JP2005076045A5 - - Google Patents
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- JP2005076045A5 JP2005076045A5 JP2003304477A JP2003304477A JP2005076045A5 JP 2005076045 A5 JP2005076045 A5 JP 2005076045A5 JP 2003304477 A JP2003304477 A JP 2003304477A JP 2003304477 A JP2003304477 A JP 2003304477A JP 2005076045 A5 JP2005076045 A5 JP 2005076045A5
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本発明者等は微粉末を大気中に放置したところ、微粉末に窒素が多く存在すると窒素量が減少するとともに、酸素量が増加しやすいこと、換言すれば微粉末の窒素量を制御することによりその後の大気との接触による酸素量の増加を抑制できることを本発明者等は確認した。具体的には、窒素量が250ppm以下の場合に酸素量の増加を抑制できることを知見した。微粉末中に窒素はRNの形態で存在すると解され、大気に接触することにより式(1)の反応あるいは式(1)の反応に伴う微粉末の表面状態変化や発熱により酸化が進むと考えられる。
RN+3H2O→R(OH)3+NH3…(1)
微粉末の窒素量を250ppm以下に制御するための手法はいくつか考えられる。例えば、微粉砕に気流粉砕機を使用する場合、その雰囲気を純窒素ではなく500〜4500ppmの濃度で酸素を混入すること、より好ましくは2000〜3500ppmの濃度で酸素を混入することが有効である。
When the present inventors left the fine powder in the atmosphere, the amount of nitrogen decreases and the amount of oxygen tends to increase if there is a lot of nitrogen in the fine powder, in other words, the amount of nitrogen in the fine powder is controlled. Thus, the present inventors have confirmed that an increase in the amount of oxygen due to subsequent contact with the atmosphere can be suppressed. Specifically, it has been found that an increase in the amount of oxygen can be suppressed when the amount of nitrogen is 250 ppm or less. It is understood that nitrogen is present in the form of RN in the fine powder, and it is thought that oxidation proceeds by contact with the atmosphere due to the reaction of formula (1) or the change in surface condition of the fine powder accompanying the reaction of formula (1) and heat generation. It is done.
RN + 3H 2 O → R (OH) 3 + NH 3 (1)
Several methods for controlling the nitrogen content of the fine powder to 250 ppm or less are conceivable. For example, when using an airflow pulverizer for fine pulverization, it is effective to mix oxygen at a concentration of 500 to 4500 ppm, more preferably 2000 to 3500 ppm, instead of pure nitrogen. .
本発明は以上の知見に基づくものであり、R−T−B(ただし、RはYを含む希土類元素の1種又は2種以上、TはFe又はFe及びCoを必須とする1種又は2種以上の遷移金属元素)系永久磁石の製造用合金粉末であって、窒素量が120〜250ppm、酸素量が4000〜5500ppmである永久磁石用合金粉末により前記課題を解決する。
また、本発明の永久磁石用合金粉末は、単一の組成を有する合金から構成することができるが、後述する混合法に適用することもできる。混合法は高磁気特性を得るために有効な手法であり、本発明を適用することにより高磁気特性を安定して得ることができるという利点を有することになる。混合法に適用する場合、永久磁石用合金粉末は、R2T14B相を主体とする第1の合金粉末と、第1の合金粉末よりRを多く含む第2の合金粉末とを少なくとも含む混合物から構成されることになる。
The present invention is based on the above findings, and R-T-B (where R is one or more of rare earth elements including Y, T is one or two essential elements of Fe, Fe and Co) The above-mentioned problems are solved by an alloy powder for producing permanent magnets having at least two kinds of transition magnets, wherein the amount of nitrogen is 120 to 250 ppm and the amount of oxygen is 4000 to 5500 ppm .
Moreover, although the alloy powder for permanent magnets of this invention can be comprised from the alloy which has a single composition, it can also apply to the mixing method mentioned later. The mixing method is an effective technique for obtaining high magnetic characteristics, and has the advantage that high magnetic characteristics can be stably obtained by applying the present invention. When applied to the mixing method, the alloy powder for permanent magnet includes at least a first alloy powder mainly composed of an R 2 T 14 B phase and a second alloy powder containing more R than the first alloy powder. It will consist of a mixture.
Claims (5)
窒素量が120〜250ppm、酸素量が4000〜5500ppmであることを特徴とする永久磁石用合金粉末。 Production of R-T-B (where R is one or more of rare earth elements including Y and T is one or more transition metal elements in which Fe or Fe and Co are essential) based permanent magnets Alloy powder for
An alloy powder for permanent magnets, wherein the nitrogen content is 120 to 250 ppm and the oxygen content is 4000 to 5500 ppm .
前記粗粉砕工程で得られる粗粉末を酸素濃度が500〜4500ppmの不活性ガス雰囲気中で気流粉砕する微粉砕工程と、
前記微粉砕工程で得られる微粉末を成形し成形体を得る工程と、
前記成形体を焼結する焼結工程と、を備えることを特徴とする希土類永久磁石の製造方法。 R-T-B (where R is one or more rare earth elements including Y and T is one or more transition metal elements in which Fe or Fe and Co are essential) based permanent magnet alloys A coarse pulverization step for coarsely pulverizing the raw materials;
A fine pulverization step in which the coarse powder obtained in the coarse pulverization step is air-flow pulverized in an inert gas atmosphere having an oxygen concentration of 500 to 4500 ppm;
Molding the fine powder obtained in the fine grinding step to obtain a molded body;
And a sintering step of sintering the molded body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003304477A JP4247977B2 (en) | 2003-08-28 | 2003-08-28 | Rare earth permanent magnet manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003304477A JP4247977B2 (en) | 2003-08-28 | 2003-08-28 | Rare earth permanent magnet manufacturing method |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2005076045A JP2005076045A (en) | 2005-03-24 |
JP2005076045A5 true JP2005076045A5 (en) | 2006-10-12 |
JP4247977B2 JP4247977B2 (en) | 2009-04-02 |
Family
ID=34408153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2003304477A Expired - Lifetime JP4247977B2 (en) | 2003-08-28 | 2003-08-28 | Rare earth permanent magnet manufacturing method |
Country Status (1)
Country | Link |
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JP (1) | JP4247977B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006283100A (en) * | 2005-03-31 | 2006-10-19 | Tdk Corp | Method for cutting rare earth alloy powder molding |
JP4640585B2 (en) * | 2005-03-31 | 2011-03-02 | Tdk株式会社 | Rare earth magnet manufacturing method |
KR102170875B1 (en) | 2011-10-24 | 2020-10-28 | 가부시키가이샤 니콘 | Illumination optical assembly, exposure apparatus, and device manufacturing method |
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2003
- 2003-08-28 JP JP2003304477A patent/JP4247977B2/en not_active Expired - Lifetime
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