Ceramic nanofiltration membrane with polymers grafted into the pores and method of producing same

Patent metadata

Field	Value
Publication number	US-12569816-B2
Application number	US-201917260444-A
Country	US
Kind code	B2
Filing date	Jul 9, 2019
Priority date	Jul 19, 2018
Publication date	Mar 10, 2026
Grant date	Mar 10, 2026

Abstract

The present disclosure relates to a nanofiltration membrane and a method of manufacturing a nanofiltration membrane. The method includes providing a support structure having a first mesoporous layer made of TiO 2 and/or ZrO 2 and a second porous layer adjacent to the mesoporous layer made of aluminum oxide. The method further includes grafting an anchoring group within pores of the first mesoporous layer, wherein the second layer is inert to the grafting step. An initiator for a surface-initiated atom transfer radical polymerization (SI-ATRP) reaction is covalently bonded to the anchoring group. The support structure is impregnated with a monomer and a solvent, and a polymerization reaction is performed, which includes passing a catalyst through the mesoporous layer, the monomer being configured to start the polymerization reaction by grafting from the initiator in the presence of the catalyst.

First claim

The invention claimed is:

1 . A method of manufacturing a nanofiltration membrane, the method comprising:
providing a support structure comprising a first mesoporous layer and a second porous layer adjacent to the first mesoporous layer, wherein the first mesoporous layer is a layer of ceramic material comprising one or a combination of: TiO 2 and ZrO 2 and wherein the second porous layer is made of an aluminum oxide; covalently attaching an anchoring group selected from the group consisting of a phosphonic acid group, a Grignard reagent, a salicylic acid group, a carbohydrate, and a phthalic acid group within pores of the first mesoporous layer, wherein the second porous layer is inert to the covalently attaching step; subsequent to the covalently attaching, covalently bonding an initiator to the anchoring group, wherein the initiator is configured to initiate a surface-initiated atom transfer radical polymerization reaction and is selected from the group consisting of α-bromoisobutyryl, α-bromoisobutyryl bromide, ethyl 2-bromoisobutyrate, α-bromoisobutyrate, m,p-halogenobenzyl derivatives, and 2-bromo-2-methylpropanamide derivatives; impregnating an entirety of the support structure, including the first mesoporous layer and the second porous layer, with a monomer and a solvent; and performing a polymerization reaction, comprising passing a feed comprising a catalyst through the first mesoporous layer, the monomer being configured to start the surface-initiated atom transfer radical polymerization reaction by grafting from the initiator in the presence of the catalyst; wherein passing the feed comprising the catalyst comprises injecting the catalyst at a first side of the support structure from the second porous layer toward the first mesoporous layer to obtain a concentration gradient; and wherein passing the feed comprising the catalyst further comprises diffusing the catalyst through the first mesoporous layer under action of the concentration gradient.

2 . The method of claim 1 , further comprising deactivating the catalyst by flushing the support structure with a deactivating agent.

3 . The method of claim 1 , wherein the feed comprising the catalyst is passed through the support structure during the polymerization reaction, wherein a flow rate of the feed through the support structure is monitored during the polymerization reaction, and wherein a deactivating agent configured to deactivate the catalyst is injected when the flow rate reaches a predetermined threshold.

4 . The method of claim 1 , wherein passing the feed comprising the catalyst comprises injecting the catalyst at a first side of the support structure from the second porous layer towards the first mesoporous layer, and at a second side of the support structure opposite to the first side.

5 . The method of claim 2 , wherein the first mesoporous layer is present on an external surface of the second porous layer.

6 . The method of claim 2 , wherein the feed comprising the catalyst is passed through the support structure during the polymerization reaction, wherein a flow rate of the feed through the support structure is monitored during the polymerization reaction, and wherein a deactivating agent configured to deactivate the catalyst is injected when the flow rate reaches a predetermined threshold.

7 . The method of claim 2 , wherein passing the feed comprising the catalyst comprises injecting the catalyst at a first side of the support structure from the second porous layer towards the first mesoporous layer, and at a second side of the support structure opposite to the first side.

8 . The method of claim 1 , wherein the catalyst is selected from the group consisting of N,N,N′,N′,N″-Pentamethyldiethylenetriamine, 2,2′-bipyridine, 4,4′-Di-5-nonyl-2,2′-bipyridine, tris(2-aminoethyl)amine, Tris(2-dimethylaminoethyl)amine, CuBr, CuCl2, and Sn(EH)2.

9 . The method of claim 1 , wherein the impregnating is subsequent to the covalently bonding.

10 . The method of claim 1 , wherein the performing the polymerization reaction is subsequent to the impregnating.

11 . The method of claim 10 , wherein the performing the polymerization reaction is subsequent to the covalently bonding.

Assignees

• Vito Nv

Inventors

• Dorbec Matthieu
• Buekenhoudt Anita
• Coloma Jimenez Maider
• Vandezande Pieter

Classifications

• B01D69/108

  Inorganic support material · CPC title

• B01D69/1214

  Chemically bonded layers, e.g. cross-linking · CPC title

• B01D2323/50

  Control of the membrane preparation process · CPC title

• B01D2323/46

  Impregnation · CPC title

• B01D2323/40

  in-situ membrane formation · CPC title