IP Library Granted Patent US 9,597,642
Granted Patent B2
US 9,597,642 · App. 14/338,543 · Granted Mar 21, 2017

Hybrid TFC RO membranes with non-metallic additives

Inventors: Jeffrey Alan Koehler (Pasadena, CA); Christopher James Kurth (Eden Prairie, MN)
Assignee: LG NANOH2O, INC.
B01D71/56B01D67/0006B01D67/0009B01D67/0079B01D69/02B01D69/10B01D69/125B01D69/148B01D61/025B01D2323/30B01D2323/36B01D2325/18Y10S977/779Y10S977/783
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Quick Facts
Patent No.
US 9,597,642
App. No.
14/338,543
Granted
Mar 21, 2017
Kind
B2
Abstract

A process for preparing a reverse osmosis membrane that includes: (A) providing a polyamine, a polyfunctional acid halide, and a flux increasing additive having the formula Z + B − , where Z + is an easily dissociable cation and B − is a beta-diketonate; (B) combining the polyamine, polyfunctional acid halide, and flux increasing additive on the surface of a porous support membrane; and (C) interfacially polymerizing the polyamine and the polyfunctional acid halide, and flux increasing additive on the surface of the porous support membrane to form a reverse osmosis membrane comprising (i) the porous support membrane and (ii) a discrimination layer comprising a polyamide. The reverse osmosis membrane is characterized by a flux that is greater than the flux of the same membrane prepared in the absence of the flux increasing additive.

Claims (14)

1. A composition, comprising:

a flux increasing additive having the formula Z + B − , wherein Z + is an easily dissociable cation selected from among H + and R 1 R 2 R 3 R 4 N + , where R 1 , R 2 , R 3 , and R 4 , each independently is H, a C 1 -C 6 hydrocarbyl group, a benzyl group, or a phenyl group, and B − is a beta-diketonate;

an aqueous phase containing a polar liquid; and

a difunctional or polyfunctional nucleophilic monomer.

2. The composition of claim 1 , wherein Z + has the formula R 1 R 2 R 3 R 4 N + , where R 1 , R 2 , R 3 , and R 4 , each independently is H, a C 1 -C 6 hydrocarbyl group, a benzyl group, or a phenyl group.

3. The composition of claim 2 , wherein R 1 , R 2 , R 3 , and R 4 are ethyl groups.

4. The composition of claim 2 , wherein R 1 , R 2 , and R 3 each is an ethyl group, and R 4 is H.

5. The composition of claim 1 , wherein B − has the formula:

where X and Y, independently, are H, a C 1 -C 6 hydrocarbyl group, a benzyl group, a phenyl group, —OR 5 , or NR 6 R 7 , each optionally substituted with fluorine, and R 5 , R 6 , and R 7 , each independently, is H, a C 1 -C 6 hydrocarbyl group, a benzyl group or a phenyl group.

6. The composition of claim 5 , wherein X and Y each independently is a C 1 -C 6 hydrocarbyl group, a benzyl group, a phenyl group, —OR 5 , or NR 6 R 7 each substituted with fluorine.

7. The composition of claim 5 , wherein X and Y are methyl groups.

8. The composition of claim 5 , wherein X and Y are trifluoromethyl groups.

9. The composition of claim 5 , wherein X and Y are selected so that B − has a 5-carbon or larger carbon framework.

10. The composition of claim 1 , wherein the nucleophilic monomer is a polyamine selected from the group consisting of diaminobenzene, triaminobenzene, m-phenylene diamine, p-phenylene diamine, 1,3,5-diaminobenzoic acid, 2-4-diaminotoluene, 2,4-diaminoanisole, xylylene diamine, ethylene diamine, propylene diamine, piperazine and tris(2-aminoethyl)amine.

Assignments (3)
CHANGE OF NAME Recorded Jun 30, 2026
From: LG NANOH2O, LLC
To: NANOH2O AMERICA, LLC
Reel/Frame 075857/0834 →
CHANGE OF NAME Recorded Jun 29, 2026
From: LG NANOH2O, INC.
To: LG NANOH2O, LLC
Reel/Frame 075853/0148 →
CHANGE OF NAME Recorded Aug 22, 2014
From: NANOH20, INC.
To: LG NANOH20, INC.
Reel/Frame 033593/0482 →
Continuity (3)
Continuation 13293744 · Nov 10, 2011
Provisional Application 61412184 · Nov 10, 2010
Related Publication 20140329010A1 · Nov 6, 2014