Polymeric-coated dielectric particles and formulation and method for preparing same

• US 5,783,614 A
• Filed: 02/21/1997
• Issued: 07/21/1998
• Est. Priority Date: 02/21/1997
• Status: Expired due to Fees

• Current Assignee: AU Optronics Corporation
• Original Assignee: Anixa Biosciences, Inc. (f/k/a ITUS Corporation)
• Inventors: Hou, Wei-Hsin, Chen, Jing Hong, Schubert, Frederic E.
• Primary Examiner(s): Michl, Paul R.
• Application Number:
  US08/803,716
• Time in Patent Office: 515 Days
• Field of Search: 523/205, 524/805, 428/407
• US Class Current: 523/205
• CPC Class Codes: C09B 67/0013 with polymeric coatings
• CPC Class Codes: G02F 1/167 by electrophoresis
• CPC Class Codes: G03G 17/04 using photoelectrophoresis
• CPC Class Codes: Y10T 428/2998 including synthetic resin or polymer

Abstract

Properly-coated pigment particles for use in an electrophoretic display include pigment particles having a pre-determined density and application of a polymeric coating to the pigment particles, wherein the coating comprises a near fluoropolymer, and wherein the density of the fluoropolymer is substantially the same as the density of the pigment particles. When a polymeric coating is applied having a density that is substantially the same as the density of the pigment particles, even though the particles comprise a distribution of particle sizes, the density of the pigment particles is not significantly altered. In a preferred embodiment, the pigment particle comprises a diarylide yellow pigment, having a density of 1.43 g/ml, coated with a polymer made from the monomer 2,3,4,5,6-Pentafluorostyrene, having a density of 1.41 g/ml.

Claims

1. An electrophoretic suspension comprising a plurality of pigment particles having a pre-determined density and suspended in a fluid medium, wherein the pigment particles are coated with polypentafluorostyrene having substantially the same density as the pigment particles.

2. The electrophoretic suspension of claim 1, wherein the pigment particles are selected from the group consisting of Diarylide yellow, Hansa yellow, Arylide yellow, Hostaperm yellow, and Novoperm yellow.

3. The electrophoretic suspension of claim 1, wherein the pigment particles comprise yellow diarylide pigment particles having a density of about 1.43 g/ml.

4. The electrophoretic suspension of claim 1, wherein the monomer is 2,3,4,5,6-Pentafluorostyrene having a density of about 1.41 g/ml.

5. The electrophoretic suspension of claim 3, wherein the fluid medium comprises a mixture of tetrachloroethylene and sec-butyl benzene balanced to a specific gravity of approximately 1.43 g/ml.

6. The electrophoretic suspension of claim 1, wherein the pigment particles comprise yellow diarylide pigment particles having a density of about 1.43 g/ml;

and wherein said polymerized pentafluorostyrene monomer is prepared from the polymerization of 2,3,4,5,6-Pentafluorostyrene monomer having a density of about 1.41 g/ml.

7. A formulation for coating pigment particles with polypentafluorostyrene for use in an electrophoretic device, comprising a mixture of:

(a) a plurality of pigment particles having a certain predetermined density;

(b) a radical polymerization initiator;

(c) a pentafluorostyrene monomer having a density substantially equal to the density of the pigment particles; and

(d) an organic solvent.

8. The formulation of claim 7, wherein the plurality of pigment particles are selected from the group consisting of Diarylide yellow, Hansa yellow, Arylide yellow, Hostaperm yellow, and Novoperm yellow;

wherein the radical polymerization initiator is selected from the group consisting of 4,4'"'"'-Azobis (4-cyanovaleric acid), 2,2'"'"'-azobis (2-methylbutyronitrile), benzoyl peroxide, lauroyl peroxide, and octanoyl peroxide; and

wherein the organic solvent comprises a mixture of aliphatic and aromatic hydrocarbon solvents selected from the group consisting of decane, sec-butylbenzene, phenylxylylethane, toluene, benzene, xylene, cyclohexane, phenyloctane, octane, and hexadecane decahydronaphthalene.

9. The formulation of claim 7, wherein the plurality of pigment particles (a) further comprises approximately 1.18 grams of diarylide yellow pigment having a density of about 1.43 g/ml.

10. The formulation of claim 9, wherein the radical polymerization initiator (b) further comprises approximately 0.02-0.06 grams 4,4'"'"'-Azobis (4-cyanovaleric acid).

11. The formulation of claim 10, wherein the pentafluorostyrene monomer©

further comprises approximately 0.50-2.00 grams 2,3,4,5,6-Pentafluorostyrene having a density of about 1.41 g/ml.

12. The formulation of claim 11, wherein the organic solvent (d) further comprises a mixture of approximately 30-35 grams decane and 3-7 grams alcohol.

13. The formulation of claim 10, wherein the pentafluorostyrene monomer©

further comprises approximately 0.50 grams 2,3,4,5,6-Pentafluorostyrene having a density of about 1.41 g/ml.

14. The formulation of claim 13, wherein the organic solvent (d) further comprises a mixture of approximately 30 grams sec-butylbenzene and 3.0 grams alcohol.

15. A method of coating pigment particles with polypentafluorostyrene for use in an electrophoretic device, comprising the steps of:

(a) combining a mixture of a plurality of pigment particles having a predetermined density;

a radical polymerization initiator;

a pentafluorostyrene monomer having a density substantially equal to the density of the pigment particles; and

an organic solvent; and

(b) heating and tumbling the mixture of step (a) such that the pentafluorostyrene monomer is polymerized and coats the pigment particles.

16. The method of claim 15, further comprising the step of cleaning the resulting particles with an organic solvent wash.

17. The method of claim 15, wherein step (a) further comprises combining a mixture of about 1.18 grams yellow diarylide pigment particles having a density of about 1.43 g/ml, 0.05 grams 4,4'"'"'-Azobis (4-cyanovaleric acid), 0.75 grams 2,3,4,5,6-Pentafluorostyrene having a density of about 1.41 g/ml;

and a mixture of approximately 30 grams decane and 5.0 grams alcohol.

18. The method of claim 15, wherein step (a) further comprises combining a mixture of about 1.18 grams yellow diarylide pigment particles having a density of about 1.43 g/ml, 0.05 grams 4,4'"'"'-Azobis (4-cyanovaleric acid), 0.50 grams 2,3,4,5,6-Pentafluorostyrene having a density of about 1.41 g/ml;

and a mixture of approximately 30 grams sec-butylbenzene and 3.0 grams alcohol.

19. The method of claim 15, wherein the step of heating and tumbling the mixture further comprises tumbling the mixture at approximately 32 revolutions per minute at about sixty degrees Celsius for twenty-four hours and then at seventy degrees Celsius for twelve hours.