Softening materials based on thiol-ene copolymers

Patent metadata

Field	Value
Publication number	US-9931771-B2
Application number	US-201414261336-A
Country	US
Kind code	B2
Filing date	Apr 24, 2014
Priority date	Apr 24, 2013
Publication date	Apr 3, 2018
Grant date	Apr 3, 2018

Abstract

Embodiments of the invention are directed to softening amorphous polymeric materials based on a combination of thiol, acrylate, ene and epoxy monomers. These materials can soften to the modulus of tissue, have a sharp transition and are highly tunable. The materials have a glassy modulus of 1-7 GPa and exhibit a rubbery plateau in modulus that can range from 100 MPa down to as low as 0.03 MPa, which is at or below the modulus of tissue. They have potential uses as materials for near net shape processing such as casting, stereolithography, reaction injection molding, fused deposition molding and various other forms of 3D printing.

First claim

What is claimed is:

1. A polymer formed from a mixture of mutually miscible monomers that can be polymerized under ambient conditions, wherein:
one of the mutually miscible monomers includes a multifunctional thiol monomer including Tris[2-(3-mercaptopropionyloxy)ethyl]isocyanurate; and
another one of the mutually miscible monomer includes one or more multifunctional alkenes of Tricyclo[5.2.1.02,6]decanedimethanol diacrylate and another multifunctional alkene selected from the group consisting of:
Poly(ethylene glycol) diacrylate; Diallyl terephthalate; Diallyl phthalate; Diallyl maleate; Trimethylolpropane diallyl ether; Ethylene glycol dicyclopentenyl ether acrylate; Diallyl carbonate; diallyl urea; 1,6- Hexanediol diacrylate; Cinnamyl cinnamate; vinyl cinnamate; allyl cinnamate; Allyl acrylate; Crotyl acrylate; Cinnamyl methacrylate; and trivinylcyclohexane.

2. The polymer of claim 1 , wherein the polymer has a tangent delta greater than 0.1 at both 20° C. and 37° C., as measured by dynamic mechanical analysis at 1Hz.

3. The polymer of claim 1 , wherein the polymer has a tangent delta greater than 0.1 at both 40° C. and 57° C., as measured by dynamic mechanical analysis at 1Hz.

4. The polymer of claim 1 , wherein the polymer has a tangent delta greater than 0.1 at both 55° C. and 72° C., as measured by dynamic mechanical analysis at 1Hz.

5. The polymer of claim 1 , wherein the polymer has a rubbery modulus at 47° C. that is between 2-50 times less than the glassy modulus of the polymer at 30° C.

6. The polymer of claim 1 , wherein the polymer has a rubbery modulus at 57° C. that is between 2-50 times less than the glassy modulus of the polymer at 40° C.

7. The polymer of claim 1 , wherein the polymer has a tangent delta in the range from 0.1 to 1.

8. The polymer of claim 1 , wherein one of the functional C═C (carbon-carbon double bonds) is 1,2-substituted in the multifunctional alkene.

9. The polymer of claim 1 , wherein two of the functional C═C (carbon-carbon double bonds) are 1,2-substituted in the multifunctional alkene.

10. The polymer of claim 1 , wherein the polymer has a rubbery modulus in a range from 10 kPa to 100 MPa.

11. A composite comprising:
the polymer of claim 1 ,
at least one particulate filler; and
at least one carbon based filler, wherein the glassy modulus of the composite is above 1 GPa.

12. The composite of claim 11 , wherein the glassy modulus of the composite is above 5 GPa.

13. The composite of claim 11 , wherein the at least one particulate filler is selected from ceramic, metallic and polymeric fillers.

14. The composite of claim 11 , wherein the at least one carbon based filler is nanocrystalline diamond.

15. The polymer of claim 1 , wherein the polymer has a rubbery modulus at 37° C. that is between 2-50 times less than the glassy modulus of the polymer at 20° C.

16. The polymer of claim 1 wherein all of the monomers have a molecular weight below 5000 g/mol.

17. The polymer of claim 1 wherein all of the monomers have a molecular weight below 750 g/mol.

18. A polymer formed from a mixture of mutually miscible monomers that can be polymerized under ambient conditions, wherein:
at least one of the mutually miscible monomers is a multifunctional thiol monomer modified such that some pendant thiol end groups of the multifunctional thiol monomer are end-capped by reaction with a monofunctional alkene monomer, and at least one of the monomers is a multifunctional alkene monomer;
the multifunctional thiol monomer includes Tris[2-(3-mercaptopropionyloxy)ethyl]isocyanurate; and
the multifunctional alkene includes 1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione and Tricyclo[5.2.1.02,6]decanedimethanol diacrylate.

19. A polymer formed from a mixture of mutually miscible monomers that can be polymerized under ambient conditions, wherein:
one of the mutually miscible monomers includes a multifunctional thiol monomer selected from the group consisting of:
Trimethylolpropane tris(2-mercaptoacetate); 2.2′-(Ethylenedioxy)diethanethiol; 1,2-Ethanedithiol; 1,4-butanedithiol; Tris[2-(3-mercaptopropionyloxy)ethyl]isocyanurate; and 3,4-ethylenedioxythiophene; and

another one of the mutually miscible monomer includes a multifunctional alkene monomer selected from the group consisting of:
Diallyl terephthalate; Diallyl phthalate; Ethylene glycol dicyclopentenyl ether acrylate; Diallyl carbonate; diallyl urea; Cinnamyl cinnamate; vinyl cinnamate; allyl cinnamate; Allyl acrylate; Crotyl acrylate; and Cinnamyl methacrylate.

20. A polymer formed from a mixture of mutually miscible monomers that can be polymerized under ambient conditions, wherein:
at least one of the mutually miscible monomers is a multifunctional thiol monomer having three or four pendant thiol end groups modified such that on average from about 0.07 to 0.1 of the pendant thiol end groups are end-capped by reaction with a monofunctional alkene monomer, and at least one of the monomers is a multifunctional alkene monomer, wherein a ratio of the monofunctional alkene monomer reacted with the multifunctional thiol monomer equals 1:3.67.

21. The polymer of claim 20 , wherein the multifunctional thiol monomer is selected from the group consisting of:
Trimethylolpropane tris(3-mercaptopropionate); Trimethylolpropane tris(2-mercaptoacetate); Pentaerythritol tetrakis(2-mercaptoacetate); Pentaerythritol tetrakis(3-mercaptopropionate); Tris[2-(3-mercaptopropionyloxy)ethyl]isocyanurate; and
the multifunctional alkene monomer is selected from the group consisting of:
1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;
Tricyclo[5.2.1.02,6]decanedimethanol diacrylate; Poly(ethylene glycol) diacrylate; Diallyl terephthalate; Diallyl phthalate; Diallyl maleate; Trimethylolpropane diallyl ether; Ethylene glycol dicyclopentenyl ether acrylate; Diallyl carbonate; diallyl urea; 1,6- Hexanediol diacrylate; Cinnamyl cinnamate; vinyl cinnamate; allyl cinnamate; Allyl acrylate; Crotyl acrylate; Cinnamyl methacrylate; and trivinylcyclohexane.

22. The polymer of claim 20 , wherein the monofunctional alkene monomer is methyl acrylate.

Assignees

• Univ Texas

Inventors

• Voit Walter
• Ware Taylor

Classifications

• B29K2105/0002

  monomers or prepolymers · CPC title

• B29L2031/7532

  Artificial members, protheses · CPC title

• B29C67/0085

  Operations & Transport · mapped topic

• B29K2105/0032

  Pigments, colouring agents or opacifiyng agents · CPC title

• B33Y80/00

  Products made by additive manufacturing · CPC title