IP Library Granted Patent US 12,515,960
Granted Patent B2
US 12,515,960 · App. 17/918,787 · Granted Jan 6, 2026

Method for producing lithium hydroxide

Inventors: Hirotaka Ariyoshi (Hitachi, JP); Isao Tomita (Hitachi, JP); Hiroshi Abe (Hitachi, JP)
Assignee: JX METALS CIRCULAR SOLUTIONS CO., LTD.
C01D15/02B09B3/35B09B3/70
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Quick Facts
Patent No.
US 12,515,960
App. No.
17/918,787
Granted
Jan 6, 2026
Kind
B2
Abstract

Provided is a method for producing lithium hydroxide, which can obtain lithium hydroxide from lithium sulfate with a relatively low cost. A method for producing lithium hydroxide from lithium sulfate includes: a hydroxylation step of allowing the lithium sulfate to react with barium hydroxide in a liquid to provide a lithium hydroxide solution; a barium removal step of removing barium ions in the lithium hydroxide solution using a cation exchange resin and/or a chelate resin; and a crystallization step of precipitating lithium hydroxide in the lithium hydroxide solution that has undergone the barium removal step.

Claims (20)

1 . A method for producing lithium hydroxide from lithium sulfate, the method comprising:

a hydroxylation step of allowing the lithium sulfate to react with barium hydroxide in a liquid to provide a lithium hydroxide solution; a barium removal step of removing barium ions in the lithium hydroxide solution using a cation exchange resin and/or a chelate resin; and a crystallization step of precipitating lithium hydroxide in the lithium hydroxide solution that has undergone the barium removal step.

2 . The method for producing lithium hydroxide according to claim 1 , wherein, in the barium removal step, the lithium hydroxide solution has a pH of 9 or more when the lithium hydroxide solution is brought into contact with the cation exchange resin and/or the chelate resin.

3 . The method for producing lithium hydroxide according to claim 1 , wherein, in the barium removal step, the lithium hydroxide solution has a space velocity (SV) of 5 to 20 when the lithium hydroxide solution is passed through the cation exchange resin and/or the chelate resin.

4 . The method for producing lithium hydroxide according to claim 1 , wherein a weakly acidic cation exchange resin having carboxyl groups as functional groups is used in the barium removal step.

5 . The method for producing lithium hydroxide according to claim 1 ,

wherein the lithium sulfate is in a form of a lithium sulfate solution; and

wherein the lithium sulfate solution is obtained by a process comprising: a lithium dissolution step of dissolving lithium in roasted lithium ion secondary battery waste in water or an acidic solution to obtain a lithium dissolved solution; and a lithium concentration step of extracting lithium ions from the lithium dissolved solution with a solvent and back-extracting the lithium ions.

6 . The method for producing lithium hydroxide according to claim 5 , wherein, in the lithium concentration step, lithium is extracted into a solvent, the solvent is then scrubbed with a lithium solution, and lithium ions are back-extracted from the scrubbed solvent.

7 . The method for producing lithium hydroxide according to claim 1 , wherein the method produces lithium hydroxide used for producing lithium ion secondary batteries.

8 . The method for producing lithium hydroxide according to claim 1 , wherein, in the hydroxylating step, the barium hydroxide is in a form of a barium hydroxide solution, and the barium hydroxide solution is brought into contact with the lithium sulfate.

9 . The method for producing lithium hydroxide according to claim 8 , wherein the barium hydroxide solution is a saturated aqueous solution.

10 . The method for producing lithium hydroxide according to claim 8 , wherein, in the hydroxylating step, the barium hydroxide solution is brought into contact with the lithium sulfate at a liquid temperature of 40° C. to 100° C.

11 . A method for producing lithium hydroxide from lithium carbonate, the method comprising:

a hydroxylation step of allowing the lithium carbonate to react with calcium hydroxide in a liquid to provide a lithium hydroxide solution; a calcium removal step of removing calcium ions in the lithium hydroxide solution using a cation exchange resin and/or a chelate resin; and a crystallization step of precipitating lithium hydroxide in the lithium hydroxide solution that has undergone the calcium removal step.

12 . The method for producing lithium hydroxide according to claim 11 , wherein, in the calcium removal step, the lithium hydroxide solution has a pH of 9 or more when the lithium hydroxide solution is brought into contact with the cation exchange resin and/or the chelate resin.

13 . The method for producing lithium hydroxide according to claim 11 , wherein, in the calcium removal step, the lithium hydroxide solution has a space velocity (SV) of 5 to 20 when the lithium hydroxide solution is passed through the cation exchange resin and/or the chelate resin.

14 . The method for producing lithium hydroxide according to claim 11 , wherein a weakly acidic cation exchange resin having carboxyl groups as functional groups is used in the calcium removal step.

15 . The method for producing lithium hydroxide according to claim 11 , wherein the lithium carbonate is obtained by a process comprising: a lithium dissolution step of dissolving lithium in roasted lithium ion secondary battery waste in water or an acidic solution to obtain a lithium dissolved solution; and a lithium concentration step of concentrating lithium ions in the lithium dissolved solution.

16 . The method for producing lithium hydroxide according to claim 11 , wherein the method produces lithium hydroxide used for producing lithium ion secondary batteries.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 23, 2024
From: JX ADVANCED METALS CORPORATION
To: JX METALS CIRCULAR SOLUTIONS CO., LTD.
Reel/Frame 068665/0857 →
CHANGE OF NAME Recorded Jul 29, 2024
From: JX METALS CORPORATION
To: JX ADVANCED METALS CORPORATION
Reel/Frame 068179/0696 →
CHANGE OF NAME Recorded Jun 27, 2024
From: JX NIPPON MINING & METALS CORPORATION
To: JX METALS CORPORATION
Reel/Frame 068050/0527 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 14, 2022
From: ARIYOSHI, HIROTAKA; TOMITA, ISAO; ABE, HIROSHI
To: JX NIPPON MINING & METALS CORPORATION
Reel/Frame 061420/0605 →
Priority Claims (2)
JP 2020-075634 · Apr 21, 2020 · national
JP 2020-075635 · Apr 21, 2020 · national
Continuity (1)
Related Publication 20230132311A1 · Apr 27, 2023
References Cited (40)
US 4154801A · Wheaton · 1979 [cited by examiner]
US 9677181B2 · Bourassa · 2017 [cited by examiner]
US 10329160B2 · Malhotra · 2019 [cited by examiner]
US 10584037B2 · Malhotra · 2020 [cited by examiner]
US 10633748B2 · Bourassa · 2020 [cited by examiner]
US 10648090B2 · Snydacker · 2020 [cited by examiner]
US 11292725B2 · Tiihonen · 2022 [cited by examiner]
US 20110044882A1 · Buckley · 2011 [cited by examiner]
US 20110135547A1 · Kobayashi et al. · 2011 [cited by applicant]
US 20190152797A1 · Liu et al. · 2019 [cited by applicant]
US 20200248283A1 · Ariyoshi et al. · 2020 [cited by applicant]
US 20210316998A1 · Ariyoshi et al. · 2021 [cited by applicant]
US 20220064757A1 · Ghahreman · 2022 [cited by examiner]
US 20230019776A1 · Bishkin · 2023 [cited by examiner]
CN 107128954A · 2017 [cited by applicant]
CN 107285345A · 2017 [cited by applicant]
CN 108658099A · 2018 [cited by applicant]
CN 109987616A · 2019 [cited by applicant]
CN 110791664A · 2020 [cited by applicant]
JP 62161973A · 1987 [cited by applicant]
JP 200946390A · 2009 [cited by applicant]
JP 2009269810A · 2009 [cited by applicant]
JP 2009270188A · 2009 [cited by applicant]
JP 2010180439A · 2010 [cited by applicant]
JP 201131232A · 2011 [cited by applicant]
JP 201132151A · 2011 [cited by applicant]
JP 2014162982A · 2014 [cited by applicant]
JP 201926531A · 2019 [cited by applicant]
JP 201926916A · 2019 [cited by applicant]
JP 201999901A · 2019 [cited by applicant]
JP 2019178395A · 2019 [cited by applicant]
JP 2019530795A · 2019 [cited by applicant]
JP 202035723A · 2020 [cited by applicant]
JP 2020164969A · 2020 [cited by applicant]
KR 1020160002578A · 2016 [cited by applicant]
KR 101975468B1 · 2016 [cited by applicant]
Extended European Search Report for European Application No. 21792875.3, dated Apr. 17, 2024. [cited by applicant]
Office Action for corresponding Japanese Application No. 2020-075634, dated Feb. 14, 2023, including an English translation. [cited by applicant]
International Preliminary Report on Patentability, dated Nov. 3, 2022, and English translation of the Written Opinion of the International Searching Authority, dated Jun. 22, 2021, for International Application No. PCT/… [cited by applicant]
International Search Report for PCT/JP2021/016223 mailed on Jun. 22, 2021. [cited by applicant]