TW201901709A - Dust core, method for producing said dust core, inductor provided with said dust core, and electronic/electrical device on which said inductor is mounted - Google Patents

Dust core, method for producing said dust core, inductor provided with said dust core, and electronic/electrical device on which said inductor is mounted Download PDF

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TW201901709A
TW201901709A TW107107258A TW107107258A TW201901709A TW 201901709 A TW201901709 A TW 201901709A TW 107107258 A TW107107258 A TW 107107258A TW 107107258 A TW107107258 A TW 107107258A TW 201901709 A TW201901709 A TW 201901709A
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powder
magnetic material
core
powder core
inductor
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TW107107258A
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TWI720292B (en
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中林亮
小島章伸
高橋利男
岡本淳
佐藤昭
佐藤桂一郎
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日商阿爾普士電氣股份有限公司
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/08Metallic powder characterised by particles having an amorphous microstructure
    • 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
    • H01F1/147Alloys characterised by their composition
    • H01F1/153Amorphous metallic alloys, e.g. glassy metals
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F27/00Details of transformers or inductances, in general
    • H01F27/24Magnetic cores
    • H01F27/25Magnetic cores made from strips or ribbons
    • 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
    • H01F41/00Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
    • H01F41/02Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C45/00Amorphous alloys
    • C22C45/02Amorphous alloys with iron as the major constituent

Abstract

Provided is a dust core which is suitable as a constituent member for a small and low inductor with a built-in coil, and which contains a powder of a crystalline magnetic material and a powder of an amorphous magnetic material. This dust core is configured such that: a first mixing ratio, which is the mass ratio of the content of the powder of the crystalline magnetic material to the sum of the content of the powder of the crystalline magnetic material and the content of the powder of the amorphous magnetic material, is from 30% by mass to 70% by mass (inclusive); the crystalline magnetic material is composed of an Fe-Si-Cr system alloy; and the median diameter D50C thereof is from 2.5 [mu]m to 6 [mu]m (inclusive).

Description

壓粉芯、該壓粉芯之製造方法、具備該壓粉芯之電感器、及安裝有該電感器之電子・電氣機器Powder core, method for producing the powder core, inductor including the powder core, and electronic/electrical machine to which the inductor is attached

本發明係關於一種壓粉芯、該壓粉芯之製造方法、具備該壓粉芯之電感器、及安裝有該電感器之電子· 電氣機器。於本說明書中,所謂「電感器」,係指具備包含壓粉芯之芯材及線圈之被動元件。The present invention relates to a powder core, a method of manufacturing the powder core, an inductor including the powder core, and an electric / electric machine to which the inductor is mounted. In the present specification, the term "inductor" means a passive component including a core material and a coil including a powder core.

於智慧型手機、平板終端、筆記型電腦等電子機器中,對小型化、輕量化、高性能化之要求提高。為了響應此種要求,電子機器內之開關電源電路必須可應對較高之頻率。因此,要求組裝至開關電源電路中之電感器亦能以高頻穩定地驅動。 以提供可應對較高之驅動頻率之磁性元件之構成材料為目的,於專利文獻1中,記載有一種金屬磁性材料粉末,其包含具有平均第1粒徑之第1粒子及具有平均第2粒徑之第2粒子,且上述平均第1粒徑與上述平均第2粒徑之比為1/8~1/3,上述第1粒子與上述第2粒子之混合比以體積比計為10/90~25/75。 [先前技術文獻] [專利文獻] [專利文獻1]日本專利特開2011-192729號公報In electronic devices such as smart phones, tablet terminals, and notebook computers, the demand for miniaturization, weight reduction, and high performance has increased. In response to this requirement, the switching power supply circuit within the electronic machine must be able to handle higher frequencies. Therefore, the inductor assembled into the switching power supply circuit is required to be stably driven at a high frequency. In order to provide a constituent material of a magnetic element capable of coping with a high driving frequency, Patent Document 1 discloses a metal magnetic material powder including a first particle having an average first particle diameter and having an average second particle. The second particle of the diameter, and the ratio of the average first particle diameter to the average second particle diameter is 1/8 to 1/3, and the mixing ratio of the first particle to the second particle is 10/by volume. 90 to 25/75. [Prior Art Document] [Patent Document] [Patent Document 1] Japanese Patent Laid-Open Publication No. 2011-192729

[發明所欲解決之問題] 近年來,開關電源電路、尤其是DC(direct current,直流)-DC轉換器中對小型化之要求特別高,作為響應該要求之結果,組裝於內部之電感器不斷小型而且流通較大之直流電流。因此,放置構成電感器之磁性材料之磁性環境成為如下環境:於因該直流電流引起之感應磁場作為偏壓被施加之狀態下,進而施加有基於高頻下之開關之電流變動(漣波電流)所引起之變動磁場。因此,要求構成電感器之磁性材料於此種磁性嚴酷之環境下,具有適當之磁性特性(例如較高之相對磁導率)。 又,對於電子機器薄型化之要求亦較強,故而機器內之基板上之零件亦被強烈要求低高度化。若於電感器、尤其是線圈嵌入型之電感器中低高度化進展,則位於線圈周圍之磁性材料之絕對量變少,故而維持電感器之絕緣特性及維持芯之機械特性變得困難。 本發明係鑒於上述現狀,目的在於提供一種適合作為小型且低高度之線圈內置電感器之構成構件之壓粉芯及能夠用作具備該壓粉芯之電感器材料之壓粉芯、該壓粉芯之製造方法、具備該壓粉芯之電感器、及安裝有該電感器之電子· 電氣機器。 [解決問題之技術手段] 為了解決上述問題而提供之本發明之一態樣係一種壓粉芯,其特徵在於:其係含有結晶質磁性材料之粉末及非晶質磁性材料之粉末者,且上述結晶質磁性材料之粉末之含量相對於上述結晶質磁性材料之粉末之含量與上述非晶質磁性材料之粉末之含量之總和的質量比率即第一混合比率為30質量%以上且70質量%以下,上述結晶質磁性材料包含Fe-Si-Cr系合金,且中值粒徑D50 C為2.5 μm以上且6 μm以下。 如上所述,於電感器中流通之電流在疊加有直流之狀態下電流值變動。因此,構成壓粉芯之磁性材料要求即便於外部磁場某種程度較高之狀態下亦具有較高之磁導率。該高磁場中之磁導率係與初始磁導率異質之參數,且稱不上與飽和磁通密度具有較強之中間相。作為評估此種高磁場中之磁導率之參數之一例,可列舉外部磁場為5500 A/m之情形時之相對磁導率即μ5500。該μ5500越高,可謂磁性材料於高磁場中具有越優異之磁性特性。又,若電感器變得小型且低高度,則位於內置線圈之周圍之芯之體積變少。作為於該情形時擔心之不良情況,可列舉芯之絕緣破壞及芯之破損(破裂、缺損)。因此,較佳為芯之絕緣耐壓(單位:V/mm)及徑向壓碎強度(radial crushing strength)(單位:MPa)較高。因此,藉由使用μ5500×絕緣耐壓×徑向壓碎強度較高之壓粉芯,可獲得即便為小型且低高度亦於強磁場中具有優異之磁性特性之電感器。 因此,對於提供μ5500×絕緣耐壓×徑向壓碎強度較高之壓粉芯之條件進行了研究,結果獲得如下知識見解:藉由使壓粉芯中所包含之磁性材料之粉末(磁性粉末)滿足以下事項,即便具有小型且低高度之形狀亦不易產生芯之絕緣破壞或破損之問題,使用該芯而成之電感器即便被用於高磁場中亦可具有適當之磁性特性。 (事項1)使磁性粉末為結晶質磁性材料之粉末與非晶質磁性材料之粉末之混合體。 (事項2)使第一混合比率為30質量%以上且70質量%以下。 (事項3)結晶質磁性材料包含Fe-Si-Cr系合金,且中值粒徑D50 C為2.5 μm以上且6 μm以下。 藉由滿足該等事項,可獲得μ5500×絕緣耐壓×徑向壓碎強度特異地較高之壓粉芯。 於上述壓粉芯中,較佳為上述非晶質磁性材料之粉末之中值粒徑D50 A為5 μm以上且8 μm以下。於滿足事項2之情形時,藉由中值粒徑D50 A為5 μm以上可特異地提高μ5500×絕緣耐壓×徑向壓碎強度。自該觀點而言,更佳為中值粒徑D50 A為5.5 μm以上。另一方面,於中值粒徑D50 A過大之情形時,μ5500×絕緣耐壓×徑向壓碎強度容易降低,或者鐵損,尤其高頻時之鐵損提高。因此,中值粒徑D50 A較佳為8 μm以下,更佳為7 μm以下。 於上述壓粉芯中,較佳為上述非晶質磁性材料之粉末之中值粒徑D50 A與上述結晶質磁性材料之粉末之中值粒徑D50 C滿足下述式(1)。藉由使2種粉末之粒徑滿足下述式(1)之關係,而更穩定地實現提高μ5500×絕緣耐壓×徑向壓碎強度。 1≦D50 A/D50 C≦3.5 (1) 於上述壓粉芯中,藉由使上述第一混合比率為40質量%以上且60質量%以下,可特異地提高μ5500×絕緣耐壓×徑向壓碎強度。 於上述壓粉芯中,存在如下情形:較佳為上述非晶質磁性材料亦可包含選自由Fe-Si-B系合金、Fe-P-C系合金及Co-Fe-Si-B系合金所組成之群中之1種或2種以上之材料,上述非晶質磁性材料包含Fe-P-C系合金。 於上述壓粉芯中,存在如下情形:藉由含有使上述結晶質磁性材料之粉末及上述非晶質磁性材料之粉末黏結於上述壓粉芯中所含有之其他材料之黏結成分,而容易提高壓粉芯之絕緣耐壓或提高徑向壓碎強度。於該情形時,上述黏結成分亦可包含基於樹脂材料之成分。 本發明之另一態樣提供一種含有上述包含基於樹脂材料之成分之黏結成分的壓粉芯之製造方法。該製造方法具備藉由包含混合物之加壓成形之成形處理而獲得成形製造物之成形步驟,該混合物包含上述結晶質磁性材料之粉末及上述非晶質磁性材料之粉末以及含有上述樹脂材料之黏合劑成分。自提高生產性之觀點等而言,較佳為此時之成形處理係於常溫左右之溫度環境下以0.5 GPa左右至2 GPa左右進行加壓之壓縮成形。 本發明之又一態樣提供一種電感器,其具備上述壓粉芯、線圈及連接於上述線圈之各自之端部之連接端子,且上述壓粉芯之至少一部分係以位於在經由上述連接端子對上述線圈流通電流時由上述電流產生之感應磁場內之方式配置。關於該電感器,基於壓粉芯之優異之特性,即便為小型且低高度,芯亦不易絕緣破壞或破損,而且直流疊加特性優異。 本發明之又一態樣提供一種電子· 電氣機器,其係安裝有上述電感器之電子· 電氣機器,且上述電感器係由上述連接端子而連接於基板。該電子· 電氣機器中之組裝有電感器之電路並不特別限定,但於使用於DC-DC轉換器等開關電源電路之情形時,容易發揮直流疊加特性優異之上述電感器之優點。又,於電子· 電氣機器為智慧型手機等可攜式機器之情形時,容易發揮易於應對小型且低高度之上述電感器之優點。 [發明之效果] 上述發明之壓粉芯被適當地調整了結晶質磁性材料之粉末之組成及粒徑分佈、以及結晶質磁性材料之粉末與非晶質磁性材料之粉末之混合比率(第一混合比率),故而關於具備該壓粉芯之電感器,即便為小型且低高度亦能夠提高直流疊加特性。又,根據本發明,提供一種上述壓粉芯之製造方法、具備該壓粉芯之電感器、及安裝有該電感器之電子· 電氣機器。[Problems to be Solved by the Invention] In recent years, switching power supply circuits, particularly DC (direct current)-DC converters, have been particularly demanding for miniaturization, and as a result of responding to such requirements, inductors are assembled inside. Constantly small and circulated large DC current. Therefore, the magnetic environment in which the magnetic material constituting the inductor is placed is an environment in which a current fluctuation (switching current) based on a switch at a high frequency is applied in a state where an induced magnetic field due to the direct current is applied as a bias voltage. The magnetic field caused by the change. Therefore, it is required that the magnetic material constituting the inductor has appropriate magnetic properties (e.g., high relative magnetic permeability) in such a magnetically harsh environment. Moreover, the requirements for the thinning of electronic devices are also strong, and the components on the substrates in the machine are also strongly required to be lowered in height. When the inductor, particularly the coil-embedded inductor, is lowered in height, the absolute amount of the magnetic material located around the coil is reduced, so that it is difficult to maintain the insulating properties of the inductor and maintain the mechanical properties of the core. The present invention has been made in view of the above circumstances, and an object thereof is to provide a powder core suitable as a constituent member of a small-sized and low-height coil-incorporated inductor, and a powder core which can be used as an inductor material having the powder core, the powder A method of manufacturing a core, an inductor including the powder core, and an electric / electrical device to which the inductor is mounted. [Technical means for solving the problem] An aspect of the present invention provided to solve the above problems is a powder core characterized in that it contains a powder of a crystalline magnetic material and a powder of an amorphous magnetic material, and The first mixing ratio is 30% by mass or more and 70% by mass based on the mass ratio of the content of the powder of the crystalline magnetic material to the total of the content of the powder of the crystalline magnetic material and the content of the powder of the amorphous magnetic material. Hereinafter, the crystalline magnetic material contains an Fe—Si—Cr-based alloy, and the median diameter D 50 C is 2.5 μm or more and 6 μm or less. As described above, the current flowing in the inductor fluctuates in a state in which DC is superimposed. Therefore, the magnetic material constituting the powder core is required to have a high magnetic permeability even in a state in which the external magnetic field is somewhat high. The magnetic permeability in the high magnetic field is a parameter that is heterogeneous with the initial magnetic permeability, and cannot be said to have a strong intermediate phase with the saturation magnetic flux density. As an example of the parameter for evaluating the magnetic permeability in such a high magnetic field, the relative magnetic permeability, that is, μ5500 when the external magnetic field is 5500 A/m is exemplified. The higher the μ5500, the more excellent the magnetic properties of the magnetic material in a high magnetic field. Further, when the inductor is small and has a low height, the volume of the core located around the built-in coil is small. As a problem that is feared in this case, insulation breakdown of the core and breakage (breakage or defect) of the core are exemplified. Therefore, it is preferable that the core insulation withstand voltage (unit: V/mm) and radial crushing strength (unit: MPa) are high. Therefore, by using a powder core having a μ5500×insistance withstand voltage×high radial crushing strength, an inductor having excellent magnetic properties even in a small magnetic field and a high magnetic field can be obtained. Therefore, the conditions for providing a powder core having a μ5500×insulation withstand voltage×high radial crushing strength have been studied, and as a result, the following knowledge has been obtained: a powder of a magnetic material contained in a powder core (magnetic powder) It satisfies the following matters, and even if it has a small and low-profile shape, it is less likely to cause insulation breakdown or breakage of the core, and the inductor using the core can have appropriate magnetic characteristics even when used in a high magnetic field. (Item 1) The magnetic powder is a mixture of a powder of a crystalline magnetic material and a powder of an amorphous magnetic material. (Item 2) The first mixing ratio is 30% by mass or more and 70% by mass or less. (Problem 3) The crystalline magnetic material contains an Fe—Si—Cr-based alloy, and the median diameter D 50 C is 2.5 μm or more and 6 μm or less. By satisfying these matters, it is possible to obtain a powder core having a μ5500 × insulation withstand voltage × radial crushing strength which is particularly high. In the above-mentioned powder core, it is preferable that the powder of the amorphous magnetic material has a median diameter D 50 A of 5 μm or more and 8 μm or less. When the case 2 is satisfied, the μ5500×insulation withstand strength×radial crushing strength can be specifically increased by the median diameter D 50 A of 5 μm or more. From this viewpoint, it is more preferable that the median diameter D 50 A is 5.5 μm or more. On the other hand, when the median diameter D 50 A is excessively large, the μ5500×insulation withstand voltage×radial crushing strength is liable to be lowered, or iron loss, particularly at high frequency, is increased. Therefore, the median diameter D 50 A is preferably 8 μm or less, more preferably 7 μm or less. In the powder core, it is preferable that the powder median diameter D 50 A of the amorphous magnetic material and the powder median diameter D 50 C of the crystalline magnetic material satisfy the following formula (1). By making the particle diameters of the two kinds of powders satisfy the relationship of the following formula (1), it is more stably achieved that the μ5500×insulation withstand voltage×radial crushing strength is improved. 1≦D 50 A/D 50 C≦3.5 (1) In the above-mentioned powder core, by setting the first mixing ratio to 40% by mass or more and 60% by mass or less, it is possible to specifically increase μ5500×insulation withstand voltage× Radial crush strength. In the above-mentioned powder core, it is preferable that the amorphous magnetic material may further comprise a material selected from the group consisting of Fe-Si-B alloy, Fe-PC alloy, and Co-Fe-Si-B alloy. One or two or more materials of the group, and the amorphous magnetic material contains an Fe-PC alloy. In the above-mentioned powder core, there is a case where it is easy to improve by containing a binder component in which the powder of the crystalline magnetic material and the powder of the amorphous magnetic material are adhered to other materials contained in the powder core. The insulation pressure of the powder core or the increase of the radial crush strength. In this case, the above-mentioned bonding component may also contain a component based on a resin material. Another aspect of the present invention provides a method of producing a powder core comprising the above-described binder component comprising a resin material-based component. The production method includes a molding step of obtaining a molded article by a molding process including press molding of a mixture, the mixture comprising a powder of the crystalline magnetic material and a powder of the amorphous magnetic material and a bond containing the resin material Ingredients. From the viewpoint of improving productivity, it is preferred that the molding treatment at this time is compression molding which is pressurized at a temperature of about 0.5 GPa to about 2 GPa in a temperature environment of about room temperature. According to still another aspect of the present invention, there is provided an inductor comprising: the powder core, a coil, and a connection terminal connected to respective ends of the coil, and at least a portion of the powder core is located via the connection terminal When the current flows through the coil, it is disposed in the induced magnetic field generated by the current. According to the excellent characteristics of the powder core, the inductor is not easily damaged or broken by insulation even if it is small in size and low in height, and is excellent in DC superposition characteristics. A further aspect of the present invention to provide a kind of electronic and electrical equipment, which is mounted based electronic and electric equipment of the inductor, the inductor and the connecting lines from the terminals connected to the substrate. The circuit in which the inductor is incorporated in the electronic / electrical device is not particularly limited. However, when it is used in a switching power supply circuit such as a DC-DC converter, it is easy to exhibit the advantages of the above-described inductor excellent in DC superposition characteristics. Moreover, when the electronic / electrical device is a portable device such as a smart phone, it is easy to provide an advantage that it is easy to cope with a small-sized and low-profile inductor. [Effects of the Invention] The powder core of the above invention is appropriately adjusted in the composition and particle size distribution of the powder of the crystalline magnetic material, and the mixing ratio of the powder of the crystalline magnetic material and the powder of the amorphous magnetic material (first Since the mixing ratio is the same, the inductor having the powder core can improve the DC superposition characteristics even in a small size and a low height. Moreover, according to the present invention, there is provided a method of manufacturing the above-described powder core, an inductor including the powder core, and an electric / electric machine to which the inductor is attached.

以下,對本發明之實施形態詳細地進行說明。 1.壓粉芯 圖1所示之本發明之一實施形態之壓粉芯1係外觀為環狀之環形芯,且含有結晶質磁性材料之粉末及非晶質磁性材料之粉末。本實施形態之壓粉芯1係藉由具備成形處理之製造方法而製造者,該成形處理包含將含有該等粉末之混合物加壓成形。作為不受限定之一例,本實施形態之壓粉芯1含有使結晶質磁性材料之粉末及非晶質磁性材料之粉末黏結於壓粉芯1中所含有之其他材料(存在為相同種類之材料之情形,亦存在為不同種類之材料之情形)之黏結成分。 (1)結晶質磁性材料之粉末 提供本發明之一實施形態之壓粉芯1所含有之結晶質磁性材料之粉末的結晶質磁性材料為結晶質(藉由通常之X射線繞射測定,而獲得在能夠特定出材料種類之程度上具有明確之峰值之繞射光譜)且強磁性,包含Fe-Si-Cr系合金。Fe-Si-Cr系合金係於結晶質磁性材料之中飽和磁通密度相對較高且軟磁性特性良好,比電阻亦較高之材料。因此,若與其他結晶質磁性材料、例如羰基鐵粉等相比,即便於高磁場及高頻之條件下損耗亦較低,容易顯示良好之磁性特性。因此,藉由使壓粉芯1中含有之結晶質磁性材料之粉末包含Fe-Si-Cr系合金,即便提高結晶質磁性材料之粉末之含量相對於壓粉芯1中之結晶質磁性材料之粉末之含量與非晶質磁性材料之粉末之含量之總和的質量比率(於本說明書中亦稱為「第一混合比率」),高磁場環境下之相對磁導率、具體而言為μ5500亦不易降低。Fe-Si-Cr系合金中之Si之含量及Cr之含量並不限定。作為不受限定之例示,可列舉將Si之含量設為2~7質量%左右,將Cr之含量設為2~7質量%左右,其餘部分設為Fe及不可避免之雜質。 本發明之一實施形態之壓粉芯1所含有之結晶質磁性材料之粉末之形狀並不限定。粉末之形狀可為球狀亦可為非球狀。於非球狀之情形時,亦可為鱗片狀、橢圓球狀、液滴狀、針狀等具有形狀各向異性之形狀。 粉末之形狀可為於製造粉末之階段獲得之形狀,亦可為藉由對所製造出之粉末進行二次加工而獲得之形狀。作為前者之形狀,例示球狀、橢圓球狀、液滴狀、針狀等,作為後者之形狀,例示鱗片狀。 關於本發明之一實施形態之壓粉芯1所含有之結晶質磁性材料之粉末之粒徑,於體積基準之粒度分佈中自小粒徑側起之累計粒徑分佈成為50%之粒徑(於本說明書中亦稱為「結晶質粉末中值粒徑」)D50 C為2.5 μm以上且6 μm以下。藉由使結晶質粉末中值粒徑D50 C處於上述範圍,而於第一混合比率為30質量%以上且70質量%以下時,可特異地提高μ5500×絕緣耐壓×徑向壓碎強度。存在如下情形:若亦進而考慮高頻、尤其是1 MHz以上之鐵損Pcv之影響,則較佳為結晶質粉末中值粒徑D50 C為2.5 μm以上且5.5 μm以下。 亦可對結晶質磁性材料之粉末之至少一部分實施表面絕緣處理。於對結晶質磁性材料之粉末實施表面絕緣處理之情形時,觀察到壓粉芯1之絕緣電阻提高之傾向。對結晶質磁性材料之粉末實施之表面絕緣處理之種類並不限定。例示有磷酸處理、磷酸鹽處理、氧化處理等。 (2)非晶質磁性材料之粉末 提供本發明之一實施形態之壓粉芯1所含有之非晶質磁性材料之粉末的非晶質磁性材料只要滿足為非晶質(藉由通常之X射線繞射測定,無法獲得可特定出材料種類之程度具有明確之峰值之繞射光譜)及為強磁性體、尤其是軟磁性體,則具體之種類並不限定。作為非晶質磁性材料之具體例,可列舉Fe-Si-B系合金、Fe-P-C系合金及Co-Fe-Si-B系合金。上述非晶質磁性材料可由1種材料構成亦可由複數種材料構成。構成非晶質磁性材料之粉末之磁性材料較佳為選自由上述材料所組成之群中之1種或2種以上之材料,該等之中,較佳為含有Fe-P-C系合金,更佳為包含Fe-P-C系合金。 作為Fe-P-C系合金之具體例,可列舉如下之Fe基非晶質合金,其組成式由Fe100 原子 % - a - b - c - x - y - z - t Nia Snb Crc Px Cy Bz Sit 表示,且0原子%≦a≦10原子%、0原子%≦b≦3原子%、0原子%≦c≦6原子%、6.8原子%≦x≦13原子%、2.2原子%≦y≦13原子%、0原子%≦z≦9原子%、0原子%≦t≦7原子%。於上述組成式中,Ni、Sn、Cr、B及Si為任意添加元素。 Ni之添加量a較佳為0原子%以上且6原子%以下,更佳為0原子%以上且4原子%以下。Sn之添加量b較佳為0原子%以上且2原子%以下,亦可於1原子%以上且2原子%以下之範圍內添加。Cr之添加量c較佳為0原子%以上且2原子%以下,更佳為1原子%以上且2原子%以下。亦存在P之添加量x較佳為8.8原子%以上之情形。亦存在C之添加量y較佳為5.8原子%以上且8.8原子%以下之情形。B之添加量z較佳為0原子%以上且3原子%以下,更佳為0原子%以上且2原子%以下。Si之添加量t較佳為0原子%以上且6原子%以下,更佳為0原子%以上且2原子%以下。 本發明之一實施形態之壓粉芯1所含有之非晶質磁性材料之粉末之形狀並不限定。關於粉末之形狀之種類,由於與結晶質磁性材料之粉末之情形時相同,故而省略說明。亦存在就製造方法之關係而言非晶質磁性材料容易形成為球狀或橢圓球狀之情形。又,一般而言,非晶質磁性材料較結晶質磁性材料更硬質,故而亦存在較佳為使結晶質磁性材料為非球狀而於加壓成形時容易變形之情形。 本發明之一實施形態之壓粉芯1所含有之非晶質磁性材料之粉末之形狀可為於製造粉末之階段獲得之形狀,亦可為藉由對所製造出之粉末進行二次加工而獲得之形狀。作為前者之形狀,例示球狀、橢圓球狀、針狀等,作為後者之形狀,例示鱗片狀。 關於本發明之一實施形態之壓粉芯1所含有之非晶質磁性材料之粉末之粒徑,於體積基準之粒度分佈中自小粒徑側起之累計粒徑分佈成為50%之粒徑(於本說明書中亦稱為「非晶質粉末中值粒徑」)D50 A較佳為5 μm以上且8 μm以下。藉由於第一混合比率為30質量%以上且70質量%以下時使非晶質粉末中值粒徑D50 A為5 μm以上,可特異地提高μ5500×絕緣耐壓×徑向壓碎強度。自該觀點而言,非晶質粉末中值粒徑D50 A更佳為5.5 μm以上。另一方面,亦存在如下情形:於非晶質粉末中值粒徑D50 A過大之情形時,具有μ5500×絕緣耐壓×徑向壓碎強度降低,或鐵損Pcv、尤其是高頻中之鐵損Pcv提高之傾向。因此,非晶質粉末中值粒徑D50 A較佳為8 μm以下,更佳為7 μm以下。 又,本發明之一實施形態之壓粉芯1所含有之非晶質磁性材料之粉末之粒徑亦可具有與壓粉芯1所含有之非晶質磁性材料之粉末之粒徑之以下關係。即,非晶質粉末中值粒徑D50 A與結晶質粉末中值粒徑D50 C亦可滿足下述式(1)。 1≦D50 A/D50 C≦3.5 (1) 藉由使D50 A/D50 C處於1至3.5之範圍內,關於壓粉芯1容易特異地提高μ5500×絕緣耐壓×徑向壓碎強度。自更穩定地實現特異地提高μ5500×絕緣耐壓×徑向壓碎強度之觀點而言,D50 A/D50 C存在較佳為處於1.2至2.5之範圍之情形,且存在較佳為處於1.3至2.0之範圍之情形。 自更穩定地實現針對壓粉芯1使μ5500×絕緣耐壓×徑向壓碎強度特異地變高之觀點而言,第一混合比率較佳為40質量%以上且60質量%以下,更佳為40質量%以上且55質量%以下。 (3)黏結成分 壓粉芯1亦可含有使結晶質磁性材料之粉末及非晶質磁性材料之粉末黏結於壓粉芯1中所含有之其他材料之黏結成分。黏結成分只要為有助於將本實施形態之壓粉芯1中所含有之結晶質磁性材料之粉末及非晶質磁性材料之粉末(於本說明書中,有時亦將該等粉末總稱為「磁性粉末」)固定之材料,則其組成並不限定。作為構成黏結成分之材料,例示樹脂材料及樹脂材料之熱分解殘渣(於本說明書中,將該等總稱為「基於樹脂材料之成分」)等有機系材料、無機系材料等。作為樹脂材料,例示丙烯酸系樹脂、矽酮樹脂、環氧樹脂、酚樹脂、尿素樹脂、三聚氰胺樹脂等。由無機系材料構成之黏結成分例示有水玻璃等玻璃系材料。黏結成分可由一種材料構成,亦可由複數種材料構成。黏結成分亦可為有機系材料與無機系材料之混合體。 作為黏結成分,通常使用絕緣性之材料。藉此,能夠提高作為壓粉芯1之絕緣性。 2.壓粉芯之製造方法 上述本發明之一實施形態之壓粉芯1之製造方法並不特別限定,但若採用以下說明之製造方法,則實現更有效率地製造壓粉芯1。 本發明之一實施形態之壓粉芯1之製造方法具備以下說明之成形步驟,亦可進而具備熱處理步驟。 (1)成形步驟 首先,準備包含磁性粉末及在壓粉芯1中提供黏結成分之成分之混合物。所謂提供黏結成分之成分(於本說明書中,亦稱為「黏合劑成分」),既存在為黏結成分本身之情形,亦存在為與黏結成分不同之材料之情形。作為後者之具體例,可列舉黏合劑成分為樹脂材料,且黏結成分為其熱分解殘渣之情形。此種熱分解殘渣如下所述係藉由繼成形步驟後進行之熱處理步驟而形成者。 可藉由包含該混合物之加壓成形之成形處理而獲得成形製造物。加壓條件並不限定,基於黏合劑成分之組成等而適當設定。例如,於黏合劑成分包括熱硬化性之樹脂之情形時,較佳為一併進行加壓及加熱,於模具內進行樹脂之硬化反應。另一方面,於壓縮成形之情形時,雖然加壓力較高,但加熱不成為必要條件,加壓之時間較短。壓縮成形之情形時之加壓力適當設定。若進行不受限定之例示,則有為0.5 GPa以上且2 GPa以下,較佳為1 GPa以上且2 GPa以下之情形。 以下,對於混合物為造粒粉且進行壓縮成形之情形稍微詳細地進行說明。造粒粉由於操作性優異,故而可提高成形時間短且生產性優異之壓縮成形步驟之作業性。 (1-1)造粒粉 造粒粉含有磁性粉末及黏合劑成分。造粒粉中之黏合劑成分之含量並不特別限定。於該含量過低之情形時,黏合劑成分不易保持磁性粉末。又,於黏合劑成分之含量過低之情形時,於經過熱處理步驟而獲得之壓粉芯1中,包含黏合劑成分之熱分解殘渣之黏結成分不易使複數個磁性粉末相互與其他磁性粉末絕緣。另一方面,於上述黏合劑成分之含量過高之情形時,經過熱處理步驟而獲得之壓粉芯1中所含有之黏結成分之含量容易變高。若壓粉芯1中之黏結成分之含量變高,則壓粉芯1之磁性特性容易降低。因此,造粒粉中之黏合劑成分之含量較佳為相對於造粒粉整體為0.5質量%以上且5.0質量%以下之量。自更穩定地減小壓粉芯1之磁性特性降低之可能性之觀點而言,造粒粉中之黏合劑成分之含量較佳為相對於造粒粉整體為1.0質量%以上且3.5質量%以下之量,更佳為1.2質量%以上且3.0質量%以下之量。 造粒粉亦可含有上述磁性粉末及黏合劑成分以外之材料。作為此種材料,例示潤滑劑、矽烷偶合劑、絕緣性之填料等。於含有潤滑劑之情形時,其種類並不特別限定。可為有機系之潤滑劑,亦可為無機系之潤滑劑。作為有機系之潤滑劑之具體例,可列舉硬脂酸鋅、硬脂酸鋁等金屬皂。認為此種有機系之潤滑劑於熱處理步驟中氣化,幾乎不殘留於壓粉芯1中。 造粒粉之製造方法並不特別限定。可將提供上述造粒粉之成分直接混練,將所獲得之混練物利用公知之方法粉碎等而獲得造粒粉,亦可藉由製備於上述成分中添加分散媒(可列舉水作為一例)而成之漿料,使該漿料乾燥並進行粉碎而獲得造粒粉。亦可於粉碎後進行篩分或分級,控製造粒粉之粒度分佈。 作為自上述漿料獲得造粒粉之方法之一例,可列舉使用噴霧乾燥器之方法。如圖2所示,於噴霧乾燥器裝置200內設置轉子201,自裝置上部將漿料S朝向轉子201注入。轉子201以特定之轉數而旋轉,於噴霧乾燥器裝置200內部之腔室使漿料S藉由離心力以小滴狀噴霧。進而,對噴霧乾燥器裝置200內部之腔室導入熱風,藉此使小滴狀之漿料S中所含有之分散媒(水)維持小滴形狀之狀態揮發。其結果,自漿料S形成造粒粉P。將該造粒粉P自噴霧乾燥器裝置200之下部回收。轉子201之轉數、導入至噴霧乾燥器裝置200內之熱風溫度、腔室下部之溫度等各參數只要適當設定即可。作為該等參數之設定範圍之具體例,轉子201之轉數可列舉4000~8000 rpm,導入至噴霧乾燥器裝置200內之熱風溫度可列舉100~170℃,腔室下部之溫度可列舉80~90℃。又,腔室內之環境及其壓力亦只要適當設定即可。作為一例,可列舉使腔室內為大氣(空氣)環境,其壓力以與大氣壓之差壓計為2 mmH2 O(約0.02 kPa)。亦可藉由篩分等進而控制所獲得之造粒粉P之粒度分佈。 (1-2)加壓條件 壓縮成形中之加壓條件並不特別限定。只要考慮造粒粉之組成、成形品之形狀等適當設定即可。於將造粒粉壓縮成形時之加壓力過低之情形時,成形品之機械強度降低。因此,容易產生成形品之操作性降低、自成形品獲得之壓粉芯1之機械強度降低等問題。又,亦存在壓粉芯1之磁性特性降低或絕緣性降低之情形。另一方面,於將造粒粉壓縮成形時之加壓力過高之情形時,難以製成能夠耐受該壓力之成形模具。自更穩定地降低壓縮加壓步驟對壓粉芯1之機械特性或磁性特性帶來不良影響之可能性,且工業上容易進行大量生產之觀點而言,將造粒粉壓縮成形時之加壓力較佳為0.3 GPa以上且2 GPa以下,更佳為0.5 GPa以上且2 GPa以下,特佳為0.8 GPa以上且2 GPa以下。 於壓縮成形中,可一面進行加熱一面進行加壓,亦可於常溫下進行加壓。 (2)熱處理步驟 藉由成形步驟而獲得之成形製造物可為本實施形態之壓粉芯1,亦可如以下所說明般對成形製造物實施熱處理步驟而獲得壓粉芯1。 於熱處理步驟中,對藉由上述成形步驟而獲得之成形製造物進行加熱,由此藉由修正磁性粉末間之距離而進行磁性特性之調整以及使在成形步驟中賦予至磁性粉末之應變緩和而進行磁性特性之調整,從而獲得壓粉芯1。 熱處理步驟如上所述目的係為了調整壓粉芯1之磁性特性,故而熱處理溫度等熱處理條件係以壓粉芯1之磁性特性變得最佳之方式設定。作為設定熱處理條件之方法之一例,可列舉使成形製造物之加熱溫度變化,使升溫速度及加熱溫度下之保持時間等其他條件固定。 設定熱處理條件時之壓粉芯1之磁性特性之評估基準並不特別限定。作為評估項目之具體例,可列舉壓粉芯1之鐵損Pcv。於該情形時,只要以壓粉芯1之鐵損Pcv成為最低之方式設定成形製造物之加熱溫度即可。鐵損Pcv之測定條件適當設定,作為一例,可列舉使頻率為2 MHz且使有效最大磁通密度Bm為15 mT之條件。 熱處理時之環境並不特別限定。於氧化性環境之情形時,黏合劑成分之熱分解過度進行之可能性或磁性粉末之氧化進展之可能性提高,故而較佳為於氮氣、氬氣等惰性環境或氫氣等還原性環境下進行熱處理。於黏合劑成分由樹脂材料形成之情形時,存在藉由如上所述之熱處理而該黏合劑成分成為熱分解殘渣之情形。一般認為於如上所述般使應變緩和時,黏合劑成分成為熱分解殘渣。 3.電感器、電子•電氣機器 本發明之一實施形態之電感器具備上述本發明之一實施形態之壓粉芯1、線圈及連接於該線圈之各端部之連接端子。此處,壓粉芯1之至少一部分係以位於經由連接端子對線圈流通電流時由該電流產生之感應磁場內之方式配置。本發明之一實施形態之電感器由於具備上述本發明之一實施形態之壓粉芯1,故而直流疊加特性優異,並且絕緣特性及機械特性優異。 作為此種電感器之一例,可列舉圖3所示之環形線圈10。環形線圈10具備藉由將被覆導電線2捲繞於環狀之壓粉芯(環形芯)1而形成之線圈2a。於位於由被捲繞之被覆導電線2構成之線圈2a與被覆導電線2之端部2b、2c之間的導電線之部分中,可定義線圈2a之端部2d、2e。如此,本實施形態之電感器亦可為,構成線圈之構件與構成連接端子之構件由相同之構件構成。 作為本發明之一實施形態之電感器之另一例,可列舉圖4所示之線圈埋設型電感器20。線圈埋設型電感器20能夠形成為數mm見方之小型之小片狀,且具備具有箱形之形狀之壓粉芯21,於其內部埋設有被覆導電線22中之線圈部22c。被覆導電線22之端部22a、22b位於壓粉芯21之表面且露出。壓粉芯21之表面之一部分藉由相互電性地獨立之連接端部23a、23b而覆蓋。連接端部23a與被覆導電線22之端部22a電性連接,連接端部23b與被覆導電線22之端部22b電性連接。於圖4所示之線圈埋設型電感器20中,被覆導電線22之端部22a藉由連接端部23a而覆蓋,被覆導電線22之端部22b藉由連接端部23b而覆蓋。 被覆導電線22之線圈部22c埋設於壓粉芯21內之方法並不限定。可將捲繞有被覆導電線22之構件配置於模具內,進而將包含磁性粉末之混合物(造粒粉)供給至模具內,進行加壓成形。或者,亦可準備將包含磁性粉末之混合物(造粒粉)事先預備成形而成之複數個構件,將該等構件組合,於此時形成之空隙部內配置被覆導電線22獲得組裝體,對該組裝體進行加壓成形。包含線圈部22c之被覆導電線22之材質並不限定。例如,可列舉銅合金。線圈部22c亦可為沿邊線圈。連接端部23a、23b之材質亦並不限定。存在如下情形:自生產性優異之觀點而言,較佳為具備由銀膏等導電膏形成之金屬化層及形成於該金屬化層上之鍍覆層。形成該鍍覆層之材料並不限定。作為該材料含有之金屬元素,例示銅、鋁、鋅、鎳、鐵、錫等。 本發明之一實施形態之電子· 電氣機器係安裝有上述本發明之一實施形態之電感器之電子· 電氣機器,且電感器係利用其連接端子連接於基板。作為具備該電感器之電路之一例,可列舉如DC-DC轉換器般之開關電源電路。開關電源電路為了響應電子· 電氣機器之小型化、輕量化、高功能化等多種要求,而具有開關頻率變高、流經電路之電流量增加之傾向。因此,作為電路之構成零件之電感器中流通之電流亦存在變動頻率變高、平均電流量增加之傾向。關於該方面,如上所述,具備本發明之一實施形態之壓粉芯之電感器即便為小型且低高度,亦能夠於高磁場環境中適當地動作。因此,於具備該電感器之開關電源電路中抑制了效率之降低,可不產生發熱問題地響應上述多種要求。如此,安裝有本發明之一實施形態之電感器之電子· 電氣機器能夠應對小型化、輕量化,且實現高功能化。 以上說明之實施形態係為了使本發明之理解容易而記載者,並非為了限定本發明而記載者。因此,上述實施形態中所揭示之各要素之主旨在於亦包含屬於本發明之技術性範圍之所有設計變更或均等物。 [實施例] 以下,藉由實施例等對本發明進而具體地進行說明,但本發明之範圍並不限定於該等實施例等。 (實施例1) (1)Fe基非晶質合金粉末之製作 以成為由Fe71 原子 % Ni6 原子 % Cr2 原子 % P11 原子 % C8 原子 % B2 原子 % 構成之組成之方式稱量原料,使用水霧化法製作出非晶質磁性材料之粉末(非晶質粉末)。將所獲得之非晶質磁性材料之粉末分級,使用日機裝公司製造「Microtrac粒度分佈測定裝置 MT3300EX」以體積分佈測定分級後之粉末之粒度分佈。於體積基準之粒度分佈中自小粒徑側起之累計粒徑分佈成為50%之粒徑(非晶質粉末中值粒徑)D50 A為6.5 μm。又,作為結晶質磁性材料之粉末,準備如下之粉末:包含Fe-Si-Cr系合金,具體為Si之含量為3.5質量%,Cr之含量為4.5質量%,其餘部分為Fe及不可避免之雜質之合金,且結晶質粉末中值粒徑D50 C為4.0 μm。因此,於實施例1之粉末中,D50 A/D50 C為1.6。 (2)造粒粉之製作 將上述非晶質磁性材料之粉末及結晶質磁性材料之粉末以成為表1所示之第一混合比率之方式混合而獲得磁性粉末。將磁性粉末97.2質量份、包含丙烯酸樹脂及酚樹脂之絕緣性黏結材2~3質量份及包含硬脂酸鋅之潤滑劑0~0.5質量份混合於作為溶劑之水中而獲得漿料。 使用圖2所示之噴霧乾燥器裝置200,以上述條件對所獲得之漿料進行造粒,獲得造粒粉。 (3)壓縮成形 將所獲得之造粒粉填充至模具,以面壓力1 GPa進行加壓成形,獲得具有外徑20 mm×內徑12 mm×厚度3 mm之環形狀之成形體。 (4)熱處理 將所獲得之成形體載置於氮氣流環境之爐內,使爐內溫度自室溫(23℃)以升溫速度10℃/分鐘加熱至最佳芯熱處理溫度即200~400℃為止,於該溫度下保持1小時,然後,於爐內進行冷卻至室溫為止之熱處理,獲得包含壓粉芯之環形芯。 [表1] (實施例2) 使用實施例1中製造出之非晶質磁性材料之粉末,變更分級條件而準備非晶質粉末中值粒徑D50 A為5.0 μm之非晶質磁性材料之粉末。又,作為結晶質磁性材料之粉末,準備如下粉末:包含Fe-Si-Cr系合金,具體為Si之含量為6.4質量%,Cr之含量為3.1質量%,其餘部分為Fe及不可避免之雜質之合金,且結晶質粉末中值粒徑D50 C為2.0 μm。因此,於實施例2之粉末中,D50 A/D50 C為2.5。將上述非晶質磁性材料之粉末及結晶質磁性材料之粉末以成為表2所示之第一混合比率之方式混合而獲得磁性粉末。以下,與實施例1同樣地獲得複數種環形芯。 [表2] (試驗例1)芯密度ρ之測定 對實施例1及實施例2中製作出之環形芯之尺寸及重量進行測定,根據該等數值算出各環形芯之密度(芯密度)ρ(單位:g/cc)。將其結果表示於表1及表2。 (試驗例2)初始磁導率μ0之測定 關於對實施例1及實施例2中製作出之環形芯分別以1次側40次、2次側10次之方式捲繞被覆銅線而獲得之環形線圈,使用阻抗分析儀(HP公司製造「4192A」),以100 kHz之條件測定初始磁導率μ0。將結果表示於表1及表2。 (試驗例3)μ5500之測定 使用試驗例2中製作出之環形線圈,以100 kHz之條件疊加直流電流,測定該疊加之直流電流之感應磁場為5500 A/m時之相對磁導率μ5500。將測定結果表示於表1。 (試驗例4)徑向壓碎強度之測定 藉由根據JIS Z2507:2000之試驗方法而測定實施例1及實施例2中製作出之環形芯,求出徑向壓碎強度。將測定結果表示於表1及表2。 (試驗例5)絕緣耐壓之測定 測定實施例1及實施例2中製作出之環形芯之絕緣破壞電壓(單位:V)(測定機器:菊水電子工業公司製造「TOS5051」)。測定係根據JISC2110-1進行,利用金屬板夾住圖1所示之環形芯之兩端面,以60秒階段升壓試驗進行。根據所獲得之絕緣破壞電壓,求出絕緣破壞電場(單位:V/mm)。將其結果表示於表1及表2。 (試驗例6)鐵損Pcv之測定 關於對實施例1及實施例2中製作出之環形芯分別以1次側15次、2次側10次之方式捲繞被覆銅線而獲得之環形線圈,使用BH分析儀(岩崎通信機公司製造「SY-8217」),以有效最大磁通密度Bm為15 mT之條件,在測定頻率為2 MHz下測定鐵損Pcv(單位:kW/m3 )。將測定結果表示於表1及表2。 (評估例1)μ5500×絕緣耐壓×徑向壓碎強度 基於由試驗例3至試驗例5而測定出之結果,算出μ5500×絕緣耐壓×徑向壓碎強度。將算出結果表示於表3及表4以及圖5。再者,關於上述表及圖中之「相對值」,於實施例1中表示藉由實施例1-1中之μ5500×絕緣耐壓×徑向壓碎強度將實施例1-2至實施例1-9之值標準化之結果,於實施例2中表示藉由實施例2-1中之μ5500×絕緣耐壓×徑向壓碎強度將實施例2-2至實施例2-8之值標準化之結果。 [表3] [表4] 如表3及表4以及圖5所示,於實施例1中,與實施例2對比可獲得如下結果:若第一混合比率成為30質量%以上且70質量%以下,則相對值特異地變高。可知尤其於40質量%以上且60質量%以下,該傾向較為明顯。 (實施例3) 使用實施例1中製造出之非晶質磁性材料之粉末,變更分級條件而準備非晶質粉末中值粒徑D50 A為表5所示之值之非晶質磁性材料之粉末。又,作為結晶質磁性材料之粉末,準備作為Fe-Si-Cr系合金且結晶質粉末中值粒徑D50 C為表5所示之值之粉末。將上述非晶質磁性材料之粉末及結晶質磁性材料之粉末以第一混合比率成為50質量%之方式混合而獲得磁性粉末。以下,與實施例1同樣地獲得複數種環形芯。關於所獲得之環形芯,與實施例1之情形同樣地進行各種測定及評估。將結果表示於表5。 [表5] (實施例4) 使用實施例1中製造出之非晶質磁性材料之粉末,變更分級條件而準備中值粒徑D50 A為5.0 μm之非晶質磁性材料之粉末。又,作為結晶質磁性材料之粉末,準備作為Fe-Si-Cr系合金且中值粒徑D50 C為表6所示之值之粉末。將上述非晶質磁性材料之粉末及結晶質磁性材料之粉末以第一混合比率成為30質量%之方式混合而獲得磁性粉末。以下,與實施例1同樣地獲得複數種環形芯。關於所獲得之環形芯,與實施例1之情形同樣地進行各種測定及評估。將結果表示於表6。 [表6] 如表5及表6以及圖示有鐵損Pcv之測定結果之圖6及圖7所示,關於非晶質磁性材料之粉末及結晶質磁性材料之粉末之任一者,均確認存在若中值粒徑增加則鐵損Pcv增加之傾向。又,如表5及表6以及圖示有相對值之測定結果之圖8及圖9所示,確認藉由非晶質磁性材料之粉末之中值粒徑D50 A為5 μm以上且8 μm以下,或結晶質磁性材料之粉末之中值粒徑D50 C為2.5 μm以上且6 μm以下,而μ5500×絕緣耐壓×徑向壓碎強度特異地變高。 (實施例5) 使用實施例1中製造出之非晶質磁性材料之粉末,變更分級條件而準備中值粒徑D50 A為5.0 μm(實施例5-1)、6.5 μm(實施例5-2)、及11.0 μm(實施例5-3)之非晶質磁性材料之粉末。又,作為結晶質磁性材料之粉末,準備作為Fe-Si-Cr系合金且中值粒徑D50 C為4.0 μm之粉末。將上述非晶質磁性材料之粉末及結晶質磁性材料之粉末以第一混合比率成為50質量%之方式混合而獲得磁性粉末。以下,與實施例1同樣地獲得複數種環形芯。關於所獲得之環形芯,與實施例1之情形同樣地進行各種測定及評估。將結果表示於表7及圖10。 [表7] (實施例6) 使用實施例1中製造出之非晶質磁性材料之粉末,變更分級條件而準備中值粒徑D50 A為6.5 μm之非晶質磁性材料之粉末。又,作為結晶質磁性材料之粉末,準備作為Fe-Si-Cr系合金且中值粒徑D50 C為2.0 μm(實施例5-1)、4.0 μm(實施例5-2)、及6.0 μm(實施例5-3)之粉末。將上述非晶質磁性材料之粉末及結晶質磁性材料之粉末以第一混合比率成為50質量%之方式混合而獲得磁性粉末。以下,與實施例1同樣地獲得複數種環形芯。關於所獲得之環形芯,與實施例1之情形同樣地進行各種測定及評估。將結果表示於表8及圖11。 [表8] 圖12表示將實施例5及實施例6之結果藉由實施例5-2(即實施例6-2)之結果而標準化,並且橫軸表示非晶質磁性材料之中值粒徑D50 A相對於結晶質磁性材料之粉末之中值粒徑D50 C之比(D50 A/D50 C)的曲線圖。如圖12所示,μ5500×絕緣耐壓×徑向壓碎強度相對於D50 A/D50 C之依存性成為具有頂點位於D50 A/D50 C為1.3至2.0之範圍之山型之傾向線的分佈。 [產業上之可利用性] 具備本發明之壓粉芯之電感器可較佳地用作成為DC-DC轉換器等開關電源電路之構成零件之電感器。Hereinafter, embodiments of the present invention will be described in detail. 1. Powder core The powder core 1 of one embodiment of the present invention shown in Fig. 1 has an annular core shape and contains a powder of a crystalline magnetic material and a powder of an amorphous magnetic material. The powder core 1 of the present embodiment is manufactured by a production method including a molding process including press molding a mixture containing the powders. The powder core 1 of the present embodiment contains a powder in which a powder of a crystalline magnetic material and a powder of an amorphous magnetic material are adhered to other materials contained in the powder core 1 (the same type of material exists). In the case of the case, there are also bonding components for the case of different kinds of materials. (1) Powder of crystalline magnetic material The crystal magnetic material of the powder of the crystalline magnetic material contained in the dust core 1 of one embodiment of the present invention is crystalline (determined by usual X-ray diffraction) A diffraction spectrum having a clear peak at a specific level of material can be obtained and ferromagnetic, including an Fe-Si-Cr alloy. The Fe-Si-Cr alloy is a material having a relatively high saturation magnetic flux density, good soft magnetic properties, and high specific resistance among crystalline magnetic materials. Therefore, compared with other crystalline magnetic materials, for example, carbonyl iron powder, the loss is low even under conditions of high magnetic field and high frequency, and it is easy to exhibit good magnetic properties. Therefore, by making the powder of the crystalline magnetic material contained in the powder core 1 contain the Fe—Si—Cr-based alloy, even if the content of the powder of the crystalline magnetic material is increased relative to the crystalline magnetic material in the powder core 1 The mass ratio of the content of the powder to the sum of the contents of the powder of the amorphous magnetic material (also referred to as "the first mixing ratio" in the present specification), and the relative magnetic permeability in a high magnetic field environment, specifically, μ5500 Not easy to reduce. The content of Si and the content of Cr in the Fe-Si-Cr alloy are not limited. By way of example, the content of Si is about 2 to 7% by mass, the content of Cr is about 2 to 7% by mass, and the rest is Fe and unavoidable impurities. The shape of the powder of the crystalline magnetic material contained in the dust core 1 according to the embodiment of the present invention is not limited. The shape of the powder may be spherical or non-spherical. In the case of an aspherical shape, it may have a shape having an anisotropic shape such as a scaly shape, an elliptical shape, a droplet shape, or a needle shape. The shape of the powder may be a shape obtained at the stage of producing the powder, or may be a shape obtained by secondary processing of the produced powder. The shape of the former is exemplified by a spherical shape, an elliptical shape, a droplet shape, a needle shape, or the like, and the shape of the latter is exemplified by a scaly shape. The particle diameter of the powder of the crystalline magnetic material contained in the dust core 1 according to the embodiment of the present invention is such that the cumulative particle diameter distribution from the small particle diameter side in the volume-based particle size distribution becomes 50% ( Also referred to as "crystallized powder median diameter" in the present specification, D 50 C is 2.5 μm or more and 6 μm or less. When the crystal powder median diameter D 50 C is in the above range, when the first mixing ratio is 30% by mass or more and 70% by mass or less, the μ5500×insulation withstand voltage×radial crushing strength can be specifically increased. . There is a case where the crystal powder median diameter D 50 C is preferably 2.5 μm or more and 5.5 μm or less, in consideration of the influence of the high frequency, particularly the iron loss Pcv of 1 MHz or more. At least a portion of the powder of the crystalline magnetic material may also be subjected to surface insulation treatment. When the surface of the crystalline magnetic material was subjected to surface insulation treatment, the tendency of the insulation resistance of the powder core 1 to be improved was observed. The type of surface insulation treatment performed on the powder of the crystalline magnetic material is not limited. Phosphoric acid treatment, phosphate treatment, oxidation treatment, and the like are exemplified. (2) Powder of amorphous magnetic material The amorphous magnetic material which provides the powder of the amorphous magnetic material contained in the powder core 1 of one embodiment of the present invention is amorphous (by the usual X) The ray diffraction measurement does not provide a diffraction spectrum having a clear peak to the extent that the material type can be specified, and is a ferromagnetic material, particularly a soft magnetic material, and the specific type is not limited. Specific examples of the amorphous magnetic material include an Fe-Si-B based alloy, an Fe-PC based alloy, and a Co-Fe-Si-B based alloy. The amorphous magnetic material may be composed of one material or a plurality of materials. The magnetic material constituting the powder of the amorphous magnetic material is preferably one or more selected from the group consisting of the above materials, and among these, it is preferable to contain an Fe-PC alloy, preferably It is an alloy containing Fe-PC. Specific examples of the Fe-PC-based alloy include Fe-based amorphous alloys having a composition formula of Fe 100 atom % - a - b - c - x - y - z - t Ni a Sn b Cr c P x C y B z Si t represents, and 0 atom% ≦ a ≦ 10 atom%, 0 atom% ≦ b ≦ 3 atom%, 0 atom% ≦ c ≦ 6 atom%, 6.8 atom% ≦ x ≦ 13 atom%, 2.2 Atomic % ≦ y ≦ 13 Atomic %, 0 Atomic % ≦ z ≦ 9 Atomic %, 0 Atomic % ≦ t ≦ 7 Atomic %. In the above composition formula, Ni, Sn, Cr, B, and Si are arbitrary added elements. The addition amount a of Ni is preferably 0 atom% or more and 6 atom% or less, more preferably 0 atom% or more and 4 atom% or less. The addition amount b of Sn is preferably 0 atom% or more and 2 atom% or less, and may be added in a range of 1 atom% or more and 2 atom% or less. The amount c of Cr added is preferably 0 atom% or more and 2 atom% or less, more preferably 1 atom% or more and 2 atom% or less. There is also a case where the addition amount x of P is preferably 8.8 atom% or more. The addition amount y of C is preferably 5.8 atom% or more and 8.8 atom% or less. The amount z of addition of B is preferably 0 atom% or more and 3 atom% or less, more preferably 0 atom% or more and 2 atom% or less. The amount t of addition of Si is preferably 0 atom% or more and 6 atom% or less, more preferably 0 atom% or more and 2 atom% or less. The shape of the powder of the amorphous magnetic material contained in the powder core 1 according to the embodiment of the present invention is not limited. The type of the shape of the powder is the same as that of the powder of the crystalline magnetic material, and thus the description thereof is omitted. There is also a case where the amorphous magnetic material is easily formed into a spherical shape or an ellipsoidal shape in terms of the manufacturing method. Further, in general, since the amorphous magnetic material is harder than the crystalline magnetic material, it is preferable that the crystalline magnetic material is non-spherical and is easily deformed at the time of press molding. The shape of the powder of the amorphous magnetic material contained in the powder core 1 according to the embodiment of the present invention may be a shape obtained at the stage of producing the powder, or may be performed by secondary processing of the produced powder. Get the shape. The shape of the former is exemplified by a spherical shape, an elliptical shape, a needle shape, or the like, and the shape of the latter is exemplified by a scaly shape. The particle size of the powder of the amorphous magnetic material contained in the powder core 1 according to the embodiment of the present invention is 50% of the particle size distribution from the small particle size side in the volume-based particle size distribution. (also referred to as "amorphous powder median diameter" in the present specification) D 50 A is preferably 5 μm or more and 8 μm or less. When the amorphous powder median diameter D 50 A is 5 μm or more when the first mixing ratio is 30% by mass or more and 70% by mass or less, the μ5500×insulation withstand strength×radial crushing strength can be specifically increased. From this viewpoint, the amorphous powder median diameter D 50 A is more preferably 5.5 μm or more. On the other hand, there is also a case where the amorphous powder has a median particle diameter D 50 A which is excessively large, and has a μ5500×insulation withstand voltage×radial crushing strength reduction, or iron loss Pcv, especially in high frequency. The tendency of the iron loss Pcv to increase. Therefore, the amorphous powder median diameter D 50 A is preferably 8 μm or less, more preferably 7 μm or less. Further, the particle diameter of the powder of the amorphous magnetic material contained in the powder core 1 according to the embodiment of the present invention may have the following relationship with the particle diameter of the powder of the amorphous magnetic material contained in the powder core 1. . That is, the amorphous powder median diameter D 50 A and the crystalline powder median diameter D 50 C may satisfy the following formula (1). 1≦D 50 A/D 50 C≦3.5 (1) By setting D 50 A/D 50 C in the range of 1 to 3.5, it is easy to specifically increase μ5500×insulation withstand voltage×radial pressure with respect to the powder core 1 Broken strength. From the viewpoint of more stably achieving a specific increase of μ5500 × insulation withstand voltage × radial crush strength, D 50 A/D 50 C preferably exists in the range of 1.2 to 2.5, and is preferably in the presence of The case of the range of 1.3 to 2.0. The first mixing ratio is preferably 40% by mass or more and 60% by mass or less, more preferably from the viewpoint that the powder core 1 is made to have a specific height of μ5500×insulation pressure×radial crushing strength. It is 40% by mass or more and 55% by mass or less. (3) Bonding Component The powder core 1 may contain a bonding component that bonds a powder of a crystalline magnetic material and a powder of an amorphous magnetic material to other materials contained in the powder core 1. The binder component is a powder which contributes to the powder of the crystalline magnetic material and the amorphous magnetic material contained in the powder core 1 of the present embodiment (in the present specification, the powder may be collectively referred to as "the powder". The material of the magnetic powder ") is not limited in its composition. Examples of the material constituting the binder component include an organic material such as a thermal decomposition residue of a resin material and a resin material (in the present specification, collectively referred to as "component based on a resin material"), and an inorganic material. Examples of the resin material include an acrylic resin, an anthrone resin, an epoxy resin, a phenol resin, a urea resin, and a melamine resin. A glass-based material such as water glass is exemplified as the binder component composed of an inorganic material. The bonding component may be composed of one material or a plurality of materials. The bonding component may also be a mixture of an organic material and an inorganic material. As the bonding component, an insulating material is usually used. Thereby, the insulation property of the powder core 1 can be improved. 2. Method for Producing Powder Core The method for producing the powder core 1 according to the embodiment of the present invention is not particularly limited. However, the production method described below is adopted to realize the production of the powder core 1 more efficiently. The method for producing the powder core 1 according to the embodiment of the present invention includes the molding step described below, and may further include a heat treatment step. (1) Forming Step First, a mixture containing a magnetic powder and a component which provides a binder component in the powder core 1 is prepared. The component that provides the bonding component (also referred to as "adhesive component" in the present specification) is either in the case of the bonding component itself or in the case of a material different from the bonding component. Specific examples of the latter include a case where the binder component is a resin material and the binder component is a thermally decomposed residue. Such a thermal decomposition residue is formed by a heat treatment step which is carried out after the forming step as described below. The shaped article can be obtained by a press forming process comprising the mixture. The pressurization conditions are not limited, and are appropriately set based on the composition of the binder component and the like. For example, in the case where the binder component includes a thermosetting resin, it is preferred to carry out pressurization and heating together to carry out a curing reaction of the resin in the mold. On the other hand, in the case of compression molding, although the pressing force is high, heating is not a necessary condition, and the pressing time is short. The pressing force in the case of compression molding is appropriately set. When it is not limited to an example, it is 0.5 GPa or more and 2 GPa or less, and preferably 1 GPa or more and 2 GPa or less. Hereinafter, the case where the mixture is a granulated powder and compression-molded will be described in some detail. Since the granulated powder is excellent in workability, workability in a compression molding step which is short in molding time and excellent in productivity can be improved. (1-1) Granulated powder The granulated powder contains a magnetic powder and a binder component. The content of the binder component in the granulated powder is not particularly limited. When the content is too low, the binder component does not easily retain the magnetic powder. Further, when the content of the binder component is too low, in the powder core 1 obtained by the heat treatment step, the binder component containing the thermal decomposition residue of the binder component is not easy to insulate the plurality of magnetic powders from each other with other magnetic powders. . On the other hand, when the content of the above-mentioned binder component is too high, the content of the binder component contained in the powder core 1 obtained by the heat treatment step tends to be high. When the content of the binder component in the powder core 1 becomes high, the magnetic properties of the powder core 1 are liable to lower. Therefore, the content of the binder component in the granulated powder is preferably 0.5% by mass or more and 5.0% by mass or less based on the total amount of the granulated powder. The content of the binder component in the granulated powder is preferably 1.0% by mass or more and 3.5% by mass based on the total amount of the granulated powder, from the viewpoint of more stably reducing the possibility that the magnetic properties of the powder core 1 are lowered. The amount below is more preferably 1.2% by mass or more and 3.0% by mass or less. The granulated powder may also contain materials other than the above magnetic powder and binder components. As such a material, a lubricant, a decane coupling agent, an insulating filler, or the like is exemplified. In the case of containing a lubricant, the kind thereof is not particularly limited. It can be an organic lubricant or an inorganic lubricant. Specific examples of the organic-based lubricant include metal soaps such as zinc stearate and aluminum stearate. It is considered that such an organic-based lubricant is vaporized in the heat treatment step and hardly remains in the powder core 1. The method for producing the granulated powder is not particularly limited. The granulated powder may be directly kneaded, and the obtained kneaded product may be pulverized by a known method to obtain a granulated powder, or a dispersing medium (for example, water may be mentioned) may be added to the above-mentioned components. The slurry is formed, and the slurry is dried and pulverized to obtain a granulated powder. It can also be sieved or classified after pulverization to control the particle size distribution of the granulated powder. An example of a method of obtaining a granulated powder from the above slurry is a method using a spray dryer. As shown in FIG. 2, a rotor 201 is provided in the spray dryer device 200, and the slurry S is injected toward the rotor 201 from the upper portion of the device. The rotor 201 is rotated at a specific number of revolutions, and the slurry S is sprayed in a droplet form by centrifugal force in a chamber inside the spray dryer device 200. Further, hot air is introduced into the chamber inside the spray dryer device 200, whereby the dispersion medium (water) contained in the droplet-shaped slurry S is volatilized in a state of maintaining a droplet shape. As a result, the granulated powder P is formed from the slurry S. This granulated powder P is recovered from the lower portion of the spray dryer unit 200. The number of revolutions of the rotor 201, the temperature of the hot air introduced into the spray dryer device 200, and the temperature of the lower portion of the chamber may be appropriately set. As a specific example of the setting range of the parameters, the number of revolutions of the rotor 201 may be 4,000 to 8,000 rpm, and the temperature of the hot air introduced into the spray dryer device 200 may be 100 to 170 ° C, and the temperature at the lower portion of the chamber may be 80 to 8%. 90 ° C. Moreover, the environment and pressure in the chamber can be set as appropriate. As an example, the chamber is an atmospheric (air) environment, and the pressure is 2 mmH 2 O (about 0.02 kPa) at a pressure difference from atmospheric pressure. The particle size distribution of the obtained granulated powder P can also be controlled by sieving or the like. (1-2) Pressurization Conditions The pressurization conditions in compression molding are not particularly limited. It suffices to appropriately set the composition of the granulated powder, the shape of the molded article, and the like. When the pressing force at the time of compression molding of the granulated powder is too low, the mechanical strength of the molded article is lowered. Therefore, problems such as a decrease in workability of the molded article and a decrease in mechanical strength of the powder core 1 obtained from the molded article are likely to occur. Further, there is a case where the magnetic properties of the powder core 1 are lowered or the insulation properties are lowered. On the other hand, in the case where the pressing force at the time of compression molding of the granulated powder is too high, it is difficult to form a molding die capable of withstanding the pressure. The pressure applied to the compression molding of the granulated powder from the viewpoint of more stably reducing the possibility that the compression and pressurization step adversely affects the mechanical or magnetic properties of the powder core 1, and is industrially easy to mass-produce. It is preferably 0.3 GPa or more and 2 GPa or less, more preferably 0.5 GPa or more and 2 GPa or less, and particularly preferably 0.8 GPa or more and 2 GPa or less. In the compression molding, the pressure may be applied while heating, or may be performed at normal temperature. (2) Heat Treatment Step The molded article obtained by the forming step may be the powder core 1 of the present embodiment, and the powder core 1 may be obtained by subjecting the molded article to a heat treatment step as described below. In the heat treatment step, the molded article obtained by the above-described forming step is heated, thereby adjusting the magnetic properties by correcting the distance between the magnetic powders and imparting strain relief to the magnetic powder in the forming step. The magnetic properties are adjusted to obtain the powder core 1. The heat treatment step is as described above in order to adjust the magnetic properties of the powder core 1, and the heat treatment conditions such as the heat treatment temperature are set such that the magnetic properties of the powder core 1 are optimized. As an example of the method of setting the heat treatment conditions, the heating temperature of the molded article is changed, and other conditions such as the temperature increase rate and the holding time at the heating temperature are fixed. The evaluation criteria of the magnetic properties of the powder core 1 when the heat treatment conditions are set are not particularly limited. As a specific example of the evaluation item, the iron loss Pcv of the powder core 1 can be mentioned. In this case, the heating temperature of the molded article may be set so that the iron loss Pcv of the powder core 1 is the lowest. The measurement conditions of the iron loss Pcv are appropriately set, and examples thereof include a condition in which the frequency is 2 MHz and the effective maximum magnetic flux density Bm is 15 mT. The environment at the time of heat treatment is not particularly limited. In the case of an oxidizing environment, the possibility of excessive thermal decomposition of the binder component or the possibility of progress of oxidation of the magnetic powder is improved. Therefore, it is preferably carried out in an inert environment such as nitrogen or argon or a reducing atmosphere such as hydrogen. Heat treatment. In the case where the binder component is formed of a resin material, there is a case where the binder component becomes a thermal decomposition residue by the heat treatment as described above. It is considered that when the strain is relaxed as described above, the binder component becomes a thermal decomposition residue. 3. Inductor, Electronic/Electrical Apparatus An inductor according to an embodiment of the present invention includes the powder core 1, the coil, and a connection terminal connected to each end portion of the coil according to an embodiment of the present invention. Here, at least a part of the powder core 1 is disposed so as to be located in an induced magnetic field generated by the current when a current flows through the coil via the connection terminal. Since the inductor according to the embodiment of the present invention includes the powder core 1 according to the embodiment of the present invention, it has excellent DC superposition characteristics and is excellent in insulation properties and mechanical properties. An example of such an inductor is the toroidal coil 10 shown in FIG. The loop coil 10 includes a coil 2a formed by winding a covered conductive wire 2 around a ring-shaped powder core (ring core) 1. The end portions 2d and 2e of the coil 2a can be defined in a portion of the conductive line between the coil 2a composed of the wound coated conductive wire 2 and the end portions 2b and 2c covering the conductive wire 2. As described above, in the inductor of the present embodiment, the member constituting the coil and the member constituting the connection terminal may be formed of the same member. Another example of the inductor according to an embodiment of the present invention includes the coil-embedded inductor 20 shown in Fig. 4 . The coil-embedded inductor 20 can be formed in a small piece shape of several mm square, and has a powder core 21 having a box shape, and a coil portion 22c covering the conductive wire 22 is buried therein. The end portions 22a and 22b of the coated conductive wire 22 are located on the surface of the dust core 21 and exposed. A portion of the surface of the powder core 21 is covered by electrically connecting the ends 23a, 23b independently of each other. The connection end portion 23a is electrically connected to the end portion 22a of the covered conductive wire 22, and the connection end portion 23b is electrically connected to the end portion 22b of the covered conductive wire 22. In the coil-embedded inductor 20 shown in FIG. 4, the end portion 22a of the covered conductive wire 22 is covered by the connection end portion 23a, and the end portion 22b of the covered conductive wire 22 is covered by the connection end portion 23b. The method of embedding the coil portion 22c of the conductive wire 22 in the powder core 21 is not limited. The member around which the coated conductive wire 22 is wound may be placed in a mold, and the mixture containing the magnetic powder (granulated powder) may be supplied into the mold to be press-formed. Alternatively, a plurality of members including a mixture of magnetic powders (granulated powder) may be prepared in advance, and the members may be combined, and the coated conductive wires 22 may be placed in the void portions formed at this time to obtain an assembly. The assembly is subjected to press forming. The material of the covered conductive wire 22 including the coil portion 22c is not limited. For example, a copper alloy can be cited. The coil portion 22c may also be an edge coil. The material of the connection end portions 23a and 23b is also not limited. There is a case where it is preferable to provide a metallized layer formed of a conductive paste such as a silver paste and a plating layer formed on the metallized layer from the viewpoint of excellent productivity. The material forming the plating layer is not limited. Examples of the metal element contained in the material include copper, aluminum, zinc, nickel, iron, tin, and the like. Electronic and electric equipment system of one embodiment of the present invention is mounted with one embodiment of the present invention, electronic and electric apparatuses form of inductors, inductor-based and which use a connection terminal connected to the substrate. An example of a circuit including the inductor is a switching power supply circuit such as a DC-DC converter. In response to various requirements such as miniaturization, weight reduction, and high functionality of electronic and electrical equipment, the switching power supply circuit has a tendency to increase the switching frequency and increase the amount of current flowing through the circuit. Therefore, the current flowing through the inductor which is a component of the circuit also tends to have a high fluctuation frequency and an increase in the average current amount. In this regard, as described above, the inductor including the powder core according to the embodiment of the present invention can be appropriately operated in a high magnetic field environment even if it is small and has a low height. Therefore, in the switching power supply circuit including the inductor, the decrease in efficiency is suppressed, and the above various requirements can be responded to without causing heat generation. In this way, the electronic / electrical device to which the inductor of one embodiment of the present invention is mounted can be reduced in size and weight, and can be realized with high functionality. The embodiments described above are described in order to facilitate the understanding of the present invention, and are not intended to limit the present invention. Therefore, it is intended that all of the elements of the embodiments disclosed herein are intended to include all modifications and equivalents. [Examples] Hereinafter, the present invention will be specifically described by way of Examples and the like, but the scope of the present invention is not limited to the Examples and the like. (Example 1) (1) The Fe-based amorphous alloy powder was produced in such a manner as to be composed of Fe 71 atom % Ni 6 atom % Cr 2 atom % P 11 atom % C 8 atom % B 2 atom % . A raw material was used to prepare a powder (amorphous powder) of an amorphous magnetic material by a water atomization method. The powder of the obtained amorphous magnetic material was classified, and the particle size distribution of the classified powder was measured by volume distribution using "Microtrac particle size distribution measuring apparatus MT3300EX" manufactured by Nikkiso Co., Ltd. The particle size distribution from the small particle size side in the volume-based particle size distribution was 50% (the amorphous powder median diameter) D 50 A was 6.5 μm. Further, as the powder of the crystalline magnetic material, a powder containing Fe-Si-Cr-based alloy, specifically, a content of Si of 3.5% by mass, a content of Cr of 4.5% by mass, and the balance being Fe and inevitable are prepared. An alloy of impurities, and the crystalline powder had a median diameter D 50 C of 4.0 μm. Therefore, in the powder of Example 1, D 50 A/D 50 C was 1.6. (2) Preparation of granulated powder The powder of the amorphous magnetic material and the powder of the crystalline magnetic material were mixed so as to have a first mixing ratio shown in Table 1, to obtain a magnetic powder. 97.2 parts by mass of the magnetic powder, 2 to 3 parts by mass of the insulating binder containing the acrylic resin and the phenol resin, and 0 to 0.5 parts by mass of the lubricant containing zinc stearate are mixed in water as a solvent to obtain a slurry. The obtained slurry was granulated under the above conditions using the spray dryer device 200 shown in Fig. 2 to obtain a granulated powder. (3) Compression molding The obtained granulated powder was filled in a mold, and subjected to press molding at a surface pressure of 1 GPa to obtain a molded body having a ring shape of an outer diameter of 20 mm × an inner diameter of 12 mm × a thickness of 3 mm. (4) Heat treatment The obtained shaped body is placed in a furnace in a nitrogen gas flow environment, and the furnace temperature is heated from room temperature (23 ° C) at a heating rate of 10 ° C / min to an optimum core heat treatment temperature of 200 to 400 ° C. The temperature was maintained at this temperature for 1 hour, and then heat-treated in a furnace to cool to room temperature to obtain a toroidal core including a powder core. [Table 1] (Example 2) Using the powder of the amorphous magnetic material produced in Example 1, the classification conditions were changed to prepare a powder of an amorphous magnetic material having an amorphous powder median diameter D 50 A of 5.0 μm. Further, as the powder of the crystalline magnetic material, a powder containing Fe-Si-Cr-based alloy, specifically, a content of Si of 6.4% by mass, a content of Cr of 3.1% by mass, and the balance of Fe and inevitable impurities were prepared. The alloy was obtained, and the crystalline powder had a median diameter D 50 C of 2.0 μm. Therefore, in the powder of Example 2, D 50 A/D 50 C was 2.5. The powder of the amorphous magnetic material and the powder of the crystalline magnetic material were mixed so as to have a first mixing ratio shown in Table 2 to obtain a magnetic powder. Hereinafter, a plurality of ring cores were obtained in the same manner as in Example 1. [Table 2] (Test Example 1) Measurement of Core Density ρ The dimensions and weights of the ring cores produced in Examples 1 and 2 were measured, and the density (core density) of each of the ring cores was calculated based on the values (unit: g /cc). The results are shown in Tables 1 and 2. (Test Example 2) Measurement of Initial Magnetic Permeability μ0 The ring-shaped cores produced in Examples 1 and 2 were obtained by winding a coated copper wire 10 times on the primary side and 10 times on the secondary side. The toroidal coil was measured for the initial magnetic permeability μ0 at 100 kHz using an impedance analyzer ("4192A" manufactured by HP Corporation). The results are shown in Tables 1 and 2. (Test Example 3) Measurement of μ5500 Using the toroidal coil produced in Test Example 2, a direct current was superimposed at 100 kHz, and the relative magnetic permeability μ5500 at which the induced magnetic field of the superimposed direct current was 5500 A/m was measured. The measurement results are shown in Table 1. (Test Example 4) Measurement of Radial Crush Strength The radial crush strength was determined by measuring the ring cores produced in Examples 1 and 2 according to the test method of JIS Z 2507:2000. The measurement results are shown in Tables 1 and 2. (Testing Example 5) Measurement of the dielectric breakdown voltage The dielectric breakdown voltage (unit: V) of the toroidal core produced in Example 1 and Example 2 (measurement equipment: "TOS5051" manufactured by Kikusui Electronics Co., Ltd.) was measured. The measurement was carried out in accordance with JIS C2110-1, and the both end faces of the annular core shown in Fig. 1 were sandwiched by a metal plate, and subjected to a 60-second step pressure test. The dielectric breakdown electric field (unit: V/mm) was obtained from the obtained insulation breakdown voltage. The results are shown in Tables 1 and 2. (Test Example 6) Measurement of Iron Loss Pcv The toroidal coil obtained by winding the coated copper wire on the primary side 15 times and the secondary side 10 times, respectively, in the ring cores produced in Example 1 and Example 2 Using a BH analyzer ("Yi-8217" manufactured by Iwasaki Communications Co., Ltd.), the iron loss Pcv (unit: kW/m 3 ) was measured at a measurement frequency of 2 MHz with an effective maximum magnetic flux density Bm of 15 mT. . The measurement results are shown in Tables 1 and 2. (Evaluation Example 1) μ5500 × insulation withstand voltage × radial crushing strength Based on the results measured by Test Example 3 to Test Example 5, μ5500 × insulation withstand voltage × radial crushing strength was calculated. The calculated results are shown in Tables 3 and 4 and FIG. Further, regarding the "relative value" in the above table and the drawings, in Example 1, the examples 1-2 to the examples were shown by the μ5500×insulation withstand strength×radial crushing strength in Example 1-1. The results of the standardization of values of 1-9 are shown in Example 2 to normalize the values of Examples 2-2 to 2-8 by the μ5500×insulation withstand strength×radial crush strength in Example 2-1. The result. [table 3] [Table 4] As shown in Table 3 and Table 4 and FIG. 5, in the first embodiment, as compared with the second embodiment, when the first mixing ratio is 30% by mass or more and 70% by mass or less, the relative value is specifically changed. high. It is understood that this tendency is remarkable particularly in the case of 40% by mass or more and 60% by mass or less. (Example 3) Using the powder of the amorphous magnetic material produced in Example 1, the classification conditions were changed, and the amorphous magnetic material having the amorphous powder median diameter D 50 A as shown in Table 5 was prepared. Powder. Further, as the powder of the crystalline magnetic material, a powder having a value of the crystal powder of the Fe-Si-Cr alloy and having a median diameter D 50 C as shown in Table 5 was prepared. The powder of the amorphous magnetic material and the powder of the crystalline magnetic material were mixed at a first mixing ratio of 50% by mass to obtain a magnetic powder. Hereinafter, a plurality of ring cores were obtained in the same manner as in Example 1. Regarding the obtained toroidal core, various measurements and evaluations were carried out in the same manner as in the case of Example 1. The results are shown in Table 5. [table 5] (Example 4) Using the powder of the amorphous magnetic material produced in Example 1, the classification conditions were changed, and a powder of an amorphous magnetic material having a median diameter D 50 A of 5.0 μm was prepared. Further, as the powder of the crystalline magnetic material, a powder having a value of the value shown in Table 6 as the Fe-Si-Cr-based alloy and having a median diameter D 50 C was prepared. The powder of the amorphous magnetic material and the powder of the crystalline magnetic material were mixed at a first mixing ratio of 30% by mass to obtain a magnetic powder. Hereinafter, a plurality of ring cores were obtained in the same manner as in Example 1. Regarding the obtained toroidal core, various measurements and evaluations were carried out in the same manner as in the case of Example 1. The results are shown in Table 6. [Table 6] As shown in Fig. 6 and Fig. 6 and the results of the measurement of the iron loss Pcv, the powder of the amorphous magnetic material and the powder of the crystalline magnetic material are confirmed to be present. When the value of the particle diameter increases, the iron loss Pcv tends to increase. Further, as shown in Figs. 8 and 9 and the measurement results of the relative values shown in Tables 5 and 9, it was confirmed that the powder of the amorphous magnetic material had a median diameter D 50 A of 5 μm or more and 8 The powder median diameter D 50 C of μm or less or the crystalline magnetic material is 2.5 μm or more and 6 μm or less, and the μ5500×insulation withstand voltage×radial crushing strength is specifically increased. (Example 5) Using the powder of the amorphous magnetic material produced in Example 1, the classification conditions were changed, and the median diameter D 50 A was prepared to be 5.0 μm (Example 5-1) and 6.5 μm (Example 5) -2), and a powder of an amorphous magnetic material of 11.0 μm (Example 5-3). Further, as the powder of the crystalline magnetic material, a powder having a median diameter D 50 C of 4.0 μm as an Fe—Si—Cr-based alloy was prepared. The powder of the amorphous magnetic material and the powder of the crystalline magnetic material were mixed at a first mixing ratio of 50% by mass to obtain a magnetic powder. Hereinafter, a plurality of ring cores were obtained in the same manner as in Example 1. Regarding the obtained toroidal core, various measurements and evaluations were carried out in the same manner as in the case of Example 1. The results are shown in Table 7 and Figure 10. [Table 7] (Example 6) Using the powder of the amorphous magnetic material produced in Example 1, the classification conditions were changed, and a powder of an amorphous magnetic material having a median diameter D 50 A of 6.5 μm was prepared. Further, as a powder of a crystalline magnetic material, an Fe-Si-Cr alloy was prepared, and the median diameter D 50 C was 2.0 μm (Example 5-1), 4.0 μm (Example 5-2), and 6.0. Powder of μm (Example 5-3). The powder of the amorphous magnetic material and the powder of the crystalline magnetic material were mixed at a first mixing ratio of 50% by mass to obtain a magnetic powder. Hereinafter, a plurality of ring cores were obtained in the same manner as in Example 1. Regarding the obtained toroidal core, various measurements and evaluations were carried out in the same manner as in the case of Example 1. The results are shown in Table 8 and Figure 11. [Table 8] Figure 12 shows the results of Example 5 and Example 6 normalized by the results of Example 5-2 (i.e., Example 6-2), and the horizontal axis represents the median diameter D 50 A of the amorphous magnetic material. A graph of the ratio of the median diameter D 50 C (D 50 A/D 50 C) of the powder of the crystalline magnetic material. As shown in Fig. 12, the dependence of μ5500×insulation withstand voltage×radial crushing strength with respect to D 50 A/D 50 C becomes a mountain type having a vertex at a range of 1.3 to 2.0 in D 50 A/D 50 C. The distribution of the trend line. [Industrial Applicability] The inductor including the powder core of the present invention can be preferably used as an inductor that is a component of a switching power supply circuit such as a DC-DC converter.

1‧‧‧壓粉芯(環形芯)1‧‧‧Powder core (ring core)

2‧‧‧被覆導電線2‧‧‧covered conductive wire

2a‧‧‧線圈2a‧‧‧ coil

2b、2c‧‧‧被覆導電線2之端部2b, 2c‧‧‧ covered end of conductive wire 2

2d、2e‧‧‧線圈2a之端部2d, 2e‧‧‧ end of coil 2a

10‧‧‧環形線圈10‧‧‧Circular coil

20‧‧‧線圈埋設型電感器20‧‧‧Coil-embedded inductors

21‧‧‧壓粉芯21‧‧‧Powder core

22‧‧‧被覆導電線22‧‧‧coated conductive wire

22a‧‧‧端部22a‧‧‧End

22b‧‧‧端部22b‧‧‧End

23a‧‧‧連接端部23a‧‧‧Connected end

23b‧‧‧連接端部23b‧‧‧Connecting end

22c‧‧‧線圈部22c‧‧‧ coil department

200‧‧‧噴霧乾燥器裝置200‧‧‧ spray dryer unit

201‧‧‧轉子201‧‧‧Rotor

P‧‧‧造粒粉P‧‧‧Powder powder

S‧‧‧漿料S‧‧‧Slurry

圖1係概念性地表示本發明之一實施形態之壓粉芯之形狀的立體圖。 圖2係概念性地表示製造造粒粉之方法之一例中使用之噴霧乾燥器裝置及其動作的圖。 圖3係概念性地表示作為具備本發明之一實施形態之壓粉芯之電感器之一種的環形線圈之形狀的立體圖。 圖4係概念性地表示作為具備本發明之一實施形態之壓粉芯之電感器之一種的線圈埋設型電感器之形狀的立體圖。 圖5係表示實施例1及實施例2中之μ5500×絕緣耐壓×徑向壓碎強度(相對值)與第一混合比率之關係之曲線圖。 圖6係表示實施例3之結果之曲線圖,且係表示鐵損Pcv與非晶質磁性材料之粉末之中值粒徑D50 A之關係之曲線圖。 圖7係表示實施例4之結果之曲線圖,且係表示鐵損Pcv與結晶質磁性材料之粉末之中值粒徑D50 C之關係之曲線圖。 圖8係表示實施例3之結果之曲線圖,且係表示μ5500×絕緣耐壓×徑向壓碎強度(相對值)與非晶質磁性材料之粉末之中值粒徑D50 A之關係之曲線圖。 圖9係表示實施例4之結果之曲線圖,且係表示μ5500×絕緣耐壓×徑向壓碎強度(相對值)與結晶質磁性材料之粉末之中值粒徑D50 C之關係之曲線圖。 圖10係表示實施例5之結果之曲線圖,且係表示μ5500×絕緣耐壓×徑向壓碎強度(相對值)與非晶質磁性材料之粉末之中值粒徑D50 A之關係之曲線圖。 圖11係表示實施例6之結果之曲線圖,且係表示μ5500×絕緣耐壓×徑向壓碎強度(相對值)與結晶質磁性材料之粉末之中值粒徑D50 C之關係之曲線圖。 圖12係將實施例5及實施例6之結果藉由實施例5-2(即實施例6-2)之結果而標準化,並且將非晶質磁性材料之中值粒徑D50 A相對於結晶質磁性材料之粉末之中值粒徑D50 C之比(D50 A/D50 C)設為橫軸而表示的曲線圖。Fig. 1 is a perspective view conceptually showing the shape of a powder core according to an embodiment of the present invention. Fig. 2 is a view conceptually showing a spray dryer device used in an example of a method for producing a granulated powder and an operation thereof. Fig. 3 is a perspective view conceptually showing the shape of a loop coil which is one type of inductor having a powder core according to an embodiment of the present invention. Fig. 4 is a perspective view conceptually showing the shape of a coil-embedded inductor including one of the inductors of the powder core according to the embodiment of the present invention. Fig. 5 is a graph showing the relationship between μ5500 × insulation withstand voltage × radial crush strength (relative value) and the first mixing ratio in Example 1 and Example 2. Fig. 6 is a graph showing the results of Example 3, and is a graph showing the relationship between the iron loss Pcv and the powder median diameter D 50 A of the amorphous magnetic material. Fig. 7 is a graph showing the results of Example 4, and is a graph showing the relationship between the iron loss Pcv and the powder median diameter D 50 C of the crystalline magnetic material. Figure 8 is a graph showing the results of Example 3, and shows the relationship between μ5500 × insulation withstand voltage × radial crush strength (relative value) and the powder median diameter D 50 A of the amorphous magnetic material. Graph. Figure 9 is a graph showing the results of Example 4, and shows a relationship between μ5500 × insulation withstand voltage × radial crushing strength (relative value) and the powder median diameter D 50 C of the crystalline magnetic material. Figure. Figure 10 is a graph showing the results of Example 5, and shows the relationship between μ5500 × insulation withstand voltage × radial crush strength (relative value) and the powder median diameter D 50 A of the amorphous magnetic material. Graph. Figure 11 is a graph showing the results of Example 6, and is a graph showing the relationship between μ5500 × insulation withstand voltage × radial crush strength (relative value) and the powder median diameter D 50 C of the crystalline magnetic material. Figure. Figure 12 is a result of normalizing the results of Example 5 and Example 6 by the results of Example 5-2 (i.e., Example 6-2), and comparing the median diameter D 50 A of the amorphous magnetic material with respect to The ratio of the powder median diameter D 50 C (D 50 A/D 50 C) of the crystalline magnetic material is a graph represented by the horizontal axis.

Claims (11)

一種壓粉芯,其特徵在於:其係含有結晶質磁性材料之粉末及非晶質磁性材料之粉末者,且 上述結晶質磁性材料之粉末之含量相對於上述結晶質磁性材料之粉末之含量與上述非晶質磁性材料之粉末之含量之總和的質量比率即第一混合比率為30質量%以上且70質量%以下, 上述結晶質磁性材料包含Fe-Si-Cr系合金,且中值粒徑D50 C為2.5 μm以上且6 μm以下。A powder core characterized in that it contains a powder of a crystalline magnetic material and a powder of an amorphous magnetic material, and the content of the powder of the crystalline magnetic material is relative to the content of the powder of the crystalline magnetic material. The mass ratio of the total content of the powders of the amorphous magnetic material, that is, the first mixing ratio is 30% by mass or more and 70% by mass or less, and the crystalline magnetic material contains Fe-Si-Cr-based alloy and has a median diameter. D 50 C is 2.5 μm or more and 6 μm or less. 如請求項1之壓粉芯,其中上述非晶質磁性材料之粉末之中值粒徑D50 A為5 μm以上且8 μm以下。The powder core of claim 1, wherein the amorphous magnetic material has a powder median diameter D 50 A of 5 μm or more and 8 μm or less. 如請求項1或2之壓粉芯,其中上述非晶質磁性材料之粉末之中值粒徑D50 A與上述結晶質磁性材料之粉末之中值粒徑D50 C滿足下述式(1), 1≦D50 A/D50 C≦3.5 (1)。The powder core of claim 1 or 2, wherein the powder median diameter D 50 A of the amorphous magnetic material and the powder median diameter D 50 C of the crystalline magnetic material satisfy the following formula (1) ), 1≦D 50 A/D 50 C≦3.5 (1). 如請求項1或2之壓粉芯,其中上述第一混合比率為40質量%以上且60質量%以下。The powder core of claim 1 or 2, wherein the first mixing ratio is 40% by mass or more and 60% by mass or less. 如請求項1或2之壓粉芯,其中上述非晶質磁性材料包含選自由Fe-Si-B系合金、Fe-P-C系合金及Co-Fe-Si-B系合金所組成之群中之1種或2種以上之材料。The powder core of claim 1 or 2, wherein the amorphous magnetic material comprises a group selected from the group consisting of Fe-Si-B alloys, Fe-PC alloys, and Co-Fe-Si-B alloys. One or more materials. 如請求項5之壓粉芯,其中上述非晶質磁性材料包含Fe-P-C系合金。The powder core of claim 5, wherein the amorphous magnetic material comprises an Fe-P-C alloy. 如請求項1或2之壓粉芯,其含有黏結成分,該黏結成分使上述結晶質磁性材料之粉末及上述非晶質磁性材料之粉末黏結於上述壓粉芯中所含之其他材料。The powder core of claim 1 or 2, which contains a binder component which bonds the powder of the crystalline magnetic material and the powder of the amorphous magnetic material to other materials contained in the powder core. 如請求項7之壓粉芯,其中上述黏結成分包含基於樹脂材料之成分。The powder core of claim 7, wherein the bonding component comprises a component based on a resin material. 一種壓粉芯之製造方法,其特徵在於:其係製造如請求項8之壓粉芯之方法,且具備藉由包含混合物之加壓成形之成形處理而獲得成形製造物之成形步驟,該混合物包含上述結晶質磁性材料之粉末及上述非晶質磁性材料之粉末以及含有上述樹脂材料之黏合劑成分。A method for producing a powder core, which is characterized by the method of producing the powder core of claim 8, and comprising a forming step of obtaining a shaped article by a press forming process comprising a mixture of a mixture, the mixture A powder comprising the crystalline magnetic material and a powder of the amorphous magnetic material and a binder component containing the resin material. 一種電感器,其具備如請求項1至8中任一項之壓粉芯、線圈及連接於上述線圈之各自之端部之連接端子,且上述壓粉芯之至少一部分係以位於在經由上述連接端子對上述線圈流通電流時由上述電流產生之感應磁場內之方式配置。An inductor comprising the powder core of any one of claims 1 to 8, a coil, and a connection terminal connected to each end of the coil, and at least a portion of the powder core is located above The connection terminal is disposed in such a manner that an electric field generated by the current is generated when the current flows through the coil. 一種電子· 電氣機器,其係安裝有如請求項10之電感器之電子· 電氣機器,且上述電感器係由上述連接端子而連接於基板。An electronic-electric machine, like mounting request entries based electronic and electric equipment of the inductors 10 and the inductor by the line connecting terminal is connected to the substrate.
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