IP Library Granted Patent US 9,217,929
Granted Patent B2
US 9,217,929 · App. 10/896,589 · Granted Dec 22, 2015

Composition for removing photoresist and/or etching residue from a substrate and use thereof

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Quick Facts
Patent No.
US 9,217,929
App. No.
10/896,589
Granted
Dec 22, 2015
Kind
B2
Abstract

Compositions containing certain organic solvents comprising at least 50% by weight of a glycol ether and a quaternary ammonium compound are capable of removing residues such as photoresist and/or etching residue from an article.

Claims (23)

1. A method for removing photoresist or etching residue or both from the substrate wherein said method comprises contacting a substrate with a composition consisting essentially of:

a) at least about 50% by weight of organic solvent consisting essentially of glycol ether and at least one of C 2 -C 20 alkane diols or C 3 -C 20 alkane triols, wherein at least about 50% of the organic solvent is said glycol ether, and wherein said glycol ether is selected from polyethylene glycol monomethyl ether, propylene glycol monopropyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monopropyl ether, diethylene glycol monoisopropyl ether, diethylene glycol monobutyl ether, diethylene glycol monoisobutyl ether, diethylene glycol monobenzyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol monomethyl ether, triethylene glycol dimethyl ether, diethylene glycol methyl ethyl ether, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, propylene glycol monomethyl ether, propylene glycol dimethyl ether, propylene glycol monobutyl ether, dipropylene glycol monopropyl ether, dipropylene glycol monoisopropyl ether, dipropylene monobutyl ether, dipropylene glycol diisopropyl ether, 1-methoxy-2-butanol, 2-methoxy-1-butanol, 2-methoxy-2-methylbutanol, 1,1-dimethoxyethane, and 2-(2-butoxyethoxy) ethanol;

b) at least about 0.5% by weight of one or more quaternary ammonium hydroxides wherein said one or more quaternary ammonium hydroxides is selected from tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrabutylammonium hydroxide, trimethylethylammonium hydroxide, (2-hydroxyethyl)trimethylammonium hydroxide, (2-hydroxyethyl)triethylammonium hydroxide, (2-hydroxyethyl)tripropylammonium hydroxide, and (1-hydroxypropyl)trimethylammonium hydroxide;

c) 0.2 to 19% by weight of corrosion inhibitor selected from the group consisting of gallic acid, lactic acid, and citric acid and salts thereof, catechol, benzotriazole (BZT), resorcinol, phenols, triazoles, hydroxylamines or acid salts thereof, or mixtures thereof; and

d) optionally water.

2. The method of claim 1 wherein the glycol ether is selected from the group consisting of propylene glycol monomethyl ether, propylene glycol monopropyl ether, and tri (propylene glycol) monomethyl ether.

3. The method of claim 1 wherein the one or more quaternary ammonium hydroxides is tetramethyl ammonium hydroxide.

4. The method of claim 1 wherein the amount of the glycol ether is about 50% to about 70% by weight of the composition.

5. The method of claim 1 wherein the amount of the glycol ether is about 50% to about 60% by weight of the composition.

6. The method of claim 1 wherein the amount of the one or more quaternary ammonium hydroxides is about 0.5% to about 15% by weight of the composition.

7. The method of claim 1 wherein the amount of the one or more quaternary ammonium hydroxides is about 0.5% to about 5% by weight of the composition.

8. The method of claim 1 wherein said corrosion inhibitor is hydroxylamines or acid salts thereof or mixtures thereof.

9. The method of claim 1 wherein said corrosion inhibitor is diethyl hydroxylamine or acid salt thereof or mixtures thereof.

10. The method of claim 1 wherein said corrosion inhibitor consists essentially of diethyl hydroxylamine or acid salt thereof.

11. The method of claim 1 wherein said C 2 -C 20 alkane diol or a C 3 -C 20 alkane triol consists essentially of propylene glycol.

12. The method of claim 11 wherein the amount of the propylene glycol is about 0.1 to about 40% by weight of the composition.

13. The method of claim 1 wherein water is present.

14. The method of claim 1 wherein the amount of said at least one of C 2 -C 20 alkane diol or C 3 -C 20 alkane triol is about 0.1 to about 20% by weight.

15. The method of claim 1 wherein the corrosion inhibitor is lactic acid, citric acid or salts thereof.

16. The method of claim 2 wherein the amount of the glycol ether is about 50% to about 70% by weight of the composition, and the amount of the one or more quaternary ammonium hydroxides is about 0.5% to about 15% by weight of the composition.

17. The method of claim 10 wherein the amount of the glycol ether is about 50% to about 70% by weight of the composition, and the amount of the one or more quaternary ammonium hydroxides is about 0.5% to about 15% by weight of the composition.

18. The method of claim 12 wherein the amount of the glycol ether is about 50% to about 70% by weight of the composition, and the amount of the one or more quaternary ammonium hydroxides is about 0.5% to about 15% by weight of the composition.

19. The method of claim 18 wherein the one or more quaternary ammonium hydroxides is tetramethyl ammonium hydroxide.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Oct 7, 2019
From: CITIBANK, N.A., AS AGENT
To: VERSUM MATERIALS US, LLC
Reel/Frame 050647/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2017
From: AIR PRODUCTS AND CHEMICALS, INC.
To: VERSUM MATERIALS US, LLC
Reel/Frame 041772/0733 →
PATENT SECURITY AGREEMENT Recorded Oct 27, 2016
From: VERSUM MATERIALS US, LLC
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 040503/0442 →