IP Library Granted Patent US 8,083,970
Granted Patent B2
US 8,083,970 · App. 10/517,748 · Granted Dec 27, 2011

Electroconductive carbon fibril-based inks and coatings

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Quick Facts
Patent No.
US 8,083,970
App. No.
10/517,748
Granted
Dec 27, 2011
Kind
B2
Abstract

The present invention relates to electroconductive inks and methods of making and using the same. The electroconductive inks include carbon fibrils and a liquid vehicle. The electroconductive ink may further include a polymeric binder. The electroconductive filler used is carbon fibrils which may be oxidized. The ink has rheological properties similar to that of commercially available electroconductive inks that use carbon black as their filler. The ink can be screen-printed, slot-coated, sprayed, brushed or dipped onto a wide variety of substrates to form an electroconductive coating.

Claims (26)

1. A method for making an electroconductive ink comprising

adding carbon fibrils to a liquid vehicle to form a solution, said carbon fibrils being substantially cylindrical, having one or more graphitic layers concentric with their cylindrical axes, being substantially free of pyrolytically deposited carbon overcoat, said carbon fibrils having a substantially uniform diameter between 0.4 nm and 100 nm, said fibrils having a length to diameter ratio greater than 5;

milling said carbon fibrils in said solution; and

filtering said solution to form said electroconductive ink having a viscosity from about 1 to about 50,000 CD5 and a thixotropic index value from about 1.0 to about 10.

2. The method of claim 1 , further comprising the step of mixing a polymeric binder with the liquid vehicle before adding said carbon fibrils.

3. The method of claim 1 , wherein said liquid vehicle is a nonhydrocarbon polar organic solvent.

4. The method of claim 1 , wherein said liquid vehicle is selected from the group consisting of carbitol, carbitol acetate, butyl carbitol, butyl carbitol acetate, butyrolactone, acetone, methyl ethyl ketone, cyclohexanone, dibasic ester solvent, diglyme, high boiling alcohols, alcohol esters, and water.

5. The method of claim 1 , wherein said liquid vehicle has a boiling point from about 150° C. to 200° C.

6. The method of claim 1 , wherein the carbon fibrils are 3.5 to 70 nm in diameter with c-axes substantially perpendicular to the fibril axis.

7. The method of claim 1 , wherein the carbon fibrils have a fishbone morphology.

8. The method of claim 1 , wherein said carbon fibrils are in the form of aggregates.

9. The method of claim 8 , where said aggregates are selected from the group consisting of combed yarn aggregates, cotton candy aggregates, bird nest aggregates, open net aggregates, single wall ropes and mixtures thereof.

10. The method of claim 1 , wherein said carbon fibrils are oxidized multiwall carbon fibrils.

11. The method of claim 1 further comprising: dispersing said carbon fibrils in said solution following the step of adding said carbon fibrils.

12. The method of claim 11 , wherein said dispersing step is performed by sonication.

13. The method of claim 2 , wherein said polymeric binder is selected from the group consisting of vinyl chloride, vinyl acetate, hydroxyalkyl acrylate, vinyl alcohol, cellulose acetate butyrate, hydroxylethyl cellulose, carboxylmethyl cellulose, acrylic-based polymers, and combinations thereof.

14. The method of claim 2 further comprising—dispersing said carbon fibrils in said solution following the step of adding said carbon fibrils.

15. The method of claim 14 , wherein said dispersing step is performed by sonication.

16. The method of claim 2 , wherein said liquid vehicle is a nonhydrocarbon polar organic solvent.

17. The method of claim 2 , wherein said liquid vehicle is selected from the group consisting of carbitol, carbitol acetate, butyl carbitol, butyl carbitol acetate, butyrolactone, acetone, methyl ethyl ketone, cyclohexanone, dibasic ester solvent, diglyme, high boiling alcohols, alcohol esters, and water.

18. The method of claim 2 , wherein said liquid vehicle has a boiling point from about 150° C. to 200° C.

19. The method of claim 2 , wherein the carbon fibrils are 3.5 to 70 nm in diameter with c-axes substantially perpendicular to the fibril axis.

20. The method of claim 2 , wherein the carbon fibrils have a fishbone morphology.

21. The method of claim 2 , wherein said carbon fibrils are in the form of aggregates.

22. The method of claim 21 , where said aggregates are selected from the group consisting of combed yarn aggregates, cotton candy aggregates, bird nest aggregates, open net aggregates, single wall ropes and mixtures thereof.

23. The method of claim 2 , wherein said carbon fibrils are oxidized multiwall carbon fibrils.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Jan 21, 2021
From: WHITE OAK GLOBAL ADVISORS, LLC, AS ADMINISTRATIVE AGENT
To: HYPERION CATALYSIS INTERNATIONAL
Reel/Frame 055058/0494 →
SECURITY AGREEMENT Recorded Sep 17, 2013
From: HYPERION CATALYSIS INTERNATIONAL
To: PDL BIOPHARMA, INC.
Reel/Frame 031227/0086 →
SECURITY AGREEMENT Recorded Aug 16, 2013
From: HYPERION CATALYSIS INTERNATIONAL
To: WHITE OAK GLOBAL ADVISORS, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 031030/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 13, 2004
From: MA, JUN; FISCHER, ALAN B.; NIU, CHUNMING; NGAW, LEIN
To: HYPERION CATALYSIS INTERNATIONAL, INC.
Reel/Frame 016818/0726 →