JPH058491B2 - - Google Patents
Info
- Publication number
- JPH058491B2 JPH058491B2 JP58250787A JP25078783A JPH058491B2 JP H058491 B2 JPH058491 B2 JP H058491B2 JP 58250787 A JP58250787 A JP 58250787A JP 25078783 A JP25078783 A JP 25078783A JP H058491 B2 JPH058491 B2 JP H058491B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- layer
- tape
- lubricant
- sample tape
- 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 - Lifetime
Links
- 230000005291 magnetic effect Effects 0.000 claims description 70
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 3
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 32
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
- 239000000314 lubricant Substances 0.000 description 20
- 239000000203 mixture Substances 0.000 description 12
- 239000003973 paint Substances 0.000 description 11
- 238000000576 coating method Methods 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- -1 fatty acid esters Chemical class 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
- 230000005294 ferromagnetic effect Effects 0.000 description 5
- 239000010409 thin film Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229910001566 austenite Inorganic materials 0.000 description 4
- 239000011247 coating layer Substances 0.000 description 4
- QBCOASQOMILNBN-UHFFFAOYSA-N didodecoxy(oxo)phosphanium Chemical compound CCCCCCCCCCCCO[P+](=O)OCCCCCCCCCCCC QBCOASQOMILNBN-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000006247 magnetic powder Substances 0.000 description 4
- 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
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 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
- OHRVKCZTBPSUIK-UHFFFAOYSA-N tridodecyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCC)OCCCCCCCCCCCC OHRVKCZTBPSUIK-UHFFFAOYSA-N 0.000 description 3
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- 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
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer 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
- 230000032683 aging Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- FLAJFZXTYPQIBY-CLFAGFIQSA-N bis[(z)-octadec-9-enyl] hydrogen phosphite Chemical compound CCCCCCCC\C=C/CCCCCCCCOP(O)OCCCCCCCC\C=C/CCCCCCCC FLAJFZXTYPQIBY-CLFAGFIQSA-N 0.000 description 2
- 239000001913 cellulose Chemical class 0.000 description 2
- 229920002678 cellulose Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920005749 polyurethane resin 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
- SVETUDAIEHYIKZ-IUPFWZBJSA-N tris[(z)-octadec-9-enyl] phosphate Chemical compound CCCCCCCC\C=C/CCCCCCCCOP(=O)(OCCCCCCCC\C=C/CCCCCCCC)OCCCCCCCC\C=C/CCCCCCCC SVETUDAIEHYIKZ-IUPFWZBJSA-N 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
- 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
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-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
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910002440 Co–Ni Inorganic materials 0.000 description 1
- 229910020674 Co—B Inorganic materials 0.000 description 1
- 229910020516 Co—V Inorganic materials 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 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
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229910018657 Mn—Al Inorganic materials 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
- 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
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 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
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 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
- 229910052797 bismuth Inorganic materials 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
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- DHZSIQDUYCWNSB-UHFFFAOYSA-N chloroethene;1,1-dichloroethene Chemical compound ClC=C.ClC(Cl)=C DHZSIQDUYCWNSB-UHFFFAOYSA-N 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
- 150000001875 compounds Chemical class 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
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- SPBMDAHKYSRJFO-UHFFFAOYSA-N didodecyl hydrogen phosphite Chemical compound CCCCCCCCCCCCOP(O)OCCCCCCCCCCCC SPBMDAHKYSRJFO-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002270 dispersing agent Substances 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
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 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
- 238000007733 ion plating Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910001337 iron nitride Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 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
- 230000001050 lubricating effect Effects 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
- 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
- 229920002037 poly(vinyl butyral) polymer Polymers 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
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 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
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 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
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- QULKPMBZSVVAJM-IUPFWZBJSA-N tris[(z)-octadec-9-enyl] phosphite Chemical compound CCCCCCCC\C=C/CCCCCCCCOP(OCCCCCCCC\C=C/CCCCCCCC)OCCCCCCCC\C=C/CCCCCCCC QULKPMBZSVVAJM-IUPFWZBJSA-N 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
- 239000008096 xylene Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Lubricants (AREA)
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
Description
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、磁気デイスクに
関するものである。
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、スプライト性が良いこと等
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、磁気ヘツ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
長時間に亘つ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ツド
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(例えば音色信号)は周波数に変化
をきたし、原周波数とは違つた音になつたり、あ
る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。
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、グラフアイト、ワツ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、耐久性に
とつ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。
他方、高級脂肪酸、高級脂肪酸エステル、パラ
フイン系炭化水素、シリコンオイル(例えばジメ
チルシリコンオイル、ジフエニルシリコンオイ
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潤滑性を付与することができ
ず、特にVTRのカセツト用には不充分である。
しかも磁性層表面へ滑剤がにじみ出すブルーミン
グが生じ易く、テープの貼付け現象、ステイツク
スリツプ等の原因となる。
本発明は上述した欠陥を是正すべくなされたも
のであつて、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。
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
記の化学式で表わされる亜リン酸エステルを保持
していることを特徴とする磁気記録媒体に関する
ものである。
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. Magnetic tapes are particularly required to have various characteristics such as a low coefficient of friction, smooth and stable running properties, a small amount of powder falling off, and good sprite properties. That is, the magnetic tape
When used in magnetic recording and reproducing devices such as VTRs,
Since the tape runs at high speed while physically contacting tape guides, magnetic heads, etc., it is important that it has excellent wear resistance and can run stably for a long time. For example, if the coefficient of friction on the tape surface changes during recording or playback, the tape will vibrate at the guide or magnetic head. As a result, the frequency of the signals recorded and played back on the tape (for example, timbre signals) changes, resulting in a sound different from the original frequency, or the vibration sound of the tape (so-called Q sound) can be directly heard. be. 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 not desirable because it is not very effective in terms of durability, and if added in a large amount, it deteriorates the magnetic properties. 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 lubricity. This is particularly inadequate for VTR cassettes.
Moreover, blooming, in which the lubricant oozes out onto the surface of the magnetic layer, is likely to occur, causing tape adhesion phenomena, stick slips, and the like. 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 new lubricant as the above-mentioned lubricant. 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 a phosphite represented by the following chemical formula. be.
【式】又は[Formula] or
【式】(但し
R1,R2、R3は炭素数8〜18個のアルキル基を示
す。)
前記した化学式で表わされる亜リン酸のトリエ
ステル又はジエステルにおいて、R1、R2、R3は
各各炭素数8〜18個のアルキル基を表わすもので
あり、R1、R2、R3は同じであつてもあるいは異
なつていてもよい。またR1、R2、R3は直鎖状の
アルキル基でもあるいは側鎖を有する分鎖状のア
ルキル基であつてもかまわないが、アルキル基の
炭素数としては8〜18個であるのが好ましい。炭
素数が8未満であると滑性付与機能が乏しくな
り、他方炭素数が18を超えるると入手が困難であ
る。
本発明で用いる潤滑剤の添加量は、磁性層に含
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(PHP)であるのが好まし
い。またベース裏面のバツクコート層(後述)に
含ませる場合にはバツクコート層中の結合剤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ツプコー
ト層又はコーテイング層(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/m2であるのが望ましい。
更に本発明による滑剤を前述した他の従来の滑
剤を併用することも可能である。
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。
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
む層は点々入り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ツ
プコート層3が形成された状態を示す。第3図
は、非磁性ベース1の裏面に本発明よる滑剤から
なるコーテイング層4が形成された状態を示す。
第4図は、非磁性ベース1の裏面に形成されたバ
ツクコート層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、バツクコート層
5上に本発明による滑剤からなるコーテイング層
6が形成された状態を示す。なおバツクコート層
5は種々の目的で設けられるが、これはバツク面
を表面荒らさを適当にコントロールすることによ
つて走行性を安定化したり、帯電防止の目的であ
つたりする。このためバツクコート層は結合剤中
にカーボンブラツ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−Fe2O3、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イスク等にも
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。
本発明の磁性層に使用可能な磁性粉としては、
γ−Fe2O3、Fe3O4、γ−Fe2O3とFe3O4との混
晶、コバルトをドープあるいは被着したγ−Fe2
O3又はFe3O4、CrO2、バリウムフエライト、
種々の合金粉末磁性体(例えばFe−Co、Co−
Ni、Fe−Co−Ni、Fe−Co−B、Fe−Co−Cr−
B、Mn−Bi、Mn−Al、Fe−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。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、フエノキシ樹脂、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、ブタジエン−アクリロニトリル共重
合体、アクリロニトリル−ブタジエン−メタクリ
ル酸共重合体、アクリロニトリル−ブタジエン−
アクリル酸共重合体、ポリビニルブチラール、ポ
リビニルアセタール、セルロース誘導体、スチレ
ン−ブタジエン共重合体、ポリエステル樹脂、フ
エノール樹脂、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、アルキツド
樹脂、尿素ホルムアルデヒド樹脂等が挙げられ
る。
磁性塗料の調製に当つては、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、シクロヘキサン等のケトン類;メタノ
ール、エタノール、プロパノール、ブタノール等
のアルコール類;酢酸エチル、酢酸ブチル、乳酸
エチル、酢酸グリコール、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
を塗布する被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イン類、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
トツプコート層及びコーテイ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
等の低沸点の溶剤を用い得る。
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
布型の磁気記録媒体に限られず、金属強磁性薄膜
型磁気記録媒体にも適用される。この金属強磁性
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つき、
蒸着、イオンプレーテイング、あるいはスパツタ
リング等により形成するものである。この金属強
磁性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。
以下本発明を実施例により説明する。
実施例 1
重量部
Co被着γ−Fe2O3 100
塩化ビニル−酢酸ビニル共重合体 15.5
(U.C.C.社製 VAGH)
ポリウレタン樹脂 6.5
(日本ポリウレタン社製N−5033)
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
上記組成物を基本組成物とし、該基本組成物に
亜リン酸トリラウリルエステルを2重量部添加し
ポールミルにて24時間混合してからフイルターを
通して取り出し、更に塗布前に硬化剤を4重量部
添加して30分間攪拌した。このようにして得られ
た磁性塗料を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、磁場配向を行なつた後乾燥し巻き取つた。
これをカレンダー処理した後1/2インチ幅に裁断
し、サンプルテープを作成した。
実施例 2
実施例1の基本組成物の亜リン酸ジラウリルエ
ステルを2重量部添加した磁性塗料を用い、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
実施例1の基本組成物を磁性塗料に用い、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。上記サンプルテープの磁性層に亜リン酸トリ
ラウリルエステルの1.0wt%n−ヘキサン溶液を、
亜リン酸トリラウリルエステルの塗布量が160
mg/cm2となるように塗布(トツプコート)してサ
ンプルテープを作成した。
実施例 4
実施例1の基本組成物を磁性塗料に用い、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。上記サンプルテープの磁性層に亜リン酸ジラ
ウリルエステルの1.0wt%/n−ヘキサン溶液を、
亜リン酸ジラウリルエステルの塗布量が160mg/
m2となるように塗布(トツプコート)してサンプ
ルテープを作成した。
実施例 5
実施例1の基本組成物を磁性塗料に用い、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。上記サンプルテープの磁性層に亜リン酸トリ
オレイルエステルの1.0wt%n−ヘキサン溶液を、
亜リン酸トリオレイルエステルの塗布量が160
mg/m2となるように塗布(トツプコート)してサ
ンプルテープを作成した。
実施例 6
実施例1の基本組成物を磁性塗料に用い、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。上記サンプルテープの磁性層に亜リン酸ジオ
レイルエステルの1.0wt%n−ヘキサン溶液を、
亜リン酸ジオレイルエステルの塗布量が160mg/
m2となるように塗布(トツプコート)してサンプ
ルテープを作成した。
実施例 7
12μ厚のポリエチレンテレフタレートベース上
に斜め蒸着法よつてCoを付着させ、1000Åの金
属強磁性薄膜を形成した。この金属強磁性薄膜表
面に亜リン酸ジラウリルエステルの0.1wt%n−
ヘキサン溶液を、亜リン酸ジラウリルエステルの
塗布量が2mg/m2となるように塗布(トツプコー
ト)してサンプルテープを作成した。
比較例 1
実施例1の基本組成物を磁性塗料に用い、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。
比較例 2
実施例1の基本組成物にリン酸トリラウリルエ
ステルを2重量部添加した磁性塗料を用い、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。
比較例 3
比較例1で得られたサンプルテープの磁性層に
リン酸トリラウリルエステルの1.0wt%n−ヘキ
サン溶液を、リン酸トリラウリルエステルの塗布
量が160mg/m2となるように塗布(トツプコート)
してサンプルテープを作成した。
比較例 4
比較例1で得られたサンプルテープの磁性層に
リン酸トリオレイルエステルの1.0wt%n−ヘキ
サン溶液を、リン酸トリオレイルエステルの塗布
量が160mg/m2となるように塗布(トツプコート)
してサンプルテープを作成した。
以上の実施例及び比較例で作成したサンプルテ
ープの諸特性を次表に示す。[Formula] (However, R 1 , R 2 and R 3 represent an alkyl group having 8 to 18 carbon atoms.) In the triester or diester of phosphorous acid represented by the above chemical formula, R 1 , R 2 , R 3 represents an alkyl group each having 8 to 18 carbon atoms, and R 1 , R 2 and R 3 may be the same or different. Furthermore, R 1 , R 2 , and R 3 may be a linear alkyl group or a branched alkyl group having a side chain, but the number of carbon atoms in the alkyl group is 8 to 18. is preferred. If the number of carbon atoms is less than 8, the lubricating property will be poor, while if the number of carbon atoms is more than 18, it will be difficult to obtain. When included in the magnetic layer, the amount of the lubricant used in the present invention 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, if it is included in the back coat layer (described later) on the back of the base, 100% of the binder in the back coat layer is added.
Preferably, 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 1.
Desirably it is 1000 mg/m 2 . Furthermore, it is also possible to use the lubricant according to the invention in combination with the other conventional lubricants mentioned above. A magnetic recording medium, such as a magnetic tape, according to the present invention is illustrated in FIGS. 1 to 5. FIG. 1 shows a non-magnetic base 1 on which a magnetic layer 2 containing the lubricant of the present invention is formed. In the following figures as well, the layer containing the lubricant according to the invention is shown in dotted cross-sections. Figure 2 shows
This figure shows a state in which a top coat layer 3 made of a lubricant according to the present invention is formed on the surface of a magnetic layer 2. FIG. 3 shows a state in which a coating layer 4 made of a lubricant according to the present invention is formed on the back surface of the nonmagnetic base 1.
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 1, and further, FIG. A state in which layer 6 is formed is shown. The back coat layer 5 is provided for various purposes, including stabilizing runnability by appropriately controlling the surface roughness of the back surface, and preventing static electricity. For this purpose, the back coat layer may be coated with a binder mixed with carbon black, or may further contain a nonmagnetic pigment such as α-Fe 2 O 3 , alumina, talc, etc. 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. Furthermore, the lubricant according to the present invention is held at a position in the magnetic layer 2 or on the surface of the magnetic layer 2 and/or
Or on the back side. Magnetic powders that can be used in the magnetic layer of the present invention include:
γ-Fe 2 O 3 , Fe 3 O 4 , mixed crystal of γ-Fe 2 O 3 and Fe 3 O 4 , γ-Fe 2 doped or coated with cobalt
O 3 or Fe 3 O 4 , CrO 2 , barium ferrite,
Various alloy powder magnetic materials (e.g. Fe-Co, Co-
Ni, Fe-Co-Ni, Fe-Co-B, Fe-Co-Cr-
B, Mn-Bi, Mn-Al, Fe-Co-V, etc.), iron nitride, etc., and two or more of these may be used in combination. Binders that can be used in the magnetic layer include vinyl chloride-vinylacetate copolymer, vinyl chloride-vinyl acetate-vinyl alcohol copolymer, vinyl chloride-vinyl acetate-maleic acid copolymer, and vinyl chloride-vinylidene chloride. copolymer, vinyl chloride-acrylonitrile copolymer, acrylic ester-acrylonitrile copolymer,
Acrylic acid ester-vinylidene chloride copolymer,
Methacrylic acid 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, acrylonitrile-butadiene-
Acrylic acid copolymer, polyvinyl butyral, polyvinyl acetal, cellulose derivative, styrene-butadiene copolymer, polyester resin, phenol resin, epoxy resin, thermosetting polyurethane resin, urea resin, melamine resin, alkyd resin, urea formaldehyde resin, etc. can be mentioned. When preparing magnetic paint, as an organic solvent,
Ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexane; alcohols such as methanol, ethanol, propanol, butanol; esters such as ethyl acetate, butyl acetate, ethyl lactate, glycol acetate, monoethyl ether; ethylene glycol dimethyl ether, ethylene glycol monoethyl ether,
Glycol ethers such as dioxane; aromatic hydrocarbons such as benzene, toluene and xylene; aliphatic hydrocarbons such as hexane and heptane; nitropropane and the like can be used alone or as a mixture. The magnetic base on which the magnetic paint prepared with this organic solvent is applied includes polyesters such as polyethylene terephthalate, polyolefins such as polypropylene, cellulose derivatives such as cellulose triacetate and cellulose diacetate, polycarbonate, polyvinyl chloride,
Examples include polyamide, polyimide, aluminum, metal materials such as copper, and paper. Further, as a solvent for coating the top coat layer and coating layer comprising a lubricant, a low boiling point solvent such as freon, hexane, ethanol, etc. can be used. Further, magnetic recording media to which the compound of the present invention is applied as a lubricant are not limited to so-called coated 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 ferromagnetic thin film type magnetic recording media. It also applies to magnetic recording media. This metal ferromagnetic thin film magnetic recording medium has a magnetic metal such as Co, Fe, Ni, or an alloy thereof plated on a non-magnetic support.
It is formed by vapor deposition, ion plating, sputtering, or the like. This metal ferromagnetic thin film magnetic recording medium has a high magnetic flux density because it does not require the use of a binder, and is useful for short wavelength, high density recording because it is formed into a very thin layer. The present invention will be explained below with reference to Examples. Example 1 Part by weight Co-adhered γ-Fe 2 O 3 100 Vinyl chloride-vinyl acetate copolymer 15.5 (VAGH manufactured by UCC) Polyurethane resin 6.5 (N-5033 manufactured by Nippon Polyurethane) Carbon (antistatic agent) 5 Lecithin (Dispersant) 1 Methyl ethyl ketone 150 Methyl isobutyl ketone 150 The above composition was used as a basic composition, 2 parts by weight of trilauryl phosphite was added to the basic composition, mixed in a Pall mill for 24 hours, and then taken out through a filter. Furthermore, 4 parts by weight of a curing agent was added before coating, and the mixture was stirred for 30 minutes. The thus obtained 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 wound up.
This was calendered and cut into 1/2 inch width to create a sample tape. Example 2 A sample tape was prepared in the same manner as in Example 1 using a magnetic paint to which 2 parts by weight of dilauryl phosphite of the basic composition of Example 1 was added. Example 3 A sample tape was prepared in the same manner as in Example 1 using the basic composition of Example 1 as a magnetic paint. A 1.0wt% n-hexane solution of phosphite trilauryl ester was added to the magnetic layer of the sample tape.
The application amount of phosphite trilauryl ester is 160
A sample tape was prepared by coating (top coat) so that the concentration was mg/cm 2 . Example 4 A sample tape was prepared in the same manner as in Example 1 using the basic composition of Example 1 as a magnetic paint. A 1.0wt%/n-hexane solution of dilauryl phosphite was applied to the magnetic layer of the sample tape.
Application amount of phosphite dilauryl ester is 160mg/
A sample tape was prepared by applying it (top coat) so that it was 2 m2. Example 5 A sample tape was prepared in the same manner as in Example 1 using the basic composition of Example 1 as a magnetic paint. A 1.0wt% n-hexane solution of trioleyl phosphorous ester was added to the magnetic layer of the sample tape.
The application amount of phosphite trioleyl ester is 160
A sample tape was prepared by coating (top coat) so that the concentration was mg/m 2 . Example 6 A sample tape was prepared in the same manner as in Example 1 using the basic composition of Example 1 as a magnetic paint. A 1.0wt% n-hexane solution of phosphite dioleyl ester was added to the magnetic layer of the sample tape.
Application amount of phosphite dioleyl ester is 160mg/
A sample tape was prepared by applying it (top coat) so that it was 2 m2. Example 7 Co was deposited on a polyethylene terephthalate base with a thickness of 12μ by an oblique evaporation method to form a metal ferromagnetic thin film with a thickness of 1000Å. 0.1wt% n- of dilauryl phosphite was applied to the surface of this metal ferromagnetic thin film.
A sample tape was prepared by applying a hexane solution (top coating) so that the coating amount of dilauryl phosphite was 2 mg/m 2 . Comparative Example 1 A sample tape was prepared in the same manner as in Example 1 using the basic composition of Example 1 as a magnetic paint. Comparative Example 2 A sample tape was prepared in the same manner as in Example 1 using a magnetic paint obtained by adding 2 parts by weight of trilauryl phosphate to the basic composition of Example 1. Comparative Example 3 A 1.0wt% n-hexane solution of trilauryl phosphate was applied to the magnetic layer of the sample tape obtained in Comparative Example 1 so that the coating amount of trilauryl phosphate was 160 mg/m 2 ( top coat)
A sample tape was created. Comparative Example 4 A 1.0wt% n-hexane solution of trioleyl phosphate was applied to the magnetic layer of the sample tape obtained in Comparative Example 1 so that the amount of trioleyl phosphate applied was 160 mg/m 2 ( top coat)
A sample tape was created. The properties of the sample tapes prepared in the above Examples and Comparative Examples are shown in the following table.
【表】
上表で◎は極めて良好、○は良好、△は不良、
×は極めて不良を示す。
またエージングは40℃、80%の条件下で3日間
行なわれた。
表より本発明による磁気記録媒体では摩擦係数
を極めて小さい値に抑えることができ、ステイツ
クスリツプを回避できる、特にトツプコート法に
よる磁気記録媒体では従来問題となつていた経日
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。[Table] In the table above, ◎ is extremely good, ○ is good, △ is poor,
× indicates extremely poor quality. Aging was carried out at 40° C. and 80% for 3 days. The table shows that the magnetic recording medium according to the present invention can suppress the coefficient of friction to an extremely small value and avoid stick slip.In particular, the running deterioration due to aging, which was a conventional problem with magnetic recording media using the top coating method, can be avoided. According to the invention, this problem 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。
1はベース、2は磁性層、3はトツプコート、
4,6は滑剤コーテイング層、5はバツクコート
層である。
1 to 5 are cross-sectional views showing embodiments of magnetic recording media according to the present invention. 1 is the base, 2 is the magnetic layer, 3 is the top coat,
4 and 6 are lubricant coating layers, and 5 is a back coat layer.
Claims (1)
体において、該磁気記録媒体は下記の化学式で表
わされる亜リン酸エステルを保持していることを
特徴とする磁気記録媒体。 【式】又は【式】(但し R1,R2,R3は炭素数8〜18個のアルキル基を示
す。)[Claims] 1. A magnetic recording medium having a magnetic layer on a non-magnetic support, characterized in that the magnetic recording medium holds a phosphite represented by the following chemical formula: . [Formula] or [Formula] (However, R 1 , R 2 , and R 3 represent an alkyl group having 8 to 18 carbon atoms.)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58250787A JPS60138728A (en) | 1983-12-27 | 1983-12-27 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58250787A JPS60138728A (en) | 1983-12-27 | 1983-12-27 | Magnetic recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60138728A JPS60138728A (en) | 1985-07-23 |
JPH058491B2 true JPH058491B2 (en) | 1993-02-02 |
Family
ID=17213038
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58250787A Granted JPS60138728A (en) | 1983-12-27 | 1983-12-27 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60138728A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63127424A (en) * | 1986-11-14 | 1988-05-31 | Matsushita Electric Ind Co Ltd | Magnetic recording medium |
JP2838162B2 (en) * | 1988-01-22 | 1998-12-16 | 富士写真フイルム株式会社 | Magnetic recording media |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58141440A (en) * | 1982-02-17 | 1983-08-22 | Hitachi Maxell Ltd | Magnetic recording medium |
JPS59165234A (en) * | 1983-03-08 | 1984-09-18 | Matsushita Electric Ind Co Ltd | Magnetic recording medium |
-
1983
- 1983-12-27 JP JP58250787A patent/JPS60138728A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58141440A (en) * | 1982-02-17 | 1983-08-22 | Hitachi Maxell Ltd | Magnetic recording medium |
JPS59165234A (en) * | 1983-03-08 | 1984-09-18 | Matsushita Electric Ind Co Ltd | Magnetic recording medium |
Also Published As
Publication number | Publication date |
---|---|
JPS60138728A (en) | 1985-07-23 |
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