JPS6059529A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS6059529A
JPS6059529A JP16732183A JP16732183A JPS6059529A JP S6059529 A JPS6059529 A JP S6059529A JP 16732183 A JP16732183 A JP 16732183A JP 16732183 A JP16732183 A JP 16732183A JP S6059529 A JPS6059529 A JP S6059529A
Authority
JP
Japan
Prior art keywords
powder
magnetic
coating layer
back coating
tape
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
JP16732183A
Other languages
Japanese (ja)
Inventor
Akira Morioka
章 森岡
Takeshi Matsuura
松浦 武志
Yoshiyuki Takahira
高平 義之
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.)
Maxell Ltd
Original Assignee
Hitachi Maxell 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 Hitachi Maxell Ltd filed Critical Hitachi Maxell Ltd
Priority to JP16732183A priority Critical patent/JPS6059529A/en
Priority to DE8383109714T priority patent/DE3373584D1/en
Priority to EP19860100267 priority patent/EP0192032B1/en
Priority to DE8686100267T priority patent/DE3378735D1/en
Priority to EP19830109714 priority patent/EP0105471B1/en
Priority to KR1019830004616A priority patent/KR910004010B1/en
Publication of JPS6059529A publication Critical patent/JPS6059529A/en
Priority to US07/013,286 priority patent/US4871606A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a magnetic recording medium having excellent running stability and wear resistance of a back coating layer and having a particularly good video characteristic by providing the back coating layer contg. specific alkaline BaSO4 powder and alpha-Fe2O3 powder on the rear of a base having a magnetic layer on the main plane. CONSTITUTION:BaSO4 powder which is the dry powder prepd. by charging, for example, neutral BaSO4 powder manufactured by various methods into an aq. NaOH soln. and mixing the same then rinsing thoroughly the powder and of which the pH when said dry powder is dispersed into water is in a 7.5-10pH range is dispersed together with alpha-Fe2O3 powder having <=0.2mu average grain size into a resin binder soln. An additive such as carbon black is added thereto for preventing electrification, etc. thereby preparing a coating liquid. Such coating liquid is coated on the rear of a base provided with a magnetic layer and is dried, by which a back coating layer is formed. The magnetic tape which has good running stability, has excellent wear resistance of the back coating layer, obviates the wear of a tape guide and has a good color SN ratio is thus obtd.

Description

【発明の詳細な説明】 この発明は主面に磁性層を有する支持体の背面にバック
コート層を設けてなる磁気テープその他の磁気記録媒体
に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic tape or other magnetic recording medium comprising a support having a magnetic layer on its main surface and a back coat layer provided on the back surface.

ポリエステルフィルムの如き支持体の主面に磁性層が投
けられた磁気テープなどにあっては、その走行安定性や
帯電防止などを図る目的で支持体の背面に適宜の充填剤
を含ませたバックコート層を設けている。このようなバ
ックコート層に含ませる充填剤のひとつに、走行安定性
や磁気特性などの各種特性面で非常に良好な結果を与え
るものとして硫酸バリウム粉末が提案されているが、こ
れによっても未だバックコート層の耐摩耗性が充分であ
るとはいえ表かった。
For magnetic tapes in which a magnetic layer is placed on the main surface of a support such as a polyester film, an appropriate filler is added to the back surface of the support in order to improve running stability and prevent static electricity. A back coat layer is provided. Barium sulfate powder has been proposed as one of the fillers to be included in such a backcoat layer, as it gives very good results in terms of various properties such as running stability and magnetic properties, but even with this, barium sulfate powder has not yet been proposed. Although the abrasion resistance of the back coat layer was sufficient, it was apparent that the abrasion resistance of the back coat layer was sufficient.

この発明者らは、上記欠点を回避するために鋭意検討し
た結果、硫酸バリウム粉末のなかでもこの粉本を水中に
投入し撹拌分散させたときにその液のPHが7.5以上
となるようなアルカリ性のものをα−Fe*Os粉末と
ともに用いたときには、バックコート層の耐摩耗性が著
しく改善されることを見い出し、この発明をなすにいカ
ニった。
As a result of intensive studies to avoid the above-mentioned drawbacks, the inventors found that among barium sulfate powders, when this powder is poured into water and stirred and dispersed, the pH of the liquid becomes 7.5 or more. It has been discovered that when an alkaline material is used together with α-Fe*Os powder, the abrasion resistance of the back coat layer is significantly improved, and this invention was made possible.

すなわち、この発明は、主面に磁性層を有する支持体の
背面にPH7,5〜10の硫酸バリウム粉末をα−Fa
mes粉末とともに含むバックコート層を設けたことを
特徴とする磁気記録媒体に係るものである。
That is, in this invention, barium sulfate powder with a pH of 7.5 to 10 is coated with α-Fa on the back surface of a support having a magnetic layer on the main surface.
The present invention relates to a magnetic recording medium characterized in that a back coat layer containing mes powder is provided.

この発明に用いるアルカリ性の硫酸バリウム粉末は、た
とえば各種の方法で製造されている中性の硫酸バリウム
粉末を水酸化ナトリウムの如きアルカリ水溶液中に投入
したのち、充分な水洗を行なうことによ9得ることがで
きる。
The alkaline barium sulfate powder used in this invention can be obtained by, for example, adding neutral barium sulfate powder produced by various methods into an alkaline aqueous solution such as sodium hydroxide, and then washing thoroughly with water. be able to.

また、下記の反応式; BaS+NagS04→BaSO4+Nam5にしたが
って硫酸バリウム粉末を得たのち、これを充分に水洗す
ることによりてもアルカリ性の硫酸バリウム粉末を得る
ことができる。すなわち、上記反応式で副生する硫化ナ
トリウムは引き続く水洗工程で分解して水酸化ナトリウ
ムを生成するため、この水酸化ナトリウムをとくに中和
処理しなければ、これが硫酸バリウム粉末に付着して上
記粉末をアルカリ性とする。
Alternatively, alkaline barium sulfate powder can also be obtained by obtaining barium sulfate powder according to the following reaction formula: BaS+NagS04→BaSO4+Nam5 and then thoroughly washing it with water. In other words, the sodium sulfide produced as a by-product in the above reaction formula decomposes in the subsequent water washing process to produce sodium hydroxide, so unless this sodium hydroxide is specifically neutralized, it will adhere to the barium sulfate powder and form the powder. is alkaline.

この発明においてアルカリ性硫酸バリウム粉末のPHを
7.5〜10に設定している理由は、PHが7.5よル
小さくなるとバックコート層の耐摩耗性の改善効果が充
分に得られなくなる一方、PHが10より大きくなると
バックコート層のバインダに対する分散性を損なったル
バインダを変質するなどのおそれがあるためである。そ
して、このような鑑点に立って最も望ましいPHの範囲
は7.9〜9.5である。
The reason why the pH of the alkaline barium sulfate powder is set to 7.5 to 10 in this invention is that if the pH becomes lower than 7.5, the effect of improving the abrasion resistance of the back coat layer will not be sufficiently obtained. This is because if the pH is greater than 10, there is a risk that the binder in the backcoat layer may lose its dispersibility in the binder and be altered in quality. In view of this, the most desirable pH range is 7.9 to 9.5.

また、上記硫酸バリウム粉末の平均粒子径は2μ−以下
が好ましいとされるが、この理由はこれよシ大きな粒子
径となると巻回状態で支持体主面の磁性層の表面性に悪
影響を与えたシ、またバックコート層のバインダへの分
散性の低下によシその本来の機能を充分に発揮させにく
いためである。
Furthermore, it is said that the average particle size of the barium sulfate powder is preferably 2μ or less, but this is because if the particle size is larger than this, the surface properties of the magnetic layer on the main surface of the support will be adversely affected in the rolled state. This is also because the dispersibility of the backcoat layer in the binder decreases, making it difficult to fully demonstrate its original function.

アルカリ性硫酸バリウム粉末の使用薦は、バインダ10
0重電部に対して一般に40〜400重麓部とするのが
よく、過少では走行安定性の改善などの本来の機能を充
分に発揮せず、また過多では層強度が低下するため好ま
しくない。
We recommend using alkaline barium sulfate powder with binder 10.
It is generally good to set the base part to 40 to 400 with respect to the 0-heavy electric part, and if it is too small, the original function such as improving running stability will not be fully demonstrated, and if it is too large, the layer strength will decrease, which is not preferable. .

また、この発明において併用するα−Fe101粉末は
、その平均粒子径が0.2μ集以下に設定することが望
ましい。この理由は、これよシ大きな粒子径となると巻
回状態で支持体主面の磁性層の表面性に悪影響を与えビ
デオ特性の低下を招きその本来の機能を充分に発揮させ
にくいためであるが、前記のアルカリ性硫酸バリウム粉
末よシも粒子径の制限が厳しいのは、α−Fe 20g
粉末の方が前記の硫酸バリウムに比し、粒子径の大きい
ものが、磁性層の表面性に与える影養がじん大なためで
ある0 α−FsvOs粉末の使用態は、前記アルカリ性硫酸バ
リウム粉末との合計麓に対して1〜50重鳳%の範囲と
するのが良く、過少では充分な走行安定性が得られず、
また過多では対接するテープガイド等を傷つけることと
なシ好ましくない〇この発明におけるバックコート層の
形成は、一般には、上述したアルカリ性硫酸バリウム粉
末とα−Fat’sとをバインダと共に有機溶剤中に混
合し、さらに例えば光透過率、帯電性を低減するために
カーボンブラックを加えるなど必要に応じて公知の各種
添加剤を加えた塗料を調製し、これを主面に磁性層が設
けられた支持体の背面に塗着することによって行なわれ
る。
Further, it is desirable that the average particle diameter of the α-Fe101 powder used in combination in this invention is set to 0.2μ or less. The reason for this is that if the particle size is larger than this, it will adversely affect the surface properties of the magnetic layer on the main surface of the support in the rolled state, resulting in deterioration of video characteristics and making it difficult to fully demonstrate its original function. , α-Fe 20g has stricter particle size restrictions than the alkaline barium sulfate powder mentioned above.
This is because the larger particle size of the powder has a greater effect on the surface properties of the magnetic layer than the above-mentioned barium sulfate powder. It is best to set the amount in the range of 1 to 50% with respect to the total foot of the foot, and if it is too low, sufficient running stability will not be obtained.
Also, if the amount is too large, it may damage the opposing tape guide, etc., which is undesirable. In general, the formation of the back coat layer in this invention involves adding the above-mentioned alkaline barium sulfate powder and α-Fat's to an organic solvent together with a binder. A paint is prepared by mixing and adding various known additives as necessary, such as adding carbon black to reduce light transmittance and chargeability. It is done by applying it to the back of the body.

上記に用いるバインダとしては、とくに限定はなく、w
4m素系桐脂、ポリウレタン樹脂、塩化ビニル−酢酸ビ
ニル共重合体、ポリエステル樹BK。
The binder used above is not particularly limited, and
4M paulownia resin, polyurethane resin, vinyl chloride-vinyl acetate copolymer, polyester resin BK.

アクリロニトリル−ブタジェン共重合体など従来汎用さ
れているものをいずれも適用できる。
Any conventionally used material such as acrylonitrile-butadiene copolymer can be used.

以上のように、この発明は、バックコート層の充填剤と
してアルカリ性硫酸バリウム粉末とα−Fag’s粉末
とをともに用いたことを特徴とするものであシ、これに
よってバックコート層の耐摩耗性にすぐれる磁気記録媒
体を提供することができる。
As described above, the present invention is characterized in that alkaline barium sulfate powder and α-Fag's powder are used together as a filler in the back coat layer, which makes the back coat layer resistant to wear. A magnetic recording medium with excellent properties can be provided.

つぎに、この発明の実施例を記載する。なお、以下にお
いて部とあるは重重部を意味する。また。
Next, examples of this invention will be described. In addition, in the following, "part" means a heavy part. Also.

以下の実施例で用いたPH9,4および8.0の硫酸バ
リウム粉末は次の方法で製造したもので4.b。
The barium sulfate powders with pH 9, 4 and 8.0 used in the following examples were manufactured by the following method. b.

〈アルカリ性硫酸バリウム粉末の製造〉平均粒子径0.
1μIII、PH7の硫酸バリウム粉末1.000部を
、1モル/11の水酸化ナトリウム水溶210,009
部中に投入し、充分に撹拌分散させたのち、約1時間熟
成した。その後、充分な水洗を行なったのち、ろ過、乾
燥して、PH9,4およびPH8,0の硫酸バリウム粉
末を得た。
<Production of alkaline barium sulfate powder> Average particle size 0.
1 μIII, 1.000 parts of barium sulfate powder with pH 7 was dissolved in 1 mol/11 sodium hydroxide aqueous solution 210,009
After thoroughly stirring and dispersing the mixture, the mixture was aged for about 1 hour. Thereafter, the mixture was thoroughly washed with water, filtered, and dried to obtain barium sulfate powders with pHs of 9.4 and 8.0.

実施例1 Co含有磁性酸化鉄粉末 250部 カーボンブラック 13.75部 粒状α−酸化鉄(粒径1.0μIII) 、13部Cr
5OI粉末 (粒径1.0μmm) 2部Ajs+Os
粉末 5部 ステアリン酸亜鉛 1.25部 硝化綿 22.6部 ポリウレタン樹脂 20.1部 三官能性イソシアネート化合物 7.5部シクロヘキサ
ノン 340部 トルエン 340部 ステアリン酸n−ブチル 3部 【リスチン酸 6.25部 上記組成からなる磁性塗料を14μ洛厚のポリエステル
ベースフィルム上に乾燥厚みが5μ集トするように塗布
、乾燥したのち、表面処理を行なって磁性層を形成した
0 得られた磁気テープの背面に下記組成からなるバックコ
ート用塗料を乾燥厚みが1μ慣となるように塗布、乾燥
したのち、所定の幅に裁断してビデオテープをつくった
0 粒状α−FesOs粉(モース硬度5〜6ノカーボンブ
ラツク(粒子径43μfi) 50部硝化綿 135部 ポリウレタン樹脂 94s 三官能性低分子重イソシアネート 40部ステアリン酸
n−ブチル 5部 ミリスチン酸 10部 シクロヘキサノン 1,000部 トルエン 1,000部 実施例2 実施例1と同様にして得た磁気テープの背面に硫酸バリ
ウム粉としてPH8,0のものを用いた以外は実施例1
と同様のバックコート用塗料を乾燥厚みが1μ噂となる
ように塗布、乾燥したのち、所定の幅に裁断してビデオ
テープをつくった。
Example 1 Co-containing magnetic iron oxide powder 250 parts Carbon black 13.75 parts Granular α-iron oxide (particle size 1.0 μIII), 13 parts Cr
5OI powder (particle size 1.0μmm) 2 parts Ajs+Os
Powder 5 parts Zinc stearate 1.25 parts Nitrified cotton 22.6 parts Polyurethane resin 20.1 parts Trifunctional isocyanate compound 7.5 parts Cyclohexanone 340 parts Toluene 340 parts n-butyl stearate 3 parts [listic acid 6.25 parts A magnetic paint having the above composition was applied onto a polyester base film with a thickness of 14 μm to a dry thickness of 5 μm, and after drying, surface treatment was performed to form a magnetic layer.0 The back side of the obtained magnetic tape A back coat paint having the following composition was applied to the surface to a dry thickness of 1 μm, dried, and then cut into a predetermined width to make a videotape. Carbon black (particle size 43 μfi) 50 parts Nitrified cotton 135 parts Polyurethane resin 94s Trifunctional low molecular weight isocyanate 40 parts n-butyl stearate 5 parts Myristic acid 10 parts Cyclohexanone 1,000 parts Toluene 1,000 parts Example 2 Example 1 except that barium sulfate powder with a pH of 8.0 was used on the back side of the magnetic tape obtained in the same manner as in Example 1.
A similar backcoat paint was applied to the tape to a dry thickness of about 1 micron, and after drying, it was cut to the specified width to make a videotape.

比較例1 実施例1と同様にして得た磁気テープの背面にPH9,
4の硫酸バリウムに代えてPH7,0の硫酸バリウムを
同重用いた以外は実施例1と同じ組成からなるバックコ
ート用塗料を、乾燥厚みが1μ愼となるように塗布、乾
燥したのち、所定の幅に裁断してビデオテープをつくっ
た。
Comparative Example 1 PH9,
A back coat paint having the same composition as in Example 1, except that barium sulfate with a pH of 7.0 was used in the same weight instead of barium sulfate in Example 4, was applied to a dry thickness of 1 μm, dried, and then coated with the specified coating material. I cut it into strips and made a videotape.

比較例2 比較例1と同様にして得た磁気テープ背面に、実施例1
におけるバックコート用塗料の組成のうち、α−Fes
Osの50部を加えなかった以外は全て比較例1と同様
の組成から成るバックコート用塗料を、乾燥厚みが1μ
錫となるように塗布、乾燥したのち、所定の幅に裁断し
てビデオテープをつくった。
Comparative Example 2 Example 1 was applied to the back of a magnetic tape obtained in the same manner as Comparative Example 1.
Among the compositions of back coat paints in
A back coat paint having the same composition as Comparative Example 1 except that 50 parts of Os was not added was used to a dry thickness of 1 μm.
The material was coated to form tin, dried, and then cut to a specified width to make video tapes.

上記各種実施例および比較例のビデオテープにき、光じ
やへい性、バックコート層の表面粗度、ビデオ特性(カ
ラーSN比)、バックコート層の耐摩耗性、走行安定性
およびテープガイドの摩耗性を調べた結果は、つぎの表
に示されるとおシであった。なお%負特性は以下の如く
測定評価した0く光じゃへい性〉 VH8方式のVTR(ビデオテープレコーダ)を用い、
供試テープに波長9,0001の光を当て、その透過率
を測定した。
The video tapes of the various Examples and Comparative Examples described above were characterized by light glare and resistance, surface roughness of the back coat layer, video characteristics (color S/N ratio), abrasion resistance of the back coat layer, running stability, and tape guide performance. The results of examining the abrasion properties are shown in the table below. In addition, the % negative characteristic is measured and evaluated as follows. Using a VH8 system VTR (video tape recorder),
The sample tape was irradiated with light having a wavelength of 9,0001, and its transmittance was measured.

〈表面粗度〉 触針式表面粗度計を用い、供試テープの中心線平均粗さ
くRa)を測定した。
<Surface Roughness> The center line average roughness (Ra) of the sample tape was measured using a stylus type surface roughness meter.

〈カラーSN比〉 VH8方式のVTRを用い、供試テープにカラービデオ
ノイズ測定器の一色クロマ信号を記録再生し、AMノイ
ズ分を測定してカラー8N比を算出し、基準テープとの
相対値で示した。
<Color SN ratio> Using a VH8 system VTR, record and play back the one-color chroma signal of the color video noise measuring device on the sample tape, measure the AM noise component, calculate the color 8N ratio, and calculate the relative value with the reference tape. It was shown in

〈耐摩耗性およびテープガイドの摩耗〉VH8方式のV
TRを用い、50%グレー信号を記録した供試テープの
実用走行試験を 100回繰返し、走行前のビデオSN
比に対する走行後のビデオSN比の低下鴬を測定した。
<Abrasion resistance and tape guide wear> VH8 system V
Using TR, a practical running test of a sample tape with a 50% gray signal recorded was repeated 100 times, and video SN was recorded before running.
The decrease in video S/N ratio after driving was measured.

また、同時にVTRのテープガイド、カセットのテープ
ガイドの摩耗状態を目視によシ判定した。
At the same time, the state of wear of the tape guide of the VTR and the tape guide of the cassette was visually determined.

〈走行安定性〉 VH8方式のVTRを用い、供試テープを1000回走
行させ、その後テープの変形を観察し、テープ変形が全
く認められない場合を良好、僅かに認められる場合をや
や不良、テープ変形が著しい場合を不良と評価した。
<Running Stability> Using a VH8 type VTR, run the sample tape 1000 times, then observe the deformation of the tape. If no tape deformation is observed, the tape is good; if only a little is observed, the tape is considered poor. Cases where the deformation was significant were evaluated as poor.

上記の表の結果から明らかなように、この発明のビデオ
テープ即ち、アルカリ性のBJLSO4とα−Fo2s
ilとを併用した実施例1、実施例2は、中性の従来の
BaSO4とα−ii”52osとを併用した比較例1
に比して走行安定性とバックコート層の耐摩耗性とに、
ともにすぐれていることがわかる。
As is clear from the results in the above table, the videotape of the present invention, that is, alkaline BJLSO4 and α-Fo2s
Example 1 and Example 2 in which il was used in combination with Comparative Example 1 in which neutral conventional BaSO4 and α-ii"52os were used in combination
In terms of running stability and abrasion resistance of the back coat layer,
It can be seen that both are excellent.

出願人 日立マクセル株式会社 代表者 永 井 厚 (11)Applicant: Hitachi Maxell, Ltd. Representative Atsushi Nagai (11)

Claims (1)

【特許請求の範囲】[Claims] (1)主面KvB性層を有する支持体の背面にPH7,
5〜10の硫酸バリウム粉末なα−Fe鵞Os粉末とと
もに、含むバックコート層を設けたことを特徴とする磁
気記録媒体。
(1) PH7 on the back side of the support having the main surface KvB layer,
1. A magnetic recording medium comprising a back coat layer containing 5 to 10 barium sulfate powder or α-Fe Os powder.
JP16732183A 1982-09-30 1983-09-09 Magnetic recording medium Pending JPS6059529A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP16732183A JPS6059529A (en) 1983-09-09 1983-09-09 Magnetic recording medium
DE8383109714T DE3373584D1 (en) 1982-09-30 1983-09-28 Magnetic recording medium
EP19860100267 EP0192032B1 (en) 1982-09-30 1983-09-28 Magnetic recording medium
DE8686100267T DE3378735D1 (en) 1982-09-30 1983-09-28 Magnetic recording medium
EP19830109714 EP0105471B1 (en) 1982-09-30 1983-09-28 Magnetic recording medium
KR1019830004616A KR910004010B1 (en) 1982-09-30 1983-09-29 Magnetic recording media
US07/013,286 US4871606A (en) 1982-09-30 1987-02-11 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16732183A JPS6059529A (en) 1983-09-09 1983-09-09 Magnetic recording medium

Publications (1)

Publication Number Publication Date
JPS6059529A true JPS6059529A (en) 1985-04-05

Family

ID=15847577

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16732183A Pending JPS6059529A (en) 1982-09-30 1983-09-09 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS6059529A (en)

Similar Documents

Publication Publication Date Title
EP0105471B1 (en) Magnetic recording medium
US4363850A (en) Magnetic recording medium
JPS6057530A (en) Magnetic recording medium
JPS6059529A (en) Magnetic recording medium
JPS6238525A (en) Magnetic recording medium
JPS5928242A (en) Magnetic recording medium
US5110658A (en) Magnetic recording medium
JPS59172151A (en) Magnetic recording medium
JPH0437483B2 (en)
JPS5914124A (en) Magnetic recording medium
JP3000650B2 (en) Magnetic recording medium and method of manufacturing the same
JPS6248297B2 (en)
JP2631523B2 (en) Magnetic recording media
JPH053049B2 (en)
JP2600796B2 (en) Magnetic recording media
JPS61180927A (en) Magnetic recording medium
JPS595428A (en) Magnetic recording medium
JPS6238534A (en) Magnetic recording medium
JPS5914128A (en) Magnetic recording medium
JPS5914123A (en) Magnetic recording medium
JPS5841435A (en) Magnetic recording medium
JPS6378334A (en) Magnetic recording medium
US4722863A (en) Magnetic recording medium
JPS61182630A (en) Production of magnetic recording medium
JPH0568007B2 (en)