JPS59201219A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS59201219A JPS59201219A JP58074548A JP7454883A JPS59201219A JP S59201219 A JPS59201219 A JP S59201219A JP 58074548 A JP58074548 A JP 58074548A JP 7454883 A JP7454883 A JP 7454883A JP S59201219 A JPS59201219 A JP S59201219A
- Authority
- JP
- Japan
- Prior art keywords
- recording medium
- magnetic
- carbon black
- back 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.)
- Pending
Links
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 43
- 239000006229 carbon black Substances 0.000 claims abstract description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000010439 graphite Substances 0.000 claims abstract description 14
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 14
- 239000000843 powder Substances 0.000 claims abstract description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 7
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 abstract description 7
- 238000006243 chemical reaction Methods 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000005056 polyisocyanate Substances 0.000 abstract description 4
- 229920001228 polyisocyanate Polymers 0.000 abstract description 4
- 239000000454 talc Substances 0.000 abstract description 4
- 229910052623 talc Inorganic materials 0.000 abstract description 4
- 230000006866 deterioration Effects 0.000 abstract description 3
- 238000012546 transfer Methods 0.000 abstract description 3
- 239000003822 epoxy resin Substances 0.000 abstract description 2
- 229920000647 polyepoxide Polymers 0.000 abstract description 2
- 239000011164 primary particle Substances 0.000 abstract 3
- 239000004848 polyfunctional curative Substances 0.000 abstract 1
- 230000003746 surface roughness Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 11
- 238000001723 curing Methods 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- -1 polyethylene terephthalate Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- MVLVMROFTAUDAG-UHFFFAOYSA-N ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 235000012222 talc Nutrition 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 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
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B5/00—Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
- G11B5/62—Record carriers characterised by the selection of the material
- G11B5/73—Base layers, i.e. all non-magnetic layers lying under a lowermost magnetic recording layer, e.g. including any non-magnetic layer in between a first magnetic recording layer and either an underlying substrate or a soft magnetic underlayer
- G11B5/735—Base layers, i.e. all non-magnetic layers lying under a lowermost magnetic recording layer, e.g. including any non-magnetic layer in between a first magnetic recording layer and either an underlying substrate or a soft magnetic underlayer characterised by the back layer
- G11B5/7356—Base layers, i.e. all non-magnetic layers lying under a lowermost magnetic recording layer, e.g. including any non-magnetic layer in between a first magnetic recording layer and either an underlying substrate or a soft magnetic underlayer characterised by the back layer comprising non-magnetic particles in the back layer, e.g. particles of TiO2, ZnO or SiO2
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Magnetic Record Carriers (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、バック層を有する磁気記録媒体に関し、その
主たる目的は、走行耐久性の改良に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium having a back layer, and its main purpose is to improve running durability.
磁気記録媒体は、その走行および巻取が高速で行なわれ
るため、高度の耐久性が要求される。この耐久性を良化
させるべく、磁気記録媒体にバック層を施こし、かつバ
ック層中にカーボンブラックおよびグラファイト粉末を
含有させる方法が提案されている(特公昭ゲタ−102
≠/号)。しかしながら、上記技術では、走行耐久性が
いまだ十分なものではなく、さらにビデオテープにおい
ては、パック層表面の凹凸が磁性層表面に転写されるこ
とにより、電磁変換特性、たとえばカラー信号雑音比(
8/N)が劣化する場合がある。そのためにバック層表
面の凹凸コントロールが重要であり、この点に関しても
改良が望まれてきた。Magnetic recording media are required to have a high degree of durability because they are run and wound at high speed. In order to improve this durability, a method has been proposed in which a magnetic recording medium is provided with a back layer and carbon black and graphite powder are contained in the back layer (Tokuko Sho Geter 102
≠ / issue). However, the running durability of the above technology is still insufficient, and in video tapes, unevenness on the surface of the pack layer is transferred to the surface of the magnetic layer, resulting in changes in electromagnetic conversion characteristics such as color signal-to-noise ratio (
8/N) may deteriorate. For this reason, it is important to control the irregularities on the surface of the backing layer, and improvements have been desired in this regard as well.
本発明の目的は、塗膜の走行耐久性を改良し、さらに電
磁変換特性の劣化を減少させた磁気記録媒体の提供にあ
る。An object of the present invention is to provide a magnetic recording medium in which the running durability of the coating film is improved and the deterioration of the electromagnetic conversion characteristics is reduced.
すなわち、本発明は、
1)非磁性支持体上に磁性層を設け、かつ他面にバック
層を設けた磁気記録媒体において、該バック層が、イ)
カーボンブラック、口)グラファイト、およびハ)タル
ク(滑石)粉を含有することを特徴とする磁気記録媒体
、
2ン非磁性支持体表面の中心線平均粗さくRa ;カッ
トオフ0.01mm)がo、o3zttm以下であるこ
とを特徴とする1)に記載された磁気記録媒体、
3)カーボンブラックの平均−次粒子サイズがo 、o
r〜0.11μmであることを特徴とするl)および2
)に記載された磁気記録媒体、。That is, the present invention provides: 1) a magnetic recording medium in which a magnetic layer is provided on a non-magnetic support and a back layer is provided on the other surface, where the back layer is a)
A magnetic recording medium characterized by containing carbon black, a) graphite, and c) talc (talcum) powder, wherein the centerline average roughness Ra of the surface of the nonmagnetic support (cutoff 0.01 mm) is o. , o3zttm or less; 3) the average particle size of carbon black is o, o3zttm or less;
l) and 2 characterized in that r~0.11 μm
), the magnetic recording medium described in .
4)バック層に硬化剤を含有することを特徴とする1)
、2)および3)に記載された磁気記録媒体に関する。4) 1) characterized by containing a hardening agent in the back layer
, 2) and 3).
本発明上、従来使用されているカーボンブラックおよび
グラファイトに加えて、モース硬度が7;ミ=4と軟ら
かいタルク粉を含有することを特徴とする。タルク粉は
、ビデオテープレコーダーの走行系をそこなうことはな
く表面に適度の凹凸を設けて走行耐久性の改良に効果を
有する。In addition to conventionally used carbon black and graphite, the present invention is characterized by containing soft talcum powder with a Mohs hardness of 7; Mi=4. Talcum powder has the effect of improving the running durability by providing appropriate unevenness on the surface without damaging the running system of the videotape recorder.
カーボンブラックは、その平均−次粒子サイズが、o、
or−o、iよμmのものが好ましく、0.07〜01
72μmのものがよシ好ましい。Carbon black has an average particle size of o,
or-o, i-μm is preferable, and 0.07 to 01
72 μm is more preferable.
これらの範囲より、小さいものは走行耐久性改良効果を
減じる傾向を示し、大きいものはバック層表面の凹凸が
磁性層表面に転写されやすい傾向を示すようになる。If it is smaller than these ranges, it tends to reduce the running durability improvement effect, and if it is larger, the unevenness on the surface of the back layer tends to be easily transferred to the surface of the magnetic layer.
グラファイトは、その形状が、ウロコ状、粒状、塊状、
土状など種々あるが、このうちウロコ状のものが走行耐
久性改良に最も効果がある。The shape of graphite is scaly, granular, lumpy,
There are various types such as soil, but scale-like is the most effective for improving running durability.
カーボンブラックとグラファイトとの含有比率は、重量
比で10二/〜/:lOが好ましく、j:/〜l:jが
よシ好ましい。さらに3:/〜l:3が好ましい。The content ratio of carbon black and graphite is preferably 102/~/:lO in terms of weight ratio, and more preferably j:/~l:j. Furthermore, 3:/~l:3 is preferable.
グラファイトの含有量が少なすぎると走行耐久性改良効
果が減じ、また多すぎるとバック層からの剥離が生じ、
剥離粉が走行系を汚し、好ましくない。If the graphite content is too low, the running durability improvement effect will be reduced, and if it is too high, it will peel off from the backing layer.
The peeling powder contaminates the running system, which is not desirable.
グラファイトの平均−次粒子サイズは10μm以下、好
ましくは0.0/−38m1よシ好ましくは0.0!〜
3μmである。これらの範囲より大きすぎると剥離が生
じやすく、小さすぎると走行耐久性改良効果が減少する
。The average particle size of the graphite is less than 10 μm, preferably 0.0/-38 m1, preferably 0.0! ~
It is 3 μm. If it is too large than these ranges, peeling tends to occur, and if it is too small, the effect of improving running durability will be reduced.
本発明に使用されるタルク粉は、その平均−次粒子サイ
ズが70μm以下、好ましくは、0.θ/−jμm1よ
シ好ましくはθ、OS〜3μmである。タルク粉の、カ
ーボンブラックおよびグラファイトの合計重量に対する
添加量は!=2!〜りj:!であシ、lO:りO〜り0
:10がよp好ましく、3θニア0〜70:30がさら
に好ましい。メルク粉含有量が多すぎると帯電防止効果
が低下し、少なすぎると走行耐久性改良効果が減少する
。The talcum powder used in the present invention has an average particle size of 70 μm or less, preferably 0.5 μm or less. θ/−jμm 1, preferably θ, OS~3 μm. What is the amount of talcum powder added to the total weight of carbon black and graphite? =2! ~Rij:! Ashi, lO: riO~ri0
:10 is more preferable, and 3θ near 0 to 70:30 is even more preferable. If the Merck flour content is too high, the antistatic effect will be reduced, and if it is too low, the running durability improving effect will be reduced.
本発明に使用される非磁性支持体としては、ポリエチレ
ンテレフタレート、ポリアミド、ポリエチレンナフタレ
ート、ポリイミド、トリアセチルセルロース等がある。Examples of the nonmagnetic support used in the present invention include polyethylene terephthalate, polyamide, polyethylene naphthalate, polyimide, triacetyl cellulose, and the like.
支持体のパック層側の表面性は、その中心線平均粗さく
RaHカットオフo、ormm)を0゜0.3jtμm
以下とすることにより、パック層表面凹凸の磁性面への
転写による電磁変換特性の劣化を減少させることができ
る。また、磁性層面側のRa も同様に0.033μm
以下とすることにより、磁性層表面がより平滑となり、
電磁変換特性、たとえばビデオS/N、カラーS/Nを
向上させることができる。The surface property of the pack layer side of the support is determined by the center line average roughness (RaH cutoff o, ormm) of 0°0.3jt μm.
By doing the following, it is possible to reduce the deterioration of electromagnetic conversion characteristics due to the transfer of the unevenness on the surface of the pack layer to the magnetic surface. Also, the Ra on the magnetic layer surface side is also 0.033 μm.
By doing the following, the surface of the magnetic layer becomes smoother,
Electromagnetic conversion characteristics such as video S/N and color S/N can be improved.
本発明に使用される硬化剤としてはポリイソシアネート
、ポリアミド、エポキシ樹脂、ポリアミン、メラミン樹
脂、フェノール樹脂、シリコーン樹脂、その他の熱硬化
性樹脂や湿気硬化型樹脂であり、磁気テープ一般に使用
されるものが用いられる。硬化剤の添加量はバインダー
総重量io。The curing agents used in the present invention include polyisocyanates, polyamides, epoxy resins, polyamines, melamine resins, phenolic resins, silicone resins, and other thermosetting resins and moisture-curing resins, which are commonly used in magnetic tapes. is used. The amount of curing agent added is based on the total binder weight io.
部に対して、10−♂O重量部が好ましく、20〜夕O
重量部がより好ましい。% by weight, preferably 10-♂O parts by weight, and 20-♂O parts by weight.
Parts by weight are more preferred.
硬化剤は本発明の効果をうるために細かな三次元網目構
造をとることが必要で、その為には分子量は2000未
満が好ましく、/ 000未満がより好ましい。また、
硬化剤は多官能基のもので、1分子中の官能基数は3以
上のものが好ましく、この場合本発明の効果が有効に得
られる。It is necessary for the curing agent to have a fine three-dimensional network structure in order to obtain the effects of the present invention, and for this purpose, the molecular weight is preferably less than 2,000, more preferably less than /000. Also,
The curing agent is polyfunctional, and the number of functional groups in one molecule is preferably three or more, in which case the effects of the present invention can be effectively obtained.
これら個々の技術を同時に組合せ使用することにより、
走行耐久性および電磁変換特性に関し、予想外の顕著な
効果を得ることができる。By combining these individual technologies at the same time,
Unexpected and significant effects can be obtained regarding running durability and electromagnetic conversion characteristics.
バック層の他の添加剤として、ケイ酸マグネシウム、炭
酸カルシウム、ケイ酸アルミニウム、硫酸バリウム、ク
レーなどの無機体質顔料、ベンゾグアナミン樹脂等の有
機粒子、後述の磁性層中に使用される研磨剤、界面活性
剤、潤滑剤等が必要に応じ使用される。Other additives in the back layer include inorganic extender pigments such as magnesium silicate, calcium carbonate, aluminum silicate, barium sulfate, and clay, organic particles such as benzoguanamine resin, abrasives used in the magnetic layer described below, and interfaces. An activator, lubricant, etc. are used as necessary.
本発明に使用される強磁性粉末、磁性塗料の製法、磁性
層およびバック層に使用されるバインダー、磁性層に使
用される添加剤(たとえば分散剤、潤滑剤、研磨剤、帯
電防止剤など)、磁気記録媒体の製法などに関しては特
公昭j[−,2t190号に記載されている。Ferromagnetic powder used in the present invention, method for producing magnetic paint, binder used in the magnetic layer and back layer, additives used in the magnetic layer (e.g. dispersant, lubricant, abrasive, antistatic agent, etc.) , the manufacturing method of magnetic recording media, etc. are described in Japanese Patent Publication No. Shoj [-, 2t190.
以下に実施例により本発明をさらに具体的に説明する。The present invention will be explained in more detail below with reference to Examples.
実施例中、「部」は[重量部1を示す。In the examples, "parts" indicate parts by weight.
実施例 1゜
磁性層組成
Co添加酸化鉄(Hc6400e )300部塩酢ビ共
重合体 30部(ビニルアルコール
10%含有)
ポリウレタン樹脂 20部ポリイソシ
アネート 20%Cr203j部
オレイン酸 7部エチルス
テアレート 7部メチルエチルケトン
too部トルエン
300部バック層組成
グラファイト 30部部(ウロコ
状、平均−次粒子サイズlμ)タルク粉(平均−次粒子
サイズ3μ)300部ニトロセルロース
110部硬化剤(ポリイソシアネート)す0部
ニトリルブタジェンゴム ≠θ部メチルエチ
ルケトン +2よ00部サンドミルを用いて磁
性層組成を調液し、ボールミルを用いてバック層を調液
し、ljμ厚のポリエステル支持体に各々!μ厚、/、
2μ厚に塗布し、磁気テープ(サンプル扁/)を調製し
た。Example 1 Magnetic layer composition Co-added iron oxide (Hc6400e) 300 parts Salt-vinyl acetate copolymer 30 parts (containing 10% vinyl alcohol) Polyurethane resin 20 parts Polyisocyanate 20% Cr203j parts Oleic acid 7 parts Ethyl stearate 7 parts Methyl ethyl ketone too much toluene
300 parts Back layer composition Graphite 30 parts (scaly, average particle size 1 μ) Talc powder (average particle size 3 μ) 300 parts Nitrocellulose
110 parts Curing agent (polyisocyanate) 0 parts Nitrile butadiene rubber ≠ θ parts Methyl ethyl ketone + 2 to 00 parts Prepare the composition of the magnetic layer using a sand mill, prepare the back layer using a ball mill, and prepare polyester with a thickness of ljμ. Each on a support! μ thickness, /,
A magnetic tape (sample plate/) was prepared by coating the sample to a thickness of 2 μm.
但しポリエステル支持体はその両面の几aが0゜030
μのものを用いた。However, the polyester support has a diameter of 0°030 on both sides.
μ was used.
実施例 2゜
サンプル煮/に於て、A1表に示す几aを有する支持体
に変更したサンプル(A、2.A3 )を調製した。Example 2 Samples (A, 2.A3) were prepared in which the support was changed to a support having a temperature a shown in Table A1.
実施例 3゜
実施例/において、バック層のカーボンブラックのサイ
ズを第1表のように変更したサンプル(A弘)を調製し
た。Example 3 Samples (Ahiro) were prepared in Example 3, except that the size of the carbon black in the back layer was changed as shown in Table 1.
実施例 4゜
実施例/におりて、バック層の硬化剤を除去したサンプ
ル(Aりを調製した。但し、硬化剤重量部ツバインf−
はニトロセルロースとニトリルブタジェンゴムに振りわ
け、バインダードータぶ重量を一定とした。Example 4 A sample (A) was prepared in which the curing agent in the back layer was removed in Example 4. However, the weight part of the curing agent was
was divided into nitrocellulose and nitrile butadiene rubber, and the weight of the binder dough was kept constant.
比較例 l。Comparative example l.
実施例1においてバック層組成中のタルク粉を除去し、
その重量部をカーボンブラックとグラファイトに振9わ
け、トータル粉末重量を一定としたサンプル(AJ)を
調製した。In Example 1, the talc powder in the back layer composition was removed,
The weight part was divided into 9 parts between carbon black and graphite to prepare a sample (AJ) with a constant total powder weight.
サンプルA/〜Alについての試験結果を第1表に示す
。The test results for samples A/~Al are shown in Table 1.
以下に評価法の概略を示す。An outline of the evaluation method is shown below.
磁気テープはV l(8方式ビデオカセットに組込み、
VH8方式ビデオテープレコーダーにて評価した。The magnetic tape is Vl (incorporated into an 8 format video cassette,
Evaluation was performed using a VH8 video tape recorder.
走行耐久性は磁気テープを繰シ返し走行させ、目視計測
にて深い傷がパック層表面に認められる回数で示した。The running durability was determined by running the magnetic tape repeatedly and measuring the number of times deep scratches were observed on the surface of the pack layer by visual measurement.
チェックは70回毎に行なった。Checks were performed every 70 times.
ビデオS/Nは標準テープと比較して表わした。Video S/N is expressed in comparison to standard tape.
信号記録後、≠r時間≠00CtO%RH下に保存して
、再生した時のビデオS/Nを第1表に示した。Table 1 shows the video S/N when the signal was recorded, stored under ≠r time≠00CtO%RH, and played back.
本発明によるサンプルAIは比較例サンプル屋乙にくら
べ、走行耐久性およびビデオS/Nがともにすぐれてい
る。Sample AI according to the present invention has superior running durability and video S/N compared to comparative sample AI.
硬化剤をバック層に有する場合、走行耐久性が顕著に改
良される。When the back layer contains a curing agent, running durability is significantly improved.
支持体のRaは0.03jμn1以下の場合、ビデオS
/Nを良化させるが、これは磁性層表面平滑化効果と、
バック層表面平滑化によるバック層表面凹凸の磁性層表
面への転写抑制効果の両方を有するためである。If the Ra of the support is 0.03jμn1 or less, video S
/N is improved, but this is due to the smoothing effect on the surface of the magnetic layer and
This is because it has the effect of suppressing the transfer of irregularities on the surface of the back layer to the surface of the magnetic layer by smoothing the surface of the back layer.
サンプル扁!の0.03μmのカーボンブラックを使用
した場合は、0,02μmのそれにくらべ走行耐久性が
やや劣る。Sample flat! When carbon black of 0.03 μm is used, the running durability is slightly inferior to that of 0.02 μm.
Claims (1)
層を設けた磁気記録媒体において、該バック層が イ)
カーボンブラック、口)グラファイト、および ハ)メ
ルク粉を含有することを特徴とする磁気記録媒体。 2)非磁性支持体表面の中心線平均粗さくRa)が0.
036μm以下であることを特徴とする特許請求の範囲
第1)項に記載された磁気記録媒体。 3)カーボンブラックの平均−次粒子サイズが0.01
〜05/!μmであることを特徴とする特許請求の範囲
第1)項および第2)項に記載された磁気記録媒体。 4)バック層に硬化剤を含有することを特徴とする特許
請求の範囲第1)項、第2)項および第3)項に記載式
れた磁気記録媒体。[Scope of Claims] l) A magnetic recording medium in which a magnetic layer is provided on a non-magnetic support and a back layer is provided on the other surface, wherein the back layer is a)
A magnetic recording medium characterized by containing carbon black, a) graphite, and c) Merck powder. 2) The centerline average roughness (Ra) of the surface of the nonmagnetic support is 0.
The magnetic recording medium according to claim 1, wherein the magnetic recording medium has a diameter of 0.036 μm or less. 3) The average particle size of carbon black is 0.01
~05/! The magnetic recording medium according to claims 1) and 2), characterized in that the magnetic recording medium is μm. 4) A magnetic recording medium according to claims 1), 2) and 3), characterized in that the back layer contains a curing agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58074548A JPS59201219A (en) | 1983-04-27 | 1983-04-27 | Magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58074548A JPS59201219A (en) | 1983-04-27 | 1983-04-27 | Magnetic recording medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS59201219A true JPS59201219A (en) | 1984-11-14 |
Family
ID=13550413
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58074548A Pending JPS59201219A (en) | 1983-04-27 | 1983-04-27 | Magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59201219A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63306522A (en) * | 1987-06-08 | 1988-12-14 | Toshiba Corp | Magnetic recording medium |
| JP2021047956A (en) * | 2019-09-19 | 2021-03-25 | 富士フイルム株式会社 | Magnetic recording medium and magnetic recording / playback device |
-
1983
- 1983-04-27 JP JP58074548A patent/JPS59201219A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63306522A (en) * | 1987-06-08 | 1988-12-14 | Toshiba Corp | Magnetic recording medium |
| JP2021047956A (en) * | 2019-09-19 | 2021-03-25 | 富士フイルム株式会社 | Magnetic recording medium and magnetic recording / playback device |
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