IP Library › Granted Patent US 10,522,808
Granted Patent B2
US 10,522,808 · App. 15/664,400 · Granted Dec 31, 2019

Cross-linked, microporous polysulfone battery electrode separator

Inventor: Ray L. Hauser (Boulder, CO)
Assignee: SAMSUNG ELECTRONICS CO., LTD
H01M2/1646H01M2/166H01M2/168H01M2/1653
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Quick Facts
Patent No.
US 10,522,808
App. No.
15/664,400
Granted
Dec 31, 2019
Kind
B2
Abstract

A cross-linked microporous polysulfone or polysulfone copolymer battery electrode separator membrane are described. Such membranes, which would otherwise be soluble above a particular, generally high temperature in selected battery electrolyte systems, once at least in part cross-linked, swell in the electrolyte at the particular higher temperature instead of dissolving. When the membrane separators are restrained between solid electrodes in a battery, the separator cannot increase in bulk volume, and the swelling occurs within the pores with the pore volume decreasing from its original bulk volume. The drop in pore volume causes the battery current density to drop, thereby reducing the heat generation within the hot area of the battery. This process provides a measure of safety against overheating and fires, and the battery is capable of continued usage if the overheating is localized.

Claims (19)

1. A method for producing a polysulfone or a polysulfone copolymer microporous membrane, comprising the steps of:

preparing a solution of polysulfone or a polysulfone copolymer comprising polysulfone or a polysulfone copolymer, a solvent for polysulfone or a polysulfone copolymer, a non-solvent for polysulfone or a polysulfone copolymer, and a thixotropic gellant, wherein the non-solvent has a higher boiling temperature than the solvent;

adding a cross-linker to the solution;

casting the solution onto a substrate; and

allowing the solvent and non-solvent of the cast solution to evaporate.

2. The method of claim 1 , wherein the solvents are chosen from tetrahydrofuran, methylene chloride, acetonitrile, cyclohexanone, and dimethyl formamide.

3. The method of claim 1 , wherein the non-solvents are chosen from tetrachloroethylene and isopropanol.

4. The method of claim 1 , wherein the thixotropic gellant comprises an aerogel.

5. The method of claim 4 , wherein the aerogel comprises fumed silica or alumina.

6. The method of claim 1 , wherein the substrate comprises a battery electrode.

7. The method of claim 6 , further comprising the step of adding an adhesion-improving additive to the solution.

8. The method of claim 7 , wherein the additive is chosen from styrene copolymer elastomers and chlorosulfonated polyethylene elastomers.

9. The method of claim 1 , further comprising the step of mixing discontinuous fibers with the solution.

10. The method of claim 9 , wherein the discontinuous fibers are chosen from glass and wollastonite.

11. The method of claim 1 , further comprising the step of mixing continuous fibers with the solution.

12. The method of claim 11 , wherein the continuous fibers comprise woven or non-woven webs.

13. The method of claim 12 , where the woven or non-woven webs are fabricated from materials chosen from polyester and polypropylene.

14. The method of claim 1 , wherein the cross-linker is chosen from dicyandiamide, benzoyl peroxide, di-glycidyl ethers, and tri-glycidyl ethers.

15. The method of claim 1 , further comprising the step of heating the cast solution, whereby cross-linking of the polysulfone or a polysulfone copolymer takes place.

Continuity (3)
Division 13473344 · May 16, 2012
Provisional Application 61486485 · May 16, 2011
Related Publication 20170331095A1 · Nov 16, 2017