JPS5921090B2 - Method for manufacturing magnetic recording media - Google Patents
Method for manufacturing magnetic recording mediaInfo
- Publication number
- JPS5921090B2 JPS5921090B2 JP53005001A JP500178A JPS5921090B2 JP S5921090 B2 JPS5921090 B2 JP S5921090B2 JP 53005001 A JP53005001 A JP 53005001A JP 500178 A JP500178 A JP 500178A JP S5921090 B2 JPS5921090 B2 JP S5921090B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic recording
- surfactant
- alkyl
- salts
- recording medium
- 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 21
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 238000000034 method Methods 0.000 title claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 23
- -1 alkyl sulfate salts Chemical class 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 10
- 239000006247 magnetic powder Substances 0.000 claims description 9
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003973 paint Substances 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 4
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 3
- 125000005907 alkyl ester group Chemical group 0.000 claims description 3
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 3
- 229960003237 betaine Drugs 0.000 claims description 3
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 3
- 238000004898 kneading Methods 0.000 claims description 3
- 150000005215 alkyl ethers Chemical class 0.000 claims description 2
- 125000005600 alkyl phosphonate group Chemical group 0.000 claims description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 15
- 230000005611 electricity Effects 0.000 description 6
- 230000003068 static effect Effects 0.000 description 6
- 239000000428 dust Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000007792 addition Methods 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 229910006297 γ-Fe2O3 Inorganic materials 0.000 description 2
- 238000010521 absorption reaction Methods 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
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000843 powder Substances 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)
- Manufacturing Of Magnetic Record Carriers (AREA)
Description
【発明の詳細な説明】 本発明は磁気記録媒体の製造方法に関する。[Detailed description of the invention] The present invention relates to a method for manufacturing a magnetic recording medium.
一般に磁気記録媒体はポリエステルベース等の基体に磁
性粉とバインダーの混合物である磁性塗料を塗布したも
のである。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γ−Fe2O3等の
比較的電気抵抗の高い金属酸化物であるため出来あがつ
た磁気記録媒体自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
なつている。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
ゞ磁性粉とバインダーの混合物に添加してそれを基体に
塗布したものであつた。Generally, a magnetic recording medium is a substrate such as a polyester base coated with a magnetic paint, which is a mixture of magnetic powder and a binder. However, since the substrate itself and the binder are insulators, and the magnetic powder used is also a metal oxide with relatively high electrical resistance, such as γ-Fe2O3, the electrical resistance of the resulting magnetic recording medium itself becomes high. As a result, static electricity is charged, which causes dirt and dust to be attracted. Therefore, anionic, cationic, nonionic, and amphoteric surfactants have traditionally been used as antistatic agents, but conventionally, these antistatic agents were only added to the mixture of magnetic powder and binder. 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つた。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ゞそのものの電気抵抗を下げる
ということのみであつた。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つた。そこで本発明
者は先に従来の帯電防止一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。その結果アルキルサルフェート塩、アルキルスルホ
ネート塩、アルキルホスフェート塩、第4級アンモニウ
ム塩、アミン塩、アルキルエーテル型、アルキルエステ
ル型、ゾルビタン誘導体、ベタイン型及びイミダゾリン
型の界面活性剤の少なくとも1種で表面をおゝつた磁性
粉とバインダーの混合物を基体上に塗布した磁気記録媒
体はそれに帯電した電荷が半分になる半減期が著しく小
さくなるという知見を得た。その知見にもとずき先に発
明した磁気記録媒体についてまず実施例にもとずき説明
する。実施例 1
γ−Fe2O3100重量部
アルキルサルフェート塩
界面活性剤 2.5重量部
(吉村油化社のPMX−3007)
水 1000重量部
以上の組成物をよく混合し、磁性粉の表面に界面活性剤
を吸収させた後、それを加熱乾燥した。In other words, the only means to prevent static electricity was to lower the electrical resistance of the material itself. Therefore, it was not possible to achieve a sufficiently satisfactory antistatic effect. Therefore, the inventor of the present invention first revised the conventional idea of preventing static electricity by 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 quickly, the inventors of the present invention focused on how to reduce the static electricity itself as quickly as possible. I thought about this. As a result, the surface was coated with at least one of alkyl sulfate salts, alkyl sulfonate salts, alkyl phosphate salts, quaternary ammonium salts, amine salts, alkyl ether type, alkyl ester type, sorbitan derivatives, betaine type and imidazoline type surfactants. We have found that a magnetic recording medium coated with a mixture of magnetic powder and binder on a substrate has a significantly shorter half-life, in which the electric charge on the medium is halved. Based on this knowledge, the previously invented magnetic recording medium will first be described based on examples. Example 1 100 parts by weight of γ-Fe2O3 2.5 parts by weight of alkyl sulfate salt surfactant (PMX-3007 manufactured by Yoshimura Yuka Co., Ltd.) A composition containing 1000 parts by weight or more of water was thoroughly mixed, and the surfactant was applied to the surface of magnetic powder. After absorption, 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バ・ イ
ンター、溶剤と共にボールミル中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て磁気記録媒体とした
。その試料を1−Aとし、界面活性剤を直接磁性粉と共
にバインダー中で分散して作つた試料を1−Bとし、そ
の両者の特性を表1に示す。実施例
以上の組成により実施例1と同様に試料2−A,2−B
を作つた。The ferromagnetic powder thus antistatically treated was dispersed in a ball mill together with a binder and a solvent, and the resulting magnetic paint was applied to a polyester base to obtain a magnetic recording medium. The sample was designated as 1-A, and the sample prepared by directly dispersing the surfactant together with magnetic powder in a binder was designated as 1-B. Table 1 shows the characteristics of both. Samples 2-A and 2-B were prepared in the same manner as in Example 1 with the compositions above.
I made it.
その結果を表2に示す。実施例
以上の組成により実施例1と同様に試料3−A,3−B
を作つた。The results are shown in Table 2. Samples 3-A and 3-B were prepared in the same manner as in Example 1 with the compositions above.
I made it.
その結果を表3に示す。実施例
以上の組成により実施例1と同様に試料4−A,4−B
を作つた。The results are shown in Table 3. Samples 4-A and 4-B were prepared in the same manner as in Example 1 with the compositions above.
I made it.
その結果を表4に示す。実施例
以上の組成により実施例1と同様に試料5−A,5−B
を作つた。The results are shown in Table 4. Samples 5-A and 5-B were prepared in the same manner as in Example 1 with the compositions above.
I made it.
その結果を表5に示す。実施例
Vjツ1,J1I卜1―
以上の組成により実施例1と同様に試料6−A,6−B
を作つた。The results are shown in Table 5. Example Vjtsu 1, J1I 卜1- With the above composition, samples 6-A and 6-B were prepared in the same manner as in Example 1.
I made it.
その結果を表6に示す。実施例
以上の組成により実施例1と同様に試料7一A,7−B
を作つた。The results are shown in Table 6. Samples 7-A and 7-B were prepared in the same manner as in Example 1 with the compositions above.
I made it.
その結果を表7に示す。実施例
以上の組成により実施例1と同様な試料8−A,8−B
を作つた。The results are shown in Table 7. Samples 8-A and 8-B similar to Example 1 with the compositions above.
I made it.
その結果を表8に示す。実施例
以上の組成により実施例1と同様に試料9−A,9−B
を作つた。The results are shown in Table 8. Samples 9-A and 9-B were prepared in the same manner as in Example 1 with the compositions above.
I made it.
その結果を表9に示す。実施例
以上の組成により実施例1と同様に試料10一A,lO
−Bを作つた。The results are shown in Table 9. Sample 101A, lO as in Example 1 with the composition above.
-I made B.
その結果を表10に示す。実施例以上の組成により実施
例1と同様に試料11−A,ll二Bを作つた。The results are shown in Table 10. Samples 11-A and 11-B were prepared in the same manner as in Example 1 using the compositions described above.
その結果を表11に示す。実施例以上の組成により実施
例1と同様に試料12一A,l2−Bを作つた。The results are shown in Table 11. Samples 12-A and 12-B were prepared in the same manner as in Example 1 using the compositions described above.
その結果を表12に示す。以上の結果から明らかな如く
先の発明になる磁気記録媒体は電気抵抗自体はさほど小
さくなつていないにもか\わらず半減期が著しく小さく
なつているので、ごみ、ほこり等の附着が著しく少ない
0このように先の発明によつてごみ、ほこり等の附着が
著しく少ない磁気記録媒体を得ることが出来たが、本発
明者はさらに研究を重ねた結果、前記界面活性剤を2回
に分けて使用すると、即ちまず磁性粉の表面を界面活性
剤でお\つた後、その磁性粉をバインダー、溶剤と混練
するとき再び前記の界面活性剤を加えれば少ない界面活
性剤の量で充分に効果を上げることが出来ることを見出
した。The results are shown in Table 12. As is clear from the above results, although the electric resistance itself of the magnetic recording medium according to the earlier invention has not been reduced that much, the half-life has been significantly shortened, so there is significantly less adhesion of dirt, dust, etc. 0 As described above, the previous invention made it possible to obtain a magnetic recording medium with significantly less adhesion of dirt, dust, etc., but as a result of further research, the inventors discovered that the surfactant was divided into two parts. In other words, if you first coat the surface of the magnetic powder with a surfactant and then add the surfactant again when kneading the magnetic powder with the binder and solvent, a small amount of surfactant will be sufficient. I found out that it is possible to increase the
本発明はこの知見にもとずくものであり、以下比較例と
実施例を示す。比較・実施例 1
先の実施例4の試料を(1)とし、試料(1)に対して
界面活性剤の量を2重量部にしたものを試料(1Yとす
る。The present invention is based on this knowledge, and comparative examples and examples will be shown below. Comparison/Example 1 The sample of Example 4 was referred to as (1), and the sample (1Y) was prepared by adding 2 parts by weight of the surfactant to sample (1).
そしてこの試秤1Yを用いて、バインダー、溶剤と混練
して磁性塗料を作る。このときさらに界面活性剤を添加
し、その磁性塗料をポリエステルベースフイルムに塗布
して磁気記録媒体を作製した。バインダーに添加した界
面活性剤の種類及び商品名、添加量、それにより作製さ
れた磁気記録媒体の試料腐を第13表に示す。以上の結
果を第14表に示す。Then, using this test scale 1Y, a magnetic paint is made by kneading it with a binder and a solvent. At this time, a surfactant was further added and the magnetic paint was applied to a polyester base film to produce a magnetic recording medium. Table 13 shows the type and brand name of the surfactant added to the binder, the amount added, and the sample corrosion of the magnetic recording medium prepared using the surfactant. The above results are shown in Table 14.
なお弾性とは、荷重をかけ、試料が破壊する限界である
。Note that elasticity is the limit at which a sample breaks when a load is applied.
又試料(1)a′について界面活性剤の添加量を変え、
半減期の変化を求めた。Also, for sample (1) a', the amount of surfactant added was changed,
Changes in half-life were determined.
その結果を第1図に示す。この図より試料716(1)
と同じ半減期なら0.75伊程度の添加量ですむことが
わかる。比較・実施例 2
比較・実施例の(1)において界面活性剤をアルキルサ
ルフエート塩(吉村油化のPMX−3007)2.5重
量部に変えたものを試料(2)とし、この試料(2)に
対して界面活性剤の量を1重量部にしたものを試粍2Y
とする。The results are shown in FIG. From this figure, sample 716 (1)
It can be seen that if the half-life is the same as , the addition amount is only about 0.75 days. Comparison/Example 2 Sample (2) was obtained by changing the surfactant to 2.5 parts by weight of alkyl sulfate salt (PMX-3007 of Yoshimura Yuka Co., Ltd.) in (1) of Comparison/Example. Test 2Y using 1 part by weight of surfactant as compared to 2).
shall be.
そして比較実施例1と同じように、さらに後で界面活性
剤を添加して作製した試料を第15表に示す。以上の結
果を第16表に示す。Table 15 shows samples prepared by adding a surfactant later in the same manner as in Comparative Example 1. The above results are shown in Table 16.
比較・実施例 3
先の実施例10の試料を(3)とし、試料(3)に対し
て界面活性剤のゾルビタン誘導体界面活性斉沿0.5重
量部、アミン塩界面活性剤を1重量部にしたものを試粍
3Yとする。Comparison/Example 3 The sample of Example 10 above was designated as (3), and 0.5 part by weight of the surfactant sorbitan derivative surfactant and 1 part by weight of the amine salt surfactant were added to sample (3). Let's call it Trial 3Y.
そして比較・実施例1と同じように後でさらに界面活性
剤を添加して作製した試料を第17表に示す。以上の結
果を第18表に示す。Table 17 shows samples prepared by adding a surfactant later in the same manner as in Comparative Example 1. The above results are shown in Table 18.
又他の界面活性剤即ちアルキルスルホネート塩(C)、
アルキルホスホネート塩(D)、アミン塩(E)、アル
キルエーテル塩(F)、アルキルエステル型(G)、ベ
タイン型11イミダゾリン型(1)の例を以下に示す。Also other surfactants, namely alkyl sulfonate salts (C),
Examples of the alkyl phosphonate salt (D), amine salt (E), alkyl ether salt (F), alkyl ester type (G), and betaine type 11 imidazoline type (1) are shown below.
なお、前処理の実施例は先に提案した実施例に対応し又
、添加は本願の実施例1〜3に対応する。又、電気抵抗
は〔Ω/Cd〕、半減期は〔SeO、弾性は〔Kg/C
d〕である。第19表に本実施例の中から代表的なもの
を選びその配向性を示す。Note that the pretreatment examples correspond to the previously proposed examples, and the additions correspond to Examples 1 to 3 of the present application. Also, electrical resistance is [Ω/Cd], half-life is [SeO], elasticity is [Kg/C
d]. Table 19 shows the orientation of representative samples selected from these examples.
さらに第21表に実施例C−1の中から代表的なものを
選び配向性を示す。Furthermore, Table 21 shows the orientation of representative samples selected from Example C-1.
このように本発明によつて製造された磁気記録媒体は帯
電現象が少ないので、ごみ.ほこり等を附着することな
く、又電磁特性.物性ともにすぐれている。As described above, since the magnetic recording medium manufactured according to the present invention has less charging phenomenon, it is free from dust. Does not attract dust, etc., and has good electromagnetic properties. It has excellent physical properties.
第1図は本発明になる磁気記録媒体の特性図である。 FIG. 1 is a characteristic diagram of the magnetic recording medium according to the present invention.
Claims (1)
、アルキルホスホネート塩、第4級アンモニウム塩、ア
ミン塩、アルキルエーテル型、アルキルエステル型、ソ
ルビタン誘導体、ベタイン型及びイミダゾリン型の界面
活性剤の少なくとも1種で表面をおゝつた磁性粉と、前
記界面活性剤を添加したバインダー及び溶剤を混練した
磁性塗料を基体に塗布することを特徴とする磁気記録媒
体の製造方法。1. Surface is treated with at least one of alkyl sulfate salts, alkyl sulfonate salts, alkyl phosphonate salts, quaternary ammonium salts, amine salts, alkyl ether type, alkyl ester type, sorbitan derivatives, betaine type and imidazoline type surfactants. 1. A method for manufacturing a magnetic recording medium, which comprises applying a magnetic paint obtained by kneading magnetic powder, a binder containing the surfactant, and a solvent onto a substrate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP53005001A JPS5921090B2 (en) | 1978-01-20 | 1978-01-20 | Method for manufacturing magnetic recording media |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP53005001A JPS5921090B2 (en) | 1978-01-20 | 1978-01-20 | Method for manufacturing magnetic recording media |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5498203A JPS5498203A (en) | 1979-08-03 |
| JPS5921090B2 true JPS5921090B2 (en) | 1984-05-17 |
Family
ID=11599328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP53005001A Expired JPS5921090B2 (en) | 1978-01-20 | 1978-01-20 | Method for manufacturing magnetic recording media |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5921090B2 (en) |
-
1978
- 1978-01-20 JP JP53005001A patent/JPS5921090B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5498203A (en) | 1979-08-03 |
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