Treatment method for enhancing coercive force of neodymium iron boron magnet

Patent metadata

Field	Value
Publication number	US-2025246367-A1
Application number	US-202418424885-A
Country	US
Kind code	A1
Filing date	Jan 29, 2024
Priority date	Dec 8, 2022
Publication date	Jul 31, 2025
Grant date	—

Abstract

A treatment method for enhancing coercive force of neodymium iron boron magnet includes the following steps: subjecting the neodymium iron boron magnet to electrochemical deposition in a diffusion water-based solution to obtain a neodymium iron boron magnet containing a heavy rare earth; and subjecting the neodymium iron boron magnet containing the heavy rare earth to heat treatment to complete enhancement of the coercive force of the neodymium iron boron magnet. The raw material used in the present invention is cheap heavy rare earth compounds which increases the selection of diffusion sources and lowers costs. Metal alloy particles are mainly obtained in a nanoscale size and can effectively enter crystal grains, and low-melting-point metal alloy components can enhance a demagnetizing coupling effect between main phase grains. According to the present invention, the coercive force of the magnet is increased by nearly 30%, and residual magnetism is almost not changed.

First claim

What is claimed is:

1 . A treatment method for enhancing a coercive force of a neodymium iron boron magnet, comprising the following steps:
(1) subjecting the neodymium iron boron magnet to electrochemical deposition in a diffusion water-based solution to obtain a neodymium iron boron magnet containing a heavy rare earth; (2) subjecting the neodymium iron boron magnet containing the heavy rare earth to a heat treatment to complete an enhancement of the coercive force of the neodymium iron boron magnet.

2 . The treatment method of claim 1 , wherein the diffusion water-based solution in step (1) comprises the following components: a chloride salt of the heavy rare earth, copper sulfate pentahydrate, aluminum chloride, boric acid, glycine, citric acid, sodium citrate, sodium sulfate, and water;
the chloride salt of the heavy rare earth is dysprosium chloride hexahydrate or terbium trichloride hexahydrate; a molar ratio of the chloride salt of the heavy rare earth, the copper sulfate pentahydrate, the aluminum chloride, the boric acid, the glycine, the citric acid, the sodium citrate, and the sodium sulfate is (0.5-1.5):(0.5-1.5):(0.5-1.5):(2.5-3.5):(2.5-3.5):(3.5-4.5):(3.5-4.5):(2.5-3.5); and a molar concentration of the heavy rare earth in the diffusion water-based solution is 4-6%.

3 . The treatment method of claim 2 , wherein the diffusion water-based solution in step (1) has a pH value of 5-6; and the electrochemical deposition is at a current of 5-10 mA.

4 . The treatment method of claim 3 , wherein the electrochemical deposition in step (1) is at a solution temperature of 45-55° C.

5 . The treatment method of claim 3 , wherein the electrochemical deposition in step (1) is for 10-30 min.

6 . The treatment method of claim 5 , wherein the heat treatment in step (2) comprises a first-stage diffusion heat treatment and a second-stage tempering heat treatment performed sequentially;
the first-stage diffusion heat treatment is at a first-stage vacuum degree of 0.55-0.60 Pa and a second-stage vacuum degree of 1×10 −5 -1×10 −4 Pa; and the second-stage tempering heat treatment is performed at a first-stage vacuum degree of 0.55-0.60 Pa and a second-stage vacuum degree of 1×10 −5 -1×10 −4 Pa.

7 . The treatment method of claim 6 , wherein the first-stage diffusion heat treatment is at a temperature of 500-950° C., and the first-stage diffusion heat treatment is for 1-8 h.

8 . The treatment method of claim 7 , wherein the second-stage tempering heat treatment is at a temperature of 400-550° C., and the second-stage tempering heat treatment is for 1-2 h.

9 . The treatment method of claim 4 , wherein the electrochemical deposition in step (1) is for 10-30 min.

10 . The treatment method of claim 9 , wherein the heat treatment in step (2) comprises a first-stage diffusion heat treatment and a second-stage tempering heat treatment performed sequentially;
the first-stage diffusion heat treatment is at a first-stage vacuum degree of 0.55-0.60 Pa and a second-stage vacuum degree of 1×10 −5 -1×10 −4 Pa; and the second-stage tempering heat treatment is performed at a first-stage vacuum degree of 0.55-0.60 Pa and a second-stage vacuum degree of 1×10 −5 -1×10 −4 Pa.

11 . The treatment method of claim 10 , wherein the first-stage diffusion heat treatment is at a temperature of 500-950° C., and the first-stage diffusion heat treatment is for 1-8 h.

12 . The treatment method of claim 11 , wherein the second-stage tempering heat treatment is at a temperature of 400-550° C., and the second-stage tempering heat treatment is for 1-2 h.

Assignees

• Univ Jiliang China

Inventors

• Wu Qiong
• Yan Jiahui
• Yang Hangfu
• Hu Xiukun
• Pan Minxiang
• Yu Nengjun

Classifications

• H01F41/0293 Primary

  diffusion of rare earth elements, e.g. Tb, Dy or Ho, into permanent magnets · CPC title

• H01F1/0577 Primary

  sintered · CPC title