Forward osmosis membrane and method of forming a forward osmosis membrane

Patent metadata

Field	Value
Publication number	US-12048897-B2
Application number	US-201213981876-A
Country	US
Kind code	B2
Filing date	Jan 25, 2012
Priority date	Jan 25, 2011
Publication date	Jul 30, 2024
Grant date	Jul 30, 2024

Abstract

A method of forming a forward osmosis membrane having a porous substrate and a rejection layer is provided. The method comprises a) forming a thin film of a polymer solution on a suitable substrate, wherein the polymer solution contains at least one polymer and optionally one or more additives in a suitable solvent, b) immersing the thin film in a coagulant bath to form the porous substrate; and c) forming a rejection layer on the porous substrate. A forward osmosis membrane is also provided.

First claim

The invention claimed is:

1. A method of forming a forward osmosis membrane comprising a porous substrate and a rejection layer, the method comprising
a) forming a thin film of a polymer solution on a substrate, wherein the polymer solution comprises at least one polymer, an organic pore former comprising 0.5 wt % polyvinyl pyrrolidone, an inorganic salt pore former comprising 3 wt % lithium chloride, and a solvent which dissolves each of the at least one polymer homogeneously, wherein each wt % is based on the polymer solution;
b) immersing the thin film and the substrate in a coagulant bath which is at room temperature, wherein the coagulant bath comprises (i) the solvent and (ii) a non-solvent to each of the at least one polymer, both of which flow in the coagulant bath to remove the solvent in the thin film and have the thin film undergo phase inversion on the substrate to form a porous substrate comprising:
an overall porosity of 30% to 80%,
a first layer having elongated shaped pores, and
a second layer having a lower porosity than the first layer and a sponge-like structure;

c) heating the porous substrate in deionized water at 60° C. to 90° C. for 1 minute to less than 5 minutes followed by cooling the porous substrate in room temperature deionized water before forming a rejection layer, wherein both the heating and the cooling structurally stabilize the porous substrate, and wherein the porous substrate has a contact angle ranging from 50° to 80°; and
d) forming the rejection layer on the second layer of the porous substrate by interfacial polymerization.

2. The method according to claim 1 , wherein the thin film is formed on a woven mesh placed on the substrate.

3. The method according to claim 2 , wherein the woven mesh has a porosity of about 20% to about 80%.

4. The method according to claim 1 , wherein the at least one polymer is selected from the group consisting of polysulfone (PSF), polyether sulfone (PES), polyetherimide (PEI), polyacrylonitrile (PAN), polyvinylidene fluoride (PVDF), a combination thereof and derivatives thereof.

5. The method according to claim 1 , wherein the solvent of the polymer solution is selected from the group consisting of 1-Methyl-2-Pyrrolidinone (NMP), dimethyl-acetamide (DMAc), dimethyl formamide (DMF), and combinations thereof.

6. The method according to claim 1 , wherein the non-solvent in the coagulant bath is water, and the solvent in the coagulant bath is selected from the group consisting of 1-Methyl-2-Pyrrolidinone (NMP), dimethyl-acetamide (DMAc), dimethyl formamide (DMF), and combinations thereof.

7. The method according to claim 1 , wherein forming the rejection layer on the porous substrate comprises contacting the porous substrate with an aqueous amine solution and an organic acyl halide solution.

8. The method according to claim 7 , wherein the aqueous amine solution comprises m-phenylenediamine (MPD).

9. The method according to claim 7 , wherein the organic acyl halide solution comprises an acyl chloride dissolved in a solvent which does not react with the acyl chloride.

10. The method according to claim 9 , wherein the acyl chloride is selected from the group consisting of trimesoyl chloride (TMC), 5-isocyanato-isophthaloyl chloride (ICIC), 5-chloroformyloxy-isophthaloyl chloride (CFIC), combinations thereof and derivatives thereof.

11. The method according to claim 9 , wherein the solvent which does not react with the acyl chloride is selected from the group consisting of aliphatic hydrocarbons, aromatic hydrocarbons, and halogenated hydrocarbons.

12. The method according to claim 1 , wherein the mean pore diameter of the pores in the first layer is in the range of about 1 μm to about 7 μm.

13. The method according to claim 1 , wherein the mean pore diameter of the pores in the second layer is in the range of about 10 nm to about 100 nm.

Assignees

• Tang Chuyang
• Qiu Changquan
• Wei Jing
• Wang Rong
• Fane Anthony G
• Univ Nanyang Tech

Inventors

• Tang Chuyang
• Qiu Changquan
• Wei Jing
• Wang Rong
• Fane Anthony G

Classifications

• B01D69/1251

  by interfacial polymerisation · CPC title

• B01D69/1071

  Woven, non-woven or net mesh · CPC title

• B01D2323/22

  Specific non-solvents or non-solvent system · CPC title

• B01D2323/18

  Pore-control agents or pore formers · CPC title

• B01D2325/026

  Sponge structure · CPC title