Method for fabricating multiphenylethynyl-containing and lightly crosslinked polyimides capable of memorizing shapes and augmenting thermomechanical stability

Patent metadata

Field	Value
Publication number	US-11577448-B1
Application number	US-202016752747-A
Country	US
Kind code	B1
Filing date	Jan 27, 2020
Priority date	Sep 30, 2019
Publication date	Feb 14, 2023
Grant date	Feb 14, 2023

Abstract

The invention generally relates to shape memory films that are tri-functionally crosslinked and that comprise multiple, non-terminal, phenylethynyl moieties. In addition, the present invention relates methods of fabricating such films. Due to the improved properties of such SMPs, the SMP designer can program in to the SMP thermomechanical property enhancements that make the SMP suitable, among other things, for advanced sensors, high temperature actuators, responder matrix materials and heat responsive packaging.

First claim

What is claimed is:

1. A method for fabricating a shape memory polymer into a three-dimensional object, comprising:
a) treating a solution comprising:
(i) a polymeric intermediate comprising repeat units and non-terminal, phenylethynyl moieties, each of said repeat units independently comprising 0 to 4 of said non-terminal, phenylethynyl moieties per repeat unit with the proviso that not all of said repeat units comprise only 0 or only 1 of said non-terminal, phenylethynyl moieties, said polymeric intermediate being selected from the group consisting of a poly(amic acid) intermediate, a poly(amide-amic acid) intermediate, a copolymer intermediate of poly(amic acid) and poly(amide-amic acid) and mixtures thereof;
(ii) a solvent;
with a multi-functional crosslinking agent to thereby form a sol-gel comprising a crosslinked poly(amic acid), a crosslinked poly(amide-amic acid) and/or a crosslinked copolymer of poly(amic acid) and poly(amide-amic acid), said crosslinked poly(amic acid), a crosslinked poly(amide-amic acid) and/or a crosslinked copolymer of poly(amic acid) and poly(amide-amic acid) comprising said non-terminal, phenylethynyl moieties, said multi-functional crosslinking agent comprising at least a tri-functionalized amine crosslinking agent when said polymeric intermediate is anhydride end-functionalized and said multi-functional crosslinking agent comprising at least a tri-functionalized anhydride crosslinking agent when said polymeric intermediate is amine end-functionalized;

b) forming a film of said sol-gel on a substrate to provide a laminated substrate;
c) evaporating at least a portion of the solvent from the sol-gel by heating the sol-gel comprising to a temperature in a range of about 50° C. to about 100° C. at a pressure less than about atmospheric pressure;
d) forming the laminated substrate into a first configuration that is in a three-dimensional form;
e) imidizing, via heating, said sol-gel to provide the shape memory polymer having a permanent shape corresponding to the first configuration, wherein the shape memory polymer comprises a crosslinked polyimide, a crosslinked poly(amide-imide) and/or a crosslinked polyimide poly(amide-imide) copolymer; and
f) removing the substrate from the laminated substrate to provide the three-dimensional object comprising the shape memory polymer, preferably said removal comprises chemically removing the substrate from the laminated substrate
g) optionally, heating said shape memory polymer to a temperature of from about 210° C. to 250° C. and then placing said shape memory polymer under tension to a new shape.

2. A method for fabricating a shape memory polymer into a three-dimensional object according to claim 1 comprising crosslinking said non-terminal, phenylethynyl moieties by heating said substrate to a temperature of from greater than 250° C. to about 400° C.

3. The method of claim 1 , wherein the substrate comprises a metal that dissolves in an aqueous acid solution, preferably said metal comprises aluminum.

4. The method of claim 1 , wherein the multi-functional anhydride crosslinking agent has the following chemical formula:
Z—(—Ar—) n —W,

wherein Z represents an anhydride functional group that is directly or indirectly bonded to Ar; Ar represents an aryl group that is directly bonded to W; and n is equal to 3 when W is P═O or N, or n is equal to 4 when W is Si or a carbon moiety.

5. The method of claim 4 , wherein Ar is a phenyleneoxy group (—OPh-) that is para- or meta-substituted with respect to oxygen, and the multi-functional anhydride crosslinking agent has the following chemical formula:
Z—(—OPh-) n —W.

6. The method of claim 4 , wherein Z and Ar in combination form a phthalic anhydride moiety that is directly bonded to W.

7. The method of claim 4 , wherein Ar is a phenyleneoxy group (—OPh-) that is para- or meta-substituted with respect to oxygen, and wherein Z is a phthalic anhydride group that is connected to the phenyleneoxy group through an ether bond.

8. The method of claim 4 , wherein W is P═O, wherein Ar is a phenyleneoxy group (—OPh-) that is para- or meta-substituted with respect to oxygen, and wherein the multi-functional anhydride crosslinking agent has the following chemical formula:
Z—(—OPh-) 3 —P═O.

9. The method of claim 8 , wherein Z is a phthalic anhydride group that is connected to the phenyleneoxy group through an ether bond, and wherein the multi-functional anhydride crosslinking agent has the following chemical formula:

wherein R 1 through R 8 are each independently selected from H or C 1 -C 4 alkyl.

10. The method of claim 9 , wherein the multi-functional anhydride crosslinking agent is selected from tris[3-(3,4-dicarboxyphenoxy)phenyl]phosphine oxide trianhydride or tris[4-(3,4-dicarboxyphenoxy)phenyl]phosphine oxide trianhydride.

11. The method of claim 4 , wherein W is N, wherein Ar is a phenyleneoxy group (—OPh-) that is para- or meta-substituted with respect to oxygen, and wherein the multi-functional anhydride crosslinking agent has the following chemical formula:
Z—(—OPh-) 3 —N.

12. The method of claim 11 , wherein Z is a phthalic anhydride group that is connected to the phenyleneoxy group through an ether bond, and wherein the multi-functional anhydride crosslinking agent has the following chemical formula:

wherein R 1 through R 8 are each independently selected from H or C 1 -C 4 alkyl.

13. The method of claim 11 , wherein the multi-functional anhydride crosslinking agent is selected from tris[3-(3,4-dicarboxyphenoxy)phenyl]amine trianhydride or tris[4-(3,4-dicarboxyphenoxy)phenyl]amine trianhydride.

14. The method of claim 4 , wherein W is N, wherein Z and Ar in combination form a phthalic anhydride moiety that is directly bonded to N, and wherein the multi-functional anhydride crosslinking agent has the following chemical formula:

wherein R 9 to R 11 are each independently selected from H or C 1 -C 4 alkyl.

15. The method of claim 1 , wherein the multi-functional amine crosslinking agent comprises a tri(oxybenzene-amine) crosslinker having following chemical formula:

wherein W is selected from a group consisting of CH 3 C, N, P═O, or BO 3 ; R is selected from a group consisting of H, F, Cl, CF 3 , or CH 3 ; and the amine groups are located meta or para with respect to R.

Assignees

• Us Gov Air Force
• Us Air Force

Inventors

• Tan Loon-Seng
• Wang David H
• Yu Zhenning

Classifications

• C08G73/12

  Unsaturated polyimide precursors · CPC title

• C08G73/1017

  in the form of (mono)amine · CPC title

• C08G73/1014

  in the form of (mono)anhydrid · CPC title

• C08G73/14

  Polyamide-imides · CPC title

• C08G73/1039

  comprising halogen-containing substituents · CPC title