JPH05135352A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPH05135352A JPH05135352A JP29744891A JP29744891A JPH05135352A JP H05135352 A JPH05135352 A JP H05135352A JP 29744891 A JP29744891 A JP 29744891A JP 29744891 A JP29744891 A JP 29744891A JP H05135352 A JPH05135352 A JP H05135352A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- less
- layer
- recording medium
- magnetic recording
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 124
- 239000000843 powder Substances 0.000 claims abstract description 41
- 230000005294 ferromagnetic effect Effects 0.000 claims abstract description 30
- 238000005259 measurement Methods 0.000 claims abstract description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 23
- 239000006229 carbon black Substances 0.000 claims description 16
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 239000006247 magnetic powder Substances 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 239000013078 crystal Substances 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 70
- 238000000576 coating method Methods 0.000 description 20
- 239000011248 coating agent Substances 0.000 description 18
- 239000011347 resin Substances 0.000 description 17
- 229920005989 resin Polymers 0.000 description 17
- 229940105289 carbon black Drugs 0.000 description 15
- -1 polyethylene terephthalate Polymers 0.000 description 13
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 125000000524 functional group Chemical group 0.000 description 12
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
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- 239000011230 binding agent Substances 0.000 description 7
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
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- GLYJVQDYLFAUFC-UHFFFAOYSA-N butyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCC GLYJVQDYLFAUFC-UHFFFAOYSA-N 0.000 description 4
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000000020 Nitrocellulose Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
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- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
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- 229920005749 polyurethane resin Polymers 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- 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
- QSSAKBZMXVUORV-UHFFFAOYSA-N 2-butoxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCOCCCC QSSAKBZMXVUORV-UHFFFAOYSA-N 0.000 description 2
- NHUXFMNHQIITCP-UHFFFAOYSA-N 2-butoxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOCCCC NHUXFMNHQIITCP-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- AMUTYVGRCVFCCD-UHFFFAOYSA-N 5,6-diaminopyridine-3-carboxylic acid Chemical compound NC1=CC(C(O)=O)=CN=C1N AMUTYVGRCVFCCD-UHFFFAOYSA-N 0.000 description 2
- HMRWHRBSEMHEFA-UHFFFAOYSA-N 6-methylheptyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCCCCC(C)C HMRWHRBSEMHEFA-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920001747 Cellulose diacetate Polymers 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 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
- 239000005642 Oleic acid Substances 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 230000003187 abdominal effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
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- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
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- 239000000945 filler Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 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
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
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- 239000002904 solvent Substances 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
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- IZTHTNFCHNNDAQ-QXMHVHEDSA-N 11-methyldodecyl (Z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCCCCCCCCC(C)C IZTHTNFCHNNDAQ-QXMHVHEDSA-N 0.000 description 1
- LGEZTMRIZWCDLW-UHFFFAOYSA-N 14-methylpentadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC(C)C LGEZTMRIZWCDLW-UHFFFAOYSA-N 0.000 description 1
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- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 1
- OPJWPPVYCOPDCM-UHFFFAOYSA-N 2-ethylhexyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC OPJWPPVYCOPDCM-UHFFFAOYSA-N 0.000 description 1
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- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
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- 238000004438 BET method Methods 0.000 description 1
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- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
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- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
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- RDOFJDLLWVCMRU-UHFFFAOYSA-N Diisobutyl adipate Chemical compound CC(C)COC(=O)CCCCC(=O)OCC(C)C RDOFJDLLWVCMRU-UHFFFAOYSA-N 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
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- 239000005639 Lauric acid Substances 0.000 description 1
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- GWFGDXZQZYMSMJ-UHFFFAOYSA-N Octadecansaeure-heptadecylester Natural products CCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC GWFGDXZQZYMSMJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
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Landscapes
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は磁気記録媒体に関し、特
に走行性の改善に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a magnetic recording medium, and more particularly to improvement of running property.
【0002】[0002]
【従来の技術】近年、ハイエイト(Hi-8)或はハイビ
ジョン用として磁気テープに対する要求も益々厳しくな
っており、超平滑支持体を用いた超平滑磁性層面、カー
ボン等のフィラーを除去し高充填化した磁性層等が必要
となって来ている。2. Description of the Related Art In recent years, the demand for magnetic tapes for high-eight (Hi-8) or high-definition has become more and more strict, and ultra-smooth magnetic layer surfaces using ultra-smooth supports, and fillers such as carbon are highly filled. There is a growing need for a magnetic layer that has been turned into a magnetic material.
【0003】しかし、磁性層面の超平滑化、磁性層から
のカーボン等のフィラー類の除去は磁性層の摩擦係数を
増大させ走行性を損い磁気テープのブロッキンを呼ぶ等
の支障を起す。However, super-smoothing of the magnetic layer surface and removal of fillers such as carbon from the magnetic layer increase the friction coefficient of the magnetic layer, impair the running property, and cause problems such as blocking of the magnetic tape.
【0004】Hi-8システムでは高周波特性が極めて重
要であるが、前述のような処置で、特に磁気テープの研
磨力が低下する低湿における初期RF出力の低下、高温
高湿における走行時のジッタの頻発等の問題が生じる。In the Hi-8 system, high-frequency characteristics are extremely important. However, the above-mentioned measures reduce the initial RF output especially in low humidity where the polishing power of the magnetic tape decreases, and the jitter during running in high temperature and high humidity. Problems such as frequent occurrence occur.
【0005】このような支障に対しては、非磁性支持体
表面に微細な突起を設けた積層支持体を用いて磁気テー
プの走行性を向上し、かつ電磁変換特性を改良すること
が提案されている(特開平3-176807,176808,176809各
号)。In order to solve such problems, it has been proposed to improve the running property of the magnetic tape and improve the electromagnetic conversion characteristics by using a laminated support having fine projections on the surface of the non-magnetic support. (Japanese Patent Laid-Open No. 3-176807, 176808, 176809).
【0006】また、積層磁性層とした最上層磁性層に強
磁性金属粉末を用い性能向上を図る技術が知られている
(特開昭64-19524号、特開平2-110823号)。Further, there is known a technique for improving performance by using a ferromagnetic metal powder for the uppermost magnetic layer which is a laminated magnetic layer (Japanese Patent Laid-Open No. 19524/64, Japanese Laid-Open Patent Publication No. 2-110823).
【0007】しかしながら磁気テープに対する性能要求
は更に精密な要因構成が必要となっている。However, the performance requirements for the magnetic tape require a more precise factor configuration.
【0008】[0008]
【発明の目的】本発明の目的は前記実情に照し;スペー
シングが少なく、しかも摩擦係数が小さく、低湿下のR
F出力低下、高温高湿下のジッタの発生を無視できかつ
耐蝕性の良好な磁気テープの提供にある。SUMMARY OF THE INVENTION The object of the present invention is, in view of the above-mentioned circumstances, that the R is under a low humidity condition with a small spacing and a small friction coefficient.
The purpose of the present invention is to provide a magnetic tape which has negligible F output reduction and jitter generation under high temperature and high humidity and has excellent corrosion resistance.
【0009】[0009]
【発明の構成】前記本発明の目的は;非磁性支持体上に
複数の磁性層を設けた磁気記録媒体において、前記磁性
層の表面うねりAsが0.022μm以下で、かつその最上層
に平均長軸長0.25μm未満、X線測定による結晶子サイ
ズ200Å未満の強磁性金属粉末を含有しており、また前
記非磁性支持体の磁性層形成面の表面うねりBsが0.020
μm以下、該形成面に存在する0.01μm以上の突起の数n
が測定長1mm当り200個以上、0.3μm以上の突起の数N
が測定長400mm当り500個以下であり、平均突起高さHmが
0.01〜0.25μm、更に最大突起高さHmaxと前記平均突起
高さHmとの比Hmax/Hmが10以下であることを特徴とする
磁気記録媒体によって達成される。前記本発明の構成に
よれば、最上層の磁性層表面は、非磁性支持体上の微細
な突起の影響で電気特性をおとさない程度にわずかに粗
面化され、例えばカーボンブラック等を極力除去した超
平滑磁性層の場合でも摩擦係数が増大しない。The object of the present invention is to provide a magnetic recording medium in which a plurality of magnetic layers are provided on a non-magnetic support, wherein the surface waviness As of the magnetic layer is 0.022 μm or less, and the average length of the uppermost layer is It contains a ferromagnetic metal powder with an axial length of less than 0.25 μm and a crystallite size of less than 200Å by X-ray measurement, and the surface waviness Bs of the magnetic layer forming surface of the non-magnetic support is 0.020.
The number n of protrusions of not more than μm and not less than 0.01 μm existing on the formation surface
Is 200 or more per 1 mm measuring length, and the number N of protrusions of 0.3 μm or more
Is less than 500 per 400 mm measuring length, and the average protrusion height Hm is
This is achieved by a magnetic recording medium characterized by having a ratio Hmax / Hm of 0.01 to 0.25 μm, and a ratio of the maximum protrusion height Hmax to the average protrusion height Hm of 10 or less. According to the configuration of the present invention, the surface of the uppermost magnetic layer is slightly roughened to the extent that the electrical characteristics are not deteriorated due to the influence of the fine protrusions on the non-magnetic support, and carbon black or the like is removed as much as possible. Even in the case of the ultra-smooth magnetic layer, the friction coefficient does not increase.
【0010】ところで、Hi-8やハイビジョンにも対応
できる電気特性、走行耐久性、耐蝕性をうるためには以
下の手段を適宜組合せるのが好ましい。By the way, it is preferable to appropriately combine the following means in order to obtain electric characteristics, running durability, and corrosion resistance that are compatible with Hi-8 and high-definition.
【0011】(1)最上層に平均長軸長0.25μm未満、
結晶子サイズ200Å未満の強磁性金属粉末を用いる、 (2)強磁性粉末がFe,Alを含み、FeとAlの原子重量比
がFe:Al=100:0.5〜100:20ならしめる、 (3)最上層以外の少なくとも1層に平均長軸長0.25μ
m未満、結晶子サイズ450Å未満の強磁性粉末を含ませ
る、 (4)最上層に軸比10未満の強磁性粉末を含ませる、 (5)最上層以外の少なくとも1層がFe2+とFe3+の原子
数比(Fe2+/Fe3+)が0.08以上であるCo-含有酸化鉄を含
む、 (6)非磁性支持体の磁性層形成面とは反対側の裏面に
も表面に微細な突起を均一にもつ層を積層でもうける、 (7)最上層に含まれるカーボンブラックの重量が磁性
粉100重量部に対して1重量部未満、 前記のより好ましい範囲としては前記(1)については
平均長軸長0.20μm未満、結晶子サイズ180Å未満の強磁
性金属粉、 (2)Fe:Al=100:1〜100:20、 (3)において、0.22μm未満、結晶子サイズ420Å未
満、 (4)において、軸比が6〜9、 (5)において、Fe2+/Fe3+が0.15〜0.45、 (7)において、カーボンブラックの重量が0.5重量部
未満、また、非磁性支持体の表面の突起において、(最
大突起高さ)/(平均突起高さ)の比が5以下であるこ
とがより好ましい。(1) In the uppermost layer, the average major axis length is less than 0.25 μm,
Use a ferromagnetic metal powder having a crystallite size of less than 200Å, (2) the ferromagnetic powder contains Fe and Al, and the atomic weight ratio of Fe and Al is Fe: Al = 100: 0.5 to 100: 20. ) Average major axis length 0.25μ in at least one layer other than the top layer
Ferromagnetic powder of less than m and crystallite size of less than 450Å is included. (4) The top layer contains ferromagnetic powder with an axial ratio of less than 10. (5) At least one layer other than the top layer is Fe 2+ and Fe. Includes Co-containing iron oxide with an atomic ratio of 3+ (Fe 2+ / Fe 3+ ) of 0.08 or more. (6) On the back surface of the non-magnetic support opposite to the surface on which the magnetic layer is formed A layer having uniform fine projections is laminated, and (7) the weight of the carbon black contained in the uppermost layer is less than 1 part by weight with respect to 100 parts by weight of the magnetic powder, and the more preferable range is (1) above. For the ferromagnetic metal powder with an average major axis length of less than 0.20 μm and a crystallite size of less than 180Å, (2) Fe: Al = 100: 1 to 100: 20, in (3), less than 0.22 μm and a crystallite size of less than 420Å , (4), the axial ratio was 6 to 9, (5) Fe 2+ / Fe 3+ was 0.15 to 0.45, and (7) carbon black. It is more preferable that the weight of the particles is less than 0.5 parts by weight, and the ratio of (maximum protrusion height) / (average protrusion height) is 5 or less in the protrusions on the surface of the non-magnetic support.
【0012】次に本発明を詳細に説明する。Next, the present invention will be described in detail.
【0013】非磁性支持体の磁性層形成面(以後、腹面
と称す)の表面うねりBsを0.020μm以下、好ましくは
0.018μm以下、さらに好ましくは0.015μm以下とするこ
とにより、磁性層の表面うねりAsを小さくして電磁変
換特性(特にクロマS/N)の向上を図ることができ
る。The surface waviness Bs of the surface of the non-magnetic support on which the magnetic layer is formed (hereinafter referred to as the abdomen) is 0.020 μm or less, preferably
By setting the thickness to 0.018 μm or less, and more preferably 0.015 μm or less, the surface waviness As of the magnetic layer can be reduced and the electromagnetic conversion characteristics (particularly the chroma S / N) can be improved.
【0014】逆に、前記腹面の表面うねりBsHmが0.020
μmを超えると、磁性層の表面うねりAsが0.022μmを超
えて大きくなりすぎ、電磁変換特性の低下を招くことに
なる。On the contrary, the surface waviness BsHm of the abdominal surface is 0.020.
When it exceeds μm, the surface waviness As of the magnetic layer exceeds 0.022 μm and becomes too large, which causes deterioration of electromagnetic conversion characteristics.
【0015】さらに本発明における非磁性支持体におい
ては、前記腹面表面に存在する高さが0.01μm以上の突
起の個数nが測定長1mm当り200個以上、好ましくは200
個以上2000個以下であり、また、高さが0.30μm以上で
ある突起の個数Nが測定長400mm当り500個以下、好まし
くは100個以下であり、平均突起高さHmを0.01〜0.25μ
m、更に非磁性支持体の腹面における(最大突起高さHma
x)/(平均突起高さHm)の比が10以下、好ましくは5
以下であることが必要である。Further, in the non-magnetic support of the present invention, the number n of protrusions present on the abdominal surface having a height of 0.01 μm or more is 200 or more, preferably 200, per 1 mm of measurement length.
The number N of protrusions is not less than 2000 and not more than 2000, and the number N of protrusions having a height of 0.30 μm or more is 500 or less, preferably 100 or less per measurement length 400 mm, and the average protrusion height Hm is 0.01 to 0.25 μm.
m, and on the ventral surface of the non-magnetic support (maximum protrusion height Hma
x) / (average protrusion height Hm) ratio is 10 or less, preferably 5
It must be:
【0016】また、非磁性支持体の磁性層形成面とは反
対側の面(以下、この面を背面と称する)に存在する高
さが0.01μm以上である突起の個数n′が測定長1mm当
り200個以上、好ましくは200個以上2000個以下であり、
また、高さが0.30μm以上である突起の個数N′が測定
長400mm当り500個以下、好ましくは100個以下であり、
前記背面表面における(最大突起高さH′max)/(平均
突起高さH′m)の比が10以下、好ましくは5以下であ
る。The number n'of protrusions having a height of 0.01 μm or more existing on the surface of the non-magnetic support opposite to the surface on which the magnetic layer is formed (hereinafter, this surface is referred to as the back surface) is 1 mm. 200 or more, preferably 200 or more and 2000 or less per
Further, the number N'of protrusions having a height of 0.30 μm or more is 500 or less, preferably 100 or less per 400 mm of measurement length,
The ratio of (maximum protrusion height H'max) / (average protrusion height H'm) on the back surface is 10 or less, preferably 5 or less.
【0017】前記本発明の如く、非磁性支持体の腹面及
び背面における表面うねり及び粗さを規制することによ
り、摺動ノイズが低く、また搬送性および走行性に優れ
た磁気記録媒体を提供することができるし、走行性に優
れ、磁気記録媒体の巻取時に非磁性支持体の背面に疵の
つきにくい磁気記録媒体を提供することができる。更に
磁性層の表面うねりAsを制御して電磁変換特性の向上
させるとともに、磁性塗料の塗布工程やカレンダ工程に
おいて、突起を保護、保存してドロップアウトの発生し
にくい磁気記録媒体を提供することができる。By controlling the surface waviness and roughness on the ventral surface and the back surface of the non-magnetic support as in the present invention, a sliding recording noise is reduced, and a magnetic recording medium excellent in transportability and runnability is provided. It is possible to provide a magnetic recording medium which is excellent in running property and is less likely to have a flaw on the back surface of the non-magnetic support when the magnetic recording medium is wound up. Further, the surface waviness As of the magnetic layer is controlled to improve electromagnetic conversion characteristics, and projections are protected and stored in the coating process and the calendar process of the magnetic paint to provide a magnetic recording medium in which dropout is unlikely to occur. it can.
【0018】このような特長を与える非磁性支持体の形
成材料としては、例えばポリエチレンテレフタレートお
よびポリエチレン-2,6-ナフタレート等のポリエステル
類;ポリプロピレン等のポリオレフィン類;セルロース
トリアセテートおよびセルロースダイアセテート等のセ
ルロース誘導体;ならびにポリカーボネート、芳香族ポ
リアミド、ポリイミドなどのプラスチックを挙げること
ができる。さらにCu,Al,Znなどの金属、ガラス、いわ
ゆるニューセラミック(例えば窒化硼素、炭化珪素等)
等の各種セラミックなども使用することができる。Examples of the material for forming the non-magnetic support which gives such characteristics are polyesters such as polyethylene terephthalate and polyethylene-2,6-naphthalate; polyolefins such as polypropylene; cellulose such as cellulose triacetate and cellulose diacetate. Derivatives; and plastics such as polycarbonate, aromatic polyamide and polyimide. Furthermore, metals such as Cu, Al, Zn, glass, so-called new ceramics (eg boron nitride, silicon carbide, etc.)
Various types of ceramics such as the above can also be used.
【0019】前記支持体の厚みは、通常、3〜150μm、
好ましくは4〜100μmである。The thickness of the support is usually 3 to 150 μm,
It is preferably 4 to 100 μm.
【0020】本発明においては非磁性支持体の背面に
は、磁気記録媒体の走行性の向上、帯電防止および転写
防止などを目的として、バックコート層を設けてもよ
い。ただし、本発明においては、バックコート層を設け
なくても良好な電磁変換特性、走行性および耐久性が得
られる。In the present invention, a back coat layer may be provided on the back surface of the non-magnetic support for the purpose of improving the running property of the magnetic recording medium, preventing charging and preventing transfer. However, in the present invention, good electromagnetic conversion characteristics, runnability and durability can be obtained without providing a back coat layer.
【0021】また、非磁性支持体における前記磁性層形
成面には、磁性層と非磁性支持体との接着性の向上等を
目的として、中間層(例えば接着剤層)を設けることも
できる。An intermediate layer (eg, an adhesive layer) may be provided on the surface of the nonmagnetic support on which the magnetic layer is formed for the purpose of improving the adhesiveness between the magnetic layer and the nonmagnetic support.
【0022】前記非磁性支持体上に、直接にあるいは適
当な中間層を介して形成される磁性層は、強磁性粉末を
バインダ中に分散して形成される。The magnetic layer formed on the non-magnetic support directly or via an appropriate intermediate layer is formed by dispersing ferromagnetic powder in a binder.
【0023】そして、本発明においては、磁性層の表面
うねりAs0.022μm以下、好ましくは0.020μm以下、さ
らに好ましくは0.018μm以下とするものであるが、磁性
層の該表面うねりAsを与えるには、磁性層を形成する
磁性塗料を前記非磁性支持体上に塗布した後、例えばス
ーパカレンダロールなどを用いた表面平滑化処理、粒径
の小さい強磁性粉末の採用等の手段を選べばよい。ま
た、バインダに官能基を有する樹脂の遍用、加圧ニーダ
等の剪断力の高い装置の使用等、強磁性粉末の分散性の
向上を図ることによっても、磁性層の表面うねりAsを
0.022μm以下にすることができる。In the present invention, the surface waviness As of the magnetic layer is 0.022 μm or less, preferably 0.020 μm or less, and more preferably 0.018 μm or less. To provide the surface waviness As of the magnetic layer, After applying the magnetic coating material for forming the magnetic layer on the non-magnetic support, a surface smoothing treatment using, for example, a super calender roll, a ferromagnetic powder having a small particle size, or the like may be selected. In addition, the surface waviness As of the magnetic layer can be improved by improving the dispersibility of the ferromagnetic powder, such as the general use of a resin having a functional group as a binder and the use of a device with high shearing force such as a pressure kneader.
It can be 0.022 μm or less.
【0024】本発明に係る複数の磁性層を形成する強磁
性粉末において、最上層磁性層においてはFe-Al系の強
磁性の合金粉末が用いられ、Fe-Al合金粉末、Fe-Al-Ni
合金粉末、Fe-Al-Ca合金粉末、Fe-Al-Ca-Ni合金粉末、F
e-Ni-Co-Al-Si合金粉末、Fe-Ni-Si-Al合金粉末、Fe-Ni-
Si-Al-Mn合金粉末等の強磁性合金粉末などが挙げられ
る。In the ferromagnetic powder forming a plurality of magnetic layers according to the present invention, Fe-Al based ferromagnetic alloy powder is used in the uppermost magnetic layer, and Fe-Al alloy powder, Fe-Al-Ni are used.
Alloy powder, Fe-Al-Ca alloy powder, Fe-Al-Ca-Ni alloy powder, F
e-Ni-Co-Al-Si alloy powder, Fe-Ni-Si-Al alloy powder, Fe-Ni-
Examples include ferromagnetic alloy powders such as Si-Al-Mn alloy powders.
【0025】これらの中でも、好ましいのは原子重量比
(Fe:Al)が(100:5)〜(100:20)の合金粉末であ
る。Among these, alloy powder having an atomic weight ratio (Fe: Al) of (100: 5) to (100: 20) is preferable.
【0026】前記強磁性合金粉末の形状は結晶子サイズ
200Å未満、好ましくは180Å未満、平均長軸長0.25μm
未満、好ましくは0.20μmが用いられる。The shape of the ferromagnetic alloy powder is the crystallite size.
Less than 200Å, preferably less than 180Å, average major axis length 0.25μm
Less than, preferably 0.20 μm is used.
【0027】前記強磁性粉末の比表面積(BET法によ
る)は、通常、25m2/g以上、好ましくは30〜80m2/gで
ある。The specific surface area of the ferromagnetic powder (by BET method) is usually, 25 m 2 / g or more, preferably 30~80m 2 / g.
【0028】前記強磁性粉末の保磁力は、500〜2,000エ
ルステッド、好ましくは600〜1.700エルステッドであ
る。The ferromagnetic powder has a coercive force of 500 to 2,000 oersteds, preferably 600 to 1.700 oersteds.
【0029】次いで、前記最上層以外の磁性層を形成す
る強磁性粉末としては、Co被着若しくはCo含有のCo-γ-
Fe2O3粉末、Co-Fe3O4粉末、Co-FeOx(4/3<x<3/2)粉
末等の酸化鉄磁性粉が挙げられる。Next, as the ferromagnetic powder for forming the magnetic layers other than the uppermost layer, Co-deposited or Co-containing Co-γ-
Examples thereof include iron oxide magnetic powders such as Fe 2 O 3 powder, Co-Fe 3 O 4 powder, and Co-FeOx (4/3 <x <3/2) powder.
【0030】またこれらの磁性層には、結晶子サイズ45
0Å未満、平均長軸長0.25μm未満でFe2+,Fe3+間の原子
数比Fe2+/Fe3+が0.08以上のCo-酸化鉄が好ましい。In addition, a crystallite size of 45 is included in these magnetic layers.
Less than 0 Å, Fe 2+ in less than an average major axis length 0.25 [mu] m, the atomic ratio between Fe 3+ Fe 2+ / Fe 3+ is preferably 0.08 or more Co- iron oxide.
【0031】本発明において使用されるバインダとして
は、一般的に平均分子量が約10,000〜200,000の範囲内
にある樹脂を用いることができる。As the binder used in the present invention, a resin having an average molecular weight of about 10,000 to 200,000 can be generally used.
【0032】具体的には、例えばウレタンポリマー、塩
化ビニル樹脂、塩化ビニル-酢酸ビニル共重合体、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、ブタジエン-アクリロニトリル共重
合体、ポリアミド樹脂、ポリビニルブチラール、セルロ
ース誘導体(例:セルロースアセテートブチレート、セ
ルロースダイアセテート、セルロースプロピオネート、
ニトロセルロース等)、スチレンブタジエン共重合体、
ポリエステル樹脂、各種の合成ゴム系バインダ、フェノ
ール樹脂、エポキシ樹脂、尿素樹脂、メラミン樹脂、シ
リコーン樹脂、アクリル系反応樹脂、高分子量ポリエス
テル樹脂とイソシアネートプレポリマーとの混合物、ポ
リエステルポリオールとポリイソシアネートとの混合
物、尿素ホルムアルデヒド樹脂、低分子量グリコールと
高分子量ジオール化合物との混合物およびこれらの混合
物などが挙げられる。Specifically, for example, urethane polymer, vinyl chloride resin, vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinylidene chloride copolymer, vinyl chloride-acrylonitrile copolymer, butadiene-acrylonitrile copolymer, polyamide Resin, polyvinyl butyral, cellulose derivative (eg: cellulose acetate butyrate, cellulose diacetate, cellulose propionate,
Nitrocellulose, etc.), styrene-butadiene copolymer,
Polyester resin, various synthetic rubber binders, phenol resins, epoxy resins, urea resins, melamine resins, silicone resins, acrylic reaction resins, mixtures of high molecular weight polyester resins and isocyanate prepolymers, mixtures of polyester polyols and polyisocyanates , Urea formaldehyde resin, a mixture of a low molecular weight glycol and a high molecular weight diol compound, and a mixture thereof.
【0033】本発明においては、これらの樹脂と併用、
或は単独で陰性官能基を有する樹脂を好適に用いること
もできる。In the present invention, these resins are used in combination,
Alternatively, a resin having a negative functional group may be preferably used alone.
【0034】この陰性官能基を有する樹脂としては、 −SO3M1,−OSO2M1, −OSO3M1 及び−〔(M2O−)PO(−OM3)〕 (但し、式中、M1は水素原子、アルカリ金属であり、
M2およびM3は、それぞれ水素原子、アルカリ金属およ
びアルキル基のいずれかである。またM2とM3とは、互
いに異なっていても良いし、同じであっても良い。)な
どが挙げられる。Examples of the resin having the negative functional groups, -SO 3 M 1, -OSO 2 M 1, -OSO 3 M 1 and - [(M 2 O-) PO (-OM 3) ] (where formula In the above, M 1 is a hydrogen atom or an alkali metal,
M 2 and M 3 are each a hydrogen atom, an alkali metal or an alkyl group. Further, M 2 and M 3 may be different from each other or may be the same. ) And the like.
【0035】前記陰性官能基を有する樹脂は、例えば、
塩化ビニル系樹脂、ポリエステル樹脂、ポリウレタン樹
脂などの樹脂を変性して、前記陰性官能基を導入するこ
とにより得ることができる。The resin having the negative functional group is, for example,
It can be obtained by modifying a resin such as a vinyl chloride resin, a polyester resin or a polyurethane resin to introduce the negative functional group.
【0036】前記陰性官能基を有する樹脂における陰性
官能基量は、0.005〜1.0mmol/gであるのが望ましい。The amount of the negative functional group in the resin having the negative functional group is preferably 0.005 to 1.0 mmol / g.
【0037】陰性官能基量が規制された樹脂中では、強
磁性粉末の分散性がよく、磁気記録媒体の出力が大き
く、走行安定性が向上する。In the resin in which the amount of negative functional groups is regulated, the dispersibility of the ferromagnetic powder is good, the output of the magnetic recording medium is large, and the running stability is improved.
【0038】逆に前記量を外れると、これらの効果が充
分に得られないことがある。On the contrary, when the amount is out of the above range, these effects may not be sufficiently obtained.
【0039】前記陰性官能基を有する樹脂を用いる場
合、その配合量は、前記強磁性粉末100重量部に対し
て、通常、2〜50重量部、好ましくは5〜40重量部であ
る。When the resin having a negative functional group is used, its amount is usually 2 to 50 parts by weight, preferably 5 to 40 parts by weight, based on 100 parts by weight of the ferromagnetic powder.
【0040】この配合割合が2重量部未満であると、前
記陰性官能基を有する樹脂を配合した場合に奏されるべ
き所期の効果が充分に奏されないことがある。50重量部
より多くすると、摺動ノイズやヘッド白濁の劣化を招く
ことがある。If this blending ratio is less than 2 parts by weight, the desired effect to be obtained when the resin having a negative functional group is blended may not be sufficiently exhibited. If the amount is more than 50 parts by weight, sliding noise and head turbidity may be deteriorated.
【0041】本発明においては、前記陰性官能基を有す
る樹脂とともにポリイソシアナート系硬化剤を併用する
ことにより、磁性層の耐久性の向上を図ることもでき
る。In the present invention, the durability of the magnetic layer can be improved by using a polyisocyanate curing agent together with the resin having the negative functional group.
【0042】このポリイソシアナート系硬化剤として
は、例えばトリレンジイソシアナート、ジフェニルメタ
ンジイソシアナート、ヘキサンジイソシアナート等の2
官能イソシアナート、コロネートL(商品名;日本ポリ
ウレタン工業(株)製)、デスモジュールL(商品名;
バイエル社製)等の3官能イソシアナート、または両末
端にイソシアナート基を含有するウレタンプレポリマー
などの従来から硬化剤として使用されているものや、ま
た硬化剤として使用可能であるポリイソシアナートであ
るものをいずれも使用することができる。Examples of the polyisocyanate type curing agent include, for example, tolylene diisocyanate, diphenylmethane diisocyanate, hexane diisocyanate, and the like.
Functional isocyanate, Coronate L (trade name; manufactured by Nippon Polyurethane Industry Co., Ltd.), Desmodur L (trade name;
A trifunctional isocyanate such as Bayer), or a urethane prepolymer having an isocyanate group at both ends, which has been conventionally used as a curing agent, or a polyisocyanate usable as a curing agent. Any one can be used.
【0043】前記硬化剤の使用量は、通常、全バインダ
量の5〜80重量部である。The amount of the above curing agent used is usually 5 to 80 parts by weight based on the total amount of the binder.
【0044】本発明では、前記各種のバインダの外に任
意成分である分散剤として、例えばレシチン、燐酸エス
テル、脂肪酸、アミン化合物、アルキルサルフェート、
脂肪酸アミド、高級アルコール、ポリエチレンオキサイ
ド、スルホ琥珀酸、スルホ琥珀酸エステル、公知の界面
活性剤等およびこれらの塩、陰性有機基(例えば-COO
H,-PO3H)重合体分散剤の塩などを用いることができ
る。In the present invention, in addition to the various binders, as a dispersant which is an optional component, for example, lecithin, phosphoric acid ester, fatty acid, amine compound, alkyl sulfate,
Fatty acid amides, higher alcohols, polyethylene oxides, sulfosuccinic acid, sulfosuccinic acid esters, known surfactants and their salts, negative organic groups (eg -COO
H, -PO 3 H) A polymer dispersant salt or the like can be used.
【0045】これらは一種単独で使用しても良いし、二
種以上を組合せて使用しても良い。また、本発明では、
任意成分である可塑剤として脂肪酸エステルを用いるこ
とができる。この脂肪酸エステルとしては、例えばオレ
イルオレート、オレイルステアレート、イソセチルステ
アレート、ジオレイルマレエート、ブチルステアレー
ト、ブチルパルミテート、ブチルミリステート、オクチ
ルミリステート、オクチルパルミテート、アミルステア
レート、アミルパルミテート、ステアリルステアレー
ト、ラウリルオレート、オクチルオレート、イソブチル
オレート、エチルオレート、イソトリデシルオレート、
ブトキシエチルパルミテート、ブトキシエチルステアレ
ート、2-エチルヘキシルステアレート、2-エチルヘキシ
ルミリステート、エチルステアレート、2-エチルヘキシ
ルパルミテート、イソプロピルパルミテート、イソプロ
ピルミリステート、イソオクチルパルミテート、イソオ
クチルミリステート、ブチルラウレート、セチル-2-エ
チルヘキサレート、ジオレイルアジペート、ジエチルア
ジペート、ジイソブチルアジペート、ジイソデシルアジ
ペートなどが挙げられる。これらの中でも、特に好まし
いのはブチルステアレート、ブチルパルミテート、ブト
キシエチルパルミテート、ブトキシエチルステアレー
ト、イソオクチルパルミテート、イソオクチルミリステ
ートである。These may be used alone or in combination of two or more. Further, in the present invention,
A fatty acid ester can be used as a plasticizer which is an optional component. Examples of the fatty acid ester include oleyl oleate, oleyl stearate, isocetyl stearate, dioleyl maleate, butyl stearate, butyl palmitate, butyl myristate, octyl myristate, octyl palmitate, amyl stearate, amyl palmitate. Tate, stearyl stearate, lauryl oleate, octyl oleate, isobutyl oleate, ethyl oleate, isotridecyl oleate,
Butoxyethyl palmitate, butoxyethyl stearate, 2-ethylhexyl stearate, 2-ethylhexyl myristate, ethyl stearate, 2-ethylhexyl palmitate, isopropyl palmitate, isopropyl myristate, isooctyl palmitate, isooctyl myristate, Butyl laurate, cetyl-2-ethyl hexalate, dioleyl adipate, diethyl adipate, diisobutyl adipate, diisodecyl adipate and the like can be mentioned. Of these, butyl stearate, butyl palmitate, butoxyethyl palmitate, butoxyethyl stearate, isooctyl palmitate, and isooctyl myristate are particularly preferred.
【0046】前記種々の脂肪酸エステルは一種単独で使
用しても良いし、二種以上を混合して使用しても良い。The above various fatty acid esters may be used alone or in combination of two or more.
【0047】このようなレシチン等の分散剤や脂肪酸エ
ステル等の可塑剤の添加量を少なくすると、特に高温高
湿下における磁気記録媒体の走行耐久性を向上させるこ
とができる。When the amount of the dispersant such as lecithin or the plasticizer such as fatty acid ester added is reduced, the running durability of the magnetic recording medium can be improved especially under high temperature and high humidity.
【0048】本発明の磁気記録媒体における磁性層は、
潤滑剤を含有していてもよい。The magnetic layer in the magnetic recording medium of the present invention is
It may contain a lubricant.
【0049】潤滑剤としては、例えば脂肪酸、シリコー
ン系潤滑剤、脂肪酸変性シリコーン系潤滑剤、弗素系潤
滑剤、流動パラフィン、スクワラン、カーボンブラッ
ク、グラファイト、カーボンブラックグラフトポリマ
ー、二硫化モリブデン、二硫化タングステンなどが挙げ
られる。Examples of the lubricant include fatty acids, silicone lubricants, fatty acid-modified silicone lubricants, fluorine lubricants, liquid paraffin, squalane, carbon black, graphite, carbon black graft polymers, molybdenum disulfide, and tungsten disulfide. And so on.
【0050】これらは一種単独で使用しても良いし、二
種以上を組み合わせて使用しても良い。These may be used alone or in combination of two or more.
【0051】本発明においては前記潤滑剤の中でも、脂
肪酸を好適に用いることができる。前記脂肪酸として
は、例えばカプロン酸、カプリル酸、カプリン酸、ラウ
リン酸、ミリスチン酸、パルミチン酸、ステアリン酸、
イソステアリン酸、リノレン酸、リノール酸、オレイン
酸、エライジン酸、ベヘン酸、マロン酸、コハク酸、マ
レイン酸、グルタル酸、アジピン酸、ピメリン酸、アゼ
ライン酸、セバシン酸、1,12-ドデカンジカルボン酸、
オクタンジカルボン酸などが挙げられる。In the present invention, fatty acids can be preferably used among the above lubricants. Examples of the fatty acid include caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid,
Isostearic acid, linolenic acid, linoleic acid, oleic acid, elaidic acid, behenic acid, malonic acid, succinic acid, maleic acid, glutaric acid, adipic acid, pimelic acid, azelaic acid, sebacic acid, 1,12-dodecanedicarboxylic acid,
Octanedicarboxylic acid and the like can be mentioned.
【0052】これらの中でも、特に好ましいのはミリス
チン酸、オレイン酸、ステアリン酸である。Of these, myristic acid, oleic acid and stearic acid are particularly preferable.
【0053】前記潤滑剤の配合割合は、前記強磁性粉末
100重量部に対して、通常、20重量部以下、好ましくは1
0重量部以下である。この配合割合が20重量部を超える
と、ブルーミングやブリードアウトが生じ易くなること
がある。The blending ratio of the lubricant is the ferromagnetic powder.
Generally, 20 parts by weight or less, preferably 1 part by weight per 100 parts by weight
It is 0 parts by weight or less. If this blending ratio exceeds 20 parts by weight, blooming and bleed-out may occur easily.
【0054】本発明においては、磁性層が平均粒径10〜
100mμのカーボンブラックを含有していても良い。In the present invention, the magnetic layer has an average particle size of 10 to 10
It may contain 100 mμ of carbon black.
【0055】磁性層が平均粒径10〜100mμ、好ましくは
20〜40mμのカーボンブラックを含有することにより、
本発明の磁気記録媒体における向上した電磁変換特性の
低下を招かないで走行耐久性をさらに向上させることが
できる。ただし、カーボンブラックの平均粒径が10mμ
未満であると、走行耐久性に劣ることがある。一方、カ
ーボンブラックの平均粒径が100mμを超えると、添加量
を多くした場合に電磁変換特性の低下を招くことがあ
る。The magnetic layer has an average particle size of 10 to 100 mμ, preferably
By containing 20 to 40 mμ of carbon black,
The running durability can be further improved without inducing the improved electromagnetic conversion characteristics of the magnetic recording medium of the present invention. However, the average particle size of carbon black is 10 mμ
If it is less than this, running durability may be poor. On the other hand, if the average particle size of carbon black exceeds 100 mμ, the electromagnetic conversion characteristics may be deteriorated when the addition amount is increased.
【0056】また、本発明において期待する効果を充分
に奏するための前記カーボンブラックの配合割合は、前
記強磁性粉末100重量部に対して0〜1重量部である。The blending ratio of the carbon black for sufficiently exhibiting the effect expected in the present invention is 0 to 1 part by weight with respect to 100 parts by weight of the ferromagnetic powder.
【0057】磁性層は、前記の種々の成分の他にさらに
研磨剤、帯電防止剤を含有していてもよい。The magnetic layer may further contain an abrasive and an antistatic agent in addition to the above various components.
【0058】なお、前記帯電防止剤あるいは前述の分散
剤等は、単独の作用のみを有するものではなく、例え
ば、一つの化合物が潤滑剤および帯電防止剤として作用
する場合がある。The antistatic agent or the dispersant described above does not have only a single action, but for example, one compound may act as a lubricant and an antistatic agent.
【0059】したがって、この発明における前述の分類
は主な作用を示したものであり、分類された化合物の作
用が分類に示す作用によって限定されるものではない。Therefore, the above-mentioned classification in the present invention shows the main action, and the action of the classified compound is not limited by the action shown in the classification.
【0060】また、本発明においては、特性の異なる複
数の磁性層を積層することにより、磁性層を多層構成と
することにより特性を整えている。In the present invention, the characteristics are adjusted by stacking a plurality of magnetic layers having different characteristics so that the magnetic layers have a multilayer structure.
【0061】本発明の磁気記録媒体は、前記強磁性粉
末、陰性官能基を有する塩化ビニル系樹脂などのバイン
ダおよびその他の磁性層形成成分を溶媒に混練分散して
磁性塗料を調製した後、この磁性塗料を前記非磁性支持
体上に塗布し、および乾燥することにより製造すること
ができる。In the magnetic recording medium of the present invention, the ferromagnetic powder, the binder such as vinyl chloride resin having a negative functional group, and the other components for forming the magnetic layer are kneaded and dispersed in a solvent to prepare a magnetic coating material. It can be produced by coating a magnetic coating on the non-magnetic support and drying.
【0062】磁性層形成成分の混練・分散に使用する溶
媒としては、例えばアセトン、メチルエチルケトン(ME
K)、メチルイソブチルケトン(MIBK)およびシクロヘキ
サノン等のケトン系;メタノール、エタノール、プロパ
ノールおよびブタノール等のアルコール系;酢酸メチ
ル、酢酸エチル、酢酸ブチル、乳酸エチル、酢酸プロピ
ルおよびエチレングリコールモノアセテート等のエステ
ル系;ジエチレングリコールジメチルエーテル、2-エト
キシエタノール、テトラヒドロフラン、ジオキサン等の
エーテル系;ベンゼン、トルエンおよびキシレン等の芳
香族炭化水素;メチレンクロライド、エチレンクロライ
ド、四塩化炭素、クロロホルム、エチレンクロルヒドリ
ンおよびジクロルベンゼン等のハロゲン化炭化水素など
を使用することができる。Examples of the solvent used for kneading / dispersing the magnetic layer forming components include acetone and methyl ethyl ketone (ME
K), ketone systems such as methyl isobutyl ketone (MIBK) and cyclohexanone; alcohol systems such as methanol, ethanol, propanol and butanol; esters such as methyl acetate, ethyl acetate, butyl acetate, ethyl lactate, propyl acetate and ethylene glycol monoacetate. System; ether system such as diethylene glycol dimethyl ether, 2-ethoxyethanol, tetrahydrofuran, dioxane; aromatic hydrocarbon such as benzene, toluene and xylene; methylene chloride, ethylene chloride, carbon tetrachloride, chloroform, ethylene chlorohydrin and dichlorobenzene And the like can be used.
【0063】磁性層形成成分の組成混練にあたっては、
前記強磁性粉末およびその他の磁性塗料成分を、同時に
または個々に順次混練機に投入する。例えば、まず分散
剤を含む溶液中に前記強磁性粉末を加え、所定時間混練
した後、残りの各成分を加えて、さらに混練を続けて磁
性塗料とする。When kneading the composition of the components for forming the magnetic layer,
The above-mentioned ferromagnetic powder and other magnetic paint ingredients are charged into a kneader simultaneously or individually. For example, first, the ferromagnetic powder is added to a solution containing a dispersant, and after kneading for a predetermined time, the remaining components are added and further kneading is performed to obtain a magnetic paint.
【0064】混練分散にあたっては、各種の混練機を使
用することができる。この混練機としては、例えば二本
ロールミル、三本ロールミル、加圧ニーダ、連続ニー
ダ、オープンニーダ、ボールミル、ペブルミル、サイド
グラインダ、Sqegvariアトライタ、高速インペラ分散
機、高速ストーンミル、高速度衝撃ミル、ディスパーニ
ーダ、高速ミキサ、ホモジナイザ、超音波分散機などが
挙げられる。For kneading and dispersing, various kneaders can be used. Examples of this kneader include a two-roll mill, a three-roll mill, a pressure kneader, a continuous kneader, an open kneader, a ball mill, a pebble mill, a side grinder, a Sqegvari attritor, a high-speed impeller disperser, a high-speed stone mill, a high-speed impact mill, and a disper. A kneader, a high speed mixer, a homogenizer, an ultrasonic disperser, etc. may be mentioned.
【0065】磁性塗料の塗布に利用することのできる塗
布方法としては、例えばグラビアロールコーティング、
マイヤバーコーティング、ドクタプレードコーティン
グ、リバースロールコーティング、ディップコーティン
グ、エアーナイフコーティング、カレンダコーティン
グ、スキーズコーティング、キスコーティング、エクス
トルージョンコーティングおよびファンティンコーティ
ングなどが挙げられる。As a coating method which can be used for coating the magnetic paint, for example, gravure roll coating,
Examples include Mayer bar coating, doctor blade coating, reverse roll coating, dip coating, air knife coating, calendar coating, skies coating, kiss coating, extrusion coating and fantin coating.
【0066】複層塗布にはウエット・オン・ドライ或は
ウェット・オン・ウェット方式が任意に用いられる。A wet-on-dry method or a wet-on-wet method is optionally used for multi-layer coating.
【0067】このようにして塗布された前記磁性層の厚
みは乾燥厚で、通常、0.1〜10μm、好ましくは0.5〜5
μmである。The thickness of the magnetic layer thus coated is a dry thickness, usually 0.1 to 10 μm, preferably 0.5 to 5
μm.
【0068】こうして、磁性層形成成分を塗布した後、
未乾燥の状態で、必要により磁場配向処理を行い、さら
に、例えばスーパカレンダロールなどを用いて表面平滑
化処理を行う。Thus, after applying the magnetic layer-forming component,
In the undried state, magnetic field orientation treatment is performed if necessary, and further surface smoothing treatment is performed using, for example, super calender rolls.
【0069】次いで、所望の形状に裁断することによ
り、磁気記録媒体を得ることができる。Then, by cutting into a desired shape, a magnetic recording medium can be obtained.
【0070】本発明の磁気記録媒体は、例えば長尺状に
裁断することにより、ビデオテープ、オーディオテープ
等の磁気テープとして、あるいは円盤状に裁断すること
により、フロッピーディスク等として使用することがで
きる。さらに、通常の磁気記録媒体と同様に、カード
状、円筒状などの形態でも使用することができる。The magnetic recording medium of the present invention can be used as, for example, a magnetic tape such as a video tape or an audio tape by cutting into a long shape, or a floppy disk or the like by cutting into a disk shape. .. Further, like a normal magnetic recording medium, it can be used in a card shape, a cylindrical shape, or the like.
【0071】[0071]
【実施例】次に、本発明の実施例および比較例を示し、
本発明についてさらに具体的に説明する。なお、以下に
記載する実施例および比較例において、「部」は「重量
部」を表すものとする。EXAMPLES Next, examples and comparative examples of the present invention will be shown.
The present invention will be described more specifically. In the examples and comparative examples described below, "part" means "part by weight".
【0072】まづ実施例及び比較例において用いる磁性
粉末、カーボンブラック及び非磁性支持体の特性につい
て列記する。First, the characteristics of the magnetic powder, carbon black and non-magnetic support used in Examples and Comparative Examples will be listed.
【0073】[0073]
【表1】 [Table 1]
【0074】[0074]
【表2】 [Table 2]
【0075】[0075]
【表3】 [Table 3]
【0076】[0076]
【表4】 [Table 4]
【0077】 :最上層用磁性塗料,処方A: GA1:[Fe-Al 系強磁性金属粉末(M)* 100 部 GA2:スルホン酸カリウム変性塩化ビニル樹脂 10 部 スルホン酸ナトリウム変性ポリウレタン樹脂 5 部 アルミナ(平均粒径0.2μm) 6 部 カーボンブラック(CB)** 0.4 部 ミリスチン酸 1 部 ブチルステアレート 1 部 メチルエチルケトン 100 部 シクロヘキサノン 100 部 トルエン 100 部 :下層用磁性塗料,処方B: GB1:[Co 被着酸化鉄(MO)* 100 部 GB2:[=GA2 :下層用磁性塗料,処方B′: GB′1:[=GB1 GB′2:ニトロセルロース 5 部 スルホン酸ナトリウム変性ポリウレタン樹脂 5 部 カーボンブラック(CB1)* 10 部 メチルエチルケトン 100 部 トルエン 100 部 * 試料により種類変更(表5〜8 参照) ** 試料により種類及び量変更(表5〜8 参照) 前記の上層用、下層用磁性塗料は各処方組成物をニーダ
及びサンドミルで混練、分散して塗料に仕上げた。: Magnetic coating for top layer, formulation A: GA1: [Fe-Al based ferromagnetic metal powder (M) * 100 parts GA2: Potassium sulfonate modified vinyl chloride resin 10 parts Sodium sulfonate modified polyurethane resin 5 parts Alumina (Average particle size 0.2 μm) 6 parts Carbon black (CB) ** 0.4 parts Myristic acid 1 part Butyl stearate 1 part Methyl ethyl ketone 100 parts Cyclohexanone 100 parts Toluene 100 parts: Magnetic coating for lower layer, formulation B: GB1: [Co coating Iron oxide (MO) * 100 parts GB2: [= GA2: magnetic coating for lower layer, formulation B ': GB'1: [= GB1 GB'2: nitrocellulose 5 parts sodium sulfonate-modified polyurethane resin 5 parts carbon black ( CB1) * 10 parts Methyl ethyl ketone 100 parts Toluene 100 parts * Change depending on the sample (see Tables 5-8) ** For samples Ri type and amount changes (see Table 5-8) wherein the upper-layer, the lower layer magnetic paint was finished each formulation composition kneaded by kneader and a sand mill, the dispersion to the paint.
【0078】次に得られた塗料に夫々ポリイソシアネー
ト(コロネートL;日本ポリウレタン社製)5部を加
え、ウェット・オン・ウェット方式により表4に掲げる
表面うねり及び表面粗さを有する厚み10μmの非磁性支
持体ポリエチレンテレフタレートに塗布した後、塗膜が
未乾燥のうちに磁場配向処理を行い、続いて乾燥後カレ
ンダで表面平滑化処理を施し磁性層を形成した。カレン
ダ条件は温度80℃,圧力300Kg/cm2であり、上層膜厚が
0.5μm、下層膜厚は2.5μmであった。Next, 5 parts of polyisocyanate (Coronate L; manufactured by Nippon Polyurethane Industry Co., Ltd.) was added to each of the obtained coating materials, and the surface waviness and the surface roughness listed in Table 4 having a thickness of 10 μm was obtained by a wet-on-wet method. After being coated on the magnetic support polyethylene terephthalate, a magnetic field orientation treatment was performed while the coating film was not dried, and subsequently, after drying, a surface smoothing treatment was performed with a calendar to form a magnetic layer. The calender conditions are a temperature of 80 ° C and a pressure of 300 kg / cm 2 , and the upper layer thickness is
The thickness was 0.5 μm and the thickness of the lower layer was 2.5 μm.
【0079】更にバックコート層(BC層)を設ける場
合には、下記処方のバックコート層用塗料を前記非磁性
支持体の背面に乾燥後の膜厚0.5μmに設ける。When a back coat layer (BC layer) is further provided, a back coat layer coating composition having the following formulation is provided on the back surface of the non-magnetic support so as to have a film thickness of 0.5 μm after drying.
【0080】 :バックコート層用塗料: カーボンブラック(平均粒径26mμ) 40 部 硫酸バリウム(平均粒径300mμ) 10 部 ニトロセルロース 25 部 ポリウレタン(N−2301;日本ポリウレタン社製) 25 部 ポリイソシアネート(コロネートL;日本ポリウレタン社製) 25 部 シクロヘキサノン 400 部 メチルエチルケトン 250 部 トルエン 250 部 以上のようにして得られたウェブを裁断して8mmのビデ
オテープを作成した。これらビデオテープ試料の構成及
び性能評価の結果を表5〜8に示した。: Coating for back coat layer: Carbon black (average particle size 26 mμ) 40 parts Barium sulfate (average particle size 300 mμ) 10 parts Nitrocellulose 25 parts Polyurethane (N-2301; Nippon Polyurethane Co.) 25 parts Polyisocyanate ( Coronate L; manufactured by Nippon Polyurethane Co., Ltd.) 25 parts cyclohexanone 400 parts methyl ethyl ketone 250 parts toluene 250 parts The web thus obtained was cut into 8 mm video tapes. The configurations and performance evaluation results of these video tape samples are shown in Tables 5-8.
【0081】[0081]
【表5】 [Table 5]
【0082】[0082]
【表6】 [Table 6]
【0083】[0083]
【表7】 [Table 7]
【0084】[0084]
【表8】 [Table 8]
【0085】尚、磁性層3層を有する実施例24におい
て、上、中及び下層の膜厚は0.3,0.3μm及び2.0μmで
あり、また単層磁性層の比較例21の膜厚は3.0μmであ
る。In Example 24 having three magnetic layers, the thicknesses of the upper, middle and lower layers were 0.3, 0.3 μm and 2.0 μm, and the thickness of Comparative Example 21 of the single magnetic layer was 3.0 μm. Is.
【0086】上記性能評価の方法を以下に示す。The method of evaluating the above performance is shown below.
【0087】(a)RF出力及びクロマ出力;シバソク
製ノイズメータ925Cを用い、8mmビデオムービ−V900
(ソニー社製)を用いて測定した。(A) RF output and chroma output; 8 mm video movie-V900 using a Shiba Soku noise meter 925C
(Manufactured by Sony Corporation).
【0088】(b)ルミS/N;試料テープ上にホワイ
ト100%の信号を基準レベルで入力し、再生ビデオ信号
を921D/1〔(株)シバソク製ノイズメータ〕に入力
し、得られるノイズ絶対値よりルミS/Nを読み取っ
た。(B) Lumi S / N: A white 100% signal was input on the sample tape at the reference level, and the reproduced video signal was input to 921D / 1 (a noise meter manufactured by Shibasoku Co., Ltd.) to obtain noise. Lumi S / N was read from the absolute value.
【0089】(c)クロマS/N;シバソク社製ノイズ
メータを使用し、基準テープとの比較においてクロマ信
号における試料テープのS/Nの差を求めた。(C) Chroma S / N: Using a noise meter manufactured by Shibasoku Co., Ltd., the difference between the S / N of the sample tape in the chroma signal was determined in comparison with the reference tape.
【0090】(d)走行後のジッタ値;40℃、RH80%の
環境下でテープを100時間全長走行させ、走行後のジッ
タ値をメグロエレクトロニクス社製のVTRジッタメー
タ「MK−6124」を使用して測定した。(測定単位:μ
s) (e)耐蝕性(目詰まり;耐候性);NO2(5ppm)環境
下にテープを30日放置後、画質評価を行うと共に、磁気
ヘッドの目詰まりの有無をチェックした(有:×,無:
○)。(D) Jitter value after running; the tape was run for 100 hours in an environment of 40 ° C. and RH80%, and the jitter value after running was measured using a VTR jitter meter “MK-6124” manufactured by Megroelectronics. Was measured. (Unit of measurement: μ
s) (e) Corrosion resistance (clogging; weather resistance); After leaving the tape in an NO 2 (5 ppm) environment for 30 days, the image quality is evaluated and the clogging of the magnetic head is checked (yes: × ,Nothing:
○).
【0091】(f)低湿下(40℃、20%RH)での出力低
下(△RF);40℃、RH20% の環境下でテープを全長
走行2パスさせ、RF出力低下を測定した。測定にはE
V−S1(ソニー社製)を用いた。(F) Output decrease (ΔRF) under low humidity (40 ° C., 20% RH); The tape was allowed to run for 2 full lengths in an environment of 40 ° C., RH 20%, and the RF output decrease was measured. E for measurement
V-S1 (manufactured by Sony Corporation) was used.
【0092】表5〜8を一瞥するだけで判るように本発
明の実施例と比較例とでは判然たる差がある本発明の効
果が明らかである。As can be seen by simply looking at Tables 5 to 8, the effects of the present invention are clearly different between the examples of the present invention and the comparative examples.
【0093】[0093]
【発明の効果】スペーシング摩擦係数が小さく、低湿下
のRF出力低下、高温高湿下のジッタ発生を防止した磁
気記録媒体の提供が可能となった。According to the present invention, it is possible to provide a magnetic recording medium having a small spacing friction coefficient, preventing RF output reduction under low humidity and preventing jitter generation under high temperature and high humidity.
Claims (7)
磁気記録媒体において、前記磁性層の表面うねりAsが
0.022μm以下で、かつその最上層に平均長軸長0.25μm
未満、X線測定による結晶子サイズ200Å未満の強磁性
金属粉末を含有しており、また前記非磁性支持体の磁性
層形成面の表面うねりBsが0.020μm以下、該形成面に
存在する0.01μm以上の突起の数nが測定長1mm当り200
個以上、0.3μm以上の突起の数Nが測定長400mm当り500
個以下であり、平均突起高さHmが0.01〜0.25μm、更に
最大突起高さHmaxと前記平均突起高さHmとの比Hmax/Hm
が10以下であることを特徴とする磁気記録媒体。1. In a magnetic recording medium having a plurality of magnetic layers provided on a non-magnetic support, the surface waviness As of the magnetic layer is
0.022 μm or less and the average major axis length of 0.25 μm on the top layer
Less than 200 .mu.m, the surface undulation Bs of the magnetic layer forming surface of the non-magnetic support is 0.020 .mu.m or less, and 0.01 .mu.m existing on the forming surface. The number n of protrusions above is 200 per 1 mm of measuring length
Number of protrusions N or more, 0.3 μm or more, N is 500 per 400 mm measuring length
The average protrusion height Hm is 0.01 to 0.25 μm, and the ratio of the maximum protrusion height Hmax to the average protrusion height Hm is Hmax / Hm.
The magnetic recording medium is characterized in that
側の背面において、該背面に存在する0.01μm以上の突
起の数n′が測定長1mm当り200個以上、0.3μm以上の
突起の数N′が測定長400mm当り500個以下であり、平均
突起高さH′mが0.01〜0.25μm、更に最大突起高さH′ma
xと前記平均突起高さH′mとの比H′max/H′mが10以下
であることを特徴とする請求項1記載の磁気記録媒体。2. The number of protrusions n ′ of 0.01 μm or more existing on the back surface of the non-magnetic support opposite to the magnetic layer forming surface is 200 or more and 0.3 μm or more per measurement length 1 mm. N'is less than 500 per 400 mm of measuring length, average protrusion height H'm is 0.01 to 0.25 μm, and maximum protrusion height H'ma
The magnetic recording medium according to claim 1, wherein a ratio H'max / H'm of x to the average protrusion height H'm is 10 or less.
ミニウム(Al)を含み、FeとAlの原子重量比(Fe:Al)
=(100:0.5)〜(100:20)である請求項1又は2記
載の磁気記録媒体。3. The ferromagnetic metal powder contains iron (Fe) and aluminum (Al), and the atomic weight ratio of Fe and Al (Fe: Al).
3. The magnetic recording medium according to claim 1, wherein: (100: 0.5) to (100: 20).
金属粉末が含まれていることを特徴とする請求項1乃至
3のいづれかに記載の磁気記録媒体。4. The magnetic recording medium according to claim 1, wherein the uppermost magnetic layer contains a ferromagnetic metal powder having an axial ratio of less than 10.
ラックの重量が磁性粉100重量部に対して1重量部未満
である請求項1乃至4のいづれかに記載の磁気記録媒
体。5. The magnetic recording medium according to claim 1, wherein the weight of carbon black contained in the uppermost magnetic layer is less than 1 part by weight with respect to 100 parts by weight of magnetic powder.
軸長0.25μm未満、X線測定による結晶子サイズ450Å未
満強磁性粉末が含まれていることを特徴とする請求項1
乃至5のいづれかに記載の磁気記録媒体。6. A ferromagnetic powder having an average major axis length of less than 0.25 μm and a crystallite size of less than 450Å by X-ray measurement is contained in at least one layer other than the uppermost layer.
6. The magnetic recording medium according to any one of 1 to 5.
とFe3+との原子数比Fe2+/Fe3+が0.08以上であるCo含有
酸化鉄を含むことを特徴とする請求項1乃至6のいづれ
かに記載の磁気記録媒体。7. Fe 2+ in at least one layer other than the top layer
The magnetic recording medium according to either of claims 1 to 6, characterized in that it comprises a Co-containing iron oxide atomic ratio Fe 2+ / Fe 3+ and Fe 3+ is 0.08 or more and.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29744891A JPH05135352A (en) | 1991-11-13 | 1991-11-13 | Magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29744891A JPH05135352A (en) | 1991-11-13 | 1991-11-13 | Magnetic recording medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH05135352A true JPH05135352A (en) | 1993-06-01 |
Family
ID=17846646
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP29744891A Pending JPH05135352A (en) | 1991-11-13 | 1991-11-13 | Magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH05135352A (en) |
-
1991
- 1991-11-13 JP JP29744891A patent/JPH05135352A/en active Pending
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