JPH0224838A - Production of magnetic recording medium - Google Patents
Production of magnetic recording mediumInfo
- Publication number
- JPH0224838A JPH0224838A JP17464088A JP17464088A JPH0224838A JP H0224838 A JPH0224838 A JP H0224838A JP 17464088 A JP17464088 A JP 17464088A JP 17464088 A JP17464088 A JP 17464088A JP H0224838 A JPH0224838 A JP H0224838A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic recording
- magnetic
- recording medium
- cyclohexanone
- solvent
- 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
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims abstract description 36
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims abstract description 30
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229920005989 resin Polymers 0.000 claims abstract description 25
- 239000011347 resin Substances 0.000 claims abstract description 25
- 239000011230 binding agent Substances 0.000 claims abstract description 19
- 238000000576 coating method Methods 0.000 claims abstract description 16
- 239000011248 coating agent Substances 0.000 claims abstract description 13
- 239000006247 magnetic powder Substances 0.000 claims abstract description 6
- 239000000758 substrate Substances 0.000 claims abstract description 5
- 239000003973 paint Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 15
- 239000003960 organic solvent Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 8
- 239000000020 Nitrocellulose Substances 0.000 claims description 6
- 239000006229 carbon black Substances 0.000 claims description 6
- 229920001220 nitrocellulos Polymers 0.000 claims description 6
- 239000012046 mixed solvent Substances 0.000 claims description 5
- 229920001228 polyisocyanate Polymers 0.000 claims description 4
- 239000005056 polyisocyanate Substances 0.000 claims description 4
- 229920005749 polyurethane resin Polymers 0.000 claims description 2
- 239000002904 solvent Substances 0.000 abstract description 15
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 230000002411 adverse Effects 0.000 abstract 1
- 239000011877 solvent mixture Substances 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 description 11
- 230000008020 evaporation Effects 0.000 description 11
- 239000002245 particle Substances 0.000 description 7
- 238000001035 drying Methods 0.000 description 6
- 239000013040 bath agent Substances 0.000 description 5
- 235000019241 carbon black Nutrition 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- 235000021360 Myristic acid Nutrition 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- ULBTUVJTXULMLP-UHFFFAOYSA-N butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCC ULBTUVJTXULMLP-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- AJCDFVKYMIUXCR-UHFFFAOYSA-N oxobarium;oxo(oxoferriooxy)iron Chemical compound [Ba]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O AJCDFVKYMIUXCR-UHFFFAOYSA-N 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920001692 polycarbonate urethane Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- FHYUCVWDMABHHH-UHFFFAOYSA-N toluene;1,2-xylene Chemical group CC1=CC=CC=C1.CC1=CC=CC=C1C FHYUCVWDMABHHH-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は磁気記録媒体に係わり、ざらに詳しくは、その
製fL法の改良に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a magnetic recording medium, and more particularly, to an improvement in the fL manufacturing method thereof.
近年、磁気記録媒体は高密度記録、高信頼性化が進み、
バックコート層を備えた磁気記録媒体が多くなってき比
。ま九磁気記録td 、バックコート71111共にそ
の表面性、耐久性等が問題となり、用いる結合剤樹脂も
ニトロセルロース、塩化ビニル系共電合体およびポリウ
レタンUB¥1、ポリエステル樹脂(ガラス転移点+5
0゛C以下、平均分子量10.000〜100,000
)とポリインシアネート等を組み合せ用いられるように
なった。それに伴い。In recent years, magnetic recording media have become more densely recorded and more reliable.
More and more magnetic recording media are equipped with a back coat layer. Both Maku Magnetic Recording TD and Backcoat 71111 have problems with their surface properties and durability, and the binder resins used are nitrocellulose, vinyl chloride co-electrolyte, polyurethane UB ¥1, and polyester resin (glass transition point +5).
0゛C or less, average molecular weight 10.000-100,000
) and polyincyanate, etc., can now be used in combination. with this.
それらを酵解する有機浴剤の選定も重要な検討課題であ
る。こnまで、一般に有ms剤はメチルエチルケトン、
メチルイソブチルケトン、トルエンキシレン、シクロヘ
キサノン、テトラヒドロン2ン等が単独または混合して
用いられてきたが。The selection of organic bath agents that ferment these substances is also an important consideration. Until now, MS drugs have generally been methyl ethyl ketone,
Methyl isobutyl ketone, toluene xylene, cyclohexanone, tetrahydrone dione, etc. have been used alone or in combination.
AS’f’MD 3539に示される蒸発速gが1゜6
以上のもの(メチルエチルケトン4メチルイノブチルケ
トン、トルエン、テトラヒドロフラン等)もしくは、そ
れに準するものを単独’!2&!混合して用いた場合の
問題点として、塗料!!遣、塗布工程に9いて、それら
の蒸発速度が速いため、m材表面の有1a溶剤が局部的
に蒸発し、記録媒体のその部分が出力変動、ドロップア
ウトの原因となり、あまり好ましくない。そこで蒸発速
度0.32のシクロヘキサノンを混合して用いることも
提案されているが、7クロヘキテノンの蒸発速度が極度
に遅いため、形成された磁気記録ノー中に残存しやすく
、耐久性の低下を招く等の問題点がろりその使用方法に
ついては、今迄十分な検討がなされていなかつ〔発明が
解決しようとする問題点〕
本発明は、塗布盤磁気記録媒体の製造時の使用有機溶剤
によって生ずる磁気記録ノー等への悪影響t−除去し、
以って鑞磁lR換峙性2よび耐久性に優れた磁気記録媒
体を提供することを目的とする。The evaporation rate g shown in AS'f'MD 3539 is 1°6
Use the above (methyl ethyl ketone, 4 methyl isobutyl ketone, toluene, tetrahydrofuran, etc.) or something similar alone! 2&! One of the problems when using them together is paint! ! During the coating process, the evaporation rate is high, so the 1A solvent on the surface of the M material evaporates locally, causing output fluctuations and dropouts in that part of the recording medium, which is not very desirable. Therefore, it has been proposed to mix and use cyclohexanone with an evaporation rate of 0.32, but since the evaporation rate of 7-chlorohexenone is extremely slow, it tends to remain in the formed magnetic recording layer, resulting in a decrease in durability. [Problems to be solved by the present invention] The present invention solves the problems of magnetic recording caused by the organic solvent used in the production of coated magnetic recording media. Eliminate negative effects on records, etc.
Therefore, it is an object of the present invention to provide a magnetic recording medium having excellent magnetic IR reciprocity 2 and durability.
C問題を解決するための手段〕
磁気塗料にしろバックコート用塗料にしろ、塗料製造工
程および塗布工程までは6局部的な有機浴剤の蒸発等が
無く2しかも良好な流動性を有し。Means for Solving Problem C] Regardless of whether it is a magnetic paint or a backcoat paint, there is no local evaporation of the organic bath agent during the paint manufacturing process and coating process, and the paint has good fluidity.
磁気塗料においては、塗布工程後の磁場配向処理時に磁
性粉が容易に配向できる程度に流l1lIiI性をMす
ることが望lしい。これに続く乾燥工程では逮fかに乾
燥することが望ましい。このような産科の乾m速度をA
揺するため、蒸発速度の異なる有機溶剤が混合して用す
られている。メチルエチルケトン(蒸発atぼ3.7.
n点79.6℃)とシクロヘキサノン(蒸発速度0.3
2 、線点155.7℃)との混合溶剤とし几り、特開
昭62−154323号に示されるように、ざらに少量
のトルエン’t−11.合し用いることも提案σルでい
る。In the magnetic coating material, it is desirable to have flowability M to such an extent that the magnetic powder can be easily oriented during the magnetic field orientation treatment after the coating process. In the subsequent drying step, it is desirable that the material be thoroughly dried. This kind of obstetric dry m rate is A
For shaking, a mixture of organic solvents with different evaporation rates is used. Methyl ethyl ketone (evaporation at 3.7.
n point 79.6°C) and cyclohexanone (evaporation rate 0.3
As shown in JP-A-62-154323, a small amount of toluene 't-11. It is also proposed to use them together.
しかしメチルエチルケトンとシクロヘキサノンは高画で
ろv、−4:の便用量は少ないほど壜ましi7、′tf
t、トルエンは混合してもその効果は十分と−えない。However, methyl ethyl ketone and cyclohexanone have high resolution v, -4: The smaller the amount of stool, the better the bottle i7,'tf
Even if toluene is mixed, the effect is not sufficient.
そこで、 1) 蒸発速度が遅く結合剤樹脂の良浴
媒でめるシクロへ午すノンの最低必要量と2)蒸発速度
が速く、賭合剤樹脂の良溶剤であるメチルエチルケトン
の短と、3)蒸発速度はjl<)鈷合剤出脂の貧溶剤で
あるが1mmココスト低減ため′#1釈剤として用いる
トルエンの最大許容盪の検討を行なり之。Therefore, 1) the minimum required amount of cyclocarbonate, which has a slow evaporation rate and is a good solvent for the binder resin; 2) the short amount of methyl ethyl ketone, which has a fast evaporation rate and is a good solvent for the binder resin; and 3) ) The evaporation rate is jl<)Although it is a poor solvent for fat extraction of the mixture, in order to reduce the cost by 1 mm, we investigated the maximum allowable amount of toluene used as the #1 diluent.
結合剤樹脂としてニトロセルロース、ボIJ ’71/
タン樹脂、ポリインシアネートを用い、混合溶剤に対す
る溶解性と、乾燥工程における有aI溶剤の蒸発性につ
いて検討した。その結果、結合剤樹脂と7クロヘキサノ
ンとの配合比として、シクロヘキサノンが40重量%以
上とし、しかも全溶剤のうち5〜25ffi量%をシク
ロヘキサノンとし、残り95〜751盪%をメチルエチ
ルケトンとトルエンの混合溶剤とする。このメチルエチ
ルケトンの混合比は60/40〜40/60とするのが
好ましい。Nitrocellulose as binder resin, BoIJ '71/
Using tan resin and polyinsyanate, the solubility in mixed solvents and the evaporability of al-containing solvents in the drying process were investigated. As a result, the blending ratio of the binder resin and 7-chlorohexanone was 40% by weight or more of cyclohexanone, and 5 to 25% of the total solvent was cyclohexanone, and the remaining 95 to 751% was a mixture of methyl ethyl ketone and toluene. Use as a solvent. The mixing ratio of methyl ethyl ketone is preferably 60/40 to 40/60.
上記混合溶剤を用い、結合剤樹脂としてニトロセルロー
ス、ポリウレタン樹脂、ポリイソシアネートを用いた塗
料では、樹脂成分の溶解性が良好で、しかも磁性粉等の
分散性も良好で、乾燥工程においても樹脂成分の沈澱、
析出等の問題点が生じないことが明らかとなった。In paints using the above mixed solvent and nitrocellulose, polyurethane resin, or polyisocyanate as the binder resin, the solubility of the resin component is good, and the dispersibility of magnetic powder is also good. precipitation,
It became clear that problems such as precipitation did not occur.
トルエンとメチルケトンとの混合比でトルエンが65以
上となると結合剤樹脂の溶解性が低下し。When the mixing ratio of toluene and methyl ketone is 65 or more, the solubility of the binder resin decreases.
一方メチルエチルケトンが65以1となると、塗料製造
工程中に壇科表面の有機溶剤が局部的に蒸発しf丁くな
る。On the other hand, when methyl ethyl ketone is 65 to 1, the organic solvent on the surface of the coating material evaporates locally during the paint manufacturing process, resulting in f.
ま几、混合浴剤中の7グロへキテノンの配合比が25重
t%以上となると乾燥し庸くlり形成され之磁気記録ノ
ーあろいは、バックコート層中に多くの7クロヘキサノ
ンが残存し、十分な塗膜強度が得られ薙ぐ、磁気記録媒
体の耐久性が低下する。However, when the compounding ratio of 7-chlorohexanone in the mixed bath agent exceeds 25% by weight, it dries and is slowly formed. If the particles remain, sufficient coating strength cannot be obtained, and the durability of the magnetic recording medium is reduced.
さらに全溶剤中でのシクロヘキサノンの配合比が3重量
%以下の場合には、塗料!I!造工程中で結合剤樹脂が
不溶状態となり形成され之misの機械的強度および非
磁性基体との接着性が低下する。Furthermore, if the blending ratio of cyclohexanone in the total solvent is 3% by weight or less, paint! I! During the manufacturing process, the binder resin becomes insoluble and is formed, reducing the mechanical strength of the material and its adhesion to the non-magnetic substrate.
本発明にもとづく磁気記録媒体の製造法は、磁性粉、結
合剤樹脂、−t″の他の辣加剤と本発明による有機浴剤
等を従来公知の分a機で分散し友後。The method for producing a magnetic recording medium according to the present invention involves dispersing magnetic powder, a binder resin, other flavoring agents such as -T'', and an organic bath agent according to the present invention using a conventionally known separator.
FA’fr、行ないポリエステルフィルムhvc塗布、
乾燥を行ない、ざらにカレンダ処理を行なり友後所望の
形状に裁断すればよい。FA'fr, conduct polyester film HVC coating,
It may be dried, roughly calendered, and then cut into a desired shape.
磁性粉末としては、7−Fe 10m、Co含有r−F
e20mバリウムフェライト、および鉄、コバルト、ニ
ッケル4を含む金I14微粉木等便米公知のものが何れ
も開用可能である。As magnetic powder, 7-Fe 10m, Co-containing r-F
Any known materials such as e20m barium ferrite and gold I14 fine powder containing iron, cobalt, and nickel 4 can be used.
結合剤樹脂としては、ニトロセルロース、塩化ビニル系
共1合体、ポリビニルブチラール樹脂。As the binder resin, nitrocellulose, vinyl chloride comonomer, and polyvinyl butyral resin are used.
ポリフレタン樹月旨、ポリエステル−刀旨、ポリカーボ
ネートウレタン樹脂。アクリル系樹脂等従来公知のもの
が何れも開用できる。Polyurethane juzuki, polyester sword, polycarbonate urethane resin. Any conventionally known resin such as acrylic resin can be used.
本発明に基づくバックコート膚はカーボンブラック、上
記結合剤樹脂、その他の一加剤および本発明による有機
浴剤の混合物を従来公知の分散機で分収後1通を行ない
塗料とする。これを−万の面に磁気記録ノーを設は非磁
性基体の他方の面に塗布乾燥して設ける。これを所望の
幅に裁断することによってバックコート層付ビデオテー
プを作製する。The back coat according to the present invention is prepared by separating a mixture of carbon black, the above-mentioned binder resin, other additives and the organic bath agent according to the present invention using a conventionally known dispersing machine and then applying the mixture to a coating. This is coated and dried on the other side of the non-magnetic substrate to form a magnetic recording mark on one side. By cutting this into a desired width, a videotape with a back coat layer is produced.
バックコートに用いるカーボンブラックとしては、ファ
ーネスブラック、チャンネルブラック。Carbon blacks used for the back coat include furnace black and channel black.
ランプブラック、グラファイト化カーボンブラック等の
平均粒子径10〜300fiμのものが使用できるO
〔実施例〕
次に本発明の¥凡例および比較例を示す。以下に2いて
部とあるのは直濾部を示す。Lamp black, graphitized carbon black, etc. having an average particle diameter of 10 to 300 fiμ can be used. [Example] Next, the ¥ legend of the present invention and comparative examples are shown. 2 below indicates a direct filtration section.
実施例1
CO含含有−FexOs (比表面積、40r//71
)100部
カーボンブラック(平均粒子径、 0.025μ嘱)4
部
α−AhOs (平均粒子径、0.4μfi)
4ilステアリン波亜鉛 0.5部
ニトロセルロース(l/2秒グレード) 9gポリウ
レタン−脂 8′:f5ポリイソ
シアネート 3aミリスチン酸
2gステアリン酸nブチル
1部M機溶剤(表1に示す組成物
) 270部を高速デイスパー、サンドミル等の
7部改機を用い分収し九〇ち平均孔径1μ渦のフィルタ
ーヲ用いて。Example 1 CO-containing -FexOs (specific surface area, 40r//71
) 100 parts carbon black (average particle size, 0.025μ嘱) 4
Part α-AhOs (average particle size, 0.4μfi)
4il stearin wave zinc 0.5 parts Nitrocellulose (l/2sec grade) 9g polyurethane-fat 8': f5 polyisocyanate 3a myristic acid
2 g n-butyl stearate 1 part M solvent (composition shown in Table 1) 270 parts were separated using a 7-part machine such as a high-speed disper or sand mill, and filtered using a filter with an average pore diameter of 1 μm.
e過したのち乾燥後の塗布厚みが約4μ溝となるように
ポリエステルフィルム(厚さ14μ鵠)上に塗布し、a
8配向処理および乾燥を行な、つた任カレンダ処4を行
ない1部2インチ幅に裁断してビデオテープを作製した
。After drying, apply it on a polyester film (thickness: 14μ) so that the coating thickness after drying is approximately 4μ, and
The film was subjected to 8 orientation treatment and drying, followed by 4 calendering treatments and cut into 2-inch width portions to produce a videotape.
実j例2〜8.比較例1〜4はV機溶剤以外の組成物は
実施例1と同様とし、有機溶剤は表1に示す組成物1w
用した。Examples 2 to 8. In Comparative Examples 1 to 4, the compositions other than the V-organic solvent were the same as in Example 1, and the organic solvent was Composition 1w shown in Table 1.
used.
表 I NIB溶剤組成比(重量比)以上のよう
にして作っなビデオテープを以下に示す方法で評価した
。Table I NIB Solvent Composition Ratio (Weight Ratio) The video tapes prepared as described above were evaluated by the method shown below.
ステル特注 VkLS方式のVTRを用い、5℃。Using a custom-made Stell VkLS system VTR, at 5°C.
40%R)Zの環境fで供試テープ をスチルモードで再生し、その再 主出力信号のレベルが初期値から 3dB低下するまでの時間を測定 し比。40%R) Test tape in environment f of Z play in still mode and then Main output signal level changes from initial value Measure the time until it drops by 3dB comparison.
耐久−e+ vms方式OV’jRe用い、40
℃。Durability - e+ vms method OV'jRe used, 40
℃.
80%R1−l0環境下で、R1i’信号を記録し九供
試テープ7fc100回走行させ、初期の再生出力信号
レベル
に対する走行後の出力低1Fjtt−測定した。Under an 80% R1-10 environment, the R1i' signal was recorded and the nine sample tapes were run 7fc 100 times, and the output low 1Fjtt after running with respect to the initial playback output signal level was measured.
摩擦係数 ステンレスビンに対する初期の摩擦係数と
、VTRで100回走行挟の
摩擦係数’を測定した。Friction Coefficient The initial friction coefficient against the stainless steel bottle and the friction coefficient' after running 100 times with a VTR were measured.
表2
ビデオテープ評価結果
以との結果1本発明に基づく配合組成の有機溶剤を用い
たa3:塗料より作製し友ビデオテーグは。Table 2 Results of Videotape Evaluation Results 1 Friend Videotague was made from a3: paint using an organic solvent having a composition based on the present invention.
結合剤樹脂の溶解性FC′dI!れ、#I剤の蒸発性に
関する問題点が無いため、各評価項目に優れ次性能を示
している。Solubility of binder resin FC'dI! Since there is no problem with the evaporability of agent #I, it shows excellent performance in each evaluation item.
次にバックコートj−用迩科についての本発明の実施例
、比較例について示t0以下の実施例、比較例での感性
Jfllは、実施例1に示し良磁性ノーを設は念。Next, Examples and Comparative Examples of the present invention for back coat J-use are shown.The sensitivity JFll in Examples and Comparative Examples below t0 is shown in Example 1, and good magnetic properties are not included.
実力例9
カーボンブラック(平均粒子径、0.0254m)50
部
炭酸カルシウム(平均粒子径0.08μta)404粒
状ベンガラ(平均粒子径0.1μm) 10部二ト
クセルロースCL/21)グレード)27gポリウレタ
ンIM脂 is@sポリイソシア
ネート 8都ミリスチン酸
1部有機圏剤(表3に示す組成物
) 5130部上紀Ij1成物を高速デイスパ
ー、テンドミル等の分散411It−用い分収した後、
平均孔径lμ惰のフィルターでf過しfI−後、乾燥後
の塗布厚みが約0.5〜1′−
幅−IJ1!断しビデオテープを作製した。Performance example 9 Carbon black (average particle size, 0.0254m) 50
part calcium carbonate (average particle size 0.08μta) 404 granular red iron (average particle size 0.1μm) 10 parts Nitoku cellulose CL/21) grade) 27g polyurethane IM resin is@s polyisocyanate 8 cities myristic acid
1 part Organospheric agent (composition shown in Table 3) 5130 parts After separating the Joki Ij1 component using a high-speed disper, Tendomill, etc.,
After passing through a filter with an average pore diameter of lμ, the coating thickness after drying is approximately 0.5 to 1'. Width: IJ1! A cut-out videotape was made.
実施例10〜14 、比#f15〜sri、 7f#m
ai剤以外は実施例9と同様にして、バックコート1−
t−設けた。有機溶剤の組成比を表3vc示す。Examples 10-14, ratio #f15-sri, 7f#m
Backcoat 1- was prepared in the same manner as in Example 9 except for the AI agent.
t-provided. Table 3vc shows the composition ratio of the organic solvent.
以とのようにして得られた実施例9〜14.比較例5〜
8のビデオテープを以下Vこ示す方法で評価した。Examples 9 to 14 obtained as follows. Comparative example 5~
The videotape No. 8 was evaluated using the method shown below.
耐久注:VH8万式(2)VTR’t”用イ、40 ”
C,80%kLHの環境下で供試テープ(+−100回
走行させ、バックコートノーの傷付き程t!tを銭祭し
、fJJIが認められないもの會○印、わずかに認めら
ルるものをΔ
印、4)しく認められるもの?l−X印で示した。Durability Note: VH 80,000 Type (2) VTR't'', 40''
C. Test tape (run +-100 times in an environment of 80% kLH, test to the extent that there is no scratch on the back coat, and no fJJI is recognized. 4) What can be recognized correctly? Indicated by l-X marks.
4擦係数の変化
前記の耐久性g験前後の供試テープよりサンプリングし
、これを直径20axφのステンレスビンの上にテープ
の長手方向がビンと直角になるように、バックコートを
接して!き、テープの一端にzOgの荷1直ヲかけ、も
う−5111を3 un/ secの送V速度でテープ
を引張った時の曲直よV摩擦糸数を求め比。4 Change in Coefficient of Friction A sample was taken from the sample tape before and after the durability g test described above, and the back coat was placed on top of a stainless steel bottle with a diameter of 20axφ so that the longitudinal direction of the tape was perpendicular to the bottle! Then, apply a load of zOg to one end of the tape, and then pull the tape with -5111 at a V feed speed of 3 un/sec. Find the number of V friction yarns and the ratio.
表4
評価結果
と記の結果より明らかなように本発明による混合溶媒を
用い九バックコート4は、走行後も傷がつきに〈<、ま
たJl[!係数の変化も少なく、耐久性に優れ之皇換が
形成されている。Table 4 As is clear from the evaluation results and the results described below, the back coat 4 using the mixed solvent according to the present invention was not easily scratched even after running. There is little change in the coefficient, and it has excellent durability.
以上説明してきたように1本発明による混合溶剤を用い
て、ldi性塗料あるいはバックコート塗料を調製し、
これを塗布、転環して作製した磁気記録媒体は表面性に
曖れ、かっi!1膜の耐久性に優れ虎!!!品であるこ
とが明らかである。As explained above, one method is to prepare an LDI paint or a back coat paint using the mixed solvent according to the present invention,
The magnetic recording medium produced by coating and rotating this material has a poor surface quality. A highly durable single film! ! ! It is clear that it is a quality product.
出願人 日立マクセル株式会社 代表者 水 井 厚Applicant: Hitachi Maxell, Ltd. Representative Atsushi Mizu
Claims (5)
剤中で分散した磁気塗料を非磁性基体上に塗着してなる
磁気記録媒体の製造法において、有機溶剤の1成分であ
るシクロヘキサノンと結合剤樹脂との比率で、シクロヘ
キサノンが40重量%以上である磁気塗料を用いること
を特徴とする磁気記録媒体の製造法。(1) In a method for manufacturing a magnetic recording medium in which a magnetic paint in which a composition containing magnetic powder, binder resin, etc. is dispersed in an organic solvent is applied onto a non-magnetic substrate, cyclohexanone, which is one component of the organic solvent, is used. 1. A method for producing a magnetic recording medium, comprising using a magnetic coating material containing cyclohexanone in a ratio of 40% by weight or more to a binder resin.
物を有機溶剤中で分散したバックコート用塗料を非磁性
基体の一方の面に磁気記録層を設けた磁気シートの反対
側の面に塗着してなる磁気記録媒体において、前記バッ
クコート用塗料有機溶剤の1成分であるシクロヘキサ ノンと結合剤樹脂との比率で、シクロヘキサノンが40
重量%以上である塗料を用いることを特徴とする磁気記
録媒体の製造法。(2) Applying a back coat paint in which a composition containing carbon black, binder resin, etc. is dispersed in an organic solvent to the opposite side of the magnetic sheet, which has a magnetic recording layer on one side of the non-magnetic substrate. In the magnetic recording medium made of
1. A method for manufacturing a magnetic recording medium, characterized by using a paint having a content of at least % by weight.
いる有機溶剤成分中に占めるシクロヘキサノンの比率が
5〜25重量%であることを特徴とする請求項(1)ま
たは請求項(2)記載の磁気記録媒体の製造法。(3) The method according to claim (1) or claim (2), characterized in that the proportion of cyclohexanone in the organic solvent component used in the magnetic recording layer paint and the back coat paint is 5 to 25% by weight. A method for manufacturing magnetic recording media.
ケトンおよびトルエンの混合物を用いた混合溶剤中でメ
チルエチルケトンとトルエンの比率が40/60〜60
/40の割合で含まれていることを特徴とする請求項(
1)、(2)または(3)記載の磁気記録媒体の製造法
。(4) In a mixed solvent using a mixture of cyclohexanone, methyl ethyl ketone and toluene as an organic solvent, the ratio of methyl ethyl ketone to toluene is 40/60 to 60.
/40
1), (2), or (3) the method for manufacturing a magnetic recording medium.
樹脂、ポリイソシアネートよりなることを特徴とする請
求項(1)または(2)記載の磁気記録媒体の製造方法
。(5) The method for manufacturing a magnetic recording medium according to claim (1) or (2), wherein the binder resin is made of nitrocellulose, polyurethane resin, or polyisocyanate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17464088A JPH0224838A (en) | 1988-07-13 | 1988-07-13 | Production of magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17464088A JPH0224838A (en) | 1988-07-13 | 1988-07-13 | Production of magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0224838A true JPH0224838A (en) | 1990-01-26 |
Family
ID=15982128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17464088A Pending JPH0224838A (en) | 1988-07-13 | 1988-07-13 | Production of magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0224838A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03288329A (en) * | 1990-04-05 | 1991-12-18 | Matsushita Electric Ind Co Ltd | Magnetic recording medium and production thereof |
US5970768A (en) * | 1998-06-08 | 1999-10-26 | Utica Enterprises, Inc. | Machine base for supporting vertical movement of forming racks for rolling power transmission formations |
US5983690A (en) * | 1998-06-08 | 1999-11-16 | Utica Enterprises, Inc. | Machine having antifriction support for forming racks for rolling power transmission formations |
US5987953A (en) * | 1998-06-08 | 1999-11-23 | Utica Enterprises, Inc. | Power transmission formation rolling machine having movable headstock and tailstock spindle supports |
US6047581A (en) * | 1998-02-27 | 2000-04-11 | Anderson Cook, Inc. | Drive system for vertical rack spline-forming machine |
US10869968B2 (en) | 2015-04-23 | 2020-12-22 | Sanofi-Aventis Deutschland Gmbh | Drug delivery device and retaining member for a drug delivery device |
-
1988
- 1988-07-13 JP JP17464088A patent/JPH0224838A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03288329A (en) * | 1990-04-05 | 1991-12-18 | Matsushita Electric Ind Co Ltd | Magnetic recording medium and production thereof |
US6047581A (en) * | 1998-02-27 | 2000-04-11 | Anderson Cook, Inc. | Drive system for vertical rack spline-forming machine |
US5970768A (en) * | 1998-06-08 | 1999-10-26 | Utica Enterprises, Inc. | Machine base for supporting vertical movement of forming racks for rolling power transmission formations |
US5983690A (en) * | 1998-06-08 | 1999-11-16 | Utica Enterprises, Inc. | Machine having antifriction support for forming racks for rolling power transmission formations |
US5987953A (en) * | 1998-06-08 | 1999-11-23 | Utica Enterprises, Inc. | Power transmission formation rolling machine having movable headstock and tailstock spindle supports |
US10869968B2 (en) | 2015-04-23 | 2020-12-22 | Sanofi-Aventis Deutschland Gmbh | Drug delivery device and retaining member for a drug delivery device |
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