JPS63124217A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS63124217A JPS63124217A JP61268625A JP26862586A JPS63124217A JP S63124217 A JPS63124217 A JP S63124217A JP 61268625 A JP61268625 A JP 61268625A JP 26862586 A JP26862586 A JP 26862586A JP S63124217 A JPS63124217 A JP S63124217A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- magnetic powder
- recording medium
- powder
- compd
- 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
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 59
- 239000006247 magnetic powder Substances 0.000 claims abstract description 41
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 9
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims description 23
- 239000000126 substance Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 9
- 230000002776 aggregation Effects 0.000 abstract description 4
- 125000000217 alkyl group Chemical group 0.000 abstract description 4
- 239000011248 coating agent Substances 0.000 abstract description 4
- 238000000576 coating method Methods 0.000 abstract description 4
- 230000004907 flux Effects 0.000 abstract description 3
- 239000000843 powder Substances 0.000 abstract description 2
- 238000004220 aggregation Methods 0.000 abstract 1
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 9
- 239000010419 fine particle Substances 0.000 description 7
- 239000003973 paint Substances 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 3
- 238000005054 agglomeration Methods 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 229940067606 lecithin Drugs 0.000 description 3
- 235000010445 lecithin Nutrition 0.000 description 3
- 239000000787 lecithin Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
Abstract
Description
本発明は、例えば磁気テープ、磁気ディスク等の磁気記
録媒体に関するものである。The present invention relates to magnetic recording media such as magnetic tapes and magnetic disks.
磁気テープ等の磁気記録媒体は、例えばポリエステル等
の非磁性支持体面上に、強磁性体の微粉末である磁性粉
、バインダ、各種の添加剤及び有機溶剤を混合分散して
得た磁性塗料を所定厚塗布し、そして乾燥、カレンダー
処理その他所定の工程を経て得られるのが通常である。
このような塗布型の磁気記録媒体にあっても、最近にお
いては記録再生装置の高密度記録の進展に伴なって高密
度記録化の要望が高まっており、このような観点から磁
気記録媒体に用いられる磁性粉は微粒子化することが求
められている。
しかし、高密度記録化の為に磁性粉を微粒子化すると、
微粒子化した磁性粉はそれだけ凝集が起きやすく、又、
バインダ等との親和性が悪く、磁性塗料中における磁性
粉の分散性が低下し、又、磁性層中での配向性が低下し
、磁気記録媒体の磁気特性及び電磁変換特性の低下をも
たらす原因になっており、磁性粉の微粒子化を図ったの
みでは不充分なものである。
この為、磁性粉の微粒子化を回った場合には分散剤を多
量に用いることが試みられているが、分散剤を多量に用
いるとそれだけ磁性層中における磁性粉の充填密度が低
下し、又、磁性層塗膜の強度の低下が大きくなり、さら
には分散剤の浸み出し等も起きるといったように欠点も
大きく現われるようになる。Magnetic recording media such as magnetic tapes are made by mixing and dispersing magnetic powder, which is fine ferromagnetic powder, a binder, various additives, and organic solvents on a non-magnetic support such as polyester. It is usually obtained by applying a predetermined thickness and then drying, calendering, and other predetermined steps. Even with such coating-type magnetic recording media, the demand for higher density recording has recently increased with the progress of high-density recording in recording and reproducing devices, and from this perspective, magnetic recording media The magnetic powder used is required to be made into fine particles. However, when magnetic powder is made into fine particles for high-density recording,
Micronized magnetic powder is more likely to agglomerate, and
Poor affinity with binders, etc., resulting in decreased dispersibility of magnetic powder in the magnetic paint and decreased orientation in the magnetic layer, leading to decreased magnetic properties and electromagnetic conversion characteristics of the magnetic recording medium. Therefore, it is insufficient to simply make the magnetic powder into fine particles. For this reason, attempts have been made to use a large amount of a dispersant when making magnetic powder into fine particles, but using a large amount of a dispersant lowers the packing density of the magnetic powder in the magnetic layer. , the strength of the magnetic layer coating is greatly reduced, and further disadvantages such as oozing of the dispersant occur.
本発明者は、高密度記録化の為に磁性粉の微粒子化を図
った場合に起きる欠点についての研究を進めていくうち
に、微粒子化した磁性粉の凝集を起きに<<、かつ、分
散性が低下しにくいようにする為には、そもそも磁性粉
の凝集が起きにくいような表面処理を磁性粉自体に施し
ておけば良いであろうとの啓示を得るに至り、磁性粉の
凝集防止の為の表面処理を各種の化合物について試みて
いくうちに、下記の化合物[A]で処理した磁性粉は凝
集が起きに<<、かつ、磁性塗料中での分散性が良く、
又、この化合物[A]で処理した磁性粉を含む磁性塗料
を塗布して得た磁気記録媒体の磁性層の塗膜強度は大き
く、さらには磁気特性及び電磁変換特性も優れており、
高密度記録に適していることを見出した。
○
ここで、上記の一般式[A]で表わされる化合物のうち
R,、R,の炭素数があまり多くなりすぎると、すなわ
ち炭素数が多いアルキル基を有する化合物[A]で処理
した磁性粉を用いて磁性層を構成した磁気記録媒体は、
その最大残留磁束密度B糟及び角型比11s等の特性が
低下し始めることから、R1はその炭素数が6以下の炭
化水素基であることが、そしてR2はその炭素数が14
以下の炭化水素基であることが大事である。
尚、R1は、その炭素数が2〜5のアルキル基であるこ
とが一層望ましいものであり、又、R2は、その炭素数
が4〜12のアルキル基であることが一層望ましい。
又、一般式[A]の化合物で処理した磁性粉は、磁性粉
100重量部に対して約0.5〜3.5重量部の一綬式
[A]で表わされる化合物を所定の溶剤中で混合分散さ
せることによって得られる。While conducting research on the drawbacks that occur when magnetic powder is made into fine particles for high-density recording, the present inventor found that due to the agglomeration of the fine magnetic powder, In order to prevent the magnetic powder from deteriorating, it was discovered that it would be best to apply a surface treatment to the magnetic powder itself to make it difficult for the magnetic powder to agglomerate. As we experimented with various compounds for surface treatment, we found that magnetic powder treated with the following compound [A] did not cause agglomeration and had good dispersibility in magnetic paint.
In addition, the coating strength of the magnetic layer of a magnetic recording medium obtained by applying a magnetic paint containing magnetic powder treated with this compound [A] is high, and furthermore, the magnetic properties and electromagnetic conversion properties are excellent.
We found that it is suitable for high-density recording. ○ Here, if the number of carbon atoms in R, R, of the compound represented by the above general formula [A] is too large, that is, the magnetic powder treated with the compound [A] having an alkyl group with a large number of carbon atoms. A magnetic recording medium whose magnetic layer is constructed using
Since its characteristics such as maximum residual magnetic flux density B and squareness ratio 11s begin to decrease, R1 is a hydrocarbon group with a carbon number of 6 or less, and R2 has a carbon number of 14
It is important that the hydrocarbon group is one of the following. In addition, it is more desirable that R1 is an alkyl group having 2 to 5 carbon atoms, and it is even more desirable that R2 is an alkyl group having 4 to 12 carbon atoms. The magnetic powder treated with the compound of the general formula [A] can be prepared by adding about 0.5 to 3.5 parts by weight of the compound represented by the formula [A] to 100 parts by weight of the magnetic powder in a predetermined solvent. It is obtained by mixing and dispersing.
【実施例1】
BET値が35+*2/gの針状の磁性粉100重量部
、及びR1=C2115、R2・Cs1l+tの上記一
般式[A]で表わされる化合物2重量部及び溶剤280
重1部を充分に混合分散し、表面に一般式[A]で表わ
される化合物が吸着した磁性粉を含む磁性塗料を得る。
次に、この磁性塗料に、所定のバインダ20重1部、研
磨剤10重量部及びカーボンブラック5重量部を添加し
、これを充分に混合分散し、その後インシアネ−1・系
の硬化剤を20重量部加えて再度混合分散し、このよう
にして得た磁性塗料をポリエステル等の非磁性支持体上
に塗布し、配向、カレンダー及び硬化処理等の通常の処
理を行なって磁気テープ等の磁気記録媒体を得る。
(実施例2〜4]
実施例1において、R,=C,IIs、R2=C5ll
+tの一般式[A]で表わされる化合物の代りに、R1
・Cs1l++、R2・C,11,、の一般式[A]で
表わされる化合物を用いて(実施例2)、R+=C5l
lz、R2・C+5llz+の一般式[A]で表わされ
る化合物を用いて(実施例3)、R1・Cs1l+8、
R2・C4I1.の一般式[A]で表わされる化合物を
用いて(実施例4)同様に行ない、磁気記録媒体を得る
。[Example 1] 100 parts by weight of acicular magnetic powder with a BET value of 35+*2/g, 2 parts by weight of a compound represented by the above general formula [A] where R1=C2115, R2・Cs1l+t, and 280 parts by weight of a solvent.
A magnetic paint containing magnetic powder having a compound represented by the general formula [A] adsorbed on the surface thereof is obtained by thoroughly mixing and dispersing 1 part of the magnetic powder. Next, 20 parts by weight of a predetermined binder, 10 parts by weight of an abrasive, and 5 parts by weight of carbon black were added to this magnetic paint, and these were thoroughly mixed and dispersed. The magnetic paint obtained in this way is coated on a non-magnetic support such as polyester, and subjected to ordinary treatments such as orientation, calendering and curing treatment to produce magnetic recording such as magnetic tape. Get medium. (Examples 2 to 4) In Example 1, R,=C,IIs, R2=C5ll
+t instead of the compound represented by the general formula [A], R1
・Cs1l++, R2・C,11, using a compound represented by the general formula [A] (Example 2), R+=C5l
Using a compound represented by the general formula [A] of lz, R2・C+5llz+ (Example 3), R1・Cs1l+8,
R2・C4I1. A magnetic recording medium is obtained in the same manner as in Example 4 using a compound represented by the general formula [A].
【比較例1】
実施例1において、一般式[A]で表わされる化合物の
代りにレシチンを用いて同様に行ない、磁気記録媒体を
得る。Comparative Example 1 A magnetic recording medium was obtained by carrying out the same procedure as in Example 1 using lecithin instead of the compound represented by the general formula [A].
【比較例2.3】
実施例1において、R,=C,Ils、R2=C5ll
+tの一般式[A]で表わされる化合物の代りに、R1
”C7+115、R2・C,l+、、の−最大[A]で
表わされる化合物を用いて(比較例2)、R+”Cs1
lz、R2・C+5llz+の一般式[A]で表わされ
る化合物を用いて(比較例3)同様に行ない、磁気記録
媒体を得る。[Comparative Example 2.3] In Example 1, R, = C, Ils, R2 = C5ll
+t instead of the compound represented by the general formula [A], R1
Using a compound represented by -maximum [A] of "C7+115, R2・C,l+," (Comparative Example 2), R+"Cs1
A magnetic recording medium is obtained in the same manner as in Comparative Example 3 using a compound represented by the general formula [A] of lz, R2·C+5llz+.
【比較例4】
実施例1において、一般式[A]で表わされる化合物を
全く用いないで同様に行ない、磁気記録媒体を得る。Comparative Example 4 A magnetic recording medium was obtained by carrying out the same procedure as in Example 1 without using any compound represented by the general formula [A].
上記各側で得た磁気記録媒体について、その最大残留磁
束密度Bn+、角型比Rs及び記録再生装置に装着して
繰り返し走行させた後に磁気ヘッドを観察し、そのヘッ
ド汚れを調べたので、その結果を表に示す。
表
これかられかるように、全く表面処理が行なわれていな
い磁性粉を用いた場合には、比較例4に示す如く、磁性
粉の微粒子化によって磁性粉の凝集が起き、BII及び
Rsが悪い磁気記録媒体になっているのに対し、一般式
[A]で表わされる化合物によって処理した磁性粉を用
いた場合には、実施例1〜4に示す如く、BIllは大
きく、かつ、Rsは高く、その磁気特性及び電磁変換特
性は優れている。
しかし、−ffi式[A]の化合物で磁性粉を処理する
にしても、一般式[A]の化合物におけるR+ 、R2
の炭素数が多くなると、比較例2,3に示す如く、Bm
は低下し、かつ、Rsも小さくなるように、その磁気特
性及び電磁変換特性の向上は小さいものである。
又、比較例2.3に示す如< 、 R1,R2の炭素数
が多すぎると、磁気特性及び電磁変換特性の向上が小さ
いのみではなく、ヘッド汚れが増大する欠点が却って認
められるようになる。
又、本実施例の磁気記録媒体は、分散剤として良く知ら
れているレシチンによって磁性粉を処理し、このレシチ
ン処理磁性粉を用いて同様に作成した比較例1の磁気記
録媒体よりも、その磁気特性及び電磁変換特性の向上度
は著しく高いものである。Regarding the magnetic recording media obtained on each side above, we observed the maximum residual magnetic flux density Bn+, the squareness ratio Rs, and the magnetic head after it was installed in a recording/reproducing device and ran it repeatedly, and examined the head dirt. The results are shown in the table. As shown in the table, when magnetic powder without any surface treatment is used, as shown in Comparative Example 4, agglomeration of the magnetic powder occurs due to atomization of the magnetic powder, resulting in poor magnetic properties due to BII and Rs. On the other hand, when magnetic powder treated with the compound represented by the general formula [A] is used as a recording medium, as shown in Examples 1 to 4, BIll is large, Rs is high, Its magnetic properties and electromagnetic conversion properties are excellent. However, even if magnetic powder is treated with the compound of -ffi formula [A], R+, R2 in the compound of general formula [A]
As the number of carbon atoms increases, as shown in Comparative Examples 2 and 3, Bm
The improvement in the magnetic properties and electromagnetic conversion properties is small, as is shown in FIG. Furthermore, as shown in Comparative Example 2.3, if the number of carbon atoms in R1 and R2 is too large, not only the improvement in magnetic properties and electromagnetic conversion properties is small, but also the drawback of increased head contamination is observed. . In addition, the magnetic recording medium of this example treated the magnetic powder with lecithin, which is well known as a dispersant, and the magnetic recording medium of Comparative Example 1 was made in the same manner using the lecithin-treated magnetic powder. The degree of improvement in magnetic properties and electromagnetic conversion properties is extremely high.
本発明に係る磁気記録媒体は、磁性層中に一般式[A]
で表わされる化合物で処理した磁性粉を含むものである
から、この磁性層中における磁性粉の分散性及び配向性
は磁性粉が微粒子化されたものであっても優れており、
従って磁気特性及び電磁変換特性の低下が磁性粉を微粒
子化しても起きず、高密度記録に対応できるものであり
、さらには磁性層の機械的強度も充分にあり、又、この
ような優れた特長を示す磁気記録媒体の製造工程は従来
からの工程を大巾に改変するものでもないから従来と同
様なコストで提供できる特長を有する。The magnetic recording medium according to the present invention has the general formula [A] in the magnetic layer.
Since it contains magnetic powder treated with a compound represented by the following, the dispersibility and orientation of the magnetic powder in this magnetic layer are excellent even if the magnetic powder is made into fine particles.
Therefore, the magnetic properties and electromagnetic conversion properties do not deteriorate even if the magnetic powder is made into fine particles, and it is compatible with high-density recording.Furthermore, the mechanical strength of the magnetic layer is sufficient, and such excellent The manufacturing process of the magnetic recording medium exhibiting this feature does not require any major modification of the conventional process, so it has the advantage of being able to be provided at the same cost as the conventional process.
Claims (1)
処理した磁性粉を含むことを特徴とする磁気記録媒体。 ▲数式、化学式、表等があります▼[A] (但し、R_1は炭素数が6以下の炭化水素基、R_2
は炭素数が14以下の炭化水素基)[Scope of Claims] A magnetic recording medium characterized in that a magnetic layer contains magnetic powder treated with a compound represented by the following general formula [A]. ▲There are mathematical formulas, chemical formulas, tables, etc.▼ [A] (However, R_1 is a hydrocarbon group with 6 or less carbon atoms, R_2
is a hydrocarbon group having 14 or less carbon atoms)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61268625A JPS63124217A (en) | 1986-11-13 | 1986-11-13 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61268625A JPS63124217A (en) | 1986-11-13 | 1986-11-13 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63124217A true JPS63124217A (en) | 1988-05-27 |
Family
ID=17461144
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61268625A Pending JPS63124217A (en) | 1986-11-13 | 1986-11-13 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63124217A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5619351A (en) * | 1992-07-13 | 1997-04-08 | Seiko Epson Corporation | Surface-type illumination device and liquid crystal display |
US5931555A (en) * | 1989-05-18 | 1999-08-03 | Seiko Epson Corporation | Background lighting apparatus for liquid crystal display |
-
1986
- 1986-11-13 JP JP61268625A patent/JPS63124217A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5931555A (en) * | 1989-05-18 | 1999-08-03 | Seiko Epson Corporation | Background lighting apparatus for liquid crystal display |
US5619351A (en) * | 1992-07-13 | 1997-04-08 | Seiko Epson Corporation | Surface-type illumination device and liquid crystal display |
US5949505A (en) * | 1992-07-13 | 1999-09-07 | Seiko Epson Corporation | Surface-type illumination device and liquid crystal display |
US6108060A (en) * | 1992-07-13 | 2000-08-22 | Seiko Epson Corporation | Surface-type illumination device and liquid crystal display |
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