JPS6076019A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS6076019A JPS6076019A JP58183533A JP18353383A JPS6076019A JP S6076019 A JPS6076019 A JP S6076019A JP 58183533 A JP58183533 A JP 58183533A JP 18353383 A JP18353383 A JP 18353383A JP S6076019 A JPS6076019 A JP S6076019A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- layer
- compd
- lubricant
- recording medium
- 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
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 239000000126 substance Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 abstract description 21
- 239000011230 binding agent Substances 0.000 abstract description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052799 carbon Inorganic materials 0.000 abstract description 5
- 239000006247 magnetic powder Substances 0.000 abstract description 5
- 230000001105 regulatory effect Effects 0.000 abstract 2
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 32
- -1 fatty acid esters Chemical class 0.000 description 20
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 14
- 239000011248 coating agent Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000003973 paint Substances 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000011247 coating layer Substances 0.000 description 5
- NVKSMKFBUGBIGE-UHFFFAOYSA-N 2-(tetradecoxymethyl)oxirane Chemical compound CCCCCCCCCCCCCCOCC1CO1 NVKSMKFBUGBIGE-UHFFFAOYSA-N 0.000 description 4
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 4
- 235000021360 Myristic acid Nutrition 0.000 description 4
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- VMSIYTPWZLSMOH-UHFFFAOYSA-N 2-(dodecoxymethyl)oxirane Chemical compound CCCCCCCCCCCCOCC1CO1 VMSIYTPWZLSMOH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- 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 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- AYTAKQFHWFYBMA-UHFFFAOYSA-N chromium dioxide Chemical compound O=[Cr]=O AYTAKQFHWFYBMA-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000000787 lecithin Substances 0.000 description 2
- 229940067606 lecithin Drugs 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- NFJRZZOZYGUSSF-UHFFFAOYSA-N CCCCCC.C(CCCCCCCCCCC)CC(=O)O Chemical compound CCCCCC.C(CCCCCCCCCCC)CC(=O)O NFJRZZOZYGUSSF-UHFFFAOYSA-N 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910020674 Co—B Inorganic materials 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 229910017061 Fe Co Inorganic materials 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 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
- 238000007259 addition reaction Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 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
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- FHTACFVZIAVFCY-UHFFFAOYSA-N buta-1,3-diene;2-methylprop-2-enoic acid;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N.CC(=C)C(O)=O FHTACFVZIAVFCY-UHFFFAOYSA-N 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- LTMGJWZFKVPEBX-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile;prop-2-enoic acid Chemical compound C=CC=C.C=CC#N.OC(=O)C=C LTMGJWZFKVPEBX-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000003795 chemical substances by application 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
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- PJWNIOJGDLTZPK-UHFFFAOYSA-N cyclohexanone;methanol Chemical compound OC.O=C1CCCCC1 PJWNIOJGDLTZPK-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910001337 iron nitride Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide 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
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide 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
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000005236 sound signal Effects 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
- Lubricants (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、非磁性支持体上に磁性層を有する磁気記録媒
体、例えば磁気テープ、磁気ディスクに関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium having a magnetic layer on a non-magnetic support, such as a magnetic tape or a magnetic disk.
磁気テープには特に摩擦係数が小さいこと及び円滑且つ
安定な走行性を有することをはじめ、粉落ち量が少ない
こと、スプライス性が良いこと等、各種の特性が要求さ
れる。即ち、磁気テープがVTR等の磁気記録再生装置
に使用される場合、テープガイド類、磁気ヘッド等と物
理的に接触しつつ高速度で走行するので耐摩耗性に優れ
しかも長時間に亘って安定に走行し得ることが重要とな
る。例えば、記録又は再生時にテープ表面の摩擦係数が
変化すると、テープはガイドや磁気ヘッドの箇所で振動
してしまう。この結果テープへの記録・再生信号(例え
ば音声信号)は周波数に変化をきたし、原周波数とは違
った音になったり、或いはテープの振動音(いわゆるQ
音)が直接聞こえてしまうという欠点がある。Magnetic tapes are particularly required to have various properties, including a low coefficient of friction, smooth and stable running properties, a small amount of powder falling off, and good splicability. That is, when magnetic tape is used in magnetic recording and reproducing devices such as VTRs, it runs at high speed while physically contacting tape guides, magnetic heads, etc., so it has excellent wear resistance and remains stable over long periods of time. It is important to be able to drive in For example, if the friction coefficient of the tape surface changes during recording or reproduction, the tape will vibrate at the guide or magnetic head. As a result, the signals recorded and played back on the tape (for example, audio signals) change in frequency, resulting in a sound different from the original frequency, or the vibration of the tape (so-called Q
The disadvantage is that the sound (sound) can be heard directly.
これを防止するために、テープに滑性を付与することが
従来から種々試みられている。例えば磁性粉末と結合剤
を含む磁性塗料中に、二硫化モリブデン、グラファイト
、ワックス等の固形滑剤を添加している。しかしこの固
形滑剤は、耐久性の向上にとってさほど効果がない上に
、多量に添加すると磁気特性を劣化させるので望ましく
ない。In order to prevent this, various attempts have been made to impart lubricity to the tape. For example, a solid lubricant such as molybdenum disulfide, graphite, or wax is added to a magnetic paint containing magnetic powder and a binder. However, this solid lubricant is undesirable because it is not very effective in improving durability and, when added in large amounts, deteriorates the magnetic properties.
他方、高級脂肪酸、高級脂肪酸エステル、パラフィン系
炭化水素、シリコンオイル(例えばジメチルシリコンオ
イル、ジフェニルシリコンオイル〉等を滑剤として使用
する場合もあるが、これでも充分な耐久性と渭lh性を
付与することができず、特にVTRのカセント用には不
充分である。しかも磁性層表面へ滑剤かにじみ出すブル
ーミングが生じ易く、テープの貼付き現象、ステインク
スリップ等の原因となる。On the other hand, higher fatty acids, higher fatty acid esters, paraffinic hydrocarbons, silicone oils (e.g. dimethyl silicone oil, diphenyl silicone oil), etc. are sometimes used as lubricants, but these also provide sufficient durability and lhability. This is particularly insufficient for use as a VTR centerpiece.Furthermore, blooming in which the lubricant oozes onto the surface of the magnetic layer is likely to occur, causing tape sticking phenomena, stain slips, and the like.
本発明は上述した欠陥を是正すべくなされたものであっ
て、上述の潤滑剤として新規なものを用いて磁気記録媒
体の走行性を向上させることを目的としている。The present invention has been made to correct the above-mentioned defects, and an object of the present invention is to improve the running properties of a magnetic recording medium by using a novel lubricant.
すなわち本発明は非磁性支持体上に磁性層を有する磁気
記録媒体において、該磁気記録媒体は下記に示される化
合物を保持していることを特徴とする磁気記録媒体にか
んするものである。That is, the present invention relates to a magnetic recording medium having a magnetic layer on a non-magnetic support, characterized in that the magnetic recording medium contains the compound shown below.
化学式
(但しR,R’はアルキル基を表わす。)おいて、Rは
直鎖状あるいは側鎖を有するアルキル基いずれでもよく
、Rの炭素数は8〜30であるのが好ましい。Rの炭素
数が7以下では潤滑効果が不充分となり、また31以上
では合成が困難となる。特にRの炭素数は12〜18で
あるのがより望ましい。In the chemical formula (where R and R' represent an alkyl group), R may be either a straight chain or an alkyl group having a side chain, and R preferably has 8 to 30 carbon atoms. If the carbon number of R is 7 or less, the lubricating effect will be insufficient, and if it is 31 or more, synthesis will be difficult. In particular, it is more desirable that R has 12 to 18 carbon atoms.
また本発明によるもう一つの化合物
直鎖状あるいは側鎖を有するアリキル基いずれでもよく
、R′の炭素数は7〜29であるのがこのましい。R′
の炭素数が6以下では潤滑効果が不充分となり、また3
0以上では合成が困難となる。特にR′の炭素数は11
〜17であるのがより望ましい。The other compound according to the present invention may be either a linear alkyl group or an alkyl group having a side chain, and R' preferably has 7 to 29 carbon atoms. R'
If the number of carbon atoms in is 6 or less, the lubricating effect will be insufficient;
If it is 0 or more, synthesis becomes difficult. In particular, the number of carbon atoms in R' is 11
It is more desirable that it is 17.
本発明で使用するR OC112CIl CH2また\
1
性層に含ませる場合には磁性層中の磁性粉末100重量
部に対して0.2〜4重量部(P HP)であるのが好
ましい。またベース裏面のバンクコート層(1&述)に
含ませる場合にはノ\・7クコ一ト層中の結合剤100
重量部に対して0.2〜20重量部(PHR)であるの
が望ましい。さらに上記滑剤からなるトップコート層又
はコーティング層(いずれも後述)を塗布形成する場合
、その滑剤の塗布量としては1〜1000mg/ rd
であるのが望ましい。R OC112CIl CH2 used in the present invention
When it is included in the magnetic layer, it is preferably 0.2 to 4 parts by weight (PHP) per 100 parts by weight of the magnetic powder in the magnetic layer. In addition, when it is included in the bank coat layer (1 & above) on the back of the base, the binder 100 in the bank coat layer (1 & 7)
It is desirable that the amount is 0.2 to 20 parts by weight (PHR). Furthermore, when forming a top coat layer or a coating layer (both described below) made of the above-mentioned lubricant, the amount of the lubricant applied is 1 to 1000 mg/rd.
It is desirable that
次に、本発明による滑剤の合成方法を説明する。。Next, a method for synthesizing a lubricant according to the present invention will be explained. .
1)高級アルコール又は脂肪酸と過剰のエピクロルヒド
リンとの付加反応をルイス酸(高級アルコール)又は第
3級アミン(脂肪酸)を触媒として還流させながら行な
う。1) An addition reaction between a higher alcohol or fatty acid and excess epichlorohydrin is carried out under reflux using a Lewis acid (higher alcohol) or a tertiary amine (fatty acid) as a catalyst.
ルイス饋触媒 (Ill
2)過剰のエピクロルヒドリンを揮発回収した後、当量
よりやや過剰の水酸化ナトリウムを加え、閉環反応を行
なう。Lewis Catalyst (Ill 2) After the excess epichlorohydrin is evaporated and recovered, a slightly excess equivalent amount of sodium hydroxide is added to carry out a ring-closing reaction.
(A) ROC+(2CHCH2Cl + Na011
(Ill
3)濾過で沈降した塩化ナトリウム水を除去して本発明
による滑剤を得る。(A) ROC+(2CHCH2Cl + Na011
(Ill 3) The precipitated sodium chloride water is removed by filtration to obtain a lubricant according to the present invention.
本発明による磁気記録媒体、例えば磁気テープを第1図
〜第5図に例示する。A magnetic recording medium, such as a magnetic tape, according to the present invention is illustrated in FIGS. 1 to 5.
第1図は、非磁性ベース(1)の表面に本発明の滑剤を
含有した磁性層(2)を形成したものを示す。以下の図
でも同様であるが、本発明による滑剤を含む層は点々大
すの断面で示している。第2図は、磁性層(2)の表面
に本発明による滑剤からなるトップコートJiif +
3)が形成された状態を示す。第3図は。FIG. 1 shows a magnetic layer (2) containing the lubricant of the present invention formed on the surface of a non-magnetic base (1). In the following figures, the layer containing the lubricant according to the invention is shown in large-scale cross-sections. FIG. 2 shows a top coat Jiif + made of a lubricant according to the present invention on the surface of the magnetic layer (2).
3) is formed. Figure 3 is.
非磁性ベース(1)の裏面に本発明による滑剤からなる
コーティング層(4)が形成された状態を示す。第4図
は、非磁性ベース(11の裏面に形成されたバックコー
ト層(5)中に本発明による滑剤を含有せしめた状態を
示し、更に第5図は、バンクコートIii (5)上に
本発明による滑剤からなるコーティング層(6)が形成
された状態を示す。なおバンクコート層(5)は種々の
目的で設けられるが、これはバンク面を表面荒らさを適
当にコントロールすることによって走行性を安定化した
り、帯電防止の目的であったりする。このためバックコ
ート層は結合剤中にカーボンブランクを混合したものを
塗布したり、更に非磁性の顔料例えばα−Fe20a−
、アルミナ、タルク等を混合してもよい。本発明の磁気
記録媒体は、こうした磁気テープのみならず、表面又は
表裏面に磁性層を有する磁気ディスク等にも適用できる
。また本発明による滑剤を保持する位置を磁性層(2)
中、或いは磁性層(2)の表面上及び/又は裏面上と様
々にすることができる。A state in which a coating layer (4) made of a lubricant according to the present invention is formed on the back surface of a non-magnetic base (1) is shown. FIG. 4 shows a state in which the lubricant according to the present invention is contained in the back coat layer (5) formed on the back surface of the non-magnetic base (11), and further, FIG. This shows a state in which a coating layer (6) made of a lubricant according to the present invention has been formed.The bank coat layer (5) is provided for various purposes, but it is possible to control the surface roughness of the bank surface to make it easier to run. The purpose is to stabilize the properties and prevent static electricity.For this reason, the back coat layer is coated with a mixture of carbon blank in a binder, and a non-magnetic pigment such as α-Fe20a-
, alumina, talc, etc. may be mixed. The magnetic recording medium of the present invention can be applied not only to such magnetic tapes but also to magnetic disks having magnetic layers on the front or back surfaces. In addition, the position where the lubricant according to the present invention is held is located in the magnetic layer (2).
It can be placed inside, or on the front and/or back side of the magnetic layer (2).
本発明の磁性層に使用可能な磁性粉としては、γ−Fe
2O3、Fe504、r Fe2O3とFe50+との
混晶、コバルトをドープあるいは被着したγ−Pe20
3又はFe504 、CrO2、バリウムフェライト、
種々の合金粉末磁性体(例えばFe −Co、 Go
−Ni、 Fe−G。As the magnetic powder that can be used in the magnetic layer of the present invention, γ-Fe
2O3, Fe504, r Mixed crystal of Fe2O3 and Fe50+, γ-Pe20 doped or coated with cobalt
3 or Fe504, CrO2, barium ferrite,
Various alloy powder magnetic materials (e.g. Fe-Co, Go
-Ni, Fe-G.
−Ni、、Fe −Co −B 、 Fe −Co −
Cr−B XMn −Bis Mn−^LFe−Co−
V等)、窒化鉄等を挙げることができ、これら2種以上
を混合して使用してもよい。-Ni,,Fe-Co-B,Fe-Co-
Cr-B XMn -Bis Mn-^LFe-Co-
V, etc.), iron nitride, etc., and two or more of these may be used in combination.
また磁性層に使用可能な結合剤としては、塩化ビニル−
酢酸ビニル共重合体、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、塩化ビニル−塩化ビニリデン共重合体、
塩化ビニル−アクリロニトリル共重合体、アクリル酸エ
ステル−アクリロニトリル共重合体、アクリル酸エステ
ル−塩化ビニリデン共重合体、メタクリル酸エステル−
塩化ビニリデン共重合体、メタクリル酸エステル−スチ
レン共重合体、熱可塑性ポリウレタン樹脂、フェノキシ
樹脂、ポリ弗化ビニル、塩化ビニリデン−アクリロニト
リル共重合体、ブタジェン−アクリロニトリル共重合体
、アクリロニトリル−ブタジェン−メタクリル酸共重合
体ゎアクリロニトリル−ブタジェン−アクリル酸共重合
体、ポリビニルブチラール、ポリビニルブチラール、セ
ルロース誘導体、スチレン−ブタジェン共重合体、ポリ
エステル樹脂、フェノール樹脂、エポキシ樹脂、熱硬化
性ポリウレタン樹脂、尿素樹脂、メラミン樹脂、アルキ
ッド樹脂、尿素ホルムアルデヒド樹脂等が挙げられる。In addition, as a binder that can be used for the magnetic layer, vinyl chloride-
Vinyl acetate copolymer, vinyl chloride-vinyl acetate-vinyl alcohol copolymer, vinyl chloride-vinyl acetate-maleic acid copolymer, vinyl chloride-vinylidene chloride copolymer,
Vinyl chloride-acrylonitrile copolymer, acrylic ester-acrylonitrile copolymer, acrylic ester-vinylidene chloride copolymer, methacrylic ester-
Vinylidene chloride copolymer, methacrylic acid ester-styrene copolymer, thermoplastic polyurethane resin, phenoxy resin, polyvinyl fluoride, vinylidene chloride-acrylonitrile copolymer, butadiene-acrylonitrile copolymer, acrylonitrile-butadiene-methacrylic acid copolymer Polymer: Acrylonitrile-butadiene-acrylic acid copolymer, polyvinyl butyral, polyvinyl butyral, cellulose derivative, styrene-butadiene copolymer, polyester resin, phenol resin, epoxy resin, thermosetting polyurethane resin, urea resin, melamine resin, Examples include alkyd resins and urea formaldehyde resins.
磁性塗料の調製に当っては、有機溶剤として、アセトン
、メチルエチルケトン、メチルイソブチルケトン、シク
ロヘキサノン等のケトン頻;メタノール、エタノール、
プロパツール、ブタノール等のアルコール頬;酢酸エチ
ル、酢酸ブチル、乳酸:1チ)Lt、酢酸クリコール、
モノエチルエーテル等のエステル類;エチレングリコー
ルジメチルエーテル、エチレングリコールモノエチルエ
ーテル、ジオキサン等のグリコールエーテル類;ベンゼ
ン、トルエン、キシレン等の芳香族炭化水素;ヘキサン
、ヘプタン等の脂肪族炭化水素;ニトロプロパン等を単
独で或いは混合物として使用することができる。この有
機溶剤で調製された磁性塗料を塗布する非磁性ベースと
しては、ポリエチレンテレフタレート等のポリエステル
類、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等のセルロ
ース誘導体、ポリカーボネート、ポリ塩化ビニル、ポリ
アミド、ポリイミド、アルミニウム、銅等の金属材料、
紙等が挙げられる。また滑剤からなるトップコート層及
びコーティング層を塗布する際の溶剤としてはフレオン
、ヘキサン、エタノール等の極性の弱い低沸点の溶剤を
用い得る。When preparing magnetic paint, organic solvents such as ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone; methanol, ethanol,
Alcohol such as propatool, butanol; ethyl acetate, butyl acetate, lactic acid: 1) Lt, glycol acetate,
Esters such as monoethyl ether; glycol ethers such as ethylene glycol dimethyl ether, ethylene glycol monoethyl ether, and dioxane; aromatic hydrocarbons such as benzene, toluene, and xylene; aliphatic hydrocarbons such as hexane and heptane; nitropropane, etc. can be used alone or as a mixture. Non-magnetic bases for applying magnetic paint prepared with this organic solvent include polyesters such as polyethylene terephthalate, polyolefins such as polypropylene, cellulose derivatives such as cellulose triacetate and cellulose diacetate, polycarbonate, polyvinyl chloride, polyamide, Metal materials such as polyimide, aluminum, copper, etc.
Examples include paper. Further, as a solvent for applying the top coat layer and the coating layer consisting of a lubricant, a weakly polar and low boiling point solvent such as Freon, hexane, and ethanol can be used.
さらに本発明の化合物を滑剤として適用される磁気記録
媒体としては、前述の如き磁性粉と結合剤とともに塗布
して磁性層を形成するいわゆる塗右型の磁気記録媒体に
限られず、金属薄膜型磁気記録媒体にも適用される。こ
の金属薄膜型磁気記録媒体は非磁性支持体上に磁性金属
、例えばCo、Fe、、 Niあるいはその合金をめっ
き、蒸着、イオンブレーティング、あるいはスパッタリ
ング等により形成するものである。この金属薄膜型磁気
記録媒体は結合剤を用いる必要がないため高い磁束密度
を有し、また非常に薄い層に形成されるため、短波長、
高密度記録に有用である。Further, magnetic recording media to which the compound of the present invention is applied as a lubricant are not limited to so-called coating-type magnetic recording media in which a magnetic layer is formed by coating together with magnetic powder and a binder as described above, but also metal thin film magnetic recording media. It also applies to recording media. This metal thin film type magnetic recording medium is one in which a magnetic metal such as Co, Fe, Ni, or an alloy thereof is formed on a nonmagnetic support by plating, vapor deposition, ion blasting, sputtering, or the like. This metal thin film magnetic recording medium has a high magnetic flux density because it does not require the use of a binder, and because it is formed into an extremely thin layer, it
Useful for high-density recording.
以下本発明を実施例により説明する。The present invention will be explained below with reference to Examples.
実施例1゜
Co被着r Fe20a 100重量部カーボン(帯電
防止剤) 5 〃
レシチン(分散剤) 1 〃
\ 1
メチルエチルケトン 150重量部
メチルイソブチルケトン 150〃
上記組成物をボールミルにて24時間混合してからフィ
ルタを通して取出し、更に塗布直前に硬化剤を1重量部
添加して30分間攪拌した。この磁性塗料を12μ厚の
ポリエチレンテレフタレートベース上に、乾燥後の厚み
が5μとなるように塗布し、磁場配向を行なった後乾燥
し巻き取った。これをカレンダー処理した後%インチ幅
に裁断し、サンプルテープを作成した。Example 1 Co deposition r Fe20a 100 parts by weight Carbon (antistatic agent) 5 Lecithin (dispersant) 1 \ 1 Methyl ethyl ketone 150 parts by weight Methyl isobutyl ketone 150 The above composition was mixed in a ball mill for 24 hours. The mixture was taken out through a filter, and immediately before coating, 1 part by weight of a curing agent was added and stirred for 30 minutes. This magnetic paint was applied onto a polyethylene terephthalate base having a thickness of 12 μm so that the thickness after drying would be 5 μm, and after magnetic field orientation, it was dried and rolled up. This was calendered and then cut to a width of 1.5 inches to prepare a sample tape.
実施例2゜
実施例1.のミリスチルグリシジルエーテルラ
ウリルグリシジルエーテル
は実施例1.と同一組成の磁性塗料を用い、実施例1、
と同様の方法によりサンプルテープを作成した・実施例
3。Example 2゜Example 1. Myristyl glycidyl ether lauryl glycidyl ether of Example 1. Using a magnetic paint with the same composition as in Example 1,
A sample tape was created in the same manner as in Example 3.
実施例1.のミリスチルグリシジルエーテルラウリン酸
のグリシジルエステル
実施例】、と同一組成の磁性塗料を用い、実施例1。Example 1. Glycidyl ester of myristyl glycidyl ether lauric acid Example 1 was prepared using a magnetic paint having the same composition as in Example 1.
と同様の方法によりサンプルテープを作成した。A sample tape was prepared in the same manner as above.
実施例4。Example 4.
実施例1.のミリスチルグリシジルエーテル○ ミリスチン酸のグリシジルエステル 実施例1.と同一組成の磁性塗料を用い、実施例1。Example 1. Myristyl glycidyl ether○ Glycidyl ester of myristic acid Example 1. Example 1 using a magnetic paint having the same composition as in Example 1.
と同様の方法によりサンプルテープを作成した。A sample tape was prepared in the same manner as above.
比較例1。Comparative example 1.
Co被着r Fe203, 100重量部カーボン(帯
電防止剤) 5 〃
レシチン(分散剤) 1 〃
メチルエチルケトン 150〃
メチルイソブチルケトン 150〃
上記組成物を用い、実施例1.と同様の方法によりサン
プルテープを作成した。Co adhesion r Fe203, 100 parts by weight Carbon (antistatic agent) 5 Lecithin (dispersant) 1 Methyl ethyl ketone 150 Methyl isobutyl ketone 150 Using the above composition, Example 1. A sample tape was prepared in the same manner as above.
実施例5。Example 5.
比較例1.で作成したサンプルテープの磁性層に、ミリ
スチルグリシジルエーテル
リ
n−ヘキサン溶液をミリスチルグリシジルエーテルの塗
布量が80mg/rrrとなるように塗布(トップコー
ト)してサンプルテープを作成した。Comparative example 1. A sample tape was prepared by applying (top coat) a myristyl glycidyl ether phosphorus n-hexane solution to the magnetic layer of the sample tape prepared in step 1 so that the coating amount of myristyl glycidyl ether was 80 mg/rrr.
実施例6。Example 6.
比較例1.で作成したサンプルテープの磁性層に、ラウ
リルグリシジルエーテル
U
n−ヘキサン溶液をラウリルグリシジルエーテルの塗布
量が8On+g/rrrとなるように塗布(トップコー
ト)シてサンプルテープを作成した。Comparative example 1. A sample tape was prepared by applying (top coating) a lauryl glycidyl ether U n-hexane solution to the magnetic layer of the sample tape prepared in step 1 in such a manner that the coating amount of lauryl glycidyl ether was 8 On+g/rrr.
実施例7゜
比較例1.で作成したサンプルテープの磁性層に、ラウ
リン酸のグリシジルエステル
n−へキサン溶液をラウリン酸のグリシジルエステルの
塗布量が80mg/ rrlとなるように塗布(トップ
コート)シてサンプルテープを得た。Example 7゜Comparative Example 1. A sample tape was obtained by applying (top coat) a solution of glycidyl ester of lauric acid in n-hexane to the magnetic layer of the sample tape prepared in the above so that the amount of glycidyl ester of lauric acid applied was 80 mg/rrl.
実施例8゜
比較例1.で作成したサンプルテープの磁性層に、ミリ
スチン酸のグリシジルエステル
n−ヘキサン溶液をミリスチン酸のグリシジルエステル
の塗布量が80a+g/nfとなるように塗布(トップ
コート)シてサンプルテープを作成した。Example 8 Comparative Example 1. A sample tape was prepared by applying (top coating) a glycidyl ester of myristic acid n-hexane solution to the magnetic layer of the sample tape prepared in step 1 so that the coating amount of glycidyl ester of myristic acid was 80a+g/nf.
実施例9゜
比較例1.で作成したサンプルテープの磁性層に、イソ
ステアリン酸のグリシジルエステルn−へキサン溶液を
イソステアリン酸のグリシジルエステルの塗布量が80
mg/rrfとなるように塗布(トップコート)してサ
ンプルテープを作成した。Example 9 Comparative Example 1. A solution of glycidyl ester of isostearic acid in n-hexane was applied to the magnetic layer of the sample tape prepared in 1.
A sample tape was prepared by coating (top coat) so that the concentration was mg/rrf.
比較例2゜
12μ厚のポリエチレンテレフタレートよりなるベース
上に斜め蒸着法によりGoを1000人の厚みとなるよ
うに真空蒸着して磁性層を形成し、所定の幅に裁断して
サンプルテープを作成した。Comparative Example 2 A magnetic layer was formed by vacuum evaporating Go to a thickness of 1000 mm using an oblique evaporation method on a base made of polyethylene terephthalate with a thickness of 12 μm, and the sample tape was cut to a predetermined width. .
実施例10゜
比較例2.で作成したサンプルテープの磁性層に、ミリ
スチルグリシジルエーテル
n−へキサン溶液をミリスチルグリシジルエーテルの塗
布量が20mg/ trrとなるように塗布(トップコ
ート)シてサンプルテープを作成した。Example 10° Comparative Example 2. A sample tape was prepared by applying (top coat) a myristyl glycidyl ether n-hexane solution to the magnetic layer of the sample tape prepared in step 1 in such a manner that the coating amount of myristyl glycidyl ether was 20 mg/trr.
実施例11゜
比較例2.で作成したサンプルテープの磁性層にミリス
チン酸のグリシジルエステル
n−へキサン溶液をミリスチン酸のグリシジルエステル
の塗布量が20mg/ cdとなるように塗布(トップ
コート)シてサンプルテープを作成した。Example 11゜Comparative Example 2. A sample tape was prepared by applying (top coat) a solution of glycidyl ester of myristic acid in n-hexane to the magnetic layer of the sample tape prepared in step 1 so that the coating amount of glycidyl ester of myristic acid was 20 mg/cd.
以上の実施例及び比較例で作成したサンプルテこの表で
◎は極めて良好、Qは良好、△は不良、×は極めて不良
を示す。In this table, ◎ indicates extremely good, Q indicates good, △ indicates poor, and × indicates extremely poor.
またエージングは60℃の温度で3日間行われた。Further, aging was performed at a temperature of 60° C. for 3 days.
表より本発明による磁気記録媒体では摩擦係数を極めて
小さな値に抑えることができ、スティックスリップを回
避できる。特にトップコート法による磁気記録媒体では
従来問題となっていた経口変化による走行劣化も本発明
によれば解消することができる。As can be seen from the table, in the magnetic recording medium according to the present invention, the coefficient of friction can be suppressed to an extremely small value, and stick-slip can be avoided. In particular, according to the present invention, running deterioration due to oral deformation, which has been a problem in the past with magnetic recording media using the top coat method, can be solved.
第1図乃至第5図は夫々本発明による磁気記録媒体の実
施例を示す断面図である。
(11はベース、(2)は磁性層、(3)はトップコー
ト、+41 (6)は滑剤コーティング層、(5)はバ
ックコート屓である。1 to 5 are cross-sectional views showing embodiments of magnetic recording media according to the present invention. (11 is the base, (2) is the magnetic layer, (3) is the top coat, +41 (6) is the lubricant coating layer, and (5) is the back coat layer.
Claims (1)
、該磁気記録媒体は下記に示される化合物を保持してい
ることを特徴とする磁気記録媒体5化学式 (但しR,R’はアルキル基を表わす。)[Scope of Claims] A magnetic recording medium having a magnetic layer on a non-magnetic support, characterized in that the magnetic recording medium has a chemical formula 5 (wherein R, R' represents an alkyl group.)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58183533A JPS6076019A (en) | 1983-09-30 | 1983-09-30 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58183533A JPS6076019A (en) | 1983-09-30 | 1983-09-30 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6076019A true JPS6076019A (en) | 1985-04-30 |
Family
ID=16137492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58183533A Pending JPS6076019A (en) | 1983-09-30 | 1983-09-30 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6076019A (en) |
-
1983
- 1983-09-30 JP JP58183533A patent/JPS6076019A/en active Pending
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