JPH0618128B2 - Magnet roll manufacturing method - Google Patents
Magnet roll manufacturing methodInfo
- Publication number
- JPH0618128B2 JPH0618128B2 JP59062549A JP6254984A JPH0618128B2 JP H0618128 B2 JPH0618128 B2 JP H0618128B2 JP 59062549 A JP59062549 A JP 59062549A JP 6254984 A JP6254984 A JP 6254984A JP H0618128 B2 JPH0618128 B2 JP H0618128B2
- Authority
- JP
- Japan
- Prior art keywords
- vinyl acetate
- magnet
- ethylene
- acetate copolymer
- weight
- 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.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 230000005291 magnetic effect Effects 0.000 claims description 34
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 27
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 26
- 239000000843 powder Substances 0.000 claims description 24
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 23
- 238000000465 moulding Methods 0.000 claims description 17
- 230000005294 ferromagnetic effect Effects 0.000 claims description 14
- 238000001746 injection moulding Methods 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 2
- 230000002093 peripheral effect Effects 0.000 claims 1
- 239000002131 composite material Substances 0.000 description 17
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 11
- 229910000859 α-Fe Inorganic materials 0.000 description 10
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 239000006247 magnetic powder Substances 0.000 description 4
- 230000035939 shock Effects 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000805 composite resin Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 150000002910 rare earth metals Chemical class 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 229910001047 Hard ferrite Inorganic materials 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910000828 alnico Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000005347 demagnetization Effects 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000013585 weight reducing agent Substances 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
- H01F1/032—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 hard-magnetic materials
- H01F1/04—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 hard-magnetic materials metals or alloys
- H01F1/06—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 hard-magnetic materials metals or alloys in the form of particles, e.g. powder
- H01F1/08—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 hard-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together
- H01F1/083—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 hard-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together in a bonding agent
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Hard Magnetic Materials (AREA)
Description
【発明の詳細な説明】 技術分野 本発明は強磁性粉末と熱可塑性樹脂とを含む異方性複合
磁石を含むマグネットロールの製造方法に関する。Description: TECHNICAL FIELD The present invention relates to a method for producing a magnet roll including an anisotropic composite magnet containing a ferromagnetic powder and a thermoplastic resin.
先行技術 電子写真複写機、ファクシミリ、プリンター等の画像再
生装置(乾式)においては、磁性現像剤(磁性キャリア
とトナーとの混合粉体である二成分現像剤あるいは一成
分系の磁性トナー等)の搬送手段として、非磁性スリー
ブの内部に複数個の磁極を有する永久磁石部材を設置
し、両者を相対的に回転させるように構成したマグネッ
トロールが一般に使用されている。2. Description of the Related Art In an image reproducing apparatus (dry type) such as an electrophotographic copying machine, a facsimile, and a printer, a magnetic developer (a two-component developer that is a mixed powder of a magnetic carrier and a toner or a one-component magnetic toner) is used. As a conveying means, a magnet roll is generally used in which a non-magnetic sleeve is provided with a permanent magnet member having a plurality of magnetic poles, and the two are relatively rotated.
上記のマグネットロールにも種々の構造のものがあり、
例えば実公昭57-9798号公報に記載されているような、
フェライト粉末を磁場中でプレス成形後焼結して得られ
る長尺の異方性ブロック磁石を軸の周囲に固定して形成
した永久磁石部材を用いるもの、あるいはハードフェラ
イトからなる円筒状永久磁石を軸に固着して形成した永
久磁石部材を用いるもの(例えば特公昭55-6907号公
報、特公昭53-47043号公報参照)などが挙げられる。し
かるに前者の場合は、組立工程数が多くなったり低温減
磁が生ずるなどの問題があり、一方後者の場合は焼結体
の密度が約5g/cm3と大きいため、重量が大となるとい
う問題がある。また焼結フェライト磁石は、一般に、焼
結中あるいは焼結後にクラックや割れが発生し易く、歩
留が悪いという問題もある。There are various structures for the above magnet rolls,
For example, as described in Japanese Utility Model Publication No. 57-9798,
Using a permanent magnet member formed by fixing a long anisotropic block magnet obtained by press-forming ferrite powder in a magnetic field and then sintering it, or a cylindrical permanent magnet made of hard ferrite. Examples thereof include those using a permanent magnet member formed by being fixedly attached to a shaft (see, for example, JP-B-55-6907 and JP-B-53-47043). However, in the former case, there are problems such as an increase in the number of assembly steps and in low temperature demagnetization, while in the latter case, the sintered body has a large density of about 5 g / cm 3 and thus is heavy. There's a problem. In addition, sintered ferrite magnets generally have a problem that cracks and fractures are likely to occur during or after sintering, resulting in poor yield.
これに対して、主として軽量化と製造の容易さのために
強磁性粉末(一般にフェライト粉末)と高分子化合物
(一般にゴム又はプラスチツク材料)とを主体とする混
練物を押出成形あるいは、射出成形の手法により円筒状
に一体に成形し、ついで冷却固化後着磁したいわゆる複
合磁石を用いたマグネットロールが提案された(特開昭
55-154707号、同56-108207号、同57-130407号、同57-16
4509号、特公昭52-12400号、同55-32206号、同56-5045
号)。これらの場合、複合磁石は焼結磁石よりも磁粉の
濃度充填密度が低いので、焼結フェライト磁石と同等の
磁気特性を得るために、異方性化工程が施されている。
この異方性化工程は磁性体粉末と樹脂との混練物を所定
の磁場中で射出成形することを含む。On the other hand, a kneaded product mainly composed of a ferromagnetic powder (generally ferrite powder) and a polymer compound (generally rubber or plastic material) is mainly used for extrusion molding or injection molding for the purpose of weight reduction and ease of manufacturing. A magnet roll using a so-called composite magnet, which is integrally molded into a cylindrical shape by a method and then magnetized after being solidified by cooling, has been proposed (Japanese Patent Laid-open No. Sho 61-206).
55-154707, 56-108207, 57-130407, 57-16
No. 4509, No. 52-12400, No. 55-32206, No. 56-5045
issue). In these cases, since the composite magnet has a lower concentration packing density of magnetic powder than the sintered magnet, an anisotropy process is performed in order to obtain magnetic characteristics equivalent to those of the sintered ferrite magnet.
This anisotropy step includes injection molding a kneaded product of the magnetic powder and the resin in a predetermined magnetic field.
これらの異方性複合磁石に使用し得る樹脂として、ポリ
エチレン、ポリプロピレン、ポリスチレン、ポリアミ
ド、エチレン−酢酸ビニル共重合体、エチレン−エチル
アクリレート共重合体等が示されている。しかしながら
これらの樹脂をマグネットロールのような長尺の異方性
磁石、特に長尺円筒状異方性複合磁石に使用する場合に
種々の問題が生じることがわかった。As resins that can be used for these anisotropic composite magnets, polyethylene, polypropylene, polystyrene, polyamide, ethylene-vinyl acetate copolymer, ethylene-ethyl acrylate copolymer and the like are shown. However, it has been found that various problems occur when these resins are used for a long anisotropic magnet such as a magnet roll, especially for a long cylindrical anisotropic composite magnet.
ポリアミド樹脂を使用した場合、磁気特性の点で優れて
おり、しかも固化速度が早く成形サイクルを大幅に短縮
できるという利点はあるが、上述した長尺の円筒磁石の
製造において、磁場異方化により生じた残留応力のベー
スレヂンであるポリアミド樹脂が応力緩和により吸収出
来ずに成形後あるいはヒートサイクルテスト中に割れを
生ずるという欠点がある。成形条件を厳密に管理するこ
とにより割れの発生の頻度を減少させることは技術的に
不可能でないが、量産には不向きである。When a polyamide resin is used, it has excellent magnetic properties, and has the advantage that the solidification rate is fast and the molding cycle can be greatly shortened.However, in the production of the long cylindrical magnet described above, the The polyamide resin, which is the base resin of the residual stress generated, cannot be absorbed due to stress relaxation and has a defect that cracks occur after molding or during a heat cycle test. Although it is technically impossible to reduce the frequency of cracking by strictly controlling the molding conditions, it is not suitable for mass production.
また低密度ポリエチレンを使用した場合はポリアミドに
比較して更に応力亀裂を発生する頻度が高く、不適であ
る。Further, when low density polyethylene is used, stress cracking occurs more frequently than polyamide and is not suitable.
エチレン−酢酸ビニル共重合体に関して、特公昭52-124
00号は酢酸ビニル含有量8%のエチレン−酢酸ビニル共
重合体を使用して製造した異方性複合磁石を開示してい
るが、この磁石は20φ×5mmの円板状である。特公昭55
-32206号は90〜96重量%のフェライト粉末(有機けい素
化合物で表面処理)と10〜4重量%のエチレン−酢酸ビ
ニル共重合体(酢酸ビニル含有量5〜25重量%)とから
なる異方性磁石を開示しているが、この磁石は界磁マグ
ネット用などに使用するものである。これらの公知技術
はいずれも電子写真複写機等のマグネットロールに使用
するための長尺の円筒状異方性磁石に関するものではな
く、長尺の円筒状異方性磁石に関連する後述の技術的問
題について何ら議論がされていない。Regarding ethylene-vinyl acetate copolymer, Japanese Patent Publication No. 52-124
No. 00 discloses an anisotropic composite magnet manufactured by using an ethylene-vinyl acetate copolymer having a vinyl acetate content of 8%, and this magnet has a disk shape of 20φ × 5 mm. Japanese Patent Office Sho 55
-32206 consists of 90-96 wt% ferrite powder (surface treated with organic silicon compound) and 10-4 wt% ethylene-vinyl acetate copolymer (vinyl acetate content 5-25 wt%). Although a direction magnet is disclosed, this magnet is used for a field magnet or the like. None of these known techniques relates to a long cylindrical anisotropic magnet for use in a magnet roll of an electrophotographic copying machine or the like. There is no discussion of the issue.
また特開昭57-130407号は強磁性粉末をエチレン−酢酸
ビニル共重合体で結合した長尺の円筒状異方性樹脂磁石
を開示している。しかしながらかかる長尺円筒状の異方
性樹脂磁石の場合、成形体のそりの問題がしばしば生じ
た。マグネットロールは長尺であり、通常スリーブに収
容されるが、僅かでもそりが生ずると種々の重大な問題
が生ずる。Further, JP-A-57-130407 discloses a long cylindrical anisotropic resin magnet in which ferromagnetic powders are bonded with an ethylene-vinyl acetate copolymer. However, in the case of such a long cylindrical anisotropic resin magnet, the problem of warpage of the molded body often occurs. Although the magnet roll is long and is usually housed in a sleeve, a slight warpage causes various serious problems.
円筒状複合磁石成形体のそりは、あらかじめ金型内にマ
グネットロールのシャフトを挿入しておくインサート成
形の場合にもしばしば生ずることがわかった。また成形
体のそりは特に磁場中で成形する場合に生ずることもわ
かった。この原因は必ずしも解明されていないが、その
一つは磁場中の金型内に磁性体・EVA樹脂組成物の溶
融物を注入する場合、溶融物が十分に均一に充填される
ものとは限らないという点である。また不均一な磁場の
下でも不均一な混練物の充填が生じうる。不均一な充填
によりシャフトは金型中で曲がる傾向がある。金型から
成形体を取り出すと曲がったシャフトの復元力により成
形体は曲げられる。その他樹脂複合磁石自身中の残留応
力も曲がりやそりに寄与すると考えられる。そりが起こ
るような条件下では、磁石の長手方向に磁力が不均一に
なるという問題も生ずる。It has been found that the warpage of the cylindrical composite magnet molded body often occurs in the case of insert molding in which the shaft of the magnet roll is previously inserted into the mold. It was also found that the warpage of the molded body occurs especially when molded in a magnetic field. The cause of this is not always clarified, but one of them is that when the melt of the magnetic material / EVA resin composition is injected into the mold in the magnetic field, the melt is not always uniformly filled. There is no point. Further, even under a non-uniform magnetic field, non-uniform filling of the kneaded material may occur. The uneven filling tends to cause the shaft to bend in the mold. When the molded body is taken out of the mold, the molded body is bent by the restoring force of the bent shaft. It is also considered that the residual stress in the resin composite magnet itself also contributes to bending and warping. Under the condition that warpage occurs, there is a problem that the magnetic force becomes non-uniform in the longitudinal direction of the magnet.
このようにEVA樹脂を使用した場合、得られた長尺磁
石は優れた耐熱衝撃性を有するが、そりや曲がり等の寸
法安定性に問題がある。When the EVA resin is used as described above, the obtained long magnet has excellent thermal shock resistance, but there is a problem in dimensional stability such as warpage and bending.
またEVA樹脂を使用した場合、成形時間が長くなる
(例えばポリアミド樹脂を使用した場合の3倍以上)と
いう問題がある。Further, when using EVA resin, there is a problem that the molding time becomes long (for example, three times or more that when using polyamide resin).
発明の要約 従って本発明の目的は、そりのない長尺の円筒状異方性
複合磁石を有するマグネットロールを能率よく製造する
方法を提供することである。SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide a method for efficiently producing a magnet roll having a long cylindrical anisotropic composite magnet without warpage.
そりのない長尺の異方性磁性体・樹脂複合磁石は、樹脂
としてエチレン−酢酸ビニル共重合体を使用し、かつ該
共重合体の酢酸ビニル含有量を4〜10重量%とし、該樹
脂と強磁性粉末とを主体とする溶融混練物を磁場のかか
った長尺の金型内に注入することにより成形することが
できることが発見された。またエチレン・酢酸ビニル共
重合体が3g/10min.以上のメルトインデックス(AS
TMD=1238)を有する場合に、混練物の成形が容易で
あることも発見された。A long anisotropic magnetic / resin composite magnet without warping uses an ethylene-vinyl acetate copolymer as a resin, and the vinyl acetate content of the copolymer is 4 to 10% by weight. It was discovered that the melt-kneaded material mainly composed of and the ferromagnetic powder can be molded by injecting it into a long mold under a magnetic field. The ethylene / vinyl acetate copolymer has a melt index (AS of 3 g / 10 min. Or more).
It was also found that the kneaded product was easy to mold when it had TMD = 1238).
かかる発見に基づき、本発明は強磁性粉末とエチレン・
酢酸ビニル共重合体とを主体とする長尺の異方性複合磁
石成形体であって、前記共重合体の酢酸ビニル含有量が
4〜10重量%であり、もってそりや曲りがないとともに
優れた磁気特性を有する成形体を有するマグレットロー
ルの製造方法を提供する。Based on these findings, the present invention provides a ferromagnetic powder and ethylene.
A long anisotropic composite magnet molding mainly composed of a vinyl acetate copolymer, wherein the vinyl acetate content of the copolymer is 4 to 10% by weight, which is excellent in that there is no warp or bending. Provided is a method for manufacturing a maglet roll having a molded body having excellent magnetic properties.
発明の構成 本発明の長尺の複合磁石は任意の断面形状を有し得る
が、製作が容易であるという理由で円筒状であるのが望
ましい。円筒状複合磁石の長さ/直径比は、マグネット
ロールに使用するものの場合、通常約5以上であるが実
質的には約10又はそれ以上である。長さ/直径比に特に
制限はないが、その比が大きくなるに従ってそりや曲り
の問題は深刻になる。Configuration of the Invention The long composite magnet of the present invention may have any cross-sectional shape, but is preferably cylindrical because it is easy to manufacture. The length / diameter ratio of the cylindrical composite magnet, when used for a magnet roll, is usually about 5 or more, but substantially about 10 or more. There is no particular limitation on the length / diameter ratio, but as the ratio increases, the problem of warping and bending becomes more serious.
酢酸ビニルの含有量が少ない程エチレン酢酸ビニル共重
合体の硬度と軟化点が高くなる傾向にあることはよく知
られているが、本発明者等は、エチレン酢酸ビニル共重
合体の硬度と軟化点が高い程短い時間で成形することが
できることおよび寸法安定性に優れている、すなわちそ
りや曲りが少ないことを発見した。従って成形能率およ
び寸法安定性の点からは、酢酸ビニルの含有量の少ない
エチレン酢酸ビニル共重合体が有利である。具体的には
10重量%以下、好ましくは8重量%以下である。酢酸ビ
ニル含有量が10重量%より高いと得られた長尺複合磁石
成形体のそりは大きくなりすぎ、マグネットロールに使
用できなくなる。また成形時間も長くなる。一方酢酸ビ
ニルの含有量が少なすぎると、残留応力を十分に緩和吸
収することが不可能になり、成形体に割れが生ずる傾向
が生ずる。従って、酢酸ビニルの含有量は4重量%以上
と(好ましくは4重量%より大きく)することが必要で
ある。It is well known that the smaller the content of vinyl acetate, the higher the hardness and softening point of the ethylene-vinyl acetate copolymer, but the present inventors have found that the hardness and softening of the ethylene-vinyl acetate copolymer. It has been discovered that the higher the point, the shorter the molding time and the better the dimensional stability, that is, the less warpage and bending. Therefore, from the viewpoint of molding efficiency and dimensional stability, an ethylene vinyl acetate copolymer having a low vinyl acetate content is advantageous. In particular
It is 10% by weight or less, preferably 8% by weight or less. If the vinyl acetate content is higher than 10% by weight, the warp of the obtained long composite magnet compact becomes too large to be used for a magnet roll. Also, the molding time becomes long. On the other hand, if the content of vinyl acetate is too low, it becomes impossible to absorb and absorb the residual stress sufficiently, and the molded product tends to crack. Therefore, it is necessary that the content of vinyl acetate is 4% by weight or more (preferably greater than 4% by weight).
また成形性の点からエチレン酢酸ビニル共重合体の流動
性が良いことが必要であり、具体的には3g/10min以上
のメルトインデックスを有することが必要である。Further, from the viewpoint of moldability, it is necessary that the ethylene-vinyl acetate copolymer has good fluidity, and specifically, it is necessary that it has a melt index of 3 g / 10 min or more.
本発明に使用できるエチレン酢酸ビニル共重合体で市販
のものとしては、三井ポリケミカル製のM−2030(酢酸
ビニル含有量6重量%、メルトインデックス70g/10mi
n)およびP−0607(酢酸ビニル含有量6重量%、メル
トインデックス25g/10min)、住友化学工業製のD−30
21(酢酸ビニル含有量6重量%、メルトインデックス7
g/10min)、日本ユニカー製のNUC−5491(酢酸ビニ
ル含有量6重量%、メルトインデックス5.5g/10min)
などが挙げられる。Commercially available ethylene vinyl acetate copolymers usable in the present invention include M-2030 (vinyl acetate content 6% by weight, melt index 70 g / 10 mi, manufactured by Mitsui Polychemicals).
n) and P-0607 (vinyl acetate content 6% by weight, melt index 25 g / 10 min), Sumitomo Chemical D-30
21 (vinyl acetate content 6% by weight, melt index 7
g / 10 min), NUC-5491 manufactured by Nippon Unicar (vinyl acetate content 6% by weight, melt index 5.5 g / 10 min)
And so on.
本発明においては強磁性粉末として、Baフェライト、
Srフェライトなどのマグネットプランバイト型結晶構
造を有するフェライト粉末、アルニコ磁石粉末、Fe−
Cr−Co系磁石粉末、希土類コバルト磁石粉末、希土
類鉄磁石粉末等の強磁性粉末を使用することができる。
これらの強磁性粉末の配合量は、強磁性粉末:樹脂の重
量比が80〜96:20〜4、好ましくは磁粉が85重量%以上
となるように定めればよい。強磁性粉末の配合量が80重
量部未満では所定の磁気特性(磁石表面での残留磁束密
度が1400G以上)が得難く、その配合量が96重量部を越
えると、成形がほぼ困難となる。強磁性粉末は樹脂との
ぬれ特性を改善するために、予めその表面を有機ケイ素
化合物もしくは有機チタネート化合物等で被覆してもよ
い。In the present invention, as the ferromagnetic powder, Ba ferrite,
Ferrite powder having magnet-plumbite type crystal structure such as Sr ferrite, alnico magnet powder, Fe-
Ferromagnetic powders such as Cr—Co based magnet powder, rare earth cobalt magnet powder, and rare earth iron magnet powder can be used.
The blending amount of these ferromagnetic powders may be determined so that the weight ratio of ferromagnetic powder: resin is 80 to 96:20 to 4, preferably 85% by weight or more of magnetic powder. When the blending amount of the ferromagnetic powder is less than 80 parts by weight, it is difficult to obtain a predetermined magnetic property (the residual magnetic flux density on the magnet surface is 1400 G or more), and when the blending amount exceeds 96 parts by weight, molding becomes almost difficult. The surface of the ferromagnetic powder may be previously coated with an organic silicon compound, an organic titanate compound or the like in order to improve the wettability with the resin.
磁性粉と樹脂のほかに、成形性を改善するためにポリエ
チレンワックス、ステアリン酸カルシウム等の滑剤若し
くは酸アミド化合物等を少量(数重量%)加えてもよ
い。In addition to the magnetic powder and resin, a small amount (several weight%) of a lubricant such as polyethylene wax, calcium stearate, or an acid amide compound may be added to improve moldability.
本発明によれば、上記の原料を用いて次のようにして異
方性を有する長尺複合磁石が得られる。まず強磁性粉末
とEVA樹脂および必要に応じ他の添加材料を含む混練
物を準備する。次に該混練物を、周囲に電磁石もしくは
永久磁石を設けた金型内に注入し、磁場を加えながらか
つ加熱しながら射出成形しついで冷却固化後金型から成
形体を取出す。異方性化を十分に行うためには、6000〜
10000G程度の磁場中で成形することが適当である。所
望の用途に応じ任意の数の磁極を設けるように異方性化
処理を行なうことができる。また設備の小形化および簡
略化の点からは、永久磁石による磁界中で射出成形する
のが有利である。このようにして得た成形体はさらに加
工する必要なくマグネットロールに使用することができ
るが、必要に応じて外形を所定の寸法に加工してもよ
い。According to the present invention, an elongated composite magnet having anisotropy can be obtained using the above raw materials as follows. First, a kneaded material containing ferromagnetic powder, EVA resin, and other additive materials as needed is prepared. Next, the kneaded product is poured into a mold provided with an electromagnet or a permanent magnet on the periphery, injection molding is performed while heating while applying a magnetic field, and after cooling and solidification, a molded product is taken out from the mold. 6000-
It is suitable to mold in a magnetic field of about 10,000 G. The anisotropy treatment can be performed so as to provide an arbitrary number of magnetic poles according to a desired application. From the viewpoint of downsizing and simplification of equipment, it is advantageous to perform injection molding in a magnetic field of a permanent magnet. The molded body thus obtained can be used for a magnet roll without further processing, but the outer shape may be processed into a predetermined dimension as necessary.
マグネットロール用の長尺複合磁石を製造する場合、成
形体を円筒状とするのが便利であるが、これは単に円筒
状金型を用いることにより達成できる。円筒状磁石にシ
ャフトを取り付けることによりマグネットロールを作成
することができる。When producing a long composite magnet for a magnet roll, it is convenient to make the molded body into a cylindrical shape, but this can be achieved by simply using a cylindrical mold. A magnet roll can be created by attaching a shaft to a cylindrical magnet.
マグネットロールはまたインサート成形により一工程で
作成することもできる。この場合、円筒状金型内にシャ
フトをあらかじめ挿入しておき、磁場をかけながら混練
物を注入する。成形体は複合磁石とシャフトとが一体と
なっているので、そのままマグネットロールとして使用
し得る。The magnet roll can also be made in one step by insert molding. In this case, the shaft is previously inserted into the cylindrical mold, and the kneaded material is injected while applying a magnetic field. Since the molded body has the composite magnet and the shaft integrated, it can be used as it is as a magnet roll.
得られたマグネットロールは異方性方向と同方向に着磁
し、適当なスリーブ内に収容した後に現像装置等に組み
込む。The obtained magnet roll is magnetized in the same direction as the anisotropic direction, housed in an appropriate sleeve, and then mounted in a developing device or the like.
発明の実施例および比較例 以下実施例および比較例により本発明を具体的に説明す
るが、これにより本発明が限定されるものではない。EXAMPLES AND COMPARATIVE EXAMPLES OF THE INVENTION Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples, but the present invention is not limited thereto.
実施例1 平均粒径1.60μmのSrフェライト粉末8.90kgにエチレ
ン酢酸ビニル共重合体(東洋曹達製メルセン900、酢ビ
含有量4重量%、メルトインデックス30g/10min)1.10
kgを加えて2軸押出機により130℃の温度で混練した。
得られた流動状混練物を、マグネットロール用軸(外径
10mmφ、sus304)を立設した金型を備えた射出成形機に
射出温度230℃、射出圧力1200kg/cm2、射出時間6sec、
金型温度80℃、冷却時間70secの条件で注入した。磁場
は成形体の磁極がNSSの3極となるように印加した。
ついで冷却固化後金型から軸付成形体(外径28mmφ、長
さ240mm)を取出した。そして同様の条件で10本の成形
体を製作した。Example 1 8.90 kg of Sr ferrite powder having an average particle size of 1.60 μm was added to ethylene vinyl acetate copolymer (Mersen 900 manufactured by Toyo Soda Co., Ltd., vinyl acetate content 4% by weight, melt index 30 g / 10 min) 1.10
Kg was added and the mixture was kneaded by a twin-screw extruder at a temperature of 130 ° C.
The resulting fluid kneaded product was used for the magnet roll shaft (outer diameter
10mmφ, sus304) standing injection molding machine equipped with an injection temperature 230 ℃, injection pressure 1200kg / cm 2 , injection time 6sec,
Injection was performed under the conditions of a mold temperature of 80 ° C. and a cooling time of 70 seconds. The magnetic field was applied so that the magnetic poles of the molded body had three NSS poles.
Then, after cooling and solidification, a molded body with a shaft (outer diameter 28 mmφ, length 240 mm) was taken out from the mold. Then, 10 molded bodies were manufactured under the same conditions.
実施例2 エチレン酢酸ビニル共重合体としてM−2030(三井ポリ
ケミカル製、酢ビ含有量6重量%、メルトインデックス
7g/10min)を用いた以外は実施例1と同様の条件で10
本の成形体を製作した。Example 2 M-2030 as an ethylene-vinyl acetate copolymer (Mitsui Polychemical, vinyl acetate content 6% by weight, melt index
10 g under the same conditions as in Example 1 except that 7 g / 10 min) was used.
A molded body of a book was produced.
実施例3 エチレン酢酸ビニル共重合体としてP−0607(三井ポリ
ケミカル製、酢ビ含有量6重量%、メルトインデックス
25g/10min)を用いた以外は実施例1と同様の条件で10
本の成形体を製作した。Example 3 P-0607 as an ethylene vinyl acetate copolymer (manufactured by Mitsui Polychemical, vinyl acetate content 6% by weight, melt index
10 g under the same conditions as in Example 1 except that 25 g / 10 min) was used.
A molded body of a book was produced.
実施例4 エチレン酢酸ビニル共重合体として(住友化学工業製、
酢ビ含有量6重量%、メルトインデックス7g/10min)
を用いた以外は実施例1と同様の条件で10本の成形体を
製作した。Example 4 As ethylene vinyl acetate copolymer (Sumitomo Chemical Co.,
Vinyl acetate content 6% by weight, melt index 7g / 10min)
Ten molded bodies were manufactured under the same conditions as in Example 1 except that was used.
実施例5 エチレン酢酸ビニル共重合体としてNUC−5491(日本
ユニカー製、酢ビ含有量6重量%、メルトインデックス
5.5g/10min)を用いた以外は実施例1と同様の条件で1
0本の成形体を製作した。Example 5 NUC-5491 as an ethylene vinyl acetate copolymer (manufactured by Nippon Unicar, vinyl acetate content 6% by weight, melt index)
1) under the same conditions as in Example 1 except that 5.5 g / 10 min) was used.
0 molded bodies were produced.
実施例6 エチレン酢酸ビニル共重合体としてNUC−3140(日本
ユニカー製、酢ビ含有量10重量%、メルトインデックス
20)を用いた以外は実施例1と同様の条件で10本の成形
体を製作した。Example 6 NUC-3140 (manufactured by Nippon Unicar, vinyl acetate content 10% by weight, melt index as ethylene vinyl acetate copolymer)
Ten compacts were manufactured under the same conditions as in Example 1 except that 20) was used.
比較例1 平均粒径1.47μmのSrフェライト粉末8.50kgにナイロ
ン6(宇部興産製1011FB)1.50kgを2軸押出機により
240℃の温度で混練した。次に得られた混練物を射出温
度280℃、射出圧力900kg/cm2で成形した以外は実施例
1と同様の条件で10本の成形体を製作した。Comparative Example 1 1.50 kg of nylon 6 (1011FB manufactured by Ube Industries) was added to 8.50 kg of Sr ferrite powder having an average particle size of 1.47 μm by a twin-screw extruder.
Kneading was performed at a temperature of 240 ° C. Next, 10 molded bodies were manufactured under the same conditions as in Example 1 except that the obtained kneaded product was molded at an injection temperature of 280 ° C. and an injection pressure of 900 kg / cm 2 .
比較例2 エチレン酢酸ビニル共重合体の代りに低密度ポリエチレ
ン(三井ポリケミカル製ミラソン68)を用いた以外は実
施例1と同様の条件で10本の成形体を製作した。Comparative Example 2 Ten molded products were manufactured under the same conditions as in Example 1 except that low density polyethylene (Mirason 68 manufactured by Mitsui Polychemical) was used instead of the ethylene-vinyl acetate copolymer.
比較例3 エチレン酢酸ビニル共重合体として三井ポリケミカル製
エバフレックスP−1207(酢酸ビニル含有量12重量%、
メルトインデックス12g/10min)を用いた以外は実施例
1と同様の条件で10本の成形体を製作した。Comparative Example 3 Evaflex P-1207 manufactured by Mitsui Polychemicals as an ethylene-vinyl acetate copolymer (vinyl acetate content 12% by weight,
Ten compacts were manufactured under the same conditions as in Example 1 except that the melt index was 12 g / 10 min).
比較例4 エチレン酢酸ビニル共重合体として三井ポリケミカル製
エバフレックス410(酢酸ビニル含有量19重量%、メル
トインデックス400g/min)を用いた以外は実施例1と
同様の条件で10本の成形体を製作した。Comparative Example 4 Ten molded products under the same conditions as in Example 1 except that Evaflex 410 (vinyl acetate content 19% by weight, melt index 400 g / min) manufactured by Mitsui Polychemical was used as the ethylene-vinyl acetate copolymer. Was produced.
比較例5 エチレン酢酸ビニル共重合体として住友化学製H−4011
(酢酸ビニル含有量20重量%、メルトインデックス20g
/10min)を用いた以外は実施例1と同様の条件で10本
の成形体を製作した。Comparative Example 5 H-4011 manufactured by Sumitomo Chemical Co., Ltd. as an ethylene-vinyl acetate copolymer
(Vinyl acetate content 20% by weight, melt index 20g
/ 10 min) was used to produce 10 compacts under the same conditions as in Example 1.
上記各実施例および比較例で得られた成形体について、
成形体の割れの有無、そり、ヒートサイクルテストによ
る耐熱衝撃性、密度および着磁後の磁気特性について測
定を行った。その結果を第1表に示す。また各々の成形
体の所要成形時間を同じく第1表に示す。なおヒートサ
イクルテストは、第1図に示す通り、室温から40℃まで
2℃/分の速度で加熱し(区間A−B)、40℃に3時間
保ち(B−C)、2℃/分の冷却速度で−40℃まで冷却
し(C−D)、−40℃に3時間保ち(D−E)、再び2
℃/分の速度で室温まで加熱する(E−F)サイクル
を、5回繰り返すことにより行った。For the molded body obtained in each of the examples and comparative examples,
The presence or absence of cracks in the molded body, warpage, thermal shock resistance by a heat cycle test, density and magnetic properties after magnetization were measured. The results are shown in Table 1. Table 1 also shows the required molding time for each molded body. In the heat cycle test, as shown in Fig. 1, the sample was heated from room temperature to 40 ° C at a rate of 2 ° C / minute (section AB), kept at 40 ° C for 3 hours (BC), and 2 ° C / minute. At a cooling rate of -40 ° C (C-D), kept at -40 ° C for 3 hours (D-E), and again 2
A (EF) cycle of heating to room temperature at a rate of ° C / min was repeated 5 times.
第1表から明らかなように、実施例1〜6で得られた成
形体は、磁気特性、耐熱衝撃性および寸法精度の点で十
分満足すべき結果が得られ、また成形能率も良好であ
る。 As is clear from Table 1, the molded products obtained in Examples 1 to 6 have sufficiently satisfactory results in terms of magnetic properties, thermal shock resistance and dimensional accuracy, and have good molding efficiency. .
第2図は実施例1で得られたNSSの3つの磁極を有す
る成形体の円周方向の磁束密度分布を示す。FIG. 2 shows the magnetic flux density distribution in the circumferential direction of the molded body having three NSS magnetic poles obtained in Example 1.
これに対して比較例1のポリアミド含有成形体では、磁
気特性および成形能率は良好であるが、第3図に示すよ
うに、シャフト2に固着された円筒状永久磁石1に残留
応力に起因すると考えられる応力亀裂3が多数発生する
傾向があり、成形歩留が著しく低い。また比較例2のポ
リエチレンを使用した場合も割れがひどい。比較例3〜
5の成形体は寸法精度および成形能率が著しく劣ること
がわかる。On the other hand, the polyamide-containing molded body of Comparative Example 1 has good magnetic properties and molding efficiency, but as shown in FIG. 3, it is considered that the residual stress is caused in the cylindrical permanent magnet 1 fixed to the shaft 2. Many possible stress cracks 3 tend to occur and the molding yield is significantly low. Also, when the polyethylene of Comparative Example 2 is used, cracking is severe. Comparative Example 3
It can be seen that the molded product of No. 5 is extremely inferior in dimensional accuracy and molding efficiency.
発明の効果 以上に記述の如く、本発明によれば、特定の特性を有す
るエチレン酢酸ビニル共重合体をベースレジンとして用
いることにより、磁気特性、寸法安定性および耐熱衝撃
性に優れた磁気特性を有する長尺円筒複合磁石を能率よ
く得ることができる。As described above, according to the present invention, by using an ethylene vinyl acetate copolymer having specific properties as a base resin, magnetic properties excellent in magnetic properties, dimensional stability and thermal shock resistance can be obtained. The long cylindrical composite magnet can be efficiently obtained.
第1図はヒートサイクル条件を示す図、第2図は本発明
法により得られた複合磁石の磁束密度分布を示す図、第
3図は従来法により得られた成形体の斜視図である。FIG. 1 is a diagram showing heat cycle conditions, FIG. 2 is a diagram showing a magnetic flux density distribution of a composite magnet obtained by the method of the present invention, and FIG. 3 is a perspective view of a molded body obtained by the conventional method.
フロントページの続き (72)発明者 萩 千敏 埼玉県熊谷市三ヶ尻5200番地 日立金属株 式会社熊谷工場内 (72)発明者 小泉 悟 埼玉県熊谷市三ヶ尻5200番地 日立金属株 式会社熊谷工場内 (56)参考文献 特開 昭57−130407(JP,A) 特公 昭52−12400(JP,B1) 特公 昭55−32206(JP,B2)Front page continued (72) Inventor Chitoshi Hagi 5200 Mikkajiri, Kumagaya, Saitama Prefecture Inside the Hitachi Metals Co., Ltd. Kumagaya Plant (72) Inventor Satoru Koizumi 5200, Mikkajiri, Kumagaya, Saitama Inside Kumagaya Plant 56) References JP-A-57-130407 (JP, A) JP-B 52-12400 (JP, B1) JP-B 55-32206 (JP, B2)
Claims (1)
重量%で、メルトインデックス(ASTM D123
8)が3g/10min以上のエチレン−酢酸ビニル共重
合体とを主体としかつ前記強磁性粉末と前記エチレン−
酢酸ビニル共重合体とを80〜96:20〜4の重量比
で含む混合物を流動化し、磁場の存在下において、長さ
/直径比が5以上の円筒状の成形空間を有しかつシャフ
トが挿入された金型内に射出成形し、得られたシャフト
付円筒状成形体の外周面に異方性方向と同方向に多極着
磁することを特徴とするマグネットロールの製造方法。1. A ferromagnetic powder and vinyl acetate content of 4-10.
In wt%, melt index (ASTM D123
8) is mainly composed of an ethylene-vinyl acetate copolymer having a content of 3 g / 10 min or more, and the ferromagnetic powder and the ethylene-
A mixture containing a vinyl acetate copolymer in a weight ratio of 80 to 96:20 to 4 is fluidized, and has a cylindrical molding space having a length / diameter ratio of 5 or more in the presence of a magnetic field, and the shaft is A method for producing a magnet roll, comprising performing injection molding in an inserted mold, and magnetizing the outer peripheral surface of the obtained cylindrical molded body with a shaft in multiple directions in the same direction as the anisotropic direction.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59062549A JPH0618128B2 (en) | 1984-03-30 | 1984-03-30 | Magnet roll manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59062549A JPH0618128B2 (en) | 1984-03-30 | 1984-03-30 | Magnet roll manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60206110A JPS60206110A (en) | 1985-10-17 |
| JPH0618128B2 true JPH0618128B2 (en) | 1994-03-09 |
Family
ID=13203435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59062549A Expired - Lifetime JPH0618128B2 (en) | 1984-03-30 | 1984-03-30 | Magnet roll manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0618128B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62199002A (en) * | 1986-02-27 | 1987-09-02 | Kanegafuchi Chem Ind Co Ltd | Composition for synthetic resinous magnet and synthetic resinous magnet and magnet roll made of the same |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5228696A (en) * | 1975-08-29 | 1977-03-03 | Toshiba Corp | Resin-ferrite composition |
| JPS57130407A (en) * | 1981-02-06 | 1982-08-12 | Daido Steel Co Ltd | Cylindrical anisotropic resin magnet |
-
1984
- 1984-03-30 JP JP59062549A patent/JPH0618128B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60206110A (en) | 1985-10-17 |
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