JP2688296B2 - Magnetic recording media - Google Patents
Magnetic recording mediaInfo
- Publication number
- JP2688296B2 JP2688296B2 JP3121764A JP12176491A JP2688296B2 JP 2688296 B2 JP2688296 B2 JP 2688296B2 JP 3121764 A JP3121764 A JP 3121764A JP 12176491 A JP12176491 A JP 12176491A JP 2688296 B2 JP2688296 B2 JP 2688296B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- weight
- parts
- undercoat layer
- magnetic recording
- 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 - Fee Related
Links
Landscapes
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、非磁性の支持体への密
着性、走行耐久性及び電磁変換特性の良好な、磁気記録
媒体に係る。特に製造工程に於ける半製品ウェブの表面
性及び非磁性支持体への磁性材料の密着性に優れ、しか
も長時間たっても磁性層中の潤滑剤成分の導電性下塗層
への移行の少ない製品として、安定した品質をもつ磁気
記録媒体に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a magnetic recording medium having good adhesion to a non-magnetic support, running durability and electromagnetic conversion characteristics. In particular, it has excellent surface properties of the semi-finished web in the manufacturing process and adhesion of the magnetic material to the non-magnetic support, and less migration of the lubricant component in the magnetic layer to the conductive undercoat layer even after a long time. As a product, the present invention relates to a magnetic recording medium having stable quality.
【0002】[0002]
【従来の技術】近時磁気記録媒体は、オーディオ、ビデ
オ、コンピュータ等の広い分野で大量の情報を記録する
記録媒体として使用されるようになってきている。これ
に伴なって、磁気記録媒体の高密度化が要求されてい
る。磁気記録媒体を高密度化する手段の一つとして、強
磁性磁性粉を高充填化する方法が検討されてきている。2. Description of the Related Art Recently, magnetic recording media have come to be used as recording media for recording a large amount of information in a wide range of fields such as audio, video and computers. Along with this, there is a demand for higher density magnetic recording media. As one of means for increasing the density of a magnetic recording medium, a method of increasing the packing density of ferromagnetic magnetic powder has been studied.
【0003】[0003]
【本発明が解決しようとする問題点】しかし、強磁性磁
性粉を高充填化しようとすると、磁性粉の非磁性支持体
への接着性や密着性が低下し、かつ磁性粉の帯電性が高
くなり、この結果磁気記録媒体の走行性が悪くなった
り、放電によるノイズが発生すると言う問題が生じてく
る。この対策として、磁性層と非磁性支持体との間に導
電性の下塗層を設ける構成が提案されているものの、従
来の導電性下塗層では、磁気記録媒体の製造工程にお
いて、均質な表面を形成し難く、非磁性支持体への密
着性が低く、結果として磁性層の表面性が不良となり、
塗布方向に塗りすじ等が現れやすく、電磁変換特性も悪
い。しかも、磁性層中に含有される液体潤滑剤成分
が、導電性下塗層へ移行しやすく経時的に走行耐久性が
劣化する問題が生じている。However, when an attempt is made to increase the loading of the ferromagnetic magnetic powder, the adhesiveness and adhesion of the magnetic powder to the non-magnetic support are deteriorated, and the charging property of the magnetic powder is reduced. As a result, the running property of the magnetic recording medium deteriorates, and noises due to discharge occur. As a countermeasure, but be provided with a conductive subbing layer between the magnetic layer and the nonmagnetic support is proposed, in conventional conductive undercoat layer, in the manufacturing process of the magnetic recording medium, a homogeneous It is difficult to form the surface, the adhesion to the non-magnetic support is low, and as a result, the surface property of the magnetic layer becomes poor,
Streaks and the like tend to appear in the coating direction, and electromagnetic conversion characteristics are poor. In addition, there is a problem that the liquid lubricant component contained in the magnetic layer easily migrates to the conductive undercoat layer and the running durability deteriorates with time.
【0004】本発明は、従来の問題を解決すべく検討し
た結果達成されたものであり、走行耐久性、非磁性支持
体への密着性、及び電磁変換特性の良好な磁気記録媒体
を提供することを目的としている。The present invention has been achieved as a result of studies to solve the conventional problems, and provides a magnetic recording medium having good running durability, adhesion to a non-magnetic support, and electromagnetic conversion characteristics. Is intended.
【0005】[0005]
【問題点を解決するための手段】すなわち、本発明の磁
気記録媒体は、非磁性の支持体と、強磁性の磁性粉を含
有する磁性層と、該支持層と該磁性層との間に導電性の
下塗層を設けてなる磁気記録媒体であって、該下塗層が
ヨウ化第一銅、ヨウ化銀及び硫化第二銅の群から選ばれ
た少なくとも1種の金属化合物の導電性の充填剤と、有
機結合剤と、要すれば低分子イソシアネート化合物とを
含むことを特徴とするものである。That is, the magnetic recording medium of the present invention comprises a non-magnetic support, a magnetic layer containing ferromagnetic magnetic powder, and a space between the support and the magnetic layer. A magnetic recording medium provided with a conductive undercoat layer, wherein the undercoat layer is
Selected from the group of cuprous iodide, silver iodide and cupric sulfide
A conductive filler of at least one metal compound,
Machine binder and, if necessary, low molecular weight isocyanate compound
It is characterized by including .
【0006】従来技術にあっては、導電性充填剤とし
て、カーボンブラック、グラファイト等々のカーボン系
の充填剤の使用が一般的であるが、カーボン系充填剤で
十分な導電機能を発揮させるには、BET法による比表
面積が100m2 /g以上と大きく、かつDBP法によ
る吸油量の大きな粒子(100g/100gカーボン以
上)のカーボンを選択する必要があった。かかる比表面
積が大きく、かつ吸油量の大きなカーボン粒子は、均一
分散が困難であるばかりでなく、導電下塗層の表面粗度
が大きくなり、磁性面の表面積を低下させ、電磁変換特
性に悪影響を与えるようになる。In the prior art, carbon-based fillers such as carbon black and graphite are generally used as the conductive fillers, but in order for the carbon-based fillers to exhibit a sufficient conductive function. It was necessary to select carbon particles having a large specific surface area of 100 m 2 / g or more by the BET method and a large oil absorption by the DBP method (100 g / 100 g or more carbon). Such carbon particles having a large specific surface area and a large oil absorption amount are not only difficult to uniformly disperse, but also increase the surface roughness of the conductive undercoat layer, reducing the surface area of the magnetic surface and adversely affecting the electromagnetic conversion characteristics. To give.
【0007】さらにかかる吸油量の大なる粒子を、導電
下塗層中に存在させると磁性層中に添加含有される低分
子量(Mn<2000)の潤滑剤成分が導電下塗層へ移
行し、表面磁性層の走行耐久性が時間と共に悪化する傾
向があった。Further, when such particles having a large oil absorption amount are present in the conductive undercoat layer, the low molecular weight (Mn <2000) lubricant component additionally contained in the magnetic layer is transferred to the conductive undercoat layer, The running durability of the surface magnetic layer tended to deteriorate with time.
【0008】さらに、潤滑剤成分の導電下塗層への移行
を防止するため、予め多量の潤滑剤成分を導電下塗層に
存在させると、この下塗層の非磁性支持体への密着性が
低下するという別な問題が発生する。Further, in order to prevent the migration of the lubricant component to the conductive undercoat layer, if a large amount of the lubricant component is present in the conductive undercoat layer in advance, the adhesion of the undercoat layer to the non-magnetic support is improved. Another problem occurs that is decreased.
【0009】これに対し、本発明で使用する導電性充填
剤は、前述のカーボンに比べ吸油量がはるかに少ないた
め、前述の如き問題は起らない。On the other hand, the conductive filler used in the present invention has a much smaller oil absorption amount than the above-mentioned carbon, so that the above-mentioned problem does not occur.
【0010】しかしながら、当然の事であるが導電性下
塗層の表面粗度を一定水準(例えば中心線平均粗さで
0.03μm以下より好ましくは0.02μm以下、さ
らに好ましくは0.015μm以下)にするため平均粒
子系(aμm)は下塗層の厚さ(cμm)をパラメータ
ーとして C> a+0.02、 好ましくは C>1.1a+0.02、 より好ましくは C>1.5a+0.03 の範囲とすべきである。However, as a matter of course, the surface roughness of the conductive undercoat layer is kept at a certain level (for example, the center line average roughness is 0.03 μm or less, preferably 0.02 μm or less, more preferably 0.015 μm or less). The average particle system (aμm) is C> a + 0.02, preferably C> 1.1a + 0.02, more preferably C> 1.5a + 0.03, with the thickness (cμm) of the undercoat layer as a parameter. Should be a range.
【0011】結合剤や上記充填剤の使用割合は、導電性
充填剤100重量部当り結合剤5〜100重量部が適切
で、その他の潤滑剤等々の成分は結合剤100重量部当
り1〜20重量部添加するのがよい。The binder and the above-mentioned filler are appropriately used in an amount of 5 to 100 parts by weight per 100 parts by weight of the conductive filler, and other components such as lubricant are 1 to 20 parts by weight per 100 parts by weight of the binder. It is recommended to add parts by weight.
【0012】また導電性充填剤の使用割合は、所望の厚
さで下塗層を作成したとき、その表面抵抗値が500M
Ω/cm2 以下の所望の値となるようにコントロールする
とよい。The ratio of the conductive filler used is such that when the undercoat layer is formed to a desired thickness, the surface resistance value is 500 M.
It is advisable to control the value to a desired value of Ω / cm 2 or less.
【0013】ここで、下塗層に使用される結合剤樹脂と
しては、塩化ビニル−酢酸ビニル系共重合体、ポリビニ
ルブチラール樹脂、繊維素系樹脂、ポリウレタン系樹
脂、ポリエステル系樹脂、エポキシ系樹脂、ポリエーテ
ル系樹脂、イソシアネート化合物、放射線硬化型樹脂な
ど従来から汎用されている結合剤樹脂がいずれも好適に
使用される。Here, as the binder resin used in the undercoat layer, vinyl chloride-vinyl acetate copolymer, polyvinyl butyral resin, fibrin resin, polyurethane resin, polyester resin, epoxy resin, Any conventionally used binder resin such as a polyether resin, an isocyanate compound, or a radiation curable resin is preferably used.
【0014】また、有機溶剤としては、アセトン、メチ
ルイソブチルケトン、メチルエチルケトン、シクロヘキ
サノン、トルエン、酢酸エチル、テトラヒドロフラン、
ジメチルホルムアミドなど従来一般に使用される有機溶
剤がいずれも単独で、或いは2種以上混合して使用され
る。As the organic solvent, acetone, methyl isobutyl ketone, methyl ethyl ketone, cyclohexanone, toluene, ethyl acetate, tetrahydrofuran,
Any of the conventionally commonly used organic solvents such as dimethylformamide may be used alone or in admixture of two or more.
【0015】本発明に於いて用いられる低分子イソシア
ネート化合物としては、2,4−トリレンジイソシアネ
ート、2,6−トリレンジイソシアネート、4,4′−
ジフェニルメタンジイソシアネート、ヘキサメチレンジ
イソシアネート、キシレンジイソシアネートなどのジイ
ソシアネート類および、これらジイソシアネート3モル
とトリオール1モルを反応させて得られる3官能性低分
子イソシアネート化合物等があり、市販品の多くのもの
を用いることができる(たとえば、日本ポリウレタン社
製コロネート2036,住友バイエル社製デスモジュー
ルL,デスモジュール14,スミジュールT−80,武
田薬品工業社製タケネートD102,タケネートM40
3等がある。)。The low molecular weight isocyanate compound used in the present invention includes 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate and 4,4'-
There are diisocyanates such as diphenylmethane diisocyanate, hexamethylene diisocyanate, and xylene diisocyanate, and trifunctional low-molecular isocyanate compounds obtained by reacting 3 mol of these diisocyanates with 1 mol of triol, and many commercially available products can be used. Possible (for example, Coronate 2036 manufactured by Nippon Polyurethane Company, Death Module L manufactured by Sumitomo Bayer, Death Module 14, Sumidule T-80, Takenate D102, Takenate M40 manufactured by Takeda Pharmaceutical Co., Ltd.)
There are 3 mag. ).
【0016】[0016]
【発明の効果】本発明は非カーボンブラック系の下塗剤
を使用しているため電導率が下塗剤の粒径等によって変
動することがなく、安定した電磁変換特性を備えてい
る。そして、バリウムフェライト等の磁性層と緊密な接
着性を有する。Since the present invention uses a non-carbon black type undercoating agent, the electric conductivity does not vary depending on the particle size of the undercoating agent and has a stable electromagnetic conversion characteristic. And, it has a close adhesiveness with a magnetic layer such as barium ferrite.
【0017】[0017]
【実施例】以下実施例によって本発明を説明する。The present invention will be described below with reference to examples.
【0018】[0018]
【実施例1】 (下塗層塗料の調製) ヨウ化第1銅 75重量部 スルホン酸ソーダ含有 25重量部 ポリエステルウレタン(東洋紡バイロン) 低分子ポリウレタン 2重量部(日本ポリウレタンコロネートL) シクロヘキサノン 200重量部 上記組成物をボールミルに入れ72時間混合分散して、
下塗塗料を調整した。この下塗層用塗料を厚さ75μm
のポリエチレンテレフタレートフイルム両面に乾燥厚
1.0μmとなる様に塗布し、乾燥し、10MΩ/cm2
の表面抵抗を有する下塗層を形成し、ついでカレンダー
処理を施した。次に、このポリエチレンテレフタレート
フイルム両面に、下記組成の磁性塗料をその乾燥厚さが
0.7μmとなるように塗布し、乾燥し、カレンダー処
理を施した。しかる後ウェブ状物を3.5″(インチ)
円板状に打抜き、みがき処理をした後、公知の方法に従
って磁気ディスクを作成した。Example 1 (Preparation of Undercoat Layer Coating Material) Cuprous iodide 75 parts by weight Sodium sulfonate-containing 25 parts by weight Polyester urethane (Toyobo Byron) Low molecular weight polyurethane 2 parts by weight (Nippon Polyurethane Coronate L) Cyclohexanone 200 parts by weight Parts The above composition was put into a ball mill, mixed and dispersed for 72 hours,
The undercoat paint was adjusted. This undercoat paint is 75 μm thick
Of polyethylene terephthalate film on both sides to a dry thickness of 1.0 μm, dried and 10 MΩ / cm 2
An undercoat layer having a surface resistance of 1 was formed and then calendered. Next, a magnetic coating composition having the following composition was applied to both surfaces of this polyethylene terephthalate film so that the dry thickness was 0.7 μm, and the coating was dried and calendered. Then 3.5 "(inch) the web
After punching into a disc shape and polishing treatment, a magnetic disk was prepared according to a known method.
【0019】磁性塗料 Ba−フェライト粉末 80重量部 BET比表面積 50m2 /g板状比 4.2 アルミナ(平均粒径0.3μm) 7重量部 スルホン酸塩含有塩ビ・酢ビ樹脂 10重量部(日本ゼオン MR110) ポリウレタン樹脂 10重量部 低分子ポリウレタン 10重量部(日本ポリウレタン社コロネートL) オレイルオレート 7重量部 シクロヘキサノン 300重量部 トルエン 100重量部Magnetic paint Ba-Ferrite powder 80 parts by weight BET specific surface area 50 m 2 / g Plate ratio 4.2 Alumina (average particle size 0.3 μm) 7 parts by weight Sulfonate-containing vinyl chloride / vinyl acetate resin 10 parts by weight ( Nippon Zeon MR110) Polyurethane resin 10 parts by weight Low molecular weight polyurethane 10 parts by weight (Nippon Polyurethane Company Coronate L) oleyl oleate 7 parts by weight Cyclohexanone 300 parts by weight Toluene 100 parts by weight
【0020】[0020]
【比較例1】下記組成のカーボン含有組成の下塗層を実
施例1と同様にして製造(塗布)した後、実施例1の磁
性塗料を塗布して、実施例1と同様にして磁気ディスク
を製造した。 カーボンブラック 30重量部(ライオンアクゾ社ケッチェンブラック) スルホン酸ソーダ含 70重量部 ポリエスターウレタン(東洋紡バイロン) 低分子ポリウレタン 2重量部(日本ポリウレタン コロネート) シクロヘキサノン 200重量部[Comparative Example 1] An undercoat layer of a carbon-containing composition having the following composition was produced (applied) in the same manner as in Example 1, and then the magnetic coating material of Example 1 was applied, followed by the same procedure as in Example 1. Was manufactured. Carbon black 30 parts by weight (Lion Akzo Ketjen black) Sodium sulfonate 70 parts by weight Polyester urethane (Toyobo Byron) Low molecular weight polyurethane 2 parts by weight (Nippon Polyurethane Coronate) Cyclohexanone 200 parts by weight
【0021】[0021]
【実施例2及び実施例3】実施例1のヨウ化銅を硫化第
2銅及びヨウ化銀に代えて実施例1と同様にして磁気デ
ィスクを製造した。この結果を実施例2及び3とする。
結果を実施例1及び比較例1と共に表1に併記する。Example 2 and Example 3 A magnetic disk was manufactured in the same manner as in Example 1 except that copper iodide in Example 1 was replaced with cupric sulfide and silver iodide. The results are referred to as Examples 2 and 3.
The results are shown in Table 1 together with Example 1 and Comparative Example 1.
【0022】[0022]
【表1】 *)塗膜剥離強度は1cm巾に磁性塗膜をカットし、該テ
ープ状の磁性面に粘着テープを張りつけテープ状磁性膜
と、粘着テープを180°方向に10cm/secで引張
った時のベースフイルムと、磁性層の剥離する時の力 **)ディスクを80℃100hr熱処理し、潤滑剤の移
行加速テストを行った。[Table 1] *) The peeling strength of the coating film is obtained by cutting the magnetic coating film to a width of 1 cm, attaching an adhesive tape to the tape-shaped magnetic surface, and the tape-shaped magnetic film and the base when the adhesive tape is pulled in the 180 ° direction at 10 cm / sec. The force of peeling the film and the magnetic layer **) The disk was heat-treated at 80 ° C. for 100 hours, and a lubricant transfer acceleration test was performed.
【0023】しかる後3.5″フロッピーディスクドラ
イブ(NEC1135c)(ヘッドテンション80g,
回転速度1200rpm)にて、塗膜キズつきまでの時
間を測定した。Then 3.5 ″ floppy disk drive (NEC1135c) (head tension 80g,
The time to scratch the coating film was measured at a rotation speed of 1200 rpm.
フロントページの続き (56)参考文献 特開 昭62−89219(JP,A) 特開 昭63−140420(JP,A) 特開 昭59−165239(JP,A) 特開 平4−195819(JP,A) 特開 平4−192111(JP,A)Continuation of front page (56) Reference JP 62-89219 (JP, A) JP 63-140420 (JP, A) JP 59-165239 (JP, A) JP 4-195819 (JP , A) JP-A-4-192111 (JP, A)
Claims (1)
る磁性層と、該支持体と該磁性層との間に設けられた導
電性下塗層とからなる磁気記録媒体であって、該下塗層
がヨウ化第一銅、ヨウ化銀及び硫化第二銅の群から選ば
れた少なくとも1種の金属化合物の導電性の充填剤と、
有機結合剤と、要すれば低分子イソシアネート化合物と
を含むことを特徴とする磁気記録媒体。1. A magnetic recording medium comprising a non-magnetic support, a magnetic layer containing ferromagnetic magnetic powder, and a conductive undercoat layer provided between the support and the magnetic layer. Te, and a conductive filler of at least one metal compound undercoat layer is selected from the group consisting of cuprous iodide Gin及 beauty sulfide cupric iodide,
And an organic binder, the magnetic recording medium you; and a low-molecular isocyanate compound optionally.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3121764A JP2688296B2 (en) | 1991-04-25 | 1991-04-25 | Magnetic recording media |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3121764A JP2688296B2 (en) | 1991-04-25 | 1991-04-25 | Magnetic recording media |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04325914A JPH04325914A (en) | 1992-11-16 |
JP2688296B2 true JP2688296B2 (en) | 1997-12-08 |
Family
ID=14819311
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3121764A Expired - Fee Related JP2688296B2 (en) | 1991-04-25 | 1991-04-25 | Magnetic recording media |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2688296B2 (en) |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59165239A (en) * | 1983-03-10 | 1984-09-18 | Fuji Photo Film Co Ltd | Magnetic recording medium |
JP2723213B2 (en) * | 1985-10-15 | 1998-03-09 | 東レ株式会社 | Film for magnetic recording media |
JPS63140420A (en) * | 1986-12-03 | 1988-06-13 | Victor Co Of Japan Ltd | Magnetic recording medium |
JPH04195819A (en) * | 1990-11-27 | 1992-07-15 | Victor Co Of Japan Ltd | Magnetic recording medium |
JPH04192111A (en) * | 1990-11-27 | 1992-07-10 | Ube Ind Ltd | Magnetic recording medium |
-
1991
- 1991-04-25 JP JP3121764A patent/JP2688296B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH04325914A (en) | 1992-11-16 |
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