IP Library Granted Patent US 10,821,433
Granted Patent B2
US 10,821,433 · App. 16/164,175 · Granted Nov 3, 2020

Ion exchange resins, purification methods and methods of making ionic resins

Inventors: Andrey Rudenko (Clinton, MA); Gerhard Pohlers (Needham, MA)
Assignee: Rohm and Haas Electronic Materials LLC
B01J45/00B01J41/05B01J41/14B01J47/016B01J47/12C07C41/36C07C67/56
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Quick Facts
Patent No.
US 10,821,433
App. No.
16/164,175
Granted
Nov 3, 2020
Kind
B2
Abstract

An ion exchange resin comprises a crosslinked resin and a salt covalently bonded to a carbon of the resin, wherein the salt comprises a first non-metallic cation and a first counteranion, wherein the first counteranion comprises a second non-metallic cation and a thiosulfate counteranion, and wherein the ion exchange resin is essentially free of metals. The ion exchange resin finds particular use in the removal of impurities from solutions that are useful in the manufacture of semiconductor devices.

Claims (19)

1. An ion exchange resin, comprising a crosslinked resin and a salt covalently bonded to a carbon of the resin, wherein the salt comprises a first non-metallic cation and a first counteranion, wherein the first counteranion comprises a second non-metallic cation and a thiosulfate counteranion, and wherein the ion exchange resin is essentially free of metals.

2. The ion exchange resin of claim 1 , wherein the second non-metallic cation is an optionally substituted ammonium cation.

3. An ion exchange medium, comprising an ion exchange resin of claim 1 .

4. The ion exchange medium of claim 3 , wherein said medium is a bead, a membrane, a filter, an ion exchange column or a combination thereof.

5. A purification method, comprising contacting a composition comprising a solvent and an impurity with an ion exchange resin of claim 1 , thereby reducing the content of the impurity in the composition.

6. The purification method of claim 5 , wherein the impurity is hydrogen peroxide or an organic peroxide.

7. The purification method of claim 5 , wherein the impurity is a metal.

8. The purification method of claim 5 , wherein the solvent is an organic solvent.

9. The purification method of claim 8 , wherein the organic solvent is diisopropyl benzene, triisopropyl benzene, methanol, isopropyl alcohol, methyl isobutyl carbinol, propylene glycol, tripropylene glycol, methyl tertbutyl ether, isoamyl ether, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, dipropylene glycol dimethyl ether, tripropylene glycol monomethyl ether, tetrahydrofuran, acetone, methyl isobutyl ketone, cyclopentanone, cyclohexanone, ethyl-3-ethoxy propionate, propylene glycol monomethyl ether acetate, gamma-butyrolactone, ethyl lactate, butyl cellosolve, or a combination thereof.

10. A method of making an ion exchange resin, comprising:

(a) providing an ionic resin comprising a crosslinked resin and a salt covalently bonded to a carbon of the crosslinked resin, wherein the salt comprises a first cation and a first counteranion; and

(b) contacting the ionic resin with a salt comprising a second cation and a second counteranion comprising a thiosulfate group, thereby exchanging the first counteranion and the second counteranion.

11. The ion exchange medium of claim 3 , wherein the second nonmetallic cation is an optionally substituted ammonium cation.

12. The ion exchange medium of claim 11 , wherein said medium is a bead, a membrane, a filter, an ion exchange column or a combination thereof.

13. The purification method of claim 5 , wherein the second nonmetallic cation is an optionally substituted ammonium cation.

14. The purification method of claim 13 , wherein the impurity is hydrogen peroxide or an organic peroxide.

15. The purification method of claim 13 , wherein the impurity is a metal.

16. The purification method of claim 13 , wherein the solvent is an organic solvent.

17. The purification method of claim 16 , wherein the organic solvent is diisopropyl benzene, triisopropyl benzene, methanol, isopropyl alcohol, methyl isobutyl carbinol, propylene glycol, tripropylene glycol, methyl tertbutyl ether, isoamyl ether, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, dipropylene glycol dimethyl ether, tripropylene glycol monomethyl ether, tetrahydrofuran, acetone, methyl isobutyl ketone, cyclopentanone, cyclohexanone, ethyl-3-ethoxy propionate, propylene glycol monomethyl ether acetate, gamma-butyrolactone, ethyl lactate, butyl cellosolve, or a combination.

Assignments (3)
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 →
CHANGE OF NAME Recorded Oct 29, 2024
From: ROHM & HAAS ELECTRONIC MATERIALS LLC
To: DUPONT ELECTRONIC MATERIALS INTERNATIONAL, LLC
Reel/Frame 069272/0383 →