JPS62192929A - Production of magnetic recording medium - Google Patents
Production of magnetic recording mediumInfo
- Publication number
- JPS62192929A JPS62192929A JP3591486A JP3591486A JPS62192929A JP S62192929 A JPS62192929 A JP S62192929A JP 3591486 A JP3591486 A JP 3591486A JP 3591486 A JP3591486 A JP 3591486A JP S62192929 A JPS62192929 A JP S62192929A
- Authority
- JP
- Japan
- Prior art keywords
- radiation
- magnetic
- magnetic recording
- atmosphere
- layer
- 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
Links
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 61
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 230000005855 radiation Effects 0.000 claims abstract description 18
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 10
- 239000011248 coating agent Substances 0.000 abstract description 5
- 238000000576 coating method Methods 0.000 abstract description 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 5
- 229920006267 polyester film Polymers 0.000 abstract description 5
- 238000001035 drying Methods 0.000 abstract description 4
- 238000005498 polishing Methods 0.000 abstract description 4
- 239000004576 sand Substances 0.000 abstract 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 abstract description 2
- 230000005294 ferromagnetic effect Effects 0.000 abstract description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000787 lecithin Substances 0.000 abstract description 2
- 229940067606 lecithin Drugs 0.000 abstract description 2
- 235000010445 lecithin Nutrition 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 229920005749 polyurethane resin Polymers 0.000 abstract description 2
- 239000011148 porous material Substances 0.000 abstract description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 238000004898 kneading Methods 0.000 abstract 1
- 239000011877 solvent mixture Substances 0.000 abstract 1
- 238000010894 electron beam technology Methods 0.000 description 11
- 239000003973 paint Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 229920001187 thermosetting polymer Polymers 0.000 description 5
- 231100000987 absorbed dose Toxicity 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- -1 polyethylene terephthalate Polymers 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 239000006247 magnetic powder Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000003847 radiation curing Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L magnesium chloride Substances [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Manufacturing Of Magnetic Record Carriers (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、オーディオ、ビデオ機器あるいはコンピュー
ター等に用いる磁気テープ、磁気ディスク等の磁気記録
媒体に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to magnetic recording media such as magnetic tapes and magnetic disks used in audio and video equipment, computers, and the like.
従来の技術
近年、上記の各磁気記録媒体は高密度記録に向かい、そ
のため記録波長は短く、記録トラック幅は狭く、記録媒
体厚は薄くという方向にある。その結果、再生出力、S
N比等の電磁変換特性は、一般に不利になってきている
。従来の磁気記録媒体は、主として磁性層の耐久性改善
の目的から、21、−
塗布直前に反応性に富んだ硬化剤を加えたいわゆる熱硬
化型磁性塗料を、非磁性支持体に塗布、乾燥、カレンダ
処理後、比較的長時間の熱処理を加えて得られていたこ
とから、特性が均質で、且つ、高平滑な表面性を有する
磁気記録媒体の製造には種々の問題が生じていた。例え
ば、磁性塗料のポットライフの短さからくる塗膜特性の
ばらつき、あるいは、磁性層の表面性が磁性粉の分散性
のみならず、磁性層の形成される非磁性粉支持体の表面
性や非磁性支持体上の形成されるバックコート層の表面
性の影響を極めて受は易く、その影響度も製品の長手方
向で傾斜をもつなどの問題があげられる。こうした従来
の熱硬化型磁気記録媒体の問題点を解決するために、放
射線硬化性結合剤を含有した磁性層に放射線照射を施し
塗膜を硬化させる、いわゆる放射線硬化型磁気記録媒体
の提案がこれまでにも数多く成されている。BACKGROUND OF THE INVENTION In recent years, the above-mentioned magnetic recording media are moving toward high-density recording, and therefore the recording wavelength is becoming shorter, the recording track width is narrower, and the recording medium thickness is becoming thinner. As a result, the playback output, S
Electromagnetic conversion characteristics such as N ratio are generally becoming disadvantageous. Conventional magnetic recording media are manufactured mainly for the purpose of improving the durability of the magnetic layer. Since these magnetic recording media were obtained by applying heat treatment for a relatively long time after calendering, various problems occurred in the production of magnetic recording media having homogeneous characteristics and highly smooth surfaces. For example, variations in coating film properties due to the short pot life of magnetic paints, or variations in the surface properties of the magnetic layer, not only due to the dispersibility of the magnetic powder but also due to the surface properties of the non-magnetic powder support on which the magnetic layer is formed. It is extremely susceptible to the influence of the surface properties of the back coat layer formed on the non-magnetic support, and there are problems such as the degree of influence being inclined in the longitudinal direction of the product. In order to solve these problems with conventional thermosetting magnetic recording media, a so-called radiation-curable magnetic recording medium was proposed, in which a magnetic layer containing a radiation-curable binder is irradiated with radiation to harden the coating. Many have already been done.
放射線硬化型樹脂は、一般には熱硬化型樹脂を放射線感
応変性したもので、具体例としては、ラジカル重合性を
有する不飽和二重結合を示すアクリル酸、メタアクリル
酸あるいは一′f、t1らの工×デル化合物のJ:つな
(メタ)アクリル系−1F結合やマレイン酸、マレイン
酸誘ノ、す体の二重結合等の放射線照射による架橋ある
いは重合する部分五で分子中に導入することである。そ
の他IJ(射線照射により架橋あるいは申合する不飽和
■−6中結合であれば用いることができる。このような
放射#1lflV!化型樹脂は、(1’i独もしくは複
数1中の組み合わせがnJ能であり、・V−璧に応じて
熱硬化型樹脂との併用も差し支えない。Radiation-curable resins are generally radiation-sensitive modified thermosetting resins, and specific examples include acrylic acid, methacrylic acid, 1'f, t1, etc., which exhibit radically polymerizable unsaturated double bonds. Noko x Dell compound J: Introducing into the molecule at the part 5 that crosslinks or polymerizes by radiation irradiation such as tuna (meth)acrylic-1F bond, maleic acid, maleic acid induction, and double bond of the body. That's true. Other IJ (unsaturated ■-6 bonds that are crosslinked or agreed by radiation irradiation can be used. Such radiation #1lflV! type resin has (1'i alone or a combination of nJ capacity, and can be used in combination with a thermosetting resin depending on the V-performance.
放射線としては、電子線加11柵”4%−線源とした電
子線、0060を線源としたr線、X線発生器を線源と
したX線等が使用される。特に照射線源と1、では吸収
線fifeの制御、製潰工稈ラインへの導入。As the radiation, an electron beam using an electron beam added as a 4% source, an r-ray using a 0060 as a source, an X-ray using an X-ray generator as a source, etc. are used. In particular, an irradiation source In 1, the absorption line fife is controlled and introduced into the crusher culm line.
電離放身1線の箇蔽雪の見地舌から、電子線加速器によ
る電子線(1Φ化法が有利である。電子−線加i土器の
具体例としてにY、米国エナジー型イエンス社にて製造
されている1氏線量タイプの電子線加速器(工1/り1
・「1カー゛jンシステム)や[−1新バイポルチーシ
ネ1製のスキャニング型低線量′タイプの電子線!h[
1速器等があlh 。From the point of view of the coverage of ionizing radiation, the electron beam (1Φ method) using an electron beam accelerator is advantageous. 1 degree dose type electron beam accelerator (engineering 1/ri 1)
・“1-carn system) and scanning type low-dose” type electron beam made by [-1 New Bipolar Cine 1]
There are 1 speed gear etc.
1だ、放射線架橋(F際t、−’rii、 N、 カ
ス、 CO。1, radiation cross-linking (Ft, -'rii, N, Kas, CO.
カス舌の不活性カス気流中でIJ(射線肴′・磁1/1
層(て照射ノーることかイ]効である。″と気中ての放
射線照射Qま、バインダー中に41−したラジカルが酸
素あるいけ放射線照射により牛L2だオゾン舌の影響で
バインダーの重合、硬化が阻害さ11る/こめ好−牛し
7〈ない。IJ (radiation appetizer'・magnetic 1/1
It is said that the 41-radicals in the binder are exposed to oxygen, and due to radiation irradiation, the binder polymerizes due to the influence of ozone. , hardening is inhibited.
従来、磁気記録媒体(たとえは、力士)[・に装着され
た劃−ディオテープ、ビデ」デーゾ)は室内の温度変化
が徳交・かな環境で使用、保管されてきた。近年、ラジ
カセ、ビデオカメラ、8m1nヒテオなどが広く使用さ
れるようになり、磁気記録媒体が屋外の高温、低温の環
境で使用、保管されることが多くな−)でいる。!持C
′高温さらには高渦高湿時において、磁気記録媒体のX
j法変11三か著しく生じ易くスギュー(Skew)の
発生−や、出力低下/(云けでなく、カール等の発生の
ため走行不良をひきおとし易い。昨今の磁気記録ンスデ
ノ・の多様化。Traditionally, magnetic recording media (for example, a sumo wrestler) have been used and stored in environments where the indoor temperature is subject to fluctuations. In recent years, radio cassette players, video cameras, 8m1n Hiteo, etc. have become widely used, and magnetic recording media are often used and stored outdoors at high or low temperatures. ! Hold C
'At high temperatures, high vortices, and high humidity, the magnetic recording medium's
It is extremely easy to cause skew, output drop/(not to mention curling, etc.), which can easily lead to poor running.The recent diversification of magnetic recording devices.
高性能化に伴い、ますます十行信幀性が中蟹規さ51、
−7
)1、かかる−I′i酷な環境下での磁気記録媒体の特
性維すが求められている。With the improvement of performance, the reliability of the ten lines is becoming more and more the norm51.
-7) 1. It is required to maintain the characteristics of magnetic recording media under such harsh environments.
従来これらを解決するために、低熱117縮率のイース
フ2イルムの使用(例えば特開昭59−11531号公
報、!特開昭59−107424号公報、特開昭60−
15830け公報、特開昭60−98524号公報)、
ベースフィルムをあらかじめ熱処理したものを使用(例
えば特開昭69−135632月公報、特開昭60−1
03517 ケ公報)する等の案がある。Conventionally, in order to solve these problems, the use of East-F2 film with a low thermal shrinkage ratio of 117 (for example, JP-A-59-11531, JP-A-59-107-424, JP-A-Sho 60-
15830, Japanese Patent Application Laid-open No. 60-98524),
Use a base film that has been heat-treated in advance (for example, JP-A No. 69-135632, JP-A No. 60-1
There is a proposal to do so.
発明が解決[7ようとする問題点
昨今、磁気記録媒体の高密度化に伴いベースフィルムの
薄膜化が進み機械的強度が弱くなる一方、放射線硬化型
樹脂を含んだ磁気記録媒体は、従来の熱硬化型樹脂を用
いたものに比べて先述の如く多くの特徴が認められるも
のの、熱硬化における残留応力の緩和の工程がないため
、磁気記録媒体の=t−t−法灯定性らに田作な物にし
ている。このため従来の方法では、放射線硬化型樹脂を
含んだ磁気記録媒体の高温時の特性維持が、不充分とな
っている。Problems to be Solved by the Invention [7] In recent years, as the density of magnetic recording media has increased, base films have become thinner and their mechanical strength has weakened. Although it has many characteristics compared to those using thermosetting resins as mentioned above, there is no process of relaxing residual stress during thermosetting, so the = t-t method characteristics of magnetic recording media are not as good. I'm making it a work of art. For this reason, conventional methods are insufficient to maintain the characteristics of magnetic recording media containing radiation-curable resins at high temperatures.
本発明は上記問題に鑑み、放射線硬化型樹脂を含有する
層を形成してなる磁気記録媒体か高温[:あるいは高温
高湿下に置かれても熱収縮による磁気記録媒体の変形が
小さく、優れた寸法安定性を有し、安定した走行性を有
する磁気記録媒体を1是供するものである。In view of the above-mentioned problems, the present invention provides a magnetic recording medium formed with a layer containing a radiation-curable resin, which is superior in that deformation of the magnetic recording medium due to heat shrinkage is small even when placed under high temperature or high temperature and high humidity. The present invention provides a magnetic recording medium having high dimensional stability and stable running performance.
問題点を解決するだめの手段
上記問題点を解決するために、本発明の磁気記録媒体の
製造法は非磁性支持体上に、放射線硬化型樹脂を含有す
る層を形成し、相対湿度60%以上の雰囲気中で放射線
硬化することを特徴とするものである。Means for Solving the Problems In order to solve the above problems, the method for manufacturing a magnetic recording medium of the present invention involves forming a layer containing a radiation-curable resin on a non-magnetic support, and forming a layer containing a radiation-curable resin at a relative humidity of 60%. It is characterized by radiation curing in the above atmosphere.
作用
本発明は上記の方法によって、01に不活性ガス気流中
で放射線を照射するだけでなく、湿度もかけることによ
り水分が可塑剤と[7て働き磁気記録媒体内部の残留歪
みを確実迅速に取り除き、高温高湿下での寸法安定性を
改善するととができる。Operation The present invention uses the method described above to not only irradiate 01 with radiation in an inert gas stream but also apply humidity so that the moisture acts with the plasticizer [7] to reliably and quickly remove residual strain inside the magnetic recording medium. It can be removed to improve dimensional stability under high temperature and high humidity conditions.
実施例
以下本発明の実施例について、磁気テープで具体的に説
明する。なお実施例で述べている成分の部数は、すべて
重量比を示すものとする。EXAMPLES Hereinafter, examples of the present invention will be specifically explained using a magnetic tape. Note that all parts of components mentioned in the examples indicate weight ratios.
非磁性支持体として、ポリエチレンテレフタレート、ポ
リエチレン−2,6−ナフタレート等のポリエステル類
;ポリエチレン、ポリプロピレン等のポリオレフィン類
;セルローストリアセテート、セルロースダイアセテー
ト、セルロースアセテートブチ−レート、セルロースア
セテートプロピオネート類のセルロース誘導体;ポリ塩
化ビニル、ポリ塩化ビニリデン等のビニル系樹脂;ポリ
カーボネート、ポリイミド、ポリエーテルイミドポリア
ミドイミド等のプラスチックフィルム等があげられるが
、どれについても適用可能である0(実施例1)
磁性層用塗料〔A〕の調整;
強磁性CO被着γ−Fe203
100部
電子線硬化型ポリウレタン樹脂 10部塩化ビニ
ール酢酸ビニル共重合体 10部カーボンブランク
3部研摩剤(A1203)
4部レシチン
1部混合溶剤[” M li: K /
l−ルエン/アノン−1/1/1)300部
上記組成物をボールミル及びザンドミルを用いて混線分
散をおこなった後、平均孔径1μmのフィルターでろ過
して磁性層用塗料(’−A:B、準備した。Non-magnetic supports include polyesters such as polyethylene terephthalate and polyethylene-2,6-naphthalate; polyolefins such as polyethylene and polypropylene; cellulose such as cellulose triacetate, cellulose diacetate, cellulose acetate butyrate, and cellulose acetate propionate. Derivatives: Vinyl resins such as polyvinyl chloride and polyvinylidene chloride; Plastic films such as polycarbonate, polyimide, polyetherimide, polyamideimide, etc., but any can be applied.0 (Example 1) For magnetic layer Adjustment of paint [A]; Ferromagnetic CO-coated γ-Fe203 100 parts Electron beam curable polyurethane resin 10 parts Vinyl chloride vinyl acetate copolymer 10 parts Carbon blank 3 parts Abrasive agent (A1203)
4 part lecithin
1 part mixed solvent [” M li: K /
300 parts of the above composition (1-luene/anone-1/1/1) was subjected to cross-dispersion using a ball mill and a sand mill, and then filtered through a filter with an average pore size of 1 μm to obtain a magnetic layer coating material ('-A:B ,Got ready.
上記磁性塗料(A)を表1のポリエステルフィルム上に
塗布、磁場配向、乾燥処理を施した後、スーパーカレン
ダロールによる鏡面加工処理、次いで加速電圧160k
v吸収線量としてs Mradとなる条件で電子線照射
全窒素気流下で相対湿度60%の雰囲気中で行い、厚さ
511mの磁性層を有する原反ロールを得た。これt’
Aインチ幅に裁断して、ビデオテープ試料(250m長
)を製造9A−1
した。The above magnetic paint (A) was applied onto the polyester film shown in Table 1, subjected to magnetic field orientation, and drying treatment, followed by mirror polishing treatment using a super calender roll, and then an accelerating voltage of 160 k.
Electron beam irradiation was carried out under conditions such that the absorbed dose was s Mrad in an atmosphere with a relative humidity of 60% under a total nitrogen flow to obtain a raw roll having a magnetic layer with a thickness of 511 m. This is t'
A videotape sample (250 m long) was manufactured by cutting it to an A inch width.
(実施例2)
」−配出性塗料(A)’e表1のポリエステルフィルム
」二に塗布、磁場配向、乾燥処理を施した後、スーパー
カレンダロールによる鏡面加工処理、次いで加速電圧1
60kV吸収線量としてsMradとなる条件で電子線
照射を窒素気流下で相対湿度80%の雰囲気中で行い、
厚さE511mの磁性層を有する原反ロールを得た○こ
れをμインチ幅に裁断して、ビデオテープ試料(260
m長)を製造したO
(比較例1)
上記磁性塗料(Al:l’を表1のポリエステルフィル
ム上に塗布、磁場配向、乾燥処理を施した後、スーパー
カレンダロールによる鏡面加工処理、次いで加速電圧1
60kv吸収線量として8 Mradとなる条件で電子
線照射を窒素気流下で相対湿度40%の雰囲気中で行い
、厚さ5μmの磁性層を有する原反ロールを得た0これ
に’Aインチ幅に裁断して、ビデオテープ試料(250
77+、長)を製造10.1.、
した。(Example 2) "-Distributable paint (A) 'e Polyester film shown in Table 1" was applied, magnetic field oriented, and dried, followed by mirror polishing treatment using a super calender roll, and then accelerated voltage 1
Electron beam irradiation was performed in an atmosphere with a relative humidity of 80% under a nitrogen stream under conditions such that the absorbed dose was sMrad at 60 kV.
A raw roll having a magnetic layer with a thickness of E511 m was obtained. This was cut into μ inch width and a videotape sample (260 mm) was obtained.
(Comparative Example 1) The magnetic paint (Al:l') was applied onto the polyester film shown in Table 1, subjected to magnetic field orientation and drying treatment, followed by mirror polishing treatment using a super calender roll, and then accelerated treatment. Voltage 1
Electron beam irradiation was carried out in an atmosphere with a relative humidity of 40% under a nitrogen stream under conditions such that the absorbed dose of 60 kV was 8 Mrad, and a raw roll having a magnetic layer with a thickness of 5 μm was obtained. Cut and cut videotape samples (250
77+, long) manufactured 10.1. , did.
(比較例2)
上記磁性塗料CAlk表1のポリエステルフィルム上に
塗布、磁場配向、乾燥処理を施した後、スーパーカレン
ダロールによる鏡面加工処理、次いで加速電圧160k
V吸収線量としてs Mradとなる条件で電子線照射
を窒素気流下で相対湿度50%の雰囲気中で行い、厚さ
1511mの磁性層を有する原反ロールを得た。これを
捧インチ幅に裁断して、ビデオテープ試料(260m長
)を製造した。(Comparative Example 2) The above magnetic paint CAlk was coated on the polyester film shown in Table 1, subjected to magnetic field orientation, and drying treatment, followed by mirror finishing treatment using a super calender roll, and then an accelerating voltage of 160 k.
Electron beam irradiation was performed in an atmosphere of 50% relative humidity under a nitrogen stream under conditions such that the V absorbed dose was s Mrad, and a raw roll having a magnetic layer with a thickness of 1511 m was obtained. This was cut into inch-wide pieces to produce videotape samples (260 m long).
表1
」ン、−にの各実施例及び比較例で得られた磁気テープ
i?’L料を用いて、表2の結束を得た。Table 1 Magnetic tape i? obtained in each of the Examples and Comparative Examples. Using L material, the bonds shown in Table 2 were obtained.
表2
1)熱収縮率
熱処理条ply;1oo″C11時間
熱収縮率−(L−L’) /L X100(%)L;熱
処理前の試料テープの長さ
くat30’c)
L′;熱処理後の試料テープの長さ
くat30℃)
2)カール
手記の熱処理条件で、[1祝検f1で判定し〜だ。Table 2 1) Heat shrinkage rate Heat treatment strip ply; 1oo''C11 hour heat shrinkage rate - (L-L') /L (The length of the sample tape is at 30°C) 2) Under the heat treatment conditions described in Carl's notes, it was determined by [1st test f1].
39走行件
VH8方式VTR(松−1−電器産業(株)製、N Y
−8200) f、60 ”(+ (7)環境1;で
走行させ安定性を:みた。39 runs VH8 type VTR (Matsu-1-manufactured by Denki Sangyo Co., Ltd., NY)
-8200) f, 60'' (+ (7) Environment 1; Run to check stability.
発明の効果
以−ヒのように本発明によれ(d、川砂4Ilダ持体上
に、放射線(1q1化型樹脂を含有する層を形成し、相
対湿度60%す、上の雰囲気中で放射線硬化−すること
に」:す、磁気記録媒体が高温下あるいは高温高湿下に
置かれても、熱II又縮による磁気記録媒体の変形か小
さく、1・ρれた・」法灯定性を・有1〜、安定した走
行性を有する磁気記録媒体を、17′I′gじ4゛るこ
とができる。According to the present invention, a layer containing a radiation (1q1) type resin is formed on a river sand 4Il da carrier, and a layer containing radiation (1q1) type resin is formed on the river sand 4Il da carrier, and radiation Curing: Even if the magnetic recording medium is placed under high temperature or high temperature and high humidity, the deformation of the magnetic recording medium due to heat II or shrinkage is small, and the stability of the magnetic recording medium is 1.ρ.・A magnetic recording medium having stable running properties can be produced as much as 17'I'g.
々お、I−記実施例では磁気テープについて説明をした
が、本発明は、磁気テープのみならず、磁気デ2イスク
、磁気カード等の他の磁気記録媒体に、応用可能である
ことは言う寸でもない。Although magnetic tape has been described in Example I, it should be noted that the present invention is applicable not only to magnetic tape but also to other magnetic recording media such as magnetic disks and magnetic cards. It's not even a size.
Claims (1)
成し、相対湿度60%以上の雰囲気中で放射線硬化する
ことを特徴とする磁気記録媒体の製造法。A method for producing a magnetic recording medium, which comprises forming a layer containing a radiation-curable resin on a non-magnetic support, and curing the layer with radiation in an atmosphere with a relative humidity of 60% or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3591486A JPH071547B2 (en) | 1986-02-20 | 1986-02-20 | Method of manufacturing magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3591486A JPH071547B2 (en) | 1986-02-20 | 1986-02-20 | Method of manufacturing magnetic recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62192929A true JPS62192929A (en) | 1987-08-24 |
JPH071547B2 JPH071547B2 (en) | 1995-01-11 |
Family
ID=12455297
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3591486A Expired - Lifetime JPH071547B2 (en) | 1986-02-20 | 1986-02-20 | Method of manufacturing magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH071547B2 (en) |
-
1986
- 1986-02-20 JP JP3591486A patent/JPH071547B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH071547B2 (en) | 1995-01-11 |
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