JPH04219902A - Dust core material and its manufacture - Google Patents
Dust core material and its manufactureInfo
- Publication number
- JPH04219902A JPH04219902A JP2412308A JP41230890A JPH04219902A JP H04219902 A JPH04219902 A JP H04219902A JP 2412308 A JP2412308 A JP 2412308A JP 41230890 A JP41230890 A JP 41230890A JP H04219902 A JPH04219902 A JP H04219902A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- iron powder
- temperature
- annealing
- core material
- 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.)
- Pending
Links
- 239000011162 core material Substances 0.000 title claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 239000000428 dust Substances 0.000 title abstract 2
- 239000000843 powder Substances 0.000 claims abstract description 51
- 230000005291 magnetic effect Effects 0.000 claims abstract description 32
- 238000000137 annealing Methods 0.000 claims abstract description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 22
- 230000005294 ferromagnetic effect Effects 0.000 claims abstract description 15
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052681 coesite Inorganic materials 0.000 claims abstract description 11
- 229910052906 cristobalite Inorganic materials 0.000 claims abstract description 11
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 11
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 11
- 229910052682 stishovite Inorganic materials 0.000 claims abstract description 11
- 229910052905 tridymite Inorganic materials 0.000 claims abstract description 11
- 239000011230 binding agent Substances 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 6
- 238000000465 moulding Methods 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 34
- 239000000463 material Substances 0.000 abstract description 4
- 229910000889 permalloy Inorganic materials 0.000 abstract description 2
- 239000011363 dried mixture Substances 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000001035 drying Methods 0.000 description 12
- 239000006247 magnetic powder Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000005389 magnetism Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- -1 but in addition Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229910000601 superalloy Inorganic materials 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets 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
- H01F1/14—Magnets 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
- H01F1/20—Magnets 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
- H01F1/22—Magnets 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
- H01F1/24—Magnets 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
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Powder Metallurgy (AREA)
- Soft Magnetic Materials (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は圧粉磁心材およびその製
造方法に関し、さらに詳しくは、ノイズフィルターおよ
びチョークコイル等の電磁気部品に使用される低鉄損の
圧粉磁心材およびその製造方法に関するものである。[Field of Industrial Application] The present invention relates to a powder magnetic core material and a method for manufacturing the same, and more particularly to a powder magnetic core material with low iron loss used for electromagnetic parts such as noise filters and choke coils, and a method for manufacturing the same. It is something.
【0002】0002
【従来技術】一般的に、磁心材はヒステリシス損および
渦電流損を生じるものであり、この二つを合わせて鉄損
になるのである。2. Description of the Related Art Generally, magnetic core materials produce hysteresis loss and eddy current loss, and the sum of these two results in iron loss.
【0003】このヒステリシス損は残留磁気を打ち消す
ために消費するエネルギーであり、保磁力(Hc)が低
いほど小さく、また、渦電流損は交番磁界において誘起
される電流により生じるため、電気抵抗が高いほど小さ
いのである。This hysteresis loss is the energy consumed to cancel residual magnetism, and the lower the coercive force (Hc), the smaller it becomes. Eddy current loss is caused by current induced in an alternating magnetic field, so when electrical resistance is high. That's how small it is.
【0004】従って、磁心材は鉄損の小さいものを必要
とし、通常、絶縁皮膜処理した薄い鉄板を重ねた積層構
造が採用されているが、複雑な形状部品を作ることは困
難であった。[0004] Therefore, the magnetic core material needs to have a low core loss, and a laminated structure of thin iron plates treated with an insulating coating is usually used, but it has been difficult to manufacture parts with complex shapes.
【0005】一方、軟磁性粉末をエポキシ樹脂により被
覆して固化成形した圧粉磁心は、通常の粉末成形法を使
用することにより複雑な形状の部品を作ることが可能で
あるが、粉末成形時に加圧されるため磁性粉末に歪が導
入され、磁心材としての磁気性能が劣化するという問題
がある。On the other hand, powder magnetic cores made by covering soft magnetic powder with epoxy resin and solidifying it can be made into parts with complex shapes by using ordinary powder molding methods, but it is difficult to make parts with complex shapes during powder molding. There is a problem that strain is introduced into the magnetic powder due to pressurization, and the magnetic performance as a magnetic core material deteriorates.
【0006】[0006]
【発明が解決しようとする課題】本発明は上記に説明し
た従来の磁心材の製造における種々の問題点に鑑み、本
発明者が鋭意研究を行った結果、磁心材を複雑な形状に
成形することが可能であり、かつ、プレス成形によって
歪を解消することができる磁気性能の優れた圧粉磁心材
およびその製造方法を開発したのである。[Problems to be Solved by the Invention] In view of the various problems in the production of conventional magnetic core materials explained above, the present inventor has conducted extensive research, and as a result, the present invention has been developed to form a magnetic core material into a complicated shape. We have developed a powder magnetic core material with excellent magnetic performance that can eliminate distortion through press forming, and a method for manufacturing the same.
【0007】[0007]
【課題を解決するための手段】本発明に係る圧粉磁心材
およびその製造方法は、600℃以下の温度において焼
鈍回復可能な強磁性粉末に、バインダーとしてSiO2
を3.9wt%以下含有させ固化成形させたことを特徴
とする圧粉磁心材を第1の発明とし、強磁性粉末に水お
よびアルコールを添加して加水分解反応を起こさせたエ
チルシリケートを混合し、混合物の表面を200℃以下
の温度において乾燥を行い、プレス成形後、600℃以
下の温度において焼鈍を行うことを特徴とする磁気性能
の優れた圧粉磁心材の製造方法を第2の発明とする2つ
の発明よりなるものである。[Means for Solving the Problems] A powder magnetic core material and a method for producing the same according to the present invention include SiO2 as a binder in a ferromagnetic powder that can be recovered by annealing at a temperature of 600°C or lower.
The first invention is a powder magnetic core material characterized by containing 3.9 wt% or less of ferromagnetic powder and solidified and molded, and mixed with ethyl silicate obtained by adding water and alcohol to ferromagnetic powder to cause a hydrolysis reaction. A second method for producing a powder magnetic core material with excellent magnetic performance, which is characterized in that the surface of the mixture is dried at a temperature of 200°C or lower, and after press forming, annealing is performed at a temperature of 600°C or lower. This invention consists of two inventions.
【0008】本発明に係る圧粉磁心材およびその製造方
法について、以下詳細に説明する。The powder magnetic core material and the method for producing the same according to the present invention will be explained in detail below.
【0009】磁心材用の磁性粉末は、保磁力(Hc)が
小さく、最大透磁率(μm)が大きいことが望ましく、
このために、焼鈍回復温度の低いものがよく、例えば、
焼鈍回復温度の低い鉄粉としては電解鉄粉があるけれど
も、この電解鉄粉はO2を0.2〜0.3wt%含有す
るために還元焼鈍を行わなければ使用することがてきず
、使用するまでの作業が繁雑となると共に、鉄粉自体が
高価である。It is desirable that the magnetic powder for the magnetic core material has a small coercive force (Hc) and a large maximum magnetic permeability (μm).
For this reason, it is best to use a material with a low annealing recovery temperature, for example,
Electrolytic iron powder is an iron powder with a low annealing recovery temperature, but since it contains 0.2 to 0.3 wt% of O2, it cannot be used without reduction annealing. The work up to this point is complicated, and the iron powder itself is expensive.
【0010】また、生産性の高い水アトマイズ鉄粉は、
焼鈍用鉄粉として多量に製造されているが、電解鉄粉に
比較して不純物の含有量が多い。しかし、溶製用原料を
厳格に選択することによって、還元焼鈍電解鉄粉と同等
の性能のものが得られる。従って、本発明に係る圧粉磁
心材およびその製造方法においては、例えば、強磁性粉
末として、高純度鉄粉、300NH鉄粉、パーマロイ等
を示したが、他にニッケル、軟磁性用アモルフアス等に
おいても優れた効果が得られるのである。[0010] In addition, water atomized iron powder with high productivity is
Although it is produced in large quantities as iron powder for annealing, it contains more impurities than electrolytic iron powder. However, by strictly selecting raw materials for melting, it is possible to obtain products with performance equivalent to reduction annealed electrolytic iron powder. Therefore, in the powder magnetic core material and the manufacturing method thereof according to the present invention, for example, high-purity iron powder, 300NH iron powder, permalloy, etc. are shown as the ferromagnetic powder, but in addition, nickel, amorphous amorphous for soft magnetism, etc. Excellent effects can also be obtained.
【0011】また、絶縁皮膜材としては、耐熱性を有し
ており、かつ、取り扱いが容易であり、量産化の行い易
い原料として、無機質系のSiO2皮膜を形成させるこ
とができるエチルシリケートを皮膜原料として使用する
。[0011] In addition, as an insulating film material, ethyl silicate, which has heat resistance, is easy to handle, and can be easily mass-produced, is used as a material for forming an inorganic SiO2 film. Use as raw material.
【0012】このエチルシリケートはSiO2を濃縮し
たエチルシリケート20、40、50等が市販されてい
るが、エチルシリケート40をアルコールを溶媒とし、
水を加え加水分解を行ったものを使用する。This ethyl silicate is commercially available as ethyl silicate 20, 40, 50 etc. made by concentrating SiO2.
Use one that has been hydrolyzed by adding water.
【0013】強磁性粉末の皮膜処理は、加水分解された
エチルシリケートの適量を強磁性粉末に添加して均一に
混合した後、100〜250℃の温度において熱風炉内
で上記粉末を流動させながら表面を乾燥させる。[0013] The coating treatment of the ferromagnetic powder is carried out by adding an appropriate amount of hydrolyzed ethyl silicate to the ferromagnetic powder, mixing it uniformly, and then fluidizing the powder in a hot air oven at a temperature of 100 to 250°C. Allow the surface to dry.
【0014】なお、未加水分解エチルシリケートは20
0〜250℃の乾燥温度を必要とするが、充分に加水分
解が行われているエチルシリケートは100℃以下の温
度で乾燥することができる。[0014] The unhydrolyzed ethyl silicate is 20
Although a drying temperature of 0 to 250°C is required, ethyl silicate that has been sufficiently hydrolyzed can be dried at a temperature of 100°C or lower.
【0015】そして、この乾燥温度は高くなるほど、強
磁性粉末の圧縮性が悪くなり、250℃の温度では圧縮
できない場合があることから、できるだけ低い温度とす
るのがよく、従って、上記の乾燥温度の説明から200
℃以下の乾燥温度とするのがよい。[0015] The higher the drying temperature, the worse the compressibility of the ferromagnetic powder becomes, and it may not be possible to compress it at a temperature of 250°C. Therefore, it is better to keep the drying temperature as low as possible. 200 from the explanation of
It is preferable to set the drying temperature to below ℃.
【0016】また、乾燥時に強磁性粉末を流動させるの
がよく、この粉末を流動させると塊状化を防止すること
ができると共に、乾燥後の粉末を容易に砕く事ができる
ためである。この乾燥後の粉末は成形性を良好にするた
めに#60の篩を通過させる。[0016] Furthermore, it is preferable to fluidize the ferromagnetic powder during drying, because fluidizing the powder can prevent agglomeration and also allows the powder to be easily crushed after drying. This dried powder is passed through a #60 sieve to improve moldability.
【0017】次に、成形は粉末プレスを用い4.5〜9
.5トン/cm2面圧により圧縮を行った。成形体はそ
の後粉末の磁気特性を回復させ、粉末の表面皮膜のSi
O2化を促進し、粉末間をより強固に結合させるために
焼鈍を行うのである。[0017] Next, molding is performed using a powder press at 4.5 to 9
.. Compression was performed using a surface pressure of 5 tons/cm2. The compact then recovers the magnetic properties of the powder and removes the Si on the surface coating of the powder.
Annealing is performed to promote O2 conversion and to create stronger bonds between powders.
【0018】通常の鉄粉では磁気特性を回復させるには
、焼鈍温度600℃以上必要とするが、高純度強磁性粉
末では600℃以下の温度、例えば、500℃の温度で
も回復する。Normal iron powder requires an annealing temperature of 600°C or higher to recover its magnetic properties, but high-purity ferromagnetic powder can recover even at a temperature of 600°C or lower, for example, 500°C.
【0019】従って、表面皮膜の加熱劣化(電気抵抗の
低下)を考慮すると、高純度鉄粉末(鉄粉)を使用する
のが有利である。この加熱劣化はエチルシリケートの場
合では650℃の温度で0.0005Ω・cmに対して
、500℃の温度では0.02〜0.03Ω・cmと小
さい。Therefore, in consideration of thermal deterioration of the surface film (reduction in electrical resistance), it is advantageous to use high-purity iron powder (iron powder). This thermal deterioration is 0.0005 Ω·cm at a temperature of 650°C in the case of ethyl silicate, whereas it is as small as 0.02 to 0.03 Ω·cm at a temperature of 500°C.
【0020】磁性粉末の焼鈍の加熱速度は、速すぎると
膨張したり、割れが発生したりするので、例えば、3℃
/min以下とするのがよい。[0020] The heating rate for annealing the magnetic powder is, for example, 3°C, because if it is too fast, it may expand or crack.
/min or less.
【0021】そして、焼鈍後の成形体密度は通常のアト
マイズ鉄粉に比較して2〜3%高くなっており、これは
、高純度強磁性粉末の方が柔らかいためであり、結果と
して、高純度鉄粉の最大透磁束密度(Bm)は高くなる
のである。[0021] The density of the compact after annealing is 2 to 3% higher than that of ordinary atomized iron powder. This is because high-purity ferromagnetic powder is softer, and as a result, The maximum permeable flux density (Bm) of pure iron powder becomes high.
【0022】[0022]
【実 施 例】本発明に係る圧粉磁心材およびその
製造方法の実施例を説明する。[Example] An example of the powder magnetic core material and the manufacturing method thereof according to the present invention will be described.
【0023】[0023]
【実 施 例】表1に粉末の種類、使用量、エチルシリ
ケートのSiO2換算量、粉末の乾燥温度、表2に成形
面圧、焼鈍温度、焼鈍後の密度、磁気特性および比抵抗
を示してある。[Example] Table 1 shows the type of powder, the amount used, the SiO2 equivalent amount of ethyl silicate, the drying temperature of the powder, and Table 2 shows the forming surface pressure, annealing temperature, density after annealing, magnetic properties, and specific resistance. be.
【0026】No.1、No.2、No.3は乾燥温度
を変えて圧粉した場合であり、乾燥温度が200℃まて
は離型を行うことができたが、乾燥温度が250℃では
型崩れを起こした。[0026]No. 1.No. 2.No. No. 3 is a case where the powder was compacted by changing the drying temperature, and it was possible to release the powder from the mold at a drying temperature of 200°C, but when the drying temperature was 250°C, the shape collapsed.
【0027】No.3、No.4、No.5、No.6
エチルシリケート量を変えて、乾燥後のSiO2量を増
加された場合であり、SiO2量が3.9wt%までは
型崩れを起こすことなく成形できたが、SiO2量が5
wt%では型崩れを起こした。[0027]No. 3.No. 4.No. 5, No. 6
This is a case where the amount of SiO2 after drying was increased by changing the amount of ethyl silicate, and molding was possible without losing the shape up to the amount of SiO2 up to 3.9 wt%, but when the amount of SiO2 was 5.
At wt%, the shape was lost.
【0028】No.6、No.7、No.8、No.9
は成形後の焼鈍温度を変えた場合であり、Hcは焼鈍温
度が250℃では不充分であり、焼鈍温度が500℃、
550℃では回復している。また、μmも焼鈍温度が高
いほど高くなっている。[0028]No. 6, No. 7.No. 8, No. 9
is the case where the annealing temperature after forming is changed; for Hc, an annealing temperature of 250°C is insufficient, and an annealing temperature of 500°C,
It recovered at 550°C. Further, the higher the annealing temperature, the higher μm becomes.
【0029】No.7、No.10は面圧を変えた場合
であり、面圧が大きいほど成形体の密度が上昇しており
、Bmも大きくなっている。[0029]No. 7.No. No. 10 shows the case where the surface pressure was changed, and the higher the surface pressure, the higher the density of the molded body and the larger Bm.
【0030】No.6、No.7、No.8、No.9
、No.10とNo.11、No.12、No.13、
No.14は粉末の種類を変えた場合であり、高純度鉄
粉のHcは焼鈍温度が500℃で回復しているが、通常
の鉄粉(300μ)は600℃以上の焼鈍温度を必要と
していることがわかる。また、高純度鉄粉は成形密度が
5%程大きいのでBmも大きくなっている。[0030]No. 6, No. 7.No. 8, No. 9
, No. 10 and no. 11, No. 12, No. 13,
No. 14 is the case where the type of powder was changed, and the Hc of high-purity iron powder recovered at an annealing temperature of 500°C, but normal iron powder (300 μ) requires an annealing temperature of 600°C or higher. I understand. Furthermore, since the compacted density of high-purity iron powder is about 5% higher, Bm is also higher.
【0031】一方、比抵抗をみると、高純度鉄粉と通常
の鉄粉とでは、焼鈍温度600℃で0.01Ω・cmと
通常のバルク材に比較して1600倍も大きいが、焼鈍
温度が650℃になると比抵抗は0.0005Ω・cm
と極端に小さくなる。よって、焼鈍温度は最高600℃
までである。On the other hand, looking at the specific resistance of high-purity iron powder and ordinary iron powder, it is 0.01 Ωcm at an annealing temperature of 600°C, which is 1600 times higher than that of ordinary bulk material. When the temperature reaches 650℃, the specific resistance becomes 0.0005Ω・cm
becomes extremely small. Therefore, the maximum annealing temperature is 600℃
That's it.
【0032】No.15のスーパーアロイは高純度鉄粉
と同じである。[0032]No. 15 super alloy is the same as high purity iron powder.
【0033】この表1、表2から、高純度鉄粉を使用し
、SiO2含有量が3.9wt%以下であり、強磁性粉
末の加水分解したエチルシリケートの混合物の表面の乾
燥温度が200℃以下、成形後の焼鈍温度は600℃以
下とすることにより、優れた圧粉磁心材を得られるので
ある。従って、この条件から外れているNo.2、No
.5、No.14は不適格である。From Tables 1 and 2, it is clear that high-purity iron powder is used, the SiO2 content is 3.9 wt% or less, and the surface drying temperature of the mixture of hydrolyzed ethyl silicate in the ferromagnetic powder is 200°C. Hereinafter, by setting the annealing temperature after forming to 600° C. or lower, an excellent powder magnetic core material can be obtained. Therefore, No. 1 that deviates from this condition. 2.No
.. 5, No. 14 is ineligible.
【0034】[0034]
【発明の効果】以上説明したように、本発明に係る圧粉
磁心材およびその製造方法は上記の構成を有しているか
ら、優れた磁気特性を有しているから、ノイズフィルタ
ーやチョークコイル、アクティブフィルタ等の電磁気部
品として好適な圧粉磁心材を得ることができという効果
を有しているものである。[Effects of the Invention] As explained above, since the powder magnetic core material and the method for manufacturing the same according to the present invention have the above-mentioned structure and have excellent magnetic properties, they can be used in noise filters and choke coils. This has the effect that powder magnetic core material suitable for use as electromagnetic components such as active filters can be obtained.
Claims (2)
可能な強磁性粉末に、バインダーとしてSiO2を3.
9wt%以下含有させ固化成形させたことを特徴とする
圧粉磁心材。1. A ferromagnetic powder that can be recovered by annealing at a temperature of 600° C. or less is mixed with SiO2 as a binder.
A powder magnetic core material containing 9 wt% or less and solidified and molded.
加して加水分解反応を起こさせたエチルシリケートを混
合し、混合物の表面を200℃以下の温度において乾燥
を行い、プレス成形後、600℃以下の温度において焼
鈍を行うことを特徴とする磁気性能の優れた圧粉磁心材
の製造方法。2. Ethyl silicate obtained by adding water and alcohol to ferromagnetic powder to cause a hydrolysis reaction is mixed, the surface of the mixture is dried at a temperature of 200°C or lower, and after press molding, the mixture is heated to a temperature of 600°C or lower. A method for producing a powder magnetic core material with excellent magnetic performance, the method comprising annealing at a temperature of .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2412308A JPH04219902A (en) | 1990-12-20 | 1990-12-20 | Dust core material and its manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2412308A JPH04219902A (en) | 1990-12-20 | 1990-12-20 | Dust core material and its manufacture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04219902A true JPH04219902A (en) | 1992-08-11 |
Family
ID=18521162
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2412308A Pending JPH04219902A (en) | 1990-12-20 | 1990-12-20 | Dust core material and its manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04219902A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5800636A (en) * | 1996-01-16 | 1998-09-01 | Tdk Corporation | Dust core, iron powder therefor and method of making |
| CN102667971A (en) * | 2009-11-05 | 2012-09-12 | 罗伯特·博世有限公司 | Method for producing a magnet, magnet, and electric machine |
-
1990
- 1990-12-20 JP JP2412308A patent/JPH04219902A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5800636A (en) * | 1996-01-16 | 1998-09-01 | Tdk Corporation | Dust core, iron powder therefor and method of making |
| CN102667971A (en) * | 2009-11-05 | 2012-09-12 | 罗伯特·博世有限公司 | Method for producing a magnet, magnet, and electric machine |
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