JPH03214417A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPH03214417A JPH03214417A JP2009106A JP910690A JPH03214417A JP H03214417 A JPH03214417 A JP H03214417A JP 2009106 A JP2009106 A JP 2009106A JP 910690 A JP910690 A JP 910690A JP H03214417 A JPH03214417 A JP H03214417A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- layer
- resin
- coating
- dummy layer
- 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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- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 239000006249 magnetic particle Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 abstract description 36
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- 101100434016 Caenorhabditis elegans gar-2 gene Proteins 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
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- 239000004593 Epoxy Substances 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
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- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
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- 230000002378 acidificating effect Effects 0.000 description 1
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- 125000005907 alkyl ester group Chemical group 0.000 description 1
- JZQOJFLIJNRDHK-CMDGGOBGSA-N alpha-irone Chemical compound CC1CC=C(C)C(\C=C\C(C)=O)C1(C)C JZQOJFLIJNRDHK-CMDGGOBGSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical group OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Chemical group 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 239000002223 garnet Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
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- 239000004814 polyurethane Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
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- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000010458 rotten stone Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- RVEZZJVBDQCTEF-UHFFFAOYSA-N sulfenic acid Chemical group SO RVEZZJVBDQCTEF-UHFFFAOYSA-N 0.000 description 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical group OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
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Landscapes
- Paints Or Removers (AREA)
- 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、磁気記録媒体関し、特に可撓性の非磁性支持
体上に磁性層を形成して成る磁気記録媒体に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a magnetic recording medium, and particularly to a magnetic recording medium comprising a magnetic layer formed on a flexible non-magnetic support.
従来、オーディオテープ、ビデオテープ等の磁気テープ
、及びフロッピィ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
。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 floppy disks, involves applying a magnetic coating liquid onto a non-magnetic support that is wider than normal products. After coating to form a magnetic layer, performing an orientation treatment and drying the magnetic layer, smoothing the surface of the magnetic layer to produce a tape material, and then cutting the tape material in a cutting process. It is manufactured by cutting the tape into a predetermined width or shape.
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.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。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. 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ッ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、前記磁気ヘ
ットは小型化され、発生磁束量が減少させられる。従っ
て、上記のように減ぜられた磁束で磁性層のるn化の方
向を所望の反転するためには、前記磁性層の体積の減少
、すなわち、前記磁性層の厚みを減少させなければ完全
な磁化反転を行うことが難しく記録再生特性の向−Eが
望めないために、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。又、例えば特開昭63
−102036号、同63−102037号、特開平1
−106333号等に開示されているように磁性層を特
性の違った2層構造にしてその性能を高めると共に磁性
層の薄層化や原材料コストの低減が行われていた。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 small area, so the magnetic head is miniaturized and the amount of generated magnetic flux is reduced. reduced. Therefore, in order to reverse the direction of nization of the magnetic layer as desired with the reduced magnetic flux as described above, it is necessary to reduce the volume of the magnetic layer, that is, reduce the thickness of the magnetic layer. Since it is difficult to perform a magnetization reversal and the recording/reproducing characteristics cannot be expected to have a -E direction, it has become necessary to make the magnetic layer of the magnetic recording medium thinner. Also, for example, JP-A-63
No.-102036, No. 63-102037, JP-A-1
As disclosed in No. 106333, etc., the magnetic layer has been made into a two-layer structure with different characteristics to improve its performance, as well as to make the magnetic layer thinner and reduce the cost of raw materials.
更に、上記の如き粉末磁性材料を有機バインダー中に分
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■。や残留
磁束密度B1が大きく磁性層の厚みを極めて薄くするこ
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。Furthermore, coercive force (1) is applied to a coating-type magnetic recording medium in which a magnetic coating solution in which the powdered magnetic material as described above is dispersed in an organic binder is coated on a non-magnetic support and dried. Ferromagnetic metal thin film type, which has a large residual magnetic flux density B1 and can make the thickness of the magnetic layer extremely thin, is made by directly depositing a metal thin film made of a ferromagnetic metal material on a nonmagnetic support by vacuum deposition, etc. Magnetic recording media are beginning to be used.
上述のように性能向上に伴って磁性層の薄層化が進む一
方で、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。このため、材料コ
スト低減の観点から磁性層の支持体厚みをその強度や走
行耐久性を満足する限度内でより薄くすることが考えら
れるが、記録再生装置のとの対応性に制約(規格例えば
、VHS方式のT−120で総厚み17.0μ麟以上)
があり、実現に到っていなかった。As mentioned above, magnetic layers are becoming thinner as performance improves, but in order to obtain magnetic recording media with good magnetic properties, it is necessary to use nonmagnetic supports with good surface smoothness. However, such nonmagnetic support materials are expensive and have the problem of increasing manufacturing costs. Therefore, from the perspective of reducing material costs, it is conceivable to make the support thickness of the magnetic layer thinner within the limits that satisfy its strength and running durability, but there are restrictions on compatibility with recording and reproducing devices (for example, , total thickness of 17.0μ or more in VHS format T-120)
However, it had not been realized.
そこで、本発明の目的は上記課題を解消することにあり
、電磁変換特性や走行耐久性を高いレベルに維持しつつ
支持体の厚みを従来では達しえなかった薄層にできコス
ト低減化のできる磁気記録媒体を提供することである。Therefore, the purpose of the present invention is to solve the above-mentioned problems.It is possible to reduce costs by making the thickness of the support thinner, which could not be achieved in the past, while maintaining electromagnetic conversion characteristics and running durability at a high level. An object of the present invention is to provide a magnetic recording medium.
本発明の上記目的は、非磁性支持体の少なくとも片面に
磁性層を設けた磁気記録媒体において、前記非磁性支持
体の片面に高分子樹脂或は高分子樹脂と非磁性の粒子を
主成分とするダミー層と、前記磁性層を順次積層して成
ることを特徴とする磁気記録媒体により達成される。The above object of the present invention is to provide a magnetic recording medium having a magnetic layer on at least one side of a non-magnetic support, in which one side of the non-magnetic support has a polymer resin or a polymer resin and non-magnetic particles as main components. This is achieved by a magnetic recording medium characterized in that the dummy layer and the magnetic layer are sequentially laminated.
(実施態様)
以下、本発明の一実施態様である磁気テープについて第
1図及び第2図を参照して説明する。(Embodiment) A magnetic tape which is an embodiment of the present invention will be described below with reference to FIGS. 1 and 2.
第1図に磁気テープの断面を示すように、比較的表面性
の悪い支持体2の上に塗布によりダミー層11を形成す
ることにより、例えばVHS方式(7)T− 1 2
0のテープのポリエチレンテレフタレートの場合前記支
持体2を0.014 mm −0.009 mm程度に
薄くできるだけでなく、磁性層l2を形成する表面の平
滑性が良くでき、しかも裏面側は粗面であるので、従来
の高品質な支持体の場合のように支持体裏面の粗面化処
理を行わなくとも、テープ走行性を良好に保つことがで
きる。なお、前記ダミー層l1の厚さは、前記支持体2
にポリエチレンテレフタレートを用いた場合に、本実施
態様においては前記支持体2の限度厚さから見ると略2
μm以上であり、この厚さ以上にすることにより強度面
で補助的機能を持たせることができテープ強度の面で規
格以上の品質を維持し且つ極めて廉価な製品を提供する
ことができる。なお、前記ダミー層l1の上限の厚みは
、記録媒体の強度や厚みの規格から略6μm程度を限界
とすることができる。As shown in the cross section of the magnetic tape in FIG. 1, by forming a dummy layer 11 by coating on a support 2 with relatively poor surface properties, for example, VHS system (7) T-12
In the case of the polyethylene terephthalate tape of No. 0, not only can the support 2 be made as thin as 0.014 mm to 0.009 mm, but the surface on which the magnetic layer 12 is formed can have good smoothness, and the back side is rough. Therefore, good tape running properties can be maintained without roughening the back surface of the support as in the case of conventional high-quality supports. Note that the thickness of the dummy layer l1 is the same as that of the support 2.
In this embodiment, when polyethylene terephthalate is used for the
By making the tape thicker than this, it is possible to provide an auxiliary function in terms of strength, maintain quality that exceeds the standard in terms of tape strength, and provide an extremely inexpensive product. Note that the upper limit of the thickness of the dummy layer l1 can be approximately 6 μm based on the strength and thickness standards of the recording medium.
前記ダミー層11を形成するのは、ロールコート、グラ
ビアコート、ロールコート或はエクストルージランプラ
スドクタ一方式など種々の塗布形式により形成すること
ができる.第2図には磁気テープを製造する工程におい
て前記ダミー層11を形成する設備の概略を示した。即
ち、支持体2が繰出口−ル1から送り出された直後に第
1塗布ヘッド3により前記ダミー1ii11を塗布して
乾燥ゾーン5にて乾燥する。この乾燥に引き続いてカレ
ンダーロール6a.6bによりカレンダー処理L、その
後、第2塗布ヘッド7により磁性層を重層塗布し、乾燥
ヅーン9にて適宜乾燥してから巻き取りロール10に巻
き取る.なお、前記両塗布ヘッド3、7にはダミー層及
び磁性層用のそれぞれの給液系4 、8a,8bにより
下記組成の磁性分散液が供給される。このようにして形
成された磁気テープを引き続いてカレンダー処理を行う
と、特に前記ダミー層11に加熱並びにお加圧によって
比較的変形し易い樹脂を使用することにより、カレンダ
処理等の平面平滑化処理の効果が高められるので、前記
支持体に用いる素材の表面性が悪くても表面平滑性の良
い良好な磁気特性を有する磁気記録媒体を得ることがで
きる。The dummy layer 11 can be formed by various coating methods such as roll coating, gravure coating, roll coating, or one-sided extrusion run plus doctor method. FIG. 2 schematically shows equipment for forming the dummy layer 11 in the process of manufacturing a magnetic tape. That is, immediately after the support 2 is fed out from the outlet 1, the dummy 1ii11 is applied by the first coating head 3 and dried in the drying zone 5. Following this drying, the calender roll 6a. 6b, the magnetic layer is subjected to calendering L, and then a magnetic layer is coated in multiple layers using the second coating head 7, and the magnetic layer is suitably dried using a drying dune 9, and then wound onto a winding roll 10. Incidentally, a magnetic dispersion liquid having the following composition is supplied to both coating heads 3 and 7 by respective liquid supply systems 4, 8a and 8b for the dummy layer and the magnetic layer. When the magnetic tape formed in this way is subsequently subjected to calender treatment, the use of a resin that is relatively easily deformed by heating and pressure for the dummy layer 11 results in surface smoothing treatment such as calender treatment. Since this effect is enhanced, it is possible to obtain a magnetic recording medium having good surface smoothness and good magnetic properties even if the surface properties of the material used for the support are poor.
尚、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10
000〜300000、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
ポリアミド樹脂、ボリフッ力ビニル、塩化ビニリデンア
クリ口ニトリル共重合体、ブタジエンアクリ口ニトリル
共重合体、ボリアミド樹脂、ポリビニルプチラール、セ
ルロース誘導体(セルロースアセテートプチレート、セ
ルロースダイアセテート、セルローストリアセテート、
セルロースブロピオネート、二トロセルロース、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 polymer resin used in the dummy layer of the present invention may be, for example, a thermoplastic resin, a thermosetting resin, a reactive resin, or a mixture thereof. The thermoplastic resin has a softening temperature of 150'C or less and an average molecular weight of 10
000 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-polyamide resin, polyfluorinated vinyl, vinylidene chloride-acrylic nitrile copolymer, butadiene-acrylic nitrile copolymer, polyamide resin, polyvinyl butyral, cellulose derivatives (cellulose acetate, cellulose diacetate, cellulose triacetate,
Cellulose propionate, ditrocellulose, ethylcellulose, methylcellulose, probilcellulose,
methyl ethyl cellulose, carboxymethyl cellulose, acetyl cellulose, etc.), styrene-butadiene copolymers, polyester resins, chlorovinyl ether acrylic acid ester copolymers, amino resins, various synthetic rubber-based thermoplastic resins, and mixtures thereof. I can do it.
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
限大のものとなる。又、これらの樹脂のなかで、樹脂が
熱分解するまでの間に軟化又は溶融しないものが好まし
い。具体的には例えばフェノール樹脂、フエノキシ樹脂
、エボキシ樹脂、ポリウレタン硬化型樹脂、尿素樹脂、
メラミン樹脂、アルキンド樹脂、シリコン樹脂、アクリ
ル系反応樹脂、エポキシーボリアミド樹脂、ニトロセル
ロースメラミン樹脂、高分子量ボリエステル樹脂とイソ
シアネートプレボリマーの混合物、メタクリル酸塩共重
合体とジイソシアネートプレボリマーの混合物、ポリエ
ステルポ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/トリフエ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。The thermosetting resin or reactive resin has a molecular weight of 200,000 or less in the state of a coating liquid, and when heated after coating and drying, the molecular weight becomes infinite due to reactions such as condensation and addition. Also, among these resins, those that do not soften or melt before the resin is thermally decomposed are preferred. Specifically, for example, phenol resin, phenoxy resin, epoxy resin, polyurethane curable resin, urea resin,
Melamine resins, alkynd resins, silicone resins, acrylic reactive resins, epoxy polyamide resins, nitrocellulose melamine resins, mixtures of high molecular weight polyester resins and isocyanate prebolimers, mixtures of methacrylate copolymers and diisocyanate prebolimers, polyester polyols and polyisocyanate, urea formaldehyde resin, mixture of low molecular weight glycol/high molecular weight diol/triphenylmethane triisocyanate, polyamine resin, polyimine resin, and mixtures thereof.
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ボン酸、スルフィ
ン酸、スルフエン酸、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、アルキルベ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
lfB、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I XIO
−’eq−I XIO−”eq含む事が好ましい。These thermoplastic resins, thermosetting resins, and reactive resins are
In addition to the main functional groups, functional groups include acidic groups such as carboxylic acid, sulfinic acid, sulfenic acid, sulfonic acid, phosphoric acid, sulfuric acid, phosphonic acid, phosphine, boric acid, sulfuric ester groups, phosphoric ester groups, and alkyl ester groups thereof, and amino acids. Aminosulfonic acids, sulfuric or phosphoric acid esters of aminoalcohols, amphoteric groups such as alkyl betaine types, amino groups, imino groups, imido groups, amide groups, eboxylfB, etc. Also, hydroxyl groups, alkosyl groups, thiol groups,
Usually one or more halogen groups, silyl groups, and siloxane groups (6)
Each functional group contains IXIO per gram of resin.
-'eq-I XIO-"eq is preferably included.
前記ダミー層11に使用した各樹脂内に適当な粒子を混
入させることにより、該ダミー層11の強度を高めるこ
とができる。この粒子としては、前記支持体2と同様に
非磁性のものが望ましく、例えば、カーボンブラック、
α−アルミナ、Tアルミナ、α一T−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一酸化鉄、ザクロ石、エ
メリー(主成分:コランダムと磁鉄K)、ガー2 y
}、ケイ石、窒化ケイ素、窒化硼素、炭化タングステン
、チタンカーハイト、クオーツ、トリポリ、ケイソウ土
、F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。また、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、
小さすぎると前記ダミー層11の補強効果がさほど期待
できないので、その粒径には適宜範囲が有り平均粒径が
0.01〜2μ一の範囲が望ましい。又、粒子の混大割
合としては、前記ダミー層l1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.
前記実施態様では第2図に示すように磁性層を形成する
直前にダミー層を形成する場合を示したが、本発明は前
記実施態様に限るものではなく、勿論、前記支持体2を
製造するときに形成するようにしてもよい.
(発明の効果)
以上述べたように、本発明は非磁性支持体と磁性層との
間に該支持体の薄層化の分だけの厚みを有した高分子樹
脂或は高分子樹脂と非磁性の粒子を主成分とする厚肉の
ダミー層が塗布にて形成されているので、材料費を大幅
に低減できるように前記支持体の厚みを薄くしても、記
録再生装置によって制限される媒体の規定厚みを保つこ
とがきる.また、前記ダミー層に加熱並びにお加圧によ
って比較的変形し易い樹脂を使用することにより、カレ
ンダー処理等の平面平滑化処理の効果が高められるので
、前記支持体に用いる素材の表面性が悪くても表面平滑
性の良い良好な磁気特性を有する磁気記録媒体を得るこ
とができ、更に、表面性が悪い前記支持体を用いること
により、支持体裏面にバックコーティングによる粗面化
処理を省くこともでき、製造コストの低減化を促進する
ことができ、しかも電磁変換特性や走行耐久性を高いレ
ヘルに維持した磁気記録媒体を提供することができる。By mixing appropriate particles into each resin used for the dummy layer 11, the strength of the dummy layer 11 can be increased. As with the support 2, these particles are preferably non-magnetic, such as carbon black,
α-alumina, T-alumina, α-T-alumina, fused alumina, silicon carbide, chromium oxide, cerium oxide, corundum, artificial diamond, α-iron monoxide, garnet, emery (main components: corundum and magnetic iron K), Gar 2 y
}, silica, silicon nitride, boron nitride, tungsten carbide, titanium carbide, quartz, tripoli, diatomaceous earth, F lomite, etc. can be used singly or in combination. In addition, if the size of these particles is too large, it will deteriorate the surface properties of the surface to which the magnetic layer is applied.
If it is too small, the reinforcing effect of the dummy layer 11 cannot be expected so much, so the particle size has an appropriate range, and the average particle size is preferably in the range of 0.01 to 2 μm. Further, it is desirable that the mixing ratio of the particles is 70% or less by weight based on the resin constituting the dummy layer l1. In the embodiment described above, as shown in FIG. 2, a case was shown in which a dummy layer was formed immediately before forming the magnetic layer, but the present invention is not limited to the embodiment described above, and of course, the support body 2 may be manufactured. It may be possible to form it sometimes. (Effects of the Invention) As described above, the present invention provides a polymer resin with a thickness corresponding to the thinning of the support between a non-magnetic support and a magnetic layer, or a polymer resin and a non-magnetic resin. Since a thick dummy layer mainly composed of magnetic particles is formed by coating, even if the thickness of the support is made thinner to significantly reduce material costs, it is limited by the recording and reproducing device. The specified thickness of the media can be maintained. Furthermore, by using a resin that is relatively easily deformed by heating and pressurizing for the dummy layer, the effect of surface smoothing treatment such as calender treatment is enhanced, so that the surface properties of the material used for the support are poor. It is possible to obtain a magnetic recording medium having good magnetic properties with good surface smoothness, and furthermore, by using the above-mentioned support with poor surface properties, it is possible to omit roughening treatment by back coating on the back surface of the support. It is also possible to provide a magnetic recording medium that can promote reduction in manufacturing costs and maintain electromagnetic conversion characteristics and running durability at a high level.
以下、本発明の効果を実施例および比較例により更に明
確にすることができる。Hereinafter, the effects of the present invention can be further clarified through Examples and Comparative Examples.
〔1隻■〕
ダミー層及び磁性層の塗布は、第1図に示す塗布設備を
用いて行う。この塗布設備は図示のごと《繰出口−ルl
から引き出された支持体2に、第1塗布ヘッドによりダ
ミー層を塗布して乾燥ゾーン5にて乾燥する。この乾燥
に引き続いてカレンダーロール6a,6bによりカレン
ダー処理し、その後、第2塗布ヘッド7により磁性層を
重層塗布し、乾燥ゾーン9にて適宜乾燥してから巻き取
り口ールlOに巻き取る。[1 ship ■] The coating of the dummy layer and the magnetic layer is performed using the coating equipment shown in FIG. This coating equipment is as shown in the figure.
A dummy layer is applied to the support 2 pulled out from the support body 2 by the first application head and dried in the drying zone 5. Following this drying, it is calendered using calender rolls 6a and 6b, and then a magnetic layer is coated in multiple layers using the second coating head 7, dried appropriately in the drying zone 9, and then wound onto the winding roll 1O.
ダミー層の塗布に用いた塗布ヘッドは特開昭60238
179号公報に開示したエクストルージョン型塗布ヘッ
ドと同じものであり、塗布ヘッド部分の概略構成はスリ
ット幅は0.6 mm,ポケット部分の径は20mmで
あり、ドクターエッジ表面の湾曲率は15mm, ド
クターエッッジ表面の有効長さは6mm、パックエッジ
表面は丸みを有した形状でその有効長さは7.5mmで
ある。また、磁性層の塗布に用いた塗布ヘッドは特開昭
63−88080号公報に示した二層同時塗布型の塗布
ヘッドと同じものを使用し、その概略構成については、
スリット幅は上層側が0.5 mmで下層側が0.6m
m、ポケット部分の径は上層側が15m mで下層側が
20mmであり、ドクターエッジ表面の湾曲率は上層側
が20mm下層側が15mm, ドクターエツツジ表
面の有効長さは上層側が6mmで下層側が5mm、バッ
クエッジ表面が丸みを有した形状でその有効長さは7.
5mmである.
使用した支持体はポリエチレンテレフタレートフィルム
で、厚みが11.5μ−、表面粗さ0.02μ麟である
。下塗層は形成しなかった.
ダミー層の組成は第1表に示した組成であり、塗布厚み
は3.3μm(平均)とした.磁性層は上層の組成が第
2表に示した組成で塗布厚みが0.8μmであり、下層
の組成は第3表に示す組成で厚みが3,2μmである.
このようにしてサンプルNo.lの磁気記録媒体を作成
した。この結果を第4表に示す。The coating head used for coating the dummy layer is JP-A-60238.
It is the same as the extrusion type coating head disclosed in Publication No. 179, and the general configuration of the coating head part is that the slit width is 0.6 mm, the diameter of the pocket part is 20 mm, and the curvature of the doctor edge surface is 15 mm. The effective length of the doctor edge surface is 6 mm, and the pack edge surface has a rounded shape and has an effective length of 7.5 mm. The coating head used for coating the magnetic layer was the same as the two-layer simultaneous coating type coating head shown in JP-A-63-88080, and its schematic configuration is as follows.
The slit width is 0.5 mm on the upper layer side and 0.6 m on the lower layer side.
m, the diameter of the pocket part is 15 mm on the upper layer side and 20 mm on the lower layer side, the curvature of the Doctor Edge surface is 20 mm on the upper layer side and 15 mm on the lower layer side, the effective length of the Doctor Edge surface is 6 mm on the upper layer side, 5 mm on the lower layer side, and 5 mm on the lower layer side. The edge surface has a rounded shape and its effective length is 7.
It is 5mm. The support used was a polyethylene terephthalate film with a thickness of 11.5 μm and a surface roughness of 0.02 μm. No undercoat layer was formed. The composition of the dummy layer was as shown in Table 1, and the coating thickness was 3.3 μm (average). The upper layer of the magnetic layer has the composition shown in Table 2 and has a coating thickness of 0.8 μm, and the lower layer has the composition shown in Table 3 and has a thickness of 3.2 μm.
In this way, sample No. 1 magnetic recording medium was prepared. The results are shown in Table 4.
磁性層の塗布は、第l図に示す塗布設備でグミ層を塗布
しない設備を用いた。The magnetic layer was coated using the coating equipment shown in FIG. 1, which does not coat the gummy layer.
使用した支持体はポリエチレンテレフタレートフィルム
で、厚みが14.8μ+w(この厚みは前記実施例の支
持体とダミー層の厚みとの合計と同じである)、表面粗
さ0.02μmである。下塗層は形成しなかった。The support used was a polyethylene terephthalate film with a thickness of 14.8 μm+w (this thickness is the same as the total thickness of the support and dummy layer in the above example) and a surface roughness of 0.02 μm. No undercoat layer was formed.
ダミー層の組成は第1表に示した組成であり、塗布厚み
は3.3μm(平均)とした。The composition of the dummy layer was as shown in Table 1, and the coating thickness was 3.3 μm (average).
磁性層は上層の組成が第2表に示した組成で塗布厚みが
0.8μ霧であり、下層の組成は第3表に示す組成で厚
みが3.2μ靖で実施例と同じである.このようにして
サンプルNl12の磁気記録媒体を作成した.この結果
を第4表に示す.
第1表
(以下余白)
第2表
(上層の磁性分散液)
第3表
(下層の磁性分散液)
第4
表
尚、嘲
印の箇所はJIS C231B
による.
第4表を見ると実施例(サンプル階1)と比較例(サン
プルNO.2)とでは表面特性、磁性層の密着強度、媒
体全体の力学的強度はほぼ同程度であることが判る.し
かも、実施例の支持体は表面性が悪く仕上げ程度の低い
ものであるので極めて廉価であり、比較例のものと比べ
ると製造コストが低いことが顕著に現れた。The composition of the upper layer of the magnetic layer was as shown in Table 2, and the coating thickness was 0.8 μm, and the composition of the lower layer was as shown in Table 3, and the thickness was 3.2 μm, the same as in the example. In this way, a magnetic recording medium of sample Nl12 was created. The results are shown in Table 4. Table 1 (blank below) Table 2 (upper layer magnetic dispersion) Table 3 (lower layer magnetic dispersion) Table 4 Note that the parts marked with a mock mark are based on JIS C231B. Looking at Table 4, it can be seen that the surface characteristics, adhesion strength of the magnetic layer, and mechanical strength of the entire medium are approximately the same between the Example (Sample Level 1) and the Comparative Example (Sample No. 2). Furthermore, the supports of Examples had poor surface properties and a low finish, so they were extremely inexpensive, and the manufacturing costs were significantly lower than those of Comparative Examples.
第1図は本発明の磁気記録媒体の断面図、第2図は本発
明の磁気記録媒体を製造するために設備の概略図である
。
(図中符号)
l ・・繰出口−ル、2・・支持体、3・・第一塗布ヘ
ッド、 4 ,8a,8b・・給液系、5.9・・乾燥
ゾーン、6a,6b ・・カレンダーロール、lO・
・巻き取りロール。FIG. 1 is a sectional view of the magnetic recording medium of the present invention, and FIG. 2 is a schematic diagram of equipment for manufacturing the magnetic recording medium of the present invention. (Symbols in the figure) l...Feeding outlet, 2...Support, 3...First coating head, 4, 8a, 8b...Liquid supply system, 5.9...Drying zone, 6a, 6b.・Calendar roll, lO・
・Take-up roll.
Claims (1)
気記録媒体において、前記非磁性支持体の片面に高分子
樹脂或は高分子樹脂と非磁性の粒子を主成分とするダミ
ー層と、前記磁性層を順次積層して成ることを特徴とす
る磁気記録媒体。 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。 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
。 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。[Scope of Claims] 1) A magnetic recording medium in which a magnetic layer is provided on at least one side of a non-magnetic support, wherein one side of the non-magnetic support has a polymer resin or a polymer resin and non-magnetic particles as main components. 1. A magnetic recording medium comprising a dummy layer and the magnetic layer sequentially laminated. 2) The 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 magnetic recording medium of claim 1, comprising particles of ~2 [mu]m. 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.
The magnetic recording medium according to claim 1, comprising particles of.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009106A JPH03214417A (en) | 1990-01-18 | 1990-01-18 | Magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009106A JPH03214417A (en) | 1990-01-18 | 1990-01-18 | Magnetic recording medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03214417A true JPH03214417A (en) | 1991-09-19 |
Family
ID=11711381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009106A Pending JPH03214417A (en) | 1990-01-18 | 1990-01-18 | Magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03214417A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0734015B2 (en) † | 1995-03-23 | 2004-08-25 | TDK Corporation | Magnetic recording medium |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6066318A (en) * | 1983-09-20 | 1985-04-16 | Fuji Photo Film Co Ltd | Base film for magnetic recording medium |
| JPS60223022A (en) * | 1984-04-18 | 1985-11-07 | Victor Co Of Japan Ltd | Magnetic recording medium |
| JPS63191315A (en) * | 1987-02-04 | 1988-08-08 | Fuji Photo Film Co Ltd | Magnetic recording medium |
-
1990
- 1990-01-18 JP JP2009106A patent/JPH03214417A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6066318A (en) * | 1983-09-20 | 1985-04-16 | Fuji Photo Film Co Ltd | Base film for magnetic recording medium |
| JPS60223022A (en) * | 1984-04-18 | 1985-11-07 | Victor Co Of Japan Ltd | Magnetic recording medium |
| JPS63191315A (en) * | 1987-02-04 | 1988-08-08 | Fuji Photo Film Co Ltd | Magnetic recording medium |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0734015B2 (en) † | 1995-03-23 | 2004-08-25 | TDK Corporation | Magnetic recording medium |
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