GB2102305A - Magnetic recording medium and process for producing the same - Google Patents

Abstract

A magnetic recording medium comprises a non-magnetic support, e.g. polyethylene terephthalate, coated with a thin layer of ferromagnetic Fe, Co or Ni or ferromagnetic alloy, and on at least one surface a layer of an epoxy resin formed by curing a two-part composition, usually a condensate of bisphenol A and epichlorohydrin, having an epoxy equivalent of 400 to 3,000, together with a curing agent. Another polymer (cellulose derivative, polyurethane or vinyl polymer) may be present in the layer. The resin layer preferably contains or is coated with a lubricant, e.g. an aliphatic acid or amide or ester thereof, higher alcohol or metal soap. The medium can be used for video recording; it has good running properties, wear resistance and electro-to-magnetic conversion.

Description

SPECIFICATION Magnetic recording medium and process for producing the same The present invention relates to a magnetic recording medium comprising a thin magnetic film as a magnetic recording layer and to a process for producing the same, more particularly, to a magnetic recording medium of the thin metal film type having good running properties, wear resistance and electro-to-magnetic conversion characteristics and to a process for producing the same.

Most conventional magnetic recording media are of the coated type which are produced by dispersing particles of magnetic oxides or ferromagnetic alloys, such as y-Fe2O3, Co-doped y-Fe203, Fe304, Co-doped Fe304, a Berthollide compound of y-Fe2O3 and Fe304 or CrO2, in an organic binder, such as a vinyl chloride/vinyl acetate copolymer, a styrene/butadiene copolymer, an epoxy resin or a polyurethane resin, applying the resulting coating composition onto a non-magnetic base and drying the coating.

However, with the recent increasing demand for higher density recording, researchers' attention has been drawn to magnetic recording media of the thin metal film type that comprise a thin ferromagnetic metal film as a magnetic recording layer, the layer being formed by a vapor deposition technique such as vacuum deposition, sputtering or ion plating, or a plating technique such as electroplating or electroless plating. Various efforts are being made to use such recording medium on a commercial scale.

Most magnetic recording media of the coated type use a metal oxide with low saturation magnetization as a magnetic material, so attempts to achieve high density recording using a thinner magnetic recording medium results in a decreased signal output. However, with magnetic recording media of the thin metal film type, a very thin magnetic recording layer can be formed using a ferromagnetic metal having a higher saturation magnetization than with a magnetic oxide without using a non-magnetic material such as binder, and such thinness is advantageous to provide good electro-to-magnetic conversion characteristics.However, such thin metal film type magnetic recording media have their own problems: (1) high friction against a magnetic head, guide poles or other transport means when run to record, reproduce or erase magnetic signals, i.e., the same wear easily; (2) easily attacked by corrosive environments; and (3) the magnetic recording layer thereof may be damaged by impact during handling.

Some attempts have been made to solve these problems by forming a protective layer on a magnetic recording media of the thin metal film type. One such proposal is described in Japanese Patent Application (OPI) 75001/75 (the term OPI as used herein means an unexamined published Japanese Patent Application) wherein a thin lubricant layer is formed on the thin metal film. According to this proposal, the coefficient of friction between the magnetic head or guide poles and the thin metal film is reduced to provide a tape that runs consistently and which is unlikely to be abraded. However, these advantages are quickly lost if the tape is used repeatedly.

Another method is described in Japanese Patent Applications (OPI) 39708/78 and 40505/78 wherein a lubricant protective layer made of a metal or metal oxide is formed on the thin metal film; however, even in this case the effect of the protective layer does not last long and, as the tape is repeatedly used, the friction coefficient increases rapidly or the thin magnetic metal film breaks.

Still another method is described in Japanese Patent Application (OPI) 155010/79 wherein an overcoat of a high molecular weight film is formed on the metal film; however, if the overcoat is made of a vinylidene chloride/acrylic ester copolymer or some other known high molecular weight substance, the resulting film thickness is at least about 0.2 m which causes spacing loss which, in turn, leads to reduced output in high density recording.

To achieve high density recording, most thin magnetic metal films are supported on a very smooth base, but no matter how smooth the base surface is, none of the lubricating methods described above can provide a magnetic recording medium having good running properties especially in very humid atmospheres, or high wear resistance.

Therefore, one object of the present invention is to provide a magnetic recording medium of the thin metal film type that has good running properties, wear resistance and electro-to-magnetic conversion characteristics.

Another object of the present invention is to provide a magnetic recording medium of the thin metal film type that retains good running properties and wear resistance for an extended period of time.

The present inventors have found that these objects can be attained by forming a thin film of a two-part epoxy resin, most preferably a thin cured epoxy resin film comprising an epoxy resin of formula (I) as later described, and a curing agent, on either the thin magnetic metal film or the surface of the non-magnetic base opposite the thin magnetic metal film or both. The epoxy resin preferably has an epoxy equivalent of from 400 to 3,000 and the curing agent is preferably an aliphatic amine having two or more amino groups and three or more amino active hydrogen atoms in the molecular chain.

The resulting magnetic recording medium has good electro-to-magnetic conversion characteristics, as well as good running properties, wear resistance and abrasion resistance, and, at the same time, these properties are exhibited for an extended period.

The present inventors have also found that better results are obtained by incorporating a lubricant in the thin film of the two part epoxy resin or forming a lubricant layer thereon.

The thin magnetic metal film used in the present invention can be formed by vapor deposition or plating; vapor deposition is preferred since it yields the desired thin metal film and involves simple manufacturing steps without effluent treatment. Vapor deposition is a process in which a substance or its compound is heated in a gaseous or vacuum enclosure until its vapor or ionized vapor condenses on the surface of a substrate, and among variations of this process are vacuum vapor deposition, sputtering, ion plating and chemical vapor phase plating.

The magnetic recording layer used in the present invention is a thin film that is formed by vapor deposition or plating of a ferromagnetic metal such as iron, cobalt or nickel, or a ferromagnetic alloy such as Fe-Co, Fe-Ni, Co-Ni, Fe-Si, Fe-Rh, Co-P, Co-B, Co-Si, Co-V, Co-Y, Co-La, Co-Ce, Co-Pr, Co-Sm, Co-Pt, Co-Mn, Fe-Co-Ni, Co-Ni-P, Co-Ni-B, Co-Ni-Ag, Co-Ni-Na, Co-Ni-Ce, Co-Ni-Zn, Co-Ni-Cu, Co-Ni W, Co-Ni-Re, or Co-Sm-Cu. The thickness of the layer as used in the magnetic recording medium is preferably in the range of from 0.05 to 2 ym, more preferably from 0.1 to 0.4,um.

The thin resin layer formed on either the thin magnetic metal film or the surface of the nonmagnetic base opposite the metal film or both is made of an epoxy resin that forms a threedimensional network structure (cross-linked structure) upon addition of a curing agent. Generally, a condensate of bisphenol A and epichlorohydrin having the following basic structure (I) is used:

Other epoxy resins that can be used in the present invention include those of the halogenated bisphenol type, resorcin type, bisphenol F type, tetrahydroxyphenylethane type, novolak type, polyalcohol/polyglycol type, glycerin triether type, polyolefin type and bisphenol A type. These resins may be used alone or in combination.

The epoxy resin used in the present invention preferably has an epoxy equivalent of from 400 to 3,000. An epoxy resin having an epoxy equivalent of less than 400 is liquid at ordinary temperatures, so the base having an epoxy resin layer formed on the thin magnetic metal film and/or on the base itself cannot be wound up before the resin layer is cured. An epoxy resin having an epoxy equivalent of more than 3,000 softens when a roll of the base having such a layer is heat cured, and blocking occurs at the interface between the epoxy layer on the metal film or the epoxy layer on the base. This makes it difficult to produce a long tape.

A preferred feature of the process of making the medium is to incorporate a curing agent in the epoxy resin to cure the same and form an insoluble and infusible resin layer. The curing agent is an aliphatic amine containing two or more amino groups and three or more amino active hydrogen atoms in its molecular chain. An aliphatic amine containing three or four amino groups and three or more amino active hydrogen atoms is preferred. Examples of such preferred amines are diethylenetriamine, N-amino-ethylpiperazine, triethylenetetramine, dipropylenetriamine, tri( 1 ,2-propylene)tetramine and bis(hexamethylene)triamine.Aliphatic amines having a molecular weight of more than 150 such as diethylenetriamine, N-aminoethylpiperazine, triethylenetetramine and dipropylenetriamine are particularly preferred. These desired amines may be used either alone or in combination. The most desired curing speed or a protective resin layer having most superior strength is obtained with amines as mentioned above.

The protective resin layer may contain 0.2 to 30 wt%, based on the resin, of a polymer such as a cellulose derivative, polyurethane or vinyl polymer to modify the physical properties of the surface of the resin layer. If more than 30 wt% of the polymer is used, one of the objects of the present invention, i.e, good tape wear resistance, is not effectively obtained.

An insoluble and infusible layer can be formed by curing the epoxy coating; and a suitable curing method can be used, such as addition of a curing agent (e.g. organic polyamine, organic acid, amino resin, phenolic resin, and isocyanate), or esterification with an aliphatic acid or modification with an alkyd resin.

The non-magnetic base on which the thin magnetic metal film is formed is generally made of a polyester film. Since polyester films deform or shrink at temperatures higher than 1 SOC C, the epoxy resin layer must be cured at temperatures not exceeding 1 500C. This requirement can be met by using an organic polyamine or isocyanate as a curing agent.Suitable organic polyamines include an aliphatic amine such as diethylenetriamine, triethylenetetramine, tetraethylenepentamine, diethylaminopropylamine or N-aminoethylpiperazine; an internal amine adduct or separable amine adduct; a polyamide resin; an aromatic amine such as metaphenylenediamine or diaminodiphenylsulfone; a complex amine compound such as dicyandiamide, xylylenediamine, tris(dimethylaminomethyl)phenol or benzyldimethylamine; and an amine salt such as tris(dimethylaminomethyl)phenol triacetate. These organic amines may be used either alone or in combination.

Illustrative isocyanates are a divalent isocyanate such as tolylene diisocyanate, 4,4'diphenyimethane diisocyanate or hexamethylene diisocyanate; a trivalent isocyanate such as triphenylmethane triisocyanate; and a polyvalent isocyanate such as an adduct of trimethylol propane or pentaerythritol and a diva lent isocyanate, e.g., tolylene diisocyanate or diphenylmethane diisocyanate. These isocyanate compounds may also be used either alone or in combination.

The objects of the present invention can be achieved more effectively by incorporating a lubricant in the resin layer or forming a lubricant layer on the resin layer. Suitable lubricants are aliphatic acids, metal soaps, aliphatic acid amides, aliphatic acid esters, mineral oils, animal oils such as whale oil, vegetable oils, higher alcohols, and silicone oils; electrically conducting fine particulate materials such as graphite; inorganic fine particulate materials such as molybdenum disulfide, and tungsten disulfide; fine particles of plastics such as polyethylene, polypropylene, polyethylene/vinyl chloride copolymers and polytetrafluoroethylene; a-olefin polymers; unsaturated aliphatic hydrocarbons that are liquid at ordinary temperatures (i.e. those compounds having an n-olefin double bond attached to a terminal carbon atom), fluorocarbons and mixtures thereof.

Aliphatic acids, metal soaps, aliphatic acid amides, aliphatic acid esters, higher alcohols and mixtures thereof are preferred, and aliphatic acids having 10 or more carbon atoms are particularly preferred.

In addition to the lubricant, a corrosion inhibitor or a mold inhibitor which is well known in the art may be used as desired.

A thin epoxy resin film can be formed on either the thin magnetic metal film or the non-magnetic base, or both by any suitable method, for example, by applying a solution of the epoxy resin and curing agent in an organic solvent onto the metal film and/or base and drying the same, or by applying a solution of the epoxy resin in an organic solvent and a solution of the curing agent in an organic solvent, one on the other, and drying the respective coatings.

Theoretically, the primary or secondary amine may be used as a curing agent in such an amount that it contains amino active hydrogen in a chemically equivalent amount to the epoxy groups in the epoxy resin while if the curing agent is an isocyanate compound, it may be used in such an amount that it contains -NCO groups in a chemically equivalent amount to the hydroxyl groups in the epoxy resin.

In practice, however, the primary or secondary amine is used in an amount equal to the chemical equivalent thereof +50% to compensate for evaporation during the subsequent drying step or for modifying the physical properties of the resin layer. The amount of the isocyanate compound can also be varied to suit the desired purpose. The tertiary amine may be used in a catalytic amount of 5 to 15 phr. Any amount of polyamide resin can be used, but practical purposes, it is generally used in an amount of from 30 to 300 wt% of the epoxy resin.

The concentration of the coating solution(s) is preferably in the range of from 0.05 to 5 wt%, and the solution is/are applied to the thin metal film and/or base in such an amount that the dry thickness of the film(s) is preferably in the range of from 5 to 1000 A, more preferably from 10 to 500 A, most preferably from 20 to 200 A.

Examples of the organic solvent in which the epoxy resin and/or curing agent is/are dissolved include ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and diacetone alcohol; esters such as methyl acetate, ethyl acetate, butyl acetate and glycol acetate monoethyl ether; glycol ethers such as glycol monoethyl ether and glycol monobutyl ether; aromatic hydrocarbons such as toluene and xylene; alcohols such as propanol and butanol; and chlorinated hydrocarbons such as methylene chloride and ethylene chloride. Alcohols are not used if the curing agent is an isocyanate compound.

When an organic polyamine compound is used as a curing agent, an alcohol or phenol (or water, as the case may be) used in a small amount accelerate the curing reaction. The preferred amount of alcohol or phenol (or water) used is 2 to 300 wt% based on the weight of the curing agent. The effect of accelerating the curing reaction is caused by a ring-opening reaction of hydrogen bonding between the hydrogen atom of hydroxyl groups thereof and the epoxy groups. Specifically, phenols tend to form the hydrogen bonding, and so the curing reaction using amine is remarkably accelerated with phenols.

To compensate for evaporation during the subsequent drying step or to modify the physical properties of the resin layer, the amount of the curing agent amine added may be varied, but, preferably, it is used in an amount that satisfies the following relation: 100a 100 a 0.5x < y < 1.5x x E x.E wherein y=the amount of curing agent amine (g) per 100 g of the epoxy resin; a=the molecular weight of the curing agent amine; x=the number of amino active hydrogen atoms in the curing agent amine; E=the epoxy equivalent of the epoxy resin.

If the curing agent is used in an amount of less than the lower limit, curing sufficient to provide a satisfactory protective layer is not achieved, while if it is used in an amount exceeding the upper limit, excess amine is emitted into air during the curing step or free amine will remain in the resin layer.

The epoxy resin layer containing the curing agent is dried and cured at a temperature higher than 1 50C, and the curing can be completed in a very short period by using a curing temperature higher than 300 C. The preferred curing temperature is higher than 300C and lower than the glass transition point of the base plus 300C.

The lubricant can be incorporated in the epoxy resin layer or can be formed as a layer on the resin layer by any suitable method, for example, by applying a solution of the epoxy resin, curing agent and lubricant in an organic solvent as earlier exemplified onto the thin metal film and/or base; by first forming a dry thin layer of the epoxy resin and curing agent in the manner earlier described and then applying a solution of the lubricant in an organic solvent onto the resin film; or by first forming a cured thin layer of epoxy resin and curing agent in the manner earlier described and then applying a solution of the lubricant in an organic solvent onto the resin film; or by any of the methods of vapor deposition described before.

Examples of the solvent used for application of the lubricant layer include ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone and cyclohexanone; alcohols having 1 to 1 0 carbon atoms such as methanol, ethanol propanol and butanol; esters such as methyl acetate, ethyl acetate, butyl acetate, ethyl lactate, and glycol acetate monoethyl ether; ether and glycol ethers such as glycol dimethyl ether, glycol monoethyl ether and dioxane; hydrocarbons such as pentane, hexane, heptane, octane, nonane and decane; tars (aromatic hydrocarbons) such as benzene, toluene and xylene; and chlorinated hydrocarbons such as methylene chloride, ethylene chloride, carbon tetrachloride, chloroform, ethylene chlorohydrin and dichlorobenzene.

The lubricant is generally used in a dry weight of from 2 to 100 mg/m2, preferably from 2 to 50 mg/m2, more preferably from 2 to 20 mg/m2 whether in layer form alone or in the epoxy layer. If the amount of the lubricant is less than 2 mg/m2, the desired consistent tape running is not obtained, while if the amount is more than 100 mg/m2, it fouls the magnetic head or guide poles on the video deck.

The recording medium of the present invention provides the following advantages: (1) When it is used on a tape deck, it undergoes only a small increase in dynamic friction coefficient. This means the medium is stable to repeated running and has very high wear resistance; (2) It retains high stability to repeated running even when it has a very smooth thin magnetic metal film and base; (3) It has a low dynamic friction coefficient and runs smoothly in humid atmospheres; (4) The epoxy resin layer does not reduce the electro-to-magnetic conversion characteristics of the magnetic recording medium of thin metal film type in which it is used; and (5) The epoxy resin layer is not substantially susceptible to corrosive attack in humid conditions and causes no reduction in the electro-to-magnetic conversion characteristics.

The present invention will now be described in greater detail by reference to the following examples and comparative examples which are given here for illustrative purposes. In the examples and comparative examples, all parts are by weight.

Example 1 A magnetic cobalt film (0.2 FL thick) was formed on a polyethylene terephthalate (PET) film (20,u thick); electron beams were used to condense vapor of cobalt (99.95% purity) which was directed onto the PET film at an angle of incidence of 700 at a pressure of 5x 10-5 Torr. A polymer coating solution I of the formulation indicated below was applied onto the Co film and the base film in a dry thickness of 100 A, dried at 300C for 10 seconds, cured at 230C for 40 hours and heated at 800C for 24 hours to provide magnetic tape A.

Polymer Coating Solution I Epikote 1009 (epoxy resin from Shell International Chemicals Corp.) 1.0 part Triethylenetetramine 0.01 part Methylene chloride 100.0 parts A lubricant coating solution ll of the formulation indicated below was applied onto the epoxy resin film of the above magnetic tape A in a weight of 10 mg/m2 and dried at 500C for 10 seconds. The dried film was slit into a video tape 1/2 inch wide which was referred to as Sample No. 1.

Lubricant Coating Solution II Myristic acid 1.0 part n-Hexane 200 parts Comparative Example 1 A video tape was prepared as in Example 1 except that the Co magnetic film was simply formed on the PET base by oblique deposition without forming an epoxy resin film or a lubricant layer. The tape was referred to as Sample C-i.

Comparative Example 2 A video tape 1/2 inch wide was prepared as in Example 1 except that only lubricant coating solution II was applied to a Co magnetic film. The magnetic surface of the tape was referred to as Sample C-2.

The three samples were subjected to the following film durability (wear resistance) test and measurement of dynamic friction coefficient.

(1) Durability Durability of a magnetic thin film was determined when pressing a magnetic tape against a magnetic head at a tension of 90 g/ inch and reciprocating at 38 cm/sec 500 times.

The number of visually observed abrasions that were formed on the tape surface was counted.

(2) Measurement of dynamic friction coefficient The magnetic tape was reciprocated on a VHS video tape recorder (Maclord 88, Model NV-8800, of Matsushita Electric Industrial Co., Ltd.) once, 20 times, 100 times and 500 times, and the change in the dynamic friction coefficient (y) was examined by the formula T2/T1=e wherein T1 was the tape tension at the supply side of the rotary cylinder and T2 was the tape tension at the takeup side.

The test and measurement results are shown in Table 1. For the surface of the base, only measurement of dynamic friction coefficient was conducted with the tape of Example 1 and that of Comparative Example 1. The surfaces of the respective bases were referred to as Sample No. 2 and C3. The results are also shown in Table 1.

Table 1 (2) Change in dynamic friction coefficient (1) Abrasion Sample Sliding after 500 1 No. face Polymer film Lubricant reciprocations Frecip. J 20 100 500 No. 1 Magnetic Epikote 1009 myristic no abrasion 0.29 0.30 0.32 0.34 surface triethylene- acid tetramine No. 2 Base do do - 0.30 0.30 0.31 0.35 surface C-1 Magnetic - - More than 10 0.48 0.55 0.58 0.67 surface deep abrasions C-2 do - do do 0.30 0.33 0.41 0.48 C-3 Base - 0.35 0.40 0.57 0.59 surface As the data in Table 1 show, the magnetic recording medium of the thin metal film type according to the present invention has very good running properties and wear resistance. Furthermore, the improvement in these properties is retained for an extended period of time. For this reason, the medium is a product having high commercial value.

Example 2 A magnetic cobalt film (0.2 Mm thick) was formed on a polyethylene terephthalate film (20 ym thick); electron beams were used to condense vapor of cobalt (99.95% purity) which was directed onto the PET film at an angle of incidence of 70C at a pressure of 5x1 0-5 Torr. A polymer coating solution X-l of the formulation indicated below was applied onto both the Co film and the base film, each layer thereof having a dry thickness of 100 A. The thus coated web was wound up into a roll, cured at 230C for 40 hours and heated at 800C for 24 hours to provide magnetic tape X-A.

Polymer Coating Solution X-l Epoxy resin (of bisphenol A/glycidyl ether type with an epoxy equivalent of 450500) 1.0 part Diethylenetriamine 0.05 part Methylene chloride 100.0 parts A lubricant coating solution X-ll of the formulation indicated below was applied onto the cured epoxy resin film of the above magnetic tape X-A in a weight of 10 mg/m2 and dried at 500C for 10 seconds. The dried film was slit into a video tape 1/2 inch wide which was referred to as Sample No. X1. The surface of the base opposite the Co film was referred to as Sample No. X-1 '.

Lubricant Coating Solution X-ll Myristic acid 1.0 part n-Hexane 200 parts Example 3 A web was prepared as in Example 2 except that polymer coating solution X-l was replaced by polymer coating solution X-lil of the formulation indicated below. The thus coated web was wound into a roll which was cured at 230C for 40 hours and heated at 800C for 24 hours to provide magnetic tape X-B. There was partial blocking at the interface of the epoxy layer on the thin metal film and the epoxy layer on the base. Lubricant coating solution X-ll was applied on each epoxy resin coating in a same weight as in Example 2 and treated as in Example 2 to provide a video tape 1/2 inch wide which was referred to as Sample No. X-2.

Polymer Coating Solution X-lll Epoxy resin (of bisphenol A/lycidyl ether type with an epoxy equivalent of 450~500) 1.0 part Diethylenetriamine 0.018 part Methylene chloride 100 parts Comparative Example 3 A magnetic tape X-C was prepared as in Example 2 except that polymer coating solution X-l was replaced by polymer coating solution X-IV of the formulation indicated below. Blocking occurred in a fairly large area at the interface of the epoxy layer on the thin metal film and the epoxy layer on the base, and this made subsequent evaluation of the properties of the tape impossible.

Polymer Coating Solution X-IV Epoxy resin (of bisphenol A/glycidyl ether type with an epoxy equivalent of 3300) 1.0 part Diethylenetriamine 0.008 part Methylene chloride 100 parts Comparative Example 4 A magnetic tape X-D was prepared as in Example 2 except that polymer coating solution X-l was replaced by polymer coating solution X-V of the formulation indicated below. Partial blocking occurred at the interface of the epoxy layer on the thin metal film and the epoxy layer on the base. A lubricant coating solution X-ll was applied onto each epoxy resin coating in a same weight as in Example 2 and treated as in Example 2 to provide a video tape 1/2 inch wide which was referred to as Sample X-R-2.

Polymer Coating Solution X-V Epoxy resin (of bisphenol A/glycidyl ether type with an epoxy equivalent of 450500) 1.0 part Diethylaminopropylamine 0.15 part Methylene chloride 100 parts Comparative Example 5 A magnetic tape X-E was prepared as in Example 2 except that polymer coating solution X-l was replaced by polymer coating solution X-VI of the formulation indicated below. Lubricant coating solution X-ll was applied onto each epoxy resin coating in a same weight as in Example 2 and treated as in Example 2 to provide a video tape 1/2 inch wide which was referred to as Sample X-R-3.

Polymer Coating Solution X-VI Vinylidene chloride/acrylic acid ester copolymer 1.0 part Methyl ethyl ketone 200 parts Comparative Example 6 A video tape Sample X-R-4 was prepared as in Example 2 except that the Co magnetic film was simply formed on the PET base by oblique deposition without forming an epoxy resin film or lubricant layer. The base surface of the Sample X-R-4 was referred to as Sample X-R-4'.

All samples except for Sample No. X-1 ' and X-R-4' were subjected to the following film durability (wear resistance) test and measurement of dynamic friction coefficient. For Sample No. X-1 ' and X-R4', only measurement of dynamic friction coefficient was conducted.

(1) Durability Durability of a magnetic thin film was determined when pressing a magnetic tape against a magnetic head at a tension of 90 9/ inch and reciprocating at 38 cm/sec 500 times. The number of visually observed abrasions that were formed on the tape surface was counted.

(2) Measurement of dynamic friction coefficient The magnetic tape was recriprocated on a VHS video tape recorder (Maclord 88, Model NV8800; Matsushita Electric Industrial Co., Ltd.) once, 20 times, 100 times and 500 times, and the change in the dynamic friction coefficient (t4) was examined by the formula T2/T1=e wherein T1 was the tape tension at the supply side of the rotary cylinder and T2 was the tape tension at the takeup side.

The results are shown in Table 2 below.

Table 2 (2) Change in dynamic (1) Abrasions friction coefficient Sample Sliding after 500 1 20 100 500 No. face Polymer film **Anti-blocking Lubricant reciprocations (recip.) No.X-1 Magnetic Epoxy (450#500 ): 1 part 0 Myristic No abrasion 0.28 0.31 0.32 0.33 surface Diethylenetriamine: 0.05 part acid No.X-1' Base do - 0 do - 0.29 0.30 0.31 0.34 surface No.X-2 Magnetic Epoxy (450#500*): 1 part # do 2 or 3 shallow 0.30 0.34 0.37 0.44 surface Diethylenetriamine: 0.018 part abrasions X-C Epoxy (3300*): 1 part X - Diethylenetriamine: 0.008 part X-R-2 Magnetic Epoxy (450#500*): 1 part # do 4 or 5 shallow 0.30 0.36 0.39 0.47 surface Diethylaminopropylamine: 0.15 part abrasions X-R-3 Magnetic Vinylidene chlorids/acrylic - - do 4 or 5 shallow 0.31 0.38 0.42 0.50 surface acid ester copolymer abrasions X-R-4 Magnetic - - - - More than 10 0.48 0.55 0.58 0.67 surface deep abrasions X-R-4' Base - - - - - 0.35 0.44 0.57 0.59 surface *:epoxy equivalent of epoxy resin **:evaluation of antiblocking O no blocking # partial blocking X blocking in a wide area As the data in Table 2 show, the magnetic recording medium of the thin metal film type according to the present invention has very good running properties and wear resistance. Furthermore, the improvement in these properties is retained for an extended period of time. For this reason, the medium is a product having high commercial value.

Claims (10)

Claims

1. A magnetic recording medium having a thin magnetic recording metal film formed on one surface of a non-magnetic base, and a thin coating of a two-part epoxy resin being formed on either the thin magnetic metal film or the other surface of the base or both.

2. A magnetic recording medium according to Claim 1 , wherein the epoxy resin consists of an epoxy resin and a curing agent wherein the epoxy resin had an epoxy equivalent of from 400 to 3,000 and the curing agent was an aliphatic amine having two or more amino groups and three or more amino active hydrogen atoms in the molecular chain.

3. A magnetic recording medium according to Claim 2, wherein the curing agent was an aliphatic amine having a molecular weight of less than 1 50, three or four amino groups in the molecular chain and three or more amino active hydrogen atoms in the molecular chain thereof.

4. A magnetic recording medium according to Claim 2 or 3, wherein the curing agent is contained in the epoxy resin in the amount that satisfies the following relation: 100.a 100.a 0.5x < y < 1.5x x.E x.E wherein y=the amount of the curing agent amine (g) per 100 g of the epoxy resin; a=the molecular weight of the curing agent amine; x=the number of amino active hydrogen atoms in the curing agent amine; and E=the epoxy equivalent of the epoxy resin.

5. A magnetic recording medium according to Claim 1 , wherein the curing agent which is one of the two parts of the epoxy resin is an organic polyamine or a compound having two or more --NCO groups in its molecule.

6. A magnetic recording medium according to any preceding claim, wherein the or each epoxy resin coating is of a thickness of 5 to 1,000 Angstroms.

7. A magnetic recording medium according to any preceding claim, wherein the coating of epoxy resin contains a lubricant, or a lubricant layer is formed on said resin coating.

8. A magnetic recording medium according to Claim 7, wherein the lubricant is an aliphatic acid having 10 or more carbon atoms.

9. A magnetic recording medium substantially as hereinbefore described in Example 1,2 or 3.

10. A process of producing a magnetic recording medium as claimed in any preceding claim, wherein the thin cured epoxy resin film is made by heating the non-magnetic base having the epoxy resin film in uncured form thereon at a temperature higher than 300C but lower than the glass transition point of the base plus 300 C.