IP Library Granted Patent US 12,502,664
Granted Patent B2
US 12,502,664 · App. 17/543,362 · Granted Dec 23, 2025

Membranes for acid-sensitive solvents

Inventors: James Hamzik (N Billerica, MA); Jad Ali Jaber (Westford, MA)
Assignee: ENTEGRIS, INC.
B01J39/05B01D69/02B01D71/261B01D71/32B01J47/12B01D2325/16B01D2325/42C02F2001/425
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 12,502,664
App. No.
17/543,362
Granted
Dec 23, 2025
Kind
B2
Abstract

This disclosure provides certain strong cation-modified ion exchange resins and membranes useful for carrying out the removal of metal and metal ion contaminants in fluid compositions. Filtered liquid compositions with significantly reduced amounts of metals can be used in a microelectronic manufacturing process, such as liquids for removing photoresist. The cation-modified ion exchange resins and membranes of the disclosure can be configured for use in a microelectronic manufacturing system, which can be utilized in the system as a point of use metal-removal feature for liquids entering the system. Advantageously, the filter materials and methods of this disclosure showed considerable improvement in preventing degradation and the formation of color bodies and dimeric and oligomeric materials from ketones (e.g., cyclohexanone) in the liquid compositions while not compromising the filter material's ability to remove undesired metal ions.

Claims (13)

1 . A method of removing one or more metals or metal ions from a liquid composition, the method comprising:

(i) contacting a filter material with the liquid composition, wherein the liquid composition comprises at least one ketone and the one or more metals or metal ions, wherein the filter material comprises at least one strong acid functional group having a cationic counterion, wherein the strong acid functional group is selected from the group consisting of sulfonic acid, phosphonic acid, and combinations thereof, and wherein the cationic counterion is selected from the group consisting of ammonium, C1-C6 alkylammonium, cyclohexylammonium, phosphonium, C 1 -C 6 alkyl phosphonium, imidazolium, pyridinium, guanidinium, sulfonium, pyrrolidinium, morpholinium, and pyrimidinium; and

(ii) reducing an amount of the one or more metals or metal ions in the liquid composition to provide a purified liquid composition.

2 . The method of claim 1 , wherein the filter material comprises a membrane.

3 . The method of claim 1 , wherein the filter material is in the form of a resin bead.

4 . The method of claim 1 , wherein said purified liquid composition maintains a water white appearance for up to 7 days upon storage in an inert atmosphere.

5 . The method of claim 1 , wherein contacting the membrane with a liquid composition comprising at least one ketone for seven days leads to the liquid composition having an increase in the sum of dimeric and oligomeric condensation species in the liquid composition in a range from greater than 0% to less than 100% as compared to the sum of dimeric and oligomeric condensation species in the liquid composition before it is contacted with the membrane.

6 . The method of claim 1 , wherein the liquid composition comprises a ketone selected from the group consisting of cyclohexanone and methyl isobutyl ketone.

7 . The method of claim 1 , wherein the liquid composition further comprises one or more of n-butyl acetate, isopropyl alcohol, 2-ethoxyethyl acetate, xylene, ethyl lactate, isopentyl ether, methyl-2-hydroxyisobutyrate, methyl isobutyl carbinol, isoamyl acetate, undecane, propylene glycol methyl ether, propylene glycol monomethyl ether acetate, and a mixed solution of propylene glycol monomethyl ether (PGME) and PGMEA having a (7:3) mixing ratio and surface tension of 27.7 mN/m.

8 . The method of claim 7 , wherein the liquid composition comprises isopropyl alcohol.

9 . The method of claim 1 , wherein the one or more metal or metal ions are selected from the group consisting of Li, B, Na, Mg, Al, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Mo, Cd, Sn, Ba, and Pb metals or metal ions, and combinations thereof.

10 . The method of claim 1 , wherein the metal ions are selected from the group consisting of iron, chromium, manganese, aluminum, and nickel cations.

11 . The method of claim 1 , wherein the strong acid functional group is sulfonic acid and wherein the cationic counterion is ammonium.

Assignments (3)
SECURITY INTEREST Recorded Jul 8, 2022
From: ENTEGRIS, INC.; ENTEGRIS GP, INC.; POCO GRAPHITE, INC.; CMC MATERIALS, INC.; INTERNATIONAL TEST SOLUTIONS, LLC; QED TECHNOLOGIES INTERNATIONAL, INC.
To: TRUIST BANK, AS NOTES COLLATERAL AGENT
Reel/Frame 060613/0072 →
SECURITY INTEREST Recorded Jul 8, 2022
From: ENTEGRIS, INC.; ENTEGRIS GP, INC.; POCO GRAPHITE, INC.
To: MORGAN STANLEY SENIOR FUNDING, INC., AS COLLATERAL AGENT
Reel/Frame 060614/0980 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 26, 2022
From: HAMZIK, JAMES; JABER, JAD A.
To: ENTEGRIS, INC.
Reel/Frame 060029/0139 →
Continuity (2)
Provisional Application 63124373 · Dec 11, 2020
Related Publication 20220184595A1 · Jun 16, 2022
References Cited (27)
US 4113922A · D'Agostino · 1978 [cited by applicant]
US 4758347A · Henz · 1988 [cited by examiner]
US 5350714A · Trefonas et al. · 1994 [cited by applicant]
US 20050167271A1 · Gajek · 2005 [cited by examiner]
US 20110082264A1 · Selifonov · 2011 [cited by examiner]
US 20160060133A1 · Vollmer · 2016 [cited by examiner]
US 20180001277A1 · Liu · 2018 [cited by applicant]
US 20180229186A1 · Yandrasits et al. · 2018 [cited by applicant]
US 20190134570A1 · Pintauro · 2019 [cited by applicant]
US 20200171442A1 · Filipancic · 2020 [cited by examiner]
US 20200360862A1 · Kamimura · 2020 [cited by examiner]
US 20220135445A1 · Moore · 2022 [cited by examiner]
CN 1688624A · 2005 [cited by applicant]
JP 2003190949A · 2003 [cited by applicant]
JP 2004330056A · 2004 [cited by applicant]
JP 2009039695A · 2009 [cited by applicant]
JP 2009110950A · 2009 [cited by applicant]
TW I710544B · 2020 [cited by applicant]
WO 0158576W · 2001 [cited by applicant]
WO 2015017972A1 · 2015 [cited by applicant]
WO 2017205722A1 · 2017 [cited by applicant]
Mahajan, Y et al.; “Self-Condensation of Cyclohexanone over Ion Exchange Resin Catalysts: Kinetics and Selectivity Aspects” Ind. Eng. Chem. Res., 2008, pp. 25-33, vol. 47, No. 1, Department of Chemical Engineering, Indi… [cited by applicant]
Purolite C1500CHA, Polystyrenic Macroporous, Strong Acid Cation Resin, Cyclohexylamine form, Strongly Acidic; Product Data Sheet; Apr. 8, 2020, p. 1 of 1, Purolite, purolite.com. [cited by applicant]
Monazam, E. et al.; “Rate analysis of sorption of Ce+3, Sm+3, and Yb+3 ions from aqueous solution using Dowex 50W-X8 as a sorbent in a continuous flow reactor” National Energy Technology Laboratory, U.S. Department of E… [cited by applicant]
Product Information, Lewatit S 100 NH4; Lanxess, Business Unit Ion Exchange Resins, Oct. 13, 2011, pp. 1/4-4/4. [cited by applicant]
Kang et al., A facile method for the preparation of poly(vinylidene fluoride) membranes filled with cross-linked sulfonated polystyrene, Reactive and Functional Polymers, vol. 99, pp. 42-48, 2016. [cited by applicant]
L. S. Ettre, Nomenclature for Chromatography, Pure & Appl. Chem., vol. 65, No. 4, pp. 819-872, 1993. [cited by applicant]