JPH0556566B2 - - Google Patents
Info
- Publication number
- JPH0556566B2 JPH0556566B2 JP85282354A JP28235485A JPH0556566B2 JP H0556566 B2 JPH0556566 B2 JP H0556566B2 JP 85282354 A JP85282354 A JP 85282354A JP 28235485 A JP28235485 A JP 28235485A JP H0556566 B2 JPH0556566 B2 JP H0556566B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- present
- carbon atoms
- durability
- magnetic 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.)
- Expired - Fee Related
Links
- -1 ester compound Chemical class 0.000 claims description 11
- 239000011230 binding agent Substances 0.000 claims description 8
- 239000006247 magnetic powder Substances 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 229910001566 austenite Inorganic materials 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 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
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 2
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 2
- 229960005235 piperonyl butoxide Drugs 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-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
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 229910017061 Fe Co Inorganic materials 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 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
- 230000035699 permeability Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Magnetic Record Carriers (AREA)
- Lubricants (AREA)
- Paints Or Removers (AREA)
Description
〔産業上の利用分野
本発明は磁気記録媒体に関する。詳しくは、耐
久性に優れた磁気記録媒体に関する。
〔従来の技術及び問題点〕
磁気記録媒体は、一般にポリエステルフイルム
などの基体上に、磁性粉末、結合剤樹脂、有機溶
剤及びその他の必要成分からなる磁性塗料を塗着
して作られるが、中でもフロツピーデイスクは記
録再生時に、磁気ヘツドやジヤケツトライナー等
と激しく摺接するために、磁性層が摩耗されやす
いので、磁性層の摩耗が少なくて耐久性に優れた
ものが要求される。
このため、磁性層の耐摩耗性を改善する一方策
として磁性層中に種々の潤滑剤を混入することが
行われている。
従来から使用されている潤滑剤としては脂肪
酸、オレイン酸オレイル、ステアリン酸ブトキシ
ド、脂肪酸アミド、流動パラフイン、ワツクス等
がある。しかしながら、これらの潤滑剤は性能面
では満足されるものとは言い難いのが現状であ
る。例えば、オレイン酸オレイル、ステアリン酸
ブトキシド等は媒体の耐久性向上に対して不十分
であり、ステアリン酸、オレイン酸等の脂肪酸や
流動パラフイン等の炭化水素系の潤滑剤は、耐久
性の向上には有効であるがバインダーとの相溶性
が悪く、多量に用いると磁性層表面からブリード
しヘツドを汚しやすい等の欠点がある。
〔問題点を解決するための手段〕
本発明者らは、良好な潤滑性が付与されて、幅
広い使用環境下でも大幅に耐久性が改善された磁
気記録媒体を得るべく鋭意研究の結果本発明に到
達した。
即ち、本発明は、磁性粉とバインダーを主たる
成分としてなる磁性層を有する磁気記録媒体にお
いて、前記磁性層が、下記一般式(1)で表されるエ
ステル化合物を含有することを特徴とする磁気記
録媒体を提供するものである。
{式中、R1及びR2は各々炭素数1〜25(ただしR1
とR2の炭素数の和は21〜32である)の直鎖又は
分岐を有する飽和アルキル基、R3はオレイル基
である。}
〔作用〕
本発明に係わる前記一般式(1)で表されるエステ
ル化合物は、ある限定された化合物であり、アル
コールに由来する部分は、炭素数23〜34の分岐ア
ルコールであり、樹脂酸に由来する部分はオレイ
ン酸であることが必要である。かかる特定のエス
テル化合物を潤滑剤に用いた場合に、磁気記録媒
体の潤滑性が大きく改善される理由については明
らかではない。
本発明者らの検討によれば、潤滑剤としてはバ
インダーとの相溶性の関係からエステル系が最適
であり、潤滑性の向上のためには分子量の比較的
大きなものがより効果的であつた。しかしなが
ら、分子量の大きな通常のエステルの多くのもの
は融点が高く、比較的高い温度領域での潤滑性は
良いが、例えば5℃といつた低い温度では流動性
と浸透性が不良となり、低温では媒体に良好な耐
久性を与えることはできなかつた。以上のことか
ら推測するに、分岐アルコールと不飽和脂肪酸の
相乗的作用で、本発明に係わるエステル化合物の
融点が低下し、これによつて、磁気記録媒体に良
好な潤滑性が付与されて耐久性が向上するものと
推測される。
本発明に係わるエステル化合物は炭素数23〜34
の分岐アルコールと、オレイン酸を用いたエステ
ル化反応によつて得ることができる。ここに用い
る分岐アルコールは、その合成方法からゲルベア
ルコールと呼ばれるものである。
本発明のエステル化合物は、磁性塗料中に添加
して用いてもよいし、適当な剤に溶解させて磁性
塗膜上に散布してもよい。又、本発明のエステル
化合物に更に通常の潤滑剤を加えることは差支え
ない。
本発明に係わる磁性粉としては針状形の微細な
γ−Fe2O3、Fe3O4、CrO2のような金属酸化物、
またCo被着γ−Fe2O3、Coドープγ−Fe2O3のよ
うな加工処理を施したγ−Fe2O3、鉄メタル粉、
微小板状のバリウムフエライト及びそのFe原子
の一部がTi、Co、Zn、V、Nb等の1種又は2種
以上で置換された磁性粉、Co、Fe−Co、Fe−
Ni等の金属又は合金の超微粉などが挙げられる。
これらのうち鉄メタル粉は特に化学的安定性が悪
いからこの改良のためニツケル、コバルト、チタ
ン、ケイ素、アルミニウムなどを金属原子、塩及
び酸化物の形で少量加えたり表面処理されること
があるが、これらを用いることもできる。鉄メタ
ル粉は又その安定化のため弱い酸化性雰囲気の中
で表面に薄い酸化皮膜を作らせることがあるが、
このように処理されたメタル粉を用いることもで
きる。
本発明において用いることができるバインダー
の例としては、ポリウレタン、ポリエステル、ポ
リ塩化ビニル、塩化ビニル酢酸ビニル共重合体、
ポリアクリロニトリル、ニトリルゴム、エポキシ
樹脂、アルキツド樹脂、ポリアミド、ポリアクリ
ル酸エステル、ポリメタクリル酸エステル、ポリ
酢酸ビニル、ポリビニルブチラール、塩化ビニリ
デン、塩化ビニリデン共重合体、硝化綿、マレイ
ン酸変性塩化ビニル/酢酸ビニル共重合体、エチ
ルセルロースなどが挙げられる。これらは単独で
用いてもよいが、通常2種類以上混合して用いら
れる。また、樹脂の硬さを調節するため可塑剤や
硬化剤を加えて使用することもできる。
また、バインダーの配合量は一般に磁性粉100
重量部に対して15〜60重量部である。最も大きな
結合力を有するバインダーであつても15重量部よ
り少ないときは磁性塗膜の強度が弱く、また基板
と磁性塗膜の接着力が不足となる。また60重量部
より多いときには磁性塗膜中の磁性粉濃度が小さ
くなつて再生出力が低下して不利である。また塗
膜特性が低下することもある。
また、前記一般式(1)で表されるエステル化合物
は通常磁性粉に対して1〜15重量%いられる。
〔実施例〕
以下、実施例により本発明を更に詳細に説明す
るが、本発明はこれらの実施例に限定されるもの
ではない。
実施例 1〜3
表1に示す潤滑剤を用い、下記に示す組成の混
合物を調製した。
Co被着γ−Fe2O3 100重量部
塩ビ/酢ビコポリマー*1 30
ニトリルブタジエンゴム*2 15
カーボンブラツク 7
酸化アルミニウム 6
トルエン 150
メチルエチルケトン 150
レシチン 1
潤滑剤 6
(注)*1 米国U.C.C.社製の商品名VAGH
*2 日本ゼオン社製の商品名1432J
次いで、上記混合物をサンドミルで15時間混練
し、その後ポリイソシアネート化合物(日本ポリ
ウレタン(株)製のコロネートL)を7重量部加えて
合計11種類の磁性塗料を調製した。次いでこれら
の塗料を厚さが75μのポリエチレンテレフタレー
トフイルム上に、乾燥膜厚が1.5μになるように塗
布し、乾燥後カレンダー処理を行つた。更に、こ
れを60℃で4日間放置して硬化反応を行つた後、
円盤状に打ち抜き、表面研磨して磁気デイスクを
製造した。
これらのデイスクをフロツピーデイスク加速耐
久製試験ドライブ中に装填し、再生出力が初期出
力の70%になるまでの走行時間を5℃において測
定することにより、各々の磁気デイスクの耐久性
を判定した。その結果を表1に示す。
[Industrial Field of Application] The present invention relates to magnetic recording media. Specifically, the present invention relates to a magnetic recording medium with excellent durability. [Prior Art and Problems] Magnetic recording media are generally made by applying a magnetic paint consisting of magnetic powder, binder resin, organic solvent, and other necessary components onto a substrate such as a polyester film. Since floppy disks come into violent sliding contact with magnetic heads, jacket liners, etc. during recording and reproduction, the magnetic layer is likely to be abraded, so a magnetic layer that is less abrasive and has excellent durability is required. Therefore, as a measure to improve the wear resistance of the magnetic layer, various lubricants are mixed into the magnetic layer. Conventionally used lubricants include fatty acids, oleyl oleate, butoxide stearate, fatty acid amides, liquid paraffin, wax, and the like. However, it is currently difficult to say that these lubricants are satisfactory in terms of performance. For example, oleyl oleate, butoxide stearate, etc. are insufficient for improving the durability of media, while fatty acids such as stearic acid and oleic acid, and hydrocarbon-based lubricants such as liquid paraffin are effective in improving durability. Although effective, it has poor compatibility with the binder, and when used in large quantities, it bleeds from the surface of the magnetic layer and tends to stain the head. [Means for Solving the Problems] The present inventors have developed the present invention as a result of intensive research in order to obtain a magnetic recording medium that is endowed with good lubricity and has significantly improved durability even under a wide range of usage environments. reached. That is, the present invention provides a magnetic recording medium having a magnetic layer containing magnetic powder and a binder as main components, wherein the magnetic layer contains an ester compound represented by the following general formula (1). It provides a recording medium. {In the formula, R 1 and R 2 each have 1 to 25 carbon atoms (however, R 1
and R 2 have a total number of carbon atoms of 21 to 32), a linear or branched saturated alkyl group, and R 3 is an oleyl group. } [Function] The ester compound represented by the general formula (1) according to the present invention is a certain limited compound, and the part derived from alcohol is a branched alcohol having 23 to 34 carbon atoms, and the resin acid The moiety derived from must be oleic acid. It is not clear why the lubricity of magnetic recording media is greatly improved when such specific ester compounds are used as lubricants. According to the studies conducted by the present inventors, ester-based lubricants are optimal in terms of compatibility with binders, and lubricants with relatively large molecular weights are more effective in improving lubricity. . However, many ordinary esters with large molecular weights have high melting points and have good lubricity at relatively high temperatures, but have poor fluidity and permeability at temperatures as low as 5°C, and at low temperatures. It was not possible to impart good durability to the media. Inferred from the above, the synergistic effect of the branched alcohol and unsaturated fatty acid lowers the melting point of the ester compound according to the present invention, thereby imparting good lubricity to the magnetic recording medium and increasing its durability. It is assumed that the performance will improve. The ester compound according to the present invention has 23 to 34 carbon atoms.
It can be obtained by an esterification reaction using a branched alcohol and oleic acid. The branched alcohol used here is called Guerbet alcohol because of its synthesis method. The ester compound of the present invention may be used by being added to a magnetic coating, or may be dissolved in a suitable agent and sprayed onto a magnetic coating. Furthermore, a conventional lubricant may be added to the ester compound of the present invention. The magnetic powder according to the present invention includes fine needle-shaped metal oxides such as γ-Fe 2 O 3 , Fe 3 O 4 , and CrO 2 ,
In addition, γ-Fe 2 O 3 treated with Co-coated γ-Fe 2 O 3 , Co-doped γ-Fe 2 O 3 , iron metal powder,
Microplate-like barium ferrite and magnetic powder in which part of its Fe atoms are replaced with one or more of Ti, Co, Zn, V, Nb, etc., Co, Fe-Co, Fe-
Examples include ultrafine powder of metals such as Ni or alloys.
Among these, iron metal powder has particularly poor chemical stability, so to improve this, small amounts of nickel, cobalt, titanium, silicon, aluminum, etc. are added in the form of metal atoms, salts, and oxides, or the surface is treated. However, these can also be used. Iron metal powder may also form a thin oxide film on its surface in a weakly oxidizing atmosphere to stabilize it.
Metal powder treated in this way can also be used. Examples of binders that can be used in the present invention include polyurethane, polyester, polyvinyl chloride, vinyl chloride vinyl acetate copolymer,
Polyacrylonitrile, nitrile rubber, epoxy resin, alkyd resin, polyamide, polyacrylic acid ester, polymethacrylic acid ester, polyvinyl acetate, polyvinyl butyral, vinylidene chloride, vinylidene chloride copolymer, nitrified cotton, maleic acid-modified vinyl chloride/acetic acid Examples include vinyl copolymers and ethyl cellulose. Although these may be used alone, two or more types are usually used in combination. Furthermore, a plasticizer or a hardening agent may be added to adjust the hardness of the resin. In addition, the amount of binder blended is generally 100% magnetic powder.
It is 15 to 60 parts by weight. Even if the binder has the highest binding strength, if it is less than 15 parts by weight, the strength of the magnetic coating will be weak and the adhesive strength between the substrate and the magnetic coating will be insufficient. On the other hand, when the amount is more than 60 parts by weight, the concentration of magnetic powder in the magnetic coating film decreases, which is disadvantageous because the reproduction output decreases. Furthermore, the properties of the coating film may deteriorate. Further, the ester compound represented by the general formula (1) is usually contained in an amount of 1 to 15% by weight based on the magnetic powder. [Examples] Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to these Examples. Examples 1 to 3 Using the lubricants shown in Table 1, mixtures having the compositions shown below were prepared. Co-adhered γ-Fe 2 O 3 100 parts by weight PVC/vinyl acetate copolymer *1 30 Nitrile butadiene rubber *2 15 Carbon black 7 Aluminum oxide 6 Toluene 150 Methyl ethyl ketone 150 Lecithin 1 Lubricant 6 (Note) *1 Manufactured by UCC, USA Product name VAGH *2 Product name 1432J manufactured by Nippon Zeon Co., Ltd. Next, the above mixture was kneaded in a sand mill for 15 hours, and then 7 parts by weight of a polyisocyanate compound (Coronate L manufactured by Nippon Polyurethane Co., Ltd.) was added to make a total of 11 types. A magnetic paint was prepared. Next, these paints were applied onto a polyethylene terephthalate film having a thickness of 75μ so that the dry film thickness was 1.5μ, and after drying, a calender treatment was performed. Furthermore, after leaving this at 60℃ for 4 days to perform a curing reaction,
A magnetic disk was manufactured by punching it into a disk shape and polishing the surface. The durability of each magnetic disk was determined by loading these disks into a floppy disk acceleration durability test drive and measuring the running time at 5°C until the playback output reached 70% of the initial output. . The results are shown in Table 1.
【表】
比較例 1〜6
実施例で用いた潤滑剤の代わりに、表2に示す
各種潤滑剤を6重量部用い、その他の成分とその
量は実施例1と同一にして、実施例の方法に準じ
て合計6種類の磁性塗料を調製した。これらの塗
料を用いて、実施例1と同じ方法で磁気デイスク
を製造し、これらデイスクの耐久性を調べた。そ
の結果は表2に示す。[Table] Comparative Examples 1 to 6 In place of the lubricant used in the example, 6 parts by weight of the various lubricants shown in Table 2 were used, and the other components and their amounts were the same as in Example 1. A total of six types of magnetic paints were prepared according to the method. Magnetic disks were manufactured using these paints in the same manner as in Example 1, and the durability of these disks was examined. The results are shown in Table 2.
Claims (1)
磁性層を有する磁気記憶媒体において、前記磁性
層が、下記一般式(1)で表されるエステル化合物を
含有することを特徴とする磁気記録媒体。 {式中、R1及びR2は各々炭素数1〜25(ただしR1
とR2の炭素数の和は21〜32である)の直鎖又は
分岐を有する飽和アルキル基、R3はオレイル基
である。}[Scope of Claims] 1. A magnetic storage medium having a magnetic layer mainly composed of magnetic powder and a binder, characterized in that the magnetic layer contains an ester compound represented by the following general formula (1). magnetic recording medium. {In the formula, R 1 and R 2 each have 1 to 25 carbon atoms (however, R 1
and R 2 have a total number of carbon atoms of 21 to 32), a linear or branched saturated alkyl group, and R 3 is an oleyl group. }
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/838,475 US4675250A (en) | 1985-03-20 | 1986-03-11 | Magnetic recording medium |
CA000504525A CA1258008A (en) | 1985-03-20 | 1986-03-19 | Magnetic recording medium |
ES553164A ES8802483A1 (en) | 1985-03-20 | 1986-03-19 | Magnetic recording medium. |
DE8686302059T DE3664969D1 (en) | 1985-03-20 | 1986-03-20 | Magnetic recording medium |
EP19860302059 EP0195675B1 (en) | 1985-03-20 | 1986-03-20 | Magnetic recording medium |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60-56554 | 1985-03-20 | ||
JP5655485 | 1985-03-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS621118A JPS621118A (en) | 1987-01-07 |
JPH0556566B2 true JPH0556566B2 (en) | 1993-08-19 |
Family
ID=13030326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60282354A Granted JPS621118A (en) | 1985-03-20 | 1985-12-16 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS621118A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2886788B2 (en) * | 1994-12-01 | 1999-04-26 | 日本板硝子株式会社 | Glass plate mounting structure |
JP2010271077A (en) | 2009-05-19 | 2010-12-02 | Toshiba Corp | Electromagnetic flow meter |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5698717A (en) * | 1980-01-11 | 1981-08-08 | Victor Co Of Japan Ltd | Magnetic recording medium |
-
1985
- 1985-12-16 JP JP60282354A patent/JPS621118A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5698717A (en) * | 1980-01-11 | 1981-08-08 | Victor Co Of Japan Ltd | Magnetic recording medium |
Also Published As
Publication number | Publication date |
---|---|
JPS621118A (en) | 1987-01-07 |
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