JPS5843813B2 - magnetic recording medium - Google Patents
magnetic recording mediumInfo
- Publication number
- JPS5843813B2 JPS5843813B2 JP5551378A JP5551378A JPS5843813B2 JP S5843813 B2 JPS5843813 B2 JP S5843813B2 JP 5551378 A JP5551378 A JP 5551378A JP 5551378 A JP5551378 A JP 5551378A JP S5843813 B2 JPS5843813 B2 JP S5843813B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic recording
- weight
- recording medium
- type surfactant
- alkyl ether
- 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
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.
ところが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γFe2O3、酸化クロム、コ
バルトドープ型、γFe2O3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、はこりを吸着する原因となっていた。However, the base itself and the binder are insulating materials, and
The magnetic powder used is also a metal oxide with relatively high electrical resistance, such as γFe2O3, chromium oxide, cobalt-doped type, γFe2O3, etc., 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.
そこで従来よりアニオン、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g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。Therefore, anionic, cationic, nonionic, and amphoteric surfactants have traditionally been used as antistatic agents. It was then 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
した静電気を即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 immediately discharge the static electricity that has been charged.
即ち帯電防止の手段はたgそのものの電気抵抗を下げる
ということのみであった。That is, the only means to prevent static electricity was to lower the electrical resistance of the tag itself.
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。For this reason, it was not possible to achieve a sufficiently satisfactory antistatic effect, but the inventors of the present invention have developed a conventional antistatic effect.
We changed the idea of reducing electrical resistance, and instead of focusing on the concept of electrical resistance, since the point is that the static electricity that has been charged should disappear as quickly as possible, we considered how to reduce the static electricity itself as quickly as possible.
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40重
量%以下とし、さらに界面活性剤としてアルキルエーテ
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戒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。As a result, when using vinyl chloride-vinyl acetate copolymer plasticized with polyurethane resin as a binder,
Magnetic recording is achieved by keeping the amount of polyurethane resin at 40% by weight or less based on the total amount of binder, using an alkyl ether type surfactant, and applying a magnetic paint, which is a mixture of these and magnetic powder, to the substrate. It was previously discovered that the half-life of a medium, during which the amount of charge charged thereon is halved, is significantly shortened.
本発明者はさらに研究をした結果、上記のアルキルエー
テル型界面活性剤と共にりん酸エステル型界面活性剤を
使用すると、アルキルエーテル単独の場合よりも磁気特
性(配向性)が改善されることを見出した。As a result of further research, the present inventor found that when a phosphate ester type surfactant is used together with the above alkyl ether type surfactant, the magnetic properties (orientation) are improved compared to the case of alkyl ether alone. Ta.
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
成る範囲でこれら活性剤の割合を変えても変わらないこ
とを見出した。Furthermore, it has been found that the effect of decreasing the half-life does not change even if the ratio of these active agents is changed within a range where the total amount of both active agents is constant.
アルキルエーテル型活性剤の添加効果は3重量部(後記
実施例における配合物のような組成に対し)以上で急激
に大きくなるが、同じ程度の半減期の減少はこの活性剤
の約5割程度までりん酸エステル型界面活性剤で置換し
ても得られる。The effect of adding an alkyl ether type activator becomes sharply greater at 3 parts by weight or more (for a composition such as the formulation in the example below), but the same degree of decrease in half-life is about 50% for this activator. It can also be obtained by replacing it with a phosphate ester type surfactant.
しかも、上記のようにりん酸エステル型界面活性剤の添
加は磁気配向性を向上させることになりすぐれた磁気記
録媒体を提供することになる。Moreover, as mentioned above, the addition of a phosphate ester type surfactant improves the magnetic orientation, thereby providing an excellent magnetic recording medium.
尚、ポリウレタン樹脂の含有量を全バインダーに対して
約40重量%以下の割合で用いるのは、界面活性剤との
相乗作用によりこの範囲で半減期が大幅に減じるからで
ある。The reason why the polyurethane resin content is about 40% by weight or less based on the total binder is that the half-life is significantly reduced in this range due to synergistic action with the surfactant.
ポリウレタン樹脂の量が約40重量%を超えると半減期
が大きくなり好ましくない。If the amount of polyurethane resin exceeds about 40% by weight, the half-life will be undesirably large.
以下実施例に関して本発明を具体的に説明する。The present invention will be specifically described below with reference to Examples.
実施例 1
γFe2O3
100重量部
熱可塑性ポリウレタン樹脂 X
(グツドリッチ社のニステ
ン5701 ) 30 //塩
化ビニルー酢酸ビニル共 y
重合体
★
1アルキル工−テル型界面活
性剤
(日本乳化剤(株)の
Neucol 1010 )
1.8重量部
C9H1oOHのりん酸ニス 1.2〃チル
ただしx+y=30重量部一定とし、Xはバインダー全
量に対して10.20.30.40及び50%(3〜1
5重量部)とした。Example 1 γFe2O3 100 parts by weight Thermoplastic polyurethane resin 1.8 parts by weight C9H1oOH phosphoric acid varnish 1.2 chilled. However, x + y = 30 parts by weight constant, and X is 10, 20, 30, 40 and 50% (3 to 1
5 parts by weight).
上記の5種の組成物をそれぞれボールミル中で混合し、
常法に従ってポリエステルベースに塗布して磁気記録媒
体を製作した。Mixing the above five types of compositions in a ball mill,
A magnetic recording medium was fabricated by applying it to a polyester base according to a conventional method.
その緒特性は第1表に示した。比較例
実施例1において、アルキルエーテル型活性剤を3重量
部用い、りん酸エステル型活性剤を用いないで5種の磁
気記録媒体を製造した。Its initial characteristics are shown in Table 1. Comparative Example In Example 1, five types of magnetic recording media were manufactured using 3 parts by weight of an alkyl ether type activator and without using a phosphate ester type activator.
その結果を第1表に示す。The results are shown in Table 1.
第1表から先ず分ることは、ポリウレタン含有率が40
%以下で半減期が非常に短かくなることである。The first thing that can be seen from Table 1 is that the polyurethane content is 40
% or less, the half-life becomes extremely short.
従って本発明は全バインダーに対するポリウレタン含有
率40%以下のものを用いる。Therefore, in the present invention, a polyurethane content of 40% or less based on the total binder is used.
次に電気抵抗はアルキルエーテル型活性剤3重量部の場
合(比較例)とその一部を1.2重量部りん酸エステル
型活性剤で置換した場合とでほとんど差がなく、また半
減期にもほとんど差がないことが分る。Next, there is almost no difference in electrical resistance between 3 parts by weight of alkyl ether type activator (comparative example) and when a part of it is replaced with 1.2 parts by weight of phosphate ester type activator. It can be seen that there is almost no difference.
従ってりん酸エステル型界面活性剤もアルキルエーテル
型と同様な半減期減少の効果を有することが理解できる
。Therefore, it can be understood that phosphate ester type surfactants also have the same half-life decreasing effect as alkyl ether type surfactants.
ただし置換には限界があることは後で説明する。However, it will be explained later that there are limits to substitution.
最後に、本発明によるときは磁気配向性が相当に向上し
、比較例に比してすぐれた磁気記録媒体が提供できたこ
とが分る。Finally, it can be seen that in the case of the present invention, the magnetic orientation was considerably improved, and a magnetic recording medium superior to that of the comparative example could be provided.
実施例 2
アルキルエーテル型界面活性剤の一部をりん酸エステル
型界面活性剤と置換した場合の効果を見るために
γFe2O3
100重量部
熱可塑性ポリウレタン樹脂 12.0 〃(ニ
ステン5701)
塩化ビニル
重合体
酢酸ビニル共
18.0
アルキルエーテル型界面活 k
性剤
(日本乳化剤(株)の
Neucol 1010 ) 3.0
重量部C9H190Hのりん酸ニス l
チル
の配合物(ただしに+1=3.0重量部)をに、 1を
変えて数種調製し、実施例1と同様にして磁気記録媒体
を製造した。Example 2 To see the effect of replacing a part of the alkyl ether type surfactant with a phosphate ester type surfactant, γFe2O3 100 parts by weight Thermoplastic polyurethane resin 12.0 (Nysten 5701) Vinyl chloride polymer Vinyl acetate co-18.0 Alkyl ether type surfactant (Neucol 1010 from Nippon Nyukazai Co., Ltd.) 3.0
Several types of mixtures of varnish phosphate having a weight part of C9H190H (+1=3.0 parts by weight) were prepared by changing 1, and magnetic recording media were manufactured in the same manner as in Example 1.
半減期を第1図に示した。同図から分るようにアルキル
エーテル型界面活性剤は単独で3重量部存在すれば充分
に短い半減期(約10秒以下)を有するが、しかし約1
.5重量部までのりん酸エステル型界面活性剤で置換し
ても半減期は十分に短いことが分る。The half-life is shown in Figure 1. As can be seen from the figure, the alkyl ether type surfactant has a sufficiently short half-life (approximately 10 seconds or less) when present alone in 3 parts by weight;
.. It can be seen that even when replaced with up to 5 parts by weight of a phosphate ester type surfactant, the half-life is sufficiently short.
一方、実施例1で示されたように配向性は一部置換によ
り改善されるのである。On the other hand, as shown in Example 1, the orientation can be improved by partial substitution.
実施例 3
rrFe203
ioo重量部
熱可塑性ポリウレタン樹脂
(ニステン5701 )
2
塩化ビニル−酢酸ビニル共重合
体
8
アルキルエーテル型界面活性剤
(日本乳化剤(株)のNeucol
lolo)
C15H27→ζ=二)OHのり l t
tん酸エステル
上記組成物を実施例1と同様にして磁気記録媒体を製造
した。Example 3 rrFe203 ioo parts by weight Thermoplastic polyurethane resin (Nysten 5701) 2 Vinyl chloride-vinyl acetate copolymer 8 Alkyl ether type surfactant (Neucol lolo from Nippon Nyukazai Co., Ltd.) C15H27→ζ=2)OH glue l t
Tonic acid ester A magnetic recording medium was produced using the above composition in the same manner as in Example 1.
その結果を第2表に示す。尚、実施例2におけるに=3
.0(アルキルエーテル3.0重量部)のものを比較例
として挙げた。The results are shown in Table 2. In addition, in Example 2 = 3
.. 0 (alkyl ether 3.0 parts by weight) was used as a comparative example.
第2表の結果はりん酸エステル型活性剤の置換により配
向性が改善されることを示している。The results in Table 2 show that substitution of the phosphate ester type activator improves orientation.
第1図は本発明の磁気記録媒体の半減期に対するアルキ
ルエーテル型及びりん酸エステル型界面活性剤の添加の
効果を示すグラフである。FIG. 1 is a graph showing the effect of the addition of alkyl ether type and phosphate ester type surfactants on the half-life of the magnetic recording medium of the present invention.
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、アルキルエーテル型の界面活性剤、りん酸エステル
型の界面活性剤、及び磁性粉を含有し、且つりん酸エス
テル型の界面活性剤を界面活性剤総量の50%以下の量
で含む磁性塗料を基体に塗布して戒る磁気記録媒体。1 Contains vinyl chloride-vinyl acetate copolymer plasticized with polyurethane resin in an amount of 40% by weight or less based on the total binder amount, an alkyl ether type surfactant, a phosphate ester type surfactant, and magnetic powder. A magnetic recording medium in which a magnetic paint containing a phosphate ester type surfactant in an amount of 50% or less of the total amount of surfactants is coated on a substrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5551378A JPS5843813B2 (en) | 1978-05-12 | 1978-05-12 | magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5551378A JPS5843813B2 (en) | 1978-05-12 | 1978-05-12 | magnetic recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS54147813A JPS54147813A (en) | 1979-11-19 |
JPS5843813B2 true JPS5843813B2 (en) | 1983-09-29 |
Family
ID=13000762
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5551378A Expired JPS5843813B2 (en) | 1978-05-12 | 1978-05-12 | magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5843813B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6043217A (en) * | 1983-08-19 | 1985-03-07 | Toshiba Corp | Magnetic recording medium |
-
1978
- 1978-05-12 JP JP5551378A patent/JPS5843813B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS54147813A (en) | 1979-11-19 |
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