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JPS63124217A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

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
Application number
JP61268625A
Other languages
Japanese (ja)
Inventor
Isao Sasaki
功 佐々木
Nobuo Ishikawa
石川 信夫
Masato Ueda
正人 上田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Victor Company of Japan Ltd
Original Assignee
Victor Company of Japan Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Victor Company of Japan Ltd filed Critical Victor Company of Japan Ltd
Priority to JP61268625A priority Critical patent/JPS63124217A/en
Publication of JPS63124217A publication Critical patent/JPS63124217A/en
Pending legal-status Critical Current

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Landscapes

  • Paints Or Removers (AREA)
  • Magnetic Record Carriers (AREA)

Abstract

PURPOSE:To improve the dispersibility and orientational property of magnetic powder even if said powder is pulverized and to prevent degradation in magnetic characteristics and electromagnetic conversion characteristic by incorporating the magnetic powder treated by a specific compd. contg. a hydrocarbon group into a magnetic layer. CONSTITUTION:The characteristics such as max. residual magnetic flux density and squareness ratio of the magnetic powder begin to degrade if the magnetic powder treated with a compd. A having an alkyl group of many carbon atoms is used for a magnetic recording medium contg. the magnetic powder treated with the compd. expressed by formula A in the magnetic layer. It is, therefore, important that R1 be the hydrocarbon group of <=6C and that R2 be the hydrocarbon group of <=14C. Aggregation hardly rises with such magnetic powder and the dispersibility of the magnetic powder is good. The coated film strength of the magnetic layer obtd. by coating the magnetic coating compd. of said magnetic powder is high and further, the magnetic characteristics and electromagnetic conversion characteristic are excellent as well. This recording medium is suitable for high-density recording.

Description

【発明の詳細な説明】[Detailed description of the invention] 【産業上の利用分野】[Industrial application field]

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.

【従来技術とその問題点】[Prior art and its problems]

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.

【発明の開示】[Disclosure of the invention]

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].

【特性】【Characteristic】

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.

【効果】【effect】

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)

【特許請求の範囲】 磁性層中に、下記の一般式[A]で表わされる化合物で
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)
JP61268625A 1986-11-13 1986-11-13 Magnetic recording medium Pending JPS63124217A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (4)

* Cited by examiner, † Cited by third party
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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