JPS6318514A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS6318514A JPS6318514A JP16257786A JP16257786A JPS6318514A JP S6318514 A JPS6318514 A JP S6318514A JP 16257786 A JP16257786 A JP 16257786A JP 16257786 A JP16257786 A JP 16257786A JP S6318514 A JPS6318514 A JP S6318514A
- Authority
- JP
- Japan
- Prior art keywords
- intermediate layer
- urethane
- carbon black
- magnetic
- nitrocellulose
- 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
- 239000006229 carbon black Substances 0.000 claims abstract description 15
- 239000011230 binding agent Substances 0.000 abstract description 10
- 239000000020 Nitrocellulose Chemical group 0.000 abstract description 6
- 229920001220 nitrocellulos Chemical group 0.000 abstract description 6
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 abstract description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000003973 paint Substances 0.000 description 9
- 238000010521 absorption reaction Methods 0.000 description 7
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- -1 polybutylene adipate Polymers 0.000 description 6
- 229920002635 polyurethane Polymers 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000006249 magnetic particle Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- CUXVCONCZJJRCS-UHFFFAOYSA-N nitrosilane Chemical class [O-][N+]([SiH3])=O CUXVCONCZJJRCS-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
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〕
本発明は磁気記録テープや7o、ビーディスク等の磁気
記録媒体に係り、ざらに詳しくは高密度記録に適しな磁
気記録媒体に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to magnetic recording media such as magnetic recording tapes, 7O disks, and B-disks, and more particularly to magnetic recording media suitable for high-density recording.
磁気記録媒体の多くは、ポリエステルなどの非磁性支持
体上に、ニトロセルロースなどの合am脂中に磁性粒子
が分散した磁性層を有する。そして磁性層中にカーボン
ブラックが含まれることが多かった。その理由は、磁気
記録媒体の帯電によるノイズの発生や、磁性層へのじん
あいの付着によるドロップアウトの発生といった問題の
防止目的、あるいはビデオテープの終端検出や、フロッ
ピーディスクのインデックスホール検出などのため磁気
記録媒体に遮光性を付与する目的で行われていた。Many magnetic recording media have a magnetic layer on a non-magnetic support such as polyester, in which magnetic particles are dispersed in synthetic resin such as nitrocellulose. Carbon black was often contained in the magnetic layer. The reason for this is to prevent problems such as noise caused by charging of the magnetic recording medium and dropout caused by dust adhering to the magnetic layer, or to detect the end of a video tape or index hole of a floppy disk. This was done for the purpose of imparting light-shielding properties to magnetic recording media.
近年8a気記録媒体は高密度記録化が計らnる傾向にあ
り、磁性層の厚み損失を逃れる之めに、磁性層を薄くす
ることが試みられている。このことは、磁性層の導電性
、遮光性、耐久性などに不利な条件となる。導電性、遮
光性を改善するには、磁性層中に含めるカーボンブラッ
クの量を多くスればよいが、そうすると急性層中の磁性
粒子比率が減少し、再生出力の低下が生じ、またバイン
ダー比率も減少し、耐久性の低下が生じる。In recent years, there has been a trend toward higher density recording in 8A recording media, and attempts have been made to make the magnetic layer thinner in order to avoid loss in the thickness of the magnetic layer. This becomes a disadvantageous condition for the conductivity, light-shielding property, durability, etc. of the magnetic layer. In order to improve conductivity and light-shielding properties, it is possible to increase the amount of carbon black contained in the magnetic layer, but this reduces the ratio of magnetic particles in the acute layer, resulting in a decrease in reproduction output, and also increases the binder ratio. is also reduced, resulting in a decrease in durability.
これらの問題を解決するため、非磁性支持体と磁性層の
中間に、ポリエステル樹脂をバインダーとし、カーボン
ブラックを含む中間層を設けることが行なわれている。In order to solve these problems, an intermediate layer containing carbon black and using a polyester resin as a binder is provided between the nonmagnetic support and the magnetic layer.
この方法によって、−導゛亀性。By this method - induction properties.
遮光性、および耐久性という問題は解決されたが、中間
層の表面平滑性が悪くなり、雑音性能が悪く、高密摩記
録には適ネなかった。そこで、本発明者らは、中間層の
表面平滑性を良好にすべく鋭意検討の結果、ニトロセル
ロースをパインダートシテ用いれば、中間層の表面平滑
性は良好になることを見出した。しかし、このようにニ
トロセルロースをバインダーとして用いた場合、中間層
と゛磁性層の接着強度は十分であるが、非磁性支持体と
中間層の接着強度が低く、このため耐久性が悪pという
問題が残った。接着強度の改善のため、ニトロセル四−
スとポリウレタン樹脂を併用したが・、この場合、ニド
胃セルロース単独に比べ中間層の表面平滑性が悪く、高
密度記録には適さなかった。Although the problems of light-shielding properties and durability were solved, the surface smoothness of the intermediate layer deteriorated and the noise performance was poor, making it unsuitable for high-density recording. Therefore, the present inventors conducted intensive studies to improve the surface smoothness of the intermediate layer and found that the surface smoothness of the intermediate layer can be improved by using nitrocellulose as a binder. However, when nitrocellulose is used as a binder in this way, although the adhesive strength between the intermediate layer and the magnetic layer is sufficient, the adhesive strength between the non-magnetic support and the intermediate layer is low, resulting in poor durability. remained. To improve adhesive strength, Nitrocell 4-
However, in this case, the surface smoothness of the intermediate layer was poorer than that of cellulose alone, making it unsuitable for high-density recording.
本発明は、上記従来製品が持っていた欠点を除き、導電
性、遮光性、耐久性に優れ、かつ高密度記録に適する磁
気記録媒体を提供することにある。An object of the present invention is to provide a magnetic recording medium that eliminates the drawbacks of the conventional products described above, has excellent conductivity, light-shielding properties, and durability, and is suitable for high-density recording.
(問題を解決するための手段〕
1 本発明者らは、上記目的を達成すべ
く鋭意検討ノ結果、ニド田七ルp−スをウレタン変性シ
て、内部可塑化して用いれば、上記目的を達成できる仁
とを見出し、本発明に至った。(Means for Solving the Problem) 1. As a result of intensive studies to achieve the above object, the present inventors found that the above object can be achieved by using urethane-modified p-su and internally plasticizing it. The inventors have discovered that this can be achieved, and have led to the present invention.
すなわち、本発明は、非磁性支持体と磁性層の中間に、
ウレタン変性ニトロセルロースをバインダーとしたカー
ボンブラックを含も中間層を設けたものである。That is, in the present invention, between the nonmagnetic support and the magnetic layer,
An intermediate layer is provided containing carbon black using urethane-modified nitrocellulose as a binder.
本発明で使用するウレタン変性ニトロセルロースは、末
端イソシアネート基のウレタンとニトロセルロースを反
応させて得られるものである。The urethane-modified nitrocellulose used in the present invention is obtained by reacting urethane with terminal isocyanate groups and nitrocellulose.
例えば、テスラツクυD、1010(日立化成ポリマー
社製ポリブチレンアジペート)6oyと2−プタノン2
00fを11の4つロフラスコに入れ加熱、溶解後、6
0’Cに加熱、撹拌を行いつ\、N2%流中で、ジフェ
ニルメタンジイソシアネート10f、オクチル酸スズ0
.05y 、2−ブタノン50pの混合溶液を滴下する
。滴下終了譚さらに60″Cで2時間攪拌した後、80
″Cで2時間攪拌を行い反応を終了する。そして2−ブ
タノンを除失、乾燥を行う。For example, Tesla Tsuk υD, 1010 (polybutylene adipate manufactured by Hitachi Chemical Polymer Co., Ltd.) 6oy and 2-ptanone 2
Put 00f into 4 flasks of 11, heat and dissolve, then 6
While heating to 0'C and stirring, 10f of diphenylmethane diisocyanate and 0% of tin octylate were added in a 2% N flow.
.. 05y, a mixed solution of 50p of 2-butanone is added dropwise. After the addition was completed, the mixture was further stirred at 60″C for 2 hours, and then heated to 80°C.
The reaction was terminated by stirring at 100° C. for 2 hours. Then, 2-butanone was removed and drying was performed.
上記生成物35g 、l・6−へキサメチレンジイソシ
アネート2.5g、シクロへ゛キサノン/トルエン(5
0150)1509を11の4ツロフラスコに入れ溶解
後、60″Cに加熱2時間攪拌を行う。35 g of the above product, 2.5 g of l.6-hexamethylene diisocyanate, cyclohexanone/toluene (5 g)
0150) After dissolving 1509 in a 4-tube flask (No. 11), heat to 60"C and stir for 2 hours.
次いで工tロセルロースSS局を乾燥後、シクロヘキサ
ノン/トルエン(50150)の20w1t%としたも
の250fを混合し、30°Cで72時間攪拌してウレ
タン変性二トロセルロースヲ得り。Next, after drying the modified nitrocellulose SS, 250f of cyclohexanone/toluene (50150) at 20w1t% was mixed and stirred at 30°C for 72 hours to obtain urethane-modified nitrocellulose.
中間層用のバインダーとしては、上記のウレタン父性ニ
トロセルロースのみならずこれにコロネー)L (日本
ポリウレタン社製ポリイソシアネート)などのポリイソ
シアネート及び/またはポリウレタン樹脂を添加しても
よい。ポリイソシアネートの添加量は全バインダーに対
して50%以下好ましくは30%以下がよい。50%よ
り多いとカーボンブラックの分散性が低下し、中間層の
表面平滑性が低下する。ポリウレタン樹脂の添加量は、
全バインダーに対して40第以下、好ましくは20%以
下がよい。As the binder for the intermediate layer, not only the above-mentioned urethane-based nitrocellulose but also polyisocyanate and/or polyurethane resin such as Coronet) L (polyisocyanate manufactured by Nippon Polyurethane Co., Ltd.) may be added thereto. The amount of polyisocyanate added is preferably 50% or less, preferably 30% or less, based on the total binder. When it is more than 50%, the dispersibility of carbon black decreases, and the surface smoothness of the intermediate layer decreases. The amount of polyurethane resin added is
It is preferably 40 or less, preferably 20% or less, based on the total binder.
中間層に用いるカーボンブラックとしては、BET (
N2)による比表面積が、10〜300〆/f! DB
Pによる吸油量が40〜200cc/ 100 gのも
のが適しており、特に、上記比表面積が25〜260イ
/I 、上記吸油量が50〜180匡/ 100 gの
ものが好ましい。このようなカーボンブラックの例とし
ては、5TERLING−1(比表面積25ゴ/f。As the carbon black used for the intermediate layer, BET (
The specific surface area due to N2) is 10 to 300〆/f! DB
A material having an oil absorption amount of 40 to 200 cc/100 g due to P is suitable, and a material having the above-mentioned specific surface area of 25 to 260 I/I and an oil absorption amount of 50 to 180 squares/100 g is particularly preferred. An example of such carbon black is 5TERLING-1 (specific surface area 25g/f).
DBP吸油t 7 lee/ 10J+ 、米国キャボ
ット社製)、5TRRLING・NS(比表面積25ゴ
/f 。DBP oil absorption t7 lee/10J+, manufactured by Cabot, USA), 5TRRLING・NS (specific surface area 25g/f).
DBP吸油量70cc7100y 、米国キャボット社
製)、MOGυいL(比表面積138ゴ/f、DBP吸
油fi 60cc/ 1007F e米国キャボット社
製)。DBP oil absorption 70cc/7100y, manufactured by Cabot, USA), MOGυL (specific surface area 138g/f, DBP oil absorption fi 60cc/1007F, manufactured by Cabot, USA).
VULCAN−XC−72(比表面積254ttf/
g 、 DBP吸油量178cc/100y 、米国キ
ャボット社製)。VULCAN-XC-72 (specific surface area 254ttf/
g, DBP oil absorption 178cc/100y, manufactured by Cabot, USA).
LAMPBLACKIOI C比表面積20ゴ/p、D
BP吸油量65cc/loog、西独デグサ社製)、ジ
ースト5H(比表面積60ゴ/y、DBP@油ff11
32cc/100y、東海カーボン社製)などがあげら
れる。LAMPBLACKIOI C specific surface area 20g/p, D
BP oil absorption 65cc/loog, made by Degussa, West Germany), GEST 5H (specific surface area 60go/y, DBP@oil ff11)
32cc/100y, manufactured by Tokai Carbon Co., Ltd.).
中間層に含ませるカーボンブラックの量は、導電性およ
び遮光性の点から、10〜79w6%、好ましくは、4
0〜59wt%がよい。カーボンブラックが10wt%
以下だと導電性が十分でなく、7Qwt%より多くなる
と中間層の空は右が多くなり、表面平滑性が低下する。The amount of carbon black to be included in the intermediate layer is 10 to 79w6%, preferably 4% from the viewpoint of conductivity and light shielding properties.
0 to 59 wt% is preferable. Carbon black is 10wt%
If it is less than 7Qwt%, the conductivity will not be sufficient, and if it is more than 7Qwt%, the middle layer will have more vacancies on the right side, and the surface smoothness will deteriorate.
本発明に用いることができる非磁性支持体には、従来公
知のポリエチレンテトラフタレート、ポリエチレン−2
・6−す7タレート等のホ゛リエステル類、ポリエチレ
ン、ポリプロピレン等のボ)ノオレフィン類、セルロー
ストリアセテート、セルロースアセテ−ドブpビオネー
ト等のセルロース誘導体、ポリ塩化ビニル、ポリ塩化ビ
ニリデン等のビニル系樹脂、メリカーボネート、ポリア
ミド、ポリイミド等のプラスチックおよび用途に応じて
アルミニウムなどの非磁性金属あるいは合金、または紙
、ポリエチレン等をラミネートした紙などがある。Non-magnetic supports that can be used in the present invention include conventionally known polyethylene tetraphthalate, polyethylene-2
・Polyesters such as 6-7 talate, boroolefins such as polyethylene and polypropylene, cellulose derivatives such as cellulose triacetate and cellulose acetate p-bionate, vinyl resins such as polyvinyl chloride and polyvinylidene chloride, and polymers. Examples include plastics such as carbonate, polyamide, and polyimide, non-magnetic metals such as aluminum or alloys, paper, and paper laminated with polyethylene, etc., depending on the purpose.
以下本発明の詳細を実施例によって説明する。 The details of the present invention will be explained below with reference to Examples.
実施例1 中間層用塗料を以下の通り調製した。Example 1 A paint for the intermediate layer was prepared as follows.
カーボンブラック(米国キャボット社製、MOGUL−
L):100重世部
ウレタン変性二トロセ/%/四−ス : 80 rシ
フ田ヘキサノン =210重胤部トルエ
ン =210 1上
記組成物をボールミルによって48時間混合分赦した後
、コロネートL(日本ポリウレタン社製、ポリイソシア
ネート)を、20重n部添加し、さらに30分間混合分
散して、中間層用塗料を得た。Carbon black (manufactured by Cabot, USA, MOGUL-
L): 100 parts urethane modified Nitrose/%/4-se: 80 r Schifta hexanone = 210 parts Toluene = 210 1 After mixing the above composition in a ball mill for 48 hours, Coronate L (Japan 20 parts by weight (n parts by weight) of Polyisocyanate (manufactured by Polyurethane Co., Ltd.) were added, and the mixture was further mixed and dispersed for 30 minutes to obtain a paint for an intermediate layer.
上記塗料をポリエステルフィルム(厚−J 75μ鴫)
表面にvJ燥換厚が1μ隻になるように塗布し中間層を
形成した。フィルム&面にも同様に塗布を行なった。Apply the above paint to a polyester film (thickness - J 75μ)
An intermediate layer was formed by coating the surface so that the vJ dry thickness was 1 μm. The film and surface were also coated in the same manner.
次き゛に磁性塗料を以下の通り調製した。Next, a magnetic paint was prepared as follows.
Co含有1−Fe2O3粉末 =100重am
塩諸ビーポリビニルアルコール共重合体: 68 l
ポリウレタン : 41 lオレイ
ルオレー) : 15 #アルミ
ナ = 1o rトルエン
:287#シクロヘキサノン
:287#硬化剤(日本ポリウレタン社製
、フロネー)L); 27重量部
からなる磁性塗料を、上記中間層を塗布したポリエステ
ルフィルム上に乾燥膜厚1μ鶏と人るように塗布し、磁
性層を表裏両面に形成後、表面平滑化処理を行った。こ
のシートを円形に打ち抜き、フ’O−)ビーディスクを
得り。Co-containing 1-Fe2O3 powder = 100 am
Polyvinyl alcohol copolymer: 68 l Polyurethane: 41 l Oleyl oleate: 15 #Alumina = 1 o r toluene
:287# cyclohexanone
: 287# hardening agent (manufactured by Nippon Polyurethane Co., Ltd., Fronay L); 27 parts by weight of a magnetic paint was applied onto the polyester film coated with the above intermediate layer so that the dry film thickness was 1 μm, and the magnetic layer was After forming on both the front and back surfaces, surface smoothing treatment was performed. This sheet was punched out into a circular shape to obtain a F'O-)B disk.
実施例2
実施例1の中間層塗料において、ウレタン変性ニトロセ
ルロースの量を80重量部から50重世部に変更し、さ
らにポリウレタン(大日本インキ化学工業社製T−52
50”)を30重量部添加した以外は、実施例1と同様
にしてフロンピーディスクを得た。Example 2 In the intermediate layer paint of Example 1, the amount of urethane-modified nitrocellulose was changed from 80 parts by weight to 50 parts by weight, and polyurethane (T-52 manufactured by Dainippon Ink and Chemicals) was added.
A floppy disk was obtained in the same manner as in Example 1, except that 30 parts by weight of 50") was added.
比較例1
実施例1の中間層塗料において、ウレタン変性ニトロセ
ルロースの代りにポリエステル(東洋u社製バイロン5
30 )80重量部に変更した以外、実施例1と同様
にしてフロッピーディスクを得た。Comparative Example 1 In the intermediate layer paint of Example 1, polyester (Vylon 5 manufactured by Toyo U Co., Ltd.) was used instead of urethane-modified nitrocellulose.
30) A floppy disk was obtained in the same manner as in Example 1 except that the amount was changed to 80 parts by weight.
比較例2
実施例2において、中間層塗料のウレタン変性ニトロセ
ルロースs o NU!Fl二) ロセl’y o −
150重量部に変更した以外は、実施例2と同様にして
7田フピーデイスクを得た〇
比較例3
実施例1において、中間層を塗布しないで、ポリエステ
ルフィルム上に直接磁性塗料を塗布した以外は実施例1
と同様にしてフロッピーディスクを得た。Comparative Example 2 In Example 2, urethane-modified nitrocellulose so NU! of the intermediate layer paint was used. Fl2) Rosel'y o -
A 7-P disk was obtained in the same manner as in Example 2, except that the amount was changed to 150 parts by weight. Comparative Example 3 In Example 1, the magnetic paint was applied directly onto the polyester film without applying the intermediate layer. Example 1
I obtained a floppy disk in the same way.
実施例および比較例で得られたフロッピーディスクにつ
いて、光透過率、寛気抵抗、変調ノイズおよび再生出力
が、初期出力の70%以下になるまでの連続実走回数す
なわち耐久性を調べた。結果を表に示す。For the floppy disks obtained in Examples and Comparative Examples, the number of continuous actual runs until the light transmittance, resistance, modulation noise, and reproduction output became 70% or less of the initial output, that is, the durability was examined. The results are shown in the table.
上記の結果から明らかなように、本発明は、非磁性支持
体と磁性層の中間に、ウレタン変性ニトロ七ル四−スを
バインダーとし、カーボンブラックを含む中間層を形成
することによって、光透過率、電気抵抗、変調ノイズ、
耐久性のすべての点で優れた磁気記録媒体を得ることが
できる。As is clear from the above results, the present invention achieves light transmission by forming an intermediate layer containing carbon black between the nonmagnetic support and the magnetic layer using urethane-modified nitrosilane as a binder. rate, electrical resistance, modulation noise,
A magnetic recording medium that is excellent in all aspects of durability can be obtained.
Claims (1)
ルロースにカーボンブラックを含ませた中間層を設けた
ことを特徴とする磁気記録媒体。A magnetic recording medium characterized in that an intermediate layer made of urethane-modified nitrocellulose containing carbon black is provided between a nonmagnetic support and a magnetic layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16257786A JPS6318514A (en) | 1986-07-09 | 1986-07-09 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16257786A JPS6318514A (en) | 1986-07-09 | 1986-07-09 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6318514A true JPS6318514A (en) | 1988-01-26 |
Family
ID=15757227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16257786A Pending JPS6318514A (en) | 1986-07-09 | 1986-07-09 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6318514A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007036132A (en) * | 2005-07-29 | 2007-02-08 | Koha Co Ltd | Field light emitting module and field light emitting device using the same |
-
1986
- 1986-07-09 JP JP16257786A patent/JPS6318514A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007036132A (en) * | 2005-07-29 | 2007-02-08 | Koha Co Ltd | Field light emitting module and field light emitting device using the same |
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