IP Library Granted Patent US 9,943,810
Granted Patent B2
US 9,943,810 · App. 15/301,981 · Granted Apr 17, 2018

Composite polyamide membrane post-treated with nitrous acid

Inventors: Mou Paul (Edina, MN); Matthew J. Jansma (Midland, MI); Abhishek Roy (Edina, MN); Ian A. Tomlinson (Midland, MI)
Assignee: Dow Global Technologies LLC
B01D69/125B01D67/0006B01D67/0093B01D71/56B05D3/107B05D3/108C08G69/48C09D177/00B01D2323/40
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Quick Facts
Patent No.
US 9,943,810
App. No.
15/301,981
Granted
Apr 17, 2018
Kind
B2
Abstract

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 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; and ii) exposing the thin film polyamide layer to nitrous acid; wherein the method is characterized by at least one of: conducting the interfacial polymerization of step i) in the presence of a subject amine compound, or applying a subject amine compound to the interfacially polymerized polyamide layer prior to step ii), wherein the subject amine compound is different from the polyfunctional acyl halide and polyfunctional amine monomers.

Claims (27)

1. A method for making a composite polyamide membrane comprising a porous support and a polyamide layer, wherein the method comprises the steps of:

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; and

ii) exposing the polyamide layer to nitrous acid; wherein the method is characterized by:

applying a subject amine compound to the interfacially polymerized polyamide layer prior to step ii) such that the subject amine compound reacts with residual acid chloride groups present on the surface of the polyamide layer,

wherein the subject amine compound is different from the polyfunctional amine monomer and is represented by the following formula:

wherein:

Z is: hydroxyl, alkoxy, ester, secondary or tertiary amine, or keto-amide;

Y is: hydrogen, carboxylic acid, sulfonic acid or salt thereof, halogen, amine or an alkyl group having from 1 to 12 carbon atoms; and

A, A′, A″ and A′″ are independently: Z, hydrogen, or amine with the proviso that at least one of A, A′, A″ and A′″ is a primary or secondary amine and that at least one of Y, A or A″ is hydrogen.

2. The method of claim 1 wherein Z and at least one of A′ or A′″ is hydroxyl with the proviso that at least one of A or Y is hydrogen.

3. The method of claim 1 wherein Z and at least one of A′ or A′″ is a secondary or tertiary amine with the proviso that at least one of A or Y is hydrogen.

4. The method of claim 1 wherein: Z is: hydroxyl or methoxy; Y is: hydrogen, halogen or carboxylic acid; and A, A′, A″ and A′″ are independently: hydrogen or amine with the proviso that at least one of A, A′, A″ and A′″ is a primary or secondary amine and that at least one of A or A″ is hydrogen.

5. The method of claim 1 wherein: Z is hydroxyl, A′ is hydroxyl, and A is hydrogen provided at least one of A″, A′″ or Y is a primary or secondary amine.

6. The method of claim 1 wherein: Z is hydroxyl, A′″ is hydroxyl, and Y is hydrogen provided at least one of A, A′ or A″ is a primary or secondary amine.

7. The method of claim 1 wherein the polyfunctional amine is a difunctional amine.

8. 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 following formula:

wherein R 1 , R 2 and R 3 are independently: hydrogen or 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.

9. The method of claim 1 wherein the subject amine compound comprises at least one of: 3,5-diaminophenol, 2,4-diaminophenol, 3-aminophenol, 2-aminophenol, 4-aminophenol, 5-aminobenzene-1,3-diol, 3-amino-5-hydroxybenzoic acid, 3-amino-5-hydroxybenzenesulfonic acid, 5-methoxybenzene-1,3-diamine, 4-methoxybenzene-1,3-diamine, 3-methoxyaniline, 2-methoxyaniline, 4-methoxyaniline, 3-amino-5-methoxybenzoic acid, 3-amino-5-methoxybenzenesulfonic acid, N1,N1-dimethylbenzene-1,3-diamine, N1,N1-dimethylbenzene-1,3,5-triamine, N1,N1,N3,N3-tetramethylbenzene-1,3,5-triamine,N,N′-(5-amino-1,3-phenylene)bis(3-oxobutanamide), N-(4-amino phenyl)-3-oxobutanamide, 5-amino-1,3-phenylene bis(2,2,2-trifluoroacetate), 5-amino-1,3-phenylene diacetate, 3,5-bis((tert-butyldimethylsilyl)oxy)aniline, (3,5-bis((tert-butyldimethylsilyl)oxy) phenyl)methanamine, and 2-(3,5-bis((tert-butyldimethylsilyl)oxy) phenyl)ethanamine.

10. A method for making a composite polyamide membrane comprising a porous support and a polyamide layer, wherein the method comprises the steps of:

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; and

ii) exposing the polyamide layer to nitrous acid; wherein the method is characterized by applying a subject amine compound to the interfacially polymerized polyamide layer prior to step ii) such that the subject amine compound reacts with residual acid chloride groups present on the surface of the polyamide layer,

wherein the subject amine compound is different from the polyfunctional amine monomer and is represented by the following formula:

wherein:

Z is: hydroxyl, alkoxy, ester, secondary or tertiary amine or keto-amide;

Y is: hydrogen, carboxylic acid, sulfonic acid or salt thereof, halogen, amine or an alkyl group having from 1 to 12 carbon atoms; and

A, A′, A″ and A′″ are independently: Z, hydrogen, or amine with the proviso that at least one of A, A′, A″ and A′″ is a primary or secondary amine and that at least one of Y, A or A″ is hydrogen; and wherein at least one of the polar and non-polar solutions further comprises a tri-hydrocarbyl phosphate compound represented by following formula:

wherein R 1 , R 2 and R 3 are independently: hydrogen or 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.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2024
From: DOW GLOBAL TECHNOLOGIES LLC
To: THE DOW CHEMICAL COMPANY
Reel/Frame 069923/0030 →
CHANGE OF LEGAL ENTITY Recorded Sep 10, 2024
From: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
To: DDP SPECIALTY ELECTRONIC MATERIALS US, LLC
Reel/Frame 068907/0881 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2024
From: THE DOW CHEMICAL COMPANY
To: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
Reel/Frame 068922/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2018
From: PAUL, MOU; ROY, ABHISHEK
To: FILMTEC CORPORATION
Reel/Frame 045102/0182 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2018
From: FILMTEC CORPORATION
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 045102/0254 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2018
From: JANSMA, MATTHEW J.; TOMLINSON, IAN A.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 045102/0381 →
Continuity (2)
Provisional Application 61992965 · May 14, 2014
Related Publication 20170203259A1 · Jul 20, 2017