JPH0610872B2 - video tape - Google Patents

Description

Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a magnetic recording medium, and more particularly to a metal thin film type video tape.

2. Description of the Related Art Prior Art and Problems There are active developments of magnetic recording media for video, audio, etc., which have a metal thin film type magnetic layer because of their compactness when formed into a tape and wound.

As a magnetic layer of such a metal thin film type medium, vapor deposition of Co-based, Co-Ni-based, or the like, which is formed by a so-called oblique vapor deposition method in which vapor deposition is performed at a predetermined inclination angle with respect to the normal line of the substrate, is characteristic. Membranes are preferred.

However, such a metal thin film has a problem of poor corrosion resistance in an atmosphere of relatively high temperature and high humidity. Especially when the tape is wound and wound, when it is subjected to a sudden temperature change under high humidity, dew condensation is likely to occur between the magnetic surface and the back surface of the wound tape, which face each other. Since the magnetic surface and the back surface are in close contact with each other, it is difficult to evaporate, and the magnetic surface is leaked for a long time.

For this reason, corrosion is likely to occur in the dew condensation portion, and when the corroded portion is dried, the magnetic surface and the back surface are easily bonded (so-called blocking) via the corrosion product.

Focusing on this point, a proposal has been made to increase the corrosion resistance of the magnetic recording medium by controlling the contact angle between the magnetic surface and the water on the back surface (Japanese Patent Laid-Open No. 57-123526).
Has been done.

In this proposal, the contact angles of water on the magnetic surface and the back surface are both 8
Blocking is improved by setting the angle to 5 ° or more, specifically 85 to 95 °.

However, when it is used for a video tape, it has been found that a contact angle of about 95 ° has a problem in running property especially at high temperature and high humidity, causes large modulation noise, and has a poor C / N ratio. Further, storage under high temperature and high humidity deteriorates running properties, deteriorates still characteristics, and frequently causes head clogging.

II Object of the invention The object of the present invention is to improve the running property under high temperature and high humidity,
Another object of the present invention is to provide a video tape that reduces noise and further prevents deterioration of running property and still characteristic after storage under high temperature and high humidity and occurrence of head clogging.

III DISCLOSURE OF THE INVENTION Such an object is achieved by the present invention described below.

That is, the present invention has a ferromagnetic metal thin film layer containing Co as a main component on one surface of a flexible substrate, a top coat layer on the surface of the ferromagnetic metal thin film layer, and further on the other surface of the substrate. Has a back coat layer, and the contact angle with water on the surface of the top coat layer is θ _t ,
When the contact angle of water on the surface of the back coat layer is θ _b , 100 ° ≦ θ _t ≦ 140 °, 100 ° ≦ θ _b ≦ 140 ° and | θ _t −θ _b | ≦ 10 ° are regulated to be still. It is a video tape with improved characteristics.

IV Specific Structure of the Invention Hereinafter, the specific structure of the present invention will be described in detail.

The video tape of the present invention has a structure that Co film is formed on one surface of the flexible substrate.
A ferromagnetic metal thin film layer containing as a main component, a top coat layer is provided on the surface of the metal thin film layer, and a back coat layer is provided on multiple surfaces of the substrate.

In the present invention, the contact angle with water on the surface of the top coat layer is θ _t , and the contact angle with water on the surface of the back coat layer is θ _t .
_When it is set to _b , both (theta) _t and (theta) _b are 100-140 degrees.

Further, there is a relationship of | θ _t −θ _b | ≦ 10 °.

If any of the theta _t and theta _b is less than 100 °, it deteriorates the runnability at high temperature and high humidity, the modulation noise increases.

More specifically, when only θ _t is less than 100 °, durability and still characteristics are deteriorated, clogging is increased, and storage stability under high temperature and high humidity is also deteriorated.

If only θ _b is less than 100 °, modulation noise increases, clogging increases, and storage stability decreases.

When both θ _t and θ _b are less than 100 °, these characteristics are further deteriorated.

Note that θ _t and θ _b are actually 14 due to material restrictions.
It rarely exceeds 0 °.

If the difference between θ _t and θ _b is within 10 °, the change in running friction over time is reduced. Further, deterioration of the still characteristics after storage under high temperature and high humidity is reduced, and head clogging is also reduced.

The top coat layer provided on the surface of the ferromagnetic metal thin film layer of the video tape of the present invention has a θ _{t of} 100 ° or more and is composed of a coating film of an antioxidant or a lubricant, a vapor deposition film, a plasma polymerization film, etc. It is desirable that the inhibitor is contained as an essential component.

As the antioxidant used in the present invention, usual antioxidants are used, and these are: 1) phenolic antioxidants 2) amine antioxidants, 3) phosphorus antioxidants, 4) sulfur compounds Structurally roughly classified as antioxidants, 5) organic acids, alcohols, ester-based antioxidants, 6) quinone-based antioxidants, 7) inorganic acids, inorganic salt-based antioxidants.

Specific examples of the above various antioxidants are as follows: 1) Phenol-based antioxidants include 2,6-di-tert-butyl-p-cresol, 2,6-di-tert-butyl-phenol, 2 , 4-di-methyl-6-
Tert-butyl-phenol, butylhydroxyanisole, 2,2'-methylenebis (4-methyl-6-tert-butylpheninol), 4,4'-butylidenebis (3-
Methyl-6-tert-butylphenol), 4,4'-thiobis (3-methyl-6-tert-butylphenol), tetrakis [methylene-3 (3,5-di-tert-butyl-4-)
Hydroxyphenyl) propionate] methane, 1,
1,3-tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butane, dibutylhydroxytoluene, propyl gallate, guaiac butter, nordihydroguaiaretic acid and the like.

As a radiation curable type, monoglycol salicylate,
Examples thereof include methacrylate and acrylate types such as 2,5-di-tert-butylhydroquinone, 2,4-dihydroxybenzophenone, 2,4,5-trihydroxybutyrophenone and hydroquinone.

2) Amine-based antioxidants include phenyl-β-naphthylamine, α-tiphtylamine, N, N′-di-tert-butyl-p-phenylenediamine, phenothiazine,
In addition to N, N'-diphenyl-p-phenylenediamine,
Examples thereof include alkanolamine and phospholipid.

Among amine-based radiation-curable types, there are radiation-curable types such as dimethylaminoethyl methacrylate and acrylate.

3) As the phosphorus-based antioxidant, a radiation-curable type or a non-radiation-curable type is used, and R of the phosphate ester portion contains an alkyl group, an alkylphenyl group, other ethylene oxide, or propylene oxide. C is preferably 1 to 26, and more preferably 1 to 22.

The phosphoric acid ester includes mono, di, and triesters, and may have a large amount of mono or di components,
Tri-type may be cut.

In addition, the phosphate ester is And those of methacrylate type and acrylate type are also included.

Specifically, phosphite such as triphenyl phosphite, trioctadecyl phosphite, tridecyl phosphite, trilauryl trithiophosphite, hexamethylphosphoric triamide, butyl phosphate, cetyl phosphate, butoxyethyl phosphate, 2 -Ethylhexyl phosphate, β-chloroethyl phosphate, butoxyethyl phosphate diethylamine salt, di (2-ethylhexyl) phosphate, ethylene glycol acid phosphate, (2-hydroxyethyl) methacrylate phosphate, butylhydroxymethacrylate phosphate, caprylhydroxymethacrylate phosphate , Myristyl hydroxymethacrylate phosphate, stearyl hydroxymethacrylate Phosphate, cetyl hydroxyethyl methacrylate phosphate, butylphenyl hydroxy methacrylate phosphate, amyl phenyl hydroxy methacrylate phosphate, nonylphenyl hydroxy methacrylate phosphate, and these acrylate types, phenyl phosphate,
Other alcohols, phenyl phosphates such as nonylphenyl, and phosphoric acid esters such as vanadium-based acidic phosphoric acid esters are included.

4) Examples of sulfur-based antioxidants include dilauryl thiodipropionate, distearyl thiodipropionate, lauryl stearyl thiodipropionate, dimyristyl thiodipropionate, distearyl β, β′-thiobutyrate, 2- In addition to mercaptobenzimidazole and dilauryl sulfide, 4,4'-
Examples of the radiation-curable type include methacrylates such as thio-bis (3-methyl-6-tert-butyl-phenol) and 2,2'-thio-bis (4-methyl-6-tert-butyl-phenol) and acrylates. To be

Moreover, these may contain ethylene oxide and propylene oxide.

5) Examples of the organic acid, alcohol, and ester-based antioxidants include sorbitol, glycerin, propylene glycol, adipic acid, citric acid, and ascorbic acid, which may be radiation-curable.

6) Examples of the quinone-based antioxidant include hydroquinone and tocopherol, and among these, radiation-curable type may be used.

7) Typical examples of inorganic acids and inorganic salt antioxidants include phosphoric acid.

Among the above antioxidants, radiation curable ones having an acrylic double bond in the molecule, for example, monoglycol salicylate methacrylate (acrylate), 4 Tert-butyl catechol methacrylate (acrylate), dimethylamine ethyl methacrylate (acrylate), ethyl hydroxymethacrylate (acrylate) phosphate, cetyl hydroxyphosphate methacrylate (acrylate), stearyl methacrylate (acrylate) phosphate, and phenyl type of the above, 2,2 'Thio-
Bis (4-methyl-6-tert-butyl-phenol) methacrylate (acrylate) and the like are preferable.

The phosphoric acid ester can be produced by a known method, and the method described in JP-B-57-44223 can also be used.

Since the radiation-curable inhibitor can be cured online on the ferromagnetic thin film, the surface property is not deteriorated due to the back mold transfer due to winding tightness at the time of heat curing, and therefore the output is not reduced.

The top coat on the ferromagnetic thin film is 100Å as described later.
The following is preferable, and if the thickness is further increased, the electromagnetic conversion characteristics are deteriorated. Also, if it is too thick, the top coat layer will be scraped. This is the first finding of the present invention. By using a radiation-curable antioxidant, there are characteristic effects such as prevention of dropout, reduction of output difference due to internal and external parts when rolled, and online manufacturing is possible. The processing effect can be improved.

As the lubricant used in the present invention, as a lubricant conventionally used in this type of magnetic recording medium, silicone oil,
Fluorine oil, fatty acid, fatty acid ester, paraffin,
Liquid paraffin, a surfactant and the like can be used, but it is preferable to use a fatty acid and / or a fatty acid ester.

Examples of the fatty acid include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, elaidic acid, linoleic acid, linolenic acid, stearic acid and the like having 12 or more carbon atoms (R
COOH and R are alkyl groups having 11 or more carbon atoms) and the like.

Examples of the fatty acid ester include fatty acid esters composed of monobasic fatty acids having 12 to 16 carbon atoms and monohydric alcohol having 3 to 12 carbon atoms, monobasic fatty acids having 17 or more carbon atoms and carbon numbers of fatty acids. In total, a fatty acid ester or the like composed of a monohydric alcohol having 21 to 23 carbon atoms is used.

As the silicone, those which are modified with fatty acids and those which are partially modified with fluorine are used.

As the alcohol, a higher alcohol is used, and as the fluorine, one obtained by electrolytic substitution, telomerization, oligomerization or the like is used.

Among the lubricants, it is convenient to use radiation-curable lubricants.

Since these suppress backside transfer to the ferromagnetic thin film, they prevent dropouts, reduce the output difference due to the inner and outer diameters when wound in a roll, and have the advantage that they can be manufactured online. have.

As the radiation-curable lubricant, a compound having a molecular chain exhibiting lubricity and an acrylic double bond in the molecule, for example, acrylic acid ester, methacrylic acid ester, vinyl acetate ester, acrylic acid amide compound, vinyl alcohol ester , Methyl vinyl alcohol ester, allyl alcohol ester, glyceride and the like.

When these lubricants are represented by structural formulas, _{CH 2 = CH-CH 2 COOR} , CH 2 = CHCONHCH 2 OCOR RCOOCH ₌ is _{CH 2, RCOOCH 2 -CH = CH} 2 and the like.

Here, R is a linear or branched saturated or unsaturated hydrocarbon group having a carbon number of 7 or more, preferably 12 or more 23
Below, these can also be made into the fluorine substitution product.

As the fluorine-substituted compound, CnF _{2n + 1} −, CnF _{2n + 1} (CH ₂ ) _m − (where m = 1 to 5), _{CnFnCH 2 CH 2 NHCH 2 CH 2} -, Etc.

Specific preferred examples of these radiation-curable lubricants include:
Examples thereof include stearic acid methacrylate (acrylate), stearyl alcohol methacrylate (acrylate), glycerin methacrylate (acrylate), glycol methacrylate (acrylate), and silicone methacrylate (acrylate).

The method of providing the topcoat layer on the surface of the ferromagnetic thin film is to dilute the additive with a solvent and apply it thinly on the ferromagnetic metal thin film, or to add the additive in the atmosphere, in an inert gas, or in a vacuum. It is possible to apply these by vaporizing with, and applying the vapor to the ferromagnetic metal surface.

The top coat layer of the present invention may contain an organic binder such as a polymer. As the polymer used in the top coat layer, a thermoplastic, thermosetting or reactive resin conventionally used for magnetic recording media or a mixture thereof is used, but it is cured from the viewpoint of the obtained coating film strength and the like. Molds, especially radiation-curable resins, are preferred.

The thermoplastic resin has a softening temperature of 150 ° C. or lower, an average molecular weight of 10,000 to 200,000, and a polymerization degree of about 200 to
Approximately 2000, for example, vinyl chloride-vinyl acetate copolymer (including carboxylic acid introduced), vinyl chloride-vinyl acetate-vinyl alcohol copolymer (including carboxylic acid introduced), vinyl chloride-chlorinated Vinylidene copolymer, vinyl chloride-acrylonitrile copolymer, acrylic ester-acrylonitrile copolymer, acrylic ester-vinylidene chloride copolymer, acrylic ester-styrene copolymer, methacrylic acid ester-acrylonitrile copolymer, Methacrylic acid ester-vinylidene chloride copolymer, methacrylic acid ester-styrene copolymer, urethane elastomer, nylon-silicone resin, nitrocellulose-polyamide resin, polyvinyl fluoride, vinylidene chloride-acrylonitrile copolymer, butadiene-acryl Nitrile copolymer, polyamide resin, polyvinyl butyral, cellulose derivative (cellulose acetate, cellulose diacetate, cellulose triacetate, cellulose propionate, nitrocellulose, etc.), styrene-butadiene copolymer, polyester resin, chlorovinyl ether-acrylic acid Ester copolymers, amino resins, various synthetic rubber-based thermoplastic resins and mixtures thereof are used, but fluororesins such as polyvinyl fluoride are particularly preferable.

The thermosetting resin or reactive resin has a molecular weight of 200,000 or less in the state of a coating liquid, and by heating after coating and drying, the molecular weight becomes infinite due to reactions such as condensation and addition. In addition, among these resins,
It is preferable that the resin does not soften or melt before being thermally decomposed.

Specifically, for example, phenol resin, epoxy resin, polyurethane softening type resin, urea resin, melamine resin, alkyd resin, silicon resin, acrylic reaction resin, epoxy-polyamide resin, nitrocellulose melamine resin, high molecular weight polyester resin and isocyanate. Prepolymer mixture, methacrylate copolymer and diisocyanate prepolymer mixture, polyester polyol and polyisocyanate mixture, urea formaldehyde resin, low molecular weight glycol / polymer diol / triphenylmethane triisocyanate mixture, polyamine resin and these Is a mixture of.

Particularly preferred are fibrin resin (nitrified cotton, etc.), vinyl chloride-vinyl acetate-vinyl alcohol copolymer, thermosetting resin composed of a combination of urethane (using a curing agent), or vinyl chloride-vinyl acetate-vinyl alcohol. A radiation-curable resin composed of a copolymer (including a carboxylic acid-introduced product) or an acrylic-modified vinyl chloride-vinyl acetate-vinyl alcohol copolymer (including a carboxylic acid-introduced product) and urethane acrylate. ,
Regarding the radiation-curable resin, in addition to the above-mentioned preferable combinations, acrylic double bonds such as acrylic acid, methacrylic acid, or ester compounds thereof having a radical polymerizable unsaturated double bond, or a diallyl phthalate It is possible to use a resin or the like which contains or introduces into the molecule of a thermoplastic resin a group capable of being crosslinked by irradiation or polymerized and dried, such as an allyl double bond, an unsaturated bond such as maleic acid or a maleic acid derivative. .

Other usable binder components include acrylic acid and methacrylic acid acrylamide as monomers. As the binder having a double bond, various polyesters, polyols, polyurethanes and the like can be modified with a compound having an acrylic double bond. Furthermore, various molecular weights can be prepared by blending a polyhydric alcohol and a polycarboxylic acid, if necessary. The above radiation-sensitive resins are a part of the above, and these can be mixed and used.

The radiation-curable monomer, radiation-curable oligomer and radiation-curable polymer used in the top coat layer of the present invention include acrylic acid and methacrylic acid having an unsaturated double bond which is sensitive to ionization energy and shows radical polymerizability. Alternatively, an acrylic double bond such as an ester compound thereof, an allyl double bond such as diallyl phthalate, a unsaturated double bond such as maleic acid or a maleic acid derivative, which is crosslinked or polymerized by irradiation with radiation, may be a group. Examples thereof include monomers, oligomers and polymers contained or introduced in the molecule.

A compound having a molecular weight of less than 2000 is used as the radiation-curable monomer, and a molecular weight of 2000 to 100 is used as the oligomer.
No. 00 is used.

These include styrene, ethyl acrylate, ethylene glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, diethylene glycol methacrylate, 1,6-hexane glycol diacrylate, 1,6-hexaglycol dimethacrylate, etc., but particularly preferred ones. As, N-vinylpyrrolidone, pentaerythritol tetraacrylate (methacrylate), pentaerythritol acrylate (methacrylate), trimethylolpropane triacrylate (methacrylate), trimethylolpropane diacrylate (methacrylate),
Polyfunctional oligoester acrylate (Aronix M-
7100, M-5400, 5500, 5700, etc., Toa Gosei), urethane elastomer (Nitzporan 4040)
Modified acrylics, or those into which functional groups such as COOH have been introduced, acrylates (methacrylates) of phenol ethylene oxide adducts, acryl groups (methacryl groups) or ε on the pentaerythritol condensed ring represented by the following general formula. -Caprolactone-a compound having an acrylic group, In the formula, a compound of m = 1, a = 2, b = 4 (hereinafter referred to as a special pentaerythritol condensate A), a compound of m = 1, a = 3, b = 3 (hereinafter referred to as a special pentaerythritol condensate B) , M = 1, a = 6, b = 0 compound (hereinafter referred to as special pentaerythritol condensate C), m = 2, a = 6, b = 0 compound (hereinafter referred to as special pentaerythritol condensate D) , And special acrylates represented by the following general formula.

_{1) (CH 2 = CHCOOH 2} ) 3 -CCH 2 OH ( special acrylate _{A) 2) (CH 2 =} CHCOOH 2) 3 -CCH 2 OH 3 ( special acrylate B) 3) [CH ₂ = CHOC (OC ₃ H ₆ ) _n- OCH ₂ ] _3- CCH ₂ CH ₃ (special acrylate C) 4) Five) 6) 7) _{8) CH 2 = CHCOO- (CH} 2 CH 2 O) 4 -COCH = CH 2 ( special acrylate H) 9) Ten) 11) Examples of radiation-curable oligomers include polyfunctional oligoester acrylates represented by the following general formula, acrylic modified urethane elastomers, and those into which a functional group such as COOH is introduced.

By using at least one organic binder of these monomers, oligomers and polymers, the topcoat layer is reinforced, the breaking strength of the coating film is increased, the coating film is reinforced, and the topcoat is less likely to be scraped off and high temperature The drivability under humidity becomes stable. Therefore, it is possible to obtain a magnetic recording medium with less dropout, less head adhesion, less topcoat abrasion, and more stable change in friction. Further, when the radiation-curable binder is used, continuous treatment is possible in the production of the top coat layer and it is possible to perform treatment online, which is useful for energy saving and cost reduction.

The thickness of the top coat layer is preferably 450 Å or less. If it is too thick, scratches will occur. If it is too small, the adsorption of the top coat layer is too weak, and clogging is expected.

A particularly preferable range is 5 to 450 Å, and 10 to 100 Å is more preferable.

On the back surface of the substrate of the video tape of the present invention on which the ferromagnetic metal thin film layer is provided, a back coat layer having θ _{b of} 100 ° or more is provided.

The organic binder used in the back coat layer of the present invention is a thermoplastic resin conventionally used for magnetic recording media,
A thermosetting or reactive resin or a mixture thereof is used, but a curable resin, particularly a radiation curable resin is preferable from the viewpoint of the strength of the resulting coating film.

The thermoplastic resin has a softening temperature of 150 ° C. or lower, an average molecular weight of 10,000 to 200,000, and a polymerization degree of about 200 to
About 2000, for example, vinyl chloride-vinyl acetate copolymer (including carboxylic acid introduced), vinyl chloride-vinyl acetate-vinyl alcohol copolymer (including carboxylic acid introduced), vinyl chloride-chlorinated Vinylidene copolymer, vinyl chloride-acrylonitrile copolymer, acrylic ester-acrylonitrile copolymer, acrylic ester-
Vinylidene chloride copolymer, acrylic ester-styrene copolymer, methacrylic acid ester-acrylonitrile copolymer, methacrylic acid ester-vinyldene chloride copolymer, methacrylic acid ester-styrene copolymer, urethane elastomer, nylon-silicone Resin, nitrocellulose-polyamide resin, polyvinyl fluoride, vinylidene chloride-acrylonitrile copolymer, butadiene-
Acrylonitrile copolymer, polyamide resin, polyvinyl butyral, cellulose derivative (cellulose acetate, cellulose diacetate, cellulose triacetate, cellulose propionate, nitrocellulose, etc.), styrene-butadiene copolymer, polyester resin, chlorovinyl ether-acrylic acid Ester copolymers, amino resins, various synthetic rubber-based thermoplastic resins, and mixtures thereof are used.

The thermosetting resin or reactive resin has a molecular weight of 200,000 or less in the state of a coating liquid, and by heating after coating and drying, the molecular weight becomes infinite due to reactions such as condensation and addition. Further, among these resins, those which do not soften or melt before the resin is thermally decomposed are preferable.

Specifically, for example, phenol resin, epoxy resin, polyurethane curable resin, urea resin, melamine resin, alkyd resin, silicone resin, acrylic resin, acrylic reaction resin, epoxy-polyamide resin, nitrocellulose melamine resin, high molecular weight polyester. Resin / isocyanate prepolymer mixture, methacrylate copolymer / diisocyanate prepolymer mixture, polyester polyol / polyisocyanate mixture, urea formaldehyde resin, low molecular weight glycol / high molecular weight diol / triphenylmethane triisocyanate mixture, polyamine Resins and mixtures thereof.

Particularly preferred are thermosetting resins (using a curing agent) consisting of fibrous resin (nitrified cotton, etc.), vinyl chloride-vinyl acetate-vinyl alcohol copolymer, urethane, or vinyl chloride-vinyl acetate-vinyl alcohol. Copolymers (including carboxylic acid-introduced) or acrylic radiation-modified vinyl chloride-vinyl acetate-vinyl accol copolymers (including carboxylic acid-introduced) and urethane acrylate is there.

Regarding the radiation-curable resin, in addition to the above preferable combinations, acrylic double bonds such as acrylic acid, methacrylic acid or their ester compounds showing an unsaturated double bond having radical polymerizability, such as diallyl phthalate. It is possible to use, for example, a resin containing or introducing a group such as an allylic double bond, an unsaturated bond such as maleic acid or a maleic acid derivative, which is crosslinked or polymerized by irradiation with radiation into the molecule of the thermoplastic resin.

Other usable binder components include acrylic acid, methacrylic acid and acrylamide as monomers.

As the binder having a double bond, various polyesters, polyols, polyurethanes and the like can be modified with a compound having an acrylic double bond. Further, if necessary, a polyhydric alcohol and a polycarboxylic acid may be mixed to obtain various molecular weights.

The above radiation-sensitive resins are a part of the above, and these can be mixed and used.

More preferred is (A) a plastic compound having a molecular weight of 5,000 to 100,000 having two or more unsaturated double bonds curable by radiation, and (B) one unsaturated double bond curable by radiation. A rubber-like compound having a molecular weight of 3,000 to 100,000, which has at least one or no radiation curability, and (C) a compound having a molecular weight of 200 to 3,000, which has at least one unsaturated double bond curable by radiation. , (A) 20 to 70% by weight, (B) 20 to 80% by weight, and (C) 10 to 40% by weight.

This increases the breaking strength of the coating film, strengthening the coating film, less backcoat abrasion, less transfer of the inorganic filler powder from the backcoat layer to the magnetic layer, and less dropout, and roll-shaped. It is possible to obtain a magnetic recording medium having uniform properties in the length direction, which is free from winding tightness when cured in a wound form.

The ferromagnetic metal thin film layer as the magnetic layer in the present invention is C
o is the main component, O is included in this, and if necessary N
It has a composition containing i and / or Cr.

That is, in a preferred embodiment, it may consist of Co alone or Co and Ni. When Ni is contained, the weight ratio Co / Ni is preferably 1.5 or more.

Further, Cr may be contained in the ferromagnetic metal thin film layer.

When Cr is contained, electromagnetic conversion characteristics are improved, output and S / N ratio are improved, and film strength is also improved.

In such a case, Cr / Co or Cr / (Co + N
The weight ratio of i) is 0.001-0.1, more preferably,
It is preferably 0.005 to 0.05.

Further, O is contained in the ferromagnetic metal thin film.

The average oxygen content in the ferromagnetic metal thin film is the atomic ratio, especially O /
The atomic ratio of (Co or Co + Ni) is preferably 0.5 or less, more preferably 0.05 to 0.5.

In this case, oxygen forms an oxide with the ferromagnetic metal (Co, NI) on the surface of the ferromagnetic metal thin film layer.

That is, a peak showing an oxide is recognized by Auger spectroscopic analysis in the surface portion, particularly in the range of 50 to 500 Å, more preferably 50 to 200 Å from the surface. The oxygen content of this oxide layer is about 0.5 to 1.0 in atomic ratio.

In such a ferromagnetic metal thin film, other trace components, especially transition elements such as Fe, Mn, V, Zr,
Nb, Ta, Ti, Zn, Mo, W, Cu, etc. may be contained.

In a preferred embodiment, such a ferromagnetic metal thin film layer is composed of an aggregate of columnar crystal grains containing Co as the main component.

In this case, the thickness of the ferromagnetic metal thin film layer is 0.05 to 0.
The thickness is 5 μm, preferably 0.07 to 0.3 μm.

The columnar crystal grains have a length extending over almost the entire area in the thickness direction of the thin film, and the longitudinal direction is inclined in the range of 10 to 70 ° with respect to the normal line of the main surface of the substrate. Is preferred.

It should be noted that oxygen is present in the form of a compound on the surface of the columnar crystal grains in the surface portion as described above.

Further, there is no particular limitation on the oxygen concentration gradient of the ferromagnetic metal thin film layer.

Further, the minor axis of the crystal grains preferably has a length of about 50 to 500 Å.

The substrate on which such a ferromagnetic metal thin film layer is formed is not particularly limited as long as it is a non-magnetic substrate, but a particularly flexible substrate, particularly a resin such as polyester or polyimide is preferable. preferable.

The thickness may be various, but especially 5
It is preferably ˜20 μm.

If necessary, various known underlayers may be interposed between the substrate and the ferromagnetic metal thin film layer.

If necessary, the ferromagnetic metal thin film layer may be divided into a plurality of layers, and the non-ferromagnetic metal thin film layer may be interposed therebetween.

In the present invention, the magnetic layer may be formed by electrolytic vapor deposition, ion plating, plating or the like, but it is preferably formed by a so-called oblique vapor deposition method.

In this case, the minimum value of the incident angle of the vapor deposition substance with respect to the normal to the substrate is preferably 20 ° or more.

If the incident angle is less than 20 °, the electromagnetic conversion characteristics deteriorate.

The vapor deposition atmosphere is usually an atmosphere containing oxygen gas in an inert atmosphere such as argon, helium, or vacuum.
And ^-5 to 10 0 ^Pa pressure of about, also deposition distance, the substrate transport direction, the structure of the can and the mask, arrangement and the like may be the same as known conditions.

Then, a metal oxide film is formed on the surface by vapor deposition in an oxygen atmosphere. The oxygen gas partial pressure at which the metal oxide is formed can be easily obtained from experiments.

Various oxidation treatments can be performed to form a metal oxide film on the surface.

The following oxidation treatments can be applied.

1) Dry treatment a. Energetic Particle Treatment As described in Japanese Patent Application No. 58-76640, in the latter stage of vapor deposition, oxygen is energized to the magnetic layer as energetic particles by an ion gun or a neutral gun.

b. Glow treatment O ₂ , H ₂ O, O ₂ + H ₂ O and the like and an inert gas such as Ar and N ₂ are used to glow discharge this to generate plasma, and the surface of the magnetic film is exposed to this plasma. .

c. Oxidizing gas A gas that blows an oxidizing gas such as ozone or heated steam.

d. Heat treatment A substance that is oxidized by heating. Heating temperature is 60-150
℃ degree.

2) Wet treatment a. Anodization b. Alkaline treatment c. Acid treatment Chromate treatment, permanganate treatment, phosphate treatment, etc. are used.

d. Oxidant treatment H ₂ O ₂ or the like is used.

According to the present invention, the running property under high temperature and high humidity is improved, noise is reduced, and the C / N ratio is improved. Further, the running property after storage under high temperature and high humidity is stable, the still characteristics are not deteriorated, and the head clogging can be prevented.

VI Specific Examples of the Invention Hereinafter, specific examples of the present invention will be shown to explain the effects of the present invention in more detail.

Example A magnetic thin film layer having a thickness of 0.15 μm was formed on a polyester film substrate (thickness: 12 μm) by an oblique vapor deposition method using an alloy having a Co / Ni weight ratio of 4/1.

The substrate is continuously transported by a can, and the incident angle of the vapor deposition substance is set to 90.
It gradually decreased from °. The distance between the evaporation source and the can is 200 mm.
And

Then, the vapor deposition was performed in an atmosphere in which P _Ar = 5 × 10 ⁻³ Pa and P ₀₂ = 2 × 10 ⁻¹ Pa oxygen were introduced into this.

A 40 Å top coat layer was formed on the surface of the magnetic thin film layer as shown below.

Topcoat layer formation Topcoat 1 part by weight Butyl (2) hydroxymethacrylate phosphate (mixture of mono and di) 2 Fluorine-modified silicone stearate 0.8 MEK 100 Apply the above mixture of topcoat composition to the ferromagnetic thin film layer. , Electrocurtain type electron beam accelerator, acceleration voltage 150KeV, electrode current 60mA, absorbed dose 3Mra
EB irradiation was performed in d and N ₂ gas to form a top coat layer.

Topcoat 2 The topcoat layer was formed under the same conditions except that the fluorine-modified silicone stearate of Topcoat 1 was 0.4 parts by weight.

Topcoat 3 parts by weight 2,6 di-tert-butyl p-cresol 0.4 pentaerythritol tetraacrylate (molecular weight 352) 0.6 myristic acid-modified silicone 0.5 oleic acid-modified silicone 0.5 butyl myristate 0.1 MEK 100 A topcoat layer was formed in the same manner as in Topcoat 1 using the above topcoat composition.

Topcoat 4 A topcoat layer was formed under the same conditions except that the myristic acid-modified silicone and oleic acid-modified silicone of Topcoat 3 were both 0.4 parts by weight.

5 parts by weight of top coat Dimethylaminoethyl methacrylate 0.5 stearic acid 0.5 MEK / toluene (1/1) 100 Using the above top coat composition, a top coat layer was formed in the same manner as in top coat 1.

Topcoat 6 parts by weight Dimethylaminoethyl methacrylate 0.5 Stearic acid 0.3 MEK / toluene (1/1) 100 Using the above topcoat composition, a topcoat layer was formed in the same manner as in Topcoat 1.

Top coat 7 The top coat layer was formed under the same conditions except that the stearic acid of the top coat 6 was 0.1 part by weight.

Further, a 1 μm back coat layer was formed on the back surface of the substrate on which the magnetic thin film layer was formed, as described below.

Formation of backcoat layer 1 part by weight of backcoat Zinc sulfide (particle size 50 nm) 30 Carbon black (particle size 25 nm) 25 Acrylic modified vinyl chloride-vinyl acetate vinyl alcohol copolymer (molecular weight 30000) 40 Acrylic modified polyurethane elastomer (molecular weight 20000) ) 40 polyfunctional acrylate (molecular weight 10,000) 20 oleic acid 4 stearyl methacrylate 2 MIBK / toluene (1/1) 250 The above mixture was dispersed in a ball mill for 5 hours, and the back surface of the polyester film on which the magnetic thin film layer and the top coat layer were formed. To a dry thickness of 1 μm and use an electron curtain type electron beam accelerator to accelerate at an acceleration voltage of 150 Ke.
V, electrode current 10mA, absorbed dose 5Mrad, E in N ₂ gas
B irradiation was performed to form a back coat layer.

Backcoat 2 A backcoat layer was formed under the same conditions except that the oleic acid of the backcoat 1 was 2 parts by weight and the stearyl methacrylate was 1 part by weight.

Backcoat 3 parts by weight Carbon black (particle size 100 nm) 50 Acrylic modified vinyl chloride-vinyl acetate-Vinyl alcohol Copolymer (molecular weight 45000) 50 Acrylic modified polyurethane elastomer (molecular weight 5000) 50 Stearic acid 4 Butyl stearate 4 MIBK / toluene ( 1/1) 300 A back coat layer was formed in the same manner as the back coat 1 using the above back coat composition.

Backcoat 4 A backcoat layer was formed under the same conditions except that the amount of both stearic acid and butyl stearate in Backcoat 3 was 2 parts by weight.

Backcoat 5 A backcoat layer was formed under the same conditions except that the amount of both stearic acid and butyl stearate in Backcoat 3 was 1 part by weight.

Backcoat 6 parts by weight Zinc oxide (particle size 80 nm) 200 Nitrified cotton 20 PVC-vinyl acetate-Vinyl alcohol copolymer (Sekisui Chemical Co., Ltd. Eleks A) 30 Polyurethane elastomer 30 (BF Goodrich, Essen 5703) Stearic acid Modified Silicone 4 Butyl Stearate 2 Hardener 20 (Nippon Polyurethane, Coronate L) MEBK / Toluene (1/1) 250 Dissolve the above mixture well and dry it on the back surface of the polyester film on which the magnetic thin film and the top coat layer are formed. Thickness 1 μm
So that the solvent becomes dry and the solvent is dried with hot air,
The surface was smoothed and kept in a roll state for 48 hours in an oven kept at 80 ° C. to accelerate the crosslinking reaction by isocyanate.

Backcoat 7 The backcoat layer was formed under the same conditions as in Backcoat 5 except that 2 parts by weight of stearic acid-modified silicone of backcoat 6 and 1 part by weight of butyl stearate were used.

Using the above magnetic thin film, top coat film and back coat film, the magnetic tapes prepared were cut into a width of 8 mm to prepare samples 1 to 13 shown in Table 1.

The contact angles with water on the surfaces of the top coat film and the back coat film are also shown in Table 1.

The following characteristics of each sample were measured with an 8-mm video deck.

The magnetic head used had a gap length of 0.25 μm,
The track length is 20 μm.

In this case, the core halves 21 and 22 are made of ferrite, and the gap end faces are made of Co and have a thickness of 3 μm.
0.8, Ni 0.1, Zr 0.1 (atomic ratio), and the gap material was glass.

(1) Still characteristic A still characteristic was measured by recording a signal of 5 MHz, reproducing it in a still state, and measuring the time until the output level became half of that at the start.

(2) Modulation noise A 5 MHz signal was recorded, and the relative value of the output level of the reproduction output at 4 MHz was used as the modulation noise.

(3) Clogging Using a video tape for 30 minutes of recording time, the number of clogging per 10 passes was measured.

The results are shown in Table 1.

Here, the initial means the measurement result immediately after the preparation of the sample, and the after storage means the result measured after being stored at 40 ° C. and 80% RH for 48 hours and then left at room temperature for 5 hours.

From the results shown in Table 1, the effect of the present invention is clear.

Claims (3)

[Claims] 1. A flexible substrate has a ferromagnetic metal thin film layer containing Co as a main component on one surface thereof, a top coat layer on the surface of the ferromagnetic metal thin film layer, and further on the other surface of the substrate. Has a back coat layer, and the contact angle with water on the surface of the top coat layer is θ _t ,
When the contact angle of water on the surface of the back coat layer is θ _b , 100 ° ≦ θ _t ≦ 140 °, 100 ° ≦ θ _b ≦ 140 ° and | θ _t −θ _b | ≦ 10 ° are regulated to be still. Video tape with improved characteristics. 2. The video tape according to claim 1, wherein the ferromagnetic metal thin film layer contains oxygen. 3. The video tape according to claim 1, wherein the flexible substrate is made of a polymer.