Process for making a monomer solution for making cation exchange membranes
View Patent ↗A method of making a monomer solution of styrene sulfonic acid or the pyridine salt of styrene sulfonic acid or mixtures of both in an organic solvent, said solution being suitable for producing cation exchange membranes. The method comprises the steps of dissolving a metal salt of styrene sulfonate in said organic solvent and pyridinium styrene sulfonate. The mixture solution is reacted under conditions that generate a salt byproduct precipitate and the reactant product solution is collected. Embodiments of the present invention provide for cation exchange membranes and processes for their manufacture. Membranes made by the processes described herein combine low resistance and high permselectivity which make them highly effective for membrane components in desalination of water by electrodialysis (ED), as a power generating sources in reverse electrodialysis and as separators in fuels cells.
1. A process for producing a cation exchange membrane, comprising:
forming a first suspension of a metal salt of styrene sulfonate in an organic solvent;
adding pyridinium chloride to said first suspension to form a second suspension;
promoting a reaction in the second suspension to form a metal chloride byproduct precipitate and a monomer solution of styrene sulfonic acid, or a pyridine salt of styrene sulfonic acid, or a mixture of both styrene sulfonic acid and a pyridine salt of styrene sulfonic acid, in said organic solvent;
collecting the monomer solution;
providing a porous substrate;
saturating porous regions of the substrate with a solution comprising the monomer solution, a crosslinking monomer, and a polymerization initiator;
removing excess solution from the saturated porous substrate; and
initiating polymerization to form a crosslinked ion transferring polymer in the porous regions of the substrate.
2. The process of claim 1 , wherein the porous substrate comprises polypropylene, high molecular weight polyethylene, ultrahigh molecular weight polyethylene, or polyvinylidene fluoride.
3. The process of claim 1 , wherein a thickness of the porous substrate is greater than about 55 microns and less than about 155 microns.
4. The process of claim 1 , wherein a thickness of the porous substrate is greater than about 20 microns and less than about 55 microns.
5. The process of claim 1 , wherein the solution further comprises 2 sulfoethylmethacrylate (2-SEM), 2-acrylamide-2-methyl propane sulfonic acid (AMPS), or acrylic acid.
6. The process of claim 1 , wherein the solution further comprises a secondary monomer selected from the group consisting of: styrene, vinyl toluene, 4-methylstyrene, t-butyl styrene, alphamethylstyrene; methacrylic anhydride, methacrylic acid, n-vinyl-2-pyrolidone, vinyltrimethoxysilane, vinyltriethoxysilane, vinyl-tris-(2-methoxyethoxy)silane, vinylidene chloride, vinylidene fluoride, vinylmethyldimethoxysilane, 2,2,2,-trifluroethyl methacrylate, maleic anhydride, glycidyl methacrylate, hydroxyethylmethacrylate, methylmethacrylate, (C 8 H 13 O) n (SiO 1.5 ) n , wherein n=8, 10, or 12, (C 6 H 11 O 2 ) n (SiO 1.5 ) n , wherein n=8, 10, or 12, (C 7 H 11 O 2 ) n (SiO 1.5 ) n , wherein n=8, 10, or 12, (C 6 H 9 O 2 ) n (SiO 1.5 ) n , wherein n=8, 10, or 12, C 56 H 104 O 30 S 3 Si 10 , and C 70 H 132 O 30 S 3 Si 10 .
7. The process of claim 1 , wherein the crosslinking monomer is selected from the group consisting of: divinylbenzene, ethylene glycol dimethacrylate, propylene glycol dimethacrylate, isobutylene glycol dimethacrylate, C 16 H 24 O 12 Si 8 , C 32 H 72 O 20 Si 16 , (CH 2 CH) n (SiO 1.5 ) n , wherein n=8, 10, or 12, C 14 H 38 O 12 Si 7 , C 28 H 66 O 12 Si 7 , C 56 H 122 O 12 Si 7 , C 16 H 56 O 20 Si 16 , and H 8 O 12 Si 8 .
8. The process of claim 1 , wherein the polymerization initiator is selected from the group consisting of organic peroxides, 2,2′-azobis[2,(2-imidazolin-2-yl)-propane]dihydrochloride, a,a′-azoisobutyronitrile, 2,2′-azobis(2-methylpropioaminidine dihydrochloride, 2,2′-azobis[2,(2-imidazolin-2-yl)-propane], and dimethyl 2,2′-azobis(2-methylpropionate).
9. The process of claim 1 , further comprising removing volatile species from the monomer solution under conditions that volatilize less than about 5% of said organic solvent by weight.
10. The process of claim 1 , wherein polymerization is initiated by the application of heat, ultraviolet light, or ionizing radiation.
11. The process of claim 1 , wherein polymerization is carried out substantially in the absence of oxygen.
12. The process of claim 1 , wherein the porous substrate comprises pores having a size of about 0.1 microns to about 0.2 microns.
13. The process of claim 1 , wherein the pyridine salt of styrene sulfonic acid is a saturated pyridine salt of styrene sulfonic acid in said organic solvent.
14. The process of claim 1 , wherein the organic solvent is a dipolar aprotic solvent.
15. The process of claim 14 , wherein the dipolar aprotic solvent is N-methylpyrrolidone (NMP).
16. The process of claim 1 , wherein promoting the reaction in the second suspension comprises heating the second suspension to a temperature above 80° C. to form the metal chloride byproduct precipitate and a monomer solution of styrene sulfonic acid in the organic solvent.
17. The process of claim 1 , wherein promoting the reaction in the second suspension is performed at a temperature below 80° C. to form the metal chloride byproduct precipitate and a monomer solution of the pyridine salt of styrene sulfonic acid in the organic solvent.
18. A process for producing a cation exchange membrane, comprising:
forming a first suspension of sodium styrene sulfonate in an organic solvent;
adding pyridinium chloride to the first suspension to form a second suspension;
promoting a reaction in the second suspension to form a sodium chloride byproduct precipitate and a monomer solution of styrene sulfonic acid, or pyridinium styrene sulfonate, or a mixture of both styrene sulfonic acid and pyridinium styrene sulfonate, in the organic solvent;
collecting the monomer solution;
providing a porous substrate;
saturating porous regions of the substrate with a solution comprising the monomer solution, a crosslinking monomer, and a polymerization initiator;
removing excess solution from the saturated porous substrate; and
initiating polymerization to form a crosslinked ion transferring polymer in the porous regions of the substrate.