JPS6029932A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS6029932A JPS6029932A JP58139067A JP13906783A JPS6029932A JP S6029932 A JPS6029932 A JP S6029932A JP 58139067 A JP58139067 A JP 58139067A JP 13906783 A JP13906783 A JP 13906783A JP S6029932 A JPS6029932 A JP S6029932A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- powder
- reinforcing material
- magnetic layer
- dispersant
- 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
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
- G11B5/68—Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent
- G11B5/70—Record 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
- G11B5/708—Record 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
- G11B5/7085—Record 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 non-magnetic abrasive particles
Abstract
Description
【発明の詳細な説明】 本発明は磁気記録媒体に関する。[Detailed description of the invention] The present invention relates to magnetic recording media.
さらに詳細には分散性の優れた補強材を用いることによ
る磁性層の耐摩耗性に優れ、磁気ヘッドの摩耗抑制作用
が改善され、かつ表面平2汁性に優れたf1俺気配録媒
体に関する。オーディオ用、ビデオ用、コンピュータ用
磁気韻Q 11i、+体は、記録再生時に磁気ヘッドと
激しく摺接するため、磁性層が摩耗し耐久性が充分なも
のとは言い難い。More specifically, the present invention relates to an f1 recording medium that has excellent abrasion resistance of the magnetic layer by using a reinforcing material with excellent dispersibility, improved abrasion suppression effect of the magnetic head, and excellent surface flatness. The magnetic head for audio, video, and computers Q11i, + body comes into violent sliding contact with the magnetic head during recording and reproduction, so the magnetic layer wears out and it cannot be said that it has sufficient durability.
従来、かかる欠点を改善するために、Cr20hA52
0. 、 SiC等の非磁性粉末を補強材として磁性層
中に混入させる方法が提案されている。Conventionally, in order to improve this drawback, Cr20hA52
0. , A method has been proposed in which non-magnetic powder such as SiC is mixed into the magnetic layer as a reinforcing material.
しかし、上記のような補強材を磁性層中へ均一に分散さ
せることは容易ではなく、分散ムラを生ずることが多く
、結果として、磁性層の耐摩耗性の低下、磁気ヘッドの
摩耗のし過ぎ、テープ表面の平滑性の低下等の問題を生
じている。However, it is not easy to uniformly disperse the reinforcing material in the magnetic layer, and uneven distribution often occurs.As a result, the wear resistance of the magnetic layer decreases, and the magnetic head becomes excessively worn. This causes problems such as a decrease in the smoothness of the tape surface.
かかる不都合を改善するために磁性層を形成させるため
の学膜形成用塗布液を調整するlid lこステアリン
酸−n−ブチlし、流リカパラフィン、アルキルベンゼ
ンスルホン酸ナトリウム等の分散剤を添加湿式混合する
ことによって補強材の分散性を改良するという方/jζ
は知られているが、目的とするに充分な分散性の向1を
図れないという欠点がある。In order to improve this inconvenience, a coating liquid for forming a magnetic layer is prepared using a wet method using n-butyl stearate and adding a dispersant such as liquid paraffin or sodium alkylbenzenesulfonate. Those who want to improve the dispersibility of reinforcing materials by mixing / jζ
is known, but it has the drawback that it cannot achieve sufficient dispersibility for the purpose.
本発明者らは先に特願昭57.−192904号にて親
油基を有する分散剤の存在下に衝5y値がIG以上の条
件下に乾式混合して得られ4た平均粒子径2μm以下及
びモース硬度5以□上の無−質粉末を用いることを提案
した。The present inventors previously filed a patent application filed in 1983. -192904, obtained by dry mixing in the presence of a dispersant having a lipophilic group under conditions where the 5y value is IG or more. It was proposed to use powder.
しかし、塗膜形成用塗布液溶媒としてトルエン又はトル
エン含有溶媒を用いる場合にはITiI記特願昭に開示
された分散剤では必ずしも十分でないことがある。However, when toluene or a toluene-containing solvent is used as a solvent for a coating solution for forming a coating film, the dispersant disclosed in ITiI Patent Application Sho may not necessarily be sufficient.
本発明は1述のような不都合を克服すべく種々検討した
結果、特定の分散剤を用い特定の手段によって補強剤に
分散性を付与した場合には公知の方法に比較してトルエ
ン又はトルエン含有溶媒に対して顕著に分散性が改善で
きることを4見出し、かかる補強剤を用いることにより
、磁性層の耐摩耗性および磁気ヘッドの耐摩耗性を改善
し、かつテープ表面の平滑性を改善することが出来るこ
とを見出し本発明を完成するに至った。As a result of various studies to overcome the above-mentioned disadvantages, the present invention has found that when dispersibility is imparted to a reinforcing agent using a specific dispersant and by a specific method, toluene or toluene-containing It has been found that dispersibility in solvents can be significantly improved, and by using such a reinforcing agent, the wear resistance of the magnetic layer and the magnetic head can be improved, and the smoothness of the tape surface can be improved. They discovered that this can be done and completed the present invention.
すなわち、本発明は、芳香族カルボン酸及び/又はシリ
コーン分散力1の存在下に衝撃値が10以上の条件下に
乾式混合して得られた平均粒子径2μm以下及びモース
硬度5以ヒの無機質粉末と磁性粉とが含まれてなる磁性
層を有する磁気記録媒体を提供するにある。That is, the present invention provides an inorganic material having an average particle diameter of 2 μm or less and a Mohs hardness of 5 or more obtained by dry mixing in the presence of an aromatic carboxylic acid and/or a silicone dispersion force of 1 under conditions of an impact value of 10 or more. The present invention provides a magnetic recording medium having a magnetic layer containing powder and magnetic powder.
本発明の実施に当り用いられる親油基を有する分散剤を
強固に圧着せしめた無機質粉末は例えば安息香酸、トル
イル酸、ジエチルベンゼンカルボン酸、エチルベンゼン
カルボン酸、ジエチルベンゼンカルボン酸、フタル酸、
インフタル酸、テレフタル酸、ナフトエ酸、ケイ皮酸等
の芳香族カルボン酸、メチルシリコーンオイル、メチル
ハイドロジエンシリコーンオイル、メチルフェニルシリ
コーンオイル、脂肪酸変性シリコーンオイル、アルキル
変性シリコーンオイル、ポリオキシアルキレン変性シリ
コーンオイル等のシリコーンオイル等の分散剤と無機質
粉末とを無機′へ粉末100重1部当り0、O1〜20
重耽部、好ましくは0,02〜l O@tRx部の割合
の混合物をIG以t、好ましくは3〜15Gの粉砕又は
摩砕条件下に混合することによって製造される。Examples of inorganic powders to which a dispersant having a lipophilic group is firmly attached are used in carrying out the present invention, such as benzoic acid, toluic acid, diethylbenzenecarboxylic acid, ethylbenzenecarboxylic acid, diethylbenzenecarboxylic acid, phthalic acid,
Aromatic carboxylic acids such as inphthalic acid, terephthalic acid, naphthoic acid, and cinnamic acid, methyl silicone oil, methylhydrodiene silicone oil, methylphenyl silicone oil, fatty acid-modified silicone oil, alkyl-modified silicone oil, polyoxyalkylene-modified silicone oil A dispersant such as silicone oil and an inorganic powder are converted into an inorganic powder of 0.0, O1 to 20 per part of 100 weight of powder.
It is produced by mixing a mixture in proportions of 0.02 to 1 O@tRx parts under grinding or milling conditions of less than IG, preferably 3 to 15 G.
特に好;Eしくは安息香酸、トルイル酸等の芳香族カル
ボン酸、メチルシリコーンオイル、メチルハイドロジエ
ンシリコーンオイル、メチルフェニルシリコーンオイル
、11811/j酸変性シリコーンオイル等のシリコー
ンオイルが挙げられる。Particularly preferred are aromatic carboxylic acids such as benzoic acid and toluic acid, and silicone oils such as methyl silicone oil, methyl hydrogen silicone oil, methylphenyl silicone oil, and 11811/j acid-modified silicone oil.
分散剤が芳香族カルボン酸及び/又はシリコーン以外の
ドデカン酸ナトリウム、ンルビタンモノドデカネートの
場合にはトルエン又はトルエン含有溶媒に対する分散性
の改良効果が僅かであり好ましくない。When the dispersant is sodium dodecanoate or nrubitan monododecanate other than aromatic carboxylic acid and/or silicone, the effect of improving dispersibility in toluene or a toluene-containing solvent is small and is not preferred.
分散剤の使用割合が0.011重部より少なくなると分
散性の改簿効果が僅かとなり好ましくない。一方、上限
は経済性を考慮して決められる。If the proportion of the dispersant used is less than 0.011 parts by weight, the effect of changing the dispersibility will be small, which is not preferable. On the other hand, the upper limit is determined in consideration of economic efficiency.
無機質粉末としては例えばr−アルミナ。An example of the inorganic powder is r-alumina.
α−アルミナ、シリカ、酸化鉄、酸化クロム、酸化ヂタ
ン、酸化ジルコニウム、酸化セリウム、酸化スズ、炭化
ケイ素、スピネル等のモース硬度が5以上のものが適用
され、これより、モース硬度が小さくなると補強剤とし
て好ましくなくなる。α-Alumina, silica, iron oxide, chromium oxide, titanium oxide, zirconium oxide, cerium oxide, tin oxide, silicon carbide, spinel, etc. with a Mohs hardness of 5 or more are used, and if the Mohs hardness is smaller than this, reinforcement is applied. It becomes undesirable as an agent.
また、該無機質粉末の粒子径は平均粒子径2μm以下が
必須であり好ましくは1.5μm以下であることが望ま
しく、2μmより粒子径が大になると磁気ヘッドの耐摩
耗性が著しく低下するようになるので好ましくない。Further, the particle size of the inorganic powder must be 2 μm or less in average particle size, preferably 1.5 μm or less. This is not desirable.
本発明の補強材は無機質粉末の表面にトルエン系溶媒に
対して親和性を有する分散剤が厚く強固に圧着されてい
るため、良好な分、散性を有し、有機溶媒中特にトルエ
ンに対して又は重合体中への分散性に優れた補強材とな
るという利点がある。The reinforcing material of the present invention has a thick and firmly bonded dispersant having an affinity for toluene-based solvents on the surface of the inorganic powder, so it has good dispersibility and is particularly resistant to toluene in organic solvents. It has the advantage that it becomes a reinforcing material with excellent dispersibility in polymers.
本発明の補強材の磁性粉に対する添加割合は一般に?、
l〜41号重蔽%、好ましくは0.5〜lO重龍%、で
感服される。補強材の添加割合が0.1重量%より少な
くなると磁性層の耐摩耗性が低下するようになり、一方
15重量%以tになると磁気ヘッドの¥耗が大となるの
で好ましくない。In general, what is the addition ratio of the reinforcing material of the present invention to the magnetic powder? ,
1 to 41%, preferably 0.5 to 10%. If the proportion of the reinforcing material added is less than 0.1% by weight, the wear resistance of the magnetic layer will decrease, while if it exceeds 15% by weight, the wear of the magnetic head will increase, which is not preferable.
本発明に用いられる磁性体としては公知の磁性材料、例
えばI Fe2O3、FegO,、Co −含有γ−F
e、、01 、還元鉄粉、Cr 02 が任意に用いら
れる。粒子径は特に限定的ではないが、一般に001〜
5μmの範囲のものが用いられる。The magnetic material used in the present invention may be a known magnetic material such as I Fe2O3, FegO, Co-containing γ-F.
e,,01, reduced iron powder, and Cr02 are optionally used. The particle size is not particularly limited, but generally 001~
A thickness in the range of 5 μm is used.
本発明に用いられるバインダーは、例えば熱iiJ塑性
樹脂、熱硬化性樹脂あるいはこれらのγ[i1合物など
である。このようなバインダーとしては例えばエポキシ
樹脂、ポリウレタンi、■脂、尿素1’J脂、ポリアミ
ド樹脂、シリコン1”jJ l脂、ポリエステル樹脂、
フェノール樹脂、尿素ホルムアルデヒド樹脂、ビニル樹
脂、セルロース誘導体、アクリル酸又はメタクリル酸の
重合体もしくはこれらの共重合体、アルキッド樹脂等の
弔独又は混合物が挙げられる。The binder used in the present invention is, for example, a thermal iiJ plastic resin, a thermosetting resin, or a γ[i1 compound thereof. Examples of such binders include epoxy resin, polyurethane resin, urea resin, polyamide resin, silicone resin, polyester resin,
Examples include phenol resins, urea formaldehyde resins, vinyl resins, cellulose derivatives, acrylic acid or methacrylic acid polymers or copolymers thereof, alkyd resins, and mixtures thereof.
以下に本発明を更に詳細に説明するために実施例を示す
が、本発明はその要旨をこえない限り以下の実施例に限
定されるものではない。Examples are shown below to explain the present invention in more detail, but the present invention is not limited to the following examples unless the gist of the invention is exceeded.
実施例1
0.6μmの平均−次粒子径を有するα−アルミナ粒子
toof及び分散剤P−)ルイル酸l?を84の内容積
を有する振動ミル(衝撃値=6G)に仕込み、20分間
粉砕混合した。Example 1 α-alumina particles toof having an average particle size of 0.6 μm and dispersant P-) Ruylic acid l? was charged into a vibrating mill (impact value = 6G) having an internal volume of 84 mm, and pulverized and mixed for 20 minutes.
このようにして得られた易分散性アルミナ粉末とド、−
7Eエレク・10 rslとを試験管(高さ10crn
)に仕込み、5分間振盪した。The easily dispersible alumina powder thus obtained and
7E Elec・10 rsl and test tube (height 10crn
) and shaken for 5 minutes.
次いで超音波分散処理を行なった後、静置し、24時間
放置後の沈降高さを測定した。その結果、沈降高さは8
.7 cmであった。Next, after performing an ultrasonic dispersion treatment, it was allowed to stand still, and the sedimentation height was measured after standing for 24 hours. As a result, the sedimentation height was 8
.. It was 7 cm.
以1のようにして製造したアルミナを用いて下記の如き
屯都、配合比で磁性塗料を製作した。Magnetic paints were produced using the alumina produced as described in 1 above, with the following tunities and compounding ratios.
強磁性酸化鉄 100重計部
前記アルミナ 5 “
ビニライトVYHH15u
(米国、U、C,C社製商品名)
ポリウレタンプレポリマー 5 〃
カーボンブラック 5 “
ステアリン酸−n−ブチル l 〃
流動パラフィン 0,2〃
メチルエチIレケトン lOθ “
ト ル エ ン 100 N
t記磁性塗料をボールミルで20時時
間分散処理した後、厚さ20μmのポリスチルベースフ
ィルムLに乾燥厚さが6となるように塗布乾燥し、所定
の幅に切しtこ。Ferromagnetic iron oxide 100 weight scale Alumina 5 Vinyrite VYHH15u (trade name manufactured by U, C, C, USA) Polyurethane prepolymer 5 Carbon black 5 n-butyl stearate l Liquid paraffin 0,2 Methyl ethyl I reketone lOθ "Toluene 100 Nt" After dispersing the magnetic paint in a ball mill for 20 hours, it was coated on a 20 μm thick polystyrene base film L to a dry thickness of 6, dried, and coated to a specified thickness. Cut it to the width of t.
比較例1
実施例1の磁性塗料組成物においてア
ミナを分散剤と共に粉砕していないα−ルミナ粒子に代
えた以外は、実施例1とく同一にして磁気テープをつく
った。Comparative Example 1 A magnetic tape was prepared in the same manner as in Example 1 except that the amine in the magnetic coating composition of Example 1 was replaced with unpulverized α-lumina particles together with the dispersant.
以tのようにして製造された磁気チー
をビデオテープレコーダーに装填してスール特性を測定
した。また磁気テープを磁気ヘッドの摩耗量を測定した
。The magnetic chip manufactured as described below was loaded into a video tape recorder, and the Soul characteristics were measured. The amount of wear on the magnetic head of the magnetic tape was also measured.
また、テープ表面を表面粗さ計で測定し中心線平均粗さ
をめた。In addition, the tape surface was measured with a surface roughness meter to determine the center line average roughness.
その結果を第1表に示す。The results are shown in Table 1.
第 1 表
混
工
μm 丈
断 辻
実施例2
ル 0.4μmの平均−成粒J″−径を有する酸化ア
全
ル11を3eの内容積を有する振動ミルプ (衝撃値=
6G)に仕込み、20分間粉砕チ 混合した。Table 1 Mixing process μm Length Tsuji Example 2 All oxide aluminum 11 having an average granulation J″ diameter of 0.4 μm was mixed with a vibrating mill having an internal volume of 3e (impact value =
6G) and ground and mixed for 20 minutes.
このようにして得られた易分散性酸化クロすると、沈降
高さは9.6 cmであった。The easily dispersible oxidized chloride thus obtained had a sedimentation height of 9.6 cm.
以とのようにして製造した酸化クロムを用いて下記の如
き市H1配合比で磁袢塗料を製作した。Using the chromium oxide produced as described above, a porcelain paint was produced with the following Ichi H1 blending ratio.
強磁性酸化鉄 ioo重量部
前記酸化クロム 7 〃
ポリウレタンプレポリマー 5 〃
カーボンブラック 5 〃
ステアリン酸−n−ブチル l #
流動パラフィン 02〃
メチルエチルケトン 100 〃
ト ル エ ン 100 〃
ト記磁性塗料をボールミルで20時間混合分散処理した
後厚さ20μmのポリエステルベースフィルムトに乾燥
厚さが6μmとなるように塗布乾燥し、所定の幅に切断
した。Ferromagnetic iron oxide ioo parts by weight Chromium oxide 7 Polyurethane prepolymer 5 Carbon black 5 N-butyl stearate 1 # Liquid paraffin 02 Methyl ethyl ketone 100 Toluene 100 20% of the magnetic paint was prepared using a ball mill. After time mixing and dispersion treatment, the mixture was coated on a polyester base film having a thickness of 20 μm and dried to a dry thickness of 6 μm, and cut into a predetermined width.
比較例2
実施例2の磁性塗料組成物において酸化クロムを分散剤
と共に粉砕していない酸化クロム粒子に代えた以外は、
実施例−2と全く同一にして磁気テープをつくった。Comparative Example 2 The magnetic coating composition of Example 2 except that chromium oxide was replaced with unpulverized chromium oxide particles together with a dispersant.
A magnetic tape was made in exactly the same manner as in Example-2.
以上のようにして製造された磁気テープを実施例1と同
一の条件でスチール特性、ヘッド摩耗量および中心線平
均粗さを測定した。The steel properties, head wear amount, and centerline average roughness of the magnetic tape manufactured as described above were measured under the same conditions as in Example 1.
その結果を第2表に示す。The results are shown in Table 2.
第2表
以とから本発明の補強材は分散性に優れ、しかも、この
補強剤を用いて作られたテープは磁性層の耐閉耗性番ビ
優れ、磁気ヘッドの摩耗抑制作用が改善されテープの表
面平滑性が改善されることが明らかである。From Table 2 onwards, it is clear that the reinforcing material of the present invention has excellent dispersibility, and tapes made using this reinforcing material have excellent abrasion resistance of the magnetic layer and improved wear-suppressing effect on the magnetic head. It is clear that the surface smoothness of the tape is improved.
Claims (1)
に衝撃値がIG以tの条件下に乾式混合して得られた平
均粒子径2μm以下及びモース硬度5以上の無機質粉末
と磁性粉とが含まれてなる磁性層を有する磁気韻1if
+ν体。Contains an inorganic powder and magnetic powder with an average particle diameter of 2 μm or less and a Mohs hardness of 5 or more obtained by dry mixing in the presence of an aromatic carboxylic acid and/or a silicone dispersant under conditions with an impact value of IG or less. A magnetic rhombus 1if having a magnetic layer consisting of
+ν body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58139067A JPS6029932A (en) | 1983-07-28 | 1983-07-28 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58139067A JPS6029932A (en) | 1983-07-28 | 1983-07-28 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6029932A true JPS6029932A (en) | 1985-02-15 |
Family
ID=15236720
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58139067A Pending JPS6029932A (en) | 1983-07-28 | 1983-07-28 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6029932A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6342025A (en) * | 1986-08-05 | 1988-02-23 | Fuji Photo Film Co Ltd | Magnetic recording medium |
JP2010049738A (en) * | 2008-08-21 | 2010-03-04 | Fujifilm Corp | Composition, magnetic recording medium, and method for manufacturing the same |
-
1983
- 1983-07-28 JP JP58139067A patent/JPS6029932A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6342025A (en) * | 1986-08-05 | 1988-02-23 | Fuji Photo Film Co Ltd | Magnetic recording medium |
US4885208A (en) * | 1986-08-05 | 1989-12-05 | Fuji Photo Film Co., Ltd. | Magnetic recording medium |
JP2010049738A (en) * | 2008-08-21 | 2010-03-04 | Fujifilm Corp | Composition, magnetic recording medium, and method for manufacturing the same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS61104427A (en) | Magnetic recording medium | |
GB2080319A (en) | Magnetic recording medium | |
JPS6029932A (en) | Magnetic recording medium | |
JPS621117A (en) | Magnetic recording medium | |
JPH0610863B2 (en) | Magnetic recording medium | |
JP3380911B2 (en) | Magnetic recording media | |
JPS5982630A (en) | Magnetic recording medium | |
JP2828248B2 (en) | Magnetic recording media | |
JPH11279231A (en) | Vinyl chloride-based copolymer and resin composition for magnetic recording | |
JPH0536059A (en) | Magnetic recording medium | |
JPH0877546A (en) | Magnetic recording medium and its production | |
JPS62219327A (en) | Solid additive for magnetic recording medium and magnetic recording medium using such additive | |
JPS6168728A (en) | Magnetic recording medium | |
JPH0235627A (en) | Magnetic recording medium | |
JPH02133475A (en) | Film reinforcing agent | |
JPH02260226A (en) | Magnetic recording medium | |
JPH01256019A (en) | Magnetic recording medium | |
JPS6226626A (en) | Magnetic recording medium | |
JPH04248119A (en) | Magnetic recording medium | |
JPS60263325A (en) | Magnetic recording medium | |
JPH0383220A (en) | Magnetic recording medium | |
JPS60246020A (en) | Magnetic recording medium | |
JPH02260119A (en) | Magnetic recording medium and abrasive used for this medium | |
JPS5984347A (en) | Magnetic recording medium | |
JPS62185235A (en) | Magnetic recording medium |