IP Library › Granted Patent US 12,540,240
Granted Patent B2
US 12,540,240 · App. 18/653,643 · Granted Feb 3, 2026

Photo-curable polyimide-like materials, and method of making

Inventors: David A. Walker (Evanston, IL); Matthew N. Pearlson (Wales, WI)
Assignee: Intrnls, Inc.
C08L33/26B29B13/02B33Y70/00C08G73/1003B29C64/129B29K2033/26B29K2079/08B29K2105/0002B29K2105/0091C08L2205/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,540,240
App. No.
18/653,643
Granted
Feb 3, 2026
Kind
B2
Abstract

A method of making a polyimide (PI)-based material. In one embodiment, the method begins by dispersing a polyamic acid (PAA) oligomer and photo-initiator into a photo-reactive monomer to form a liquid resin. In contrast to the above-described prior art, the liquid resin is substantially devoid of any non-reactive solvents. Electromagnetic radiation is then applied (e.g., in a 3D printing operation) to solidify the liquid resin and to substantially form a interpenetrating polymer network (IPN) in which the PAA oligomer is entangled within the network formed by the photo-reactive monomer but remains substantially independent and un-crosslinked from the PAA oligomer. Thereafter, the PAA-based IPN is thermally cycled to form a polyimide-based IPN.

Claims (18)

1 . A method of making a polyimide (PI) based material, comprising:

dispersing a polyamic acid (PAA) oligomer and a photo-initiator into a photo-reactive monomer to form a liquid resin, wherein the liquid resin is substantially devoid of any non-photoreactive solvents;

applying electromagnetic radiation to solidify the liquid resin and to substantially form a PAA-based interpenetrating polymer network (IPN) in which the polyamic acid oligomer is entangled within the network formed by the photo-reactive monomer; and

thermally cycling the PAA-based IPN to form a PI-based IPN.

2 . The method as described in claim 1 , wherein the polyamic acid and the photo-reactive monomer in the PAA-based IPN are substantially independent and un-crosslinked.

3 . The method as described in claim 1 , wherein the photo-reactive monomer comprises one or more photo-reactive components.

4 . The method as described in claim 3 , wherein the photo-reactive monomer is one of: N,N-dimethyacrylamide (DMAA), and a photo-reactive amine.

5 . The method as described in claim 1 , wherein a loading of the PAA oligomer in the liquid resin is about 70%.

6 . The method as described in claim 1 , wherein a wavelength of the electromagnetic radiation is between about 350 nm and 7000 nm and is applied in association with an additive manufacturing operation.

7 . The method as described in claim 6 , wherein the additive manufacturing operation is a vat photopolymerization.

8 . The method as described in claim 1 , wherein thermal cycling is at or below one of: 200° C., 250° C. and 300° C.

9 . The method as described in claim 8 , wherein pyrolysis of a polymer formed from the photo-reactive monomer is avoided.

10 . The method as described in claim 1 , wherein the IPN is a semi-IPN.

11 . The method as described in claim 1 , wherein the electromagnetic radiation is one of: deep UV, light UV, visible and near IR.

12 . A polyimide (PI) based material manufactured according to the following process steps:

dispersing a polyamic acid (PAA) oligomer and a photo-initiator into a photo-reactive monomer to form a liquid resin, wherein the liquid resin is substantially devoid of any non-photoreactive solvents;

applying electromagnetic radiation to solidify the liquid resin and to substantially form a PAA-based interpenetrating polymer network (IPN) in which the polyamic acid oligomer is entangled within the network formed by the photo-reactive monomer; and

thermally cycling the PAA-based IPN to form a PI-based IPN.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2025
From: WALKER, DAVID A.; PEARLSON, MATTHEW N.
To: INTRNLS, INC.
Reel/Frame 073297/0799 →
Continuity (2)
Provisional Application 63463523 · May 2, 2023
Related Publication 20240368392A1 · Nov 7, 2024
References Cited (3)
US 20140272358A1 · Meador · 2014 [cited by examiner]
US 20150141544A1 · Meador · 2015 [cited by examiner]
US 20210115279A1 · Rau · 2021 [cited by examiner]