JPS63166009A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS63166009A JPS63166009A JP31222986A JP31222986A JPS63166009A JP S63166009 A JPS63166009 A JP S63166009A JP 31222986 A JP31222986 A JP 31222986A JP 31222986 A JP31222986 A JP 31222986A JP S63166009 A JPS63166009 A JP S63166009A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- vinyl chloride
- resin
- polyurethane resin
- chloride resin
- 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
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 31
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- 229920005749 polyurethane resin Polymers 0.000 claims abstract description 17
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000006185 dispersion Substances 0.000 claims abstract description 14
- 239000011248 coating agent Substances 0.000 claims abstract description 7
- 238000000576 coating method Methods 0.000 claims abstract description 7
- 239000003973 paint Substances 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 238000001179 sorption measurement Methods 0.000 abstract description 4
- 239000006247 magnetic powder Substances 0.000 abstract description 2
- 239000000696 magnetic material Substances 0.000 description 10
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 8
- 229920002554 vinyl polymer Polymers 0.000 description 8
- 239000000956 alloy Substances 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- -1 Ketchinplak E Chemical compound 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000005294 ferromagnetic effect Effects 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000001270 Allium sibiricum Nutrition 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- ULBTUVJTXULMLP-UHFFFAOYSA-N butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCC ULBTUVJTXULMLP-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229910001337 iron nitride Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000702 sendust Inorganic materials 0.000 description 1
- 125000000542 sulfonic acid group Chemical class 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【発明の詳細な説明】
磁気ディスク等に用いることができる磁気記録媒体に関
するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium that can be used for magnetic disks and the like.
従来の技術
近年、特にビデオテープの分野においては高密度記録を
めざすために従来の酸化鉄から金属2合金系へと磁性体
の研究開発が進んでいる。そのなかで、金属1合金系磁
性体については、均一な微粒子化を達成するために組成
、製造条件の改良が進められBET比表面積が60m2
/g以上のものが安定に製造できるようになった。さら
に、酸化鉄磁性体についてもBET比表面積が50 m
2/i以上のものが製造されるようになっている。この
ような微粒子の磁性体を用いて耐久性に優れた高密度記
録媒体を得るためにはテープとヘッドのインターフェイ
スの問題が重要となる。BACKGROUND OF THE INVENTION In recent years, particularly in the field of video tapes, research and development of magnetic materials has progressed from conventional iron oxide to metal-2 alloy systems in order to achieve high-density recording. Among these, the composition and manufacturing conditions of metal 1 alloy magnetic materials have been improved to achieve uniform fine particles, and the BET specific surface area has been reduced to 60 m2.
/g or more can now be stably produced. Furthermore, the BET specific surface area of iron oxide magnetic material is 50 m
Products with a ratio of 2/i or higher are now being manufactured. In order to obtain a high-density recording medium with excellent durability using such fine-grained magnetic material, the problem of the interface between the tape and the head becomes important.
このなかで耐摩耗性と電磁変換特性を決定するものとし
てバインダシステムと分散順序がある。Among these, the binder system and dispersion order determine wear resistance and electromagnetic conversion characteristics.
ポリウレタン樹脂と塩化ビニル樹脂を用いた系では特開
昭56−167771に開示されているようにポリウレ
タン樹脂で一次分散する方が塩化ビニル樹脂で一次分散
するよりも耐摩耗性に優れている。In a system using a polyurethane resin and a vinyl chloride resin, primary dispersion using a polyurethane resin is superior to primary dispersion using a vinyl chloride resin, as disclosed in JP-A-56-167771.
発明が解決しようとする問題点
しかしこのような従来の方法では表面性が悪く、BET
比表面積が30m279以下では満足できる電磁変換特
性であっても50 m27 g 以上のものでは電磁変
換特性が低下してしまうという問題点が、あった。Problems that the invention attempts to solve However, such conventional methods have poor superficiality, and the BET
If the specific surface area is 30 m279 or less, the electromagnetic conversion characteristics are satisfactory, but if the specific surface area is 50 m27 g or more, the electromagnetic conversion characteristics deteriorate.
本発明は、BET比表面積が50m2/g以上の微粒子
の磁性体を用いて耐摩耗性と電磁変換特性のいずれも満
足する磁気記録媒体を提供することを目的とするもので
ある。An object of the present invention is to provide a magnetic recording medium that satisfies both wear resistance and electromagnetic conversion characteristics by using fine particle magnetic material having a BET specific surface area of 50 m2/g or more.
問題点を解決するための手段
この問題点を解決するために、本発明の磁気記録媒体は
親水基を導入したポリウレタン樹脂で一次分散した後、
塩化ビニル樹脂で二次分散した磁性塗料を非磁性支持体
上に塗布して磁性層を形成したことを特徴とするもので
ある。Means for Solving the Problem In order to solve this problem, the magnetic recording medium of the present invention is made by first dispersing the polyurethane resin into which hydrophilic groups have been introduced, and then
It is characterized in that a magnetic layer is formed by coating a magnetic paint secondary dispersed with vinyl chloride resin on a non-magnetic support.
作 用
この構成によシ、分散性に基づく電磁変換特性と塗膜強
度に基づく耐摩耗性のいずれも満足させることが可能と
なる。Function: This configuration makes it possible to satisfy both electromagnetic conversion characteristics based on dispersibility and abrasion resistance based on coating film strength.
BET表面積が50 m279以上の微粒子の磁性体を
用いて高密度記録媒体を達成するためには、高分散によ
って表面粗度を小さくし電磁変換特性を向上させ、また
塗膜強度を向上させて走行耐久性を満足させなければな
らない。本発明者はポリウレタン樹脂と塩化ビニル樹脂
のバインダシステムを磁性体に対する樹脂の吸着という
観点から鋭意検討し、親水基を有するポリウレタン樹脂
で一次分散し、塩化ビニル樹脂で二次分散する方が、そ
の逆よりも、C/Nは殆んど変らずに耐久性において優
れた磁性塗膜が得られることを見い出したものである。In order to achieve a high-density recording medium using fine particle magnetic material with a BET surface area of 50 m279 or more, high dispersion reduces the surface roughness and improves electromagnetic conversion characteristics, and the coating strength is improved to improve running performance. Durability must be satisfied. The present inventor has intensively studied the binder system of polyurethane resin and vinyl chloride resin from the viewpoint of adsorption of the resin to the magnetic material, and found that it is better to perform primary dispersion with polyurethane resin having hydrophilic groups and secondary dispersion with vinyl chloride resin. It has been found that, rather than the reverse, a magnetic coating film with excellent durability can be obtained with almost no change in C/N.
これは耐摩耗性において塩化ビニル樹脂よりも優れてい
るポリウレタン樹脂が分子内の親水基によって磁性粉に
強固に吸着することが可能となったためである。従来、
ポリウレタン樹脂は塩化ビニル樹脂に比べて吸着量が少
ないものが多かったがその分子内に親水基を導入するこ
とにより吸着量を塩化ビニル樹脂と同等以上にすること
が可能となっており、本発明は耐久性の良い結果に基づ
いて分散順序を決定したものである。This is because polyurethane resin, which has better abrasion resistance than vinyl chloride resin, can be strongly adsorbed to magnetic powder by the hydrophilic groups in its molecules. Conventionally,
Many polyurethane resins have a lower adsorption amount than vinyl chloride resins, but by introducing hydrophilic groups into their molecules, it has become possible to make the adsorption amount equal to or higher than that of vinyl chloride resins, and the present invention The distribution order was determined based on the results with good durability.
本発明に用いられる磁性体としては、酸化鉄。The magnetic material used in the present invention is iron oxide.
CO被着酸化鉄、窒化鉄、金属もしくは合金磁性体など
があげられ、BET比表面積は50W12/、!9以上
のものである。Examples include CO-adhered iron oxide, iron nitride, metal or alloy magnetic material, and the BET specific surface area is 50W12/! 9 or higher.
結合剤としての親水基を導入したポリウレタン樹脂とは
分子内にリン酸基もしくはスルホン酸基又はそれらの金
属塩を有するものである。A polyurethane resin into which a hydrophilic group as a binder is introduced has a phosphoric acid group, a sulfonic acid group, or a metal salt thereof in the molecule.
塩化ビニル樹脂とは、塩化ビニル−酢酸ビニル−ビニル
アルコール共重合体、塩化ビニル−酢酸ビニル−マレイ
ン酸共重合体1分子内に親水基を有する塩化ビニル樹脂
誘導体などが用いられる。Examples of the vinyl chloride resin include vinyl chloride-vinyl acetate-vinyl alcohol copolymer, vinyl chloride-vinyl acetate-maleic acid copolymer, and vinyl chloride resin derivatives having a hydrophilic group in one molecule.
分散剤としてはレシチン、オレイン酸などが用いられる
。Lecithin, oleic acid, etc. are used as the dispersant.
潤滑剤としてはミリスチン酸、パルミチン酸、ステアリ
ン酸、ベヘン酸などの高級脂肪酸が使用できる。Higher fatty acids such as myristic acid, palmitic acid, stearic acid, and behenic acid can be used as lubricants.
研磨材としてはアルミナ、ベンガラ、酸化クロム。Alumina, red iron oxide, and chromium oxide are used as abrasive materials.
酸化チタンなどが用いられる。Titanium oxide or the like is used.
帯電防止剤としてはケッチンプラックE、C,のような
導電性カーボンを添加することもできる。さらにグラフ
ァイト化カーボンブラックを使用することもできる。磁
性塗料の混線分散にあたっては各種の分散機が使用され
る。As an antistatic agent, conductive carbon such as Ketchinplak E, C, etc. can also be added. Furthermore, graphitized carbon black can also be used. Various types of dispersion machines are used to disperse crosstalk in magnetic paint.
例えば、三本ロール、加圧ニーダ−、ダブルプラネタリ
ーミキアー、ボールミルヘンシェルミキサー、W動ミル
、ディスパーミル、ペブルミル。For example, a three-roll mill, a pressure kneader, a double planetary mill, a ball mill Henschel mixer, a double moving mill, a disper mill, and a pebble mill.
アジテータミルアトライタ、サンドグラインダー。Agitator mill attritor, sand grinder.
コボールミル、コンビミックス、ラインミル、ラインフ
ロ〜、ビンミルなどが単独もしくは組み合かせて用いら
れる。Coball mill, Combimix, line mill, line flow, bottle mill, etc. are used alone or in combination.
実施例 以下さらに本発明を具体的に説明する。Example The present invention will be further explained in detail below.
実施例1
強磁性Co被着r F e20s
スルホン酸ナトリウム基を有する 10重量部ポリウ
レタン樹脂
α−アルミナ(平均粒径 0.3μm) 5重量
部ステアリン酸 2重量部ステ
アリン酸n−ブチル 1重量部MEK−)
ルエンーシクロへキサ 1ooit量部ノン(2:2:
1 )
上記組成物を加圧ニーダ−で混線後コポールミルで一次
分散スる。次に塩化ビニル−ビニルアルコール−マレイ
ン酸共重合体10重量部とMEK−トルエン−シクロヘ
キサノン(2:2:1 )100重量部を加えてサンド
グラインダで二次分散して磁性塗料とした。コロネート
L(日本ポリウレタン製ポリイソシアネート)4重量部
を加えディスパーで混合分散した後、平均孔径1μmの
フィルターで濾過し、14μm厚のポリエチレンテレフ
タレートフィルム上に塗布、配向、乾燥。Example 1 Ferromagnetic Co-coated r Fe20s 10 parts by weight Polyurethane resin α-alumina (average particle size 0.3 μm) having sodium sulfonate group 5 parts by weight Stearic acid 2 parts by weight n-butyl stearate 1 part by weight MEK −)
Luene-cyclohexane 1 ooit part non(2:2:
1) The above composition is mixed in a pressure kneader and then primary dispersed in a Copol mill. Next, 10 parts by weight of vinyl chloride-vinyl alcohol-maleic acid copolymer and 100 parts by weight of MEK-toluene-cyclohexanone (2:2:1) were added and secondary dispersed using a sand grinder to obtain a magnetic paint. After adding 4 parts by weight of Coronate L (polyisocyanate manufactured by Nippon Polyurethane) and mixing and dispersing with a disper, the mixture was filtered through a filter with an average pore size of 1 μm, coated on a 14 μm thick polyethylene terephthalate film, oriented, and dried.
鏡面加工後硬化した。さらに磁性層と反対側のポリエチ
レンテレフタレートフィルム上ニカーボンブラックを主
成分とするバックコート層を設けて磁気テープを得た。Hardened after mirror polishing. Furthermore, a back coat layer containing carbon black as a main component was provided on the polyethylene terephthalate film on the side opposite to the magnetic layer to obtain a magnetic tape.
比較例1
実施例1において、スルホン酸ナトリウム基を有するポ
リウレタン樹脂と塩化ビニル−ビニルアルコール−マレ
イン酸共重合体を取シ換える以外は同様にして磁気テー
プを得た。Comparative Example 1 A magnetic tape was obtained in the same manner as in Example 1, except that the polyurethane resin having a sodium sulfonate group and the vinyl chloride-vinyl alcohol-maleic acid copolymer were replaced.
実施例2
実施例1において強磁性CO被着r−Fe2o3を強磁
性合金粉末に変更する以外は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 the ferromagnetic CO-coated r-Fe2o3 was changed to ferromagnetic alloy powder.
比較例2
実施例2において、スルホン酸ナトリウム基を有するポ
リウレタン樹脂と塩化ビニル−ビニルアルコール−マレ
イン酸共重合体を取り換える以外は同様にして磁気テー
プを得た。Comparative Example 2 A magnetic tape was obtained in the same manner as in Example 2, except that the polyurethane resin having a sodium sulfonate group and the vinyl chloride-vinyl alcohol-maleic acid copolymer were replaced.
得られ走者磁気テープをイインチに裁断し、カセットハ
ーフに巻きこんで5 MHzにおけるC/Nを測定した
。C/N測定用ビデオテープはVHSビデオテープレコ
ーダー(松下電器産業(株)製NV−8800)で合金
磁性体の場合には記録再生ヘッドはセンダスト合金に改
めた。標準テープとしてはナショナルビデオチーブ、ス
ーパーHGテープ(NV−TI 20HGA)松下電器
産業(株)夷を用い、そのC/NをOdBとした。耐久
性はテープを40℃、ao%RHの環境のもとで200
パス走行させた後の状態を観察した。表面粗度はランク
テーラーホプソン社のタリサーフで測定し、Raで表示
した。Raとは表面粗度の中心線よりの偏差の算術平均
を意味するものである。The obtained runner magnetic tape was cut into inch pieces, wound into a cassette half, and the C/N at 5 MHz was measured. The video tape for C/N measurement was a VHS video tape recorder (NV-8800, manufactured by Matsushita Electric Industrial Co., Ltd.), and in the case of alloy magnetic material, the recording/reproducing head was changed to Sendust alloy. National Video Chive and Super HG tape (NV-TI 20HGA) manufactured by Matsushita Electric Industrial Co., Ltd. were used as standard tapes, and the C/N was set to OdB. The durability of the tape is 200℃ under an environment of 40℃ and ao%RH.
The condition was observed after passing. The surface roughness was measured using Talysurf manufactured by Rank Taylor Hopson and expressed in Ra. Ra means the arithmetic mean of the deviations of the surface roughness from the center line.
実施例と対応する比較例から明らかなように、親水基を
有するポリウレタン樹脂で一次分散し、塩化ビニル樹脂
で二次分散する方が、その逆よシも、C/Nは殆んど変
らずに耐久性において優れている。As is clear from the examples and corresponding comparative examples, C/N hardly changes when primary dispersion is performed using a polyurethane resin having hydrophilic groups and secondary dispersion is performed using vinyl chloride resin, and vice versa. It has excellent durability.
発明の効果
以上のように本発明によれば電磁変換特性上耐久性の双
方を満足する磁気記録媒体を得ることができる。Effects of the Invention As described above, according to the present invention, a magnetic recording medium that satisfies both electromagnetic characteristics and durability can be obtained.
なお、上記実施例では磁気テープについて説明したが、
本発明は磁気テープのみならず、磁気ディスク、磁気カ
ード等の磁気記録媒体にも応用可能であることはいうま
でもない。In addition, in the above embodiment, a magnetic tape was explained, but
It goes without saying that the present invention is applicable not only to magnetic tapes but also to magnetic recording media such as magnetic disks and magnetic cards.
Claims (1)
塩化ビニル樹脂で二次分散した磁性塗料を非磁性支持体
上に塗布して磁性層を形成したことを特徴とする磁気記
録媒体。After primary dispersion using polyurethane resin with hydrophilic groups introduced,
A magnetic recording medium characterized in that a magnetic layer is formed by coating a magnetic paint secondary dispersed with vinyl chloride resin on a non-magnetic support.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31222986A JPS63166009A (en) | 1986-12-26 | 1986-12-26 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31222986A JPS63166009A (en) | 1986-12-26 | 1986-12-26 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63166009A true JPS63166009A (en) | 1988-07-09 |
Family
ID=18026734
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31222986A Pending JPS63166009A (en) | 1986-12-26 | 1986-12-26 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63166009A (en) |
-
1986
- 1986-12-26 JP JP31222986A patent/JPS63166009A/en active Pending
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