IP Library Granted Patent US 12,722,983
Granted Patent B2
US 12,722,983 · App. 18/396,373 · Granted Sep 1, 2026

Acid treatment of LiNiO

Inventors: Dieter G. Von Deak (Solon, OH); Tinoush Dinn (Beachwood, OH); William C. Mays (Farmington Hills, MI); Martin Lawrence Panchula (Eastlake, OH)
Assignee: BASF CORPORATION
C01G53/42C01P2002/72C01P2006/11C01P2006/40
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Quick Facts
Patent No.
US 12,722,983
App. No.
18/396,373
Granted
Sep 1, 2026
Kind
B2
Abstract

Disclosed is a process for producing a battery material including contacting a first intermediate product of a battery material with an acidic medium under conditions sufficient to dissolve low-lithium-containing oxide present on a surface of the first intermediate product to obtain a second intermediate product such that a weight of the second intermediate product is 0.2% to 5% less than a weight of the first intermediate product.

Claims (25)

1 . A process for producing a battery material, the process comprising:

contacting a first intermediate product of a battery material with an acidic medium under conditions sufficient to dissolve low-lithium-containing oxide present on a surface of the first intermediate product to obtain a second intermediate product,

wherein a weight of the second intermediate product is from about 0.2% to about 5% less than a weight of the first intermediate product, and

wherein the first intermediate product comprises Li x Ni z O 2 , wherein x ranges from about 0 to about 0.2 and z ranges from about 0.1 to about 1.

2 . The process according to claim 1 , wherein a weight of the second intermediate product is from about 1% to about 3% less than a weight of the first intermediate product.

3 . The process according to claim 1 , wherein the battery material after stabilization has a ratio of a first x-ray diffraction peak intensity at a 2Θ of about 12.5° and a second x-ray diffraction peak intensity at a 2Θ of about 37.3° of 50% or less after stabilization.

4 . The process according to claim 1 , wherein the battery material after stabilization has a ratio of a first x-ray diffraction peak intensity at a 2Θ of about 12.5° and a second x-ray diffraction peak intensity at a 2Θ of about 37.3° of 25% or less after stabilization.

5 . The process according to claim 1 , wherein the first intermediate product is Li x Ni z MO 2 , and wherein M is one or more of Co, Mn, Al, Mg, Ti, Zr, Nb, Hf, V, Cr, Sn, Cu, Mo, W, Fe, Si, Zn, B, or a rare earth element.

6 . The process according to claim 1 , wherein the conditions of contacting the first intermediate product with an acidic medium comprise a ratio of mol H+/mol of the first intermediate product of from about 0.025 to about 0.2.

7 . The process according to claim 1 , wherein the conditions of contacting the first intermediate product with an acidic medium comprise a ratio of mol H+/mol of the first intermediate product of about 0.07 or less.

8 . The process according to claim 1 , wherein the conditions of contacting the first intermediate product with an acidic medium comprise a temperature in a range of about 20° C. to about 150° C.

9 . The process according to claim 1 , wherein the conditions of contacting the first intermediate product with an acidic medium comprise a treatment time of up to about 3 hours.

10 . The process according to claim 1 , wherein the first intermediate product is separated from an aqueous slurry comprising the first intermediate product and an acid prior to the contacting step.

11 . The process according to claim 1 , wherein the acidic medium comprises at least one of HCl, H 2 SO 4 , nitric acid, acetic acid, phosphoric acid, hydrobromic acid, hydroiodic acid, perchloric acid, chloric acid, or a combination thereof.

12 . The process according to claim 1 , further comprising filtering the second intermediate product from the acidic medium using a membrane filter press with a gauge feed pressure ranging from about −0.5 bar to about 7 bar.

13 . The process according to claim 1 , further comprising stabilizing the second intermediate product by contacting the second intermediate product with one or more of a Bronsted base optionally selected from Ba(OH)2, Ni(OH)2, CsOH, Sr(OH)2, RbO, NaOH, LiGH, KOH, Ca(OH) 2 , or Mg(OH) 2 , or a combination thereof, to obtain the battery material.

14 . The process according to claim 13 , wherein a yield of the battery material is greater than about 90%.

15 . The process according to claim 13 , wherein the battery material is K y Li x Ni z O 2 , wherein y ranges from about 0 to about 0.3, x ranges from about 0 to about 0.2, z ranges from about 0.1 to about 1, and x+y ranges from about 0 to about 0.5.

16 . The process according to claim 13 , wherein the battery material comprises:

from about 0.7 weight % to about 1.1 weight % lithium by total weight of the battery material,

from about 50 weight % to about 70 weight % nickel by total weight of the battery material, and

from about 2 weight % to about 6 weight % potassium by total weight of the battery material.

17 . The process according to claim 13 , wherein the battery material has a tap density ranging from about 1.5 g/cm 3 to about 2.8 g/cm 3 .

18 . The process according to claim 13 , wherein the battery material has a capacity at 0.8V of from about 300 mAh/g to about 400 mAh/g.

19 . The process according to claim 13 , wherein the battery material has a capacity at 1.4V of from about 100 mAh/g to about 300 mAh/g.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 26, 2023
From: VON DEAK, DIETER G.; DINN, TINOUSH; MAYS, WILLIAM C.; PANCHULA, MARTIN LAWRENCE
To: BASF CORPORATION
Reel/Frame 065955/0408 →
Continuity (2)
Provisional Application 63477679 · Dec 29, 2022
Related Publication 20240217840A1 · Jul 4, 2024
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