R-Fe-B sintered magnet and making method

Patent metadata

Field	Value
Publication number	US-11315710-B2
Application number	US-201715617510-A
Country	US
Kind code	B2
Filing date	Jun 8, 2017
Priority date	Jun 20, 2016
Publication date	Apr 26, 2022
Grant date	Apr 26, 2022

Abstract

An R—Fe—B base sintered magnet is provided consisting essentially of R (which is at least two rare earth elements and essentially contains Nd and Pr), M1 which is at least two of Si, Al, Mn, Ni, Cu, Zn, Ga, Ge, Pd, Ag, Cd, In, Sn, Sb, Pt, Au, Hg, Pb, and Bi, M2 which is at least one of Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, and W, boron, and the balance of Fe, and containing an intermetallic compound R2(Fe,(Co))14B as a main phase. The magnet contains an R—Fe(Co)-M1 phase as a grain boundary phase, the R—Fe(Co)-M1 phase contains A phase which is crystalline with crystallites of at least 10 nm formed at grain boundary triple junctions, and B phase which is amorphous and/or nanocrystalline with crystallites of less than 10 nm formed at intergranular grain boundaries and optionally grain boundary triple junctions.

First claim

The invention claimed is:

1. An R—Fe—B base sintered magnet of a composition consisting essentially of 12 to 17 at % of R which contains Nd and Pr, and optionally contains one or more elements selected from the group consisting of yttrium and rare earth elements other than Nd and Pr, 0.1 to 3 at % of M 1 which is at least two elements selected from the group consisting of Si, Al, Mn, Ni, Cu, Zn, Ga, Ge, Pd, Ag, Cd, In, Sn, Sb, Pt, Au, Hg, Pb, and Bi, 0.05 to 0.5 at % of M 2 which is at least one element selected from the group consisting of Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, and W, 4.5+2×m to 5.9+2×m at % of boron wherein m is at % of M 2 , up to 10 at % of Co, up to 0.5 at % of carbon, up to 1.5 at % of oxygen, up to 0.5 at % of nitrogen, and the balance of Fe, and containing an intermetallic compound R 2 (Fe,(Co)) 14 B as a main phase, wherein
the magnet contains an R—Fe(Co)-M 1 phase consisting essentially of 25 to 35 at % of R, 2 to 8 at % of M 1 , up to 8 at % of Co, and the balance of Fe as a grain boundary phase, the R—Fe(Co)-M 1 phase contains an A phase which is crystalline with crystallites having a grain size of at least 10 nm formed at grain boundary triple junctions, and a B phase which is amorphous and/or nanocrystalline with crystallites having a grain size of less than 10 nm formed at intergranular grain boundaries or intergranular grain boundaries and grain boundary triple junctions, the B phase having a different composition from the A phase,
in the A phase, M 1 consists of 20 to 80 at % of at least one element selected from the group consisting of Si, Ge, In, Sn, and Pb and the balance of at least one element selected from the group consisting of Al, Mn, Ni, Cu, Zn, Ga, Pd, Ag, Cd, Sb, Pt, Au, Hg and Bi,
in the B phase, M 1 consists of more than 80 at % of at least one element selected from the group consisting of Si, Al, Ga, Ag, and Cu and the balance of at least one element selected from the group consisting of Mn, Ni, Zn, Ge, Pd, Cd, In, Sn, Sb, Pt, Au, Hg, Pb and Bi, and
the magnet does not contain an R 1.1 Fe 4 B 4 compound phase,
the narrowest portion of the grain boundary phase interposed between two adjacent crystal grains of the main phase has an average thickness of at least 50 nm.

2. The sintered magnet of claim 1 wherein a total content of Dy, Tb and Ho is up to 5 at % of the total of R.

3. The sintered magnet of claim 1 wherein the grain boundary phase containing the R—Fe(Co)-M 1 phase containing the A phase and B phase is distributed such as to surround individual crystal grains of the main phase at intergranular grain boundaries and grain boundary triple junctions.

4. A method for preparing the R—Fe—B base sintered magnet of claim 1 , comprising the steps of:
providing an alloy fine powder having a predetermined composition,
compression shaping the alloy fine powder in an applied magnetic field into a compact,
sintering the compact at a temperature of 900 to 1,250° C. into a sintered body,
high-temperature aging treatment including cooling the sintered body to a temperature of 400° C. or below, heating the sintered body at a temperature in the range of 700 to 1,000° C. and not higher than the peritectic point of the A phase, and cooling again to a temperature of 400° C. or below at a rate of 5 to 100° C./min, or high-temperature aging treatment including lowering, holding or elevating the temperature of the sintered body for thereby heating it at a temperature in the range of 700 to 1,000° C. and not higher than the peritectic point of the A phase, and cooling to a temperature of 400° C. or below at a rate of 5 to 100° C./min, and
low-temperature aging treatment including heating the sintered body, after the high-temperature aging treatment, at a temperature in the range of 400 to 600° C. and cooling to a temperature of 200° C. or below.

5. The method of claim 4 wherein the A phase is formed at grain boundary triple junctions during the high-temperature aging treatment, and the B phase is formed at intergranular grain boundaries or intergranular grain boundaries and grain boundary triple junctions during the low-temperature aging treatment.

6. The sintered magnet of claim 1 wherein the A phase is segregated at grain boundary triple junctions.

7. The sintered magnet of claim 1 wherein the grain boundary triple junction includes M 2 boride phase.

8. The sintered magnet of claim 1 wherein the A phase comprises, as the element M 1 , at least one element selected from the group consisting of Si, Ge, In, Sn and Pb.

Assignees

• Shinetsu Chemical Co

Inventors

• Hirota Koichi
• Kume Tetsuya
• Kamata Masayuki

Classifications

• H01F1/0577

  sintered · CPC title

• H01F41/0273

  Imparting anisotropy (methods and devices for magnetising permanent magnets H01F13/003) · CPC title

• C22C38/06

  containing aluminium · CPC title

• H01F1/059 Primary

  and Va elements, e.g. Sm2Fe17N2 · CPC title

• C22C38/02

  containing silicon · CPC title