Additive manufacturing of aromatic thermoplastics from photocurable precursor salts

Patent metadata

Field	Value
Publication number	US-12018127-B2
Application number	US-201916969826-A
Country	US
Kind code	B2
Filing date	Feb 13, 2019
Priority date	Feb 13, 2018
Publication date	Jun 25, 2024
Grant date	Jun 25, 2024

Abstract

In various aspects, a polymer resin is provided for vat photopolymerization. The resin can include a polyamic acid salt formed from the addition of a photocrosslinkable amine to a polyamic acid. The resin can include a photoinitiator suitable for initiating crosslinking of the photocrosslinkable amine when exposed to a light source of a suitable wavelength and intensity. The polyamic acid can be formed, for instance, by the addition of a diamine to a suitable dianhydride. Methods of additive manufacturing using the resins are also provided.

First claim

We claim:

1. A polymer resin for vat photopolymerization, the polymer resin comprising:
(i) a polyamic acid salt comprising repeat units having a structure according to the following formula

where each occurrence of R″ comprises a photocrosslinkable group; where each occurrence of R is independently selected from the group consisting of H, substituted and unsubstituted alkyl, substituted and unsubstituted heteroalkyl, and substituted and unsubstituted alkenyl; where each occurrence of Ar is independently selected from the group

where each occurrence of X is a substituted or unsubstituted aryl or heteroaryl group;
where each occurrence of Y is independently selected from the group consisting of O, S, C═O, C(CF 3 ) 2 , C(CH 3 ) 2 , SO 2 , and C≡C;

(ii) a photoinitiator suitable for initiating crosslinking of the photocrosslinkable groups when exposed to a light source of a suitable wavelength and intensity; and
(iii) a suitable solvent; and
wherein the polyamic acid salt comprises a polyether ether ketone, a polystyrene, or a polyallylamine.

2. The polymer resin according to claim 1 , wherein each occurrence of X is selected from the group

where each occurrence of Y is independently selected from a bond, —O—, —CH 2 —, —CH 2 CH 2 —, —C(CF 3 ) 2 —, —C(CH 3 ) 2 —, —S(O) 2 —, —S—, —S—S—, —CH═CH—, —C(O)—, —NH—, —O—Si(CH 3 ) 2 —O—,

where each occurrence of Y 1 is independently selected from —Cl, —OH, —OCH 3 , —CH 2 , —CH 2 CH 3 ;
where each occurrence of Y 2 is independently selected from —CH 3 , —OCH 3 , —OH, —CF 3 , —SO 3 H; and
where each occurrence of n is independently 1, 2, or 3.

3. The polymer resin according to claim 2 , wherein each occurrence of R″ is selected from the group

4. The polymer resin according to claim 1 , wherein the polymer has an average molecular weight of about 40000 g/mol to about 60000 g/mol.

5. The polymer resin according to claim 4 , wherein the polymer has a polydispersity of about 2 or less.

6. The polymer resin according to claim 1 , wherein the photocrosslinkable groups have a thermal decomposition temperature of about 350° C. or less.

7. The polymer resin according to claim 6 , wherein the photocrosslinkable groups comprise an acrylate, a methacrylate, or a combination thereof.

8. The polymer resin according to claim 1 , wherein the suitable solvent is selected from the group consisting of N-methyl-2-pyrrolidone (NMP), dimethylacetamide (DMAC), dimethylformamide (DMF), y-butyrolactone, mixtures with hydrocarbon solvents/aromatic hydrocarbon solvents, water, ammonia, and mixtures thereof.

9. The polymer resin according to claim 8 , wherein the suitable solvent is N-methyl-2-pyrrolidone (NMP).

10. The polymer resin according to claim 1 , wherein the suitable wavelength is about 300 nm to 500 nm.

11. The polymer resin according to claim 1 , wherein the photointiator is a phosphine oxide such as phenylbis(2,4,6-trimethylbenzoyl)phosphine.

12. The polymer resin according to claim 1 , wherein the photoinitiator is present in an amount from about 1.5 wt % to about 5 wt % based upon a total weight of the polymer resin.

13. A polymer resin according to claim 1 , further comprising a UV blocker selected from the group consisting of: a benzophenone, a benzotriazole, a diazine, a triazine, a benzoate, an oxalanilide, an azobenzone, a metal oxide, and any combination thereof.

14. A method of making an article, the method comprising:
(a) applying an effective amount of a light to a polymer resin according to claim 1 ;
(b) repeating step (a) a number of times to form the precursor article in a layer-by-layer fashion; and heating the precursor article to a first elevated temperature for a period of time to form the article.

15. The method according to claim 14 , wherein the articles comprises polyimide repeat units having a structure according to the following formula

wherein each occurrence of X is a substituted or unsubstituted aromatic group, and
wherein each occurrence of A is a substituted or unsubstituted aromatic group.

16. The method according to claim 14 , the method further comprising drying the precursor article to remove the solvent prior to forming the polyimide repeat units.

17. The method according to claim 16 , wherein the drying is performed by drying the precursor article in a vacuum oven for about 1 h, at one or more temperatures between 25° C. and 150° C.

18. The method according to claim 14 , wherein the article does not comprise a layered structure.

Assignees

• Virginia Tech Intellectual Properties Inc

Inventors

• Herzberger Jana
• Long Timothy E
• Meenakshisundaram Viswanath
• Williams Christopher B

Classifications

• B29K2105/0002

  monomers or prepolymers · CPC title

• B29K2079/08

  PI, i.e. polyimides or derivatives thereof · CPC title

• B33Y40/20

  Post-treatment, e.g. curing, coating or polishing · CPC title

• B29C64/30

  Auxiliary operations or equipment · CPC title

• B29C64/124

  using layers of liquid which are selectively solidified · CPC title