JPS6032887B2 - magnetic recording medium - Google Patents
magnetic recording mediumInfo
- Publication number
- JPS6032887B2 JPS6032887B2 JP5551678A JP5551678A JPS6032887B2 JP S6032887 B2 JPS6032887 B2 JP S6032887B2 JP 5551678 A JP5551678 A JP 5551678A JP 5551678 A JP5551678 A JP 5551678A JP S6032887 B2 JPS6032887 B2 JP S6032887B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- weight
- magnetic recording
- recording medium
- surfactant
- 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.)
- Expired
Links
- 230000005291 magnetic effect Effects 0.000 title claims description 23
- 239000004094 surface-active agent Substances 0.000 claims description 21
- 150000005215 alkyl ethers Chemical class 0.000 claims description 14
- -1 sorbitan ester Chemical class 0.000 claims description 14
- 239000011230 binding agent Substances 0.000 claims description 11
- 239000006247 magnetic powder Substances 0.000 claims description 10
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 4
- 229920005749 polyurethane resin Polymers 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 238000004898 kneading Methods 0.000 claims description 2
- 239000003973 paint Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 230000005611 electricity Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000003068 static effect Effects 0.000 description 6
- 239000000843 powder Substances 0.000 description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000012190 activator Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- CSPVUHYZUZZRGF-RNFRBKRXSA-N (4R,6R)-hydroxy-2,2,6-trimethylcyclohexanone Chemical compound C[C@@H]1C[C@@H](O)CC(C)(C)C1=O CSPVUHYZUZZRGF-RNFRBKRXSA-N 0.000 description 2
- 229930185327 Actinol Natural products 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 230000005294 ferromagnetic effect Effects 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- IUWCPXJTIPQGTE-UHFFFAOYSA-N chromium cobalt Chemical compound [Cr].[Co].[Co].[Co] IUWCPXJTIPQGTE-UHFFFAOYSA-N 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
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.
一般に磁気記録媒体はポリエステルベース等の高分子材
料製基体に磁性粉と高分子材料製バインダーとの混合物
である磁性塗料を塗布したものである。Generally, a magnetic recording medium is a substrate made of a polymeric material such as a polyester base coated with a magnetic paint, which is a mixture of magnetic powder and a binder made of a polymeric material.
ところで基体自体及びバインダーが絶縁物であるうえ、
使用する磁性粉も例えばrFe203、酸化クロム、コ
バルトドープ型がe203等の比較的電気抵抗の高い金
属酸化物であるため、出来上った磁気記録媒体の電気抵
抗が高くなり、そのために静電気が帯電し、これがごみ
、ほこりを吸着する原因となっていた。そこで従釆より
アニオン、カチオン、非イオン、両性系の界面活性剤が
帯電防止剤として使用されていたが、従来はこれらの帯
電防止剤を使用するのにた)、磁性粉とバインダーの混
合物に添加してそれを基体に塗布したものであった。By the way, the base itself and the binder are insulators, and
The magnetic powder used is a metal oxide with relatively high electrical resistance, such as rFe203, chromium oxide, and cobalt-doped e203, so the electrical resistance of the finished magnetic recording medium is high, which causes static electricity to build up. However, this caused dirt and dust to be absorbed. Therefore, anionic, cationic, nonionic, and amphoteric surfactants have traditionally been used as antistatic agents. It was added and applied to the substrate.
従来の磁気記録媒体の帯電防止に対する考え方は、帯電
した静電気を則放電させてしまうためには磁気記録媒体
の電気抵抗を下げるということであった。The conventional approach to preventing charging of magnetic recording media has been to lower the electrical resistance of the magnetic recording media in order to regularly discharge the static electricity that has been charged.
即ち帯電防止の手段はたゞそのものの電気抵抗を下げる
ということのみであった。そのために充分に満足いく帯
電防止効果をあげることが出来なかったのであるが、本
発明者は従来の帯電防止−電気抵抗低下という考え方を
改め、要は帯電した静電気が早くなくなれば良いのであ
るから電気抵抗という考え方にこだわる事なく、静電気
そのものをいかに早く少くするかという事を検討して見
た。その結果バインダーとしてポリウレタン樹脂で可塑
化された塩化ビニル−酢酸ビニル共重合体を使用する場
合、ポリウレタン樹脂の量を全バインダー量に対して4
の重量%以下とし、さらに界面活性剤としてアルキルヱ
ーテル型のものを用いこれらと磁性粉の混合物である磁
性塗料を基体に塗布して成る磁気記録媒体は帯電した電
荷の量が半分になる半減期が著しく小さくなるという事
を先きに見出した。In other words, the only way to prevent static electricity was to lower the electrical resistance of the material itself. For this reason, it was not possible to achieve a sufficiently satisfactory antistatic effect, but the inventor of the present invention revised the conventional concept of preventing static electricity - reducing electrical resistance, and realized that the point is that the static electricity that has been charged should be eliminated quickly. Rather than focusing on the idea of electrical resistance, we considered how to quickly reduce static electricity itself. As a result, when using vinyl chloride-vinyl acetate copolymer plasticized with polyurethane resin as a binder, the amount of polyurethane resin is 4% relative to the total amount of binder.
% by weight or less, and further uses an alkyl ether type surfactant and coats a magnetic paint, which is a mixture of these and magnetic powder, on the substrate. We have previously discovered that the size of the particle size becomes significantly smaller.
本発明者はさらに研究した結果、上記のアルキルェーテ
ル型界面活性剤と共にソルピタンヱステル型の界面活性
剤を使用するとアルキルェーテル型単独の場合よりも磁
気配向性が改善されることを見出した。As a result of further research, the inventors of the present invention found that when a sorpitan ester type surfactant is used together with the above-mentioned alkyl ether type surfactant, the magnetic orientation is improved more than when the alkyl ether type is used alone.
さらに半減期減少の効果は両活性剤の総量を一定として
或る範囲でこれら活性剤の割合を変えても変わらないこ
とが分った。さらに、これらの活性剤は酸性でないから
、高温多温の条件下でもヘッドにさびを生じたりしない
。これはァルキルェーテル型の界面活性剤の一部をりん
酸ェステル型の界面活性剤と置換して半減期を長くしな
いで配向性を改善する場合に生じうるヘッドのさびの発
生くりん酸ェステル型のものは強酸性である)の可能性
と比べて有利である。しかしながら、アルキルェーテル
型及びソルビタンェステル型の界面活性剤の添加が、磁
性粉とバインダーとに単に混合濠練りすることにより行
われるため、バインダー間の強度の劣化をある程度きた
し、磁気ヘッドとの摩擦により磁性膜の剥離粉が生じて
ヘッドに付着する。Furthermore, it has been found that the effect of reducing half-life does not change even if the ratio of these active agents is varied within a certain range, keeping the total amount of both active agents constant. Furthermore, since these activators are not acidic, they do not cause rust on the head even under high temperature conditions. This is because head rust occurs when a part of the alkyl ether type surfactant is replaced with a phosphate ester type surfactant to improve orientation without increasing the half-life. This is advantageous compared to the possibility that the substance is strongly acidic. However, since the addition of alkyl ether type and sorbitan ester type surfactants is carried out by simply mixing and kneading the magnetic powder and binder, the strength between the binders deteriorates to some extent, and friction with the magnetic head occurs. Peeling powder from the magnetic film is generated and adheres to the head.
そこで本発明はアルキルェーテル型及びソルビタンェス
テル型(ソルビタン脂肪酸ェステル、ポリオキシ脂肪酸
ェステル)の界面活性剤にて予め表面を覆った磁性粉を
用い、バインダー間の強度を低下させることなく半減期
を大幅に減少させ、同時にヘッド付着の問題を無くし、
さらには配向性を向上させ、またさびの発生を防ぎ、す
ぐれた磁気媒体を提供する。Therefore, the present invention uses magnetic powder whose surface is covered in advance with an alkyl ether type and sorbitan ester type (sorbitan fatty acid ester, polyoxy fatty acid ester) surfactant, thereby greatly increasing the half-life without reducing the strength between the binders. At the same time, it eliminates the problem of head adhesion.
Furthermore, it improves orientation, prevents rust, and provides an excellent magnetic medium.
尚、バインダー全量に対して4の重量%以下のポリウレ
タン樹脂を用いる理由は、この範囲で界面活性剤との相
乗的な半減期減少の効果が達成できるからである。The reason why the polyurethane resin is used in an amount of 4% by weight or less based on the total amount of the binder is that a synergistic half-life reduction effect with the surfactant can be achieved within this range.
この範囲を超えると、半減期は急激に増大する。以下実
施例に関連して本発明を具体的に述べる。Beyond this range, the half-life increases rapidly. The present invention will be specifically described below with reference to Examples.
実施例 1
rFe203 10の重量
部アルキルヱーテル型界面活性剤(日本乳化剤■のNe
比oilolo) 1.8〃ソルビタンェステル
型界面活性剤(松本製薬■のシルバーS−80)
1.2〃水 1000
〃を良く混合し、磁性粉の表面に界面活性剤を吸着させ
た後、それを加熱乾燥した。Example 1 rFe203 10 parts by weight of an alkyl ether type surfactant (Ne of Nippon Nyukazai ■)
1.8 Sorbitan ester type surfactant (Silver S-80 from Matsumoto Pharmaceutical ■)
1.2 Water 1000
After mixing well and adsorbing the surfactant on the surface of the magnetic powder, it was heated and dried.
このようにして帯電防止処理した強磁性粉末を01
‘21
rFe203 10の重量部 10の雲
量部熱可塑性ポリウレタン樹脂4.5 〃 12 〃
(グッドリッチ社のェステン5701)
塩化ビニルー酢酸ピニル共重合体
25.5 〃 18 〃
なる2種の配合でバインダー及び溶剤と共に分散機で分
散させ、その磁性塗料をポリエステルベースに塗布した
。The ferromagnetic powder subjected to antistatic treatment in this way is
'21 rFe203 10 parts by weight 10 parts by weight Thermoplastic polyurethane resin 4.5 〃 12 〃 (Goodrich Esten 5701) Vinyl chloride-pinyl acetate copolymer 25.5 〃 18 〃 Binder and It was dispersed with a solvent using a dispersion machine, and the magnetic paint was applied to a polyester base.
諸特性の測定結果は表に示した通りであった。実施例
2
rFe203 10の重量
部アルキルェーテル型界面活性剤 2〃(松本
製薬■のアクチノールRIOO)ポリオキシエチレンソ
ルビタンエステル 1″(松本製薬■のT一80)M旧
K IOOO
〃なる配合物を良く混合して表面処理を行い乾燥した。The measurement results of various characteristics were as shown in the table. Example
2 rFe203 10 parts by weight Alkyl ether type surfactant 2 (actinol RIOO from Matsumoto Pharmaceutical ■) Polyoxyethylene sorbitan ester 1'' (T-80 from Matsumoto Pharmaceutical ■) M old K IOOO
The mixture was thoroughly mixed, surface treated, and dried.
このように処理した磁性粉を‘11 ‘21
rFe203 10の重量部 10の重
量部熱可塑性ポリウレタン樹脂4.5 〃 12
〃
(エステン5701)
塩化ビニル−酢酸ビニル共重合体
25.5 〃 18 〃
なる2種の配合で磁性塗料を作り、磁気記録媒体を製造
した。The magnetic powder treated in this way was prepared by adding: '11 '21 rFe203 10 parts by weight Thermoplastic polyurethane resin 4.5 〃 12
(Esten 5701) Vinyl chloride-vinyl acetate copolymer 25.5 and 18 Magnetic paints were made with two types of compositions, and magnetic recording media were manufactured.
測定結果を下の表に示す。比較例 1
比較のため、磁性粉の前処理を行わないで直接混合によ
り磁性塗料を製造した。The measurement results are shown in the table below. Comparative Example 1 For comparison, a magnetic paint was produced by direct mixing without pre-treating the magnetic powder.
未処理の強磁性粉末を01 ‘2’
rFe203 10の重量部 10の重
量部アルキルェーテル型活性剤18 〃 1.8 〃
(Neucoilolo)
ソルビタンェステル型活性剤
12 〃 1.2 〃
(シルバS−80)
熱可塑性ポリウレタン樹脂
4.5 〃 12 〃
(エステン5701)
塩化ビニルー酢酸ビニル共重合体22.5〃 18〃な
る2つの配合で混練りして磁性塗料を作り、ベースに塗
布した。Untreated ferromagnetic powder 01 '2' rFe203 10 parts by weight 10 parts by weight Alkyl ether type activator 18 〃 1.8 〃 (Neucoilolo) Sorbitan ester type activator 12 〃 1.2 〃 (Silva S-80 ) Thermoplastic polyurethane resin 4.5 12 (Esten 5701) Vinyl chloride-vinyl acetate copolymer 22.5 18 were kneaded to make a magnetic paint, which was applied to the base.
諸特性は下の表に示す。本比較例は実施例1に対照され
る。Characteristics are shown in the table below. This comparative example is compared to Example 1.
比較例 2
○) ■
rFe203 10の重量部 10の重
量部アルキルェーテル型界面活性剤2〃2〃
(アクチノールRIOO)
ポリオキシエチレンソルビタン
1〃1〃
エステル(T−80)
熱可塑性ポリウレタン樹脂
4.5 〃 12 〃
(エステン5701)
塩化ビニル−酢酸ビニル共重合体
22.5 〃 18 〃
なる2つの配合物を混練りして磁性塗料を製造し、これ
をベースに塗布した。Comparative example 2 ○) ■ rFe203 10 parts by weight 10 parts by weight Alkyl ether type surfactant 2〃2〃 (Actinol RIOO) Polyoxyethylene sorbitan 1〃1〃 Ester (T-80) Thermoplastic polyurethane resin 4.5〃 12 〃 (Esten 5701) Vinyl chloride-vinyl acetate copolymer 22.5 〃 18 〃 Two compositions were kneaded to produce a magnetic paint, and this was applied as a base.
諸特性は下表の通りであった。表
注:ヘッド付着は肉眼により磁性塗膜の剥脱粉のヘッド
への付着を5点法で評価したものこの表から分かるよう
に、本発明の磁気記録媒体は比較例の添加物と比べると
、電気抵抗はほぼ同一であり、半減期も同様であるが、
ヘッド付着性及び配向度がいずれも改善され、機械的に
も電気的にもすぐれていることが分る。The various characteristics were as shown in the table below. Table note: Head adhesion is determined by visually evaluating the adhesion of exfoliated powder from the magnetic coating film to the head using a 5-point method.As can be seen from this table, the magnetic recording medium of the present invention has a higher Although the electrical resistance is almost the same and the half-life is similar,
It can be seen that both the head adhesion and the degree of orientation are improved, and it is excellent both mechanically and electrically.
実施例 3
実施例1においてアルキルェーテル型1.紅重量部、ソ
ルビタンヱステル型1.a重量部の割合で界面活性剤を
用いる代りに、両者の総量を3重量部とし、両者の比を
色々に変えた。Example 3 In Example 1, alkyl ether type 1. Beni weight part, sorbitan ester type 1. Instead of using a surfactant in a proportion of 1 part by weight, the total amount of both was 3 parts by weight, and the ratio of both was varied.
バインダーとの配合は実施例1の■の処方に従った。半
減期測定の結果を第1図に×で示す。同時に、前処理を
しない磁性粉100重量部、界面活性剤総量3.0重量
部、ポリウレタン(ェステン5701)IZ重量部及び
塩−酢ビ共重合体18重量部を用いた結果を第1図のo
で示した。図から分るように、アルキルェーテル型の約
5割までソルビタンェステル型と置換しても効果は変わ
らない。また添加型よりも半減期がやや短い。置換によ
り半減期が変わらないことは配向性及びヘッド付着の点
で重要である。即ち本例中アルキルェーテル型3.の重
量部を用いた場合にはヘッド付着が悪く、配向性も悪い
が、置換によりこれらを向上させることができる。なお
ソルビタンェステル型の界面活性剤はりん酸ェステル型
のもの(同様な効果をもつ)等の酸性の強い界面活性剤
とちがつてへッド‘こ対する腐蝕性を有さないから、こ
の点でも有利である。The formulation with the binder followed the recipe (2) of Example 1. The results of half-life measurements are shown in FIG. 1 with an x. At the same time, the results using 100 parts by weight of magnetic powder without pretreatment, 3.0 parts by weight of total surfactant, parts by weight of polyurethane (Esten 5701) IZ, and 18 parts by weight of salt-vinyl acetate copolymer are shown in Figure 1. o
It was shown in As can be seen from the figure, the effect remains unchanged even if approximately 50% of the alkyl ether type is replaced with the sorbitan ester type. It also has a slightly shorter half-life than the additive type. It is important from the viewpoint of orientation and head adhesion that the half-life remains unchanged upon substitution. That is, in this example, alkyl ether type 3. When using a weight part of 1, the adhesion to the head is poor and the orientation is poor, but these can be improved by substitution. Note that sorbitan ester type surfactants do not have corrosive properties against heads, unlike strongly acidic surfactants such as phosphate ester type surfactants (which have similar effects). It is also advantageous in that respect.
第1図は界面活性剤の半減期に及ぼす効果を示す図であ
る。
第1図FIG. 1 is a diagram showing the effect of surfactants on half-life. Figure 1
Claims (1)
タン樹脂で可塑化された塩化ビニル−酢酸ビニル共重合
体と、アルキルエーテル型及びソルビタンエステル型の
界面活性剤(ソルビタンエステル型は界面活性剤の全量
に対して50%以下)で表面を予め覆つた磁性粉とを混
練りした磁性塗料を基体に塗布して成る磁気記録媒体。1 Vinyl chloride-vinyl acetate copolymer plasticized with polyurethane resin in an amount of 40% by weight or less based on the total amount of the binder, and an alkyl ether type and sorbitan ester type surfactant (sorbitan ester type is included in the total amount of the surfactant). A magnetic recording medium is a magnetic recording medium formed by coating a substrate with a magnetic coating material, which is prepared by kneading magnetic powder, the surface of which has been previously covered with 50% or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5551678A JPS6032887B2 (en) | 1978-05-12 | 1978-05-12 | magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5551678A JPS6032887B2 (en) | 1978-05-12 | 1978-05-12 | magnetic recording medium |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54147816A JPS54147816A (en) | 1979-11-19 |
| JPS6032887B2 true JPS6032887B2 (en) | 1985-07-31 |
Family
ID=13000852
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5551678A Expired JPS6032887B2 (en) | 1978-05-12 | 1978-05-12 | magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6032887B2 (en) |
-
1978
- 1978-05-12 JP JP5551678A patent/JPS6032887B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54147816A (en) | 1979-11-19 |
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