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JPS5928219A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS5928219A
JPS5928219A JP13496282A JP13496282A JPS5928219A JP S5928219 A JPS5928219 A JP S5928219A JP 13496282 A JP13496282 A JP 13496282A JP 13496282 A JP13496282 A JP 13496282A JP S5928219 A JPS5928219 A JP S5928219A
Authority
JP
Japan
Prior art keywords
recording medium
magnetic recording
binder
ferromagnetic powder
diamine
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.)
Granted
Application number
JP13496282A
Other languages
Japanese (ja)
Other versions
JPH0159647B2 (en
Inventor
Masatoshi Tanahashi
棚橋 正敏
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.)
JNC Corp
Original Assignee
Chisso Corp
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 Chisso Corp filed Critical Chisso Corp
Priority to JP13496282A priority Critical patent/JPS5928219A/en
Publication of JPS5928219A publication Critical patent/JPS5928219A/en
Publication of JPH0159647B2 publication Critical patent/JPH0159647B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • G11B5/68Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent
    • G11B5/70Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer
    • G11B5/702Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the bonding agent
    • G11B5/7021Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the bonding agent containing a polyurethane or a polyisocyanate

Landscapes

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

Abstract

PURPOSE:To obtain a magnetic recording medium contg. a binder having superior dispersing power by using a cross-linked product prepared by cross-linking a copolymer consisting of polycaprolactone polyol, diamine and isocyanate with a curing agent as the principal component of a binder component for ferromagnetic powder. CONSTITUTION:Polycaprolactone polyol (PC), diamine (DI) and isocyanate (IS) are used as starting materials for manufacturing a copolymer. The mol.wt. of said PC and the number of terminal hydroxyl groups are not especially restricted, and commercially available PC may be used as it is. Said DI is required only to have one or two primary amino groups or two secondary amino groups, and phenylenediamine or alkylenediamine is preferably used. A general isocyanate compound such as tolylene diisocyanate or diphenylmethane diisocyanate is used as said IS. The preferred amount of PC is 20-80wt% of the total amount of PC, DA and IS, that of DA is 10-40wt%, and that of IS is 10-40wt%. The kind of ferromagnetic powder is not especially restricted, and powder of gamma-Fe2O3, Co-gamma-Fe2O3, CrO2, Cu or the like is used.

Description

【発明の詳細な説明】 この発明は、磁気記録媒体に関するものであり、その目
的とするところは、強磁性粉末の分散性に優れる磁気記
録媒体を提供することにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium, and an object thereof is to provide a magnetic recording medium with excellent dispersibility of ferromagnetic powder.

磁気記録体は、通常、強磁性粉末、結合剤、溶剤および
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非磁性基体に塗着してつくられる。
Magnetic recording bodies are usually made by applying a magnetic paint consisting of ferromagnetic powder, a binder, a solvent, and optionally other additives to a non-magnetic substrate such as a polyester film.

強磁性粉末としては、従来より用いられている酸化鉄系
微粉末、および近年、その飽和磁化及び保磁力が高いた
め、磁気記録密度の向上、再生出力の向上を目的に用い
られはじめた金属粉末等がある。溶剤としては1トルエ
ン1メチルエチルケトン(M B K)、メチルイソブ
デルケトン(M I’ B K ) 、イソプロピルア
ルコール、シクロへ++/ン等(7) −fi又は二種
以上の混合物が一般に用いられる。他の添加剤としては
、分散剤、研磨剤・充填剤、帯電防止剤、防錆剤等が必
要に応じて用いられる。分散剤は強磁性粉末を被覆して
用いる場合もある。結合剤については、強磁性粉末の分
散性の面で、磁気記録媒体の特性上、極めて重要な働き
を担っている。それ故強磁性粉末の分散性が良好で磁気
記録媒体に高感度、高SN比などの優れた電磁気特性を
付与できるものを選定する必要がある。これらの背景か
ら現在実際に使用されている結合剤の代表として、塩化
ビニル系共重合体樹脂およびポリウレタン系樹脂の2種
類がある。
Examples of ferromagnetic powder include iron oxide fine powder, which has traditionally been used, and metal powder, which has recently begun to be used to improve magnetic recording density and reproduction output due to its high saturation magnetization and coercive force. etc. As the solvent, 1-toluene, 1-methyl ethyl ketone (MBK), methyl isobuterketone (MI'BK), isopropyl alcohol, cyclohe++/-fi, etc. (7) -fi, or a mixture of two or more are generally used. . As other additives, dispersants, abrasives/fillers, antistatic agents, rust preventives, etc. may be used as necessary. The dispersant may be used by coating ferromagnetic powder. The binder plays an extremely important role in terms of the dispersibility of the ferromagnetic powder and the characteristics of the magnetic recording medium. Therefore, it is necessary to select a ferromagnetic powder that has good dispersibility and can impart excellent electromagnetic properties such as high sensitivity and high S/N ratio to the magnetic recording medium. Based on these backgrounds, there are two types of binders currently in actual use: vinyl chloride copolymer resins and polyurethane resins.

しかるに塩化ビニル系共重合体樹脂の場合、強磁性粉末
を分散させる能力については比較的硬れているがなお充
分でない。一方ポリウレタン系樹脂においては、走向特
性並びに耐久性の面では優れているが、強磁性粉末に対
する分散性が劣り、結果として感度、8N比などの電磁
気特性の悪化をまねいている。
However, in the case of vinyl chloride copolymer resin, although it is relatively hard, its ability to disperse ferromagnetic powder is still insufficient. On the other hand, polyurethane resins are excellent in terms of strike characteristics and durability, but have poor dispersibility with respect to ferromagnetic powder, resulting in deterioration of electromagnetic properties such as sensitivity and 8N ratio.

本発明は、従来の樹脂を用いた場合に生ずるこれらの欠
点を克服するためになされたものであって、分散性が優
れた結合剤を含む磁気記録媒体を提供することを目的と
する。
The present invention was made to overcome these drawbacks that occur when conventional resins are used, and an object of the present invention is to provide a magnetic recording medium containing a binder with excellent dispersibility.

即ち、本発明は、非磁性基体上印強磁性粉末及び結合剤
を含む磁性層を設けた磁気記録媒体において、該結合剤
成分がポリカプロラクトンポリオール、ジアミン及びイ
ンシアネートからなる共電体をその硬化剤で架橋してな
る架橋体を主成分とするものである。
That is, the present invention provides a magnetic recording medium having a magnetic layer containing a ferromagnetic powder and a binder printed on a nonmagnetic substrate, in which the binder component cures a coelectric material consisting of a polycaprolactone polyol, a diamine, and an incyanate. The main component is a crosslinked product formed by crosslinking with an agent.

本発明で使用する共重合体の製造原料である前記ポリカ
プロラクトンポリオール(以下「PC」と略記する。)
は分子量及び末端水酸基の数に特に制約はなく、市販さ
れているものをそのまま使用することができる。例えば
ダイヤル社製Placcel (同社商標)、UCC社
製NIAXPCP (同社商標)などが挙げられる。
The polycaprolactone polyol (hereinafter abbreviated as "PC"), which is a raw material for producing the copolymer used in the present invention.
There are no particular restrictions on the molecular weight or the number of terminal hydroxyl groups, and commercially available products can be used as they are. Examples include Placcel (trademark) manufactured by Dial Corporation and NIAXPCP (trademark) manufactured by UCC Corporation.

前記ジアミン(以下「DI」と略記する。)としては、
−級アミノ基を1個もしくは2個有する化合物又は二級
アミノ基を2個有するものであればよく、中でもフェニ
レンジアミン、アルキレンジアミンなどが好ましい。
The diamine (hereinafter abbreviated as "DI") includes:
Any compound having one or two -class amino groups or two secondary amino groups may be used, and among them, phenylene diamine, alkylene diamine, etc. are preferable.

前記インシアネート(以下「IS」と略記する。)とし
ては、トリレンジイソシアネート、ジフェニルメタンジ
イソンアネート、ヘキサメテンンジイソンアネートなど
一般的なインシネート化合物を使用することができる。
As the incyanate (hereinafter abbreviated as "IS"), common insinate compounds such as tolylene diisocyanate, diphenylmethane diisonanate, hexamethene diisonanate, etc. can be used.

前記共重合体の製造方法は、具体例を実施例に示すが、
特に限定されるものではなく、溶液重合、乳化重合等公
知の方法を採用することができる。
Specific examples of the method for producing the copolymer are shown in Examples,
There are no particular limitations, and known methods such as solution polymerization and emulsion polymerization can be employed.

前記共重合体の製造において使用するPClDA及びI
sの割合は、これらの合計量に対してPCが20〜80
重量%、DAが10〜40重量%、Isが10〜40重
量%とするのがよい。
PCIDA and I used in the production of the copolymer
The ratio of s is 20 to 80 PC for these total amounts.
It is preferable that DA be 10 to 40% by weight and Is be 10 to 40% by weight.

前記共重合体と共に強磁性粉末と混合され、該共重合体
の硬化剤としての役割をもつものとしては、ポリイソシ
アネート(以下1’−PI 8Jと略記する。)とエポ
キシ樹脂を挙げることができる。硬化反応が早い点で前
者が好ましい。
Examples of materials that are mixed with the ferromagnetic powder together with the copolymer and serve as a curing agent for the copolymer include polyisocyanate (hereinafter abbreviated as 1'-PI 8J) and epoxy resin. . The former is preferred because the curing reaction is quick.

FISとして、例えばトリメチロールプロパン1モルと
トリレンジイソシアネート3モルとの反応物である三官
能性低分子量イソシアネート化合物等があげられる。該
反応物は、バイエル社からは商品名「デスモジュールL
」として、日本ポリウレタン工業■からは商品名[コロ
ネ5− 一トL」として市販されている。
Examples of FIS include a trifunctional low molecular weight isocyanate compound which is a reaction product of 1 mole of trimethylolpropane and 3 moles of tolylene diisocyanate. The reactant is available from Bayer under the trade name "Desmodur L".
'' and is commercially available from Nippon Polyurethane Industry ■ under the trade name ``Corone 5-Ito L''.

PI8の前記共重合体への混入量は、多すぎると最終的
に得られる塗膜が脆くなり、少な過ぎると耐溶剤性等に
問題が生じるので、該共重合体100重量部に対し5〜
30重量部が適当である。
The amount of PI8 mixed into the copolymer is 5 to 5 parts by weight per 100 parts by weight of the copolymer, because if it is too large, the final coating film will become brittle, and if it is too small, problems will arise in solvent resistance, etc.
30 parts by weight is suitable.

本発明における前記強磁性粉末としては、特ニli、l
定されず、たとえば1−Fe2O3、Co−1−Fe2
0B、CrO2、金属鉄、コバルト、ニッケル、銅、ク
ロム、けい素等の鉄合金等を挙げることができる。
The ferromagnetic powder in the present invention is particularly li, l.
For example, 1-Fe2O3, Co-1-Fe2
Examples include iron alloys such as 0B, CrO2, metallic iron, cobalt, nickel, copper, chromium, and silicon.

結合剤を溶剤に溶解し、これに強磁性粉末を添加、混合
して分散させれば、磁性塗料を得るが、結合剤と強磁性
粉末の添加順、分散手段等は何ら限定されない。次1″
−1本発明を実施例につき更に詳細に説明するが本願発
明はこれらに限定されるものではない。
A magnetic paint is obtained by dissolving a binder in a solvent, adding ferromagnetic powder thereto, mixing and dispersing it, but there are no limitations on the order of addition of the binder and ferromagnetic powder, the dispersion means, etc. Next 1″
-1 The present invention will be explained in more detail with reference to Examples, but the present invention is not limited to these.

実施例 撹拌棒、接縮器、滴下装置、窒素吹込管、温度計を備え
た反応容器を用いる。
EXAMPLE A reaction vessel equipped with a stirring bar, a condenser, a dropping device, a nitrogen blowing tube, and a thermometer is used.

まず反応器を50℃に加温し、窒素置換をし、6一 ジフェニルメタンジイソシアネートを10重量部および
平均分子量1250のポリカプロラクトンジオールを2
5重量部添加し、内容物を攪拌しながら窒素雰囲気下8
0℃、4時間反応を行なう。反応終了後50℃まで冷却
し、ジメチルフォルムアマイド28重置部を添加し30
分攪拌し・均一に溶解させる。一方ジメチルフォルムア
マイド28重量部にピヌアミノプロビルビペラジン9重
量部を溶解させたものを調整し、前記反応生成物に添加
し攪拌しながら窒素雰囲気下50℃、2時間反応させ、
反応後室部まで冷却させる。得られた反応物の樹脂濃度
は44重量パーセントであった。この反応生成物を用い
、表1に示す如く、硬化剤と共に各種の強磁性粉末を種
々変えた場合の各種配合により、ボールミルを用い、4
8時間混合分散し磁性塗料を調整した。又この塗料を公
知の方法にて、厚さ12μのポリエステルフィルム基体
上に塗布した後、80℃で30分乾燥・硬化処理して厚
さ4μの磁性層を形成せしめ、巾10■に裁断して磁気
テープを作った。
First, the reactor was heated to 50°C, purged with nitrogen, and 10 parts by weight of 6-diphenylmethane diisocyanate and 2 parts of polycaprolactone diol with an average molecular weight of 1250 were added.
5 parts by weight was added, and the contents were heated for 8 hours under a nitrogen atmosphere while stirring.
The reaction is carried out at 0°C for 4 hours. After the reaction was completed, the mixture was cooled to 50°C, and 28 parts of dimethylformamide was added.
Stir for a minute to dissolve uniformly. On the other hand, prepare a solution of 9 parts by weight of pinuaminoprobyl biperazine in 28 parts by weight of dimethylformamide, add it to the reaction product, and react at 50°C for 2 hours under a nitrogen atmosphere with stirring,
After the reaction, the chamber is cooled down. The resin concentration of the resulting reaction product was 44% by weight. Using this reaction product, as shown in Table 1, using a ball mill, 4
The mixture was mixed and dispersed for 8 hours to prepare a magnetic paint. This paint was applied to a 12μ thick polyester film base by a known method, dried and cured at 80°C for 30 minutes to form a 4μ thick magnetic layer, and cut into 10μ width pieces. and made magnetic tape.

比較例 実施例の配合組成物のうち、本発明における結合剤に代
えて、塩化ビニル、酢酸ビニル、ビニルアルコール共重
合体(UCC社製;商品名:VAGH;樹脂分10CI
)又はポリウレタン樹脂(日本ポリウレタン工業■製;
商品名:ニラポラン2304;樹脂分35型量パーセン
ト)をおのおの使用した以外は、実施例と全く同様の方
法で磁気テープを作製した。
Comparative Examples Among the blended compositions of Examples, vinyl chloride, vinyl acetate, and vinyl alcohol copolymer (manufactured by UCC; trade name: VAGH; resin content: 10 CI) was used instead of the binder in the present invention.
) or polyurethane resin (manufactured by Nippon Polyurethane Industries ■;
Magnetic tapes were produced in exactly the same manner as in the examples, except that each product had a product name: Niraporan 2304 (resin content: 35% mold weight).

配合表は表2にまとめて示す。但し実施例と対比する為
に結合剤及び溶剤の量を合わせである。
The formulation table is summarized in Table 2. However, for comparison with Examples, the amounts of binder and solvent are the same.

実施例および比較例において得られた磁気テープの磁気
特性並びに光沢度のデータを表3にまとめて示す。この
表から磁性粉として、1 Fe2O3、Co 1 Fe
20B及びFa金合金用いた場合のいずれにおいても磁
気特性(残留磁束密度(Br)、角形比(Br / B
m ) )および表面光沢性において、高分散性記録媒
体としての本発明による磁気テープの優秀性が明らかで
ある。
Table 3 summarizes data on the magnetic properties and glossiness of the magnetic tapes obtained in Examples and Comparative Examples. From this table, as magnetic powder, 1 Fe2O3, Co 1 Fe
Both when using 20B and Fa gold alloys, the magnetic properties (residual magnetic flux density (Br), squareness ratio (Br / B
The superiority of the magnetic tape according to the invention as a highly dispersive recording medium is evident in terms of m)) and surface gloss.

表  3 以上Table 3 that's all

Claims (3)

【特許請求の範囲】[Claims] (1)  非磁性基体上に強磁性粉末および結合剤を含
む磁性層を設けた磁気記録媒体において、該結合剤成分
がポリカプロラクトンポリオール、ジアミン及びイソシ
アネートからなる共重合体をその硬化剤で架橋してなる
架橋体を主成分とすることを特徴とする前記磁気記録媒
体。
(1) In a magnetic recording medium in which a magnetic layer containing ferromagnetic powder and a binder is provided on a nonmagnetic substrate, the binder component crosslinks a copolymer consisting of polycaprolactone polyol, diamine, and isocyanate with its curing agent. The magnetic recording medium is characterized in that the main component is a crosslinked body consisting of:
(2)前記架橋体が、前記硬化剤としてポリイソシアネ
ートを使用したものであることを特徴とする第(1)項
記載の磁気記録媒体。
(2) The magnetic recording medium according to item (1), wherein the crosslinked body uses polyisocyanate as the curing agent.
(3)前記架橋体が、前記硬化剤としてエポキン樹脂を
使用したものであることを特徴とする第+11項記載の
磁気記録媒体。
(3) The magnetic recording medium according to item +11, wherein the crosslinked body uses an Epoquine resin as the curing agent.
JP13496282A 1982-08-02 1982-08-02 Magnetic recording medium Granted JPS5928219A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13496282A JPS5928219A (en) 1982-08-02 1982-08-02 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13496282A JPS5928219A (en) 1982-08-02 1982-08-02 Magnetic recording medium

Publications (2)

Publication Number Publication Date
JPS5928219A true JPS5928219A (en) 1984-02-14
JPH0159647B2 JPH0159647B2 (en) 1989-12-19

Family

ID=15140648

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13496282A Granted JPS5928219A (en) 1982-08-02 1982-08-02 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS5928219A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4708199A (en) * 1985-02-28 1987-11-24 Kabushiki Kaisha Tsuchiya Seisakusho Heat exchanger
US4722231A (en) * 1985-05-14 1988-02-02 Yamatake-Honeywell Co., Ltd. Electromagnetic flowmeter
US4836276A (en) * 1987-03-09 1989-06-06 Nippondenso Co., Ltd. Heat exchanger for engine oil
US4892136A (en) * 1986-12-31 1990-01-09 Kabushiki Kaisha Tsuchiya Seisakusho Heat exchanger
JPH02113421A (en) * 1988-10-21 1990-04-25 Dainichiseika Color & Chem Mfg Co Ltd Magnetic recording medium
EP0519177A2 (en) * 1991-06-21 1992-12-23 Chisso Corporation A thermosetting adhesive film and a process for applying the same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4708199A (en) * 1985-02-28 1987-11-24 Kabushiki Kaisha Tsuchiya Seisakusho Heat exchanger
US4722231A (en) * 1985-05-14 1988-02-02 Yamatake-Honeywell Co., Ltd. Electromagnetic flowmeter
US4892136A (en) * 1986-12-31 1990-01-09 Kabushiki Kaisha Tsuchiya Seisakusho Heat exchanger
US4836276A (en) * 1987-03-09 1989-06-06 Nippondenso Co., Ltd. Heat exchanger for engine oil
JPH02113421A (en) * 1988-10-21 1990-04-25 Dainichiseika Color & Chem Mfg Co Ltd Magnetic recording medium
EP0519177A2 (en) * 1991-06-21 1992-12-23 Chisso Corporation A thermosetting adhesive film and a process for applying the same

Also Published As

Publication number Publication date
JPH0159647B2 (en) 1989-12-19

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