JP7059594B2 - Soft magnetic materials, cores and inductors - Google Patents

Soft magnetic materials, cores and inductors Download PDF

Info

Publication number
JP7059594B2
JP7059594B2 JP2017229182A JP2017229182A JP7059594B2 JP 7059594 B2 JP7059594 B2 JP 7059594B2 JP 2017229182 A JP2017229182 A JP 2017229182A JP 2017229182 A JP2017229182 A JP 2017229182A JP 7059594 B2 JP7059594 B2 JP 7059594B2
Authority
JP
Japan
Prior art keywords
particle group
soft magnetic
particle size
particle
peak
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
Application number
JP2017229182A
Other languages
Japanese (ja)
Other versions
JP2018113436A (en
Inventor
芳浩 新海
真仁 小枝
暁太朗 阿部
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TDK Corp
Original Assignee
TDK Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by TDK Corp filed Critical TDK Corp
Priority to US15/868,363 priority Critical patent/US10573442B2/en
Priority to CN201810026596.0A priority patent/CN108364767B/en
Publication of JP2018113436A publication Critical patent/JP2018113436A/en
Application granted granted Critical
Publication of JP7059594B2 publication Critical patent/JP7059594B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F27/00Details of transformers or inductances, in general
    • H01F27/24Magnetic cores
    • H01F27/255Magnetic cores made from particles
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/20Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of particles, e.g. powder
    • H01F1/22Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together
    • H01F1/24Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together the particles being insulated

Landscapes

  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Soft Magnetic Materials (AREA)
  • Powder Metallurgy (AREA)
  • Coils Or Transformers For Communication (AREA)

Description

本発明は、軟磁性材料、コア及びインダクタに関する。 The present invention relates to soft magnetic materials, cores and inductors.

近年、電子機器の高密度実装化と高速処理化に伴い、インダクタにおいても小型化及び高出力化が求められているが、この小型化によって、インダクタのコア(磁性材料から成るコア)の体積が減少してしまうため、インダクタンスの低下と直流重畳特性(直流電流負荷時のインダクタンス)の悪化を招きやすくなっている。 In recent years, along with the high-density mounting and high-speed processing of electronic devices, there is a demand for smaller and higher output inductors, and this miniaturization has increased the volume of the inductor core (core made of magnetic material). Since it decreases, it tends to cause a decrease in inductance and deterioration of DC superimposition characteristics (inductance at the time of DC current load).

したがって、小型化した場合でも、インダクタンスの低下と直流重畳特性の悪化を招かないコア、すなわち、高透磁率、且つ直流重畳特性にも優れた軟磁性材料が求められている。 Therefore, there is a demand for a core that does not cause a decrease in inductance and deterioration of DC superimposition characteristics even when the size is reduced, that is, a soft magnetic material having high magnetic permeability and excellent DC superimposition characteristics.

従来の軟磁性材料に関する発明としては、例えば、特許文献1に記載の軟磁性材料、コア及びインダクタが知られている。該軟磁性材料はそれぞれ絶縁被覆されている、20μm以上50μm以下の粒径を有する第1の軟磁性金属粉末と、1μm以上10μm以下の粒径を有する第2の軟磁性金属粉末と、樹脂とを含む軟磁性材料である。そして、前記第1の軟磁性金属粉末の質量%と前記第2の軟磁性金属粉末の質量%との比は、A:Bであり、A+B=100、15≦A≦35及び65≦B≦85である。 As inventions relating to conventional soft magnetic materials, for example, the soft magnetic materials, cores and inductors described in Patent Document 1 are known. The soft magnetic material is an insulating coating of a first soft magnetic metal powder having a particle size of 20 μm or more and 50 μm or less, a second soft magnetic metal powder having a particle size of 1 μm or more and 10 μm or less, and a resin. It is a soft magnetic material containing. The ratio of the mass% of the first soft magnetic metal powder to the mass% of the second soft magnetic metal powder is A: B, and A + B = 100, 15 ≦ A ≦ 35 and 65 ≦ B ≦. 85.

特開2014-204108号公報Japanese Unexamined Patent Publication No. 2014-204108

特許文献1の技術では粗粉である20μm以上50μm以下の粒径を有する第1の軟磁性金属粉末より、微粉である1μm以上10μm以下の粒径を有する第2の軟磁性金属粉末の比率が大きい構成であるため、十分に軟磁性材料の充填率を上げることができない。特許文献1と同様の構成でコアを作製したところ、透磁率が小さく、近年の小型化要求に応えることができるほどの高い透磁率と良好な直流重畳特性を得るには不十分であった。 In the technique of Patent Document 1, the ratio of the second soft magnetic metal powder having a particle size of 1 μm or more and 10 μm or less, which is a fine powder, is higher than that of the first soft magnetic metal powder having a particle size of 20 μm or more and 50 μm or less, which is a coarse powder. Due to the large configuration, the filling rate of the soft magnetic material cannot be sufficiently increased. When the core was produced with the same configuration as in Patent Document 1, the magnetic permeability was small, and it was insufficient to obtain a high magnetic permeability and good DC superimposition characteristics that could meet the recent demand for miniaturization.

そこで、本発明は上記課題に鑑みてなされたものであり、高い透磁率を有し、直流重畳特性にも優れた軟磁性材料、コア及びインダクタを提供することを目的とするものである。 Therefore, the present invention has been made in view of the above problems, and an object of the present invention is to provide a soft magnetic material, a core, and an inductor having high magnetic permeability and excellent DC superimposition characteristics.

本発明の軟磁性材料は、軟磁性金属粉末と樹脂とを含み、前記軟磁性金属粉末は、粒子群αと粒子群βで構成され、粒子群αのピーク強度をIA、粒子群αの体積をVα、粒子群βのピーク強度をIB、粒子群βの体積をVβ、粒子群αと粒子群βの間に存在する最小値の強度をICとしたときに、強度比IC/IAが0.12以下、体積比Vα/Vβが2.0以上5.1以下となることを特徴とする。ただし、前記軟磁性金属粉末の粒度分布において、粒子群αは最大のピーク強度を含む粒子群であり、粒子群αのピーク粒径PAは粒子群βのピーク粒径PBよりも大きいこととする。また、粒子群αのピーク強度を大きい順にIA1、IA2、・・・、IAx(xは1以上)としたとき、粒子群αのピーク強度IAをIA1とし、粒子群αのピーク粒径PAをPA1とする。さらに、粒子群βのピーク強度を大きい順にIB1、IB2、・・・、IBy(yは1以上)としたとき、粒子群βのピーク強度IBをIB1とし、粒子群βのピーク粒径PBをPB1とする。 The soft magnetic material of the present invention contains a soft magnetic metal powder and a resin, and the soft magnetic metal powder is composed of a particle group α and a particle group β, the peak intensity of the particle group α is IA, and the volume of the particle group α. Is Vα, the peak intensity of the particle group β is IB, the volume of the particle group β is Vβ, and the minimum intensity existing between the particle group α and the particle group β is IC, the intensity ratio IC / IA is 0. It is characterized by having a volume ratio of .12 or less and a volume ratio of Vα / Vβ of 2.0 or more and 5.1 or less. However, in the particle size distribution of the soft magnetic metal powder, the particle group α is a particle group containing the maximum peak intensity, and the peak particle size PA of the particle group α is larger than the peak particle size PB of the particle group β. .. Further, when the peak intensities of the particle group α are set to IA1, IA2, ..., IAx (x is 1 or more) in descending order, the peak intensity IA of the particle group α is set to IA1 and the peak particle size PA of the particle group α is set. Let it be PA1. Further, when the peak intensities of the particle group β are set to IB1, IB2, ..., IBy (y is 1 or more) in descending order, the peak intensity IB of the particle group β is set to IB1 and the peak particle size PB of the particle group β is set. Let it be PB1.

すなわち、粒子群αと粒子群βの中間粒径の粒子が少ない。このため、粒子群αの大粒径粒子同士の間にできる空隙に、効率よく粒子群βの小粒径粒子を充填させることができる。また、粒子群αと粒子群βを合わせた軟磁性粒子の充填率を高くすることができる。この結果として、高い透磁率と良好な直流重畳特性を得ることができたと推察される。ただし、作用はこれに限定されない。 That is, there are few particles having an intermediate particle size between the particle group α and the particle group β. Therefore, the small particle size particles of the particle group β can be efficiently filled in the voids formed between the large particle size particles of the particle group α. In addition, the filling rate of the soft magnetic particles in which the particle group α and the particle group β are combined can be increased. As a result, it is presumed that high magnetic permeability and good DC superimposition characteristics could be obtained. However, the action is not limited to this.

前記粒子群αのピーク粒径PAが60μm以下であることが好ましい。この範囲とすることで、直流重畳特性が向上し、樹脂部や空隙部の分布状態が偏析しにくい組織状態となり、試料中の組織が均一になると推察される。ただし、作用はこれに限定されない。 The peak particle size PA of the particle group α is preferably 60 μm or less. Within this range, it is presumed that the DC superimposition characteristic is improved, the distribution state of the resin portion and the void portion becomes a structure state in which segregation is difficult to occur, and the structure in the sample becomes uniform. However, the action is not limited to this.

前記粒子群αを構成する軟磁性金属粉末は、Fe又はFeを含有する金属であり、絶縁材料で被覆されていることが好ましい。飽和磁化の高いFeまたはFeを含有する金属を用いることで、透磁率が高く、直流重畳特性が良好になる傾向が見られる。また、絶縁材料を被覆することで、直流重畳特性が良好となる傾向が見られる。なお、ここでいう被覆とは、粒子の一部または全部を覆うことを意味する。 The soft magnetic metal powder constituting the particle group α is a metal containing Fe or Fe, and is preferably coated with an insulating material. By using Fe or a metal containing Fe having a high saturation magnetization, there is a tendency that the magnetic permeability is high and the DC superimposition characteristic is good. Further, by covering with an insulating material, the DC superimposition characteristic tends to be improved. The coating referred to here means covering a part or all of the particles.

本発明の一形態に係るコアは、前記軟磁性材料により作製されていることを特徴とする。 The core according to one embodiment of the present invention is characterized in that it is made of the soft magnetic material.

本発明の一形態に係るインダクタは、前記コアを備えていることを特徴とする。 The inductor according to one embodiment of the present invention is characterized by including the core.

本発明によれば、高い透磁率を有し、直流重畳特性にも優れた軟磁性材料、コア及びインダクタを提供することができる。 According to the present invention, it is possible to provide a soft magnetic material, a core and an inductor having high magnetic permeability and excellent DC superimposition characteristics.

実施例5の軟磁性材料の粒度分布(頻度分布)を示す図The figure which shows the particle size distribution (frequency distribution) of the soft magnetic material of Example 5. 実施例15の軟磁性材料の粒度分布(頻度分布)を示す図The figure which shows the particle size distribution (frequency distribution) of the soft magnetic material of Example 15. 比較例1の軟磁性材料の粒度分布(頻度分布)を示す図The figure which shows the particle size distribution (frequency distribution) of the soft magnetic material of the comparative example 1. 比較例3の軟磁性材料の粒度分布(頻度分布)を示す図The figure which shows the particle size distribution (frequency distribution) of the soft magnetic material of the comparative example 3. 薄膜インダクタの内部構造を説明するための概念図である。It is a conceptual diagram for demonstrating the internal structure of a thin film inductor. 薄膜インダクタの外観を説明するための概念図である。It is a conceptual diagram for demonstrating the appearance of a thin film inductor.

以下に、本発明の実施形態について説明するが、本発明はこれらの実施形態に限定されるものではない。また、下記の実施形態における構成要素には、当業者が容易に想定できるもの、実質的に同一のもの、いわゆる均等の範囲のものが含まれる。 Hereinafter, embodiments of the present invention will be described, but the present invention is not limited to these embodiments. Further, the components in the following embodiments include those that can be easily assumed by those skilled in the art, those that are substantially the same, and those that are in a so-called equal range.

実施形態の軟磁性材料は、軟磁性金属粉末と樹脂を含み、前記軟磁性金属粉末は、粒子群αと粒子群βで構成され、粒子群αのピーク強度をIA、粒子群αの体積をVα、粒子群βのピーク強度をIB、粒子群βの体積をVβ、粒子群αと粒子群βの間に存在する最小値の強度をICとしたときに、強度比IC/IAが0.12以下、体積比Vα/Vβが2.0以上5.1以下となることを特徴とする。ただし、前記軟磁性金属粉末の粒度分布において、粒子群αは最大のピーク強度を含む粒子群であり、粒子群αのピーク粒径PAは粒子群βのピーク粒径PBよりも大きいこととする。また、粒子群αのピーク強度を大きい順にIA1、IA2、・・・、IAx(xは1以上)としたとき、粒子群αのピーク強度IAをIA1とし、粒子群αのピーク粒径PAをPA1とする。さらに、粒子群βのピーク強度を大きい順にIB1、IB2、・・・、IBy(yは1以上)としたとき、粒子群βのピーク強度IBをIB1とし、粒子群βのピーク粒径PBをPB1とする。そして、粒子群αと粒子群βの間に存在する最小値の強度ICをもつ点をCとし、その粒径をPCとする。 The soft magnetic material of the embodiment contains a soft magnetic metal powder and a resin, and the soft magnetic metal powder is composed of a particle group α and a particle group β, and has a peak intensity of the particle group α of IA and a volume of the particle group α. When Vα, the peak intensity of the particle group β is IB, the volume of the particle group β is Vβ, and the minimum intensity existing between the particle group α and the particle group β is IC, the intensity ratio IC / IA is 0. It is characterized in that the volume ratio Vα / Vβ is 12 or less and the volume ratio is 2.0 or more and 5.1 or less. However, in the particle size distribution of the soft magnetic metal powder, the particle group α is a particle group containing the maximum peak intensity, and the peak particle size PA of the particle group α is larger than the peak particle size PB of the particle group β. .. Further, when the peak intensities of the particle group α are set to IA1, IA2, ..., IAx (x is 1 or more) in descending order, the peak intensity IA of the particle group α is set to IA1 and the peak particle size PA of the particle group α is set. Let it be PA1. Further, when the peak intensities of the particle group β are set to IB1, IB2, ..., IBy (y is 1 or more) in descending order, the peak intensity IB of the particle group β is set to IB1 and the peak particle size PB of the particle group β is set. Let it be PB1. Then, the point having the minimum intensity IC existing between the particle group α and the particle group β is defined as C, and the particle size thereof is defined as PC.

ピークA1、A2、・・・、Ax(xは1以上)、B1、B2、・・・、By(yは1以上)、及び点Cは、例えば、レーザー回折・散乱法での測定によって求めた体積基準の粒度分布から判定することができ、そのピークと点からピーク粒径PA1、PA2、・・・、PAx(xは1以上)、PB1、PB2、・・・、PBy(yは1以上)とピーク強度IA1、IA2、・・・、IAx(xは1以上)、IB1、IB2、・・・、IBy(yは1以上)、及び点Cの粒径PC、強度ICを算出できる。また、その体積基準の粒度分布において、PCより大粒径側を粒子群α、小粒径側を粒子群βとし、粒子群αの体積Vα及び粒子群βの体積Vβを算出できる。 Peaks A1, A2, ..., Ax (x is 1 or more), B1, B2, ..., By (y is 1 or more), and point C are obtained by measurement by, for example, a laser diffraction / scattering method. It can be determined from the volume-based particle size distribution, and the peak particle sizes PA1, PA2, ..., PAx (x is 1 or more), PB1, PB2, ..., PBy (y is 1) from the peaks and points. IA1, IA2, ..., IAx (x is 1 or more), IB1, IB2, ..., IBy (y is 1 or more), particle size PC at point C, and strength IC can be calculated. .. Further, in the volume-based particle size distribution, the volume Vα of the particle group α and the volume Vβ of the particle group β can be calculated by setting the particle group α on the large particle size side and the particle group β on the small particle size side from the PC.

図1は代表的な本発明の実施形態を示した粒度分布の例である。図1はVα/Vβが2.0以上5.1以下であり、粒子群αの大粒径粒子同士の間にできる空隙に、効率よく粒子群βの小粒径粒子を充填させることで、粒子群αと粒子群βを合わせた軟磁性粒子の充填率を高くすることができる。図2のように強度比IC/IAが0.12より大きくなると、粒子群αと粒子群βの中間サイズの粒子が増えるので、高い充填率を得ることができない。また、体積比Vα/Vβが5.1より大きいと、粒子群βの小粒径粒子が不足して空隙ができ易く、また、体積比Vα/Vβが2.0よりも小さいと、粒子群βの小粒径粒子が過剰となり、これらの粒子が充填率の低下を招くと推測される。 FIG. 1 is an example of a particle size distribution showing a typical embodiment of the present invention. In FIG. 1, Vα / Vβ is 2.0 or more and 5.1 or less, and the voids formed between the large particle size particles of the particle group α are efficiently filled with the small particle size particles of the particle group β. It is possible to increase the filling rate of the soft magnetic particles in which the particle group α and the particle group β are combined. When the intensity ratio IC / IA is larger than 0.12 as shown in FIG. 2, particles having an intermediate size between the particle group α and the particle group β increase, so that a high filling rate cannot be obtained. Further, when the volume ratio Vα / Vβ is larger than 5.1, the small particle size particles of the particle group β are insufficient and voids are likely to be formed, and when the volume ratio Vα / Vβ is smaller than 2.0, the particle group It is presumed that the small particle size particles of β become excessive and these particles cause a decrease in the filling rate.

強度比IC/IAは0.008以上0.08以下がより好ましく、0.01以上0.06以下がさらに好ましい。強度比IC/IAが小さいと高い充填率が得られる傾向が見られるが0.003以下になると充填率の低下が見られる。 The intensity ratio IC / IA is more preferably 0.008 or more and 0.08 or less, and further preferably 0.01 or more and 0.06 or less. When the strength ratio IC / IA is small, a high filling rate tends to be obtained, but when it is 0.003 or less, a decrease in the filling rate is seen.

体積比Vα/Vβは2.5以上4.4以下が好ましく、3.0以上4.0以下がより好ましい。このような構成とすることで充填率が高く、特流重畳特性の悪化を抑えられる傾向が見られる。 The volume ratio Vα / Vβ is preferably 2.5 or more and 4.4 or less, and more preferably 3.0 or more and 4.0 or less. With such a configuration, the filling rate is high, and there is a tendency that deterioration of the special current superimposition characteristic can be suppressed.

粒子群αのピーク粒径PAは60μm以下であることが好ましく、ピーク粒径PAが大きくなると直流重畳特性が悪化する傾向が見られ、ピーク粒径PAが小さくなると透磁率が小さくなる傾向が見られる。透磁率と直流重畳特性の観点から、粒子群αのピーク粒径PAは10~60μmがより好ましく、15~60μmがさらに好ましい。粒子群αに用いる粉末のピーク粒径は、分級により粗粒と微粉を取り除いて粒度分布を調整することができる。 The peak particle size PA of the particle group α is preferably 60 μm or less, and the DC superimposition characteristic tends to deteriorate as the peak particle size PA increases, and the magnetic permeability tends to decrease as the peak particle size PA decreases. Be done. From the viewpoint of magnetic permeability and DC superimposition characteristics, the peak particle size PA of the particle group α is more preferably 10 to 60 μm, still more preferably 15 to 60 μm. The peak particle size of the powder used in the particle group α can be adjusted by removing coarse particles and fine powder by classification.

粒子群αの粒子は、水アトマイズ法やガスアトマイズ法などのアトマイズ法により作製された粒子を使用することができる。一般にガスアトマイズ法を用いる方、円形度の高い粒子が得られやすいが、水アトマイズ法を用いる場合であっても、噴霧条件などを適度に調整することによって円形度の高い粒子を得ることができる。 As the particles of the particle group α, particles produced by an atomizing method such as a water atomizing method or a gas atomizing method can be used. Generally, it is easier to obtain particles with a high circularity when the gas atomizing method is used, but even when the water atomizing method is used, particles with a high circularity can be obtained by appropriately adjusting the spraying conditions and the like.

粒子群αを構成する軟磁性金属粉末は、Fe又はFeを含有する金属(合金を含む)が好ましく、表面は絶縁材料で被覆されていることが好ましい。Feを含有する金属としては、Fe-B-Si-Cr系、Fe-Si-Cr系、Fe-Ni-Si-Co系、およびFe-Si-B-Nb-Cu系のアモルファス合金が挙げられる。また、絶縁被覆材料としては、リン酸塩ガラス、MgO、CaO及びZnOから選んだ1種又は2種以上含む化合物、並びに、ホウ酸を含む水溶液又は水分散液と混合ホウ素化合物、チタンアルコキシド類から形成された酸化チタン、ケイ素酸化物等、任意の被膜材料を選ぶことができる。 The soft magnetic metal powder constituting the particle group α is preferably Fe or a metal containing Fe (including an alloy), and the surface is preferably coated with an insulating material. Examples of the Fe-containing metal include Fe-B-Si-Cr-based, Fe-Si-Cr-based, Fe-Ni-Si-Co-based, and Fe-Si-B-Nb-Cu-based amorphous alloys. .. In addition, as the insulating coating material, a compound containing one or more kinds selected from phosphate glass, MgO, CaO and ZnO, an aqueous solution containing boric acid or an aqueous dispersion and a mixed boron compound, and titanium alkoxides are used. Any coating material such as formed titanium oxide and silicon oxide can be selected.

また、粒子群αを構成する軟磁性金属粉末は、複数の金属の粒子を混ぜて使用しても良い。例えば、Feからなる粒子とFe-B-Si-Cr系アモルファス合金からなる粒子の表面をホウ素化合物により絶縁被覆したものを混合して用いることができる。 Further, the soft magnetic metal powder constituting the particle group α may be used by mixing a plurality of metal particles. For example, particles made of Fe and particles made of Fe—B—Si—Cr-based amorphous alloy whose surface is insulated and coated with a boron compound can be mixed and used.

粒子群βのピーク粒径PBは、軟磁性金属粒子の充填率向上の観点から、0.5μm~5μmであることが好ましく、0.7μm~4μmがより好ましく、0.7μm~2μmがさらにより好ましい。粒子群βに用いる粉末のピーク粒径は、分級により粗粒と微粉を取り除いて粒度分布を調整することにより所望のピーク粒径とすることができる。 The peak particle size PB of the particle group β is preferably 0.5 μm to 5 μm, more preferably 0.7 μm to 4 μm, and even more preferably 0.7 μm to 2 μm from the viewpoint of improving the filling rate of the soft magnetic metal particles. preferable. The peak particle size of the powder used for the particle group β can be set to a desired peak particle size by removing coarse particles and fine powder by classification and adjusting the particle size distribution.

粒子群βの粒子は、粒子群αと同様に水アトマイズ法やガスアトマイズ法などのアトマイズ法により作製された粒子、また、カルボニル法により作製した数μmの粒子、噴霧熱分解法より作製したサブミクロンの粒子などを用いることができる。 The particles of the particle group β are particles produced by an atomization method such as a water atomization method or a gas atomization method, particles of several μm produced by the carbonyl method, and submicrons prepared by a spray pyrolysis method, as in the particle group α. Particles and the like can be used.

粒子群βを構成する軟磁性金属粉末は、Fe又はFeを含有する金属(合金を含む)を用いることができ、粒子群αと異なった組成でも良い。Feを含有する金属としては、例えばFe-Ni系合金が挙げられる。粒子群βも、前述の粒子群αと同様に表面は絶縁材料により被覆されている粒子を用いることができる。絶縁被覆材料としては、前述の材料等、任意の被膜材料を選ぶことができる。 As the soft magnetic metal powder constituting the particle group β, a metal (including an alloy) containing Fe or Fe can be used, and the composition may be different from that of the particle group α. Examples of the metal containing Fe include Fe—Ni based alloys. As for the particle group β, particles whose surface is covered with an insulating material can be used as in the case of the above-mentioned particle group α. As the insulating coating material, any coating material such as the above-mentioned material can be selected.

また、粒子群βを構成する軟磁性金属粉末は、前述の粒子群αと同様に複数の金属の粒子を混ぜて使用しても良い。 Further, the soft magnetic metal powder constituting the particle group β may be used by mixing a plurality of metal particles in the same manner as in the above-mentioned particle group α.

本実施形態の軟磁性材料は樹脂により軟磁性粒子間の絶縁性は保たれているが、軟磁性粒子自体の粒子表面に絶縁処理を施した紛末を使うことにより、更に高い絶縁性と良好な直流重畳特性を得ることができ、インダクタとして使用した場合にも更に好ましい絶縁性と耐圧性及び直流重畳特性を得ることができる。 In the soft magnetic material of the present embodiment, the insulating property between the soft magnetic particles is maintained by the resin, but by using the powder obtained by applying the insulating treatment to the particle surface of the soft magnetic particles themselves, the insulating property is further improved. Excellent DC superimposition characteristics can be obtained, and even more preferable insulating properties, withstand voltage and DC superimposition characteristics can be obtained when used as an inductor.

また、本実施形態の軟磁性材料は、粒子群αの粒子を65~83wt%、粒子群βの粒子を15~30wt%、樹脂を1.5~5wt%であることが好ましい。この構成とすることで、粒子群αの粒子と粒子群βの粒子の間を樹脂で埋めることができ、空隙を少なくすることができる。 Further, the soft magnetic material of the present embodiment preferably contains 65 to 83 wt% of particles of the particle group α, 15 to 30 wt% of particles of the particle group β, and 1.5 to 5 wt% of the resin. With this configuration, the space between the particles of the particle group α and the particles of the particle group β can be filled with the resin, and the voids can be reduced.

樹脂は、例えば、シリコーン樹脂、フェノール樹脂、アクリル樹脂及びエポキシ樹脂等の各種有機高分子樹脂が挙げられるが、これらに特に限定されない。これらは1種を単独で使用することができ、また、2種以上を組み合わせて用いることができる。さらに、必要に応じて、公知の硬化剤や架橋剤、潤滑剤等を配合してもよい。また、液状の樹脂や、有機溶剤に溶解した樹脂を使用しても良いが、液状のエポキシ樹脂が好ましい。 Examples of the resin include various organic polymer resins such as silicone resin, phenol resin, acrylic resin and epoxy resin, but the resin is not particularly limited thereto. One of these can be used alone, or two or more of them can be used in combination. Further, if necessary, a known curing agent, cross-linking agent, lubricant or the like may be blended. Further, a liquid resin or a resin dissolved in an organic solvent may be used, but a liquid epoxy resin is preferable.

他方、本実施形態の軟磁性材料は、印刷塗布等が可能なペーストとして使用することが好ましく、必要に応じて溶剤や分散剤等によりペーストの粘度調整をすることも可能である。 On the other hand, the soft magnetic material of the present embodiment is preferably used as a paste capable of printing and coating, and the viscosity of the paste can be adjusted with a solvent, a dispersant or the like, if necessary.

本実施形態のコアは、前述軟磁性材料を含有するペーストを任意の形状の型に充填し、熱硬化することで作製することができる。溶剤などの揮発成分を含有する場合は、半硬化状に乾燥させ、加圧した後、さらに熱硬化させ、作製することができる。なお、コアの作製において軟磁性金属粉末の粒度に変化は生じないため、コアの状態であっても、粒子群αおよび粒子群βは、前述の軟磁性材料における粒度分布を維持している。 The core of the present embodiment can be produced by filling a paste containing the above-mentioned soft magnetic material in a mold having an arbitrary shape and heat-curing it. When it contains a volatile component such as a solvent, it can be produced by drying it in a semi-cured state, pressurizing it, and then heat-curing it. Since the particle size of the soft magnetic metal powder does not change in the production of the core, the particle group α and the particle group β maintain the particle size distribution in the above-mentioned soft magnetic material even in the state of the core.

本実施形態のコアは薄膜インダクタ、積層インダクタ、巻線インダクタ等、種々のタイプのインダクタに使用することができる。その一例として、薄膜インダクタについての構成を示す。図5は薄膜インダクタ10の素子本体5における内部構造の概念図であり、図6は薄膜インダクタ10の外観の概念図である。図5の符号1は、樹脂、セラミック、フェライト等から任意に選ぶことができる材料を用いた基板であり、その上下面に、銀または銅で形成されたスパイラル状の内部導体2が形成され、上下面の導体は基板1に形成されたスルーホールにより接続されている。更に符号3は磁性層であり、本実施形態のコアである。図6の符号4は、符号2の内部電極と接続された外部電極となっており、銀の下地電極の表面にニッケル、更にその上に錫めっきが施されている。 The core of this embodiment can be used for various types of inductors such as thin film inductors, laminated inductors, and wound inductors. As an example, the configuration of a thin film inductor is shown. FIG. 5 is a conceptual diagram of the internal structure of the element body 5 of the thin film inductor 10, and FIG. 6 is a conceptual diagram of the appearance of the thin film inductor 10. Reference numeral 1 in FIG. 5 is a substrate using a material that can be arbitrarily selected from resin, ceramic, ferrite, and the like, and a spiral inner conductor 2 made of silver or copper is formed on the upper and lower surfaces thereof. The conductors on the upper and lower surfaces are connected by through holes formed in the substrate 1. Further, reference numeral 3 is a magnetic layer, which is the core of the present embodiment. Reference numeral 4 in FIG. 6 is an external electrode connected to the internal electrode of reference numeral 2, and the surface of the silver base electrode is nickel-plated and tin-plated on the surface.

次にインダクタの一例として薄膜インダクタの製造方法について説明する。 Next, a method for manufacturing a thin film inductor will be described as an example of the inductor.

樹脂基板の上下面にスパッタリング法、またはフォトリソグラフィー法によりスパイラル状の内部電極を形成する。更に本実施形態のペースト状の軟磁性材料を前記基板面に印刷して磁性層を形成し、150~200℃の温度で加熱硬化させて、スパイラル状の内部電極が複数形成された母基板を得る。この母基板には複数個の内部電極パターンが形成されており、スライサーによる切断工程を経て個々のチップに分割し、内部電極と外部電極が接続しやすいようにバレル研磨等をおこなう。こうして得られたチップを内部電極が露出した面を上にして固定し、スパッタ等の薄膜工程により外部電極を形成する。更に、外部電極表面にニッケルめっき、錫めっきを施す工程を経て薄膜インダクタを作製することができる。 A spiral internal electrode is formed on the upper and lower surfaces of the resin substrate by a sputtering method or a photolithography method. Further, the paste-like soft magnetic material of the present embodiment is printed on the substrate surface to form a magnetic layer, which is then heat-cured at a temperature of 150 to 200 ° C. to form a mother substrate on which a plurality of spiral-shaped internal electrodes are formed. obtain. A plurality of internal electrode patterns are formed on this mother substrate, and the chips are divided into individual chips through a cutting process using a slicer, and barrel polishing or the like is performed so that the internal electrodes and the external electrodes can be easily connected. The chip thus obtained is fixed with the surface where the internal electrode is exposed facing up, and the external electrode is formed by a thin film process such as sputtering. Further, the thin film inductor can be manufactured through the steps of nickel plating and tin plating on the surface of the external electrode.

以下、実施例及び比較例を挙げて、本発明を更に詳細に説明するが、本発明はこれらの実施例に限定されるものではない。 Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.

軟磁性金属粉末として、水アトマイズ法により作製された球状のFe-2.5mass%B-6.4mass%Si-2.1mass%Cr系アモルファス合金からなる、表面はリン酸塩ガラスで絶縁被覆された平均粒径D50がそれぞれ72.9μm(D10:27.8μm、D90:173μm)、56.4μm(D10:21.3μm、D90:134μm)、51.8μm(D10:19.7μm、D90:124μm)、49.0μm(D10:26.5μm、D90:87.2μm)、47.5μm(D10:17.9μm、D90:113μm)、21.8μm(D10:8.2μm、D90:52.1μm)、19.6μm(D10:9.4μm、D90:30.8μm)、9.1μm(D10:3.8μm、D90:21.6μm)、の粉末、カルボニル法により作製されたカルボニル鉄粉で平均粒径D50がそれぞれ3.2μm(D10:1.9μm、D90:5.1μm)、1.3μm(D10:0.7μm、D90:2.0μm)の粉末、噴霧熱分解法により作製された鉄粉で平均粒径D50が0.52μm(D10:0.30μm、D90:0.84μm)である粉末、を準備した。
なお、上記「Fe-2.5mass%B-6.4mass%Si-2.1mass%Cr」とは、全体を100mass%としたとき、Bが2.5mass%、Siが6.4mass%、Crが2.1mass%であり、残部がFeであることを表す。以下の実施例についても同様である。
(実施例1)
粒子群α、粒子群βとして平均粒径D50がそれぞれ9.1μm、0.52μmの粉末を重量比において35:10で配合し、表1のピーク粒径となる実施例1の軟磁性金属粉末を得た。次に、液状のエポキシ樹脂を2.5wt%を添加し、有機溶剤を加えて粘度調整を行いながら十分に混練して、実施例1のペースト状の軟磁性材料を得た。更に、ペースト状の軟磁性材料をトロイダル形状の溝が開いた金型に充填し、半硬化状に乾燥させて加圧した後、金型から取り出し、恒温槽内で更に熱硬化させ、外径15mm、内径9mm、厚さ0.7mmのトロイダル形状の実施例1のコアを得た。
As a soft magnetic metal powder, it is made of a spherical Fe-2.5 mass% B-6.4 mass% Si-2.1 mass% Cr-based amorphous alloy produced by a water atomization method, and its surface is insulated and coated with phosphate glass. The average particle size D50 is 72.9 μm (D10: 27.8 μm, D90: 173 μm), 56.4 μm (D10: 21.3 μm, D90: 134 μm), 51.8 μm (D10: 19.7 μm, D90: 124 μm, respectively). ), 49.0 μm (D10: 26.5 μm, D90: 87.2 μm), 47.5 μm (D10: 17.9 μm, D90: 113 μm), 21.8 μm (D10: 8.2 μm, D90: 52.1 μm) , 19.6 μm (D10: 9.4 μm, D90: 30.8 μm), 9.1 μm (D10: 3.8 μm, D90: 21.6 μm), average grain size of carbonyl iron powder prepared by the carbonyl method. Powder with a diameter D50 of 3.2 μm (D10: 1.9 μm, D90: 5.1 μm) and 1.3 μm (D10: 0.7 μm, D90: 2.0 μm), respectively, and iron powder produced by the spray thermal decomposition method. A powder having an average particle size D50 of 0.52 μm (D10: 0.30 μm, D90: 0.84 μm) was prepared.
The above "Fe-2.5 mass% B-6.4 mass% Si-2.1 mass% Cr" means that B is 2.5 mass%, Si is 6.4 mass%, and Cr is 100 mass% as a whole. Is 2.1 mass%, indicating that the balance is Fe. The same applies to the following examples.
(Example 1)
The soft magnetic metal powder of Example 1 in which powders having an average particle size D50 of 9.1 μm and 0.52 μm as particle group α and particle group β, respectively, are blended at a weight ratio of 35:10 to obtain the peak particle size in Table 1. Got Next, 2.5 wt% of a liquid epoxy resin was added, an organic solvent was added, and the mixture was sufficiently kneaded while adjusting the viscosity to obtain a paste-like soft magnetic material of Example 1. Further, a paste-like soft magnetic material is filled in a mold having a toroidal-shaped groove, dried in a semi-cured state and pressed, then taken out from the mold and further thermoset in a constant temperature bath to have an outer diameter. A toroidal-shaped core of Example 1 having a thickness of 15 mm, an inner diameter of 9 mm, and a thickness of 0.7 mm was obtained.

(実施例2~4)
粒子群α、粒子群βとして平均粒径D50がそれぞれ21.8μm、1.3μmの粉末を重量比において、それぞれ30:10、40:10、23:10で配合すること以外は実施例1と同様の条件で実施例2、3、及び4の軟磁性粉末、軟磁性材料、及びコアを得た。
(Examples 2 to 4)
Example 1 except that powders having an average particle size D50 of 21.8 μm and 1.3 μm as the particle group α and the particle group β are blended in weight ratios of 30:10, 40:10, and 23:10, respectively. Under the same conditions, the soft magnetic powders, soft magnetic materials, and cores of Examples 2, 3 and 4 were obtained.

(実施例5~7、9、比較例4、5)
粒子群α、粒子群βとして平均粒径D50がそれぞれ47.5μm、1.3μmの粉末を重量比においてそれぞれ27:10、35:10、45:10、20:10、50:10、15:10で配合すること以外は実施例1と同様の条件で実施例5、6、7、9、及び比較例4、5の軟磁性粉末、軟磁性材料、及びコアを得た。
(Examples 5 to 7, 9, Comparative Examples 4, 5)
As the particle group α and the particle group β, powders having an average particle size D50 of 47.5 μm and 1.3 μm, respectively, in weight ratios of 27:10, 35:10, 45:10, 20:10, 50:10, 15 :, respectively. The soft magnetic powders, soft magnetic materials, and cores of Examples 5, 6, 7, 9 and Comparative Examples 4 and 5 were obtained under the same conditions as in Example 1 except that they were blended in 10.

(実施例8)
粒子群α、粒子群βとして平均粒径D50がそれぞれ47.5μm、3.2μmの粉末を重量比において40:10で配合すること以外は実施例1と同様の条件で実施例8の軟磁性粉末、軟磁性材料、及びコアを得た。
(Example 8)
The soft magnetism of Example 8 under the same conditions as in Example 1 except that powders having an average particle size D50 of 47.5 μm and 3.2 μm as the particle group α and the particle group β are mixed at a weight ratio of 40:10, respectively. Powders, soft magnetic materials, and cores were obtained.

(実施例10)
粒子群α、粒子群βとして平均粒径D50がそれぞれ51.8μm、1.3μmの粉末を重量比において33:10で配合すること以外は実施例1と同様の条件で実施例10の軟磁性粉末、軟磁性材料、及びコアを得た。
(Example 10)
The soft magnetism of Example 10 under the same conditions as in Example 1 except that powders having an average particle size D50 of 51.8 μm and 1.3 μm, respectively, were blended as the particle group α and the particle group β at a weight ratio of 33:10. Powders, soft magnetic materials, and cores were obtained.

(実施例11)
粒子群α、粒子群βとして平均粒径D50がそれぞれ56.4μm、1.3μmの粉末を重量比において33:10で配合すること以外は実施例1と同様の条件で実施例11の軟磁性粉末、軟磁性材料、及びコアを得た。
(Example 11)
The soft magnetism of Example 11 under the same conditions as in Example 1 except that powders having an average particle size D50 of 56.4 μm and 1.3 μm as the particle group α and the particle group β are mixed at a weight ratio of 33:10, respectively. Powders, soft magnetic materials, and cores were obtained.

(実施例12)
粒子群α、粒子群βとして平均粒径D50がそれぞれ72.9μm、1.3μmの粉末を重量比において40:10で配合すること以外は実施例1と同様の条件で実施例12の軟磁性粉末、軟磁性材料、及びコアを得た。
(Example 12)
The soft magnetism of Example 12 under the same conditions as in Example 1 except that powders having an average particle size D50 of 72.9 μm and 1.3 μm as the particle group α and the particle group β were mixed at a weight ratio of 40:10, respectively. Powders, soft magnetic materials, and cores were obtained.

(実施例13、15)
粒子群α、粒子群βとして平均粒径D50がそれぞれ49.0μm、19.6μm、1.3μm、0.52μmの粉末を重量比においてそれぞれ27:33:12:8、33:327:12:8で配合すること以外は実施例1と同様の条件で実施例13、15の軟磁性粉末、軟磁性材料、及びコアを得た。
(Examples 13 and 15)
Powders having an average particle size D50 of 49.0 μm, 19.6 μm, 1.3 μm, and 0.52 μm as the particle group α and the particle group β, respectively, in weight ratios of 27: 33: 12: 8, 33: 327: 12 :, respectively. The soft magnetic powder, soft magnetic material, and core of Examples 13 and 15 were obtained under the same conditions as in Example 1 except that they were blended in 8.

(実施例14、比較例1)
粒子群α、粒子群βとして平均粒径D50が49.0μm、19.6μm、3.2μm、1.3μmの粉末を重量比において28:30:12:8、27:33:12:8で配合すること以外は実施例14と同様の条件で実施例13、及び比較例1の軟磁性粉末、軟磁性材料、及びコアを得た。
(Example 14, Comparative Example 1)
Powders having an average particle size D50 of 49.0 μm, 19.6 μm, 3.2 μm, and 1.3 μm as the particle group α and the particle group β at 28:30:12: 8, 27:33:12: 8 in weight ratio. The soft magnetic powder, soft magnetic material, and core of Example 13 and Comparative Example 1 were obtained under the same conditions as in Example 14 except that they were blended.

(比較例2)
軟磁性金属粉末として平均粒径D50が1.3μmの粉末のみ用いること以外は実施例1と同様の条件で比較例2の軟磁性材料、及びコアを得た。
(Comparative Example 2)
The soft magnetic material and core of Comparative Example 2 were obtained under the same conditions as in Example 1 except that only the powder having an average particle size D50 of 1.3 μm was used as the soft magnetic metal powder.

(比較例3)
軟磁性金属粉末として平均粒径D50が47.5μmの粉末のみを用いること以外は実施例1と同様の条件で比較例3の軟磁性材料、及びコアを得た。
(Comparative Example 3)
The soft magnetic material and core of Comparative Example 3 were obtained under the same conditions as in Example 1 except that only a powder having an average particle size D50 of 47.5 μm was used as the soft magnetic metal powder.

(実施例16)
以下に示す以外は、実施例1と同様の条件で実施例16の軟磁性金属粉末、軟磁性材料、及びコアを得た。すなわち、実施例16では、粒子群αとして水アトマイズ法により作製された球状のFe-2.5mass%B-6.4mass%Si-2.1mass%Cr系アモルファス合金からなる平均粒径D50が45.2μm(D10:16.9μm、D90:114.0μm)の粉末、粒子群βとしてカルボニル法により作製されたカルボニル鉄粉で平均粒径D50が1.3μm(D10:0.7μm、D90:2.0μm)の粉末を準備し、粒子群αと粒子群βとを重量比において40:10で配合した。
(Example 16)
Except for the following, the soft magnetic metal powder, soft magnetic material, and core of Example 16 were obtained under the same conditions as in Example 1. That is, in Example 16, the average particle size D50 made of a spherical Fe-2.5 mass% B-6.4 mass% Si-2.1 mass% Cr-based amorphous alloy produced by the water atomization method as the particle group α is 45. .2 μm (D10: 16.9 μm, D90: 114.0 μm) powder, carbonyl iron powder prepared by the carbonyl method as the particle group β, with an average particle size D50 of 1.3 μm (D10: 0.7 μm, D90: 2). A powder of .0 μm) was prepared, and the particle group α and the particle group β were mixed at a weight ratio of 40:10.

(実施例17)
粒子群αとして水アトマイズ法により作製された球状のFe-2.5mass%B-6.4mass%Si-2.1mass%Cr系アモルファス合金からなる、表面はシリカで絶縁被覆された平均粒径D50が23.6μm(D10:8.8μm、D90:57.0μm)の粉末を用いる以外は、実施例16と同様の条件で実施例17の軟磁性金属粉末、軟磁性材料、及びコアを得た。
(Example 17)
The surface is made of a spherical Fe-2.5 mass% B-6.4 mass% Si-2.1 mass% Cr-based amorphous alloy produced by the water atomization method as the particle group α, and the surface is insulated and coated with silica. The soft magnetic metal powder, soft magnetic material, and core of Example 17 were obtained under the same conditions as in Example 16 except that the powder of 23.6 μm (D10: 8.8 μm, D90: 57.0 μm) was used. ..

(実施例18)
粒子群αとして水アトマイズ法により作製された球状のFe-6.5mass%Si-2.5mass%Cr系アモルファス合金からなる、表面はリン酸塩ガラスで絶縁被覆された平均粒径D50が43.6μm(D10:16.2μm、D90:79.2μm)の粉末を用いる以外は、実施例16と同様の条件で実施例18の軟磁性金属粉末、軟磁性材料、及びコアを得た。
(Example 18)
The surface is made of a spherical Fe-6.5 mass% Si-2.5 mass% Cr-based amorphous alloy produced by the water atomization method as the particle group α, and the surface is insulated and coated with phosphate glass. The average particle size D50 is 43. The soft magnetic metal powder, soft magnetic material, and core of Example 18 were obtained under the same conditions as in Example 16 except that a powder of 6 μm (D10: 16.2 μm, D90: 79.2 μm) was used.

(実施例19)
粒子群αとして水アトマイズ法により作製された球状のFe-44mass%Ni-2.1mass%Si-4.5mass%Co系アモルファス合金からなる、表面はリン酸塩ガラスで絶縁被覆された平均粒径D50が23.0μm(D10:8.1μm、D90:56.7μm)の粉末を用いる以外は、実施例16と同様の条件で実施例19の軟磁性金属粉末、軟磁性材料、及びコアを得た。
(Example 19)
The surface is made of a spherical Fe-44 mass% Ni-2.1 mass% Si-4.5 mass% Co-based amorphous alloy produced by the water atomization method as the particle group α, and the surface is insulated and coated with phosphate glass. The soft magnetic metal powder, soft magnetic material, and core of Example 19 were obtained under the same conditions as in Example 16 except that the powder having a D50 of 23.0 μm (D10: 8.1 μm, D90: 56.7 μm) was used. rice field.

(実施例20)
以下に示す以外は、実施例16と同様の条件で実施例20の軟磁性金属粉末、軟磁性材料、及びコアを得た。すなわち、実施例20では、粒子群αとして水アトマイズ法により作製された球状のFe-13.0mass%Si-9.0mass%B-3.0mass%Nb-1.0mass%Cu系アモルファス合金からなる、表面はリン酸塩ガラスで絶縁被覆された平均粒径D50が21.8μm(D10:8.0μm、D90:51.9μm)の粉末を用いて、粒子群αと粒子群βとを重量比において35:10で配合した。
(Example 20)
Except for the following, the soft magnetic metal powder, soft magnetic material, and core of Example 20 were obtained under the same conditions as in Example 16. That is, in Example 20, it is made of a spherical Fe-13.0 mass% Si-9.0 mass% B-3.0 mass% Nb-1.0 mass% Cu-based amorphous alloy produced by the water atomization method as the particle group α. The surface is insulated and coated with phosphate glass, and a powder having an average particle size of D50 of 21.8 μm (D10: 8.0 μm, D90: 51.9 μm) is used, and the particle group α and the particle group β are weight-ratio. At 35:10.

(実施例21)
以下に示す以外は、実施例16と同様の条件で実施例21の軟磁性金属粉末、軟磁性材料、及びコアを得た。すなわち、実施例21では、粒子群αとして水アトマイズ法により作製された球状のFe-2.5mass%B-6.4mass%Si-2.1mass%Cr系アモルファス合金からなる、表面はリン酸塩ガラスで絶縁被覆された平均粒径D50が47.5μm(D10:17.9μm、D90:113μm)の粉末、粒子群βとしてカルボニル法により作製されたカルボニル鉄粉からなる、表面はシリカで絶縁被覆された平均粒径D50が1.3μm(D10:0.8μm、D90:2.2μm)の粉末を準備し、粒子群αと粒子群βとを重量比において30:10で配合した。
(Example 21)
Except for the following, the soft magnetic metal powder, soft magnetic material, and core of Example 21 were obtained under the same conditions as in Example 16. That is, in Example 21, the surface is made of a spherical Fe-2.5 mass% B-6.4 mass% Si-2.1 mass% Cr-based amorphous alloy produced by the water atomization method as the particle group α, and the surface is a phosphate. The surface is insulated with silica, consisting of a powder having an average particle size D50 of 47.5 μm (D10: 17.9 μm, D90: 113 μm) insulated and coated with glass, and carbonyl iron powder prepared by the carbonyl method as the particle group β. A powder having an average particle size D50 of 1.3 μm (D10: 0.8 μm, D90: 2.2 μm) was prepared, and the particle group α and the particle group β were blended at a weight ratio of 30:10.

(実施例22)
粒子群βとして噴霧熱分解法により作製されたFe-50mass%Ni系合金からなる、表面はシリカで絶縁被覆された平均粒径D50が0.8μm(D10:0.5μm、D90:1.3μm)の粉末を用いる以外は、実施例21と同様の条件で実施例22の軟磁性金属粉末、軟磁性材料、及びコアを得た。
(Example 22)
The average particle size D50, which is made of Fe-50mass% Ni-based alloy produced by the spray thermal decomposition method as the particle group β and whose surface is insulated and coated with silica, is 0.8 μm (D10: 0.5 μm, D90: 1.3 μm). ) Was used, and the soft magnetic metal powder, soft magnetic material, and core of Example 22 were obtained under the same conditions as in Example 21.

(実施例23)
粒子群αとして水アトマイズ法により作製された球状のFeからなる、平均粒径D50が38.2μm(D10:9.4μm、D90:92.5μm)の粉末を用いる以外は、実施例16と同様の条件で実施例23の軟磁性金属粉末、軟磁性材料、及びコアを得た。
(Example 23)
Same as Example 16 except that a powder having an average particle size D50 of 38.2 μm (D10: 9.4 μm, D90: 92.5 μm) composed of spherical Fe produced by the water atomization method is used as the particle group α. The soft magnetic metal powder, soft magnetic material, and core of Example 23 were obtained under the conditions of.

粒度分布測定方法、軟磁性金粉末の充填率、及びトロイダル形状のコアの透磁率と直流重畳特性の測定条件は以下の通りである。 The measurement conditions for the particle size distribution measurement method, the filling rate of the soft magnetic gold powder, the magnetic permeability of the toroidal-shaped core, and the DC superimposition characteristics are as follows.

(粒度分布測定)
水と粉末、分散剤を入れ、ホモジナイザー(日本精機社製)で分散し、湿式レーザー回折粒子径分布測定機(日機装社製Microtrac MT3300EXII)により求めた体積基準の粒度分布よりピークA1、A2、・・・、Ax(xは1以上)、B1、B2、・・・、By(yは1以上)、及び点Cを判定した。そのピークと点からピーク粒径PA1、PA2、・・・、PAx(xは1以上)、PB1、PB2、・・・、PBy(yは1以上)とピーク強度(頻度)IA1、IA2、・・・、IAx(xは1以上)、IB1、IB2、・・・、IBy(yは1以上)、及び点Cの粒径PC、強度(頻度)ICを算出した。また、その体積基準の粒度分布において、PCより大粒径側を粒子群α、小粒径側を粒子群βとし、粒子群αの体積Vα及び粒子群βの体積Vβを算出した。
なお、得られた軟磁性材料およびコアに含まれる軟磁性金属粉末について同様に粒度分布測定を行ったところ、軟磁性材料およびコアに用いる前の軟磁性金属粉末と同様の粒度分布が得られた。
(Measurement of particle size distribution)
Add water, powder, and dispersant, disperse with a homogenizer (manufactured by Nippon Seiki Co., Ltd.), and peak A1, A2, ... ..., Ax (x is 1 or more), B1, B2, ..., By (y is 1 or more), and point C were determined. From the peaks and points, peak particle sizes PA1, PA2, ..., PAx (x is 1 or more), PB1, PB2, ..., PBy (y is 1 or more) and peak intensities (frequency) IA1, IA2 ,. ..., IAx (x is 1 or more), IB1, IB2, ..., IBy (y is 1 or more), particle size PC at point C, and intensity (frequency) IC were calculated. Further, in the volume-based particle size distribution, the volume Vα of the particle group α and the volume Vβ of the particle group β were calculated by setting the particle group α on the large particle size side and the particle group β on the small particle size side from the PC.
When the particle size distribution of the obtained soft magnetic material and the soft magnetic metal powder contained in the core was measured in the same manner, the same particle size distribution as that of the soft magnetic metal powder before being used for the soft magnetic material and the core was obtained. ..

(軟磁性金属粉末の充填率)
トロイダル形状のコアを用いてアルキメデス法により密度を測定し、各種材料の比重から求めた。
(Filling rate of soft magnetic metal powder)
The density was measured by the Archimedes method using a toroidal-shaped core, and was determined from the specific gravity of various materials.

(透磁率の測定条件)
トロイダル形状のコアのサイズ:外径:15mm×内径:9mm×厚み:0.7mm
測定器:E4991A(Agilent社製) RFインピーダンス/マテリアル・アナライザ
測定周波数:3MHz
(Measurement conditions for magnetic permeability)
Toroidal core size: outer diameter: 15 mm x inner diameter: 9 mm x thickness: 0.7 mm
Measuring instrument: E4991A (manufactured by Agilent) RF impedance / material analyzer Measurement frequency: 3MHz

(直流重畳特性の測定条件)
トロイダル形状のコアのサイズ:外径:15mm×内径:9mm×厚み:0.7mm
巻線数:30回
測定器:4284A(Agilent社製)プレシジョンLCRメータ
高周波信号の周波数:100kHz
直流重畳特性は、直流バイアス電流を0Aから10Aとした時のインダクタンス値の低下率により評価した。
(Measurement conditions for DC superimposition characteristics)
Toroidal core size: outer diameter: 15 mm x inner diameter: 9 mm x thickness: 0.7 mm
Number of windings: 30 times Measuring instrument: 4284A (manufactured by Agilent) Precision LCR meter Frequency of high frequency signal: 100kHz
The DC superimposition characteristic was evaluated by the rate of decrease in the inductance value when the DC bias current was changed from 0 A to 10 A.

表1に粒度分布測定より算出した粒子群α、βのピーク粒径PA1、PA2、PB1、PB2、ピーク強度IA、IB、最小値の強度IC、強度比IC/IA、体積比Vα/Vβ、トロイダル形状のコアより測定した軟磁性粉末の充填率、透磁率、及びインダクタンス低下率の結果を示す。 Table 1 shows the peak particle sizes PA1, PA2, PB1, PB2, peak intensity IA, IB, minimum intensity IC, intensity ratio IC / IA, and volume ratio Vα / Vβ of the particle groups α and β calculated from the particle size distribution measurement. The results of the filling rate, the magnetic permeability, and the inductance reduction rate of the soft magnetic powder measured from the toroidal-shaped core are shown.

Figure 0007059594000001
Figure 0007059594000001

表1の実施例1~23は、何れの試料も粒子群αと粒子群βの間で、強度比IC/IAが0.12以下、体積比Vα/Vβが2.0以上5.1以下の条件を満たしており、透磁率は30を超えた高い値を示した。 In Examples 1 to 23 of Table 1, the intensity ratio IC / IA is 0.12 or less and the volume ratio Vα / Vβ is 2.0 or more and 5.1 or less between the particle group α and the particle group β in each sample. The above condition was satisfied, and the magnetic permeability showed a high value exceeding 30.

表1によれば、比較例1、4、5は粒子群αと粒子群βの間で、強度比IC/IAが0.12以下、体積比Vα/Vβが2.0以上5.1以下の条件を満たしておらず、軟磁性金属粉末の充填率は低く、透磁率も30未満であった。特に、比較例2、3のように、粒子群αしか持たない単一粒度分布の試料ではトロイダルコアにした時の軟磁性金属粉末の充填率は70vol%を超えることができず、3MHz時における透磁率も20以下となっていた。 According to Table 1, in Comparative Examples 1, 4 and 5, the intensity ratio IC / IA is 0.12 or less and the volume ratio Vα / Vβ is 2.0 or more and 5.1 or less between the particle group α and the particle group β. The filling rate of the soft magnetic metal powder was low, and the magnetic permeability was less than 30. In particular, in a sample having a single particle size distribution having only a particle group α as in Comparative Examples 2 and 3, the filling rate of the soft magnetic metal powder when made into a toroidal core cannot exceed 70 vol%, and at 3 MHz. The magnetic permeability was also 20 or less.

実施例2、5、6、13、15、20、21は、強度比IC/IAが0.01以上0.06以下、体積比Vα/Vβが3.0以上4.0以下であり、充填率は81vol%を超え、透磁率も39を超える高い値を示し、特流重畳特性も良好であり、インダクタンス低下率は33%以下となった。 In Examples 2, 5, 6, 13, 15, 20, and 21, the intensity ratio IC / IA is 0.01 or more and 0.06 or less, the volume ratio Vα / Vβ is 3.0 or more and 4.0 or less, and the filling is performed. The ratio exceeded 81 vol%, the magnetic permeability also showed a high value exceeding 39, the special current superimposition characteristic was good, and the inductance reduction rate was 33% or less.

粒子群αのピークの粒径PAが60μmを超える実施例11、12では、表1に示すように比透磁率は比較的高い値を示すものの、インダクタンスの低下率が40%を超えており、直流重畳特性の悪化が目立ち始める。しかしながら、粒子群αのピーク粒径PAが60μm以下であれば比較的良好な直流重畳特性となった。直流重畳特性の悪化の原因は、試料中の組織の不均一性に因るところが大きいものと推察される。なぜなら、粒子群αのピーク粒径PAが大きくなると、試料内にできる空隙も大きくなる傾向を示しており、樹脂部や空隙部の分布状態が偏析し易い組織状態となっていると推察されるからである。 In Examples 11 and 12 in which the particle size PA of the peak of the particle group α exceeds 60 μm, the relative permeability shows a relatively high value as shown in Table 1, but the rate of decrease in inductance exceeds 40%. Deterioration of DC superimposition characteristics begins to be noticeable. However, when the peak particle size PA of the particle group α was 60 μm or less, relatively good DC superimposition characteristics were obtained. It is presumed that the cause of the deterioration of the DC superimposition characteristic is largely due to the non-uniformity of the structure in the sample. This is because, as the peak particle size PA of the particle group α increases, the voids formed in the sample also tend to increase, and it is presumed that the distribution state of the resin portion and the void portion is in a textured state in which segregation is likely to occur. Because.

尚、表1に示した軟磁性材料の代表的な試料について、その試料の粒度分布図を図1~4に示した。 For the representative samples of the soft magnetic materials shown in Table 1, the particle size distribution maps of the samples are shown in FIGS. 1 to 4.

図1は実施例5の粒度分布(頻度分布)を示す図である。粒子群αは比較的ブロードな粒度分布を持っているが、粒子群αのピーク粒径PA(52.3μm)と粒子群βのピーク粒径PB(1.3μm)が離れているので、粒子群αと粒子群βの間に存在する最小値の強度ICは小さくなり、この時の軟磁性金属粉末の充填率は82.6vol%と高くなり、透磁率も41.4と高い値を示した。 FIG. 1 is a diagram showing a particle size distribution (frequency distribution) of Example 5. The particle group α has a relatively broad particle size distribution, but since the peak particle size PA (52.3 μm) of the particle group α and the peak particle size PB (1.3 μm) of the particle group β are separated, the particles The minimum intensity IC existing between the group α and the particle group β becomes small, the filling rate of the soft magnetic metal powder at this time becomes as high as 82.6 vol%, and the magnetic permeability also shows a high value of 41.4. rice field.

図2は実施例15の粒度分布(頻度分布)を示す図である。粒子群αはピークを2つ持つ比較的ブロードな粒度分布を持っているが、粒子群αのピーク粒径PA(52.3μm)と粒子群βのピーク粒径PB(1.3μm)が離れているので、粒子群αと粒子群βの間に存在する最小値の強度ICは小さくなり、この時の軟磁性金属粉末の充填率は81.8vol%と高くなり、透磁率も40.1と高い値を示した。 FIG. 2 is a diagram showing a particle size distribution (frequency distribution) of Example 15. The particle group α has a relatively broad particle size distribution having two peaks, but the peak particle size PA (52.3 μm) of the particle group α and the peak particle size PB (1.3 μm) of the particle group β are separated. Therefore, the minimum intensity IC existing between the particle group α and the particle group β becomes small, the filling rate of the soft magnetic metal powder at this time becomes as high as 81.8 vol%, and the magnetic permeability is also 40.1. Showed a high value.

図3は比較例1の粒度分布(頻度分布)を示す図である。粒子群αはピークを2つ持つブロードな粒度分布を持っておりピーク粒径PAも18.5μmと小さい。このため、粒子群βのピーク粒径PBは3.3μmと比較的小さな軟磁性金属粉末を使用しているが粒子群αと粒子群βは接近しており、粒子群αと粒子群βの間に存在する最小値の強度ICは大きくなり強度比IC/IAが0.12を超えた。この時の軟磁性金属粉末の充填率は74.7vol%と実施例よりも低くなり、透磁率も23.2と低い値であった。 FIG. 3 is a diagram showing a particle size distribution (frequency distribution) of Comparative Example 1. The particle group α has a broad particle size distribution having two peaks, and the peak particle size PA is as small as 18.5 μm. Therefore, although the peak particle size PB of the particle group β is 3.3 μm, which is a relatively small soft magnetic metal powder, the particle group α and the particle group β are close to each other, and the particle group α and the particle group β The minimum intensity IC existing between them became large and the intensity ratio IC / IA exceeded 0.12. At this time, the filling rate of the soft magnetic metal powder was 74.7 vol%, which was lower than that of the examples, and the magnetic permeability was also a low value of 23.2.

図4は比較例3の粒度分布(頻度分布)を示す図である。粒子群αのみで最小値の強度ICを持たず、この時の軟磁性金属粉末の充填率は68.8vol%と実施例よりも低くなり、透磁率も19.5と低い値であった。 FIG. 4 is a diagram showing a particle size distribution (frequency distribution) of Comparative Example 3. Only the particle group α did not have the minimum strength IC, and the filling rate of the soft magnetic metal powder at this time was 68.8 vol%, which was lower than that of the examples, and the magnetic permeability was also a low value of 19.5.

本発明の軟磁性材料は、高い透磁率を有し直流重畳特性にも優れているため、インダクタ、各種トランス等の電気・磁気デバイス、及びそれらを備える各種機器、設備、システム等に幅広く利用可能である。 Since the soft magnetic material of the present invention has high magnetic permeability and excellent DC superimposition characteristics, it can be widely used for electric / magnetic devices such as inductors and various transformers, and various devices, equipments, systems, etc. equipped with them. Is.

1 基板
2 内部導体
3 磁性層
4 外部電極
5 素子本体
10 薄膜インダクタ
1 Substrate 2 Internal conductor 3 Magnetic layer 4 External electrode 5 Element body 10 Thin film inductor

Claims (5)

軟磁性金属粉末と樹脂とを含む軟磁性材料であって、
レーザー回折・散乱法での測定によって求めた体積基準の粒度分布において、
前記軟磁性金属粉末は、粒子群αと粒子群βで構成され、粒子群αのピーク強度をIA、粒子群αの体積をVα、粒子群βのピーク強度をIB、粒子群βの体積をVβ、粒子群αと粒子群βの間に存在する最小値の強度をICとしたときに、強度比IC/IAが0.12以下、体積比Vα/Vβが2.5以上5.1以下となり、
前記軟磁性金属粉末の粒度分布において、粒子群αは最大のピーク強度を含む粒子群であり、粒子群αのピーク粒径PAは粒子群βのピーク粒径PBよりも大きく、
粒子群βのピーク粒径PBは0.5~5μmであり、
粒子群αのピーク強度を大きい順にIA1、IA2、・・・、IAx(xは1以上)としたとき、粒子群αのピーク強度IAをIA1とし、粒子群αのピーク粒径PAをPA1とし、
粒子群βのピーク強度を大きい順にIB1、IB2、・・・、IBy(yは1以上)としたとき、粒子群βのピーク強度IBをIB1とし、粒子群βのピーク粒径PBをPB1とすることを特徴とする軟磁性材料。
A soft magnetic material containing soft magnetic metal powder and resin.
In the volume-based particle size distribution obtained by measurement by the laser diffraction / scattering method,
The soft magnetic metal powder is composed of a particle group α and a particle group β, the peak intensity of the particle group α is IA, the volume of the particle group α is Vα, the peak intensity of the particle group β is IB, and the volume of the particle group β. When the minimum intensity existing between Vβ, the particle group α and the particle group β is taken as IC, the intensity ratio IC / IA is 0.12 or less, and the volume ratio Vα / Vβ is 2.5 or more and 5.1 or less. Next,
In the particle size distribution of the soft magnetic metal powder, the particle group α is a particle group containing the maximum peak intensity, and the peak particle size PA of the particle group α is larger than the peak particle size PB of the particle group β.
The peak particle size PB of the particle group β is 0.5 to 5 μm, and the peak particle size PB is 0.5 to 5 μm.
When the peak intensities of the particle group α are IA1, IA2, ..., IAx (x is 1 or more) in descending order, the peak intensity IA of the particle group α is IA1 and the peak particle size PA of the particle group α is PA1. ,
When the peak intensities of the particle group β are IB1, IB2, ..., IBy (y is 1 or more) in descending order, the peak intensity IB of the particle group β is IB1 and the peak particle size PB of the particle group β is PB1. A soft magnetic material characterized by
前記粒子群αのピーク粒径PAが60μm以下であることを特徴とする請求項1に記載の軟磁性材料。 The soft magnetic material according to claim 1, wherein the peak particle size PA of the particle group α is 60 μm or less. 前記粒子群αを構成する軟磁性金属粉末は、Fe又はFeを含有する金属であり、絶縁材料で被覆されていることを特徴とする請求項1又は請求項2に記載の軟磁性材料。 The soft magnetic material according to claim 1 or 2, wherein the soft magnetic metal powder constituting the particle group α is a metal containing Fe or Fe and is coated with an insulating material. 請求項1~3のいずれかに記載の軟磁性材料により作製されていることを特徴とするコア。 A core made of the soft magnetic material according to any one of claims 1 to 3. 請求項4に記載のコアを備えていることを特徴とするインダクタ。
An inductor comprising the core according to claim 4.
JP2017229182A 2017-01-12 2017-11-29 Soft magnetic materials, cores and inductors Active JP7059594B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US15/868,363 US10573442B2 (en) 2017-01-12 2018-01-11 Soft magnetic material, core, and inductor
CN201810026596.0A CN108364767B (en) 2017-01-12 2018-01-11 Soft magnetic material, magnetic core, and inductor

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017003007 2017-01-12
JP2017003007 2017-01-12

Publications (2)

Publication Number Publication Date
JP2018113436A JP2018113436A (en) 2018-07-19
JP7059594B2 true JP7059594B2 (en) 2022-04-26

Family

ID=62912448

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017229182A Active JP7059594B2 (en) 2017-01-12 2017-11-29 Soft magnetic materials, cores and inductors

Country Status (2)

Country Link
JP (1) JP7059594B2 (en)
CN (1) CN108364767B (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7211727B2 (en) * 2018-07-20 2023-01-24 古河電子株式会社 LIQUID COMPOSITION FOR CASTING, METHOD FOR PRODUCING MOLDED PRODUCT, AND MOLDED PRODUCT
WO2020090405A1 (en) * 2018-10-30 2020-05-07 アルプスアルパイン株式会社 Powder compression-molded core, method for producing powder compression-molded core, inductor having powder compression-molded core, and electronic/electrical device having said inductor
JP7119979B2 (en) * 2018-12-20 2022-08-17 Tdk株式会社 Composite magnetic material and magnetic core
JP7300288B2 (en) * 2019-03-22 2023-06-29 日本特殊陶業株式会社 dust core
JP2021021097A (en) * 2019-07-25 2021-02-18 Tdk株式会社 Composite magnetic powder, powder magnetic core using the same, and manufacturing method for composite magnetic powder
WO2021066089A1 (en) * 2019-10-04 2021-04-08 住友ベークライト株式会社 Resin composition and molded article
CN111081466A (en) * 2019-12-13 2020-04-28 浙江工业大学 Amorphous nanocrystalline soft magnetic composite material and preparation method and application thereof
CN111151740B (en) * 2020-01-21 2022-03-18 柯昕 Manufacturing method of integrally formed inductor
JPWO2021157274A1 (en) * 2020-02-05 2021-08-12
JP7192826B2 (en) * 2020-05-01 2022-12-20 株式会社村田製作所 Magnetic cores for inductors and inductors
JP2022057927A (en) * 2020-09-30 2022-04-11 株式会社村田製作所 Magnetic powder, magnetic molding body, and inductor
JP7563087B2 (en) 2020-09-30 2024-10-08 株式会社村田製作所 Magnetic compact and inductor
JPWO2022138734A1 (en) * 2020-12-25 2022-06-30
TWI841957B (en) * 2021-04-28 2024-05-11 乾坤科技股份有限公司 Electrical component and the method to make the same
JP2023123169A (en) * 2022-02-24 2023-09-05 味の素株式会社 resin composition
CN114464388A (en) * 2022-03-07 2022-05-10 北京科技大学 Iron-based amorphous composite magnetic powder core and preparation method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000294418A (en) 1999-04-09 2000-10-20 Hitachi Ferrite Electronics Ltd Powder molded magnetic core
JP2008081779A (en) 2006-09-27 2008-04-10 Hitachi Metals Ltd Powder of coated metal particulate and magnetic bead
JP2012077363A (en) 2010-10-05 2012-04-19 Sumitomo Electric Ind Ltd Method of producing powder for metallurgy, and method for production of powder magnetic core
JP2014204108A (en) 2013-04-10 2014-10-27 株式会社村田製作所 Soft magnetic material, core, and inductor
JP2015185758A (en) 2014-03-25 2015-10-22 Ntn株式会社 Amorphous dust core and production method therefor
JP2016208002A (en) 2015-04-24 2016-12-08 サムソン エレクトロ−メカニックス カンパニーリミテッド. Coil electronic component and method of manufacturing the same
WO2016204008A1 (en) 2015-06-19 2016-12-22 株式会社村田製作所 Magnetic-substance powder and production process therefor, magnetic core and production process therefor, and coil component

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003188009A (en) * 2001-12-17 2003-07-04 Matsushita Electric Ind Co Ltd Compound magnetic material
WO2010084812A1 (en) * 2009-01-22 2010-07-29 住友電気工業株式会社 Process for producing metallurgical powder, process for producing powder magnetic core, powder magnetic core, and coil component
JP5958571B1 (en) * 2015-01-29 2016-08-02 Tdk株式会社 Soft magnetic metal dust core

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000294418A (en) 1999-04-09 2000-10-20 Hitachi Ferrite Electronics Ltd Powder molded magnetic core
JP2008081779A (en) 2006-09-27 2008-04-10 Hitachi Metals Ltd Powder of coated metal particulate and magnetic bead
JP2012077363A (en) 2010-10-05 2012-04-19 Sumitomo Electric Ind Ltd Method of producing powder for metallurgy, and method for production of powder magnetic core
JP2014204108A (en) 2013-04-10 2014-10-27 株式会社村田製作所 Soft magnetic material, core, and inductor
JP2015185758A (en) 2014-03-25 2015-10-22 Ntn株式会社 Amorphous dust core and production method therefor
JP2016208002A (en) 2015-04-24 2016-12-08 サムソン エレクトロ−メカニックス カンパニーリミテッド. Coil electronic component and method of manufacturing the same
WO2016204008A1 (en) 2015-06-19 2016-12-22 株式会社村田製作所 Magnetic-substance powder and production process therefor, magnetic core and production process therefor, and coil component

Also Published As

Publication number Publication date
CN108364767B (en) 2020-12-15
CN108364767A (en) 2018-08-03
JP2018113436A (en) 2018-07-19

Similar Documents

Publication Publication Date Title
JP7059594B2 (en) Soft magnetic materials, cores and inductors
JP7059593B2 (en) Soft magnetic materials, cores and inductors
US9659704B2 (en) Chip electronic component
US10573442B2 (en) Soft magnetic material, core, and inductor
CN106816277B (en) Coil component
US9583251B2 (en) Chip electronic component and board having the same
JP7222220B2 (en) Magnetic core and coil parts
CN111755199A (en) Composite magnetic body and inductor using the same
JP2019117898A (en) Multilayer coil type electronic component
US9875839B2 (en) Magnetic composition and inductor including the same
KR20150118020A (en) Electronic component, method of manufacturing the electronic component, and electronic apparatus
KR20170142974A (en) Inductor and manufacturing method thereof
CN111986880B (en) Laminated coil component
JP6825374B2 (en) Soft magnetic materials, cores and inductors
JP6825373B2 (en) Soft magnetic materials, cores and inductors
JP6825372B2 (en) Soft magnetic materials, cores and inductors
US10763019B2 (en) Soft magnetic material, core, and inductor
JP6242568B2 (en) High-frequency green compact and electronic parts using the same
JP6291789B2 (en) Multilayer coil parts
JP7251468B2 (en) Composite magnetic materials, magnetic cores and electronic components
KR20160014936A (en) Composite magnetic powder and chip coil component using thereof
JP2022177573A (en) Coil encapsulated magnetic core and coil component
CN113242774B (en) Silver paste
KR20170089188A (en) Coil electronic component
US20200273610A1 (en) Composite magnetic material, magnetic core, and electronic component

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20200702

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20210518

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20210525

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20210706

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20210914

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20211112

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: 20220315

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20220328

R150 Certificate of patent or registration of utility model

Ref document number: 7059594

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150