JP2001006149A - Magnetic recording medium - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an application type keeper medium, and to provide a magnetic recording medium whose electromagnetic conversion characteristics, especially, recording characteristics at the time of magnetic recording using short recording wavelength are made excellent, and whose reproduction output can be made high, and whose productivity and keeping quality can be made excellent. SOLUTION: In a magnetic recording medium in which magnetic layers in not less than two layers are formed on a non-magnetic flexible supporting body, the magnetic layers in not less than two layers are constituted of a hard magnetic layer in which ferromagnetic powder and bonding agent are contained, and Hc is 8000e or more, and any non-magnetic powder is not substantially contained and a soft magnetic layer in which soft magnetic powder whose magnetic permeability is high and the bonding agent are contained, and the hard magnetic layer is arranged so as to be made closer to the supporting body than the soft magnetic layer.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

[0001] The present invention relates to a magnetic recording medium having at least two or more magnetic layers. The magnetic recording medium of the present invention relates to a magnetic recording medium suitable for high-density recording.

[0002]

2. Description of the Related Art
Magnetic recording media such as video tapes, audio tapes, and magnetic disks include a magnetic layer in which ferromagnetic iron oxide, Co-modified ferromagnetic iron oxide, CrO ₂ , ferromagnetic alloy powder, and the like are dispersed in a binder. Is widely used. In recent years, higher recording densities and higher recording densities have been promoted. As a result, the recording wavelength has become shorter, and the track width has also become narrower. However, in magnetic recording using a short recording wavelength, when the thickness of the magnetic layer is large, the self-demagnetization loss at the time of recording and the thickness loss at the time of reproduction are serious problems. For this reason, the thickness of the magnetic layer has been reduced so as to be compatible with a short recording wavelength. However, the conventional coating type magnetic recording medium is required to have a higher reproduction output from the viewpoint of compensating for the output loss due to the narrow track.

As a thin magnetic layer, a so-called thin-film medium mainly made of a metal thin film formed by a sputtering method or a vapor deposition method for a hard disk or the like has been put to practical use. Further, in order to make these thin film media correspond to high recording density, it has been proposed from the early 1990s to form a high magnetic permeability layer such as permalloy on a high Hc thin film,
Also known as "keeper media". Such a thin film keeper medium has excellent electromagnetic conversion characteristics, particularly high reproduction output. However, since it is necessary to form a multilayer film in a vacuum, it has been studied only for a hard disk made of a metal thin film, and has not been studied or applied to a coating type magnetic recording medium. Further, the thin-film keeper medium requires a DLC film and an overcoat of a lubricant in order to ensure durability, and therefore has lower productivity than a coating-type medium. Furthermore, since it is a metal thin film, it is easily rusted, and there is a problem in usability such as use in a closed system.

Accordingly, an object of the present invention is to provide a coating type keeper medium. That is, an object of the present invention is to provide a magnetic recording medium that has excellent electromagnetic conversion characteristics, particularly, excellent recording characteristics in magnetic recording using a short recording wavelength, has high reproduction output, and is excellent in productivity and storage stability. It is in.

[0005]

According to the present invention, there is provided a magnetic recording medium having two or more magnetic layers provided on a non-magnetic flexible support, wherein the two or more magnetic layers comprise a ferromagnetic powder and a binder. , Wherein Hc is 800 Oe or more, and includes a hard magnetic layer containing substantially no non-magnetic particles and a soft magnetic layer containing a soft magnetic powder having a high magnetic permeability and a binder. The present invention relates to a magnetic recording medium, which is arranged at a position closer to the support than the soft magnetic layer. In the magnetic recording medium of the present invention, the `` hard magnetic layer containing substantially no non-magnetic particles '' means that non-magnetic particles are not contained in a coating solution for preparing a hard magnetic layer,
The hard magnetic layer generated when a part of the non-magnetic particles contained in the soft magnetic layer located on the upper layer of the hard magnetic layer penetrates into the lower hard magnetic layer (e.g., pressed by a calendaring process) includes Hard magnetic layer containing substantially no non-magnetic particles. "

The magnetic recording medium of the present invention is provided with an underlayer containing a non-magnetic powder and a binder between the support and the magnetic layer closest to the support among the two or more magnetic layers. That the thickness of the hard magnetic layer is 0.01
And the thickness of the soft magnetic layer is 0.01 to 1 μm.
It is preferable that In the magnetic recording medium of the present invention, the hard magnetic layer is a layer for holding the recorded magnetization, and the soft magnetic layer plays a role of guiding the magnetic flux from the magnetization holding layer to the reproducing head. Therefore, the hard magnetic layer, which is the magnetization preserving layer, is preferably thin from the viewpoint of improving resolution and reducing self-demagnetization loss, and the thickness of the hard magnetic layer is preferably in the range of 0.01 to 1 μm. Further, if the soft magnetic layer is too thick, the bias current at the time of reproduction becomes excessively large, which may cause overwriting. Therefore, the thickness of the soft magnetic layer is 0.01 to 1
It is preferably in the range of μm. As described above, since it is preferable to make both the hard magnetic layer and the soft magnetic layer thin, it is necessary to make the magnetic layer thin as a whole. Therefore, when a keeper medium is prepared by a coating method, it is preferable to provide an underlayer mainly composed of a nonmagnetic powder and a binder from the viewpoint of improving productivity. It is preferable to provide a soft magnetic layer, which is a keeper layer, on the uppermost layer of the magnetic recording medium from the viewpoint of improving the reproduction output.

Further, the soft magnetic layer in the magnetic recording medium of the present invention contains nonmagnetic particles having an average particle size of 0.3 μm or less and a Mohs hardness of 5 or more, thereby improving the durability of the magnetic recording medium. It is preferable from the viewpoint of performing the above. Further, the soft magnetic layer in the magnetic recording medium of the present invention preferably contains a carbon black having an average particle size in the range of 10 μm to 200 μm from the viewpoint of improving running durability and preventing static charge. The soft magnetic layer in the magnetic recording medium of the present invention may contain the above-mentioned non-magnetic particles and carbon black. The soft magnetic layer in the magnetic recording medium of the present invention has a relative magnetic permeability of 20 or more and an Hc of 150.
It is preferably Oe or less. When the relative magnetic permeability is 20 or more, the effect of the keeper layer is easily exerted. Further, by setting the Hc of the soft magnetic layer to 150 Oe or less, there is an advantage that the bias current at the time of reproduction is prevented from becoming excessive, and overwriting is less likely to occur. The hard magnetic layer contains substantially no non-magnetic particles. That is, the hard magnetic layer does not include a non-magnetic powder such as an abrasive and a carbon black which are preferably contained in the soft magnetic layer. Since the hard magnetic layer substantially does not contain nonmagnetic particles, the degree of filling of the magnetization holding layer can be improved, and noise can be reduced by reducing disturbance of magnetization.

In the magnetic recording medium of the present invention, a thickness of 0.005 to 0.1 μm is provided between the hard magnetic layer and the soft magnetic layer.
It is preferable to further provide a non-magnetic layer. In the case of a multilayered medium having a plurality of magnetic layers in which magnetic particles are dispersed in a binder, the magnetic coupling between the layers is smaller than that of a multilayered thin film. However, in order to more reliably break this magnetic coupling,
It is preferable to provide a thin nonmagnetic layer as described above between the hard magnetic layer and the soft magnetic layer.

Hereinafter, the operation mechanism of the magnetic recording medium of the present invention will be described. As described above, in the thin film medium, the keeper medium is already known. Its action mechanism is described in, for example, IEEE TRANS.MAG. Vol27, No6, p4549 (199
1), J. Appl. Phys. 75 (10), 15, p6150 (1994), IEICE Technical Report M
It is reported in R98-56 (1999). That is, in the keeper medium, the soft magnetic layer adjacent to the hard magnetic layer is provided to reduce the demagnetizing field of recording magnetization, and furthermore, a DC bias magnetic field is applied to the soft magnetic layer during reproduction to reduce the virtual gap. The output is increased by forming and reducing substantial steam loss.

[0010] As described above, a keeper medium has been hitherto known only as a thin film medium. As a coating type medium, a keeper medium is not known. This is because, when a magnetic layer having a thickness of less than 1 μm, such as a thin film, is directly applied to a support, coating defects are likely to occur due to support projections or dust in the air.
This was because it was considered that production was not easy. However, although production is not always easy, it has been found that a keeper medium can provide a predetermined effect even with a coating type medium like the magnetic recording medium of the present invention. Furthermore, as described as one embodiment of the magnetic recording medium of the present invention, by providing an underlayer mainly composed of a non-magnetic powder and a binder between the support and the magnetic layer, a thin film can be formed even on a coating type medium. A similar layer configuration can be easily obtained. Furthermore, in a coating type medium, the leveling and calendering effect of the coating film are reduced, the surface roughness is increased, and the durability is easily deteriorated due to a decrease in the amount of lubricant added.
However, by providing the above-described underlayer and making the thickness of the coating layer composed of the underlayer and the magnetic layer substantially thick, these adverse effects can be easily avoided.

[0011]

DESCRIPTION OF THE PREFERRED EMBODIMENTS Each layer will be described in detail below. [Soft Magnetic Layer] A magnetic layer that can be used as a soft magnetic layer in a magnetic recording medium is a layer in which fine particles having high magnetic permeability are dispersed in a binder and applied. The relative magnetic permeability of the soft magnetic layer is suitably 20 or more, and preferably 50 or more, from the viewpoint of stabilizing the recording magnetization. From the viewpoint that overwriting is unlikely to occur, it is appropriate that Hc is 150 Oe or less, preferably 100 Oe or less, more preferably 50 Oe or less. The thickness of the soft magnetic layer is 0.001 to 1
Suitably, it is in the range of μm, preferably in the range of 0.003 to 0.5 μm, more preferably in the range of 0.005 to 0.2 μm. If the thickness is too small, the effect of the keeper layer is hardly exhibited, and if the thickness is too large, overwriting may be caused.

The fine particles having high magnetic permeability used for the soft magnetic layer include pure iron, Ni-Fe alloy, Fe-Al alloy, Si-A
alloys such as l-Fe alloy, ferrimagnetic oxide mainly composed of Fe ₂ O _3, for example, Ni-Zn ferrite, Mn-Zn ferrite, and a Cu-Zn ferrite. For details, see "Magnetic Hunt Hook" Asakura Shoten (19
80.8.20), which can be referred to. Among the fine particles having a high magnetic permeability, Vamaalloy (Ni35-80-Fe65-20), which has high magnetic permeability, and center paste (Si9.
6-Al5.4-Fe) and Mn-Zn ferrite are preferred. The average primary particle size of the fine particles having high magnetic permeability is 1 μm or less, preferably 0.5 μm.
m or less, more preferably 0.2 μm. The shape of the fine particles may be any shape as long as the shape magnetic anisotropy does not occur. In addition, the surface treatment can be performed with an organic or inorganic substance as long as the magnetic properties are not impaired. For example, to improve the hardness of particles, Al ₂ O ₃
And to and coating the surface with SiO _2, in order to improve the dispersibility in binder, silane Kaffu ° link Bu agents, titanate Kaffu ° link Bu agents, organic acid compounds, such as surface treatment with lecithin known dispersants Conventionally, effective means can be applied with hard magnetic powder.

When the soft magnetic layer is disposed as the uppermost layer, that is, a layer which is in direct contact with the magnetic head, it is preferable to use a means for improving durability in combination. For example, durability can be improved by adding a known abrasive and / or carbon black to the soft magnetic layer. As the abrasive, fine powder having a Mohs hardness of 5 or more is preferable. For example, α-Al ₂ O ₃ , α-Fe ₂ O ₃ , ZrO ₂ , Cr ₂ O ₃ , TiO ₂ , TiC, SiO ₂ , Si
C, carbon horn night light, diamond, CeO ₂ , Si ₃ N _{4 and the} like can be used. The shape of the abrasive particles can be granular, needle-like or dice-like, and the average of the maximum diameter of the primary particles (for example, the diameter of the primary particle, the long axis length of the needle-like) is 0.3 μm or less,
Preferably 0.25 μm or less, more preferably 0.2
Suitably, it is less than μm. By using an abrasive having a relatively small particle size, it is possible to prevent the abrasive particles in the upper soft magnetic layer from entering the lower hard magnetic layer by the calendaring treatment, and to suppress the increase in noise. The carbon black has an average particle size of 10 μm to 200 μm, preferably 40 μm to 150 μm.
It is preferably in the range of mμ. The carbon black is also preferably relatively small, like the abrasive particles. However, in the case of carbon black, if it is too small, dispersion tends to be poor. A known lubricant can be added to the soft magnetic layer. As these, perfluoropolyether, higher fatty acids, fatty acid esters, fatty acid amides, liquid paraffin and the like can be used according to the purpose.

As the binder used for the soft magnetic layer, a known binder can be used as it is. Examples thereof include a strong polyvinyl chloride polymer, a polyurethane resin, a nitrocellulose, a phenoxy resin, an epoxy resin, a vinyl acetal, and a polyvinyl chloride polyvinylidene. In order to enhance the dispersibility of the fine-particle soft magnetic powder, the binder preferably contains, in the molecule, a functional group which promotes resin adsorption on the surface of the powder. -SO ₃ M as the functional _{group, -OSO 3 M, -COOM, -P} = O (O
_{M) 2, -O-P =} O (OM) 2, (M is a hydrogen atom or alkali metal _{^{atom), - NR + R 3 (}} R is an alkyl group), epoxy group, SH, at least one selected from such CN Types can be mentioned. The amount of such functional groups is between 10 ^{-1 and} 1
Suitably, it is 0 ^-8 equivalents / g, preferably 10 ^-2 to 10 ^-6 equivalents / g. The amount of the binder contained in the soft magnetic layer is appropriately in the range of 1 to 100% by weight, preferably in the range of 5 to 70% by weight based on the soft magnetic powder. Further, the soft magnetic layer may contain a solid lubricant.

[Hard Magnetic Layer] The hard magnetic layer of the magnetic recording medium of the present invention has an Hc of 800 Oe or more. Hc of the preferred hard magnetic layer is 1000 Oe or more, more preferably 1500 Oe or more. If Hc is too low, the data will be erased by the bias magnetic field during reproduction. It is common knowledge of those skilled in the art that Hc is generally preferably as high as possible, but is generally optimized according to Bs of the head to be used.

The orientation of the magnetic particles includes longitudinal orientation, vertical orientation, oblique orientation, and the like, and the effects of the present invention are exhibited in any orientation. In a disk-shaped magnetic recording medium, it is desirable that the axis of easy magnetization of the magnetic particles be randomly distributed in the plane (generally called random orientation). The Bm of the hard magnetic layer is 500 G or more, preferably 1000 G or more, more preferably 150 G or more, measured in the easy axis direction.
Suitably, it is 0 G or more. However, when an MR head is used as the reproducing head, Bm is reduced, for example, to 150
It is preferable to be in the range of 0 to 3000G.

The thickness of the hard magnetic layer is 0.01 to 1 μm, preferably 0.02 to 0.5 μm, and more preferably 0.1 to 0.5 μm.
It is appropriate that the thickness is 03 to 0.3 μm. Based on the principle of magnetic recording, the thinner the magnetic layer, the better. But,
In practice, it is appropriate that the thickness of the magnetic layer is optimized according to the recording signal and the head used. The ferromagnetic powder used for the hard magnetic layer has an Hc equivalent to the Hc of the magnetic layer, and has a s50 emu / g to 170 emu / g, a particle shape of a needle,
It is appropriate to use a spindle, flat needle, plate, or die. If the particle size is needle-shaped, the major axis length is 0.03 to 0.3
μm, preferably 0.05 to 0.2 μm, and a needle ratio of 3 to 2
Suitably, it is zero. In the case of a plate, the plate diameter is 0.03 to 0.
It is suitably 3 μm, preferably 0.05 to 0.2 μm, and the plate ratio (plate diameter / plate thickness) is 3 to 20. Examples of these magnetic powders include Co-modified gamma iron oxide, CrO ₂ , Fe
Powder or a hexagonal ferrite. Particularly preferred are an alloy powder containing Fe as a main component and hexagonal ferrite such as Ba ferrite. These ferromagnetic powders may also contain alloy components such as Co, Ni, Cr, Mn, and Sm for adjusting magnetic properties. In particular, Co is suitable for obtaining an alloy having high s as fine particles. Co is 2 to Fe
The content can be 40 at%, preferably 5 to 35 at%. Also, Al, Si, B, rare group 2 elements (Ca, Mg, Zn), and other group 3 elements (Sc) such that the content of Fe is within the above range for the purpose of preventing sintering and controlling the shape. , Y, La, Nd, etc.)
Can be solid-solved or adhered to the surface. In the case of an alloy powder, σs is suitably from 100 to 170 emu / g, preferably from 110 to 160 emu / g. The crystallite size is suitably less than 250 angstroms, preferably less than 200 angstroms. The magnetic powder can be surface-treated with an organic or inorganic substance as long as the magnetic properties are not impaired. For example, to coat the surface with Al ₂ O ₃ or SiO ₂ to improve the hardness of the magnetic powder, or to improve dispersibility in a binder, a silane-based coupling agent, a titanate-based coupling agent, an organic Conventionally effective means for hard magnetic powders such as surface treatment with a known dispersant such as an acid compound and lecithin can be applied.

The hard magnetic layer of the magnetic recording medium of the present invention contains substantially no non-magnetic particles. Substantially not included
As described above, this means that the non-magnetic particles are not contained in the coating solution for preparing the hard magnetic layer, and one of the non-magnetic particles contained in the soft magnetic layer located above the hard magnetic layer. The hard magnetic layer that is generated when the part invades the lower hard magnetic layer (for example, is pressed by the calendaring process)
It is meant to be included in the “hard magnetic layer substantially containing no nonmagnetic particles”.

A known lubricant is added to the hard magnetic layer.
Can also be contained. Perfect as a lubricant
Oropolyethers, higher fatty acids, fatty acid esters, fats
Fatty acid amides, such as liquid paraffin
Compounds can be used. Used for hard magnetic layer
As the binder, use a known binder as it is
Can be. For example, phenol chloride-based strong polymer, polyurethane resin
Fat, nitrocellulose, phenoxy resin, epoxy resin, vinyl acetal, poly
Chlorinated chloride and the like. Ferromagnetic powder for binder
In order to improve the dispersibility of the powder, resin adsorption on the powder surface
It is preferred that the molecule contain a promoting functional group. these
The functional group of -SO_ThreeM, -OSO_ThreeM, -COO
M, -P = O (OM)_Two, -OP = O (OM)_Two, (M
Is a hydrogen atom or an alkali metal atom), -NR + R_Three(R is a
Alkyl), ethoxy, SH, CN, etc.
And one type. Such functional groups
Quantity is 10 ^-1-10^-8Equivalent / g, preferably 10^-2-10
^-6Suitably, it is equivalent / g. Hard magnetic layer bonding
The amount of the agent is in the range of 1 to 100% by weight based on the ferromagnetic powder.
Surrounding, preferably 5-70, more preferably 8-30
It is appropriate that the amount is in the range of%.

[Underlayer] The underlayer used in the magnetic recording medium of the present invention contains a nonmagnetic powder and a binder. The nonmagnetic powder can be selected from, for example, inorganic compounds such as metal oxides, metal carbonates, metal sulfates, metal nitrides, metal carbides, and metal sulfides. Examples of the inorganic compound include α-alumina, β-alumina, γ-alumina, silicon carbide, chromium oxide, cerium oxide, α-iron oxide, corundum, silicon nitride, titanium carbide, titanium carbide having an α conversion of 90% or more. Titanium, silicon dioxide, magnesium oxide, magnesium oxide, magnesium oxide, silicon oxide, boron nitride, zinc oxide, calcium carbonate, calcium sulfate, barium sulfate, molybdenum sulfide and the like are used alone or in combination. Particularly preferred are titanium dioxide, zinc oxide, iron oxide and barium sulfate, and more preferred are titanium dioxide and α-iron oxide. The particle size of these nonmagnetic powders is preferably in the range of 0.005 to 2 μm.
Further, if necessary, non-magnetic powders having different particle sizes may be combined, or even a single non-magnetic powder may have the same effect by broadening the particle size distribution. Particularly preferred particle sizes range from 0.01 μm to 0.2 μm. The tap density is suitably from 0.05 to 2 g / ml, preferably from 0.2 to 1.5 g / ml. The water content is 0.1 to 5% by weight, preferably 0.2 to 3% by weight.
It is appropriate that The pH is suitably between 2 and 11, but is particularly preferably between 6 and 9.
The specific surface area is 1 to 100 m ² / g, preferably 5 to 50 m ² /
g, more preferably 7 to 40 m ² / g. The crystallite size is preferably in the range of 0.01 μm to 2 μm. Oil absorption using DBP (dibutyl phthalate)
Suitably, it is 5 to 100 ml / 100 g, preferably 10 to 80 ml / 100 g, and more preferably 20 to 60 ml / 100 g. The specific gravity is suitably from 1 to 12, preferably from 3 to 6. The shape may be any of a needle shape (including a spindle shape), a spherical shape, a polyhedral shape, and a plate shape. The ignition loss is preferably 20% by weight or less.

The inorganic powder used as the non-magnetic powder contained in the underlayer of the magnetic recording medium of the present invention preferably has a Mohs hardness of 4 or more. The roughness factor of the surface of these powders is preferably 0.8 to 1.5, and more preferably 0.9 to 1.2.
It is suitable that the stearic acid (SA) adsorption amount is 1 to 20 μmol / m ² , more preferably ² to 15 μmol / m ² . The heat of wetting of the nonmagnetic powder for the underlayer in water at 25 ° C.
It is preferably in the range of 200 erg / cm ^{2 to} 600 erg / cm ² . Further, when forming the underlayer, a solvent having a range of the heat of wetting can be used. The amount of water molecules on the surface of the nonmagnetic powder for the underlayer at 100 to 400 ° C is 1 to 10
Suitably, it is 100 / angstrom. The pH of the isoelectric point in water is preferably between 3 and 6. Al ₂ O ₃ , SiO ₂ , TiO ₂ , Zr
It is preferable to perform a surface treatment with O ₂ , SnO ₂ , Sb ₂ O ₃ , and ZnO.
Particularly preferred for dispersibility are Al ₂ O ₃ , SiO ₂ , TiO ₂ , ZrO ₂ ,
However, more preferred are Al ₂ O ₃ , SiO ₂ and ZrO ₂ . These may be used in combination or may be used alone. Further, a surface treatment layer coprecipitated may be used according to the purpose, or a structure in which the surface layer is treated with alumina and then the surface layer is treated with silica, or the reverse structure may be adopted. Although the surface treatment layer may be a porous layer depending on the purpose, it is generally preferable that the surface treatment layer be homogeneous and dense.

For the preparation of other pigments, see "Characte
Rization of Powder Surfaces "Academic Press can be referred to. Also, carbon black can be mixed in the underlayer to reduce Rs, which is a known effect. Thermal for rubber,
Color black, acetylene black, and the like can be used. The specific surface area of carbon black is 100 to 5
00 m ² / g, preferably 150 to 400 m ² / g,
The DBP oil absorption is suitably from 20 to 400 ml / 100 g, preferably from 30 to 200 ml / 100 g. The particle size is suitably from 5 m to 80 m, preferably from 10 to 50 m, and more preferably from 10 to 40 m.
It is preferable that the pH is 2 to 10, the water content is 0.1 to 10%, and the tap density is 0.1 to 1 g / ml. Specific examples of carbon black used in the present invention include BLACK PEARLS manufactured by Cabot Corporation.
2000, 1300, 1000, 900, 800, 8
80,700, VULCANXC-72, manufactured by Mitsubishi Kasei Kogyo Co., Ltd., # 3050B, 3150B, 3250B, # 37
50B, # 3950B, # 950, # 650B, # 97
0B, # 850B, MA-600, manufactured by Konrombia Carbon, CONDUCTEX SC, RAVEN 880
0,8000,7000,5750,5250,3500,2100,2000,1800,1500,125
5,1250, and Axpo Ketchen Perak EC. Carbon black may be used after being surface-treated with a dispersant or the like or grafted with a resin, or may be used after a part of the surface is graphitized. The carbon black may be dispersed with a binder before adding the carbon black to the paint. These carbon blacks are contained in an amount not exceeding 50% by weight based on the inorganic powder, that is, 4% of the total weight of the underlayer.
It can be used within a range not exceeding 0%. These carbon blacks can be used alone or in combination.
The carbon black usable in the present invention can be referred to, for example, "Carbon Black Handbook" edited by Carbon Black Association.

The organic powder used as the non-magnetic powder used in the underlayer of the magnetic recording medium of the present invention includes, for example, acrylic styrene resin powder, benzoquinamine resin powder, melamine resin powder, and phthalocyanine pigment. , Polyolefin-based resin powder, polyester-based resin powder, polymer-based resin powder,
Polyimid-based resin powder, polyfluoroethylene resin and the like can be mentioned. The method for producing the organic powder used as the non-magnetic powder is described in, for example, JP-A-62-18564 and JP-A-60-255827.
Can be used.

These non-magnetic powders are
It is suitable to use in the range of 20 to 0.1 in weight ratio and 10 to 0.1 in volume ratio. It is particularly preferable that the volume ratio of the binder is 2. compared to the volume of the powder contained in the lower layer.
The range is from 0 to 0.3 times.

An undercoat layer is provided on a general magnetic recording medium. This is provided to improve the adhesive strength between the support and the magnetic layer. Is different from Further, in the present invention, it is preferable to provide an undercoat layer in order to improve the adhesion between the underlayer and the support. The binder, lubricant, dispersant, additive, solvent, dispersion method and the like of the underlayer can be applied to those of the magnetic layer. In particular, with respect to the amount and type of the binder, the amount of the additive and the type of the dispersant, and the like, the known technology for the magnetic layer can be applied.

As the binder used in each layer of the present invention (especially, an underlayer, a magnetic layer other than a hard magnetic layer and a soft magnetic layer, etc.), a known thermoplastic resin, thermosetting resin, reactive type Resins and mixtures thereof can be used. As the thermoplastic resin, the glass transition temperature is −100 to 150 ° C., and the number average molecular weight is 1,000 to 200,000, preferably 10,000.
It is suitable that the polymerization degree is about 50 to 1,000. Examples of such thermoplastic resins include vinyl chloride, vinyl acetate, vinyl alcohol, maleic acid, acuric acid, acrylate, vinylidene chloride, acrylonitrile, methacrylic acid, methacrylate, styrene, butadiene, ethylene, Examples thereof include polymers or copolymers containing vinyl butyral, vinyl acetal, vinyl ether, and the like as constituent units, polyurethane resins, and various rubber resins. Examples of the thermosetting resin or the reactive resin include a phenol resin, an epoxy resin, a polyurethane curable resin, a urea resin, a melamine resin, an alkyd resin, an acrylic reaction resin, a formaldehyde resin, a silicone resin, and an epoxy resin. Examples thereof include a polyamide resin, a mixture of a polyester resin and an isocyanate prepolymer, a mixture of a polyester polyol and a polyisocyanate, and a mixture of a polyurethane and a polyisocyanate.
These resins are described in detail in "Plastic Handbook" published by Asakura Shoten. Also, a known electron beam-curable resin can be used for the non-magnetic layer and the magnetic layer. These examples and the production method thereof are described in detail, for example, in JP-A-62-256219. The above resins can be used alone or in combination, but are preferably selected from vinyl chloride resin, vinyl chloride vinyl acetate resin, vinyl chloride vinyl acetate vinyl alcohol resin, and vinyl chloride vinyl acetate maleic anhydride copolymer. Examples include a combination of at least one kind with a polyurethane resin, or a combination of these with a polyisocyanate. Examples of the structure of the polyurethane resin include known materials such as polyester polyurethane, polyether polyurethane, polyether polyester polyurethane, polycarbonate polyurethane, polyester polycarbonate polyurethane, and polycaprolactone polyurethane. For all the binders shown here, COOM, SO ₃ M, OSO ₃ M, P = O (O
_{M) 2, O-P =} O (OM) 2, M per (or a hydrogen atom or an alkali metal _{salt,), OH, NR 2,} N + R 3
(R is a hydrocarbon group) It is preferable to use one obtained by copolymerizing or adding at least one or more polar groups selected from an epoxy group, SH, CN, and the like. The amount of such a polar group is 10 ^-1 to 10 ^-8 mol / g, preferably 10 ^-2 to 10 ^-6 mol / g.

The magnetic recording medium of the present invention has at least two magnetic layers including a hard magnetic layer and a soft magnetic layer. Accordingly, the amount of the binder, the amount of the vinyl chloride resin, the polyurethane resin, the polyisocyanate or the other resin in the binder, the molecular weight of each resin forming the magnetic layer, the amount of the polar group, or the amount described above. It is of course possible to change the physical properties of the resin between the hard magnetic layer and the soft magnetic layer, and between the hard magnetic layer and the soft magnetic layer if there is an underlayer, if necessary. In that case, a known technique for the multilayer magnetic layer can be applied. For example, when the amount of the binder is changed between the hard magnetic layer and the soft magnetic layer, and further between the underlayer, the amount of the binder in the upper magnetic layer may be increased in order to reduce scratches on the surface of the magnetic layer. Valid and
In order to improve the head touch to the head, it is preferable to increase the amount of the binder in the magnetic layer other than the upper layer or in the underlayer to have flexibility.

The polyisocyanate includes tolylene diisocyanate, 4-4'-diphenylmethane diisocyanate, hexamethylene diisocyanate,
Isocyanates such as xylylene diisocyanate, naphthylene-1,5-diisocyanate, o-toluidine diisocyanate, isophorone diisocyanate and triphenylmethane triisocyanate; Products of these isocyanates and polyalcohols, and polyisocyanates formed by condensation of isocyanates can be used. Commercially available trade names of these isocyanates include those manufactured by Nippon Polyurethane Co., Ltd., Coronate L, Coronate HL, Coronate 2
030, Coronate 2031, Millionate MR, Millionate MTL, Takedate Pharmaceutical Co., Ltd., Takenate D-10
2, Takenet D-110N, Takenet D-200,
Takenum D-202, manufactured by Sumitomo Bayer Ltd., Desmodule L, Desmodur IL, Desmodur N, Desmodur HL, and the like. These alone or in combination of two or more utilizing the difference in curing reactivity,
It can be used for both the underlayer and the magnetic layer.

Examples of the carbon black used in each layer (especially magnetic layers other than the hard magnetic layer) of the present invention include, for example, furnace for rubber, thermal for rubber, black for color, acetylene black. And the like.
Carbon black has a specific surface area of 5 to 500 m ² / g, a DBP oil absorption of 10 to 400 ml / 100 g, a particle size of 5 to 300 mμ, and a pH of 2 to 1.
0, the water content is 0.1 to 10% by weight, and the tap density is preferably 0.1 to 1 g / ml. Surface treatment of carbon black with a dispersant,
It may be used by grafting with a resin, or by partially graphitizing the surface. Also, the car
Before adding the bon black to the magnetic paint, it may be dispersed in a binder in advance. These carbon blacks can be used alone or in combination. When carbon black is used, it is preferably used in an amount of 0.1 to 30% by weight based on the amount of the ferromagnetic powder or the soft magnetic powder. Carbon black has functions such as preventing the magnetic layer from being charged, reducing the coefficient of friction, imparting light-shielding properties, and improving film strength. These properties vary depending on the carbon black used. Therefore, these carbon blacks used in the present invention may be used in a magnetic layer other than the hard magnetic layer and in the underlayer, by changing the type, amount, and combination thereof, before the particle size, oil absorption, conductivity, pH, etc. It is, of course, possible to use them properly according to the purpose based on the various characteristics shown. The carbon black that can be used in the magnetic layer other than the hard magnetic layer can be referred to, for example, "Carbon Black Handbook" edited by Carbon Black Association.

Examples of abrasives used for magnetic layers other than the hard magnetic layer include α-alumina, β-alumina, silicon carbide, chromium oxide, cerium oxide, α-iron oxide having an α conversion of 90% or more. Known materials such as corundum, artificial diamond, silicon nitride, silicon carbide, titanium carbide, titanium oxide, silicon dioxide, boron nitride, etc., mainly having a Mohs hardness of 6 or more, can be used alone or in combination. . Further, a composite of these abrasives (abrasive whose surface is treated with another abrasive) may be used. These abrasives may contain compounds or elements other than the main component, but the effect remains unchanged if the main component is 90% by weight or more. The particle size of these abrasives is preferably from 0.01 to 2 μm. However, if necessary, abrasives having different particle sizes may be combined, or even a single abrasive may have the same effect by broadening the particle size distribution. The tap density is 0.3-2 g / ml, the water content is 0.1-5% by weight, and the pH is 2-11.
The specific surface area is preferably ¹ to 30 m ² / g. The shape of the abrasive used in the present invention may be, for example, any of a needle shape, a spherical shape, and a die shape. However, those having corners in a part of the shape are preferable because of high abrasiveness. Specific examples of the abrasive used in the present invention,
AKP-20, AKP-30, AKP-, manufactured by Sumitomo Chemical Co., Ltd.
50, HIT-50, HIT-100, manufactured by Nippon Chemical Industry Co., Ltd., G
5, G7, S-1, TF-100, TF, manufactured by Toda Kogyo
-140 and the like.

The abrasive used in the present invention can be of different types, amounts and combinations for the magnetic layer (other than the hard magnetic layer) and the underlayer, and can be used properly according to the purpose. These abrasives may be added to the magnetic paint after being subjected to dispersion treatment with a binder in advance. The abrasive present on the surface of the magnetic layer and the end face of the magnetic layer of the magnetic recording medium of the present invention is preferably 5/100 μm ² or more.

In each layer of the magnetic recording medium of the present invention, a substance having a lubricating effect, an antistatic effect, a dispersing effect, a plasticizing effect, and the like can be appropriately contained as an additive.
Examples of these additives include molybdenum disulfide,
Tungsten disulfide graphite, boron nitride, fluorinated graphite, silicone oil, silicone having a polar group, fatty acid-modified silicone, fluorine-containing silicone, fluorine-containing alcohol, fluorine-containing ester, polyolefin,
Polyglycols, alkyl phosphates and alkali metal salts thereof, alkyl sulfates and alkali metal salts thereof, polyphenyl ether, fluorine-containing alkyl sulfates and alkali metal salts thereof, having 10 to 2 carbon atoms
4 monobasic fatty acids (which may contain an unsaturated bond or may be branched), and metal salts thereof (L
i, Na, K, Cu, etc. or monovalent, divalent, trivalent, tetravalent, pentavalent, hexavalent alcohols having 12 to 22 carbon atoms (although containing unsaturated bonds, they are also branched) C12 to C22 alkoxy alcohols, C10 to C24 monobasic fatty acids (which may contain unsaturated bonds or may be branched) and C2 to C12
A monofatty acid ester comprising a monovalent, divalent, trivalent, tetravalent, pentavalent, or hexavalent alcohol (which may contain an unsaturated bond or may be branched) or Examples thereof include difatty acid esters or trifatty acid esters, fatty acid esters of monoalkyl ethers of alkylene oxide polymers, fatty acid amides having 8 to 22 carbon atoms, and aliphatic amines having 8 to 22 carbon atoms.

More specifically, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, butyl stearate, oleic acid, linoleic acid, linolenic acid, elaidic acid, octyl stearate, amyl stearate, Isooctyl stearate, octyl myristate, butoxyethyl stearate, anhydrosorbitan monostearate, anhydrosorbitan distearate, anhydrosorbitan tristearate, oleyl alcohol, lauryl alcohol Can be Further, nonionic surfactants such as alkylene oxides, glycerin, glycidols, alkylphenol ethylene oxide adducts, cyclic amines, ester amides, quaternary ammonium salts, hydantoin derivatives,
Cationic surfactants such as heterocycles, phosphoniums or sulfoniums, anionic surfactants containing acidic groups such as carboxylic acid, sulfonic acid, phosphoric acid, sulfate group, phosphate group, etc., amino acids, aminosulfonic acids Sulfuric acid or phosphoric acid esters of amino alcohol,
An amphoteric surfactant such as an alkylbedine type can be used.

For details of these surfactants, see
Reference can be made to the description in “Surfactant Handbook” (published by Sangyo Tosho Co., Ltd.). These lubricants, antistatic agents and the like are not necessarily 100% pure, and may contain impurities such as isomers, unreacted materials, by-products, decomposition products, oxides and the like in addition to the main components. These impurities are preferably 30% or less, more preferably 10% or less.

The types and amounts of these lubricants and surfactants used in the present invention can be properly used in each layer as needed. For example, to control bleeding to the surface using fatty acids having different melting points in the underlayer and the magnetic layer (including the hard magnetic layer and the soft magnetic layer), and to bleed to the surface using esters having different boiling points and polarities. It is possible to improve the stability of coating by controlling the amount of the surfactant, and to improve the lubricating effect by increasing the amount of the lubricant added to the underlayer. However, it is not limited to the example shown here. All or some of the additives used in the present invention may be added at any step of the production of the magnetic paint. For example, when mixing with the ferromagnetic powder before the kneading step, when adding in the kneading step with a ferromagnetic powder and a binder and a solvent, when adding in the dispersion step,
There is a case where it is added after the dispersion or a case where it is added just before the application. In some cases, the purpose may be achieved by applying a part or all of the additive simultaneously or sequentially after applying the magnetic layer according to the purpose. Depending on the purpose, a lubricant may be applied to the surface of the magnetic layer after calendering or after the slit is completed.

The thickness of the magnetic recording medium of the present invention is suitably such that the nonmagnetic flexible support has a thickness of, for example, 1 to 100 μm, preferably 4 to 80 μm. The combined thickness of the magnetic layer and the underlayer (however, only the magnetic layer in the magnetic recording medium (1)) is 1/500 to the thickness of the nonmagnetic flexible support.
Suitably, the range is twice as large. Further, an undercoat layer for improving adhesion may be provided between the nonmagnetic flexible support and the magnetic layer or between the nonmagnetic flexible support and the underlayer. The thickness of the undercoat layer is, for example, 0.01 to 2 μm, preferably 0.02 to 0.5 μm. Further, a back coat layer may be provided on the side of the non-magnetic support opposite to the side of the magnetic layer. This thickness is, for example, 0.1 to
Suitably, it is 2 μm, preferably 0.3 to 1.0 μm. Known undercoat layers and backcoat layers can be used.

The non-magnetic flexible support used in the present invention includes polyesters such as polyethylene terephthalate and polyethylene naphthalate, polyolefins, cellulostriacetate, polycarbonate, polyamide, polyimide and polyamide. Known films such as imide, polysulfone, aramid, and aromatic polyamide can be used. These supports may be subjected to corona discharge treatment, plasma treatment, easy adhesion treatment, heat treatment, dust removal treatment, or the like in advance. In order to achieve the object of the present invention, the nonmagnetic flexible support has a center line average surface roughness (cutoff value 0.25 mm) of 0.03 μm or less, preferably 0.03 μm or less.
It is suitable to use one having a size of 2 μm or less, more preferably 0.01 μm or less. Also, these non-magnetic supports not only have a small center line average surface roughness,
It is preferable that there is no coarse projection of 1 μm or more. The surface roughness may be adjusted by the filler added to the support if necessary.
Can be freely controlled depending on the size and amount of. Examples of these fillers include Ca, S
In addition to oxides and carbonates such as i and Ti, organic fine powders such as acryl-based can be used. The F-5 value of the non-magnetic support used in the present invention in the tape running direction is preferably 5 to 50.
kg / mm ² , and the F-5 value in the tape width direction is preferably 3
３０30 kg / mm ² , F-5 in long hand direction
Generally, the value is higher than the F-5 value in the tape width direction, but this is not particularly necessary when it is necessary to increase the strength in the width direction.

The heat shrinkage of the support in the tape running direction and the width direction at 100 ° C. for 30 minutes is preferably 3% or less, more preferably 1.5% or less, at 80 ° C. for 30 minutes. The heat shrinkage is preferably 1% or less, more preferably 0.5% or less. Breaking strength 5-100 in both directions
kg / mm ^2, it is preferred that the elastic modulus is 100 to 2,000 kg / mm ^2.

The step of producing a magnetic paint used for producing the coating layer of the magnetic recording medium of the present invention comprises at least a kneading step, a dispersing step, and a mixing step provided before and after these steps as necessary. . Each step may be divided into two or more steps. All the raw materials such as the ferromagnetic powder, binder, carbon black, abrasive, antistatic agent, lubricant and solvent used in the present invention may be added at the beginning or during any step. Further, individual raw materials may be added in two or more steps in a divided manner.
For example, polyurethane may be divided and supplied in a kneading step, a dispersing step, and a mixing step for adjusting the viscosity after dispersion.

In the method of manufacturing a magnetic recording medium of the present invention, it is a matter of course that a known manufacturing technique can be used as a part of the steps. However, in order to obtain a high residual magnetic flux density (Br), a material having a strong kneading force such as a continuous kneader or a pressure kneader can be used in the kneading step. When a continuous kneader or a pressure kneader is used, the ferromagnetic powder and the binder all or a part thereof (however, preferably 30% or more of the total binder) and 15 to 500 parts by weight based on 100 parts by weight of the ferromagnetic powder. It is kneaded in the range of parts by weight. Details of these kneading processes are described in JP-A-1-106338 and JP-A-64-79274. When adjusting the underlayer liquid, it is desirable to use a dispersion medium having a high specific gravity, and zirconia beads are preferable.

An organic solvent is used when producing the coating layer of the magnetic recording medium of the present invention. Examples of the organic solvent include ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone, isophorone, and tetrahydrofuran in any ratio, methanol, ethanol, propanol, butanol, and isobutyl alcohol. Alcohols such as methyl, isopropyl alcohol, methylcyclohexanol, etc., esters such as methyl acetate, butyl acetate, isobutyl acetate, isopropyl acetate, ethyl lactate, glycol acetate, glycol dimethyl ether, glycol monoethyl ether, Glycol ethers such as dioxane, aromatic hydrocarbons such as benzene, toluene, xylene, cresol, chlorobenzene, methylene chloride, ethylene chloride, carbon tetrachloride, chloroform, ethylene chloride Ruhidorin, dichlorobenzene, chlorinated hydrocarbons and the like, N,
N-dimethylformamide, hexane and the like can be used. These organic solvents are not necessarily 100% pure, and may contain impurities such as isomers, unreacted products, by-products, decomposed products, oxides, and moisture in addition to the main components. These impurities are preferably 30% or less, more preferably 10% or less. The type of the organic solvent used in the present invention is preferably the same for the magnetic layer and the underlayer. The amount added may be changed. It is preferable that a solvent having a high surface tension (such as cyclohexanone or dioxane) is used for the underlayer to improve coating stability. Specifically, it is preferable that the arithmetic average value of the upper solvent composition does not fall below the arithmetic average value of the lower solvent composition. In order to improve the dispersibility, it is preferable that the polarity is somewhat strong, and it is preferable that the solvent composition contains 50% or more of a solvent having a dielectric constant of 15 or more. Also,
The dissolution parameters are preferably 8-11.

In the magnetic recording medium (1) of the present invention, when two or more magnetic layers are of the coating type, in the magnetic recording medium (2), the underlayer and at least the magnetic layer in contact with the underlayer are of the coating type. The following configuration can be used as an example of an apparatus and a method for applying a coating layer. 1, the lower layer is first applied by a gravure coating, a roll coating, a blade coating, an extrusion coating device, etc., which are generally used in the application of magnetic paint, and the lower layer is wet while the lower layer is in a wet state. The upper layer is applied by a support-pressing-type extrusion coating apparatus disclosed in JP-A-60-238179 and JP-A-2-265672. 2, the upper and lower layers are formed by one coating head having two built-in slits for passing the coating liquid as disclosed in JP-A-63-88080, JP-A-2-17971, and JP-A-2-265672. Are applied almost simultaneously. 3. The upper and lower layers are applied almost simultaneously by an extrusion coating apparatus with a back-up roll disclosed in Japanese Patent Application Laid-Open No. 2-174965.

Incidentally, in order to prevent the electromagnetic conversion characteristics and the like of the magnetic recording medium from deteriorating due to the aggregation of the magnetic particles, Japanese Patent Laid-Open No. 62-951 discloses
It is desirable to apply shear to the coating liquid inside the coating head by a method as disclosed in Japanese Patent Application Laid-Open No. 74-136 or Japanese Patent Application Laid-Open No. 1-236968. Furthermore, regarding the viscosity of the coating liquid,
It is necessary to satisfy the numerical range disclosed in JP-A-3-8471. If strong alignment is required, 10
A solenoid of 00G or more and a cobalt magnet of 2000G or more can be used together in the same polarity opposition. Further, it is preferable to provide an appropriate drying step before the orientation so that the orientation after the drying becomes the highest. When the present invention is applied to a disk medium, an orientation method for randomizing the orientation is required. The orientation of the hard magnetic layer and the soft magnetic layer in order to change the orientation is not necessarily longitudinal and in-plane, but can be oriented in the vertical and width directions.

Further, a heat-resistant plastic roll such as epoxy, polyimide, polyamide, or polyimide amide is used as the calendering roll. Further, the treatment can be carried out by metal rolls. The treatment temperature is preferably 70 ° C. or higher, more preferably 80 ° C. or higher. The linear pressure is preferably 200 kg /
cm, more preferably 300 kg / cm or more.
S of the magnetic layer surface and the opposite surface of the magnetic recording medium of the present invention
The friction coefficient with respect to US420J is preferably 0.5 or less, more preferably 0.3 or less, the surface resistivity is preferably 10 ⁴ to 10 ¹² ohm / sq, and the surface resistivity of the magnetic layer is 0.1 to 10 ¹² ohm / sq.
The elastic modulus at 5% elongation is preferably 100 to 2000 kg / mm ² in both the running direction and the width direction.
Preferably, it is 1 to 30 kg / cm ² , and the elastic modulus of the magnetic recording medium is preferably 100 in both the running direction and the long direction.
1500 kg / mm ² , the residual elongation is preferably 0.5% or less, and the heat shrinkage at any temperature of 100 ° C. or less is preferably 1% or less, more preferably 0.5% or less. And most preferably 0.1%
The following are appropriate respectively. The glass transition temperature of the magnetic layer (the maximum point of the loss elastic modulus in dynamic viscoelasticity measurement measured at 110 Hz) is preferably from 50 ° C to 120 ° C, and the glass transition temperature of the lower nonmagnetic layer is from 0 ° C to 100 ° C. Is preferred. The loss modulus is preferably in the range of 1 × 10 ⁸ to 8 × 10 ⁹ dyne / cm ² , and the loss tangent is preferably 0.2 or less from the viewpoint of preventing adhesion failure.

The residual solvent contained in the magnetic layer is preferably 100 mg / m ² or less, more preferably 10 mg / m ² or less.
m ² or less. The porosity of the magnetic layer is preferably 30% by volume or less, more preferably 20% by volume or less for the magnetic layer including the underlayer, the hard magnetic layer and the soft magnetic layer. The porosity is preferably small in order to achieve high output, but it may be better to secure a certain value depending on the purpose. For example, in a magnetic recording medium for data recording in which repetitive use is emphasized, a higher porosity is often preferable in running durability. When the magnetic properties of the magnetic recording medium of the present invention are measured at a magnetic field of 5 KOe, the squareness ratio in the tape running direction is 0.70 or more, preferably 0.80 or more, and more preferably 0.90 or more. Appropriate. It is preferable that the squareness ratio in the two directions perpendicular to the tape running direction is 80% or less of the squareness ratio in the running direction. The SFD (Swiching Field Distribution) of the magnetic layer is 0.
It is preferably 6 or less. The center line surface roughness (cutoff value 0.25 mm) Ra of the magnetic layer is 1 nm to 10 nm.
Is preferred, but the value can be appropriately set according to the purpose. In order to improve the electromagnetic conversion characteristics, Ra is preferably smaller. However, in order to improve running durability, it is more preferable to increase Ra. It is preferable that the RMS (root mean square) surface roughness RRMS obtained by evaluation with an AFM (Atomic Force Micro Scope) is in the range of 2 nm to 15 nm.

The magnetic recording medium of the present invention has a magnetic layer including a hard magnetic layer and a soft magnetic layer, and further has an underlayer in the magnetic recording medium (2). These physical properties can be changed. For example, the elastic modulus of the magnetic layer is increased to improve running durability, and at the same time, the elastic modulus of the underlayer is made lower than that of the magnetic layer to improve the contact of the magnetic recording medium with the head. What physical properties each brings to two or more magnetic layers is
It is possible to refer to a known technique regarding the magnetic layer overlay.

[0047]

Next, the details of the present invention will be specifically described with reference to examples. In the examples, "parts" indicates "parts by weight".
Means Underlayer Non-magnetic powder α-Fe ₂ O ₃ 80 parts Average major axis length 0.1 μm Specific surface area by BET method 48 m ² / g pH 8, Fe ₂ O ₃ content 90% or more DBP oil absorption 27-38 ml / 100g Surface Treatment agent Al ₂ O ₃ carbon black 20 parts Average primary particle diameter 16 μm DBP oil absorption 80 ml / 100 g pH 8.0 Specific surface area by BET method 250 m ² / g Volatile content 1.5% Vinyl chloride copolymer 12 parts Nippon Seon Co., Ltd. MR-110 polyester polyurethane resin 5 parts Neopentyl glycol / caprolactone polyol / MDI = 0.9 / 2.6 / 1 -SO ₃ Na group 1 × 10 ^-4 eq / g butyl stearate 1 part Stearic acid 1 part Methyl ethyl ketone 100 parts Cyclohexanone 50 parts Toluene 50 parts

Hard magnetic layer Ferromagnetic metal powder Composition Fe / Co = 90/10 100 parts Hc 2300 Oe, specific surface area by BET method 54 m ² / g Crystallite size 165 A, surface treatment agent Al ₂ O ₃ , particle size (length Shaft diameter) 0.1 μm, needle ratio 8 σs: 110 emu / g Vinyl chloride copolymer 5 parts MR-110 polyester polyurethane resin manufactured by Nippon Seon Co., Ltd. 2 parts Neopentyl alcohol / caprolactone polyol / MDI = 0.9 / 2 0.6 / 1 -SO ₃ Na group 1 × 10 ^-4 eq / g containing butyl stearate 1 part Stearic acid 5 parts Methyl ethyl ketone 90 parts Cyclohexanone 30 parts Toluene 60 parts Soft magnetic layer Ni-Fe fine powder composition Ni / Fe = 78 / 22 100 parts Hc 0.5 Oe, Bs10000G Initial permeability 9000 Specific surface area by BET method 48 m ² / g Average particle size 0.08 μm Vinyl chloride copolymer 12 parts Nippon Seon MR-110 POLYE Stell polyurethane resin 5 parts Neopentyl glycol / caprolactone polyol / MDI = 0.9 / 2.6 / 1-SO ₃ Na group 1 × 10 ^-4 eq / g containing α-alumina (particle size 0.2 μm) 5 parts -Bon black (particle size 0.09 μm) 5 parts Butyl stearate 1 part Stearic acid 2 parts Methyl ethyl ketone 90 parts Cyclohexanone 30 parts Toluene 60 parts

Each of the above two paints was kneaded with a continuous kneader and dispersed using a sand mill. To the resulting dispersion, 1 part of polyisocyanate was added to the underlayer coating solution, and 3 parts to the hard magnetic layer and soft magnetic layer coating solutions.
40 parts of a cyclohexanone mixed solvent was added, and the mixture was filtered using a filter having an average pore size of 1 μm to prepare coating solutions for the underlayer, the hard magnetic layer, and the soft magnetic layer. The thickness of the obtained underlayer coating solution after drying is 1.
0 μm, and immediately after that, the center line surface roughness is 62 μm so that the thickness of the hard magnetic layer is 0.08 μm and the thickness of the soft magnetic layer is 0.05 μm. A simultaneous multi-layer coating was carried out on a polyethylene naphthalate support having a cut-off value of 0.25 mm (0.01 μm), and a frequency of 50 H was applied while each layer was still wet.
z-field strength 200G, frequency 120Hz field strength 130
G was passed through to perform a random orientation process. Thereafter, it was dried and treated at a temperature of 90 ° C. with a seven-stage calender composed of only metal rolls, and punched into a 3.5-inch diameter to prepare a disk.

Evaluation method (1) Using an Hc, Br vibration data type magnetometer (manufactured by Toei Kogyo), Hm10 kOe
Was measured. (2) The reproduction output was measured using RWA1 manufactured by Guzik
A gap length of 0.25 μm was measured with a 001 type disk evaluation device and a spin stand LS-90 manufactured by Kyodo Electronic System Co., Ltd.
Using a m thin film head, a reproduction output at a linear recording density of 90 KFCI was obtained at a position of a radius of 24.6 mm. At the time of reproduction, a direct current was applied to the head so that the gap magnetic field intensity was 300 Oe.

[0051]

[Table 1]

Description of Examples / Comparative Examples A coating solution obtained by adding 5 parts of α-alumina having an average particle size of 0.2 μm to the composition of the hard magnetic layer was applied alone to a non-magnetic support at 1.2 μm.
(Comparative Example 1) was used as a reference for output and CNR. The first embodiment corresponds to claims 1 to 6 of the present application.
This sample satisfies the requirements described in (1). Example 2
Means that the soft magnetic layer has a center dust powder (relative initial permeability of 30,000, Bs80
00G, Hc0.01 Oe) and the same abrasive as in Example 1 except that the abrasive used was α-hematite having an average particle size of 0.1 μm. Higher output and CNR than in Example 1 were obtained. In Example 3, the soft magnetic layer was made of Mn-Zn ferrite (specific initial permeability 1).
4000, Bs3000G, Hc0.4Oe) and the same sample as in Example 1 except that the particle size of the carbon black used was 20 mμ. Since Bn of the Mn-Zn ferrite was smaller than that of the alloy powder, the output was lower than those of the samples of Examples 1 and 2. In Example 4, the magnetic material of the hard magnetic layer was Hc1200Oe, σs60
The sample is the same as that in Example 1 except that the emu / g of ferrite was changed to emu / g. Since the Hc and σs of the magnetic material were lower than the permalloy powder used in Example 1, the output was lower. Example 5 is a sample similar to Example 1 except that the underlayer was not provided. The output and CNR are lower than in Example 1 due to a decrease in the moldability and the surface properties are deteriorated. However, a higher output and CNR are obtained as compared with the sample of Comparative Example 2 having an underlayer but not having a soft magnetic layer. Was done. Example 6
Means that the thickness of each of the hard magnetic layer and the soft magnetic layer is 0.8
The sample was the same as in Example 1 except that the thickness was set to μm. Although the value was lower than the value obtained with the sample of Example 1, a sufficient output / CNR was obtained. Example 7 is a sample similar to Example 1 except that the thicknesses of the hard magnetic layer and the soft magnetic layer were larger than 1 μm, and the size of the alumina particles in the soft magnetic layer was 0.4 μm. In this case, the demagnetizing field is large and the output is reduced as compared with Example 1, and the abrasive particles of the soft magnetic layer affect the lower hard magnetic layer to increase noise.
NR tends to decrease. However, higher output and higher CNR were obtained as compared with the sample of Comparative Example 2 having the underlayer but not the soft magnetic layer. Example 8 is a sample having a non-magnetic layer (break layer) formed by applying the same coating solution as the non-magnetic underlayer so as to have a dry film thickness of 0.02 μm between the soft magnetic layer and the hard magnetic layer. It is. Although there is no significant effect as is known in the thin film medium, the output and the CNR are improved by the presence of the flake layer as compared with the first embodiment.
Comparative Example 2 is a sample similar to Example 1 except that the soft magnetic layer was not provided. Comparative Example 3 shows that Hc of the hard magnetic layer
The sample was the same as in Example 1 except that the sample was changed to 700 Oe.

Claims (6)

[Claims] 1. A magnetic recording medium in which two or more magnetic layers are provided on a non-magnetic flexible support, wherein the two or more magnetic layers contain a ferromagnetic powder and a binder, and Hc is 800 Oe or more. And comprising a hard magnetic layer containing substantially no nonmagnetic particles and a soft magnetic layer containing a soft magnetic powder having a high magnetic permeability and a binder, wherein the hard magnetic layer is more of a support than the soft magnetic layer. A magnetic recording medium, wherein the magnetic recording medium is arranged at a position close to the magnetic recording medium. 2. The magnetic recording medium according to claim 1, wherein an underlayer containing a nonmagnetic powder and a binder is provided between the support and the magnetic layer closest to the support among the two or more magnetic layers. 3. The soft magnetic layer has an average particle size 平均 of 0.3.
The magnetic recording medium according to claim 1, further comprising nonmagnetic particles having a μm or less and a Mohs hardness of 5 or more. 4. The soft magnetic layer has an average particle size of 10 μm.
The magnetic recording medium according to any one of claims 1 to 3, wherein the magnetic recording medium contains a carbon black in the range of -200 m [mu]. 5. The soft magnetic layer has a relative initial magnetic permeability of 20 or more and an Hc of 150 Oe or less.
The magnetic recording medium according to any one of the above items. 6. The magnetic recording medium according to claim 1, further comprising a nonmagnetic layer having a thickness of 0.005 to 0.1 μm between said hard magnetic layer and said soft magnetic layer.