JP6511862B2 - Manganese magnet - Google Patents
Manganese magnet Download PDFInfo
- Publication number
- JP6511862B2 JP6511862B2 JP2015039798A JP2015039798A JP6511862B2 JP 6511862 B2 JP6511862 B2 JP 6511862B2 JP 2015039798 A JP2015039798 A JP 2015039798A JP 2015039798 A JP2015039798 A JP 2015039798A JP 6511862 B2 JP6511862 B2 JP 6511862B2
- Authority
- JP
- Japan
- Prior art keywords
- manganese
- calcium
- magnesium
- based magnet
- mass
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Landscapes
- Powder Metallurgy (AREA)
- Hard Magnetic Materials (AREA)
Description
本発明は、高い電気抵抗率を有するマンガン系磁石に関するものである。 The present invention relates to a manganese-based magnet having high electrical resistivity.
現在、フェライト磁石よりも磁気特性が高く、希土類磁石よりも安価な磁石が求められている。このため希土類を含まないマンガン系磁石が注目されている。 At present, magnets having higher magnetic properties than ferrite magnets and cheaper than rare earth magnets are required. For this reason, manganese-based magnets that do not contain rare earths are attracting attention.
マンガン系磁石の中でもマンガンアルミニウム磁石は有望であり、鋳造の後に熱間塑性加工というプロセスにより作製されており（特公昭５４−３１４４８）、高い磁気特性や機械的強度を有する異方性磁石として知られている。 Among manganese-based magnets, manganese aluminum magnets are promising, and they are manufactured by a process called hot plastic working after casting (Japanese Patent Publication No. 54-31448), and are known as anisotropic magnets having high magnetic properties and mechanical strength. It is done.
磁石は使用環境下で時間変化する磁場にさらされると、その磁場を打ち消すために磁石内部に渦電流が流れ、この渦電流がジュール熱を発生させて渦電流損になる。マンガン系磁石では電流が流れ易いため、渦電流損が大きい。 When the magnet is exposed to a time-varying magnetic field in an operating environment, an eddy current flows inside the magnet to cancel the magnetic field, and this eddy current generates Joule heat to become an eddy current loss. In the case of a manganese-based magnet, the current easily flows, so the eddy current loss is large.
特許文献１ではマンガン系磁石の電気抵抗率を十分に高めることができていないので、渦電流損を低減できない。
本発明は、このような実情に鑑みてなされ、その目的は、高い電気抵抗率を有するとともに、良好な磁気特性を併せ持つマンガン系磁石を提供することである。 The present invention has been made in view of such circumstances, and an object thereof is to provide a manganese-based magnet having high electrical resistivity and good magnetic characteristics.
本発明に係るマンガン系磁石は、カルシウムもしくはマグネシウムを０．０１ｍａｓｓ％〜１１ｍａｓｓ％含むことを特徴とする。 The manganese-based magnet according to the present invention is characterized by containing 0.01 mass% to 11 mass% of calcium or magnesium.
マンガン系磁石内の隣り合う２つ以上の主相粒子によって形成された粒界にカルシウムもしくはマグネシウムが存在することで、電子伝導を妨げ、渦電流損を低減できると共に、良好な磁気特性を有することができる。本発明は、かかる知見に基づいて完成されたものである。 Presence of calcium or magnesium at grain boundaries formed by two or more adjacent main phase particles in a manganese-based magnet prevents electronic conduction, reduces eddy current loss, and has good magnetic properties. Can. The present invention has been completed based on such findings.
カルシウムやマグネシウムは酸素と結合し易いため、それらの酸化物である酸化カルシウムや酸化マグネシウムがマンガン系磁石内部に安定して存在でき、マンガン系磁石の電気抵抗率を上げることができると考えられる。 Since calcium and magnesium easily bind to oxygen, it is thought that calcium oxide and magnesium oxide which are oxides thereof can be stably present inside the manganese-based magnet, and the electrical resistivity of the manganese-based magnet can be increased.
マンガン系磁石に含まれるカルシウムもしくはマグネシウムが０．０１ｍａｓｓ％未満では電気抵抗率を高くすることができない。また、マンガン系磁石に含まれるカルシウムもしくはマグネシウムが１１ｍａｓｓ％を超えると磁気特性の低下が大きい。本発明では、マンガン系磁石に含まれるカルシウムもしくはマグネシウムを０．０１〜１１ｍａｓｓ％の割合で構成したので、電気抵抗率の増大と磁気特性の維持の両立を図ることができる。 If the content of calcium or magnesium contained in the manganese-based magnet is less than 0.01 mass%, the electrical resistivity can not be increased. In addition, when the content of calcium or magnesium contained in the manganese-based magnet exceeds 11 mass%, the magnetic properties significantly decrease. In the present invention, since calcium or magnesium contained in the manganese-based magnet is composed of 0.01 to 11 mass%, it is possible to achieve both the increase in the electrical resistivity and the maintenance of the magnetic characteristics.
本発明によれば、高い電気抵抗率を有するとともに、良好な磁気特性を併せ持つマンガン系磁石を得ることができる。 According to the present invention, it is possible to obtain a manganese-based magnet having high electrical resistivity and good magnetic characteristics.
以下、本発明の好適な実施形態について説明する。なお、本発明は以下に記載の実施形態および実施例の内容により限定されるものではない。また、以下に記載の実施形態および実施例にて示された構成要素は適宜組み合わせてもよいし、適宜選択してもよい。 Hereinafter, preferred embodiments of the present invention will be described. The present invention is not limited by the contents of the embodiments and examples described below. In addition, the components shown in the embodiments and examples described below may be combined as appropriate or selected as appropriate.
本発明の実施形態に係るマンガン系磁石の実施形態について説明する。本実施形態に係るマンガン系磁石はＭｎＸ（ここで、ＸはＡｌ、Ｂ、Ｂｉ、Ｃ、Ｃｏ、Ｃｒ、Ｆ、Ｉｒ、Ｇａ、Ｎ、Ｎｉ、Ｒｈ、Ｐｔ、Ｐｄの少なくとも１種である。）結晶粒を有するマンガン系磁石であり、内部にカルシウムやマグネシウムを含んでいる。高電気抵抗率を有するカルシウムやマグネシウムの酸化物がマンガン系磁石内部に含まれることで、電子伝導を妨げることができ、交流磁場にさらされたときに誘起される渦電流損を低減することができる。一方、マンガン系磁石の磁気特性が高いのはカルシウムもしくはマグネシウム量が低い割合で構成している場合である。 An embodiment of a manganese-based magnet according to an embodiment of the present invention will be described. The manganese-based magnet according to the present embodiment is MnX (here, X is at least one of Al, B, Bi, C, Co, Cr, F, Ir, Ga, N, Ni, Rh, Pt, and Pd). 2.) It is a manganese based magnet having crystal grains, and contains calcium and magnesium inside. By containing calcium and magnesium oxides having high electrical resistivity inside the manganese-based magnet, it is possible to block electron conduction and reduce eddy current loss induced when exposed to an alternating magnetic field. it can. On the other hand, the magnetic properties of the manganese-based magnet are high when the amount of calcium or magnesium is low.
マンガン系磁石に含まれるカルシウムもしくはマグネシウムが０．０１ｍａｓｓ％未満になるとカルシウムもしくはマグネシウムが少ないため、十分に主相粒子間の電子伝導を妨げることができず、高い電気抵抗率を得られない。また、マンガン系磁石に含まれるカルシウムもしくはマグネシウムが１１％を超えてしまうとＭｎＸ相の比率が小さくなり過ぎて、十分な磁化を得ることができない。そこで、マンガン系磁石に含まれるカルシウムもしくはマグネシウムを０．０１〜１１ｍａｓｓ％とすることで、電気抵抗率の向上と磁化の維持の両立を図るようにした。 If the amount of calcium or magnesium contained in the manganese-based magnet is less than 0.01 mass%, the amount of calcium or magnesium is small, so that the electron conduction between the main phase particles can not be sufficiently prevented, and a high electrical resistivity can not be obtained. In addition, if the content of calcium or magnesium contained in the manganese-based magnet exceeds 11%, the proportion of the MnX phase becomes too small to obtain sufficient magnetization. Therefore, by setting the content of calcium or magnesium contained in the manganese-based magnet to 0.01 to 11 mass%, both the improvement of the electrical resistivity and the maintenance of the magnetization are achieved.
また、本発明に係るマンガン系磁石に含まれるカルシウムは、ＣａＯ、Ｃａ−Ｘ−Ｏ、Ｃａ−Ｍｎ−Ｏ、Ｃａ−Ｘ−Ｍｎ−Ｏ化合物またはそれらの化合物として存在し、マグネシウムはＭｇＯ、Ｍｇ−Ｘ−Ｏ、Ｍｇ−Ｍｎ−Ｏ、Ｍｇ−Ｘ−Ｍｎ−Ｏ化合物またはそれらの混合物として存在する。 In addition, calcium contained in the manganese-based magnet according to the present invention is present as CaO, Ca-X-O, Ca-Mn-O, Ca-X-Mn-O compound or compounds thereof, and magnesium is MgO, Mg. Present as -X-O, Mg-Mn-O, Mg-X-Mn-O compounds or mixtures thereof.
マンガン系磁石の主相粒子であるＭｎＸ結晶粒の粒径は１．０μｍ未満であることが好ましい。粒径が１．０μｍ以下であると主相粒子内の電子伝導が起こりにくくなるので、電気抵抗率を十分に上げることが容易となる。カルシウムもしくはマグネシウムはマンガン系磁石全体に均一に分布していることが好ましい。 It is preferable that the particle size of the MnX crystal grain which is a main phase particle of a manganese system magnet is less than 1.0 micrometer. When the particle size is 1.0 μm or less, electron conduction in the main phase particles is difficult to occur, so it is easy to sufficiently increase the electrical resistivity. Preferably, calcium or magnesium is uniformly distributed throughout the manganese-based magnet.
本発明に係るマンガン系磁石の製造方法を説明する。本発明に係るマンガン系磁石は、マンガン合金粉末を製造し、得られたマンガン系合金粉体とカルシウム源もしくはマグネシウム源を、混合・粉砕し、得られた粉体を圧縮成型し、温間押出加工する事により得られる。 A method of manufacturing a manganese based magnet according to the present invention will be described. The manganese-based magnet according to the present invention manufactures a manganese alloy powder, mixes and pulverizes the obtained manganese-based alloy powder and a calcium source or a magnesium source, compresses and molds the obtained powder, and warm extrusion It is obtained by processing.
本発明におけるマンガン系合金粉末はＭｎＸ（ここで、ＸはＡｌ、Ｂ、Ｂｉ、Ｃ、Ｃｏ、Ｃｒ、Ｆ、Ｉｒ、Ｇａ、Ｎ、Ｎｉ、Ｒｈ、Ｐｔ、Ｐｄの少なくとも１種である。）を主相とし、ガスアトマイズ法にて製造される。 The manganese-based alloy powder in the present invention is MnX (wherein X is at least one of Al, B, Bi, C, Co, Cr, F, Ir, Ga, N, Ni, Rh, Pt, and Pd). As a main phase and manufactured by gas atomization.
このマンガン系合金粉末とカルシウム源もしくはマグネシウム源を所定量秤量し混合する。カルシウム源としてＣａＯ、Ｃａ（ＯＨ）２、ＣａＣＯ３などが挙げられるが、特にＣａＯが好ましい。マグネシウム源としてＭｇＯ、Ｍｇ（ＯＨ）２、ＭｇＣＯ３などが挙げられるが、特にＭｇＯが好ましい。 Predetermined amounts of the manganese-based alloy powder and the calcium source or magnesium source are weighed and mixed. As a calcium source, CaO, Ca (OH) 2 , CaCO 3 and the like can be mentioned, and CaO is particularly preferable. Examples of the magnesium source include MgO, Mg (OH) 2 and MgCO 3, and MgO is particularly preferable.
本発明におけるカルシウム源およびマグネシウム源の粒子形状は特に限定はないが、球状、針状、粒状、紡錘状、直方体状などいずれでもよい。本発明におけるカルシウム源およびマグネシウム源の粒径は１００μｍ以下が好ましい。粒径が１００μｍ以下のカルシウムもしくはマグネシウムは磁石内部で偏らずに存在するため、十分高い電気抵抗率を得ることが容易となる。 The particle shape of the calcium source and the magnesium source in the present invention is not particularly limited, but may be spherical, needle-like, granular, spindle-like, rectangular solid or the like. The particle size of the calcium source and magnesium source in the present invention is preferably 100 μm or less. Since calcium or magnesium having a particle size of 100 μm or less is evenly present inside the magnet, it is easy to obtain a sufficiently high electrical resistivity.
次にマンガン系合金粉末とカルシウム源およびマグネシウム源を混合して微粉砕を行う。粉砕時間などの条件を適宜調整しながら、ジェットミル、ボールミル、振動ミルなどの微粉砕機を用いて粉砕を行うことで実施される。 Next, the manganese-based alloy powder is mixed with a calcium source and a magnesium source and pulverized. It implements by grind | pulverizing using pulverizers, such as a jet mill, a ball mill, a vibration mill, adjusting conditions, such as a grinding time, suitably.
マンガン合金粉体とカルシウム源およびマグネシウム源の粉砕時間は５時間以上が好ましい。粉砕時間が５時間未満の場合には、マンガン合金粉体とカルシウム源およびマグネシウム源の混合度が不十分となり、十分な電気抵抗率を有するマンガン系磁石を得ることができない。 The grinding time of the manganese alloy powder and the calcium source and magnesium source is preferably 5 hours or more. If the grinding time is less than 5 hours, the degree of mixing of the manganese alloy powder, the calcium source and the magnesium source will be insufficient, and a manganese based magnet having sufficient electrical resistivity can not be obtained.
振動ミルを使用する場合、マンガン合金粉体とカルシウム源およびマグネシウム源の振動ミルの使用する容器とボールは特に限定しないが、ステンレス、アルミナ、メノウ製が好ましい。さらにはＦｅ不純物の混入を避けることができるアルミナ、メノウ製が特に好ましい。 When a vibration mill is used, the container and balls used for the manganese alloy powder, the calcium source and the magnesium source vibration mill are not particularly limited, but stainless steel, alumina, and agate are preferable. Furthermore, alumina and agate that can avoid mixing of Fe impurities are particularly preferable.
混合で得られる混合粉末を所定量計量し、ダイスに投入し油圧プレスにて圧縮成形する。圧縮成型温度は６００℃〜７００℃が好ましい。圧縮成型温度が６００℃未満では十分な密度が得られない。圧縮成型圧力は１０ｋｇ／ｍｍ２以上であることが好ましい。１０ｋｇ／ｍｍ２未満では十分な密度が得られない。 A predetermined amount of the mixed powder obtained by mixing is measured, put into a die, and compression molded by a hydraulic press. The compression molding temperature is preferably 600 ° C to 700 ° C. If the compression molding temperature is less than 600 ° C., sufficient density can not be obtained. The compression molding pressure is preferably 10 kg / mm 2 or more. If it is less than 10 kg / mm 2 , sufficient density can not be obtained.
得られたビレットを７００℃〜８００℃、押出比Ｒ（押出加工前後のビレットの断面積比）２〜４で温間押出加工する事により、目的とするマンガン系磁石が得られる。 By hot-extruding the obtained billet at 700 ° C. to 800 ° C. and an extrusion ratio R (cross-sectional area ratio of billet before and after extrusion processing) 2 to 4, a target manganese-based magnet is obtained.
＜評価方法＞
本実施例と比較例の測定方法について説明する。作製したマンガン系磁石の電気抵抗率は４探針法にて測定した。４探針法とは４つの探針を試料表面に接触させ、外側の探針に電流を流した時に内側の探針に生じる電圧から電気抵抗率を求める方法である。試料の形状は２ｍｍ×２ｍｍ×５ｍｍに成形した。評価は１００μΩ・ｃｍ以上を合格とした。
<Evaluation method>
The measuring method of a present Example and a comparative example is demonstrated. The electrical resistivity of the manufactured manganese-based magnet was measured by the four-point probe method. The four-probe method is a method of obtaining the electrical resistivity from the voltage generated at the inner probe when the four probes are brought into contact with the sample surface and current is supplied to the outer probe. The shape of the sample was 2 mm × 2 mm × 5 mm. The evaluation passed 100 μΩ · cm or more.
マンガン系磁石の磁化は玉川製作所のＶＳＭ（振動試料型磁力測定：Ｖｉｂｒａｔｉｎｇ Ｓａｍｐｌｅ Ｍａｇｎｅｔｏｍｅｔｅｒ）で測定した。磁場範囲は０〜３３０００Ｏｅであり、温度は２５℃である。飽和磁化の評価はマンガンアルミニウム系磁石では８０ｅｍｕ／ｇ以上、マンガンビスマス系磁石では４０ｅｍｕ／ｇ以上を合格とした。 The magnetization of the manganese-based magnet was measured with a Tamagawa VSM (Vibrating Sample Magnetometer). The magnetic field range is 0-33000 Oe and the temperature is 25 ° C. In the evaluation of the saturation magnetization, 80 emu / g or more for the manganese aluminum based magnet and 40 emu / g or more for the manganese bismuth based magnet were accepted.
マンガン系磁石に含まれる相をＸ線回折法で同定した。マンガン系磁石のカルシウムおよびマグネシウムの含有量は誘導結合プラズマ質量分析法（ＩＣＰ−ＭＳ法）で測定した。 The phase contained in the manganese-based magnet was identified by X-ray diffraction. The calcium and magnesium contents of the manganese-based magnet were measured by inductively coupled plasma mass spectrometry (ICP-MS method).
実施例１
Ｍｎ（純度９９．９ｍａｓｓ％以上）、Ａｌ（純度９９．９ｍａｓｓ％以上）をＭｎ：Ａｌ＝７１：２９ｍａｓｓ％の割合で秤量し、ガスアトマイズ法でマンガンアルミニウム合金粉末を作製した。得られた粉体にＣａＯを０．０２ｍａｓｓ％添加し、ボールミルで６時間混合・粉砕を行った。
Example 1
Mn (purity of 99.9 mass% or more) and Al (purity of 99.9 mass% or more) were weighed at a ratio of Mn: Al = 71: 29 mass%, and a manganese aluminum alloy powder was produced by gas atomization. 0.02 mass% of CaO was added to the obtained powder, and it mixed and grind | pulverized for 6 hours with the ball mill.
この粉体を所定量計量後、ダイスに投入し油圧プレスにて温度６００℃、３０ｋｇ／ｍｍ２の条件で圧縮成型し、温間押し出し加工を行い、マンガンアルミニウム系磁石を得た。 A predetermined amount of this powder was measured, and then charged into a die and compression molded under conditions of a temperature of 600 ° C. and 30 kg / mm 2 with a hydraulic press, and warm extrusion processing was performed to obtain a manganese aluminum based magnet.
得られたマンガンアルミニウム系磁石のＸＲＤ測定を行うとＭｎＡｌ相のピークとわずかなＣａＯのピークが観測された。製造された磁石の主相粒子がＭｎＡｌ相になっており、カルシウムはＣａＯとして存在していることが分かる。ＩＣＰ−ＭＳ法でカルシウム量を測定すると添加したＣａＯの仕込み比から換算した値と一致していた。 When the XRD measurement of the obtained manganese aluminum based magnet was performed, the peak of MnAl phase and the peak of slight CaO were observed. It can be seen that the main phase particles of the manufactured magnet are in the MnAl phase, and calcium is present as CaO. When the amount of calcium was measured by the ICP-MS method, it was in agreement with the value converted from the preparation ratio of added CaO.
得られたマンガンアルミニウム系磁石の測定を行ったところ電気抵抗率ρが１０２μΩ・ｃｍ、飽和磁化Ｍｓが９５．２ｅｍｕ／ｇであり、十分な電気抵抗率と磁気特性が得られた。 As a result of measurement of the obtained manganese aluminum-based magnet, the electric resistivity μ was 102 μΩ · cm, the saturation magnetization Ms was 95.2 emu / g, and sufficient electric resistivity and magnetic characteristics were obtained.
実施例２〜５ではＣａＯの添加量のみを変えたこと以外は実施例１と同様にしてマンガンアルミニウム系磁石を作製した。ＩＣＰ−ＭＳ法で測定したカルシウム量は添加したＣａＯの仕込み比から換算した値と一致していた。実施例２〜５では、ＸＲＤ測定を行ったところＭｎＡｌとＣａＯのピークが観測された。電気抵抗率と飽和磁化を測定すると、十分な電気抵抗率と飽和磁化を有することが分かった。 In Examples 2 to 5, a manganese aluminum magnet was produced in the same manner as in Example 1 except that only the addition amount of CaO was changed. The amount of calcium measured by the ICP-MS method was in agreement with the value converted from the feed ratio of added CaO. In Examples 2 to 5, when XRD measurement was performed, peaks of MnAl and CaO were observed. Measurement of the electrical resistivity and the saturation magnetization revealed that it had sufficient electrical resistivity and saturation magnetization.
実施例６、７では添加剤をＣａＯからＭｇＯに変えたこと以外は実施例１と同様にしてマンガンアルミニウム系磁石を作製した。ＩＣＰ−ＭＳ法で測定したマグネシウム量は添加したＭｇＯの仕込み比から換算した値と一致していた。ＸＲＤ測定を行ったところ、ＭｎＡｌとＭｇＯのピークが観測された。電気抵抗率と飽和磁化を測定すると、十分な電気抵抗率と飽和磁化を有することが分かった。 In Examples 6 and 7, a manganese aluminum magnet was produced in the same manner as in Example 1 except that the additive was changed from CaO to MgO. The amount of magnesium measured by the ICP-MS method was in agreement with the value converted from the charging ratio of added MgO. When XRD measurement was performed, peaks of MnAl and MgO were observed. Measurement of the electrical resistivity and the saturation magnetization revealed that it had sufficient electrical resistivity and saturation magnetization.
実施例８ではＣａＯのみではなくＣａＯとＭｇＯを添加したこと以外は実施例１と同様にしてマンガンアルミニウム系磁石を作製した。ＩＣＰ−ＭＳ法で測定したカルシウム量およびマグネシウム量は添加したＣａＯおよびＭｇＯの仕込み比から換算した値と一致していた。ＸＲＤ測定を行ったところ、ＭｎＡｌ、ＣａＯおよびＭｇＯのピークが観測された。電気抵抗率と飽和磁化を測定すると、十分な電気抵抗率と飽和磁化を有することが分かった。 In Example 8, a manganese aluminum magnet was produced in the same manner as in Example 1 except that CaO and MgO were added in addition to CaO. The amounts of calcium and magnesium measured by the ICP-MS method were in agreement with the values converted from the feed ratio of added CaO and MgO. When XRD measurement was performed, peaks of MnAl, CaO and MgO were observed. Measurement of the electrical resistivity and the saturation magnetization revealed that it had sufficient electrical resistivity and saturation magnetization.
実施例１〜８で添加したＣａＯとＭｇＯの量とＩＣＰ−ＭＳ分析で検出したＣａとＭｇ量を表１に示す。
実施例１〜８で電気抵抗率と磁化の測定を行った結果を表２に示す。
The amounts of CaO and MgO added in Examples 1 to 8 and the amounts of Ca and Mg detected by ICP-MS analysis are shown in Table 1.
The results of measurement of the electrical resistivity and the magnetization in Examples 1 to 8 are shown in Table 2.
比較例１では添加剤を入れなかったこと以外は実施例１と同様にしてマンガンアルミニウム系磁石を作製した。 In Comparative Example 1, a manganese aluminum magnet was produced in the same manner as in Example 1 except that no additive was added.
比較例２ではＣａＯを０．０１ｍａｓｓ％添加し、比較例３ではＣａＯを１８ｍａｓｓ％添加したこと以外は実施例１と同様にしてマンガンアルミニウム系磁石を得た。 A manganese aluminum based magnet was obtained in the same manner as in Example 1 except that 0.01 mass% of CaO was added in Comparative Example 2 and 18 mass% of CaO was added in Comparative Example 3.
比較例４ではＣａＯの代わりにＭｇＯを０．０１ｍａｓｓ％添加し、比較例５ではＭｇＯを１８ｍａｓｓ％添加したこと以外は実施例１と同様にしてマンガンアルミニウム系磁石を得た。 A manganese aluminum based magnet was obtained in the same manner as in Example 1 except that in Comparative Example 4, 0.01 mass% of MgO was added instead of CaO and in Comparative Example 5, 18 mass% of MgO was added.
比較例１〜５で電気抵抗率と磁化の測定を行った結果を表１に示す。
電気抵抗率測定および磁化測定いずれの評価でも合格と評価できるマンガンアルミニウム系磁石は実施例１〜８であるといえる。カルシウムもしくはマグネシウムの添加量が多いほど電気抵抗率の増大の効果が強くなっていることが分かる。また、実施例１〜８のカルシウムもしくはマグネシウム量の範囲では十分な飽和磁化を持つことが分かる。 The manganese aluminum-based magnets that can be evaluated as pass in either of the electrical resistivity measurement and the magnetization measurement can be said to be Examples 1 to 8. It can be seen that the effect of increasing the electrical resistivity is stronger as the amount of addition of calcium or magnesium is larger. Moreover, it turns out that it has sufficient saturation magnetization in the range of the amount of calcium or magnesium of Examples 1-8.
一方、比較例１、２のようにカルシウムの添加量が０．０１ｍａｓｓ％未満ではカルシウム量が少ないため主相粒子間の電子伝導を抑えられず、電気抵抗率を十分に高めることができなかったと考えられる。また、比較例３のようにカルシウム量が１１ｍａｓｓ％を超えると磁石の飽和磁化が低くなる。 On the other hand, when the addition amount of calcium is less than 0.01 mass% as in Comparative Examples 1 and 2, the amount of calcium is small, so that the electron conduction between main phase particles can not be suppressed and the electrical resistivity can not be sufficiently increased. Conceivable. In addition, when the amount of calcium exceeds 11 mass% as in Comparative Example 3, the saturation magnetization of the magnet decreases.
比較例４のようにマグネシウム量が０．０１ｍａｓｓ％未満では十分電気抵抗を高めることができず、比較例５のようにマグネシウム量が１１ｍａｓｓ％を超えると磁石の飽和磁化が低くなる。 If the amount of magnesium is less than 0.01 mass% as in Comparative Example 4, the electrical resistance can not be sufficiently increased, and if the amount of magnesium exceeds 11 mass% as in Comparative Example 5, the saturation magnetization of the magnet becomes low.
実施例９
Ｍｎ（純度９９．９ｍａｓｓ％以上）、Ｂｉ（純度９９．９ｍａｓｓ％以上）をそれぞれＭｎを１７ｍａｓｓ％、Ｂｉを８３ｍａｓｓ％の割合で秤量し、ガスアトマイズ法でマンガンビスマス合金粉末を作製し、Ａｒ雰囲気中２７０℃で３日間加熱した。
Example 9
17 mass% of Mn (purity of 99.9 mass% or more) and Bi (purity of 99.9 mass% or more) are weighed at a ratio of 17 mass% of Mn and 83 mass% of Bi, manganese bismuth alloy powder is produced by gas atomizing method, and in Ar atmosphere Heated at 270 ° C. for 3 days.
得られた粉体にＣａＯを０．０２ｍａｓｓ％添加し、振動ミルで６時間混合・粉砕を行い、１００μｍ以下の粉体を得た。 0.02 mass% of CaO was added to the obtained powder, and mixing and grinding were performed for 6 hours with a vibrating mill to obtain a powder of 100 μm or less.
この粉体を所定量計量後、ダイスに投入し油圧プレスにて温度６００℃、３０ｋｇ／ｍｍ２の条件で圧縮成型し、温間押し出し加工によりマンガンビスマス系磁石を得た。 A predetermined amount of this powder was measured, and then charged into a die and compression molded at a temperature of 600 ° C. and 30 kg / mm 2 with a hydraulic press to obtain a manganese bismuth based magnet by warm extrusion processing.
ＸＲＤ測定を行うとＭｎＡｌ相のピークとわずかなＣａＯのピークが観測された。製造されたマンガン系磁石では、主相粒子がＭｎＢｉになっており、カルシウムはＣａＯとして存在していることが分かる。ＩＣＰ−ＭＳ法でカルシウム量を測定すると添加したＣａＯの仕込み比から換算した値と一致していた。 As a result of XRD measurement, a peak of MnAl phase and a peak of slight CaO were observed. In the manufactured manganese-based magnet, it is understood that the main phase particles are MnBi, and calcium is present as CaO. When the amount of calcium was measured by the ICP-MS method, it was in agreement with the value converted from the preparation ratio of added CaO.
得られた磁石の測定を行ったところ電気抵抗率ρが１０２μΩ・ｃｍ、飽和磁化Ｍｓが５０．０ｅｍｕ／ｇであり、十分な電気抵抗率と磁気特性が得られた。 As a result of measurement of the obtained magnet, the electric resistivity ρ was 102 μΩ · cm, the saturation magnetization Ms was 50.0 emu / g, and sufficient electric resistivity and magnetic characteristics were obtained.
実施例１０〜１３ではＣａＯの添加量のみを変えたこと以外は実施例９と同様にしてマンガン系磁石を作製した。ＩＣＭ−ＭＳ法で測定したカルシウム量は添加したＣａＯの仕込み比から換算した値と一致していた。実施例１０〜１３では、ＸＲＤ測定を行ったところＭｎＢｉとＣａＯのピークが観測された。電気抵抗率と飽和磁化を測定すると、十分な電気抵抗率と飽和磁化を有することが分かった。 In Examples 10 to 13, a manganese-based magnet was produced in the same manner as in Example 9 except that only the addition amount of CaO was changed. The amount of calcium measured by the ICM-MS method was in agreement with the value converted from the feed ratio of added CaO. In Examples 10 to 13, when XRD measurement was performed, peaks of MnBi and CaO were observed. Measurement of the electrical resistivity and the saturation magnetization revealed that it had sufficient electrical resistivity and saturation magnetization.
実施例１４、１５では添加剤をＣａＯからＭｇＯに変えたこと以外は実施例９と同様にしてマンガンビスマス系磁石を作製した。ＩＣＰ−ＭＳ法で測定したマグネシウム量は添加したＭｇＯの仕込み比から換算した値と一致していた。実施例１４、１５ではＸＲＤ測定を行ったところ、ＭｎＢｉとＭｇＯのピークが観測された。電気抵抗率と飽和磁化を測定すると、十分な電気抵抗率と飽和磁化を有することが分かった。 In Examples 14 and 15, a manganese bismuth based magnet was produced in the same manner as in Example 9 except that the additive was changed from CaO to MgO. The amount of magnesium measured by the ICP-MS method was in agreement with the value converted from the charging ratio of added MgO. When XRD measurement was performed in Examples 14 and 15, peaks of MnBi and MgO were observed. Measurement of the electrical resistivity and the saturation magnetization revealed that it had sufficient electrical resistivity and saturation magnetization.
実施例９〜１６で添加したＣａＯとＭｇＯの量とＩＣＰ−ＭＳ分析で検出したＣａとＭｇ量を表３に示す。
実施例９〜１６で電気抵抗率と磁化の測定を行った結果を表４に示す。
The amounts of CaO and MgO added in Examples 9 to 16 and the amounts of Ca and Mg detected by ICP-MS analysis are shown in Table 3.
The results of measurement of the electrical resistivity and the magnetization in Examples 9 to 16 are shown in Table 4.
比較例６では添加剤を入れなかったこと以外は実施例９と同様にしてマンガンビスマス系磁石を作製した。 In Comparative Example 6, a manganese bismuth based magnet was produced in the same manner as in Example 9 except that no additive was added.
比較例７ではＣａＯを０．０１ｍａｓｓ％添加し、比較例８ではＣａＯを１８ｍａｓｓ％添加したこと以外は実施例１と同様にしてマンガンビスマス系磁石を得た。 In Comparative Example 7, 0.01 mass% of CaO was added, and in Comparative Example 8, a manganese bismuth based magnet was obtained in the same manner as Example 1, except that 18 mass% of CaO was added.
比較例９ではＣａＯの代わりにＭｇＯを０．０１ｍａｓｓ％添加し、比較例１０ではＭｇＯを１８ｍａｓｓ％添加したこと以外は実施例９と同様にしてマンガンビスマス系磁石を得た。 In Comparative Example 9, 0.01 mass% of MgO was added instead of CaO, and in Comparative Example 10, a manganese bismuth based magnet was obtained in the same manner as Example 9, except that 18 mass% of MgO was added.
比較例６〜１０で電気抵抗率と磁化の測定を行った結果を表４に示す。
一方、比較例６、７のようにカルシウムの添加量が０．０１ｍａｓｓ％未満ではカルシウム量が少ないため主相粒子間の電子伝導を抑えられず、電気抵抗率を十分に高めることができなかったと考えられる。また、比較例８のようにカルシウム量が１１ｍａｓｓ％を超えると磁石の飽和磁化が低くなる。 On the other hand, when the added amount of calcium is less than 0.01 mass% as in Comparative Examples 6 and 7, the amount of calcium is small, so that the electron conduction between the main phase particles can not be suppressed and the electrical resistivity can not be sufficiently increased. Conceivable. In addition, when the amount of calcium exceeds 11 mass% as in Comparative Example 8, the saturation magnetization of the magnet decreases.
比較例９のようにマグネシウム量が０．０１ｍａｓｓ％未満では十分電気抵抗を高めることができず、比較例１０のようにマグネシウム量が１１ｍａｓｓ％を超えると磁石の飽和磁化が低くなる。 If the amount of magnesium is less than 0.01 mass% as in Comparative Example 9, the electrical resistance can not be sufficiently increased, and if the amount of magnesium exceeds 11 mass% as in Comparative Example 10, the saturation magnetization of the magnet decreases.
本発明はマンガン系磁石においてカルシウムもしくはマグネシウムを含むことで渦電流損を低減することができる。よって、本発明のマンガン系磁石は交流磁界を受けたときの渦電流損を抑え、渦電流に伴う発熱を抑えることができ、磁石モータなどの回転機に使用することができる。 The present invention can reduce eddy current loss by containing calcium or magnesium in a manganese-based magnet. Therefore, the manganese-based magnet of the present invention can suppress the eddy current loss when receiving an alternating magnetic field, can suppress heat generation due to the eddy current, and can be used for a rotating machine such as a magnet motor.
Claims (1)
カルシウムもしくはマグネシウムをカルシウムおよびマグネシウムの合計で０．０１４ｍａｓｓ％〜１０．８５４ｍａｓｓ％含み、
カルシウムは、ＣａＯ、Ｃａ−Ｘ−Ｏ、Ｃａ−Ｍｎ−Ｏ、Ｃａ−Ｘ−Ｍｎ−Ｏ化合物またはそれらの化合物として存在し、
マグネシウムは、ＭｇＯ、Ｍｇ−Ｘ−Ｏ、Ｍｇ−Ｍｎ−Ｏ、Ｍｇ−Ｘ−Ｍｎ−Ｏ化合物またはそれらの化合物として存在し、
ＸはＡｌ、Ｂ、Ｂｉ、Ｃ、Ｃｏ、Ｃｒ、Ｆ、Ｉｒ、Ｇａ、Ｎ、Ｎｉ、Ｒｈ、Ｐｔ、Ｐｄの少なくとも１種であり、
電気抵抗率が１００μΩ・ｃｍ以上であることを特徴とするマンガン系磁石。 A manganese based magnet,
0.014mass% ~10.854mass% viewing including the calcium or magnesium in the sum of calcium and magnesium,
Calcium is present as CaO, Ca-X-O, Ca-Mn-O, Ca-X-Mn-O compound or compounds thereof,
Magnesium is present as MgO, Mg-X-O, Mg-Mn-O, Mg-X-Mn-O compound or their compounds,
X is at least one of Al, B, Bi, C, Co, Cr, F, Ir, Ga, N, Ni, Rh, Pt, and Pd,
A manganese based magnet characterized by having an electrical resistivity of 100 μΩ · cm or more .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2015039798A JP6511862B2 (en) | 2015-03-02 | 2015-03-02 | Manganese magnet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2015039798A JP6511862B2 (en) | 2015-03-02 | 2015-03-02 | Manganese magnet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016162873A JP2016162873A (en) | 2016-09-05 |
| JP6511862B2 true JP6511862B2 (en) | 2019-05-15 |
Family
ID=56845599
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015039798A Active JP6511862B2 (en) | 2015-03-02 | 2015-03-02 | Manganese magnet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP6511862B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2025105244A1 (en) * | 2023-11-14 | 2025-05-22 | Ａｇｃ株式会社 | Method for producing magnetic particles, magnetic particles, and permanent magnet using same |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3138192B2 (en) * | 1995-08-10 | 2001-02-26 | 山陽特殊製鋼株式会社 | Manganese aluminum magnet with far-infrared radiation effect |
| JPH09186010A (en) * | 1995-08-23 | 1997-07-15 | Hitachi Metals Ltd | Large electric resistance rare earth magnet and its manufacture |
| JPH10261514A (en) * | 1997-03-19 | 1998-09-29 | Hitachi Maxell Ltd | Magnetic material |
| JP2001257110A (en) * | 2000-03-09 | 2001-09-21 | Hitachi Maxell Ltd | Magnetic material and magnetic recording medium using the same |
| JP2003022905A (en) * | 2001-07-10 | 2003-01-24 | Daido Steel Co Ltd | High resistance rare earth magnet and method of manufacturing the same |
| JP2007208017A (en) * | 2006-02-02 | 2007-08-16 | Nec Tokin Corp | Permanent magnet and method for manufacturing the same |
| JP2011030341A (en) * | 2009-07-24 | 2011-02-10 | Hitachi Ltd | Rotating electrical machine |
-
2015
- 2015-03-02 JP JP2015039798A patent/JP6511862B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| JP2016162873A (en) | 2016-09-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2905485T3 (en) | Sintered magnet based on R-Fe-B with low B content and preparation method thereof | |
| JP4540076B2 (en) | Bond magnet, compound, magnet roll, ferrite powder used therefor, and method for producing the same | |
| US11521769B2 (en) | Ferrite sintered magnet and rotary electrical machine comprising the same | |
| CN105895286B (en) | Rare earth element permanent magnet | |
| CN107622854B (en) | R-T-B based rare earth element permanent magnet | |
| WO2007105398A1 (en) | Rotating machine, bonded magnet, magnet roll, and process for producing ferrite sintered magnet | |
| KR20130130766A (en) | Ferrite sintered magnet and method for producing same | |
| KR20050050681A (en) | Anisotropic, sintered ferrite magnet and method for producing the same | |
| CN102050619A (en) | Method for preparing permanent magnet oxysome material | |
| CN110323027A (en) | The manufacturing method of ferrite sintered magnet and ferrite sintered magnet | |
| JP6152854B2 (en) | Ferrite sintered magnet and manufacturing method thereof | |
| CN110323026A (en) | Ferrite sintered magnet | |
| JP6828027B2 (en) | A method for producing an R-Fe-B-based rare earth sintered magnet containing a composite of Pr and W. | |
| CN105047344B (en) | R T B system's permanent magnets and electric rotating machine | |
| US20200312496A1 (en) | Ferrite sintered magnet and rotary electrical machine comprising the same | |
| JP6511862B2 (en) | Manganese magnet | |
| CN102129906B (en) | Permanent ferrite material additive and preparation method and application thereof | |
| CN108695036A (en) | R-T-B systems permanent magnet | |
| JPWO2018101409A1 (en) | Rare earth sintered magnet | |
| Mahmoudi et al. | The effect of nano-SiO2 on magnetic and dielectric properties of Li–Zn ferrite | |
| Chae et al. | Effects of Ga substitution on crystallographic and magnetic properties of Co ferrites | |
| CN104464998B (en) | A kind of high energy product sintered Nd-Fe-B permanent magnetic material and preparation method | |
| WO2019181056A1 (en) | Ferrite calcined body, ferrite sintered magnet, and method for manufacturing same | |
| JP2016162872A (en) | Manganese-based magnet | |
| Septiani et al. | Preparation of barium hexaferrite powders using oxidized steel scales waste |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20160714 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20171115 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20180926 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20181003 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20181203 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20190312 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20190325 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6511862 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |