Thixotropic polysiloxane pastes for additive manufacturing

Patent metadata

Field	Value
Publication number	US-11512201-B2
Application number	US-202117317486-A
Country	US
Kind code	B2
Filing date	May 11, 2021
Priority date	Feb 10, 2021
Publication date	Nov 29, 2022
Grant date	Nov 29, 2022

Abstract

Shelf-stable, rapid crosslinking, “all-in-one” pastes useful as “inks” in additive manufacturing are provided. These pastes exhibit desirable rheological flow properties and crosslinking upon exposure to UV light. The pastes are based on vinylsilyl-functionalized, completely amorphous, linear terpolysiloxanes containing predominantly dimethylsiloxy-repeat units with small amounts of diphenylsiloxy-, methylphenylsiloxy-, diethylsiloxy-, and/or methyltrifluoroalkylsiloxy-crystallization disruptors. The base polymers are preferably compounded with a trimethylsilylated-hydrophobic silica filler, thixotropic flow agent, hydrosilyl-functionalized oligomeric crosslinker, and a catalytic system comprising platinum(II) acetylacetonate or trimethyl(methylcyclopentadienyl)-platinum(IV), and diethyl azodicarboxylate.

First claim

We claim:

1. A method of forming a three-dimensional structure, said method comprising one or more of the following:
(i) curing a first composition to form a first layer, wherein said first composition was entirely formed at least 3 days prior to said curing (i) and comprises:
at least 50% by weight of a polymer that comprises the following monomers:

and
a crystallization disruptor monomer comprising:

where:
each R 1 can be the same or different and is chosen from C 1 to C 6 alkyls and C 1 to C 6 fluoroalkyls;
R 2 is chosen from C 1 to C 6 alkyls;
each R 3 can be the same or different and is chosen from phenyl, C 1 to C 6 alkyls, and C 1 to C 6 fluoralkyls, wherein at least one R 3 is phenyl, ethyl, or a fluoroalkyl;
the molar percentage of (I) in the polymer is from about 90% to about 98%;
the molar percentage of (II) in the polymer is from about 0.1% to about 10%; and
the molar percentage of (III) in the polymer is from about 2% to about 10%;

a hydrosilylation crosslinker;
a thixotropic additive;
a catalyst;
a catalyst inhibitor; and
a filler;

(ii) curing a second composition to form a second layer on said first layer, wherein said first and second compositions can be the same as or different from one another; and
(iii) repeating (ii) one or more times with further compositions that can be the same as the first composition or different from the first composition so as to form one or more additional layers, wherein (ii) or (iii) results in the formation of the three-dimensional structure.

2. The method of claim 1 , wherein each R 1 is methyl, R 2 is methyl, and (III) is chosen from one or more of:

3. The method of claim 1 , wherein:
said hydrosilylation crosslinker comprises a methylhydridosiloxane-dimethylsiloxane copolymer;
said catalyst comprises a platinum catalyst;
said catalyst inhibitor comprises diethyl azodicarboxylate;
said thixotropic additive comprises a polydimethylsiloxane main chain backbone and poly(ethyl ether-co-propyl ether) pendant chains ending in carbinol end groups, methylether end groups, or both; and
said filler comprises a silica filler.

4. The method of claim 1 , wherein said curing (i) and curing (ii) comprise exposing said first and second compositions to electromagnetic radiation so as to crosslink said polymer and form cured first and second layers.

5. The method of claim 1 , wherein said first layer is formed on a support.

6. The method of claim 1 , wherein said curing (i) takes place at room temperature.

7. The method of claim 1 , wherein said first composition is shelf-stable in a dark environment for at least 30 days and in ambient light for at least 4 days.

8. A three-dimensional structure formed according to the method of claim 1 .

9. A method of forming a three-dimensional structure, said method comprising one or more of the following:
(i) curing a first composition to form a first layer, wherein said first composition was entirely formed at least 3 days prior to said curing (i) and comprises:
at least 50% by weight of a polymer that comprises the following monomers:

and
a crystallization disruptor monomer chosen from one or more of:

where:
each R 1 can be the same or different and is chosen from C 1 to C 6 alkyls and C 1 to C 6 fluoroalkyls;
R 2 is chosen from C 1 to C 6 alkyls;
the molar percentage of (I) in the polymer is from about 90% to about 98%;
the molar percentage of (II) in the polymer is from about 0.1% to about 10%; and
the molar percentage of (III) in the polymer is from about 2% to about 10%;

a hydrosilylation crosslinker;
a transition metal hydrosilylation catalyst; and
a thixotropic additive;

(ii) curing a second composition to form a second layer on said first layer, wherein said first and second compositions can be the same as or different from one another; and
(iii) repeating (ii) one or more times with further compositions that can be the same as the first composition or different from the first composition so as to form one or more additional layers, wherein (ii) or (iii) results in the formation of the three-dimensional structure.

10. The method of claim 9 , wherein:
said hydrosilylation crosslinker comprises a methylhydridosiloxane-dimethylsiloxane copolymer;
said hydrosilylation catalyst comprises a platinum catalyst; and
said thixotropic additive comprises a polydimethylsiloxane main chain backbone and poly(ethyl ether-co-propyl ether) pendant chains ending in carbinol end groups, methylether end groups, or both.

11. The method of claim 9 , wherein said curing (i) and curing (ii) comprise exposing said first and second compositions to electromagnetic radiation so as to crosslink said polymer and form cured first and second layers.

12. The method of claim 9 , wherein said first layer is formed on a support.

13. The method of claim 9 , wherein said curing (i) takes place at room temperature.

14. The method of claim 9 , wherein said first composition is shelf-stable in a dark environment for at least 30 days and in ambient light for at least 4 days.

15. A three-dimensional structure formed according to the method of claim 9 .

Assignees

• Honeywell Federal Mfg & Tech Llc

Inventors

• Messman Jamie Michael
• Patterson Steven Michael
• Dvornic Petar
• Zlatanic Alisa
• Beach James

Classifications

• C08G77/80

  Siloxanes having aromatic substituents, e.g. phenyl side groups · CPC title

• C08G77/20

  containing silicon bound to unsaturated aliphatic groups · CPC title

• C08L83/04 Primary

  Polysiloxanes · CPC title

• C08G77/12

  containing silicon bound to hydrogen · CPC title