Formulations for 3D printing of hydrosilylation-modified polysilazanes

Patent metadata

Field	Value
Publication number	US-10961354-B1
Application number	US-201816029526-A
Country	US
Kind code	B1
Filing date	Jul 6, 2018
Priority date	Sep 6, 2017
Publication date	Mar 30, 2021
Grant date	Mar 30, 2021

Abstract

Some variations provide a preceramic resin precursor formulation comprising: first molecules comprising at least one Si—C bond and/or at least one Si—N bond, wherein the first molecules include at least one silyl hydride group (Si—H) available for hydrosilylation; and second molecules with at least one unsaturated carbon-carbon bond attached to a UV-active functional group. The first molecules and second molecules may be reacted, via hydrosilylation with a homogeneous or heterogeneous metal-containing catalyst, to produce third molecules comprising a hydrosilylation-modified polysilazane that contains the UV-active functional group. Many possible starting formulations are described, and methods are disclosed for carrying out the chemical reactions to generate the hydrosilylation-modified polysilazanes. The hydrosilylation-modified polysilazanes may then be 3D-printed and thermally treating to fabricate a ceramic material.

First claim

What is claimed is:

1. A preceramic radiation-curable resin composition comprising a metal-containing hydrosilylation catalyst and a molecule having the formula:

wherein:
x=1 to 100 when repeat units are connected linearly or x=1 to 10 when repeat units are connected cyclically;
y=0 to 100 when repeat units are connected linearly or are not present, or y=0 to 10 when repeat units are connected cyclically or are not present;
R 1 is selected from the group consisting of hydrogen, a C 1 -C 18 unsubstituted or substituted group, a halide, an ester group, an amine group, a hydroxyl group, a cyano group, and combinations thereof;
R 2 is selected from the group consisting of hydrogen, a C 1 -C 18 unsubstituted or substituted group, a halide, an ester group, an amine group, a hydroxyl group, a cyano group, and combinations thereof;
R 3 is selected from the group consisting of hydrogen, a C 1 -C 18 unsubstituted or substituted group, a halide, an ester group, an amine group, a hydroxyl group, a cyano group, and combinations thereof;
R 4 is a UV-active functional group that is capable of free-radical polymerization, cationic polymerization, or both of these; and
the carbon-carbon bond between R 4 and Si, depicted as , is a single bond (C—C) or a double bond (C═C).

2. The composition of claim 1 , wherein R 4 is selected from the group consisting of acrylate, methacrylate, vinyl ether, epoxide, cycloaliphatic epoxide, oxetane, thiol, alkyne, and combinations, analogues, or derivatives thereof.

3. The composition of claim 2 , wherein R 4 is a thiol, said composition further comprising an additional molecule comprising two or more unsaturated C═X double bonds, two or more C≡X triple bonds, or at least one C═X double bond and at least one C≡X triple bond, wherein X is selected from C, S, O, N, or combinations thereof.

4. The composition of claim 1 , said composition further comprising a photoinitiator that is effective to initiate polymerization at said UV-active functional group.

5. The composition of claim 4 , said composition further comprising a radiation-trigger free-radical initiator active at a second wavelength that is substantially different from a first wavelength for which said photoinitiator is active.

6. The composition of claim 1 , said composition further comprising a free-radical inhibitor.

7. The composition of claim 1 , said composition further comprising a 3D-printing resolution agent selected from the group consisting of UV absorbers, fluorescent molecules, optical brighteners, and combinations thereof.

8. The composition of claim 1 , said composition further comprising from about 0.1 vol % to about 70 vol % of solid-phase fillers.

9. A preceramic resin precursor formulation comprising:
(a) a first material containing first molecules comprising at least one Si—C bond, at least one Si—N bond, or at least one Si—C bond and at least one Si—N bond, wherein at least one of said first molecules comprises a silyl hydride group (Si—H) available for hydrosilylation;
(b) a second material containing second molecules with at least one unsaturated carbon-carbon double bond attached to an R 4 group (R 4 —C═C), and/or at least one carbon-carbon triple bond attached an R 4 group (R 4 —C≡C), wherein R 4 is a UV-active functional group; and
(c) a homogeneous or heterogeneous metal-containing catalyst.

10. The formulation of claim 9 , wherein said first molecules contain side groups selected from the group consisting of hydrogen, halides, substituted or unsubstituted cyclic or acyclic alkyl groups, aryl groups, hydrocarbon groups containing C═X double bonds or C≡X triple bonds (X is C, S, O, and/or N), and combinations thereof.

11. The formulation of claim 9 , wherein said first molecules further contain one or more atoms selected from the group consisting of B, Al, Ti, Zn, Zr, O, N, P, S, Ge, and combinations thereof.

12. The formulation of claim 9 , wherein said first molecules have the formula:

wherein:
n=1 to 100 when repeat units are connected linearly, or n=2 to 10 when repeat units are connected cyclically;
R 1 is selected from the group consisting of hydrogen, a C 1 -C 18 unsubstituted or substituted group, a halide, an ester group, an amine group, a hydroxyl group, a cyano group, and combinations thereof;
R 2 is selected from the group consisting of hydrogen, a C 1 -C 18 unsubstituted or substituted group, a halide, an ester group, an amine group, a hydroxyl group, a cyano group, and combinations thereof; and
R 3 is selected from the group consisting of hydrogen, a C 1 -C 18 unsubstituted or substituted group, a halide, an ester group, an amine group, a hydroxyl group, a cyano group, and combinations thereof, with the proviso that at least one R 3 group is hydrogen.

13. The formulation of claim 9 , wherein R 4 is selected from the group consisting of acrylate, methacrylate, vinyl ether, epoxide, cycloaliphatic epoxide, oxetane, thiol, and combinations, analogues, or derivatives thereof.

14. The formulation of claim 9 , said formulation further comprising an aprotic organic solvent in a concentration from about 1 wt % to about 99 wt % in said formulation.

15. The formulation of claim 9 , said formulation further comprising an inhibitor in a concentration from about 0.001 wt % to about 10 wt % in said formulation.

16. A method of making a preceramic radiation-curable resin composition, said method comprising:
(a) obtaining a first material containing first molecules comprising at least one Si—C bond, at least one Si—N bond, or at least one Si—C bond and at least one Si—N bond, wherein at least one of said first molecules comprises a silyl hydride group (Si—H) available for hydrosilylation;
(b) obtaining a second material containing second molecules with at least one unsaturated carbon-carbon double bond attached to an R 4 group (R 4 —C═C), and/or at least one carbon-carbon triple bond attached an R 4 group (R 4 —C≡C), wherein R 4 is a UV-active functional group; and
(c) reacting, via hydrosilylation in the presence of a homogeneous or heterogeneous metal-containing catalyst, said first material with said second material, to generate a third material containing third molecules comprising at least one Si—C bond, at least one Si—N bond, or at least one Si—C bond and at least one Si—N bond, wherein said third molecules further comprise a R 4 —C—C—Si sequence and/or a R 4 —C═C—Si sequence as a hydrosilylation reaction product.

17. The method of claim 16 , wherein in step (c), the molar ratio of said second molecules to said first molecules is selected from about 1 to about n, wherein n is the average number of silyl hydride groups present in each of said first molecules.

18. The method of claim 16 , said method further comprising combining said third material with a catalyst quencher to capture or poison said metal-containing catalyst.

19. The method of claim 16 , wherein said first molecules have the formula:

and wherein said third molecules have the formula:

wherein:
m=1 to 100 and is the number of said second molecules that react with each of said first molecules;
n=1 t

Assignees

• Hrl Lab Llc

Inventors

• Eckel Zak C
• Dustin Ashley M
• Rodriguez April R
• Bui Phuong

Classifications

• C08L83/16

  in which all the silicon atoms are connected by linkages other than oxygen atoms · CPC title

• C08G77/62 Primary

  Nitrogen atoms · CPC title

• C04B2235/6026

  Computer aided shaping, e.g. rapid prototyping · CPC title

• C04B2235/483

  Si-containing organic compounds, e.g. silicone resins, (poly)silanes, (poly)siloxanes or (poly)silazanes · CPC title

• C04B35/6269

  Curing of mixtures · CPC title