JPH01212702A - Manufacture of magnetic material - Google Patents
Manufacture of magnetic materialInfo
- Publication number
- JPH01212702A JPH01212702A JP3610188A JP3610188A JPH01212702A JP H01212702 A JPH01212702 A JP H01212702A JP 3610188 A JP3610188 A JP 3610188A JP 3610188 A JP3610188 A JP 3610188A JP H01212702 A JPH01212702 A JP H01212702A
- Authority
- JP
- Japan
- Prior art keywords
- binder
- metal powder
- magnetic material
- injection molding
- sintering
- 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
- 239000000696 magnetic material Substances 0.000 title claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000011230 binding agent Substances 0.000 claims abstract description 46
- 239000000843 powder Substances 0.000 claims abstract description 28
- 239000002184 metal Substances 0.000 claims abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 19
- 238000001746 injection moulding Methods 0.000 claims abstract description 15
- 238000005245 sintering Methods 0.000 claims abstract description 12
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 8
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 8
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 8
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 8
- 238000002156 mixing Methods 0.000 claims abstract description 5
- 229920000193 polymethacrylate Polymers 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims description 17
- 238000002347 injection Methods 0.000 claims description 14
- 239000007924 injection Substances 0.000 claims description 14
- 239000007822 coupling agent Substances 0.000 claims description 7
- 239000012188 paraffin wax Substances 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000000243 solution Substances 0.000 claims description 3
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims 1
- 239000002245 particle Substances 0.000 abstract description 11
- 239000000463 material Substances 0.000 abstract description 8
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 abstract description 6
- 238000000465 moulding Methods 0.000 abstract description 5
- 150000002148 esters Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 description 10
- 230000000694 effects Effects 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- 239000002994 raw material Substances 0.000 description 3
- 238000005979 thermal decomposition reaction Methods 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- 238000007088 Archimedes method Methods 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001739 density measurement Methods 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000005389 magnetism Effects 0.000 description 2
- 230000005415 magnetization Effects 0.000 description 2
- 229910000889 permalloy Inorganic materials 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 229910000976 Electrical steel Inorganic materials 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 229910000979 O alloy Inorganic materials 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000003648 hair appearance Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、金属粉末を射出成形して焼結する磁性材料の
製造方法と射出成形用のバインダーに関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for producing a magnetic material by injection molding and sintering metal powder, and a binder for injection molding.
[従来の技術]
磁性材料には、純鉄、パーマロイ、けい素鋼、パーメン
ジュールなどがあるが、多くは圧延鋼を必要形状にプレ
スにて打ち抜きや積層、曲げなどにより加工して使用さ
れている。また一部には粉末冶金法を用いてプレス成形
後焼結したものも使用されている。[Conventional technology] Magnetic materials include pure iron, permalloy, silicon steel, permendur, etc., but most are made by processing rolled steel into the required shape by punching, laminating, bending, etc. using a press. ing. In addition, some materials are also used that are press-formed and sintered using a powder metallurgy method.
[発明が解決しようとする課題]
しかし前述のような従来の技術では板材を利用した形状
では複雑1ヨ状のものができない。この点を改良した方
法として焼結法があるがこの場合に於いても上下方向(
加圧方向)のに対してはある程度適応できるが横方向(
加圧方向に対して直角方向)に対してはその製法上制約
があるという問題点を有する。そこで本発明はそのよう
な問題点を解決するものでその目的とするところは形状
自由度が大きく安価にて容易に製造する方法を提供する
ところにある。[Problems to be Solved by the Invention] However, with the conventional techniques as described above, it is not possible to create a complicated 1-way shape using a plate material. There is a sintering method as a method that improves this point, but in this case also the vertical direction (
It can be applied to some extent in the pressure direction (pressure direction), but it can be adapted to a certain extent in the lateral direction (pressure direction).
There is a problem in that there are restrictions on the manufacturing method in the direction perpendicular to the pressing direction. The present invention is intended to solve such problems, and its purpose is to provide a method of manufacturing easily at low cost with a large degree of freedom in shape.
[課題を解決するための手段]
本発明の磁性材料の製造方法の第1は、400メツシュ
アンダーの金属粉末と、重量%にて15〜40%のバイ
ンダーを配合、混合した後、混合物を射出成形し、射出
成形体を還元性雰囲気中にて脱バインダーを行い、続い
て脱バインダー後の成形体を焼結することを特徴とする
。[Means for Solving the Problems] The first method of manufacturing a magnetic material of the present invention is to blend and mix 400 mesh under metal powder and a binder of 15 to 40% by weight, and then mix the mixture. The method is characterized by injection molding, removing the binder from the injection molded body in a reducing atmosphere, and then sintering the molded body after the binder has been removed.
また、本発明の磁性材料の製造方法の第2は、重量%で
、エチレン酢酸ビニル共重合体(以下EVAと略j)お
よび低密度ポリエチレン(以下LDPEと略す)のうち
1種もしくは2種を40〜60%、ポリメタクリル酸エ
ステル共重合体(以下PMEと略す)25〜35%、ジ
ブチルフタレート(以下DBPと略す)もしくはジエチ
ルフタレート(以下DEPと略す)のうち1種を5〜1
0%、パラフィンワックスを残りの配合組成からなる射
出成形用バインダーであることを特徴とする。The second method for producing a magnetic material of the present invention is to use one or two of ethylene-vinyl acetate copolymer (hereinafter abbreviated as EVA) and low-density polyethylene (hereinafter abbreviated as LDPE) in weight%. 40 to 60%, 25 to 35% of polymethacrylic acid ester copolymer (hereinafter abbreviated as PME), and 5 to 1% of one of dibutyl phthalate (hereinafter abbreviated as DBP) or diethyl phthalate (hereinafter abbreviated as DEP).
The binder is characterized by being an injection molding binder consisting of 0% paraffin wax and the remainder being paraffin wax.
更に、本発明の磁性材料の製造方法の第3は、金属粉末
の表面をアルコール溶液中に希釈されたカップリング剤
により処理することを特徴とする。Furthermore, the third method of manufacturing a magnetic material according to the present invention is characterized in that the surface of the metal powder is treated with a coupling agent diluted in an alcohol solution.
[作用]
金属粉末としては、還元法、電気分解法、噴霧法、粉砕
法、等の製造方法で得られる各種金属粉末の適応が可能
であり、金属粉末の粒径は射出成形する場合流動性がな
ければならないため400メツシユ以下が望ましい。複
雑な形状の物を得ることや製造装置かかる負荷を低減し
流動性を良くするすることと、焼結性をよくするために
は10μm以下の粒径の粉末が望ましい。400メツシ
ュ以上の粒径の粉末では、金属粉末とバインダーの混合
物の流れが悪く射出成形が困難となるため望ましくない
。[Function] As the metal powder, various metal powders obtained by manufacturing methods such as reduction method, electrolysis method, spraying method, pulverization method, etc. can be applied, and the particle size of the metal powder is determined by the fluidity when injection molding. 400 meshes or less is desirable. Powder having a particle size of 10 μm or less is desirable in order to obtain a product with a complicated shape, reduce the load on the manufacturing equipment, improve fluidity, and improve sinterability. Powder having a particle size of 400 mesh or more is not desirable because the mixture of metal powder and binder will not flow well and injection molding will be difficult.
バインダーについては、原料粉末と良くなじみ成形性が
良好であると同時に焼結に当たっては容易に短時間で成
形体に悪影響を与えずに分解、気、化し除去される必要
がある。バインダーの量については少なすぎれば流動性
が悪くなり射出成形機に大きな負荷を与えるばかりが所
定形状に成形できない。また一方バインダーの量が多す
ぎれば成形の問題はないが、脱ワツクスから焼結の工程
で脱バインダーが充分できずバインダーが残留し成形体
の性能に悪影響を与えることと、バインダーが発泡し成
形体の形状を損傷するといったことに・ なる。本発明
では、金属粉末の表面をカップリング剤により表面改質
しより低バインダーで流動性をもたことによりバインダ
ーの量を、15〜40%とした。The binder must be compatible with the raw material powder and have good moldability, and at the same time, it must be easily decomposed, vaporized, and removed during sintering in a short period of time without adversely affecting the molded product. If the amount of binder is too small, the fluidity will be poor and the injection molding machine will be subjected to a large load, but the molding will not be able to be molded into the desired shape. On the other hand, if the amount of binder is too large, there will be no problem with molding, but the binder may not be removed sufficiently during the process from wax removal to sintering, and the binder may remain, adversely affecting the performance of the molded product, and the binder may foam and mold. This can result in damage to the shape of the body. In the present invention, the surface of the metal powder is modified with a coupling agent to obtain fluidity with a lower binder, thereby increasing the amount of binder to 15 to 40%.
バインダーは、金属粉末とのぬれ性が良くて均一に混ざ
り合い流動性がよく射出成形が容易にできることと、熱
分解が連続的に進行且つ分解性の良いこと、また分解に
当たっては成形対の形状を保持すること、分解後には残
留物を残さないことなどが必要である。The binder has good wettability with the metal powder, mixes uniformly, has good fluidity, and can be easily injection molded.The binder also has to be thermally decomposed continuously and has good decomposition properties. It is necessary to maintain the content and leave no residue after decomposition.
以下これの観点からバインダーについて説明する。The binder will be explained from this point of view below.
a)EVA、 LDPE
これらは熱可塑性樹脂であり、流動性、脱脂製に優れて
いることと、脱バインダー時にはこれ以外の成分が熱分
解して除去される間射出成形体の形状を保持する作用を
有する。これらの配合量が、40%未満では、流動性や
脱バインダー時の射出成形体の形状保持能力を得られな
くなる。また、61%以上では脱バインダー後に焼結体
に残留して磁気性能を悪化させることや、脱バインダー
時に発泡等などで射出成形体の形状保持に悪影響を与え
ることから、40〜60%とした。a) EVA, LDPE These are thermoplastic resins, and have excellent fluidity and degreasing properties, and also have the ability to maintain the shape of the injection molded product while other components are thermally decomposed and removed during binder removal. has. If the blending amount is less than 40%, it becomes impossible to obtain fluidity or the ability to maintain the shape of the injection molded product during binder removal. In addition, if it is more than 61%, it will remain in the sintered body after debinding and deteriorate the magnetic performance, and it will cause foaming etc. during debinding, which will have a negative effect on the shape retention of the injection molded product, so it was set at 40 to 60%. .
b)PME
この成分も、EVA、LDPEと同様に熱可塑性樹脂で
あり、その毛質も前記樹脂と同様な作用を持つがこの成
分の特徴は、EVAやLDPEと比較して低い熱分解温
度を持つ点である。これらの成分を調整することにより
、脱バインダー時のバインダーの熱分解が徐々に進行し
、射出成形体の形状を保持しながらバインダーを除去す
る作用を持つ。このことから、25%未満36%以上で
は熱分解が連続的に行なわれなくなり、射出成形体に損
傷を与えるため、25〜35%とした。b) PME This component is also a thermoplastic resin like EVA and LDPE, and its hair quality also has the same effect as the above resins, but the characteristic of this component is that it has a lower thermal decomposition temperature than EVA and LDPE. It is a point to have. By adjusting these components, thermal decomposition of the binder during binder removal progresses gradually, and the binder is removed while maintaining the shape of the injection molded article. From this, if the content is less than 25% or more than 36%, thermal decomposition will not occur continuously and the injection molded product will be damaged, so the content was set at 25 to 35%.
c)DBP、DEP
これらの成分は、前記バインダーとの相溶性を向上させ
バインダーの均質化を図る作用がある。5%以下ではそ
の効果が認められず、11%以上では脱バインダー時に
射出成形体に損傷を与えるため、 5〜10%とした。c) DBP, DEP These components have the effect of improving compatibility with the binder and homogenizing the binder. If it is less than 5%, no effect will be observed, and if it is more than 11%, the injection molded product will be damaged when the binder is removed, so the content was set at 5 to 10%.
d)パラフィンワックス
射出成形時の流動性を向上させるとともに、金属粉末と
バインダーのぬれ性を向上し、配合混合物の均質化を図
る作用がある。10%未満ではその効果がなく、16%
以上では射出成形時に於けるワックスの収縮が吠きくな
り寸法精度が悪くなるため、 10〜15%が望ましい
。d) Paraffin wax It has the effect of improving the fluidity during injection molding, improving the wettability of the metal powder and binder, and homogenizing the blended mixture. Less than 10% has no effect, and 16%
If the content is above 10% to 15%, the wax shrinks rapidly during injection molding, resulting in poor dimensional accuracy.
e)カップリング剤
2種類以上の異なる材質間の結合を促進させ金属粉末と
バインダーとのぬれ性を向上させる作用により、流動性
を高め成形性を向上させるとともに低バインダー化と脱
バインダー性の向上を図る目的で金属粉末の表面処理を
行なう。シラン系、チタン系等あるが、流動性を向上さ
せより低バインダー化を図るにはチタン系の方が効果が
大きい。e) Coupling agent By promoting the bonding between two or more different materials and improving the wettability between the metal powder and the binder, it increases fluidity and improves moldability, as well as lowering the binder content and improving binder removal properties. Surface treatment of metal powder is carried out for the purpose of achieving this. There are silane-based and titanium-based materials, but titanium-based materials are more effective in improving fluidity and reducing binder content.
一方、シラン系は焼結後に灰分を残さないことから、よ
り低不純物化が望ましい場合に適応すれば良い。On the other hand, since silane-based materials do not leave ash after sintering, they can be used when lower impurity levels are desired.
[実施例] 以下実施例にもとすき詳細に説明する。[Example] This will be explained in detail in the following examples.
[実施例−1コ
原料粉末として、10μm以下のカーボニル鉄粉(平均
粒径3.2μm(フィッシャー、サブ、シブ、サイザー
(F、 S、 S、 S))以下すべて同じ)、
同ニッケール粉末(平均粒径2.5μm)、同コバルト
粉末(平均粒径1.5μm)を用意し、各々粉末をチタ
ン系カップリング剤をアルコールに希釈した溶液中に浸
積した後乾燥して金属粉末の表面処理を行なった。これ
らの金属粉末を表−1に示す組成に調合し、同じく表−
1に示される配合組成のバインダーを、同じく表−1に
示される配合量で加え加圧式ニーダを用いて135℃で
1時間混合し冷却後粉砕して平均粒径2mmの混合物を
得た。次に得られた混合物を射出成形機を用いて、射出
温度160°C1射出圧カフ00Kg/cm2にてφ3
3×φ45xt5mmのリング形状の試料を成形した。[Example-1 As the raw material powder, carbonyl iron powder of 10 μm or less (average particle size of 3.2 μm (Fisher, Sub, Siv, Sizer (F, S, S, S)) or less is the same),
The same nickel powder (average particle size 2.5 μm) and the same cobalt powder (average particle size 1.5 μm) were prepared, and each powder was immersed in a solution of a titanium-based coupling agent diluted in alcohol, and then dried. Surface treatment of metal powder was performed. These metal powders were mixed into the composition shown in Table 1, and the composition shown in Table 1 was also prepared.
A binder having the composition shown in Table 1 was added in the amount shown in Table 1, mixed for 1 hour at 135° C. using a pressure kneader, cooled and pulverized to obtain a mixture with an average particle size of 2 mm. Next, the obtained mixture was molded using an injection molding machine with an injection temperature of 160°C, an injection pressure cuff of 00 kg/cm2, and a diameter of 3 mm.
A ring-shaped sample of 3×φ45×t5 mm was molded.
リング試料を水素雰囲気中にて20°C/hの昇温条件
で500℃まで加熱し脱バインダーした後、1200°
Cで4時間焼結を行なった。尚、脱バインダーの終了後
には温度キープをせず、約12°C/minの昇温条件
で焼結温度まで昇温にした。得られた焼結体に、励磁コ
イル及びサーチコイルを各50タ一ン巻き直流磁化測定
機で磁気、測定をした。またアルキメデス法にて密度測
定した結果を表−2に示す。本発明との比較は、溶製材
あ純鉄、パーマロイ(45Ni−Fe)、パーメンジュ
ール(50Co−Fe)を用いた。The ring sample was heated to 500°C in a hydrogen atmosphere at a temperature increase of 20°C/h to remove the binder, and then heated to 1200°C.
Sintering was performed at C for 4 hours. After the binder removal was completed, the temperature was not maintained and the temperature was raised to the sintering temperature at a rate of about 12°C/min. The magnetism of the obtained sintered body was measured using a DC magnetization measuring machine using an excitation coil and a search coil each wound with 50 turns. Table 2 shows the results of density measurement using the Archimedes method. For comparison with the present invention, molten pure iron, permalloy (45Ni-Fe), and permendur (50Co-Fe) were used.
本発明の方法では、いずれも成形、脱ワツクス、焼結の
行程では、成形体に異常は認められながった。また焼結
体は相対密度で約95%のものを得ることができ、磁気
特性も溶性材に比べ遜色のない性能のものが得られてい
る。In the method of the present invention, no abnormality was observed in the molded product during the molding, wax removal, and sintering steps. Furthermore, a sintered body with a relative density of about 95% can be obtained, and its magnetic properties are comparable to those of soluble materials.
[実施例−2]
原料粉末として、水噴霧法を用いて、45Ni−Fe合
金粉末(平均粒径4. 6μm)、50Fe−Co (
平均粒径4.9μm)合金粉末を得た0合金粉末をチタ
ン系のカップリング剤で表面処理し、表−3に示す配合
組成のバインダーを、同じく表−3に示される量で加え
、加圧式ニーダを用いて135°Cで1時間混合し冷却
後粉砕して平均粒径2mmの混合物を得た。次に得られ
た混合物を射出成形機を用いて、射出温度160°C1
射出圧カフ00Kg/cm2 にて、 φ33×φ45
xt5mmのリング形状の試料を成形した。リング試料
を水素雰囲気中にて20℃/hの昇温条件で500°C
まで加熱し脱バインダーした後、1200°Cで4時間
焼結を行なった。得られた焼結体に、励磁コイル及びサ
ーチコイルを各50タ一ン巻き直流磁化測定機で磁気測
定をした。またアルキメデス法にて密度測定した結果を
表−4に示す。[Example-2] As raw material powders, 45Ni-Fe alloy powder (average particle size 4.6 μm), 50Fe-Co (
The obtained 0 alloy powder (average particle size 4.9 μm) was surface-treated with a titanium-based coupling agent, and a binder having the composition shown in Table 3 was added in the amount also shown in Table 3. The mixture was mixed for 1 hour at 135°C using a pressure kneader, cooled, and then ground to obtain a mixture with an average particle size of 2 mm. Next, the obtained mixture was molded using an injection molding machine at an injection temperature of 160°C.
Injection pressure cuff 00Kg/cm2, φ33×φ45
A ring-shaped sample with xt5mm was molded. The ring sample was heated to 500°C in a hydrogen atmosphere at a rate of 20°C/h.
After the binder was removed by heating to 1,200° C., sintering was performed at 1200° C. for 4 hours. Magnetism was measured on the obtained sintered body using a DC magnetization measuring machine with an excitation coil and a search coil each wound with 50 turns. Table 4 shows the results of density measurement using the Archimedes method.
合金粉末を用いても、実施例−1と同等のものが得られ
ている。Even when alloy powder was used, a product equivalent to Example 1 was obtained.
表−3
表−4
[発明の効果]
以上述べてきたーように本発明によれば、400メツシ
ユ以下の金属粉末をカップリング剤にて表面処理し、熱
可塑性樹脂を主成分とするバインダーと配合混合した後
、射出成形によって必要形状を得、成形体を焼結する事
により優れた磁気性能を有する焼結磁性材料を得ること
ができる。このことにより、例えばステッピングモータ
ーのコアヨークやCD等のレンズアクチュエータヨーク
等の薄肉で複雑な形状の部品も容易に安価に製造するこ
とが可能となる。Table 3 Table 4 [Effects of the Invention] As described above, according to the present invention, metal powder of 400 mesh or less is surface-treated with a coupling agent and blended with a binder whose main component is a thermoplastic resin. After mixing, the required shape is obtained by injection molding, and the molded body is sintered to obtain a sintered magnetic material having excellent magnetic performance. This makes it possible to easily and inexpensively manufacture thin, complex-shaped parts such as the core yoke of a stepping motor or the lens actuator yoke of a CD, etc.
尚本発明は、磁性材料の製造方法について述べてきたが
この方法を応用すれば機械部品などにも適応可能である
。Although the present invention has been described with respect to a method for manufacturing magnetic materials, this method can also be applied to mechanical parts and the like.
以上 出願人 セイコーエプソン株式会社 代理人弁理士 最 上 務 他1名that's all Applicant: Seiko Epson Corporation Representative Patent Attorney Mogami and 1 other person
Claims (3)
て15〜40%のバインダーを配合、混合した後、混合
物を射出成形し、射出成形体を還元性雰囲気中にて脱バ
インダーを行い、続いて脱バインダー後の成形体を焼結
することを特徴とする磁性材料の製造方法。(1) After blending and mixing 400 mesh under metal powder and 15 to 40% binder by weight, the mixture is injection molded, the injection molded body is debindered in a reducing atmosphere, and then A method for producing a magnetic material, comprising: sintering the molded body after removing the binder.
ビニル共重合体および低密度ポリエチレンのうち1種も
しくは2種を40〜60%、ポリメタクリル酸エステル
共重合体25〜35%、ジブチルフタレートもしくはジ
エチルフタレートのうち1種を5〜10%、パラフィン
ワックスを残りの配合組成からなる射出成形用バインダ
ーを用いることを特徴とする第1項記載の磁性材料の製
造方法。(2) As the binder, in weight percent, 40 to 60% of one or two of ethylene vinyl acetate copolymer and low density polyethylene, 25 to 35% of polymethacrylate copolymer, dibutyl phthalate or diethyl 2. The method for producing a magnetic material according to claim 1, characterized in that an injection molding binder is used which has a blend composition of 5 to 10% of one kind of phthalate and the remainder of paraffin wax.
カップリング剤により処理することを特徴とする第1項
記載の磁性材料の製造方法。(3) The method for producing a magnetic material according to item 1, characterized in that the surface of the metal powder is treated with a coupling agent diluted in an alcohol solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3610188A JPH01212702A (en) | 1988-02-18 | 1988-02-18 | Manufacture of magnetic material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3610188A JPH01212702A (en) | 1988-02-18 | 1988-02-18 | Manufacture of magnetic material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01212702A true JPH01212702A (en) | 1989-08-25 |
Family
ID=12460376
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3610188A Pending JPH01212702A (en) | 1988-02-18 | 1988-02-18 | Manufacture of magnetic material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01212702A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04329847A (en) * | 1991-04-30 | 1992-11-18 | Sumitomo Metal Mining Co Ltd | Manufacture of fe-ni alloy soft magnetic material |
CN107344236A (en) * | 2017-06-21 | 2017-11-14 | 徐州明润磁材有限公司 | A kind of manufacture method of miniature motor rotor |
CN108380863A (en) * | 2017-02-03 | 2018-08-10 | 株式会社神户制钢所 | Mixed powder for powder metallurgy and its manufacturing method |
-
1988
- 1988-02-18 JP JP3610188A patent/JPH01212702A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04329847A (en) * | 1991-04-30 | 1992-11-18 | Sumitomo Metal Mining Co Ltd | Manufacture of fe-ni alloy soft magnetic material |
CN108380863A (en) * | 2017-02-03 | 2018-08-10 | 株式会社神户制钢所 | Mixed powder for powder metallurgy and its manufacturing method |
CN107344236A (en) * | 2017-06-21 | 2017-11-14 | 徐州明润磁材有限公司 | A kind of manufacture method of miniature motor rotor |
CN107344236B (en) * | 2017-06-21 | 2019-06-14 | 徐州明润磁材有限公司 | A kind of manufacturing method of miniature motor rotor |
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