JPH03214422A - Production of magnetic recording medium - Google Patents
Production of magnetic recording mediumInfo
- Publication number
- JPH03214422A JPH03214422A JP910790A JP910790A JPH03214422A JP H03214422 A JPH03214422 A JP H03214422A JP 910790 A JP910790 A JP 910790A JP 910790 A JP910790 A JP 910790A JP H03214422 A JPH03214422 A JP H03214422A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- layer
- magnetic layer
- coating
- recording medium
- 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
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Landscapes
- Manufacturing Of Magnetic Record Carriers (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、磁気記録媒体の製造方法に関し、特に非磁性
支持体上に磁性層を形成して成る磁気記録媒体の製造方
法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for manufacturing a magnetic recording medium, and particularly to a method for manufacturing a magnetic recording medium in which a magnetic layer is formed on a nonmagnetic support.
従来、オーディオテープ、ビデオテープ等の磁気テープ
、及びフロノピイディスク等の磁気ディスク等といった
磁気記録媒体の一般的な製造方法としては、通常の製品
よりも幅広の非磁性支持体上に磁性塗布液を塗布して磁
性層を形成し、配向処理等を行い磁性層を乾燥させた後
、前記磁性層の表面平滑化処理を行ってテープ原反を作
製し、その後、裁断工程において前記テープ原反を所定
のテープ幅或いは所定の形状に裁断して製造されている
.
前記表面平滑化処理は、前記磁性層表面の艶出し、平滑
化、充填密度の向上あるいは塗布厚みの均一化等のため
に行われており、特に前記磁性層表面の平滑化は、磁気
記録媒体の再生出力向上やテープノイズの減少に対して
有効である。Conventionally, the general manufacturing method for magnetic recording media, such as magnetic tapes such as audio tapes and video tapes, and magnetic disks such as Fronopy disks, has been to apply magnetic coating onto a non-magnetic support that is wider than normal products. After applying a liquid to form a magnetic layer, performing an orientation treatment and drying the magnetic layer, the surface of the magnetic layer is smoothed to produce a tape material, and then, in a cutting process, the tape material is It is manufactured by cutting the tape into a predetermined tape width or shape. The surface smoothing treatment is performed to polish or smooth the surface of the magnetic layer, improve the packing density, or make the coating thickness uniform. This is effective for improving playback output and reducing tape noise.
更に、近年に至り、磁気記録媒体の記憶容量を高めるこ
とが強く要望されており、磁気記録媒体の単位面積当た
りの情報記録密度を高める必要がある。Furthermore, in recent years, there has been a strong demand for increasing the storage capacity of magnetic recording media, and it is necessary to increase the information recording density per unit area of magnetic recording media.
そこで、前記情報記録密度を高めるためには、情報の記
録及び再生を行う磁気ヘノドから発生する書き込み磁束
を微小な面積に集中させる必要があるので、…I記侑気
ヘノトは小型化され、発生磁束蟹が滅少させられる。従
って、■−記のように滅せられた磁束で磁性層の磁化の
力向を反転するためには、前記磁性層の体積の減少、す
なわち萌記るn性層の厚みを滅少させなければ完全な磁
化反転を行うことができないので、前記磁気記録媒体の
磁性層を薄層化することが必要となってきている。Therefore, in order to increase the information recording density, it is necessary to concentrate the write magnetic flux generated from the magnetic head that records and reproduces information in a minute area. Magnetic flux crabs will become extinct. Therefore, in order to reverse the direction of magnetization of the magnetic layer with the extinguished magnetic flux as shown in (1)--, the volume of the magnetic layer must be reduced, that is, the thickness of the n-type layer must be decreased. Since it is not possible to perform complete magnetization reversal, it has become necessary to reduce the thickness of the magnetic layer of the magnetic recording medium.
また、上記の如き粉末るd性材料を有機ハインダ中に分
散せしめた磁性塗布液を非磁性支持体上に塗布、乾燥さ
せる塗布型の磁気記録媒体に対して、抗磁力しや残留磁
束密度B,が大きく磁性層の厚みを極めて薄《すること
ができ、非磁性支持体上に強磁性金属材料からなる金属
薄膜を真空蒸着法等によって直接被着形成した強磁性金
属薄膜型の磁気記録媒体が使用され始めている。In addition, for coated magnetic recording media in which a magnetic coating solution in which the above-described powdery d-material is dispersed in an organic binder is coated on a non-magnetic support and dried, the coercive force and residual magnetic flux density B , is large, and the thickness of the magnetic layer can be made extremely thin. A ferromagnetic metal thin film type magnetic recording medium in which a metal thin film made of a ferromagnetic metal material is directly deposited on a nonmagnetic support by vacuum evaporation or the like. is starting to be used.
しかしながら、磁気記録媒体の再生出力向上やテープノ
イズの減少に対して有効な前記磁性層表面の平滑性は、
該磁性層が形成される前記非磁性支持体表面の平滑性と
密接な関係に有るので、平滑な磁性層表面を得る為には
表面平滑性の良い非磁性支持体を用いる必要があり、特
に上記の如く薄層化された磁性層表面ほど前記非磁性支
持体表面の平滑性の影響を受け易い.
従って、良好な磁気特性を有する磁気記録媒体を得る為
には、表面平滑性の良好な非磁性支持体を用いる必要が
あるが、このような非磁性支持体材料は高価であり、製
造コストが高くなるという問題がある.
そこで、本発明の目的は上記課題を解消することにあり
、表面平滑性の良くない安価な非磁性支持体表面の上に
も、再生出力が高くテープノイズが低い表面平滑性の良
好な磁性層を薄層形成できる製造コストの安価な磁気記
録媒体の製造方法を提供することである。However, the smoothness of the surface of the magnetic layer is effective for improving the reproduction output of magnetic recording media and reducing tape noise.
Since the magnetic layer is closely related to the smoothness of the surface of the non-magnetic support on which the magnetic layer is formed, it is necessary to use a non-magnetic support with good surface smoothness in order to obtain a smooth magnetic layer surface. As mentioned above, the thinner the surface of the magnetic layer is, the more easily it is affected by the smoothness of the surface of the nonmagnetic support. Therefore, in order to obtain a magnetic recording medium with good magnetic properties, it is necessary to use a nonmagnetic support with good surface smoothness, but such nonmagnetic support materials are expensive and the manufacturing cost is high. The problem is that it gets expensive. Therefore, an object of the present invention is to solve the above problems, and to provide a magnetic layer with good surface smoothness, high playback output, low tape noise, even on the surface of an inexpensive non-magnetic support with poor surface smoothness. An object of the present invention is to provide a method for manufacturing a magnetic recording medium that can form a thin layer of magnetic recording media at low manufacturing cost.
本発明の上記目的は、非磁性支持体上に該非磁性支持体
よりも表面の平滑化処理をし易い高分子樹脂或いは該高
分子樹脂と非磁性の粒子を主成分とするダミー層を形成
し、該ダミー層の表面を平滑化処理した後に、前記ダミ
ー層上に磁性層を形成することを特徴とする磁気記録媒
体の製造方法により達成される.
尚、上記の如き表面の平滑化処理をし易い高分子樹脂と
は、加熱しながら加圧ローラによって加圧をする際にヅ
性変形が可能となる軟化温度が低い高分子樹脂(l50
゜C以下)、又は加圧ロールによる加圧力が低い高分子
樹脂のことであり、一般に前記非磁性支持体として使用
されているポリエチレンテレフタレート(PET)等よ
りも表面の平滑化処理をし易い高分子樹脂が好ましく、
本発明のダミー層に使用する前記高分子樹脂としては、
例えば熱可塑性樹脂、熱硬化性樹脂、反応型樹脂やこれ
らの混合物を使用することができる。熱可塑性樹脂とし
ては軟化温度が150゜C以下、平均分子量が1000
0〜300000、重合度が約50〜2000程度のも
ので、例えば塩化ビニル酢酸ビニル共重合体、塩化ビニ
ル重合体、塩化ビニル塩化ビニリデン共重合体、塩化ビ
ニルアクリロニトリル共重合体、アクリル酸エステルア
クリロニトリル共重合体、アクリル酸エステル塩化ビニ
リデン共重合体、アクリル酸エステルスチレン共重合体
、メタクリル酸エステルアクリロニトリル共重合体、メ
タクリル酸エステル塩化ビニリデン共重合体、メタクリ
ル酸エステルスチレン共重合体、ウレタンエラストマー
、ナイロンーシリコン系樹脂、ニトロセルロースーボリ
アミド樹脂、ボリフッカビニル、塩化ビニリデンアクリ
口ニトリル共重合体、ブタジエンアクリロニトリル共重
合体、ポリアミド樹脂、ポリビニルブチラール、セルロ
ース誘導体(セルロースアセテートブチレート、セルロ
ースダイアセテート、セルローストリアセテート、セル
ロースブロビオフ一ト、ニトロセルロース、エチルセル
ロース、メチルセルロース、プロビルセルロース、メチ
ルエチルセルロース、カルボキシメチルセルロース、ア
セチルセルロース等)、スチレンブタジエン共重合体、
ポリエステル樹脂、クロロビニルエーテルアクリル酸エ
ステル共重合体、アミノ樹脂、各種の合成ゴム系の熱可
塑性樹脂及びこれらの混合物等を使用することができる
。The above object of the present invention is to form on a non-magnetic support a polymer resin whose surface is easier to smoothen than the non-magnetic support, or a dummy layer mainly composed of the polymer resin and non-magnetic particles. This is achieved by a method of manufacturing a magnetic recording medium, which comprises forming a magnetic layer on the dummy layer after smoothing the surface of the dummy layer. In addition, the polymer resin whose surface can be easily smoothed as described above is a polymer resin with a low softening temperature (l50
℃ or less), or a polymer resin with a low pressure applied by a pressure roll, and whose surface is easier to smoothen than polyethylene terephthalate (PET), which is generally used as the non-magnetic support. Molecular resins are preferred;
The polymer resin used in the dummy layer of the present invention includes:
For example, thermoplastic resins, thermosetting resins, reactive resins, and mixtures thereof can be used. As a thermoplastic resin, the softening temperature is 150°C or less and the average molecular weight is 1000.
0 to 300,000, and the degree of polymerization is about 50 to 2,000, such as vinyl chloride vinyl acetate copolymer, vinyl chloride polymer, vinyl chloride vinylidene chloride copolymer, vinyl chloride acrylonitrile copolymer, acrylic acid ester acrylonitrile copolymer Polymer, acrylic acid ester vinylidene chloride copolymer, acrylic acid ester styrene copolymer, methacrylic acid ester acrylonitrile copolymer, methacrylic acid ester vinylidene chloride copolymer, methacrylic acid ester styrene copolymer, urethane elastomer, nylon Silicone resin, nitrocellulose-bolyamide resin, polyfukkavinyl, vinylidene chloride acrylonitrile copolymer, butadiene acrylonitrile copolymer, polyamide resin, polyvinyl butyral, cellulose derivatives (cellulose acetate butyrate, cellulose diacetate, cellulose triacetate, cellulose) brobiofluorite, nitrocellulose, ethylcellulose, methylcellulose, probilcellulose, methylethylcellulose, carboxymethylcellulose, acetylcellulose, etc.), styrene-butadiene copolymer,
Polyester resins, chlorovinyl ether acrylate copolymers, amino resins, various synthetic rubber-based thermoplastic resins, and mixtures thereof can be used.
熱硬化性樹脂又は反応型樹脂としては塗布液の状態では
200000以下の分子量であり、塗布、乾燥後に加熱
することにより、縮合、付加等の反応により分子量は無
限人のものとなる.又、これらの樹脂のなかで、樹脂が
熱分解するまでの間に溶融しないものが好ましい。具体
的には例えばフェノル樹脂、フェノキン樹脂、エボキン
樹脂、ポリウレタン硬化型樹脂、尿素樹脂、メラミン樹
脂、アルキノド樹脂、シリコン樹脂、アクリル系反応樹
脂、エボキシ−ボリアミド樹脂、ニトロセルロースメラ
ミン樹脂、高分子量ポリエステル樹脂とイソシアネート
プレポリマーの混合物、メタクリル酸塩共重合体とジイ
ソシアネートプレポリマーの混合物、ポリエステルボリ
オールとポリイソシアネートとの混合物、尿素ホルムア
ルデヒド樹脂、低分子量グリコール/高分子量ジオール
/トリフェニルメタントリイソシアネートの混合物、ポ
リアミン樹脂、ボリイミン樹脂及びこれらの混合物等で
ある.
これらの熱可塑性樹脂、熱硬化性樹脂、反応型樹脂は、
主たる官能基以外に官能基としてカルホン酸、スルフィ
ン酸、スルフェン酸、スルホン酸、燐酸、硫酸、ホスホ
ン、ホスフィン、ホウ酸、硫酸エステル基、燐酸エステ
ル基、これらのアルキルエステル基等の酸性基、アミノ
酸類;アミノスルホン酸類、アミノアルコールの硫酸ま
たは燐酸エステル類、アルキルヘタイン型等の両性類基
、アミノ基、イミノ基、イミド基、アミド基、エボキシ
基、等また、水酸基、アルコシル基、チオール基、ハロ
ゲン基、シリル基、シロキサン基を通常1種以上6種以
内含み、各々の官能基は樹脂lgあたりl XIO−’
eq−I XIO−”eq含む事が好ましい。Thermosetting resins or reactive resins have a molecular weight of 200,000 or less in the form of a coating solution, and when heated after coating and drying, the molecular weight becomes infinite due to reactions such as condensation and addition. Among these resins, those that do not melt before the resin is thermally decomposed are preferred. Specifically, for example, phenol resin, phenokine resin, evoquine resin, polyurethane curable resin, urea resin, melamine resin, alkynod resin, silicone resin, acrylic reaction resin, epoxy-bolyamide resin, nitrocellulose melamine resin, high molecular weight polyester resin. and isocyanate prepolymers, mixtures of methacrylate copolymers and diisocyanate prepolymers, mixtures of polyester polyols and polyisocyanates, urea formaldehyde resins, mixtures of low molecular weight glycols/high molecular weight diols/triphenylmethane triisocyanates, These include polyamine resins, polyimine resins, and mixtures thereof. These thermoplastic resins, thermosetting resins, and reactive resins are
In addition to the main functional groups, functional groups include acidic groups such as carbonic acid, sulfinic acid, sulfenic acid, sulfonic acid, phosphoric acid, sulfuric acid, phosphonic acid, phosphine, boric acid, sulfuric acid ester groups, phosphoric ester groups, and alkyl ester groups thereof, and amino acids. Classes: Aminosulfonic acids, sulfuric or phosphoric acid esters of amino alcohols, amphoteric groups such as alkylhetaine types, amino groups, imino groups, imido groups, amide groups, eboxy groups, etc. Also, hydroxyl groups, alkosyl groups, thiol groups , a halogen group, a silyl group, and a siloxane group, usually containing one to six types, and each functional group contains 1 XIO-' per 1 g of resin.
It is preferable to include eq-I XIO-"eq.
又、前記非磁性の粒子としては、例えば、カーポンプラ
ンク、α−アルミナ、T−アルミナ、αr−アルミナ、
溶融アルミナ、炭化ケイ素、酸化クロム、酸化セリウム
、コランダム、人造ダイヤモンド、α−酸化鉄、ザクロ
石、エメリー(主成分:コランダムと磁鉄鉱)、ガーネ
ント、ケイ石、窒化ケイ素、窒化硼素、炭化タングステ
ン、チタンカーバイト、クオーツ、トリポリ、ケイソウ
土、Vロマイト等を一種あるいは複数種組み合わせて用
いることができる。更に、これらの粒子の大きさは、大
きすぎると磁性層を塗布する面の表面性を悪くする一方
、小さずぎると前記ダミー層の補強効果がさほど期待で
きないので、その平均粒径が0.Ol〜2μ一の粒子が
望ましい。又、該粒子の混入割合としては、前記ダミー
層を構成する樹脂に対して重量で70%以下とすること
が望ましい。Further, examples of the non-magnetic particles include carpon blank, α-alumina, T-alumina, αr-alumina,
Fused alumina, silicon carbide, chromium oxide, cerium oxide, corundum, artificial diamond, α-iron oxide, garnet, emery (main components: corundum and magnetite), garnite, silica, silicon nitride, boron nitride, tungsten carbide, titanium Carbide, quartz, tripoli, diatomaceous earth, Vlomite, etc. can be used singly or in combination. Furthermore, if the size of these particles is too large, the surface properties of the surface to which the magnetic layer is coated will deteriorate, while if they are too small, the reinforcing effect of the dummy layer cannot be expected to be so great. Particles of 1 to 2 μm are desirable. Further, the mixing ratio of the particles is desirably 70% or less by weight of the resin constituting the dummy layer.
更に、前記ダミー層の形成手段としては、ロールコート
、グラビアコート、エクストルージョンヘンド及びドク
ターブレード方式等種々の塗布形式により形成すること
ができる。Furthermore, the dummy layer can be formed by various coating methods such as roll coating, gravure coating, extrusion hend, and doctor blade method.
以下、本発明に基づく磁気記録媒体の製造方法の一実施
態様を添付図面に基づいて詳細に説明する.
第1図は本発明の製造方法に基づく磁気記録媒体の製造
工程を示す概略図である.
繰出口−ルlから送り出された支持体2は、第2図の(
a)に示す様に、比較的表面性の悪い非磁性支持体であ
る.そこで、該支持体2の表面に第1塗布ヘッド3によ
って表面の平滑化処理をし易い高分子樹脂からなるダミ
ー層11を厚さ1〜4μm程度に塗布した後、乾燥ゾー
ン5にて該ダミー層11を乾燥固化する.前記第1塗布
ヘノド3には、前記高分子樹脂を連続的にかつ一定の流
量で送液する給液系4が連通しており、前記支持体上に
前記高分子樹脂を均一な塗布厚みで塗布する.この時、
前記ダミー層11の表面は第2図の(+))に示す様に
、比較的表面性の悪いままである.
次に、前記ダミー層l1を塗布された支持体2の表面を
一対のカレンダーロール6a,6bによってカレンダー
処理する。この時、前記カレンダーロール6a,6bは
約80゜C程度に加熱されると共に、約150〜400
kgw/cmの加圧力で、前記支持体2を加圧ニノブ
ずる。ずると、前記ダミ−Rillを構成している高分
子樹脂は、軟化温度が150゜C以下という比較的表面
の平滑化処理をし易い高分子樹脂を主成分としているの
で、第2図の(Clに示す様に、前記支持体2の表面6
こ塗布されたダミー層11の表面は平滑化処理されて良
好な表面性を有することができる。Hereinafter, one embodiment of the method for manufacturing a magnetic recording medium according to the present invention will be described in detail with reference to the accompanying drawings. FIG. 1 is a schematic diagram showing the manufacturing process of a magnetic recording medium based on the manufacturing method of the present invention. The support body 2 fed out from the feed-out port l is shown in FIG.
As shown in a), it is a non-magnetic support with relatively poor surface properties. Therefore, after coating the surface of the support 2 with a dummy layer 11 made of a polymer resin whose surface can be easily smoothed to a thickness of about 1 to 4 μm, the dummy layer 11 is coated in a drying zone 5. Dry and solidify layer 11. A liquid supply system 4 that feeds the polymer resin continuously and at a constant flow rate is connected to the first coating nozzle 3, and the polymer resin is coated on the support body with a uniform coating thickness. Apply. At this time,
The surface of the dummy layer 11 remains relatively poor in surface properties, as shown by (+) in FIG. Next, the surface of the support 2 coated with the dummy layer 11 is calendered using a pair of calender rolls 6a and 6b. At this time, the calender rolls 6a and 6b are heated to about 80°C and heated to about 150 to 400°C.
The support 2 is pressed with a pressure of kgw/cm. In other words, the polymer resin constituting the dummy rill is mainly composed of a polymer resin with a softening temperature of 150°C or less, which is relatively easy to smooth the surface of, and therefore As shown in Cl, the surface 6 of the support 2
The surface of the applied dummy layer 11 is smoothed to have good surface properties.
そして、iiI記支持体2の表面に第2塗布ヘノ1′7
によって磁性塗布液を塗布し、乾燥ヅーン9にて乾燥固
化して磁性層l2を形成する。iク記第2塗布へ,ト7
には、前記磁性塗布液を連続的にかつ一定の流量で送液
する給液系8が連通しており、前記支持体上に前記磁性
塗布液を均一な塗布厚みで塗布する。Then, a second coating layer 1'7 is applied to the surface of the support 2 described in iii.
A magnetic coating liquid is applied thereto and dried and solidified in a drying zone 9 to form a magnetic layer 12. To the second application of I, G7
A liquid supply system 8 for feeding the magnetic coating liquid continuously and at a constant flow rate communicates with the magnetic coating liquid, and the magnetic coating liquid is coated onto the support body with a uniform coating thickness.
ここで、前記磁性層l2は、良好な表面性を有する前記
ダミー層11の表面上に塗布されるので、前記支持体2
が比較的表面性の悪い非磁性支持体であっても、該磁性
層l2の表面は第2図の(dlに示す様に良好な表面性
を有することができる.そして、前記乾燥ゾーン9にて
乾燥された支持体2は巻き取り口ールlOに巻き取られ
て、磁性層のカレンダー処理工程等の次工程に送られる
。Here, since the magnetic layer l2 is coated on the surface of the dummy layer 11 having good surface properties, the magnetic layer l2
Even if it is a non-magnetic support with relatively poor surface properties, the surface of the magnetic layer l2 can have good surface properties as shown in (dl) in FIG. The dried support 2 is wound up on a take-up roll 10 and sent to the next process such as a calendering process for the magnetic layer.
従って、表面性が比較的良《ない安価な非磁性支持体上
にも、再生出力が高《テープノイズが低い表面平滑性の
良好な磁性層を薄層形成できる。Therefore, it is possible to form a thin magnetic layer with high reproduction output, low tape noise, and good surface smoothness even on an inexpensive nonmagnetic support with relatively poor surface properties.
また、前記ダミー層11を構成する比較的表面の平滑化
処理をし易い高分子樹脂にα−A1.03等の非磁性粒
子を添加することにより、前記ダミ層11の表面平滑化
処理時の樹脂の欠落といった欠陥発生に対する膜強度の
向上及び該ダミー層樹脂の前記カレンダーロールへの付
着防止が可能となる.
更に、従来は表面が平滑な非磁性支持体を用いていたの
で、記録再生装置内における磁気テープの走行性を改善
するためにバノクコート層を設けて支持体の反磁性層表
面を粗面化処理し、摩擦抵抗を下げなければならなかっ
た。しかしながら、本発明の塗布方法によれば表面の表
面性が比較的良くない非磁性支持体上に磁性層を形成す
ることができるので、表面の粗い非磁性支持体を用いれ
ば、該支持体の反磁性層表面は始めから粗く、粗面化処
理する必要がない。In addition, by adding non-magnetic particles such as α-A1.03 to the polymer resin constituting the dummy layer 11 whose surface is relatively easy to smooth, it is possible to It is possible to improve the film strength against defects such as resin missing and to prevent the dummy layer resin from adhering to the calender roll. Furthermore, since conventionally a non-magnetic support with a smooth surface was used, a banok coat layer was provided to roughen the surface of the diamagnetic layer of the support in order to improve the running properties of the magnetic tape in recording and reproducing devices. Therefore, frictional resistance had to be lowered. However, according to the coating method of the present invention, it is possible to form a magnetic layer on a non-magnetic support whose surface properties are relatively poor. The surface of the diamagnetic layer is rough from the beginning, and there is no need for roughening treatment.
尚、上記実施B欅においては、前記ダミー層Itがエク
ストルージョンヘノドによって塗布されているが、本発
明はこれに限定されるものではなく、ロールコート、グ
ラビアコート等の他の塗布手段を用いることができる。In the above-mentioned Example B, the dummy layer It is applied by extrusion, but the present invention is not limited to this, and other application methods such as roll coating and gravure coating may be used. be able to.
また、前記磁性層I2もエクストルージョンヘッドによ
って塗布されているが、他の塗布手段を用いることがで
きることは勿論であり、例えば強磁性金属材料からなる
金属薄膜を真空蒸着法等によって直接被着形成する強磁
性金属薄膜型の磁気記録媒体についても応用できる.又
、前記磁性層が多層構造に構成することができることは
勿論である.
更に、磁気記録媒体の製造工程も上記実施態様の製造工
程に限るものではな《、例えば上記実施態様における磁
性層の塗布工程と乾燥工程の間にオリエンテーション(
磁界配向処理)を行っても良い.
〔発明の効果〕
本発明の磁気記録媒体の製造方法は、非磁性支持体上に
該非磁性支持体よりも表面の平滑化処理をし易い高分子
樹脂或いは咳高分子樹脂と非磁性の粒子を主成分とする
ダミー層を形成し、該ダミー層の表面を平滑化処理した
後に、前記ダミー層上に磁性層を形成するので、前記非
磁性支持体が比較的表面性の悪い支持体であっても、該
非磁性支持体上に形成される磁性層の表面は良好な表面
性を有することができる。Further, although the magnetic layer I2 is also applied using an extrusion head, it is of course possible to use other application means. It can also be applied to ferromagnetic metal thin film type magnetic recording media. Furthermore, it goes without saying that the magnetic layer can have a multilayer structure. Furthermore, the manufacturing process of the magnetic recording medium is not limited to the manufacturing process of the above embodiment. For example, the orientation (
(magnetic field orientation treatment) may also be performed. [Effects of the Invention] The method for manufacturing a magnetic recording medium of the present invention comprises coating a polymer resin whose surface is easier to smoothen than the non-magnetic support, or a polymer resin and non-magnetic particles on a non-magnetic support. After forming a dummy layer containing the main component and smoothing the surface of the dummy layer, a magnetic layer is formed on the dummy layer, so that the non-magnetic support is a support with relatively poor surface properties. However, the surface of the magnetic layer formed on the nonmagnetic support can have good surface properties.
従って、表面平滑性の良《ない安価な非磁性支持体表面
の上にも、再生出力が高くテープノイズが低い表面平滑
性の良好な磁性層を薄層形成できる製造コストの安価な
磁気記録媒体の製造方法を提供できる.
〔実施例〕
以下、本発明の一実施例により本発明の新規な効果をよ
り明蹟にする.
迫五1日負色
下記第1表及び第2表に示す組成成分の磁性塗布l&を
ボールミルに入れて10.5時間混合分散して磁性塗布
液A,Bを調製した。こうして得られた磁性塗布液A,
Hの平衡粘度を測定したところ、剪断速度がl X I
O’sec− ’においてはそれぞれ0.25pois
e及び0.30poiseを示した。Therefore, this is an inexpensive magnetic recording medium that can produce a thin magnetic layer with high playback output, low tape noise, and good surface smoothness even on the surface of an inexpensive non-magnetic support with poor surface smoothness. We can provide a manufacturing method for [Example] Hereinafter, the novel effects of the present invention will be made clearer by way of an example of the present invention. Magnetic Coating Liquids A and B were prepared by placing magnetic coating l& having the composition shown in Tables 1 and 2 below in a ball mill and mixing and dispersing for 10.5 hours. Magnetic coating liquid A thus obtained,
When the equilibrium viscosity of H was measured, the shear rate was l
0.25 pois for each O'sec-'
e and 0.30 poise.
第 1 表
組成
r −Fe20,, tj〕未 10
0重量部( S .Et値: 35rrr/ g )・
二l・ロセルロース lo 重M 部・
ポリイソシア不一ト
・カーボンブラノク
(平均粒径=20mμm)
8重量部
2重量部
・メチルエチルケトン
300重量部
第
2
表
組成
ニトロセルロース
10重量部
ポリイソシアネート
8重量部
・Cr.03
2重量部
・ステアリン酸 1重量部・ステ
アリン酸ブチル l重量部・メチルエチ
ルケトン 300重量部久ま二11蚕血
次に、下記第3表及び第4表に示す組成成分のダミー層
塗布液をボールミルに入れてIO.5時間混合分散して
ダミー層塗布液A.Bを調製した。こうして得られたダ
ミーN塗布液A,Bの平衡粘度を測定したところ、剪断
速度がl X 10’sec− ’においてはそれぞれ
0.24poise及び0.32poiseを示し第
3
表
組成
・ニトロセルロース
50
重量部
・ポリイソシアネート
・メチルエチルケトン
8重量部
300重量部
第
4
表
組成
・α一A N z O x
・ニトロセルロース
10重量部
40重量部
・ポリイソシア不一ト 8重量部・メチ
ルエチルケトン 300重量部(実施例1
)
搬送達度:200m/分で走行させた厚さ: 11.7
μm1幅=300論、表面粗さ:O.tSμmのポリエ
チレンテレフタレート支持体上に、上記実施態様に記載
した磁気記録媒体の製造工程に基づいて上記ダミー層塗
布液Aを塗布、乾燥して乾燥厚み3,3μmのダミー層
を形成した後に上記磁性塗布液Aを乾燥厚みが4.2μ
mとなる様に塗布して磁性層を形成した.
但し、前記ダミー層の塗布に用いた塗布へ・ンドは特開
昭60−238179号公報に開示したエクストルージ
ゴン型塗布ヘッドと同しものであり、塗布ヘ7r部分の
概略構成はスロット幅二〇.6m、ポケット部分の径:
20閣、ドクターエッジ表面の曲率半径:l5閣、ドク
ターエノジ表面の有効長さ二6一、パックエッジ表面の
有効長さ:7.5m,塗布幅:250■となる樺にした
.また、前記ダミー層の乾燥固化は80゜Cの垂直空気
流乾燥により行うと共に、前記ダミー層のカレンダー処
理は直径=250閣、表面相さ: 0.01μmのハー
ドクロムメッキロールを2本用いてカレンダー線圧:
200 kgw /cm、カレンダー温度80℃で行っ
た.
更に、前記磁性層の塗布に用いた塗布ヘッドも特開昭6
0−238179号公報に開示したエクストルジョン型
塗布へ冫ドと同しものであり、塗布へンド部分の概略構
成はスロノト幅=0.6閣、ボケノト部分の径: 20
mm、ドクターエノジ表面の曲率半径: IO+μm、
トクターエノジ表面の有効長さ;5閤、バックエノジ表
面の有効長さ: 7 . 5 IIlm、塗布幅:25
0画となる様にした。また、前記磁性層の乾燥固化も前
記ダミー層の乾燥固化と同様に行い、該磁性層のカレン
ダー処理は一旦、巻き取りロールに巻き取った後に、前
記ダミー層のカレンダー処理と同様に行った。Table 1 Composition r −Fe20,, tj〕10
0 parts by weight (S.Et value: 35rrr/g)・
2L・Locellulose lo heavy M part・
Polyisocyanate carbon black (average particle size = 20 mμm) 8 parts by weight 2 parts by weight Methyl ethyl ketone 300 parts by weight Second Table Composition Nitrocellulose 10 parts by weight Polyisocyanate 8 parts by weight Cr. 03 2 parts by weight Stearic acid 1 part by weight Butyl stearate 1 part by weight Methyl ethyl ketone 300 parts by weight Put it in IO. After mixing and dispersing for 5 hours, dummy layer coating solution A. B was prepared. When the equilibrium viscosities of the thus obtained dummy N coating solutions A and B were measured, they were 0.24 poise and 0.32 poise, respectively, at a shear rate of l x 10'sec-', as shown in Table 3 Composition Nitrocellulose 50 Weight Parts by weight Polyisocyanate 8 parts by weight Methyl ethyl ketone 300 parts by weight Table 4 Composition α1A N z O x 10 parts by weight Nitrocellulose 40 parts by weight Polyisocyanate 8 parts by weight Methyl ethyl ketone 300 parts by weight (Example 1
) Conveyance efficiency: Thickness when traveling at 200 m/min: 11.7
μm1 width = 300 theory, surface roughness: O. The above-mentioned dummy layer coating solution A was applied onto a polyethylene terephthalate support having a thickness of tS μm based on the manufacturing process of the magnetic recording medium described in the embodiment above, and dried to form a dummy layer with a dry thickness of 3.3 μm. Dry thickness of coating solution A is 4.2μ
A magnetic layer was formed by coating the material in an amount of m. However, the coating head used for coating the dummy layer is the same as the extrusion type coating head disclosed in Japanese Patent Application Laid-Open No. 60-238179, and the general configuration of the coating head 7r section is the slot width 2. 〇. 6m, diameter of pocket part:
The birch has a radius of curvature of 20 mm, a radius of curvature of the doctor edge surface: 15 mm, an effective length of the doctor edge surface of 261 mm, an effective length of the pack edge surface: 7.5 m, and a coating width of 250 cm. The dummy layer was dried and solidified by vertical air flow drying at 80°C, and the dummy layer was calendered using two hard chrome plated rolls with a diameter of 250 mm and a surface texture of 0.01 μm. Calendar linear pressure:
The test was carried out at 200 kgw/cm and a calendar temperature of 80°C. Furthermore, the coating head used for coating the magnetic layer was also manufactured by Japanese Patent Application Laid-open No. 6
It is the same as the extrusion-type coating tool disclosed in Publication No. 0-238179, and the approximate configuration of the coating end part is width of width = 0.6mm, diameter of blurring part: 20mm.
mm, Radius of curvature of Doctor Enoji surface: IO+μm,
Effective length of Tokuta Enoji surface: 5. Effective length of back Enoji surface: 7. 5 IIlm, coating width: 25
I made it so that it was 0 strokes. Further, the drying and solidification of the magnetic layer was performed in the same manner as the drying and solidification of the dummy layer, and the calendering treatment of the magnetic layer was performed in the same manner as the calendering treatment of the dummy layer after it was once wound up on a take-up roll.
この様にして得られた磁気記録媒体における磁性層の表
面ネHさを測定した。その結果を第5表に示した。The surface roughness of the magnetic layer in the magnetic recording medium thus obtained was measured. The results are shown in Table 5.
(実施例2)
」一記実施例lにおけるダミー層塗布液八の代わりに、
非磁性粒子を添加したダミー層塗布液Bを用いた以外は
上記実施例1と同条件で磁気記録媒体を作成し、この磁
気記録媒体における磁性層の表面粗さを測定した。その
結果を第5表に示した.(実施例3)
搬送速度:200m/分で走行させた厚さ: 11.7
μm、輻: 300ms、表面粗さ:0.15μmの
ポリエチレンテレフタレート支持体上に、上記実施態様
に記載した磁気記録媒体の製造工程に基づいて上記ダミ
ー層塗布液Aを塗布、乾燥して乾燥厚み3.3μmのダ
ミー層を形成した後に、上記磁性塗布液八を乾燥厚みが
3.5 μrnの下層、上記磁性塗布液Bを乾燥厚みが
0.7 μmの上層となる様に重層塗布して二層構造の
磁性層を形成した。(Example 2) Instead of the dummy layer coating liquid 8 in Example 1,
A magnetic recording medium was prepared under the same conditions as in Example 1, except that dummy layer coating liquid B containing non-magnetic particles was used, and the surface roughness of the magnetic layer in this magnetic recording medium was measured. The results are shown in Table 5. (Example 3) Conveyance speed: Traveled at 200 m/min Thickness: 11.7
μm, convergence: 300 ms, surface roughness: 0.15 μm On a polyethylene terephthalate support, the above dummy layer coating solution A is applied based on the manufacturing process of the magnetic recording medium described in the above embodiment, and dried to obtain a dry thickness. After forming a dummy layer of 3.3 μm, the above magnetic coating liquid 8 was applied in layers so that the lower layer had a dry thickness of 3.5 μrn, and the above magnetic coating liquid B was applied as an upper layer with a dry thickness of 0.7 μrn. A magnetic layer with a two-layer structure was formed.
但し、前記ダミー層の塗布に用いた塗布へノドは上記実
施例lに用いたものと同様であり、カレンダー処理も同
様に行った.
更に、前記磁性層の重層塗布に用いた塗布ヘノドは特開
昭63−88080号公報に開示したエクス]・ルジョ
ン型塗布ヘノドと同しものであり、塗布ヘノド部分の概
略構成は下層用スロノト幅:0.6mm、上層用スロッ
ト幅+0.5m、下層用ポケット部分の径:20−、上
層用ポケノト部分の径:15m、第1ドクターエッジ表
面の曲率半径:15■、第2ドクターエノジ表面の曲率
半径:20m、第1ドクターエ,ジ表面の有効長さ:5
閣、第2ドクターエノジ表面の有効長さ:6μm,塗布
輻:250mとなる様にした。また、前記磁性層の乾燥
固化も前記ダミー層の乾燥固化と同様に行い、該磁性層
のカレンダー処理は一旦、巻き取りロールに巻き取った
後に、前記ダミー層のカレンダー処理と同様に行った。However, the coating nozzle used for coating the dummy layer was the same as that used in Example 1 above, and the calendering was performed in the same manner. Further, the coating helix used for the multilayer coating of the magnetic layer is the same as the EX] Lujon type coating hept disclosed in JP-A No. 63-88080, and the general configuration of the coating helix portion is the width of the slot for the lower layer. : 0.6mm, upper layer slot width + 0.5m, lower layer pocket diameter: 20-, upper layer pocket diameter: 15m, radius of curvature of first doctor edge surface: 15■, curvature of second doctor edge surface Radius: 20m, effective length of first doctor surface: 5
The effective length of the surface was set to 6 μm, and the coating radius was set to 250 m. Further, the drying and solidification of the magnetic layer was performed in the same manner as the drying and solidification of the dummy layer, and the calendering treatment of the magnetic layer was performed in the same manner as the calendering treatment of the dummy layer after it was once wound up on a take-up roll.
この様にして得られた磁気記録媒体における磁性層の表
面粗さを測定した.その結果を第5表に示した.
(比較例l)
搬送速度:200m/分で走行させた厚さ: 11.7
gm、幅: 300wa、表面相さ:0.15μmの
ポリエチレンテレフタレート支持体上に、上記磁性塗布
液Aを乾燥厚みが4.2 μmとなる様に塗布して磁性
層を形成した。The surface roughness of the magnetic layer in the magnetic recording medium thus obtained was measured. The results are shown in Table 5. (Comparative Example 1) Thickness when traveling at conveyance speed: 200 m/min: 11.7
On a polyethylene terephthalate support having gm, width: 300 wa, and surface thickness: 0.15 μm, the magnetic coating solution A was applied to a dry thickness of 4.2 μm to form a magnetic layer.
但し、前記磁性層の塗布に用いた塗布ヘノドは上記実施
例lで磁性層を塗布したエクストルージョン型塗布ヘノ
トと同じものであり、前記磁性層の乾燥固化も上記実施
例1における磁性層の乾燥固化と同様に行い、該磁性層
のカレンダー処理も上記実施例lにおける磁性層のカレ
ンダー処理と同様に行った.
この様にして得られた磁気記録媒体における磁性層の表
面粗さを測定した。その結果を第5表に示した.
(比較例2)
搬送速度:200m/分で走行させた厚さ:I1.7p
m、幅: 300m、表面粗さ:0.15μmのポリ
エチレンテレフタレート支持体上に、上記磁性塗布液A
を乾燥厚みが3.5μmの下層、上記磁性塗布液Bを乾
燥厚みが0.7μmの上層となる様に重層塗布して二層
構造の磁性層を形成した.但し、前記磁性層の重層塗布
に用いた塗布へ・7ドは上記実施例3に使用したものと
同様であり、前記磁性層の乾燥固化も上記実施例3にお
ける磁性層の乾燥固化と同様に行い、該磁性層のカレン
ダー処理も上記実施例3における磁性層のカレンダー処
理七同欅に行った.
この様にして得られた磁気記録媒体における磁性層の表
面粗さを測定した.その結果を第5表に示した。However, the coating nozzle used for coating the magnetic layer is the same as the extrusion type coating nozzle used to coat the magnetic layer in Example 1 above, and the drying and solidification of the magnetic layer is also the same as that used for drying the magnetic layer in Example 1. The solidification was carried out in the same manner as the calendering of the magnetic layer, and the calendering of the magnetic layer was carried out in the same manner as that of the magnetic layer in Example 1 above. The surface roughness of the magnetic layer in the magnetic recording medium thus obtained was measured. The results are shown in Table 5. (Comparative Example 2) Conveyance speed: Traveled at 200 m/min Thickness: I1.7p
The above magnetic coating liquid A was applied onto a polyethylene terephthalate support having a width of 300 m and a surface roughness of 0.15 μm.
A two-layer magnetic layer was formed by applying the magnetic coating solution B as a lower layer with a dry thickness of 3.5 μm and an upper layer with a dry thickness of 0.7 μm. However, the coating method used for the multilayer coating of the magnetic layer was the same as that used in Example 3 above, and the drying and solidification of the magnetic layer was also performed in the same manner as the drying and solidification of the magnetic layer in Example 3. The calender treatment of the magnetic layer was also carried out on the same calender treatment of the magnetic layer as in Example 3 above. The surface roughness of the magnetic layer in the magnetic recording medium thus obtained was measured. The results are shown in Table 5.
第
5
表
上記第5表から明らかな様に、本発明に基づく塗布方法
により得られた磁気記録媒体は、同条件で得られた比較
例の磁気記録媒体に比べて磁性層表面が平滑になってい
ることがわかる。Table 5 As is clear from Table 5 above, the magnetic recording medium obtained by the coating method based on the present invention has a smoother magnetic layer surface than the magnetic recording medium of the comparative example obtained under the same conditions. You can see that
第1図は本発明の製造方法に基づく磁気記録媒体の製造
工程の一実施態様を示す概略図、第2図は本発明の製造
方法に基づく磁気記録媒体の製造過程における状態を示
す拡大断面図である。
(図中の符号)
l一繰出口−ル 2 −支持体3 一第1塗布
ヘッド 4一給液系5 乾燥ゾーン
6a,6b カレンダーロール
7 第2塗布ヘノド 8一給液系FIG. 1 is a schematic diagram showing an embodiment of the manufacturing process of a magnetic recording medium based on the manufacturing method of the present invention, and FIG. 2 is an enlarged sectional view showing the state in the manufacturing process of a magnetic recording medium based on the manufacturing method of the present invention. It is. (Symbols in the figure) 1 - Feeding outlet - 2 - Support 3 - 1st coating head 4 - Liquid supply system 5 Drying zones 6a, 6b Calendar roll 7 2nd coating nozzle 8 - Liquid supply system
Claims (1)
化処理をし易い高分子樹脂或いは該高分子樹脂と非磁性
の粒子を主成分とするダミー層を形成し、該ダミー層の
表面を平滑化処理した後に、前記ダミー層上に磁性層を
形成することを特徴とする磁気記録媒体の製造方法。 2)前記ダミー層が熱可塑性樹脂、熱硬化性樹脂、反応
型樹脂の内の少なくとも一種の樹脂から成る請求項1に
記載の磁気記録媒体の製造方法。 3)前記ダミー層内の非磁性の粒子が平均粒径0.01
〜2μmの粒子から成る請求項1に記載の磁気記録媒体
の製造方法。 4)前記ダミー層が熱可塑性樹脂、熱硬化性樹脂、反応
型樹脂の内の少なくとも一種の樹脂から成ると共に、該
ダミー層内の非磁性の粒子が平均粒径0.01〜2μm
の粒子から成る請求項1に記載の磁気記録媒体の製造方
法。[Claims] 1) Forming on a non-magnetic support a polymer resin whose surface is easier to smoothen than the non-magnetic support, or a dummy layer mainly composed of the polymer resin and non-magnetic particles. A method for manufacturing a magnetic recording medium, comprising: forming a magnetic layer on the dummy layer after smoothing the surface of the dummy layer. 2) The method for manufacturing a magnetic recording medium according to claim 1, wherein the dummy layer is made of at least one type of resin selected from thermoplastic resin, thermosetting resin, and reactive resin. 3) The non-magnetic particles in the dummy layer have an average particle size of 0.01
2. The method of manufacturing a magnetic recording medium according to claim 1, wherein the magnetic recording medium comprises particles of ~2 μm. 4) The dummy layer is made of at least one type of resin selected from thermoplastic resin, thermosetting resin, and reactive resin, and the nonmagnetic particles in the dummy layer have an average particle size of 0.01 to 2 μm.
2. The method for manufacturing a magnetic recording medium according to claim 1, comprising particles of.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP910790A JPH03214422A (en) | 1990-01-18 | 1990-01-18 | Production of magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP910790A JPH03214422A (en) | 1990-01-18 | 1990-01-18 | Production of magnetic recording medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03214422A true JPH03214422A (en) | 1991-09-19 |
Family
ID=11711407
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP910790A Pending JPH03214422A (en) | 1990-01-18 | 1990-01-18 | Production of magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03214422A (en) |
-
1990
- 1990-01-18 JP JP910790A patent/JPH03214422A/en active Pending
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