JPS5894B2 - magnetic recording medium - Google Patents
magnetic recording mediumInfo
- Publication number
- JPS5894B2 JPS5894B2 JP52030648A JP3064877A JPS5894B2 JP S5894 B2 JPS5894 B2 JP S5894B2 JP 52030648 A JP52030648 A JP 52030648A JP 3064877 A JP3064877 A JP 3064877A JP S5894 B2 JPS5894 B2 JP S5894B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- recording medium
- weight
- polyvinyl butyral
- magnetic recording
- 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し、更に詳しくは磁性層の結
合剤成分がポリビニルブチラール、ウレタンプレポリマ
ー及び低分子量インシアネート化合物からなる磁気記録
媒体に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium, and more particularly to a magnetic recording medium in which the binder component of the magnetic layer comprises polyvinyl butyral, a urethane prepolymer, and a low molecular weight incyanate compound.
一般に、磁気記録媒体は、磁性粉末、結合剤成分、有機
溶剤及び必要に応じて他の添加剤からなる磁性塗料をポ
リエステルフィルムなどの基体に塗着、乾燥することに
より製造される。Generally, a magnetic recording medium is manufactured by applying a magnetic paint consisting of magnetic powder, a binder component, an organic solvent, and other additives as necessary to a substrate such as a polyester film, and drying the coating.
この際使用する結合剤成分としては、磁性粉末の分散性
に優れ、磁気記録媒体に高感度、高SN比などの優れた
電気的特性を附与できるとともに磁性層の耐摩耗性に優
れ、磁気記録媒体の耐久性を向上できるものを選ぶ必要
がある。The binder component used in this case has excellent dispersibility of the magnetic powder, can impart excellent electrical properties such as high sensitivity and high S/N ratio to the magnetic recording medium, and has excellent abrasion resistance of the magnetic layer. It is necessary to choose one that can improve the durability of the recording medium.
現在使用されている各種結合剤のうち、ポリビニルブラ
チールは特に分散性に優れるものとして知られている。Among various binders currently used, polyvinylbratyl is known to have particularly excellent dispersibility.
ところが、ポリビニルブチラールを結合剤成分として磁
性層は、一般に柔軟性に欠けるため、磁気記録テープな
どにおいては、その保管、取扱い時にテープにカールが
生じたり、また記録再生時にテープガイドや磁気ヘッド
との摺接により傷、摩耗が生じやすく耐久性に劣るとい
う欠点がある。However, magnetic layers containing polyvinyl butyral as a binder component generally lack flexibility, so in magnetic recording tapes, etc., the tape may curl during storage and handling, and may not be easily connected to tape guides or magnetic heads during recording and playback. It has the drawback of being easily scratched and abraded due to sliding contact and having poor durability.
この欠点を解消するために、従来よりジオクチルフタレ
ート、ジブチルフタレートなどの低分子可塑剤を併用す
るという試みがなされているが、このような可塑剤を使
用すると磁性層の耐熱性が低下し、特に高温での保存時
にテープ表面に可塑剤が滲出してテープの層間粘着を起
こしやすくなる。In order to overcome this drawback, attempts have been made to use low-molecular plasticizers such as dioctyl phthalate and dibutyl phthalate in combination, but the use of such plasticizers reduces the heat resistance of the magnetic layer. When stored at high temperatures, plasticizers ooze out onto the tape surface, making it easier for tape layers to stick together.
本発明者は、先に、ポリビニルブチラールと直鎖状の両
末端にインシアネート基を有するウレタンプレポリマー
を併用することにより上記の諸欠点が解消されることを
見出したが、更に引続く研究の結果、ポリビニルブチラ
ール及びウレタンプレポリマーの他に三官能性低分子量
のインシアネート化合物を併用すると、磁性層の耐摩耗
性及び耐熱性が更に向上することを見出し、本発明を完
成したものである。The present inventors have previously found that the above-mentioned drawbacks can be overcome by using polyvinyl butyral in combination with a urethane prepolymer having incyanate groups at both ends of the linear chain. As a result, the present invention was completed by discovering that the abrasion resistance and heat resistance of the magnetic layer can be further improved when a trifunctional low molecular weight incyanate compound is used in combination with polyvinyl butyral and urethane prepolymer.
すなわち、本発明の磁気記録媒体は、磁性層の結合剤成
分としてポリビニルブチラール、直鎖状の両末端にイン
シアネート基を有するウレタンプレポリマー及び三官能
性低分子量イソシアネート化合物を含有することを特徴
とするものであり、本発明によればポリビニルブチラー
ル特有の優れた電気特性を有するとともに耐摩耗性及び
耐熱性に優れた磁気記録媒体が得られる。That is, the magnetic recording medium of the present invention is characterized by containing polyvinyl butyral, a urethane prepolymer having incyanate groups at both ends of a linear chain, and a trifunctional low molecular weight isocyanate compound as binder components of the magnetic layer. According to the present invention, a magnetic recording medium having excellent electrical properties unique to polyvinyl butyral as well as excellent wear resistance and heat resistance can be obtained.
本発明で使用するポリビニルブチラールとじては、現在
市販されているものがいずれも使用できるが、ポリビニ
ルアルコールとして10〜40モル%に相当する水酸基
含量を有し、平均重合度が約200〜1000程度のも
のが好ましく用いられる。As the polyvinyl butyral used in the present invention, any currently commercially available polyvinyl butyral can be used, but it has a hydroxyl group content equivalent to 10 to 40 mol% as polyvinyl alcohol, and an average degree of polymerization of about 200 to 1000. Those are preferably used.
市販品の具体例としては、種水化学社製商品名工スレツ
クBM−8,BL−3,BL−1、電気化学工業社製デ
ンカブチラール#3000になどが挙げられる。Specific examples of commercially available products include Meiko Sletsku BM-8, BL-3, and BL-1 (manufactured by Tanemizu Kagaku Co., Ltd.), and Denka Butyral #3000 (manufactured by Denki Kagaku Kogyo Co., Ltd.).
ポリビニルブチラールの使用量は、結合剤成分全量に対
し40〜90重量%、好ましくは50〜70重量%であ
る。The amount of polyvinyl butyral used is 40 to 90% by weight, preferably 50 to 70% by weight, based on the total amount of binder components.
ポリビニルブチラールの量が多い程磁性粉末の分散性は
よいが、90重量%を越えると耐摩耗性の改善効果が認
められない傾向にある。The greater the amount of polyvinyl butyral, the better the dispersibility of the magnetic powder, but if it exceeds 90% by weight, there is a tendency for no improvement in wear resistance to be observed.
また、40重量%より低くなるとポリビニルブチラール
特有の優れた分散性が期待できなくなる。Moreover, if it is less than 40% by weight, the excellent dispersibility peculiar to polyvinyl butyral cannot be expected.
本発明で使用するウレタンプレポリマーとしては、イソ
シアネート基を直鎖状の両末端に有する分子量約100
0〜3000のものが好ましく用いられ、具体例として
は武田薬品工業社製タケネートL−1007、タケネー
トL−1006、タケネートL−2710、日本ポリウ
レタン工業社製コロネート#4095、コロネート#4
090、コロネーH#4048、大日本インキ社製パン
デツクスP−538、パンデツクス305Eなどが挙げ
られる。The urethane prepolymer used in the present invention has an isocyanate group at both linear ends and has a molecular weight of about 100.
0 to 3000 are preferably used, and specific examples include Takenate L-1007, Takenate L-1006, Takenate L-2710, manufactured by Takeda Pharmaceutical Co., Ltd., Coronate #4095, Coronate #4, manufactured by Nippon Polyurethane Industries, Ltd.
090, Coronae H#4048, Pandex P-538, Pandex 305E manufactured by Dainippon Ink Co., Ltd., and the like.
上記のポリビニルブチラール及びウレタンプレポリマー
と併用する三官能性低分子量イソシアネート化合物とは
、通常1モルのトリオールと3モルのジイソシアネート
との反応物からなるものである。The trifunctional low molecular weight isocyanate compound used in combination with the above-mentioned polyvinyl butyral and urethane prepolymer usually consists of a reaction product of 1 mol of triol and 3 mol of diisocyanate.
このインシアネート化合物中に含まれる三官能のイソシ
アネート基がポリビニルブチラールに含まれるOH基と
反応して網状の架橋結合を作るため、磁性層の塗膜強度
が萬くなり耐摩耗性及び耐熱性が向上するものと考えら
れる。Since the trifunctional isocyanate group contained in this incyanate compound reacts with the OH group contained in polyvinyl butyral to form a network crosslink, the strength of the coating film of the magnetic layer is 10,000, and the abrasion resistance and heat resistance are improved. This is expected to improve.
これに対して前記ウレタンプレポリマーに含まれるイソ
シアネート基は三官能であるため、立体的な網状の架橋
結合が十分には得られずこのプレポリマーだけを添加し
たものでは耐摩耗性、耐熱性にいまひとつ充分でなかっ
た。On the other hand, since the isocyanate groups contained in the urethane prepolymer are trifunctional, sufficient steric network cross-linking cannot be obtained, and the addition of only this prepolymer has poor wear resistance and heat resistance. It just wasn't enough.
このような低分子量イソシアネート化合物の具体例とし
ては、日本ポリウレタン工業社製コロネートL、バイエ
ル社製デスモジュールL、武田薬品社製タケネートD1
02などが挙げられる。Specific examples of such low molecular weight isocyanate compounds include Coronate L manufactured by Nippon Polyurethane Industries, Desmodur L manufactured by Bayer, and Takenate D1 manufactured by Takeda Pharmaceutical Co., Ltd.
Examples include 02.
三官能性低分子量インシアネート化合物の使用量は、結
合剤成分全量に対し、1〜20重量%の範囲が好ましい
。The amount of the trifunctional low molecular weight incyanate compound used is preferably in the range of 1 to 20% by weight based on the total amount of the binder component.
20重量%を越えると架橋密度が高くなって磁性層を硬
くし、脆くするおそれがあり、また1重量%以下の量で
は所期の効果が得られない。If the amount exceeds 20% by weight, the crosslinking density may increase, making the magnetic layer hard and brittle, and if the amount is less than 1% by weight, the desired effect may not be obtained.
本発明に使用する磁性粉末としては、例えば1−Fe2
O3粉末、Fe3O4粉末、Co含含有−Fe203粉
末、Co含有Fe3O4粉末、CrO2粉末など従来公
知の各種粉末が広く包含される。Examples of magnetic powder used in the present invention include 1-Fe2
A wide variety of conventionally known powders are included, such as O3 powder, Fe3O4 powder, Co-containing -Fe203 powder, Co-containing Fe3O4 powder, and CrO2 powder.
本発明の磁気記録媒体は常法に準じて製造することがで
き、例えばポリエステルフィルムなどの基体上に、磁性
粉末、ポリビニルブチラール、ポリウレタンプレポリマ
ー及び三官能性低分子量インシアネート化合物からなる
結合剤成分:有機溶剤:及びその他の添加剤を含む磁性
塗料を吹付けもしくはロール塗りなどの任意の手段で塗
布し乾燥すればよい。The magnetic recording medium of the present invention can be manufactured according to a conventional method. For example, a binder component consisting of magnetic powder, polyvinyl butyral, a polyurethane prepolymer, and a trifunctional low molecular weight incyanate compound is placed on a substrate such as a polyester film. A magnetic paint containing an organic solvent and other additives may be applied by any means such as spraying or roll coating and dried.
次に実施例により本発明を更に詳細に説明する。Next, the present invention will be explained in more detail with reference to Examples.
なお、以下において部とあるは重量部を示す。In addition, in the following, parts indicate parts by weight.
実施例1
γ−Fe203磁性粉末80部、エスレツクBM−8(
ポリビニルブチラール)10部、タケネートL(ポリウ
レタンプレポリマー)8部及びコロネートしく三官能性
低分子量イソシアネート化合物)2部をトルエンとメチ
ルエチルケトンの1:1の混合溶剤100部に加え、ボ
ールミル中で70時間混合分散して磁性塗料を調製した
。Example 1 80 parts of γ-Fe203 magnetic powder, Eslec BM-8 (
10 parts of polyvinyl butyral), 8 parts of Takenate L (polyurethane prepolymer), and 2 parts of Coronate L (trifunctional low molecular weight isocyanate compound) were added to 100 parts of a 1:1 mixed solvent of toluene and methyl ethyl ketone, and mixed for 70 hours in a ball mill. A magnetic paint was prepared by dispersing it.
この磁性塗料を厚さ21μのポリエステルフィルムに乾
燥厚が10μとなるように塗布、乾燥した。This magnetic paint was applied to a polyester film having a thickness of 21 μm to a dry thickness of 10 μm and dried.
次いで、磁性層表面をカレンダー処理し鏡面加工した後
、所定の幅に裁断して磁気テープを作製した。Next, the surface of the magnetic layer was calendered to give a mirror finish, and then cut into a predetermined width to produce a magnetic tape.
実施例2
実施例1のコロネートLの代りにデスモジュールLを使
用した以外は実施例1と同様にして磁気テープを得た。Example 2 A magnetic tape was obtained in the same manner as in Example 1 except that Desmodur L was used instead of Coronate L in Example 1.
比較例
実施例1のコロネートLを使用せず、結合剤成分として
エスレツクBM−8;10部及びタケネートL;10部
を使用した以外は実施例1と同様にして磁気テープを得
た。Comparative Example A magnetic tape was obtained in the same manner as in Example 1, except that Coronate L of Example 1 was not used, and 10 parts of Eslec BM-8 and 10 parts of Takenate L were used as binder components.
上記各磁気テープのSN比及び摩耗減量を測定したとこ
ろ、下記第1表に示す如き結果が得られた。When the SN ratio and abrasion loss of each of the above magnetic tapes were measured, the results shown in Table 1 below were obtained.
但し、摩耗減量は、一定の長さの磁気テープをテープデ
ツキを用いて、76cm/秒の走行速度で磁気ヘッドと
摺接させながら300回走行させた後の摩耗減量を比較
例を100として指数で示したものである。However, the abrasion loss is calculated as an index of the abrasion loss after running a fixed length of magnetic tape 300 times using a tape deck while slidingly contacting a magnetic head at a running speed of 76 cm/sec, with the comparative example being 100. This is what is shown.
また、上記各磁気テープの耐熱性を調べるために各磁気
テープを1kgの張力を加えてガラス管に巻きつけ、6
0℃、80%RHで24時間保存し、さらに常温で24
時間放置したのち、ガラス管から磁気テープを巻き解い
た際に磁気テープ巻回層間で粘着があるか否かを観察し
た。In addition, in order to examine the heat resistance of each magnetic tape, each magnetic tape was wound around a glass tube with a tension of 1 kg.
Store at 0℃, 80%RH for 24 hours, then store at room temperature for 24 hours.
After leaving the glass tube for a while, it was observed whether there was any adhesion between the layers of the magnetic tape when the magnetic tape was unwound from the glass tube.
その結果は第1表に示す通りであった。The results were as shown in Table 1.
上記の結果より明らかな如く、本発明の磁気テープは高
SN比を示し、耐摩耗性及び耐熱性についても比較例に
比べて一段と改善されていることが判る。As is clear from the above results, the magnetic tape of the present invention exhibits a high signal-to-noise ratio, and it can be seen that the abrasion resistance and heat resistance are further improved compared to the comparative example.
Claims (1)
ラール40〜90重量%、三官能性低分子量インシアネ
ート化合物1〜20重量%および直鎖状の両末端にイソ
シアネート基を有するウレタンプレポリマーを残部で構
成し、かつ磁性粉末が結合剤と磁性粉末の合計量に対し
て、80重量%以上含まれてなる磁気記録媒体。1 The binder for the magnetic layer is 40 to 90% by weight of polyvinyl butyral, 1 to 20% by weight of a trifunctional low molecular weight incyanate compound, and the balance is a urethane prepolymer having isocyanate groups at both straight chain ends. A magnetic recording medium comprising 80% by weight or more of magnetic powder based on the total amount of the binder and the magnetic powder.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52030648A JPS5894B2 (en) | 1977-03-18 | 1977-03-18 | magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52030648A JPS5894B2 (en) | 1977-03-18 | 1977-03-18 | magnetic recording medium |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53116116A JPS53116116A (en) | 1978-10-11 |
| JPS5894B2 true JPS5894B2 (en) | 1983-01-05 |
Family
ID=12309620
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52030648A Expired JPS5894B2 (en) | 1977-03-18 | 1977-03-18 | magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5894B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9038267B2 (en) | 2010-06-10 | 2015-05-26 | Modine Manufacturing Company | Method of separating heat exchanger tubes and an apparatus for same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4919506A (en) * | 1989-02-24 | 1990-04-24 | General Electric Company | Single mode optical fiber coupler |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5248004A (en) * | 1975-10-15 | 1977-04-16 | Hitachi Ltd | Rotor for synchronous machines |
-
1977
- 1977-03-18 JP JP52030648A patent/JPS5894B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9038267B2 (en) | 2010-06-10 | 2015-05-26 | Modine Manufacturing Company | Method of separating heat exchanger tubes and an apparatus for same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53116116A (en) | 1978-10-11 |
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