JPS5956222A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS5956222A
JPS5956222A JP57166661A JP16666182A JPS5956222A JP S5956222 A JPS5956222 A JP S5956222A JP 57166661 A JP57166661 A JP 57166661A JP 16666182 A JP16666182 A JP 16666182A JP S5956222 A JPS5956222 A JP S5956222A
Authority
JP
Japan
Prior art keywords
running
orange peel
recording medium
magnetic recording
back 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
Application number
JP57166661A
Other languages
Japanese (ja)
Inventor
Yasuyuki Tanaka
庸之 田中
Takahito Miyoshi
孝仁 三好
Toshimitsu Okutsu
俊光 奥津
Masaaki Fujiyama
正昭 藤山
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 JP57166661A priority Critical patent/JPS5956222A/en
Publication of JPS5956222A publication Critical patent/JPS5956222A/en
Pending 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
    • G11B5/73Base 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
    • G11B5/735Base 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
    • G11B5/7356Base 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
    • G11B5/7358Base 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 specially adapted for achieving a specific property, e.g. average roughness [Ra]
    • 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
    • G11B5/73Base 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
    • G11B5/739Magnetic recording media substrates
    • G11B5/73923Organic polymer substrates
    • G11B5/73927Polyester substrates, e.g. polyethylene terephthalate

Landscapes

  • Paints Or Removers (AREA)
  • Magnetic Record Carriers (AREA)

Abstract

PURPOSE:To improve both of an electromagnetic conversion characteristic and running and sustained running characteristics, by forming the back layer provided on the rear of a substrate for a magnetic recording medium into an orange peel surface. CONSTITUTION:The back layer provided on the rear of a substrate for a magnetic recording medium is formed into an orange peel surface. The projecting parts (a) in the orange peel surface are coninuously formed in a nearly hexagonal shape. Such orange peel surface is formed with preferably 0.02-0.3mum the depth (d) of a trough part (c) and preferably 2-200mum pitch (p) between the projecting parts facing to each other. If the pitch (p) is <2mum, there is no effect and when it exceeds 100mum, the running and sustained running characteristic are further slightly improved but the deterioration in the electromagnetic conversion characteristic is accelerated. When the thickness T of the back layer (b) is increased, the deterioration in the electromagnetic conversion characteristic occuring in the the depth (d) in the trough part (c) of the orange peel surface and the roughening of the surface is accelerated. The thickness T of the back layer is required to be <=2mum, and the lower limit is required to be >=0.3mum in order to provide the orange peel surface.

Description

【発明の詳細な説明】 細には支持体裏面に設けたバック層を改良した磁気記録
媒体に関するものであイ)、1一般に磁気記録媒体は、
その′llJ,磁変16f!特性、例えば感度φ比等を
向」二するlrめに磁性層の表面を平滑化する必要があ
るがこの.1 =>な平滑比に伴ない磁気記録媒体の走
行特性及び走行耐久特性は悪化する。このため従来t,
1、ザンドブラスト、アルカリ溶液中のエツチング、又
は固体粒子の充填等によシバソク層の粗面化が行なわれ
ていた。しかしながらいずれの方法によっても、走行特
性および走行耐久特性を充分な程度にバック面を粗面化
すると、テープ巻込時又はディスク積重ね時にバック層
粗面が磁性面に転写してその平滑さが損なわれ、電磁変
換特性の劣化が避けられなかった。
[Detailed Description of the Invention] In particular, it relates to a magnetic recording medium with an improved back layer provided on the back surface of a support.1) In general, magnetic recording media include:
That'llJ, magnetic variation 16f! It is necessary to smooth the surface of the magnetic layer to improve the characteristics, such as the sensitivity φ ratio. As the smoothing ratio becomes 1 =>, the running characteristics and running durability of the magnetic recording medium deteriorate. For this reason, conventionally t,
1. The surface of the shibasoku layer has been roughened by sand blasting, etching in an alkaline solution, or filling with solid particles. However, with either method, if the back surface is roughened to a sufficient degree to improve running characteristics and running durability, the rough surface of the back layer will be transferred to the magnetic surface during tape winding or stacking of disks, impairing its smoothness. Therefore, deterioration of electromagnetic conversion characteristics was unavoidable.

他方、電磁変換特性を重視したバンク層の粗面化におい
ては、得られる走行特性および走行耐久性には限界があ
り、電磁変換特性と走行特性、走行耐久特性の双方に優
れた磁気記録媒体は得られなかった。
On the other hand, when roughening the bank layer with emphasis on electromagnetic conversion characteristics, there is a limit to the running characteristics and running durability that can be obtained. I couldn't get it.

そこで、本発明者等は上記のような欠点のない磁気記録
媒体を提供すべく研究を行なった結果、次のような知見
を得た。
The inventors of the present invention conducted research to provide a magnetic recording medium that does not have the above-mentioned drawbacks, and as a result, they obtained the following knowledge.

すなわち、磁気記録媒体において、電磁変換特性のみを
重視する場合磁性mjおよびバック層表面のいずれも平
滑であることが望ましいが、良好な走行特性、走行耐久
性を維持するにはバック層表面の粗面化が必要であり、
こ;ti−に伴ない磁性面も転写によるある程度の粗面
化を受ける。しかしこのバンク層表面がゆず肌状態を呈
している場合には、そのバンク層素地と同等の面性を有
し、かつゆず肌状態を呈していないノくツク層を有する
磁気記録媒体と比較して、磁性面・\の転写が抑制され
、電磁変換特性の劣化が軽減されると共に走行特性、走
行i1久性が良くなる傾向があることが認められた。
In other words, in a magnetic recording medium, if only the electromagnetic conversion characteristics are important, it is desirable that both the magnetic mj and the back layer surface be smooth, but in order to maintain good running characteristics and running durability, the back layer surface should be rough. It is necessary to face the
Along with this, the magnetic surface also undergoes some degree of roughening due to the transfer. However, when the surface of this bank layer exhibits an orange-skinned condition, it is compared with a magnetic recording medium that has a texture layer that has the same surface properties as the bank layer substrate but does not exhibit an orange-skinned condition. It was found that the transfer of the magnetic surface was suppressed, the deterioration of the electromagnetic conversion characteristics was reduced, and the running characteristics and running durability tended to be improved.

本明細岩て使用する「ゆず肌面」なる用語は、第1図お
よび第2図に示すように突部、1が略六角形状、すなわ
ちノ・ニカム状又は網1−1状に連続して形成された表
面状態を称する3、(二のゆず肌面は、谷部(の深さく
1が05μ771以1・(好士しくは002〜06μ7
71 ) 、互いに対向J゛る突i’%l−間のピッチ
pが2〜1000μm1好−1L < &:、l、2〜
20074771とし−C形成される。このゆず肌面の
突部Jlのピッチl〕が2μm未満であると、電磁変換
特性・走行特性および走行耐久性共にゆノー肌面状態を
呈していないものと同等になり、口したピンチが100
0μ771を越えると、走行特性及び走行耐久性はさら
に若干向上するが、電磁変換特性の劣化が顕著となる。
The term "Yuzu surface" as used in this specification refers to the protrusion 1 having a substantially hexagonal shape, i.e., a continuation of the shape of a no-nikum or a net 1-1, as shown in FIGS. 1 and 2. 3, which refers to the formed surface condition, (the second yuzu skin surface has a valley (depth 1 of 05 μ771 or more) (preferably 002 to 06 μ7
71), pitch p between mutually opposing protrusions i'%l- is 2 to 1000 μm1L<&:,l,2~
20074771 and -C is formed. When the pitch l] of the protrusions Jl on the Yuzu skin surface is less than 2 μm, the electromagnetic conversion characteristics, running characteristics, and running durability are equivalent to those not exhibiting the Yuzu skin surface condition, and the pinch of the mouth is 100 μm.
If it exceeds 0 μ771, the running characteristics and running durability will further improve slightly, but the electromagnetic conversion characteristics will deteriorate significantly.

バンク層すの厚さTを増していくと、ゆず肌面の谷部C
の深さdと素地の面荒れに起因する電磁変換特性の劣化
が顕在化し、バンク層の厚さTは2 it%下とする必
要がある。バック層の厚さ′1゛の下限は従来のバック
層の一般的下限にもはソ支配されるが、ゆず肌面化する
ためには、03μm以上必要である。なお本発明におけ
るゆず肌面は通常のいわゆる粗面とは異った規則的な表
面形状を有する。
As the thickness T of the bank layer increases, the valley C of the yuzu skin surface
Deterioration of the electromagnetic conversion characteristics due to the depth d and surface roughness of the substrate becomes obvious, and the thickness T of the bank layer needs to be 2 it% or less. The lower limit of the thickness of the back layer '1' is determined by the general lower limit of conventional back layers, but in order to obtain an orange skin surface, it is necessary to have a thickness of 03 μm or more. Note that the citron skin surface in the present invention has a regular surface shape different from a normal so-called rough surface.

谷部Cの深さく1は0.02μn1未満の場合、実際上
ゆず肌面としての有効性が十分用ない。
If the depth 1 of the troughs C is less than 0.02 μn1, the effectiveness of the surface of the citron skin will not be sufficiently utilized.

本発明は、」−記のような知見に基づきなされたもので
あり、非磁性支持体の一力の而に磁性層を崩し、他方の
面に厚さ2μm以千のバンク層を有する磁気記録媒体に
おいて、・・ツク層表面をゆず肌状としたことを特徴と
する。
The present invention has been made based on the knowledge as described in "-", and provides a magnetic recording medium in which a magnetic layer is broken by the force of a non-magnetic support, and a bank layer with a thickness of 2 μm or more is provided on the other surface. The medium is characterized in that the surface of the Tsuku layer is shaped like Yuzu skin.

本発明に係る磁気記録媒体のバ・ツク層は従来公知の結
合剤を用い、粗面化のための固体粉末(無機質粉末等)
から成り、導電性付与のだめの粉状物質(カーボンブラ
ック、グラノアイト粉末、金属粉末等)を加えてもよい
The back layer of the magnetic recording medium according to the present invention uses a conventionally known binder and solid powder (such as inorganic powder) for roughening the surface.
A powder substance (carbon black, granoite powder, metal powder, etc.) may be added to impart conductivity.

本発明に用いる結合剤として目5、従来当業界で知られ
た結合剤、たとえば熱可塑性樹脂、熱硬(ヒ性樹脂、反
応型樹脂或い11 i−れらの混合物が使用される。
As the binder used in the present invention, binders conventionally known in the art, such as thermoplastic resins, thermosetting resins, reactive resins, or mixtures thereof, are used.

熱可塑性樹脂としては、塩化ビニ/L・−酢酸ビニル共
重合体、塩化ビニル−3’;1漬化ビ=リデン共重合体
、塩化ビニルーアクリロニトリル体、アクリル酸エステ
ル−アクリI1.=トリル重合体、−アクリル酸エステ
ル−1晶化ビニリデン共電合体、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一つ′クリ1
1ニトリル共! 合体、メタクリル酸エスデ)シ□ −
 1u’を化ビニリチン共重合体、メタクリル酸:1−
スノールースチレン共重合体、ウレタンエラス11ー,
ポリ弗化ビニル、塩化ビニリデン−アクリにトリル共重
合体、ブタジェン−アクリIに1リル共共電体、ポリア
ミド樹脂、ポリビニノ1、ノ゛f−ラール、繊Mf. 
素糸樹脂(セルロースアセ−7− −− 1・、、+ 
f−レート、セルロースダイアセテ−1・、 l=. 
tL1+ −  X)“ロピオネート、ニトロセルロー
ス等)、スチレン−ブタジェン共重合体、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、各種ゴム系樹脂などである。
Examples of the thermoplastic resin include vinyl chloride/L.-vinyl acetate copolymer, vinyl chloride-3'; monochlorinated bi-lydene copolymer, vinyl chloride-acrylonitrile, and acrylic ester-acrylic I1. =Tolyl polymer, -acrylic ester-1 crystallized vinylidene coelectrolyte, acrylic ester-
Styrene copolymer, methacrylic acid ester 1'Cry1
1 nitrile! Coalescence, methacrylic acid ester) C□ −
Vinyritine copolymer, methacrylic acid: 1-
Snow loose styrene copolymer, urethane elas 11-,
Polyvinyl fluoride, vinylidene chloride-acrylic to tolyl copolymer, butadiene-acrylic I to monolyl coelectric, polyamide resin, polyvinino 1, Noral, fiber Mf.
Thread resin (cellulose ace-7- -- 1.,,+
f-rate, cellulose diacetate-1, l=.
(tL1+ -

熱硬化型樹脂又は反応型樹脂としては、フェノール樹脂
、エポキシ樹脂、ポリウレタン硬化型樹脂、尿素樹脂、
メラミン樹脂、アルキッド樹脂、アクリル系反応樹脂、
ポリイソ′/アネート、ポリアミンなどである。
Examples of thermosetting resins or reactive resins include phenolic resins, epoxy resins, polyurethane curable resins, urea resins,
Melamine resin, alkyd resin, acrylic reactive resin,
These include polyiso'/anate and polyamine.

以上の中でも特に好ましくは、繊維素系樹脂、熱可塑性
ポリウレタンエラストマー及びポ1ノイノシアネートの
6成分系である。
Among the above, particularly preferred is a six-component system consisting of a cellulose resin, a thermoplastic polyurethane elastomer, and a poly-inocyanate.

繊維素系樹脂としては、ニド「1セル「J−ス等のセル
ロース誘導体が適当で、これらは、耐熱性、靭性、耐ブ
ロッキング性をイ」与するのにイ9立つ。
Suitable cellulose resins include cellulose derivatives such as Nido 1Cell J-S, which provide heat resistance, toughness, and blocking resistance.

熱可塑性ポリウレタンエラストマーとしては、はとんど
全ての市販品を使用てきる。、即ち、ノタル酸、アジピ
ン酸、二量化すルイン自(ン、マレイ室酸の如き有機二
塩基酸と、「−f”レンゲリコール、プロピレングリコ
ール5.グf−1/ングリコール、ジエチレンクリコー
ル1.ニド(1) りIJニフール類又はトリメチロー
ルプロパン、−\キサントリオール、グリセリン、トリ
メチ1J−ル・コニタン、ペンタエリスリト−ルなどの
多価アルコール類との反応によって得られるポリエステ
ルポリオールをトリレンジイソシアネート、4,4−ジ
フェニルノクンジイソンアネ−1・、ヘキサメチレンジ
イノ7アネー1 、メタキシリレンジイソン゛アネート
の如きポリイソシアネート化合物によってウレタン化し
たポリエスデルボリウレタ〔←(’)−4t。、uoe
−+(−co>−oI+、ooCN1+、+1. N+
+Co−)I 19式 但l、 mは5〜100の整数、Il、 &;l炭、(
・スジ1〜4個のヒドロキソアルキル基又tま炭素数1
〜4個のヒドロキシアルコキシル基を少く−も2個有し
た脂環族又は芳香族化合物によって導入され又は←(3
1−12→n、+1は4〜6の整数である。
As the thermoplastic polyurethane elastomer, almost all commercially available products can be used. , i.e., organic dibasic acids such as notaric acid, adipic acid, dimerized ruin acid, maleic acid, and "-f" lengelicol, propylene glycol, diethylene glycol, 1. Nid (1) Polyester polyol obtained by reaction with polyhydric alcohols such as Nifurs or trimethylolpropane, -\xanetriol, glycerin, trimethylconitane, and pentaerythritol. Polyester polyurethane urethanized with a polyisocyanate compound such as diisocyanate, 4,4-diphenylnocundiisonane-1, hexamethylene diisonane-1, metaxylylene diisonane-1 [←(')- 4t., uoe
-+(-co>-oI+, ooCN1+, +1.N+
+Co-)I Formula 19, where m is an integer from 5 to 100, Il, &;l carbon, (
・Hydroxoalkyl group with 1 to 4 streaks or 1 carbon number
introduced by an alicyclic or aromatic compound having at least 2 to 4 hydroxyalkoxyl groups or ←(3
1-12→n, +1 is an integer from 4 to 6.

これらの分子量は5.000〜soo、ooo好捷しく
は10.000〜200,000のものが有効である。
These molecular weights are preferably 5,000 to soo, preferably 10,000 to 200,000.

これらのポリウレタンについては特願昭54−2688
 [1号に記載されている。1 更に、ポリイノ7−)′ネートとしてr[,2,4−ト
リレンジイソシアネート、1,6−ヘキザノチレンジイ
ソシアネー!・、トリイソソアネート(たとえば、日本
ポリウレタン工業■製造の°コ「jネート■、”)など
が使III−Cきる。。
Regarding these polyurethanes, patent application No. 54-2688
[Described in No. 1. 1 Furthermore, as polyino7-)'ates, r[,2,4-tolylene diisocyanate, 1,6-hexanotylene diisocyanate!・Triisoocyanates (for example, "J-nate", manufactured by Nippon Polyurethane Industries, Ltd.) can be used. .

結合剤の組成比は、バインダ−1uO重111部に対し
て、繊S・11、素糸樹脂が20−ε(0市111部(
特に好1しくに3D〜60重情部)、り、4〜iTJ’
塑性ポリウレタンエラストマーが20〜50 重量部(
特に好捷しくは30〜40重−111部)、ポリイソシ
アネートが10〜50重量部(!!力に好1しくは20
〜40重量部)が好ましい3、本発明、で使用される固
体粉末の一例としての無機質粉末には、炭酸カル/1ク
ム、二酸化ケイ素、酸化チタン、二硫化タングツブ/、
−硫化モリブデン、窒化ホウ素、酸化jノ1ミ;;ウム
、酸化鉄、酸化亜鉛、酸化カルシラノ・、酸化スズ、カ
ーボンブランク、グラファイト等があり、好ましくは炭
酸カルシウム、L酸化々イ素、酸化グ゛タン等であり、
さらに好斗しく 1.+1、炭酸カルンウムである。
The composition ratio of the binder is 111 parts by weight of binder 1uO, 20-ε (0 city 111 parts) of fiber S・11, and fiber resin.
Especially preferably 3D~60 Jujobu), ri, 4~iTJ'
20 to 50 parts by weight of plastic polyurethane elastomer (
Particularly preferably 30 to 40 parts by weight - 111 parts of polyisocyanate (10 to 50 parts by weight, preferably 20 parts by weight)
3. The inorganic powder as an example of the solid powder used in the present invention preferably includes calcium carbonate/1 cum, silicon dioxide, titanium oxide, tungsten disulfide/,
- Molybdenum sulfide, boron nitride, aluminum oxide, iron oxide, zinc oxide, calcyanotin oxide, tin oxide, carbon blank, graphite, etc., preferably calcium carbonate, nitride oxide, graphite, etc.゛tan et al.
Even more friendly 1. +1, carunium carbonate.

これらの固体粉末は、−神父1t、1.−1 fΦ以上
混合して用い、粉末によって形成されるバンク層表面の
粗さが磁性面に転写されるの(L抑制するため平均粒径
がO,U2〜Q、 51Lnt、好t t、 < &l
l、0.02〜02μmのものを使用する。
These solid powders are - Father Itt, 1. The roughness of the bank layer surface formed by the powder is transferred to the magnetic surface (to suppress L, the average particle size is O, U2~Q, 51Lnt, preferably tt, <&l
1, 0.02-02 μm is used.

ゆず肌面を有するバンク層は−に記成分に溶剤(夫々の
結合剤に対応して選択する)を加えた組成物を混線分散
し、支持体表面に塗布し、乾燥することによって形成さ
れる。このバンク層は、単位体積当りの記録密度を上げ
るために、磁気記録媒体の総厚みをできる限り薄くする
様に選ばれている。この様なバンク層の厚さは好捷しく
け03〜2μm、特に好ましくは05〜1μntである
The bank layer having a yuzu skin surface is formed by cross-dispersing a composition in which a solvent (selected according to each binder) is added to the ingredients listed in -, applying it to the surface of the support, and drying it. . This bank layer is selected to make the total thickness of the magnetic recording medium as thin as possible in order to increase the recording density per unit volume. The thickness of such a bank layer is preferably 0.3 to 2 .mu.m, particularly preferably 0.5 to 1 .mu.nt.

なお、磁性層は公知のものを用いることができる。Note that a known magnetic layer can be used.

次に本発明の実施例について説明するが、実施例中に示
す「部」は「重量部」を示す。
Next, examples of the present invention will be described, and "parts" shown in the examples indicate "parts by weight."

実施例1 14μ771厚のポリエチレンテレフタレート支持体の
表面に5μ7n厚の磁性層を設け、下記の組成物をボー
ルミルにて10時間分散混合し−C成る液状塗布組成物
を支持体層の裏面に塗布した後適宜乾燥することにより
約50 finlのピッチpのゆず肌1n1を有する1
μm11厚のバンク層を設け、総厚20μmの磁気テー
プ試月へを作成し/こ。
Example 1 A magnetic layer with a thickness of 5μ7n was provided on the surface of a polyethylene terephthalate support with a thickness of 14μ771, the following composition was dispersed and mixed in a ball mill for 10 hours, and a liquid coating composition consisting of -C was applied to the back side of the support layer. After that, by drying appropriately, it becomes 1 which has a citron skin 1n1 with a pitch p of about 50 fins.
A bank layer with a thickness of 11 μm was provided to create a magnetic tape with a total thickness of 20 μm.

バンク層組成物 ニトロセルロース        25部ボリウレクン
          10部(日本ポリウレタン■製ニ
ッポジン7 K II ’l )ポリイノシアネ−1・
        25部(同上■製コロネートL) エチルメチルケトン       300部炭酸カルシ
ウム         ioo部この試料Aのバンク層
表面を顕微鏡を使って観察したところ、ゆず肌面が認め
られ、表面粗さ計で表面粗さを測定したところカットオ
フ0、 Q 8mmでR,;に0.02411mであっ
た。訃だ、次の測定法により、電磁変換特性としてい比
を寸だ走行耐久特性として出力変動、巻姿および摩耗に
ついて測定し下記表の結果を得た。
Bank layer composition Nitrocellulose 25 parts Polyurekne 10 parts (Nippojin 7 K II 'l manufactured by Nippon Polyurethane) Polyinocyanate-1.
25 parts (Coronate L manufactured by ■ above) Ethyl methyl ketone 300 parts Calcium carbonate Ioo part When the surface of the bank layer of this sample A was observed using a microscope, a citrus skin surface was observed, and the surface roughness was measured using a surface roughness meter. When measured, the R was 0.02411 m at a cutoff of 0 and a Q of 8 mm. Using the following measurement method, we measured the electromagnetic conversion characteristics, ratio, running durability characteristics, output fluctuation, winding shape, and wear, and obtained the results shown in the table below.

1Sハ比差 測定器はシバツクKK社製ノイズメーター(925C)
を使用し、基準テープを比較試料Cとし、それに対する
Sハ比の差を求めた。
The 1S ratio difference measuring device is a noise meter (925C) made by Sibaku KK.
was used, and the reference tape was used as comparative sample C, and the difference in S/c ratio with respect to it was determined.

バイパスフィルター10 KHz 、ローパスフィルタ
ー4 Ml−1zでノイズレベルを測定した。
The noise level was measured using a bypass filter of 10 KHz and a low-pass filter of 4 Ml-1z.

V1’RU、松下N V −8300ヲ用イタ。V1'RU, for Matsushita N V-8300.

2 出力変動 バージンテープと100パス走行テープの出力を比較し
た。
2. The output of the variable output virgin tape and the 100-pass running tape were compared.

6 巻姿及び摩耗 試料テープおよび上記テープデツキを用いて100パス
させたテープを観察し、その結果は良好を5、不良を1
として5段階に評価した平均値として示しである。
6 Observe the tape after 100 passes using the winding and abrasion sample tape and the above tape deck, and the results are 5 for good and 1 for bad.
It is shown as an average value evaluated in 5 stages.

実施例2 実施例1と同じ組成物をボールミルで50時間分散させ
た塗布組成物を実施例1ヒ同じ支持体層に塗布し、乾燥
することによって、ゆず肌面を有するバック層を備えた
磁気記録テープ試料13を作成した。このテープ試料I
3について実施例1と同様力測定を行ないその結果を表
に示す。
Example 2 A coating composition prepared by dispersing the same composition as in Example 1 in a ball mill for 50 hours was applied to the same support layer as in Example 1 and dried, thereby producing a magnetic material with a back layer having a citrus skin surface. Recording tape sample 13 was prepared. This tape sample I
Force measurements were performed on Sample No. 3 in the same manner as in Example 1, and the results are shown in the table.

比較例1,2 実施例1と同じ組成物を用い分jgQ 111」間を夫
々10時間および50時間とした塗4i組成物を塗布し
、通常の乾燥により普通の+11 +fii (従来法
通り、ゆず皿形成なし)のバック層をイJする試料C及
び平滑面のバンク層を有する試i:’l l)をそれぞ
れ作成した。各試料につき、実施1+111と同様の測
定を行ない、その結果をト表に小ず。
Comparative Examples 1 and 2 Coating 4i compositions were applied using the same composition as in Example 1 and the intervals were 10 hours and 50 hours, respectively. A sample C having a back layer (without plate formation) and a sample I having a bank layer with a smooth surface were prepared, respectively. The same measurements as in Example 1+111 were carried out for each sample, and the results were summarized in the table.

試料 分散時間 ゆず肌 Fシヘ比差 出力変動 巻姿
 摩耗A、10時間  有  4−1odB0.2dl
l   5  513 50     有   +1.
1    0.6     4   4C10無   
OfJ、3     5   5D   so    
 無  + 1.2     ’1.3     1 
  1上記表に小した各試料の牛−性イ、:、It較1
−ると、次の点が明らかとなる。すなわ1ハ従来法に従
いバンク層組成物の分散時間をtυ縮してバンク層表面
をゆず肌面を形成することなく単に粗面化すると、試料
Cの測定、評価結果から明らかなように走行特性及び走
行耐久性は向上するが、電磁変換特性は大幅に低下する
ことeこなる。これに対し、試料J) lま分散時間が
長いためバンク層表面は平滑(ゆず肌面形成もなし)で
あるが、この場合電磁変換特性は向上するが、走行特性
及び走行耐久性は低下する。
Sample Dispersion time Yuzu skin F-shihe ratio difference Output fluctuation Winding form Abrasion A, 10 hours Yes 4-1odB0.2dl
l 5 513 50 Yes +1.
1 0.6 4 No 4C10
OfJ, 3 5 5D so
None + 1.2 '1.3 1
1 Comparison of bovine sex of each sample listed in the table above: 1
−, the following points become clear. In other words, if the dispersion time of the bank layer composition is shortened by tυ in accordance with the conventional method and the bank layer surface is simply roughened without forming an orange skin surface, it is clear from the measurement and evaluation results of sample C that the running Although the characteristics and running durability are improved, the electromagnetic conversion characteristics are significantly reduced. On the other hand, sample J) has a long dispersion time, so the surface of the bank layer is smooth (no citron surface formation), but in this case, the electromagnetic conversion characteristics are improved, but the running characteristics and running durability are reduced. .

これに対し、試料1)に相当するバック層表面を素地と
し、ゆず肌面を形成した試料I3の場合、電磁変換特性
をほとんど損うことなく走行特性および走行耐久特性が
改善されている。この試料Bに対してゆず肌面を形成し
かつ素地を粗面化した試料Aは電磁変換特性の劣化を妥
当なところに抑えたまま走行特性及び走行耐久特性を若
干改善している。
On the other hand, in the case of sample I3, in which the surface of the back layer corresponding to sample 1) was used as the base material and a citrus skin surface was formed, the running characteristics and running durability characteristics were improved without substantially impairing the electromagnetic conversion characteristics. Compared to this sample B, sample A, which has a citrus skin surface and roughened base surface, has slightly improved running characteristics and running durability while suppressing deterioration of electromagnetic conversion characteristics to an appropriate level.

即ち、本発明において、バック層はゆず肌面を有すると
共にその素地は平滑面でも粗面ても従来法に対するバッ
ク層のゆず肌面化による改善が認められる。バンク層の
素地を粗面とするか又は平滑面とするかは目的に応じて
選択できる。
That is, in the present invention, the back layer has a citron-like surface, and whether the substrate is smooth or rough, an improvement over the conventional method is recognized due to the citron-like surface of the back layer. Whether the bank layer has a rough surface or a smooth surface can be selected depending on the purpose.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、ゆず肌面の模様を示す平面図、第2図は、ゆ
ず肌面の凹凸を示す磁気記録媒体の一断面図(第1図矢
視II −II断面)を示す。 a 突 部    b バック層  C谷 部d 谷部
深さ  p ピッチ   e 支持体f 磁性層 出願人 富士写真フィルム株式会社 代理人 弁理士別 藤 朝 道 第1図 第2図 手続補正害 昭和58年73B22日 特許庁長官  若杉和夫 殿 1 事件の表示 昭JI757年特詐願第166661号(昭和57年9
月271」出願) 2 発明の名称 磁気記録媒体 3 補正をする者 事件との関係  特許出願人 住5.9j (居所) 氏名(名称)  富士写真フィルム株式会社6 補iE
により増加する発明の数  なしレイン酸の如き有機二
塩基酸と、:T′、チレングリコール、プロピレングリ
コール、ブチ1/ングリコール、’/:”二f−レンク
リコ・−ル:’i: ト(、t) り!Jコール2bQ
 又i+、j t・す7ノチロー・ルプロパ:/、−\
キサントリオール、グリセリン、トリメチロールエタン
、ペンタエリスリト・−ルなどの多面アルコール類との
反応によっ−C得られるポリエヌテルボリオールをトリ
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、ヘキザメチレンジイソシアネート、メ
タキシリレンジイソシアネートの如きポリイソシアネー
ト化合物によってウレタン化し、たポリエステルボリウ
レタ環を不し:ケものなどが使用される。 (←o−1←oO0−r(、Co > 、1l−or+
、oo(IN + 1−+’C−N11r3o−)(1
)式 但しIllは5へ100の整数、It &よ炭ス・1数
1〜4個のヒドロキシアルキル基又は炭素数1〜4個の
ヒドロキシアルキル基を少くとも2個有した脂環族又は
芳香族化合物によって導入され又は←(J−1,−)−
n、  nは4〜6の整数で冴2る。 コiLらの分子itま5.00 [1へ500,000
好寸シ<は10、OO[1〜200.000のものが有
効である。これらのポリウレタンにソい′?、は特願昭
54−26880号に記載されている。
FIG. 1 is a plan view showing the pattern of the citron skin surface, and FIG. 2 is a sectional view of a magnetic recording medium (cross section taken along arrow II-II in FIG. 1) showing the unevenness of the yuzu skin surface. a Projection b Back layer C Valley d Valley depth p Pitch e Support f Magnetic layer Applicant Fuji Photo Film Co., Ltd. Agent Patent attorney Asahi Fuji Do Figure 1 Figure 2 Procedural Amendment No. 73B22, 1982 Mr. Kazuo Wakasugi, Commissioner of the Patent Office 1 Case Description Special Fraud Application No. 166661 of 1982 (Showa JI 757)
271 (Application filed) 2 Name of the invention Magnetic recording medium 3 Relationship to the case of the person making the amendment Patent applicant's residence 5.9j (Residence) Name Fuji Photo Film Co., Ltd. 6 Supplementary iE
The number of inventions increases due to organic dibasic acids such as oleic acid: T', ethylene glycol, propylene glycol, butylene glycol, '/:' dif-lene glycol: 'i: t( ,t) Ri!J call 2bQ
Also i+, j t・su7 nochiro・rupropa:/、−\
Polyesterboliol obtained by reaction with polyhedral alcohols such as xanetriol, glycerin, trimethylolethane, and pentaerythritol is converted into tolylene diisocyanate, 4,4-diphenylmethane di-
Polyester polyurethane which has been urethanized with a polyisocyanate compound such as isocyanate, hexamethylene diisocyanate, metaxylylene diisocyanate, and the like is used. (←o-1←oO0-r(, Co > , 1l-or+
,oo(IN+1-+'C-N11r3o-)(1
) formula, where Ill is an integer from 5 to 100, It & y carbon is an alicyclic or aromatic group having 1 to 4 hydroxyalkyl groups or at least 2 hydroxyalkyl groups having 1 to 4 carbon atoms. introduced by a group compound or ←(J-1,-)-
n, n is an integer from 4 to 6. The molecule of coiL et al. is 5.00 [1 to 500,000
Values of 10 and OO[1 to 200,000 are valid. What about these polyurethanes? is described in Japanese Patent Application No. 54-26880.

Claims (1)

【特許請求の範囲】[Claims] 非磁性体の一方の面に磁性層を有し、他方の面に厚さ2
μnt以下のバック層を有する磁気記録媒体において、
バンク層表面をゆノ“肌状としたことを特徴とする磁気
記録媒体。
The non-magnetic material has a magnetic layer on one side and a thickness of 2 on the other side.
In a magnetic recording medium having a back layer of μnt or less,
A magnetic recording medium characterized by a bank layer surface having a "skin-like" texture.
JP57166661A 1982-09-27 1982-09-27 Magnetic recording medium Pending JPS5956222A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57166661A JPS5956222A (en) 1982-09-27 1982-09-27 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57166661A JPS5956222A (en) 1982-09-27 1982-09-27 Magnetic recording medium

Publications (1)

Publication Number Publication Date
JPS5956222A true JPS5956222A (en) 1984-03-31

Family

ID=15835388

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57166661A Pending JPS5956222A (en) 1982-09-27 1982-09-27 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS5956222A (en)

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