Resin formulations for polymer-derived ceramic materials

Patent metadata

Field	Value
Publication number	US-10745525-B2
Application number	US-201816190313-A
Country	US
Kind code	B2
Filing date	Nov 14, 2018
Priority date	Jan 15, 2016
Publication date	Aug 18, 2020
Grant date	Aug 18, 2020

Abstract

This disclosure enables direct 3D printing of preceramic polymers, which can be converted to fully dense ceramics. Some variations provide a preceramic resin formulation comprising a molecule with two or more C═X double bonds or C≡X triple bonds, wherein X is selected from C, S, N, or O, and wherein the molecule further comprises at least one non-carbon atom selected from Si, B, Al, Ti, Zn, P, Ge, S, N, or O; a photoinitiator; a free-radical inhibitor; and a 3D-printing resolution agent. The disclosed preceramic resin formulations can be 3D-printed using stereolithography into objects with complex shape. The polymeric objects may be directly converted to fully dense ceramics with properties that approach the theoretical maximum strength of the base materials. Low-cost structures are obtained that are lightweight, strong, and stiff, but stable in the presence of a high-temperature oxidizing environment.

First claim

What is claimed is:

1. A preceramic resin formulation comprising:
(a) first molecules comprising two or more C═X double bonds, two or more CX triple bonds, or at least one C═X double bond and at least one CX triple bond, wherein X is selected from the group consisting of C, S, N, O, and combinations thereof, and wherein said first molecules further comprise at least one non-carbon atom selected from the group consisting of Si, B, Al, Ti, Zn, P, Ge, S, N, O, and combinations thereof;
(b) second molecules comprising R—Y—H,
wherein R is an organic group or an inorganic group containing an element selected from the group consisting of B, Al, Ti, Zn, P, Ge, S, N, and combinations thereof, and wherein R does not contain O, and
wherein Y is selected from the group consisting of S, N, O, and combinations thereof;
(c) a photoinitiator;
(d) a free-radical inhibitor; and
(e) a 3D-printing resolution agent.

2. The preceramic resin formulation of claim 1 , wherein said first molecules are present from about 3 wt % to about 97 wt % of said formulation.

3. The preceramic resin formulation of claim 1 , wherein at least one of said double bonds or said triple bonds is located at a terminal position of said first molecules.

4. The preceramic resin formulation of claim 1 , wherein said first molecules comprise one or more functional groups selected from the group consisting of vinyl, ethynyl, vinyl ether, vinyl ester, vinyl amide, vinyl triazine, vinyl isocyanurate, acrylate, methacrylate, diene, triene, and functional analogs thereof.

5. The preceramic resin formulation of claim 4 , wherein said first molecules comprise two or more functional groups selected from the group consisting of vinyl, ethynyl, vinyl ether, vinyl ester, vinyl amide, vinyl triazine, vinyl isocyanurate, acrylate, methacrylate, diene, triene, and functional analogs thereof.

6. The preceramic resin formulation of claim 1 , wherein said second molecules are present from about 0.1 wt % to about 97 wt % of said formulation.

7. The preceramic resin formulation of claim 6 , wherein said second molecules contain, or are contained within, one or more functional groups selected from the group consisting of thiol, alkyl, ester, amine, hydroxyl, and functional analogs thereof.

8. The preceramic resin formulation of claim 1 , wherein at least 10% of said R is inorganic.

9. The preceramic resin formulation of claim 1 , wherein said photoinitiator is present from about 0.001 wt % to about 10 wt % of said formulation.

10. The preceramic resin formulation of claim 1 , wherein said photoinitiator is selected from the group consisting of 2,2-dimethoxy-2-phenylacetophenone, 2-hydroxy-2-methylpropiophenone, camphorquinone, bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide, benzophenone, benzoyl peroxide, dicumyl peroxide, 2,2′-azobisisobutyronitrile, and combinations or derivatives thereof.

11. The preceramic resin formulation of claim 1 , wherein said formulation further includes a thermal free-radical initiator.

12. The preceramic resin formulation of claim 1 , wherein said formulation further includes a radiation-trigger free-radical initiator active at a wavelength substantially different from said photoinitiator.

13. The preceramic resin formulation of claim 1 , wherein said free-radical inhibitor is present from about 0.001 wt % to about 10 wt % of said formulation.

14. The preceramic resin formulation of claim 1 , wherein said free-radical inhibitor is selected from the group consisting of hydroquinone, methylhydroquinone, ethylhydroquinone, methoxyhydroquinone, ethoxyhydroquinone, monomethylether hydroquinone, propylhydroquinone, propoxyhydroquinone, tert-butylhydroquinone, n-butylhydroquinone, and combinations or derivatives thereof.

15. The preceramic resin formulation of claim 1 , wherein said 3D-printing resolution agent is present from about 0.001 wt % to about 10 wt % of said formulation.

16. The preceramic resin formulation of claim 1 , wherein said 3D-printing resolution agent is selected from UV absorbers, fluorescent molecules, optical brighteners, or combinations thereof.

17. The preceramic resin formulation of claim 1 , wherein said 3D-printing resolution agent is selected from the group consisting of 2-(2-hydroxyphenyl)-benzotriazole, 2-hydroxyphenyl-benzophenones, 2-hydroxyphenyl-s-triazines, 2,2′-(2,5- thiophenediyl)bis(5-tert-butylbenzoxazole), 2,2′-(1,2-ethenediyl)bis(4,1-phenylene)bisbenzoxazole, and combinations or derivatives thereof.

18. A preceramic resin formulation comprising:
(a) first molecules comprising two or more C═X double bonds, two or more CX triple bonds, or at least one C═X double bond and at least one CX triple bond, wherein X is selected from the group consisting of C, S, N, O, and combinations thereof, and wherein said first molecules further comprise at least one non-carbon atom selected from the group consisting of Si, B, Al, Ti, Zn, P, Ge, S, N, O, and combinations thereof;
(b) second molecules comprising R—Y—H,
wherein R is an inorganic group,
wherein for at least one of said second molecules, R contains an element selected from the group consisting of B, Al, Ti, Zn, P, Ge, S, N, and combinations thereof, wherein R does not contain O, and wherein Y is selected from the group consisting of S, N, O, and combinations thereof;
(c) a photoinitiator;
(d) a free-radical inhibitor; and
(e) a 3D-printing resolution agent.

19. The preceramic resin formulation of claim 18 , wherein said first molecules are present from about 3 wt % to about 97 wt % of said formulation.

20. The preceramic resin formulation of claim 18 , wherein said first molecules comprise one or more functional groups selected from the group consisting of vinyl, ethynyl, vinyl ether, vinyl ester, vinyl amide, vinyl triazine, vinyl isocyanurate, acrylate, methacrylate, diene, triene, and functional analogs thereof.

21. The preceramic resin formulation of claim 20 , wherein said first molecules comprise two or more functional groups selected from the group consisting of vinyl, ethynyl, vinyl ether, vinyl ester, vinyl amide, vinyl triazine, vinyl isocyanurate, acrylate, methacrylate, diene, triene, and functional analogs thereof.

22. The preceramic resin formulation of claim 18 , wherein said second molecules are present from about 0.1 wt % to about 97 wt % of said formulation.

23. The preceramic resin formulation of claim 18 , wherein said photoinitiator is present from about 0.001 wt % to about 10 wt % of said formulation.

24. The preceramic resin formulation of claim 18 , wherein said photoinitiator is selected from the group consisting of 2,2-dimethoxy-2-phenylacetophenone, 2-hydroxy-2-methylpropiophenone, camphorquinone, bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide, benzophenone, benzoyl peroxide, dicumyl peroxide, 2,2′-azobisisobutyronitrile, and combinations or derivatives thereof.

25. The preceramic resin formulation of claim 18 , wherein said formulation further includes a thermal free-radical initiator.

26. The preceramic resin formulation of claim 18 , wherein said formulation further includes a radiation-trigger free-radical initiator active at a wavelength substantially different from said photoinitiator.

27. The preceramic resin formulation of claim 18 , wherein said free-radical inhibitor is present from about 0.001 wt % to about 10 wt % of said formulation.

28. The preceramic resin formulation o

Assignees

• Hrl Lab Llc

Inventors

• Eckel Zak C

Classifications

• B33Y70/00 Primary

  Materials specially adapted for additive manufacturing · CPC title

• C04B35/622

  Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products · CPC title

• G03F7/0042

  with inorganic or organometallic light-sensitive compounds not otherwise provided for, e.g. inorganic resists (G03F7/075 takes precedence) · CPC title

• G03F7/031

  Organic compounds not covered by group G03F7/029 · CPC title

• G03F7/027

  Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds (G03F7/075 takes precedence) · CPC title