JPS5975432A - Magnetic recording body - Google Patents

Magnetic recording body

Info

Publication number
JPS5975432A
JPS5975432A JP18541782A JP18541782A JPS5975432A JP S5975432 A JPS5975432 A JP S5975432A JP 18541782 A JP18541782 A JP 18541782A JP 18541782 A JP18541782 A JP 18541782A JP S5975432 A JPS5975432 A JP S5975432A
Authority
JP
Japan
Prior art keywords
carbon black
magnetic
durability
particle size
sample
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.)
Granted
Application number
JP18541782A
Other languages
Japanese (ja)
Other versions
JPH0479059B2 (en
Inventor
Nobutaka Yamaguchi
信隆 山口
Eiichi Tadokoro
田所 栄一
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Holdings Corp
Original Assignee
Fuji Photo Film Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd
Priority to JP18541782A priority Critical patent/JPS5975432A/en
Publication of JPS5975432A publication Critical patent/JPS5975432A/en
Publication of JPH0479059B2 publication Critical patent/JPH0479059B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • G11B5/68Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent
    • G11B5/70Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer
    • G11B5/708Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by addition of non-magnetic particles to the layer

Abstract

PURPOSE:To obtain a magnetic recording body having excellent electromagnetic conversion characteristics and durability and an improved color S/N ratio, etc. by incorporating carbon black having an average primary particle size and pH respectively of specific values, a polishing agent having hardness of a specific value or above and a hardner in a magnetic layer. CONSTITUTION:A magnetic layer contg. carbon black having <30mmu average primary particle size and <6pH (for example, ''Ma-8'' produced by Mitsubishi Chemical Industries Ltd.), a thermosetting resin, etc. such as polyisocyanate, epoxy resin or the like as a hardener, and a polishing agent having >6 Morse hardness and 0.1-1.5mu particle size is provided on a substrate of polyethylene terephthalate or the like. A magnetic tape having excellent color S/N, running durability for 100hr, a good antistatic property, and excellent surface smoothness and durability is thus obtd.

Description

【発明の詳細な説明】 本発明は磁気記録体に関し、その主たる目的は電磁変換
特性及び耐久性の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium, and its main purpose is to improve electromagnetic conversion characteristics and durability.

従来、磁気記録体の磁性J@は、帯電防止を主たる目的
として、カーボンブラックに1有t、ている。
Conventionally, the magnetic properties of magnetic recording bodies are mainly contained in carbon black for the purpose of preventing static electricity.

しかしながら、カーボンブラックの添加は磁性層の塗膜
表面の平滑性を悪化させる為、qをに高密度記録を必要
とするビデオテープに於ては、電S変換特性を顕著に劣
化せしめるので、その改S、が待ち望まれてい罠。し刀
1しながら、表面平滑性會増した場合、耐久性が劣化す
るため、その両方の特性1に満足することが不可欠であ
るが、従来技術(例えば、持分57−1..220に号
、行公jコー1rs6i号、%公5J−33,zaY号
)T:n不満足な状態であつfco 本発明の目的は磁気記録体の電磁変換特性及び耐久性、
よυ具体的にけカラーF3 / 、N 、  / 00
時間短行耐久性の改良された磁気記録体全提供するにあ
る。
However, the addition of carbon black deteriorates the smoothness of the coating film surface of the magnetic layer, so in video tapes that require high-density recording, the addition of carbon black significantly deteriorates the electrical-to-solar conversion characteristics. Revised S is a long-awaited trap. However, if the surface smoothness increases, the durability will deteriorate, so it is essential to satisfy both characteristics 1. , Gyoko J CO 1RS6I, %Ko 5J-33, ZAY) T:n unsatisfactory condition and fco
Please be specific Color F3 / , N , / 00
The aim is to provide an improved magnetic recording medium with reduced time and durability.

本発明の上記の目的は、非磁性支持体上にS性膚を設け
てなる磁気記録体でちって、該磁性層が、旬平均−次粒
子すイズJOmμ以−ト% pHx未満のカーボンブラ
ック、 コ)モース硬度ル以上の研磨剤、及び 3)硬化剤 を含む磁気記録体によって達成できることを見い出した
The above-mentioned object of the present invention is to provide a magnetic recording material comprising an S layer on a non-magnetic support, in which the magnetic layer is made of carbon black having an average particle diameter of JOmμ or more and a pH of less than %. It has been found that this can be achieved by a magnetic recording material containing a) an abrasive having a Mohs hardness of 1 or higher, and 3) a hardening agent.

本発明に使用されるカーホンブラックF、に平均−次粒
子サイズがJamμ以下でpHが6未満のカーボンブラ
ックであればよい。粒子“νイズは好甘しくはコ!mμ
以下、よシ好ましくはコomμ以下、更に好ましくばi
smμ以下である。pHは好ましくijj未満、よシ好
ましくはμ未満、更に好ましくけ3未満である。磁性体
ioo重量部に対する添加量としては/−,20部景部
が好ましく、よシ好ましくは3〜is重角部である。添
加量が少ないと帯電防止効果が減少し、又反対に多いと
、磁性体の磁性層中の充填度が低下し、かつ塗膜表面性
が劣化する。
The carbon black F used in the present invention may be any carbon black having an average particle size of Jamμ or less and a pH of less than 6. Particle ``ν is sweetly ko!mμ
The following is preferably less than 0mμ, more preferably i
smμ or less. The pH is preferably less than ijj, more preferably less than μ, more preferably less than 3. The amount added to ioo parts by weight of the magnetic material is preferably /-, 20 parts by weight, and more preferably 3 to 10 parts by weight. If the amount added is small, the antistatic effect will be reduced, and if the amount added is too large, the degree of filling of the magnetic material in the magnetic layer will be reduced and the surface properties of the coating film will be deteriorated.

本発明に使用されるカーボンブラックの具体例としては
、(:abot製” BlackpearI  / J
 00″コロンビヤンカーボンF!”li、aven 
jλjO”三菱化成工業製”MA−J”等がある。
Specific examples of the carbon black used in the present invention include ("Blackpear I/J" manufactured by Abot).
00″Columbian Carbon F!”li, aven
There are "MA-J" manufactured by Mitsubishi Chemical Industries, Ltd.

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1.磁気テープ一般に使
用されるものが用いられる。硬化ハリの添加量は)(イ
ンダー総重量100部に対して、io、io部が好まし
く1.20 、30部がよシ好ましい。
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.1. A commonly used magnetic tape is used. The amount of hardening firmness added is preferably 1.20 to 30 parts, and preferably 1.20 to 30 parts, based on 100 parts of the total weight of the inder.

硬化剤は本発明の効果をつ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、1000未満がよシ好ましい。捷た、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。中でも低分子量多官能性ポリイソシアネートが特
に推奨される。
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, and more preferably less than 1,000. The curing agent used is a polyfunctional one, 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. Among them, low molecular weight polyfunctional polyisocyanates are particularly recommended.

本発明に使用される研磨剤はモース硬夙が6以上である
ことが不可欠で、を以上のものが好ましい。またその粒
子ザイズはO07〜/、jμが好ましく、Oo、2〜l
μがより好ましい。添加量に01S−10重量部が好ま
しく、より好ましくはi、io重量部、より一層好ブし
く 1−13〜j重量部である。研磨剤としては、例え
ば酸化マグネシウム(モーy、硬度6)、Cr2O3(
モース硬度r〜り)、α−A120a  (モース硬u
t rン、5iC(モース硬yly、s)等がある、こ
れらを混合使用しても良い〇 磁性体けr−Fe203.FeOx (t 、J J<
X<i、s)、Cr 02、CO象加1−Fe2O3、
CO添加FeOx (i 、 3 j(x(/ 、 s
 )、平板状Baフェライト、Fe−Co−Ni合金粉
末、Fe−20合金粉末等の通常磁気記録体に使用出来
る強磁性粉末が本発明に於ても何等異なることなく使用
出来る。
It is essential that the abrasive used in the present invention has a Moh's hardness of 6 or more, preferably 6 or more. Further, the particle size is preferably O07~/, jμ, Oo, 2~l
μ is more preferred. The amount added is preferably 01S-10 parts by weight, more preferably i and io parts by weight, and even more preferably 1-13 to j parts by weight. Examples of abrasives include magnesium oxide (hardness: 6), Cr2O3 (
Mohs hardness r~ri), α-A120a (Mohs hardness u
trn, 5iC (Mohs hardness, s), etc., these may be used in combination 〇Magnetic material r-Fe203. FeOx (t, J J<
X < i, s), Cr 02, CO inlaid 1-Fe2O3,
CO-added FeOx (i, 3 j(x(/ , s
), tabular Ba ferrite, Fe-Co-Ni alloy powder, Fe-20 alloy powder, and other ferromagnetic powders that can be used for normal magnetic recording materials can be used in the present invention without any difference.

酸化鉄系磁性体の形状については粒状、針状、紡錘状、
平板状等のどれであってもよく、必要により混合使用し
ても支障ない。
The shape of iron oxide magnetic material is granular, needle-like, spindle-like,
They may be in any shape, such as a flat plate, and may be used in combination if necessary.

硬化剤以外のバインダーについては、例えはポリ塩酢ビ
、セルロース誘導体、ポリウレタン、ニトリル−ブタジ
ェンゴム、スチレン−ブタジェンゴム、ポリエステル、
アクリル樹脂、塩化ビニリデン系樹脂等が使用出来るが
、これらのみに限定されるべきではなく、磁気記録体用
として通常用いられているものが本発明に於ても用いら
れる。
Examples of binders other than hardening agents include polyvinyl acetate, cellulose derivatives, polyurethane, nitrile-butadiene rubber, styrene-butadiene rubber, polyester,
Acrylic resins, vinylidene chloride resins, etc. can be used, but they are not limited to these, and those commonly used for magnetic recording media can be used in the present invention.

磁性層中に飽加される潤滑剤としては、脂肪酸エステル
、ソルビタン脂肪酸エステルの如きエステル%名種脂肪
酸、各種シリコンオイル、各種フッ素系オイル、流動パ
ラフィン、スクワラン、その他通常磁気記録体に使用出
来るものが用いられる。
Examples of lubricants that can be saturated in the magnetic layer include fatty acid esters, ester% fatty acids such as sorbitan fatty acid esters, various silicone oils, various fluorine-based oils, liquid paraffin, squalane, and other materials that can be normally used in magnetic recording media. is used.

磁性層中に心機に応じて安定剤、無機フィラー、可塑剤
等を加えても支障ない。
There is no problem in adding stabilizers, inorganic fillers, plasticizers, etc. to the magnetic layer depending on the core material.

支持体に関してはポリエチレンテレフタレート、ポリエ
チレンナフタレート、ポリアミド、ポリイミド、塩ビ系
フィルム等が用いられ、これらにノくツクコートを施し
1こフイルノ・でも支障なく使用出来る。支持体の表面
性は高密度小形ビデオテープ用としては、カラー87N
’cよくするため乎清なものが好ましい°。特に中心線
平均粗さく几a)が0.03jlt以f”(Cu”  
off  0.01mm)のものが好ましく、0.02
μ以下のものはよシ好ましい0また、支持体の両面の平
滑性の異なるものを必要に応じて用いてもよい。支持体
の片面(反磁性面)にFJ滑剤または界面活性剤を塗布
したものを用いズ、磁性層を塗設してもよい。磁性層塗
設後またはカレンダー処理等の表面成形処理後、反磁性
面(Nilの支持体表面に旧渭剤または界面活性剤を塗
布してもよい。
As for the support, polyethylene terephthalate, polyethylene naphthalate, polyamide, polyimide, vinyl chloride film, etc. are used, and if these are coated with a coating, they can be used without any problem even in a single film. The surface quality of the support is Color 87N for high-density small video tapes.
'c It is preferable to have something clean to make it look better. Especially when the center line average roughness (a) is 0.03 jlt or more f” (Cu”
Off 0.01 mm) is preferable, and 0.02
It is preferable to use a support having a thickness of less than 0. If necessary, supports having different smoothness on both sides may be used. The magnetic layer may be coated on one side (diamagnetic side) of the support using a FJ lubricant or surfactant coated. After coating the magnetic layer or after surface forming treatment such as calendering, an anti-polyming agent or a surfactant may be applied to the diamagnetic surface (Nil) of the support.

本発明に使用でさる組成及び製法は特公昭j6−コ≦r
り0号に記載されている。
The composition and manufacturing method used in the present invention are as follows:
It is described in No. 0.

以下に実施例を示し、本発明を更に具体的に説明する。EXAMPLES The present invention will be explained in more detail with reference to Examples below.

実施例中「部」は「重量部」を示す。In the examples, "parts" indicate "parts by weight."

実施例 / Co添加γ−pe2o3        / 00部カ
ーボンブラック(サイズ/f”mμ、pHJ)    
  l’部 α−A120g  (モース硬度Y)      1部
硬化剤 ポリイソシアネート、バイエル鯛1デスモジュ
ールL−7,、t”6部 塩酢ビ樹脂              is部塩化ビ
ニリデン/アクリロニトリル P重合体            4’、  j部オレ
イン酸メレイル        o、s部溶剤(シクロ
へキサノン/メチ ルエチルケトン=i7i)       適量上記組成
でボールミル分散により磁性液管潤製後、7μ厚のカー
ボンブラックとバインダーよシ成るバックコート層を施
し友ljμ厚のポリエチレンテレフタレートフィルム(
RR=θ、θj lt )上にドクター法にて塗布した
Example / Co-added γ-pe2o3 / 00 parts carbon black (size/f”mμ, pHJ)
1 part α-A 120 g (Mohs hardness Y) 1 part Curing agent Polyisocyanate, Bayer Tai 1 Desmodur L-7, t" 6 parts Salt vinyl acetate resin IS part Vinylidene chloride/acrylonitrile P polymer 4', J part Meleyl oleate o, s part Solvent (cyclohexanone/methyl ethyl ketone = i7i) Appropriate amount After preparing a magnetic liquid tube with the above composition by ball mill dispersion, a back coat layer consisting of carbon black and binder with a thickness of 7 μm was applied, and a layer with a thickness of 7 μm was applied. Polyethylene terephthalate film (
RR=θ, θj lt ) by a doctor method.

しかる後、カレンダー処理を施し、l/、2吋幅に裁断
し、VH8用小型ビデオテープ(サンプルA/)を得た
。また、α−A120gをMgO(モース硬度6)に代
えて同様の操作によりビデオテープ(サンプルA、2)
を得た。
Thereafter, it was calendered and cut into 1/2 inch wide pieces to obtain a small VH8 videotape (sample A/). In addition, by replacing 120 g of α-A with MgO (Mohs hardness 6), a videotape (sample A, 2) was prepared by the same operation.
I got it.

比較例 l 実施例1に於てカーボンブラックの平均−次粒子サイズ
’l<j Omμに代える以外は実施例1のサンプルA
Iと同様にしてサンプルA J f:得1こ。
Comparative Example l Sample A of Example 1 except that the average particle size of carbon black in Example 1 was replaced with 'l<j Omμ.
Sample A J f: obtained 1 piece in the same manner as I.

比較例 λ 実施例1に於てカーボンブラックに代えてrlH70カ
ーボンブラックを使用゛f′る以外同様にし−℃ザンプ
ル屋弘、を得た。
Comparative Example λ A -℃ sample was obtained in the same manner as in Example 1 except that rlH70 carbon black was used instead of carbon black.

比較flI3 実施例1のサンプルA/に於てα〜Al2O5に代えて
粒状α−Fe203  (モース硬度!#)金柑いる以
外同様にしてサンプルAjf得た。
Comparison flI3 Sample Ajf was obtained in the same manner as in Sample A/ of Example 1 except that granular α-Fe203 (Mohs hardness! #) kumquat was used instead of α-Al2O5.

比較例 グ 実施例1のサンプルA/に於て硬化剤を除く以外実施例
1のサンプルA/と同様にしてサンプル煮6を得た。
Comparative Example Sample 6 was obtained in the same manner as Sample A/ of Example 1 except that the curing agent was omitted from Sample A/ of Example 1.

実施例 一 実施例1のサンプルA/に於て支持体表面性をna=0
.0μμのものに変えたサンプル扁7を得た。
Example In Sample A/ of Example 1, the surface properties of the support were na=0
.. A sample plate 7 was obtained which was changed to a 0 μμ sample plate.

この様にして得られたサンプルA/=A、7の評価結果
全第1表に示す。なお、第1表に示すデータの測定法は
次の通りである。カラーS/N%700時間走行耐久性
、ドロップアウトの副定に用いたVTRはVH8方式V
TRであシ、當温にて実施した。カラーS/Nは相対値
で示した。
The evaluation results for sample A/=A, 7 obtained in this way are all shown in Table 1. The method for measuring the data shown in Table 1 is as follows. The VTR used for color S/N% 700 hour running durability and dropout determination was VH8 system V.
The test was carried out at TR and Toon. Color S/N is expressed as a relative value.

また、ioo時間走行耐久性はVTRにテープ2ioo
時間走行させた後のテープ磁性面のスリキズ本数’i/
/、2吋テープ幅につき目視計測した。
In addition, the running durability of the tape is 2ioo on the VTR.
Number of scratches on the tape magnetic surface after running for a time 'i/
/, 2 inch tape width was visually measured.

なお、カラーS/Nは主として磁性層の比較的長波長領
域の表面平滑性に、ioo時間走行耐久性は磁性層塗膜
耐久性に対応すると考えられるものであシ前者は大なる
程、後者は少ない程優れている。一方、ドロップアウト
は主として帯電性と関係があシカ−ボンプラックによる
W電防上効果が大なる損少なく、少ない程優れている。
Note that the color S/N is thought to correspond mainly to the surface smoothness of the magnetic layer in a relatively long wavelength region, and the IOO time running durability corresponds to the durability of the magnetic layer coating. The less the better. On the other hand, dropout is mainly related to chargeability, and the effect on W electric protection due to carbon black is less loss, and the smaller the dropout, the better.

、また磁性層Jl?強度が弱くともドロップアウトは多
くなる。
, and the magnetic layer Jl? Even if the strength is low, there will be more dropouts.

第1表から明炉な如く、サンプルA/(本発明)は比較
サンプルAJ(サイズjomμのカーボンブラックを使
用)、A4’ (pH7のカーボンブラック使用)にく
らべてカラーS/N、ドロップアウトの点で優れている
。、またioo時間走行耐久性、カラーS/N、  ド
ロップアウトの点で硬化剤を使用しない比較サンプルA
6よシ大幅に良好な特性を示している。サンプルAj 
、A、2はモース硬度りの研磨剤α−A7203の代υ
に粒状α−Fe203(モース硬度r、r)、Mg0(
モース硬に6)音用いたサンプルである。A/にくらべ
比較例サンプルA!は/ 00Ff#間の走行耐久性が
極端に劣化し、”i 7cカラーS/N、Drop  
outも劣化しておυ、研磨剤のモース硬度は6以上で
ある事が不可欠である。実施例サンプルA7は支持体表
面性の劣るものを使用した場合であり、サンプルA/の
方がカラー8/Nが優れていることが判る。
As shown in Table 1, sample A/(invention) has better color S/N and dropout than comparative samples AJ (using carbon black of size jomμ) and A4' (using carbon black of pH 7). Excellent in that respect. , Comparative sample A that does not use a hardening agent in terms of ioo hour running durability, color S/N, and dropout.
6 shows significantly better characteristics. Sample Aj
, A, 2 is the Mohs hardness abrasive α-A7203 υ
granular α-Fe203 (Mohs hardness r, r), Mg0 (
This is a sample using 6) sound for Mohs hardness. Comparative example sample A compared to A/! The running durability between /00Ff# has deteriorated extremely, and the "i7c color S/N, Drop
It is essential that the Mohs hardness of the abrasive is 6 or higher to avoid deterioration of the abrasive. Example Sample A7 is a case where a support with poor surface properties was used, and it can be seen that Sample A/ has better color 8/N.

以上まとめると、+l+  平均−次粒子サイズが30
 mμ以下でpHが6未満のカーボンブラック、(2)
モース硬度6以上の研磨剤、及び(3)P化剤と組合せ
たときのみ良好な雷、ftX変換特性及び耐久性を持つ
磁気記録体を得ることが出来る。
To summarize the above, +l+ average -order particle size is 30
Carbon black having a pH of less than mμ and less than 6, (2)
Only when combined with an abrasive having a Mohs hardness of 6 or more and (3) a phosphorizing agent can a magnetic recording medium with good lightning and ftX conversion characteristics and durability be obtained.

Claims (1)

【特許請求の範囲】 非磁性支持体上に磁性層を設けて成る磁気記録体に於て
、該磁性層が l)平均−次粒子すイズ30mμ以下p H6未満のカ
ーボンブラック、 −)モース硬度6以上の研磨剤、及び 3)硬化剤 を含むことを特徴とする磁気記録体。
[Claims] A magnetic recording body comprising a magnetic layer provided on a non-magnetic support, wherein the magnetic layer is l) carbon black with an average particle size of 30 mμ or less and a pH of less than 6; -) Mohs hardness 1. A magnetic recording material comprising: 6 or more abrasives; and 3) a hardening agent.
JP18541782A 1982-10-22 1982-10-22 Magnetic recording body Granted JPS5975432A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18541782A JPS5975432A (en) 1982-10-22 1982-10-22 Magnetic recording body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18541782A JPS5975432A (en) 1982-10-22 1982-10-22 Magnetic recording body

Publications (2)

Publication Number Publication Date
JPS5975432A true JPS5975432A (en) 1984-04-28
JPH0479059B2 JPH0479059B2 (en) 1992-12-14

Family

ID=16170417

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18541782A Granted JPS5975432A (en) 1982-10-22 1982-10-22 Magnetic recording body

Country Status (1)

Country Link
JP (1) JPS5975432A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62239320A (en) * 1986-04-09 1987-10-20 Konika Corp Magnetic recording medium
JPS63241720A (en) * 1987-03-30 1988-10-07 Fuji Photo Film Co Ltd Magnetic recording medium

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50147308A (en) * 1974-05-15 1975-11-26
JPS5238201A (en) * 1975-09-20 1977-03-24 Hitachi Maxell Ltd Magnetic recording body
JPS5415978A (en) * 1977-06-28 1979-02-06 Teijin Ltd Polyester film
JPS5434207A (en) * 1977-08-23 1979-03-13 Teijin Ltd Polyester film
JPS54124716A (en) * 1978-03-20 1979-09-27 Hitachi Maxell Magnetic disk cartridge
JPS5517816A (en) * 1978-07-19 1980-02-07 Hitachi Maxell Ltd Magnetic recording media
JPS5610455A (en) * 1979-07-09 1981-02-02 Toray Industries Polyester film
JPS5651025A (en) * 1979-10-02 1981-05-08 Hitachi Maxell Ltd Magnetic recording medium
JPS5651027A (en) * 1979-10-02 1981-05-08 Hitachi Maxell Ltd Magnetic recording medium
JPS5683842A (en) * 1979-12-13 1981-07-08 Toray Ind Inc Base film for magnetic recording
JPS56124123A (en) * 1980-03-01 1981-09-29 Hitachi Maxell Ltd Magnetic recording medium
JPS56143522A (en) * 1980-04-07 1981-11-09 Fuji Photo Film Co Ltd Magnetic recording medium
JPS5794928A (en) * 1980-12-03 1982-06-12 Matsushita Electric Ind Co Ltd Magnetic recording medium
JPS57130233A (en) * 1981-02-04 1982-08-12 Fuji Photo Film Co Ltd Magnetic recording medium
JPS57135436A (en) * 1981-02-14 1982-08-21 Sony Corp Magnetic recording medium
JPS57150130A (en) * 1981-03-12 1982-09-16 Fuji Photo Film Co Ltd Magnetic recording medium

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50147308A (en) * 1974-05-15 1975-11-26
JPS5238201A (en) * 1975-09-20 1977-03-24 Hitachi Maxell Ltd Magnetic recording body
JPS5415978A (en) * 1977-06-28 1979-02-06 Teijin Ltd Polyester film
JPS5434207A (en) * 1977-08-23 1979-03-13 Teijin Ltd Polyester film
JPS54124716A (en) * 1978-03-20 1979-09-27 Hitachi Maxell Magnetic disk cartridge
JPS5517816A (en) * 1978-07-19 1980-02-07 Hitachi Maxell Ltd Magnetic recording media
JPS5610455A (en) * 1979-07-09 1981-02-02 Toray Industries Polyester film
JPS5651025A (en) * 1979-10-02 1981-05-08 Hitachi Maxell Ltd Magnetic recording medium
JPS5651027A (en) * 1979-10-02 1981-05-08 Hitachi Maxell Ltd Magnetic recording medium
JPS5683842A (en) * 1979-12-13 1981-07-08 Toray Ind Inc Base film for magnetic recording
JPS56124123A (en) * 1980-03-01 1981-09-29 Hitachi Maxell Ltd Magnetic recording medium
JPS56143522A (en) * 1980-04-07 1981-11-09 Fuji Photo Film Co Ltd Magnetic recording medium
JPS5794928A (en) * 1980-12-03 1982-06-12 Matsushita Electric Ind Co Ltd Magnetic recording medium
JPS57130233A (en) * 1981-02-04 1982-08-12 Fuji Photo Film Co Ltd Magnetic recording medium
JPS57135436A (en) * 1981-02-14 1982-08-21 Sony Corp Magnetic recording medium
JPS57150130A (en) * 1981-03-12 1982-09-16 Fuji Photo Film Co Ltd Magnetic recording medium

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62239320A (en) * 1986-04-09 1987-10-20 Konika Corp Magnetic recording medium
JPS63241720A (en) * 1987-03-30 1988-10-07 Fuji Photo Film Co Ltd Magnetic recording medium

Also Published As

Publication number Publication date
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