Granted Patent B2

US 8,486,579 · App. 12/821,961 · Granted Jul 16, 2013

Abstract

Claims (15)

1. A method for manufacturing a polymer blend proton exchange membrane comprising the following steps:

a) dissolving a soluble polymer in an organic solvent and obtaining a uniform solution, wherein the soluble polymer is at least one polymer selected from the group consisting of polysulfone, polyethersulfone and polyvinylidene fluoride;

b) dissolving a sulfonated polymer in the solution obtained in step a) and obtaining a polymer blend membrane forming solution,

wherein the sulfonated polymer is at least one polymer selected from the group consisting of sulfonated poly(ether-ether-ketone), sulfonated poly(ether-ketone-ether-ketone-ketone), sulfonated poly(phthalazinone ether ketone), sulfonated phenolphthalein poly (ether sulfone), sulfonated polyimide, sulfonated polyphosphazene and sulfonated polybenzimidazole,

wherein the sulfonated polymer is prepared by directly dissolving an unsulfonated polymer in concentrated sulfuric acid, Nordhausen acid, or chlorosulfonic acid and sulfonating the unsulfonated polymer,

wherein the sulfonated polymer is prepared by two steps: the first step is to carry out reaction for 3 to 5 hours at 20 to 40° C.; the second step is to carry out reaction for 1 to 4 hours at 70 to 100° C., and

wherein the degree of sulfonation of the sulfonated polymer is in the range of 96% to 118%; and

c) forming a polymer blend proton exchange membrane by tape casting the polymer blend membrane forming solution, then removing the polymer blend proton exchange membrane after being dried and heat-treated.

2. The method according to claim 1 , wherein the method further includes a step: d) immersing the polymer blend proton exchange membrane in sulfuric acid aqueous solution for a whole day and taking out the membrane for later use.

3. The method according to claim 1 , wherein the degree of sulfonation of the sulfonated polymer is 98 to 116%, preferably 100 to 114%, more preferably 106 to 110%.

4. The method according to claim 1 , wherein the sulfonated polymer is made from an unsulfonated polymer with melt viscosity of 100 to 550 centipoise, preferably 300 to 450 centipoise, more preferably 350 to 400 centipoise, at 300 to 500° C.

5. The method according to claim 1 , wherein the resulting sulfonated polymer is shaped through a water-cooling process, preferably through a process in which the resulting sulfonated polymer slurry is poured into a screen with 1 to 4 mm mesh size and flows into deionized water beneath the screen and a strip-like sulfonated polymer is obtained after stirring.

6. The method according to claim 5 , wherein the resulting strip-shaped sulfonated polymer is washed to remove remaining sulfuric acid, then is dried at a temperature of 100 to 120° C. for at least 1 hour, preferably at least 4 hours.

7. The method according to claim 1 , wherein the weight-average molecular weight of the soluble polymer is in the range of 35000 to 65000, preferably 45000 to 55000, more preferably 48000 to 52000.

8. The method according to claim 1 , wherein the content of the soluble polymer is 10% to 50%, preferably 13% to 38%, more preferably 18% to 35%, most preferably 22% to 32%, based on the total weight of the membrane.

Assignments (8)