Electro-optic media including encapsulated pigments in gelatin binder
US-10983410-B2 · Apr 20, 2021 · US
US12130534B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12130534-B2 |
| Application number | US-202318118483-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 7, 2023 |
| Priority date | Dec 23, 2019 |
| Publication date | Oct 29, 2024 |
| Grant date | Oct 29, 2024 |
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A capsule comprising a capsule wall and an electrophoretic fluid encapsulated by the capsule wall. The capsule wall comprises a cross-linked nonionic, water-soluble or water-dispersible polymer. The electrophoretic fluid comprises a suspending fluid, first pigment particles, second pigment particles, and third pigment particles. In some embodiments, the electrophoretic fluid includes a fourth electrophoretic particle. The first, second, and third particles are electrically charged, suspended in the suspending fluid, and capable of moving through the suspending fluid upon application of an electric field to the capsule.
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We claim: 1. A method for producing a capsule encapsulating an electrophoretic medium, the method comprising: providing a first polymer solution comprising a nonionic, water-soluble or water-dispersible first starting polymer in an aqueous solvent, wherein the first starting polymer is a polyol; providing a second polymer solution comprising a polyvinyl lactam in an aqueous solvent; mixing the first polymer solution with the second polymer solution to form a third polymer solution; providing an electrophoretic fluid comprising a suspending solvent and pigment particles; mixing the third polymer solution and the electrophoretic fluid to create a reaction mixture; heating the reaction mixture to a temperature above the lowest critical solution temperature of the third polymer solution to form a coacervate, thereby forming an oil-in-water emulsion including the electrophoretic fluid; adding a cross-linking agent to the oil-in-water emulsion, thereby forming a curing mixture; and heating the curing mixture to form capsules encapsulating an electrophoretic medium. 2. The method according to claim 1 , further comprising a step of cooling the curing mixture after the heating step. 3. The method according to claim 1 , wherein the first starting polymer is a polyvinyl alcohol. 4. The method according to claim 3 , wherein the mean molecular weight of the polyvinyl alcohol is at least about 10,000 Daltons. 5. The method according to claim 3 , wherein the mean molecular weight of the polyvinyl alcohol is 100,000 Daltons or lower. 6. The method according to claim 1 , wherein the first polymer solution comprises a copolymer of vinyl acetate. 7. The method according to claim 1 , wherein the second polymer solution comprises polyvinylpyrrolidone. 8. The method according to claim 1 , wherein the cross-linking agent is a glutaraldehyde. 9. The method according to claim 1 , further comprising adding a coacervation inducer to the third polymer solution. 10. The method according to claim 9 , wherein the coacervation inducer is a water-soluble or water-dispersible salt. 11. The method according to claim 1 , wherein the electrophoretic fluid comprises a first, a second, and a third types of pigment particles. 12. The method according to claim 11 , wherein two of the three types of pigment particles carry opposite charge polarities and the third type of pigment particles is slightly charged. 13. The method according to claim 12 , wherein the third type of pigment particles has larger size than the size of the first type of particles and the second type of particles. 14. The method according to claim 11 , wherein the electrophoretic fluid further comprises a fourth type of pigment particles. 15. The method according to claim 14 , wherein the electrophoretic fluid comprises white, cyan, yellow, and magenta pigment particles. 16. The method according to claim 14 , wherein the electrophoretic fluid comprises black, red, yellow and blue pigment particles. 17. The method according to claim 1 , wherein the suspending solvent comprises a hydrocarbon. 18. The method according to claim 1 , wherein the suspending solvent has a dielectric constant in the range of about 2 to about 30. 19. The method according to claim 18 , wherein the suspending solvent has a dielectric constant in the range of about 2 to about 15. 20. The method according to claim 1 , wherein the capsules have an average diameter between 15 μm and 50 μm, and wherein less than one third of the capsules (by number) are smaller than 15 μm or larger than 50 μm.
Electrodes · CPC title
characterised by the composition or particle type · CPC title
Polymerisation; cross-linking · CPC title
dye · CPC title
by electrophoresis · CPC title
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