IP Library Granted Patent US 12,077,730
Granted Patent B2
US 12,077,730 · App. 17/270,881 · Granted Sep 3, 2024

Quaternary ammonium hydroxides of polyamines

Inventors: Donald H. Champion (The Woodlands, TX); David C. Lewis (The Woodlands, TX); Juventino Uriarte (The Woodlands, TX); Hui Zhou (The Woodlands, TX); Ke Zhang (The Woodlands, TX); Chai Zheng (The Woodlands, TX)
Assignee: HUNTSMAN PETROCHEMICAL LLC
C11D3/30C11D3/20C11D7/26C11D7/3209G03F7/425C11D2111/16C11D2111/22
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Quick Facts
Patent No.
US 12,077,730
App. No.
17/270,881
Granted
Sep 3, 2024
Kind
B2
Abstract

The present disclosure provides a quaternary ammonium hydroxide solution comprising a reaction product of a polyamine and an organic oxirane. The quaternary ammonium hydroxide solution may be used in various applications, such as in removing chemical residue from a metal or dielectric surface.

Claims (20)

1. A quaternary ammonium hydroxide solution comprising the reaction product of (i) a polyamine having a formula:

where each R 1 is independently hydrogen, an alkyl group, a cycloalkyl group, an aryl group, an alkyloxyalkyl group, a hydroxylated alkyl group, a hydroxylated alkyloxyalkyl group or two R 1 groups may be joined to form a cyclic amine, with the proviso that the R 1 groups are selected in such a combination that at least one tertiary nitrogen is formed and that each R1 group has less than 6 carbon atoms; x is 0 or an integer of 1 to 10; n is an integer of at least 2; R′ is an alkyl group with 2 to 10 carbon atoms, an aryl group, alkaryl group, or unsaturated hydrocarbyl with 2 to 10 carbon atoms, or a group containing O or N in combination with C and H and may form a cyclic structure; and (ii) an organic oxirane having the formula

where each R is independently hydrogen, an alkyl group having 1 to 6 carbon atoms, an unsaturated alkyl group, an aryl group an aralkyl group or one or more R groups may form a cyclic structure containing 3 to 12 carbon atoms and optionally the R groups may contain one or more oxygen atoms wherein the concentration of quaternized amines in the quaternary ammonium hydroxide solution ranges from 10% by weight to 70% by weight, based on the total amount of the quaternized ammonium hydroxide solution.

2. The quaternary ammonium hydroxide solution of claim 1 wherein the polyamine is bis(3-dimethylaminopropyl) ether.

3. The quaternary ammonium hydroxide solution of claim 1 wherein the polyamine is bis(2-morpholinoethyl) ether.

4. The quaternary ammonium hydroxide solution of claim 1 wherein the polyamine is bis(2-dimethylaminoethyl)amine.

5. The quaternary ammonium hydroxide solution of claim 1 wherein the polyamine is N, N, N-tris(3-dimethylaminopropyl)amine.

6. The quaternary ammonium hydroxide solution of claim 1 wherein the polyamine is N, N, N′, N″, N″-pentamethyldiethylenetriamine.

7. The quaternary ammonium hydroxide solution of claim 1 wherein the polyamine is N, N, N′, N″, N″-pentamethyldipropylenetriamine.

8. The quaternary ammonium hydroxide solution of claim 1 wherein the organic oxirane is ethylene oxide.

9. The quaternary ammonium hydroxide solution of claim 1 wherein the organic oxirane is propylene oxide.

10. The quaternary ammonium hydroxide solution of claim 1 wherein the quaternary ammonium hydroxide solution contains 1 mole percent or more of quaternary ammonium compounds having at least two quaternary groups compared to the total moles of quaternary compounds.

11. The quaternary ammonium hydroxide solution of claim 1 further comprising water.

12. The quaternary ammonium hydroxide solution of claim 1 further comprising a miscible organic solvent.

13. A composition for removing chemical residue from a metal surface or dielectric surface comprising the quaternary ammonium hydroxide solution of claim 1 .

14. A method for removing chemical residue from a metal surface or dielectric surface comprising contacting the metal surface or dielectric surface with the composition of claim 1 .

15. A method of forming quaternary ammonium hydroxide solution of claim 1 comprising (i) contacting the polyamine with the organic oxirane in situ to convert the polyamine to a polyamine comprising a tertiary group and (ii) allowing the polyamine comprising the tertiary amine group to further react with the organic oxirane to form the quaternary ammonium hydroxide.

16. The method of claim 15 wherein the polyamine is N,N′-bis(2-aminoethyl)piperazine.

17. The method of claim 15 wherein the polyamine is N,N′-bis(3-aminopropyl)piperazine.

18. The method of claim 15 wherein the polyamine is bis(2-dimethylaminoethyl) ether.

Assignments (3)
SECURITY INTEREST Recorded May 4, 2026
From: HUNTSMAN INTERNATIONAL LLC; HUNTSMAN ADVANCED MATERIALS AMERICAS LLC; HUNTSMAN NANOCOMP LLC; HUNTSMAN PETROCHEMICAL LLC
To: CITIBANK N.A.
Reel/Frame 075498/0663 →
PATENT SECURITY AGREEMENT Recorded Mar 10, 2026
From: HUNTSMAN INTERNATIONAL LLC; HUNTSMAN ADVANCED MATERIALS AMERICAS LLC; HUNTSMAN NANOCAMP LLC; HUNTSMAN PETROCHEMICAL LLC
To: CITIBANK, N.A.
Reel/Frame 075106/0238 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2021
From: ZHENG, CHAI; LEWIS, DAVID C.; CHAMPION, DONALD H; JUVENTINO, URIARTE; ZHOU, HUI; ZHANG, KE
To: HUNTSMAN PETROCHEMICAL LLC
Reel/Frame 055383/0805 →
Continuity (2)
Provisional Application 62724849 · Aug 30, 2018
Related Publication 20210179972A1 · Jun 17, 2021