from: amide and ether. 5. The method of claim 1 wherein the non-polar solution further comprises an acid-containing monomer comprising a C 2 -C 20 hydrocarbon moiety substituted with at least one carboxylic acid functional group or salt thereof and at least one amine-reactive functional group selected from: acyl halide, sulfonyl halide and anhydride, wherein the acid-containing monomer is distinct from the polyfunctional acyl halide monomer. 6. 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 exposing the thin film polyamide layer to nitrous acid. 7. The method of claim 1 wherein at least one of the polar and non-polar solutions further comprises a tri-hydrocarbyl phosphate compound represented by Formula (I): wherein R 1 , R 2 and R 3 are independently selected from hydrogen and hydrocarbyl groups comprising from 1 to 10 carbon atoms, with the proviso that no more than one of R 1 , R 2 and R 3 are hydrogen. 8. The method of claim 1 wherein the dihydroxyaryl compound is selected from at least one of: N,N′-(benzene-1,3-diyldimethanediyl)bis(3,5-dihydroxybenzamide) N,N′-(1,4-phenylenebis(methylene))bis(3,5-dihydroxybenzamide) N,N′-[5-(trifluoromethyl)benzene-1,3-diyl]bis(3,5-dihydroxybenzamide) N,N′-biphenyl-4,4′-diylbis(3,5-dihydroxybenzamide) N,N′-ethane-1,2-diylbis(3,5-dihydroxybenzamide) 3,5-bis[(3,5-dihydroxybenzoyl)amino]benzoic acid. 9. The method of claim 1 wherein the dihydroxyaryl compound is represented by at least one of: wherein Y is selected from the aliphatic and arylene. 10. The method of claim 1 wherein the dihydroxyaryl compound is represented by at least one of:

Assignees

Inventors

Classifications

  • Cross-linking · CPC title

  • B01D69/125Primary

    In situ manufacturing by polymerisation, polycondensation, cross-linking or chemical reaction · CPC title

  • Polyamides, e.g. polyester-amides · CPC title

  • Storing or preservation · CPC title

  • Drying · CPC title

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What does patent US9452391B1 cover?
A method for making a composite polyamide membrane comprising a porous support and a polyamide layer, including the steps of: i) applying a polar solution including a polyfunctional amine monomer and a non-polar solution including a polyfunctional acyl halide monomer to a surface of a porous support and interfacially polymerizing the monomers to form a polyamide layer; ii) applying a dihydroxya…
Who is the assignee on this patent?
Dow Global Technologies Llc
What technology area does this patent fall under?
Primary CPC classification B01D69/125. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Sep 27 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 11 related publications on this page (citations in our corpus or others sharing the same primary CPC).