Preceramic 3d-printing monomer and polymer formulations

Patent metadata

Field	Value
Publication number	US-2024124364-A1
Application number	US-202318393913-A
Country	US
Kind code	A1
Filing date	Dec 22, 2023
Priority date	Nov 30, 2016
Publication date	Apr 18, 2024
Grant date	—

Abstract

This disclosure provides resin formulations which may be used for 3D printing and thermally treating to produce a ceramic material. The disclosure provides direct, free-form 3D printing of a preceramic polymer, followed by converting the preceramic polymer to a 3D-printed ceramic composite with potentially complex 3D shapes. A wide variety of chemical compositions is disclosed, and several experimental examples are included to demonstrate reduction to practice. For example, preceramic resin formulations may contain a carbosilane in which there is at least one functional group selected from vinyl, allyl, ethynyl, unsubstituted or substituted alkyl, ester group, amine, hydroxyl, vinyl ether, vinyl ester, glycidyl, glycidyl ether, vinyl glycidyl ether, vinyl amide, vinyl triazine, vinyl isocyanurate, acrylate, methacrylate, alkacrylate, alkyl alkacrylate, phenyl, halide, thiol, cyano, cyanate, or thiocyanate. The resin formulations may contain a solid-phase filler, to provide high thermal stability and mechanical strength (e.g., fracture toughness) in the final ceramic material.

First claim

What is claimed is:

1 . A preceramic cured polymer composition comprising functionalized polycarbosilane having the polymer structure:

wherein:
R 1 is selected from the group consisting of an allyl group, an ethynyl group, an ester group, a vinyl ether group, a vinyl ester group, a glycidyl group, a glycidyl ether group, a vinyl glycidyl ether group, a vinyl amide group, a vinyl triazine group, a vinyl isocyanurate group, a cyano group, a cyanate group, a thiocyanate group, and combinations thereof;
R 2 is selected from the group consisting of an allyl group, an ethynyl group, an ester group, a vinyl ether group, a vinyl ester group, a glycidyl group, a glycidyl ether group, a vinyl glycidyl ether group, a vinyl amide group, a vinyl triazine group, a vinyl isocyanurate group, a cyano group, a cyanate group, a thiocyanate group, and combinations thereof;
n=2 to 200;
said preceramic polymer composition is in the form of a 3D-printed polymer, wherein said 3D-printed polymer contains a plurality of physically distinct 3D-printed and cured polymer layers, and wherein adjacent 3D-printed polymer layers are contiguously disposed with each other; and
said preceramic polymer composition further contains a selected 3D-printing resolution agent.

2 . The preceramic cured polymer composition of claim 1 , wherein said preceramic cured polymer composition contains at least two distinct functionalized polycarbosilanes that are each in accordance with said polymer structure, wherein R 2 , and n are independently selected for said distinct functionalized polycarbosilanes.

3 . The preceramic cured polymer composition of claim 1 , wherein said preceramic polymer composition comprises a functionalized polycarbosilane copolymer having the copolymer structure:

wherein:
R 3 and R 4 are independently selected from the group consisting of hydrogen, a vinyl group, an allyl group, an ethynyl group, a C 1 -C 18 unsubstituted or substituted alkyl group, an ester group, an amine group, a hydroxyl group, a vinyl ether group, a vinyl ester group, a glycidyl group, a glycidyl ether group, a vinyl glycidyl ether group, a vinyl amide group, a vinyl triazine group, a vinyl isocyanurate group, an acrylate group, an alkacrylate group, an alkyl alkacrylate group, a phenyl group, a halide group, a thiol group, an alkylthiol group, a thiol-containing group, a cyano group, a cyanate group, a thiocyanate group, a mercaptopropionate group, a mercaptoactetate group, an aromatic group, and combinations thereof;
at least one of R 3 and R 4 is different than R 1 or R 2 ;
n=2 to 200; and
m=1 to 200.

4 . The preceramic cured polymer composition of claim 3 , wherein said copolymer structure is:

wherein R 3 is selected from C 1 -C 18 unsubstituted or substituted alkyl groups.

5 . The preceramic cured polymer composition of claim 3 , wherein said copolymer structure is:

wherein R 3 is selected from C 1 -C 18 unsubstituted or substituted alkyl groups.

6 . The preceramic cured polymer composition of claim 3 , wherein said copolymer structure is:

wherein R 3 is selected from C 1 -C 18 unsubstituted or substituted alkyl groups.

7 . The preceramic cured polymer composition of claim 1 , wherein said preceramic cured polymer composition further contains a crosslinking agent.

8 . The preceramic cured polymer composition of claim 1 , wherein said preceramic cured polymer composition comprises copolymer repeat units that are different from repeat units contained in said functionalized polycarbosilane.

9 . The preceramic cured polymer composition of claim 8 , wherein said copolymer repeat units are polycarbonitrosilane repeat units containing nitrogen bonded to silicon and/or carbon.

10 . The preceramic cured polymer composition of claim 9 , wherein said nitrogen is bonded to a functional group selected from the group consisting of hydrogen, a vinyl group, an allyl group, an ethynyl group, a C 1 -C 18 unsubstituted or substituted alkyl group, an ester group, an amine group, a hydroxyl group, a vinyl ether group, a vinyl ester group, a glycidyl group, a glycidyl ether group, a vinyl glycidyl ether group, a vinyl amide group, a vinyl triazine group, a vinyl isocyanurate group, an acrylate group, a methacrylate group, an alkacrylate group, an alkyl alkacrylate group, a phenyl group, a halide group, a thiol group, an alkylthiol group, a thiol-containing group, a cyano group, a cyanate group, a thiocyanate group, a mercaptoproprionate group, a mercaptoacetate group, an aromatic group, and combinations thereof.

11 . The preceramic cured polymer composition of claim 1 , wherein said preceramic cured polymer composition further comprises from about 0.1 vol % to about 70 vol % of solid-phase fillers.

12 . The preceramic cured polymer composition of claim 1 , wherein said selected 3D-printing resolution agent is selected to structurally limit curing to a desired region of light exposure via absorbing said light at a first wavelength and converting energy produced therefrom into thermal energy or radiation at a higher wavelength.

13 . The preceramic cured polymer composition of claim 1 , wherein said 3D-printing resolution agent is selected from the group consisting of 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 thereof.

Assignees

• Hrl Lab Llc

Inventors

• Eckel Zak C
• Nowak Andrew P
• Dustin Ashley M
• Rodriguez April R
• Bui Phuong
• Schaedler Tobias A

Classifications

• C04B35/571 Primary

  obtained from {Si-containing} polymer precursors {or organosilicon monomers} · CPC title

• B28B1/001

  Rapid manufacturing of 3D objects by additive depositing, agglomerating or laminating of material (selective deposition modelling of metallic powder B22F10/00; rapid manufacturing of 3D objects in general and in particular of plastics B29C64/00) · CPC title

• B33Y70/00

  Materials specially adapted for additive manufacturing · CPC title

• B33Y80/00

  Products made by additive manufacturing · CPC title

• C08G77/50

  by carbon linkages · CPC title