IP Library Granted Patent US 11,643,515
Granted Patent B2
US 11,643,515 · App. 17/739,548 · Granted May 9, 2023

Polyimide compositions and polyimide solutions

Inventors: Joseph Casey Johnson (Pickerington, OH); Kostantinos Kourtakis (Media, PA)
Assignee: DUPONT ELECTRONICS, INC.
C08J5/18C08G73/1082C08J2379/08
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 11,643,515
App. No.
17/739,548
Granted
May 9, 2023
Kind
B2
Abstract

In a first aspect, a polyimide corn position has a glass transition temperature of less than 300° C. and includes a polyimide derived from a dianhydride, a fluorinated aromatic diamine and an aliphatic diamine. A polyimide film made from the polyimide composition has a b* of less than one for a film thickness of at least 30 microns.

Claims (17)

1. A polyimide composition having a glass transition temperature of less than 300° C. and comprising a polyimide derived from:

a dianhydride;

a fluorinated aromatic diamine; and

an aliphatic diamine, wherein a polyimide film made from the polyimide composition has a b* of less than one for a film thickness of at least 30 microns.

2. The polyimide composition of claim 1 , wherein the dianhydride comprises 4,4″-(hexafluoroisopropylidene)diphthalic anhydride.

3. The polyimide composition of claim 2 , wherein the dianhydride further comprises an alicyclic dianhydride.

4. The polyimide composition of claim 3 , wherein the alicyclic dianhydride is is selected from the group consisting of cyclobutane dianhydride, cyclohexane dianhydride, 1,2,3,4-cyclopentanetetracarboxylic, dianhydride, hexahydro-4,8-ethano-1H,3H-benzo[1,2-c:4,5-c′]difuran-1,3,57-tetrone, 3-(carboxymethyl)-1,2,4-cyclopentanetricarboxylic acid 1,4:2,3-dianhydnde and mesd-butane-1,2,3,4-tetracarboxylic acid dianhydride.

5. The polyimide composition of claim 1 , wherein the fluorinated aromatic diamine comprises 2,2′-bis(trifluoromethyl) benzidine.

6. The polyimide composition of claim 1 , wherein the aliphatic diamine is selected from the group consisting of 1,2-diaminoethane, 1,6-diaminohexane, 1,4-diaminobutane, 1,7-diaminoheptane, 1,8-diaminooctane, 1,9-diaminononane, 1,10-diaminodecane, 1,11-diaminoundecane, 1,12-diaminododecane, 1,16-hexadecamethylenediamine, 1,3-bis(3-aminopropyl)-tetramethyldisiloxane, isophoronediamine, bicyclo[2.2.2]octane-1,4-diamine and mixtures thereof.

7. The polyimide composition of claim 1 , wherein the fluorinated aromatic diamine is present in a range of from 40 to 95 mole percent, based on the total diamine content of the polyimide.

8. The polyimide composition of claim , wherein the fluorinated aromatic diamine is present in a range of from 50 to 75 mole percent, based on the total diamine content of the polyimide.

9. The polyimide composition of claim 1 , wherein the glass transition temperature is less than 275° C.

10. The polyimide composition of claim 9 , wherein the glass transition temperature is less than 250° C.

11. The polyimide composition of claim 1 , wherein the polyimide is a soluble polyimide.

12. The polyimide composition of claim 11 , wherein the polyimide is soluble in a solvent selected from the group consisting of N-methylpyrrolidone, dimethylacetamide, N,N′-dimethyl-formamide, dimethyl sulfoxide, tetramethyl urea, diethyleneglycol diethyl ether, 1,2-dimethoxyethane, diethylene glycol dimethyl ether, 1,2-bis-(2-methoxyethoxy) ethane, bis [2-(2-methoxyethoxy)ethyl)] ether, gamma-butyrolactone, and bis-(2-methoxyethyl) ether, tetrahydrofuran and mixtures thereof.

13. A polyimide solution comprising the polyimide composition of claim 11 .

14. The polyimide solution of claim 13 , further comprising a solvent selected from the group consisting of N-methylpyrrolidone, dimethylacetamide, N,N′-dimethyl-formamide, dimethyl sulfoxide, tetramethyl urea, diethyleneglycol diethyl ether, 1,2-dimethoxyethane, diethylene glycol dimethyl ether, 1,2-bis-(2-methoxyethoxy) ethane, bis [2-(2-methoxyethoxy) ethyl)] ether, gamma-butyrolactone, and bis-(2-methoxyethyl) ether, tetrahydrofuran and mixtures thereof.

Assignments (2)
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 073515/0243 →
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 073517/0298 →
Continuity (3)
Continuation 16794853 · Feb 19, 2020
Provisional Application 62809090 · Feb 22, 2019
Related Publication 20220259391A1 · Aug 18, 2022