Process for production of ferromagnetic powder

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a process for the production of a powdery magnetic material for a magnetic recording medium. More particularly, the present invention relates to a process for the production of a novel powdery metal magnetic material.
2. Description of the Prior Art
Hitherto, .gamma.-Fe.sub.2 O.sub.3, Co containing .gamma.-Fe.sub.2 O.sub.3, Fe.sub.3 O.sub.4, Co containing Fe.sub.3 O.sub.4, CrO.sub.2, and the like have been used as a ferromagnetic powder for use in a magnetic recording medium. These ferromagnetic powders, however, have not been suitable for magnetic recording of a signal of a short recording wave length, e.g., 10 microns or less. That is, the magnetic properties such as coercive force (Hc), maximum residual magnetic flux density (Br), and the like are insufficient for use in the so-called high density recording. Recently, ferromagnetic powders having properties suitable for high density recording have been extensively investigated. One of these ferromagnetic powders is a ferromagnetic metal powder. The powder is made of a metal or a metal alloy. Metals such as iron, cobalt, and nickel are mainly used, and, if desired, chromium, manganese, rare earth elements, zinc, and the like are added.
The following methods are known for producing a ferromagnetic substance.
(1) A method comprising decomposing an organic salt of a ferromagnetic metal by heating followed by a reduction thereof in a reducing atmosphere, as described in, for example, Japanese Patent Publication Nos. 11412/1961, 22230/1961, 8027/1965, 14818/1966, 22394/1968, 38417/1972, etc., and The Record of Electrical and Communication Engineering Conversazione Tohoku University, Vol. 33, No. 2, page 57 (1964).
(2) A method comprising reducing a needle-like oxyhydroxide compound or those compounds containing other metals in addition to the needle-like oxyhydroxide compound, or needle-like iron oxide produced from the oxyhydroxide compound, as described in, for example, Japanese Patent Publication Nos. 3862/1960, 20939/1964, 39477/1972, etc., German Patent Laid Open No. 2,130,921, British Pat. No. 1,192,167, U.S. Pat. No. 3,681,018, etc.
(3) A method comprising evaporating a ferromagnetic metal in an inert gas, as described in, for example, Japanese Patent Publication No. 27718/1972, and Ohyo Butsuri (Applied Physics), Vol. 40, No. 1, page 110 (1971).
(4) A method comprising decomposing a metal carbonyl compound, as described in, for example, U.S. Pat. Nos. 2,983,997, 3,172,776, 3,200,007, 3,228,882, etc.
(5) A method comprising electro-depositing a ferromagnetic metal using a mercury cathode followed by the separation of the metal from the mercury, as described in, for example, Japanese Patent Publication No. 15525/1964, 8123/1965, etc., and U.S. Pat. No. 3,156,650.
(6) A method comprising reducing a salt of a ferromagnetic metal in a solution thereof, as described in, for example, Japanese Patent Publication Nos. 20520/1963, 26555/1963, 20116/1968, 41718/1972, etc., U.S. Pat. Nos. 3,206,338, 3,494,760, 3,567,525, 3,535,104, 3,607,218, 3,663,318, 3,669,643, 3,672,867, 3,756,866, German Patent Laid Open No. 2,132,430, 2,326,258, 2,326,261, etc.
The present invention is concerned with the Method (6) wherein a ferromagnetic metal salt is reduced in a solution thereof, and particularly, a borohydride compound or a derivative thereof is used as a reducing agent.
Method (6) of reducing a ferromagnetic metal salt in a solution thereof using a borohydride compound or a derivative thereof, has the following defects. That is, in general, in order to provide magnetic anisotropy, the reaction is effected in a magnetic field to thereby cause the particles to form a chain, and thus shape anisotropy is obtained. However, when the particle chains are mixed with and dispersed in a binder, they are broken, resulting in a reduction in the shape anisotropy. Thus, a tape produced using particle chains has tended to be inferior in the orientation in magnetic field, and poor in squareness ratio, Br/Bs, (where Br is the residual magnetic flux density and Bs is the saturated magnetic flux density).
Furthermore, a powder produced by the above described method is not humidity-resistant, particularly in the case where Fe is present, and thus the powder is gradually oxidized even though the powder is stored in an aqueous reaction solution or in air at an ordinary temperature, and, in the extreme cases, the magnetic properties are lost.
Moreover, the surface activity of the particles produced by the above described method is high, i.e., the particles are highly reactive, and thus they are industrially disadvantageous from the standpoint of process control.
Hitherto, various methods have been proposed in order to remove the above described drawbacks. For instance, Japanese Patent Publication No. 20520/1963 describes Fe-B based magnetic recording materials containing Co, Ni, Mn, and Cr prepared by a process which comprises applying either of the solutions of a hydrophilic high molecular weight material containing a salt of a ferromagnetic metal or a hydrophilic high molecular weight material containing a borohydride to a support to form a layer of the hydrophilic high molecular weight material on the support, applying the other solution onto the layer to precipitate the ferromagnetic metal particles in a dispersed state in the hydrophilic high molecular weight material. Japanese Patent Publication No. 7820/1972 describes Fe-B based materials containing Co, Ni, Mn, Cu, and Ag, prepared by a process which comprises reducing a solution of at least one ferromagnetic metal salt with a borohydride with the improvement comprising adding a surface active agent to the solution. Further Japanese Patent Publication No. 20116/1968 describes a process for preparing an oxidation-resistant wet-process magnetic metal powder which comprises adding sodium or potassium borohydride to a mixture (A) an aqueous solution of a salt of iron, cobalt, nickel, etc.) and (B) a dispersion of a higher aliphtic acid which is liquid at ambient temperature in the presence or absence of an additive which is capable of liberating a higher aliphatic acid upon hydrolysis of the additive thereby reducing the magnetic metal salt to precipitate the metal particles and at the same time saponify the surface of the metal particles with the higher aliphatic acid. However, it has been difficult to remove the above described drawbacks using these methods.
SUMMARY OF THE INVENTION
An object of the present invention is to remove the drawbacks using a magnetic material having a novel composition.
A further object of the present invention is to provide a powdery magnetic material whose magnetic properties are improved.
Another object of the present invention is to provide a powdery magnetic material which is humidity-resistant and is difficult to be oxidized.
An even further object of the present invention is to provide a powdery magnetic material which is relatively stable in production and thus which can be easily produced.
The present invention provides a process for producing a ferromagnetic material which comprises reducing in the presence of a titanium compound, a metal salt containing at least Fe and capable of forming a ferromagnetic substance in an aqueous solution thereof using at least one member selected from the group consisting of a borohydride compound and a derivative thereof.
The present invention will be fully understood from the following detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS
The FIGURE shows the relation between the processing time and the decrease in the Bs value where the powdery magnetic materials produced in the Examples and the Comparison Examples are processed in an atmosphere of 60.degree. C. and 90% RH, in which the Bs value prior to the processing is set at 100%.

DETAILED DESCRIPTION OF THE INVENTION
The term "metal salt containing at least Fe and capable of forming a ferromagnetic substance" designates those metal salts which contain any one of Fe, Fe-Co, Fe-Ni, and Fe-Co-Ni, and furthermore can contain, if desired, a suitable amount of at least one metal salt selected from the group consisting of Al, P, Sc, Cr, Mn, Cu, Zn, Ga, As, Se, Sr, Y, Zr, Nb, Mo, Rh, Pd, Ag, Sn, Te, La, Ce, Pr, Nd, Pm, Sm, W, Re, Os, Ir, Pt, Au, Hg, Pb, Bi, and the like for improving the magnetic properties and oxidation-stability.
Representative examples of these metal salts are the sulfates, chlorides, sulfides, nitrates, formates, acetates, pyrophosphates, sulfinates, and the like of the above described metals.
The reducing agent used in the present invention comprises one or more compounds selected from the group consisting of borohydride compounds and deratives thereof, e.g., borane, borazane, borohydride, sodium borohydride, potassium borohydride, dimethylaminoborane, diethylaminoborane, and the like.
The titanium compound as added to the reaction bath of the present invention includes water-soluble inorganic salts or organic salts of titanium. Representative examples of titanium compounds are titanium halides, e.g., titanium chloride, titanium bromide, and the like, titanium sulfate, titanium nitrate oxide, potassium titanyl oxalate, sodium titanyl oxalate, titanium sulfide, and the like. It is preferred that the molar ratio of the titanium to metal ion (Ti/metal ion) ranges from 0.001:1 to 0.5:1.
To the metal salt solution, in addition to the above described components, a complexing agent, a pH buffer agent, a pH controlling agent, and the like can be, if desired, added. Suitable pH buffer agents and complexing agents include monocarboxylic acids, e.g., formic acid, acetic acid, propionic acid, butyric acid, valeric acid, acrylic acid, trimethylacetic acid, benzoic acid, chloroacetic acid, and the like, and the salts thereof. Examples of complexing agents are dicarboxylic acids, e.g., oxalic acid, succinic acid, malonic acid, maleic acid, itaconic acid, p-phthalic acid, and the like, and the salts thereof; and oxycarboxylic acids, e.g., glycolic acid, lactic acid, salicylic acid, tartaric acid, citric acid, and the like, and the salts thereof. Illustrative pH buffer agents and pH controlling agents, are boric acid, carbonic acid, sulfurous acid, and the like and suitable examples of ph controlling agent are organic acids, ammonia, alkali metal hydroxides, and the like in addition to inorganic acids, e.g., hydrochloric acid, sulfuric acid, phosphoric acid, nitric acid, and the like. In addition, some of these additives may be employed for more than one function. For example, some compounds act as a pH buffer agent as well as a complexing agent, and thus the action of these additives is not restricted.
If desired, soluble proteins, carbohydrates, organic acids and the like can be added to the reaction bath. It is effective for the improvement of the properties to conduct the reaction while applying supersonic agitation to the reaction bath. The chemical oxidation-reduction reaction occurs in an appropriately selected reaction bath by applying, if desired, a magnetic field of several tens of oersteds or more to thereby produce a powdery ferromagnetic material. Although the reaction conditions in the present invention are not restricted, a preferred pressure range is from 0.5 to 5 atmospheres. A preferred reaction temperature and pH are 65.degree. C. or less, and 12 or less, respectively. A magnetic field of several tens of oersteds or more is effective and a stronger magnetic field is preferred.
The magnetic field is applied during the period of from the beginning of the reaction to the end thereof, and the strength of the magnetic field is generally several hundred oersteds or more. A preferred magnetic field ranges from about 500 to 3000 oe, which is effective in improving the coercive force and the squareness ratio.
The frequency of the supersonic agitation applied preferably ranges from about 1.6.times.10.sup.4 to 1.times.10.sup.6 Hz, and the supersonic agitation is applied during the period of reaction.
It has been found that the metal ion concentration is desirably about 0.002 to 2 mole/1, and preferably 0.01 to 0.5 mole/1.
It has been found that the concentration of the borohydride compound or derivative thereof desirably ranges from about 0.0002 to 10 mole/1, and that the molar ratio of the reducing agent to the metal ion (reducing agent/metal ion) desirably ranges from about 0.1 to 5.
The ferromagnetic powder as produced by conducting the chemical oxidation-reduction reaction using the composition of the reaction bath and under the conditions as selected appropriately comprises particles of a size of about 100 to 20,000 A in the longitudinal direction and about 50 to 1,000 A in the width direction and it has been observed that about 2 to about 20, more generally 3 to 10, particles are connected to thereby produce a string-like, rod-like, or necklace-like form.
The particle size and the degree of chaining as produced by the present invention can be controlled by the amount of the titanium compound added, the kind of the composition, and the strength of the magnetic field applied.
The ferromagnetic powder produced by the present invention has a coercive force (Hc) of about 100 to 2,000 oe and a Bm value of about 8,000 G or more. The effect of the present invention can be increased by heating the ferromagnetic powder in a nonoxidizing atmosphere such as an atmosphere of helium, argon, nitrogen, carbon monoxide, carbon dioxide, hydrogen, etc. or in the presence of a small amount of H.sub.2 O or O.sub.2, e.g., 10 volume % or less of water vapor or oxygen.
The powdery magnetic material for a magnetic recording medium as produced above is mixed with a binder, if desired, together with any additives, and coated on a support using an organic solvent and dried, and thus a magnetic recording medium can be obtained.
Hitherto known thermoplastic resins, thermosetting resins or mixtures thereof can be used as the binder as used in the present invention together with the powdery magnetic material of the present invention.
Suitable thermoplastic resins are those resins which have a softening point of about 150.degree. C. or less, an average molecular weight of about 10,000 to 200,000 and a degree of polymerization of about 200 to 2,000, e.g., a vinyl chloride-vinyl acetate copolymer, a vinyl chloride-vinylidene chloride copolymer, a vinyl chloride-acrylonitrile copolymer, an acrylic acid ester-acrylonitrile copolymer, an acrylic acid ester-vinylidene chloride copolymer, an acrylic acid ester-styrene copolymer, a methacrylic acid ester-acrylonitrile copolymer, a methacrylic acid ester-vinylidene chloride copolymer, a methacrylic acid ester-styrene copolymer, a urethane elastomer, a polyvinyl fluoride resin, a vinylidene chloride-acrylonitrile copolymer, a butadiene-acrylonitrile copolymer, a polyamide resin, polyvinyl butyral, a cellulose derivative, a styrene-butadiene copolymer, a polyester resin, a chlorovinylether-acrylic acid ester copolymer, an amino resin, various synthetic rubber based thermoplastic resins, mixtures thereof, and the like.
These resins are described in Japanese Patent Publication Nos. 6877/1962, 12528/1964, 19282/1964, 5349/1965, 20907/1965, 9463/1966, 14059/1966, 16985/1966, 6428/1967, 11621/1967, 4623/1968, 15206/1968, 2889/1969, 17947/1969, 18232/1969, 14020/1970, 14500/1970, 18573/1972, 22063/1972, 22064/1972, 22068/1972, 22069/1972, 22070/1972, 27886/1972, U.S. Pat. Nos. 3,144,352, 3,419,420, 3,499,789, 3,713,887, etc.
The thermosetting resin or reactive type resin has a molecular weight of about 200,000 or less as a coating solution, and when heated after coating and drying, the molecular weight becomes infinity due to reactions such as condensation, addition, and the like. Of these resins, preferred resins are resins which do not soften or melt before the thermal decomposition thereof. Representative examples of these resins are a phenol resin, an epoxy resin, a polyurethane hardening type resin, a urea resin, a melamine resin, a silicone resin, an acryl based reactive resin, an epoxy-polyamide resin, a mixture of a high molecular weight polyester resin and an isocyanate prepolymer, a mixture of a methacrylic acid salt copolymer and a diisocyanate prepolymer, a mixture of a polyesterpolyol and a polyisocyanate, a ureaformaldehyde resin, a mixture of a low molecular weight glycol, a high molecular weight diol, and triphenylmethane triisocyanate, a polyamine resin, mixtures thereof, and the like.
These resins are described in Japanese Patent Publication Nos. 8103/1964, 9779/1965, 7192/1966, 8016/1966, 14275/1966, 18179/1967, 12081/1968, 28023/1969, 14501/1970, 24902/1970, 13103/1971, 22065/1972, 22066/1972, 22067/1972, 22072/1972, 22073/1972, 28045/1972, 28048/1972, 28922/1972, U.S. Pat. Nos. 3,144,353, 3,320,090, 3,437,510, 3,597,273, 3,781,210, 3,781,211, etc.
The weight ratio of the thermosetting resin binder, thermoplastic resin binder, or reactive type resin binders, used alone or in combination, to the ferromagnetic powder is about 30:300 to 300:300, and preferably 50:300 to 150:300. In this case, the dry thickness of the magnetic recording layer is in the range of about 1 to 10.mu..
Suitable additives which can be used include a dispersing agent, a lubricant, an abrasive agent, and the like.
Suitable dispersing agents are fatty acids containing about 12 to 18 carbon atoms (e.g., having the formula R.sub.1 COOH wherein R.sub.1 is an alkyl group containing about 11 to 17 carbon atoms), e.g., caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, eladic acid, linolic acid, linolenic acid, stearolic acid, and the like. Metallic soaps comprising linolenic acid, stearolic acid, the alkali metal (Li, Na, K, etc.) salts or the alkali earth metal (Mg, Ca, Ba, etc.) salts of the above described fatty acids; and lecithin, etc. can be used. In addition, higher alcohols containing about 12 or more carbon atoms and the sulfuric acid esters thereof can be used. These dispersing agents are generally used in a proportion of about 1 to 20 parts by weight per 100 parts by weight of the binder.
Suitable lubricants include silicone oil, graphite, molybdenum disulfide, tungsten disulfide, fatty acid esters produced from a monobasic fatty acid containing about 12 to 16 carbon atoms and a monovalent alcohol containing about 3 to 12 carbon atoms, fatty acid esters produced from a monobasic fatty acid containing about 17 or more carbon atoms and a monovalent alcohol, in which the total number of carbon atoms ranges from about 15 to 28, and the like can be used. These lubricants are generally used in a proportion of about 0.2 to 20 parts by weight per 100 parts by weight of the binder. These lubricants are described in Japanese Patent Publication No. 23889/1968, Japanese Patent Publication Nos. 24041/1973 and 81543/1968, 18482/1973, etc.
Typical abrasive agents include the generally used materials, e.g., fused alumina, silicon carbide, chromium oxide, corundum, synthetic corundum, diamond, synthetic diamond, garnet, emery (main component: corundum and magnetite), and the like. Those abrasive agents are used which have an average particle size of from about 0.05 to 5.mu., preferably from 0.1 to 2.mu.. The lubricant is generally used in a proportion of from about 7 to 20 parts by weight per 100 parts by weight of the binder. These abrasive agents are described in Japanese Patent Application OPI No. 115510/1974.
The magnetic recording layer is formed by dissolving the above described components in an organic solvent and coating the resulting solution on a support.
The thickness of the support is generally about 5 to 50.mu., preferably about 10 to 40.mu.. Suitable supports include polyester, e.g., polyethylene terephthalate, and the like, polyolefins, e.g., polypropylene, and the like, cellulose derivatives, e.g., cellulose triacetate, cellulose diacetate, and the like, polycarbonate, and the like.
The magnetic recording layer can be formed on the support using air doctor coating, blade coating, air knife coating, squeeze coating, dip coating, reverse roll coating, transfer roll coating, gravure coating, kiss coating, cast coating, spray coating, and the like, and other methods can be also used. These methods are described in Coating Kogaku (Coating Engineering), pages 253 to 277, published by Asakura Shoten (March 20, 1971).
Typical organic solvents which can be used in the present invention include ketones, e.g., acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, and the like; alcohols, e.g., methanol, ethanol, propanol, butanol, and the like; esters, e.g., methyl acetate, ethyl acetate, butyl acetate, ethyl lactate, glycol monoethyl ether acetate and the like; ethers and glycol ethers e.g., diethyl ether, glycol monoethyl ether, glycol dimethyl ether, dioxane, and the like; aromatic hydrocarbons, e.g., benzene, toluene, xylene, and the like; chlorinated hydrocarbons, e.g., methylene chloride, ethylene chloride, carbon tetrachloride, chloroform, ethylene chlorohydrin, dichlorobenzene, and the like, etc. and these solvents can be used alone or in combination with each other.
The present invention will be explained in detail by referance to the following Examples and Comparison Examples. It is to be understood that many variations can be made in the components, proportions, operation sequence, and the like without departing from the spirit of the present invention, and thus the present invention is not to be considered as being restricted to the following Examples. Unless otherwise indicated, all parts, percents, ratios and the like are by weight.
______________________________________EXAMPLE 1 Quantity (mole/liter)______________________________________M.sub.1 LiquidFerrous Chloride 0.36Cobalt Chloride 0.04Titanium (II) Sulfate 0.004(40% by weight aqueous solution)R.sub.1 LiquidNaBH.sub.4 1.60______________________________________ Note: Water was used as the solvent in both of the M.sub.1 and R.sub.1 Liquids, hereinafter the same.
80 parts of the M.sub.1 liquid was charged to a non-magnetic vessel and a direct current magnetic field of 1000 oe was applied to all of the vessel. 20 parts of the R.sub.1 Liquid was added to the M.sub.1 Liquid over a ten second period while stirring gently to effect the reaction, and thus a ferromagnetic powder was obtained. The powder was washed, and then with acetone, and dried in a drying oven at 60.degree. C., and a ferromagnetic powder was obtained. This sample is designated #P-1.
The following composition containing powder #P-1 was charged to a ball mill and sufficiently mixed and dispersed to thereby prepare a magnetic coating composition.
______________________________________ Quantity (parts)______________________________________Ferromagnetic Powder (# P-1) 300Polyester Polyol.sup.1 40Polyisocyanate Compound.sup.2 20Nitrocellulose.sup.3 20Chromium Oxide (Cr.sub.2 O.sub.3 : particle 5size about 0.5 micron)Lecithin 450Methyl Isobutyl Ketone 400______________________________________ .sup.1 Condensate of adipic acid and butanediol, having terminal hydroxy groups and a molecular weight of about 1800. .sup.2 Desmodur L: trade name, produced by Bayer A.G.; 75 wt. % ethyl acetate solution; adduct of 3 moles of toluene diisocyanate and 1 mole of trimethylol propane. .sup.3 Molecular weight of about 800.
The composition was coated on one side of a polyethylene terephthalate film having a thickness of 25 microns in a dry thickness of 5 microns while applying a magnetic field and dried by heating. The thus prepared wide magnetic web was calendered and slit to a 1/2 inch width, and thus a video tape was obtained. The surface property of the video tape was quite excellent. This sample is designated #T-1.
______________________________________EXAMPLE 2 Quantity (mole/liter)______________________________________M.sub.2 LiquidFerrous Chloride 0.40Titanium Trichloride 0.004(40% by weight aqueous solution)Boric Acid 0.10R.sub.2 LiquidNaBH 1.60______________________________________
The procedure of Example 1 was repeated using the M.sub.2 and R.sub.2 Liquids to thereby obtain a ferromagnetic powder. This sample is designated #P-2. Also, the procedure of Example 1 was repeated using the powder (#P-2) to thereby prepare a video tape. The surface property of the thus produced video tape was quite excellent. This sample is designated #T-2.
______________________________________EXAMPLE 3 Quantity (mole/liter)______________________________________M.sub.3 LiquidFerrous Chloride 0.36Cobalt Chloride 0.04Titanium (II) Sulfate 0.01(40% by weight aqueous solution)Zinc Chloride 0.005R.sub.3 LiquidNaBH.sub.4 1.60Diethylaminoborane 0.20______________________________________
The procedure of Example 1 was repeated using the R.sub.3 and M.sub.3 Liquids to thereby obtain a ferromagnetic powder. This sample is designated #P-3. Also, the procedure of Example 1 was repeated using the powder (#P-3) to thereby prepare a video tape. The appearance of the thus prepared video tape was substantially the same as that of Example 1. This sample is designated #T-3.
______________________________________COMPARISON EXAMPLE 1 Quantity (mole/liter)______________________________________Mc.sub.1 LiquidFerrous Chloride 0.36Cobalt Chloride 0.04Rc.sub.1 LiquidNaBH.sub.4 1.60______________________________________
A ferromagnetic powder was produced using the Mc.sub.1 and Rc.sub.1 Liquids under the same conditions and in the same manner as in Example 1. This sample is designated #P-4. A video tape was produced using the powder (#P-4) in the same manner as in Example 1. This sample is designated #T-4.
______________________________________COMPARISON EXAMPLE 2 Quantity (mole/liter)______________________________________Mc.sub.2 LiquidFerrous Chloride 0.40Boric Acid 0.10Rc.sub.2 LiquidNaBH.sub.4 1.60______________________________________
A ferromagnetic powder was produced using the Mc.sub.2 and Rc.sub.2 Liquids under the same conditions and in the same manner as in Example 2. This sample is designated #P-5. A video tape was produced using the powder (#P-5) in the same manner as in Example 2. This sample is designated #T-5.
______________________________________COMPARISON EXAMPLE 3 Quantity (mole/liter)______________________________________Mc.sub.3 LiquidFerrous Chloride 0.36Cobalt Chloride 0.04Zinc Chloride 0.005Mc.sub.3 LiquidNabH.sub.4 1.60Diethylaminoborane 0.20______________________________________
A ferromagnetic powder was produced using the Mc.sub.3 and Rc.sub.3 Liquids under the same conditions and in the same manner as in Example 3. This sample is designated #P-6. A video tape was produced using the powder (#P-6) in the same manner as in Example 3. This sample is designated #T-6.
The properties of the six samples as obtained in Examples 1 to 3 and Comparison Examples 1 to 3 were compared and the results obtained are shown in Table 1 below.
Table 1______________________________________ Output**Example Hc Surface* Disper-* of 5 MHzNo. Sample (oe) Br/Bs property sibility (dB)______________________________________Example1 # T-1 950 0.84 Good Good + 3.62 # T-2 780 0.85 Excellent Good + 3.93 # T-3 1050 0.82 Good Good + 0.8Com-parisonExample1 # T-4 1100 0.80 Good Average 02 # T-5 900 0.82 Good Average + 0.33 # T-6 1250 0.78 Bad Bad - 2.5______________________________________ *Measured with # T4 as a standard **Measured with the output of # T4 as 0 dB
Furthermore, the composition, the particle size, and the Bs value of the powders are shown in Table 2, and the decrease in magnetism in an atmosphere of 60.degree. C. and 90% RH (Bs value decreases due to the oxidation of the sample) is shown in the figure.
Table 2______________________________________Example Bs Value Particle Composition (%)No. Sample (G) Size (A) Fe B Ti Co Zn______________________________________Example1 # P-1 11,300 250 72.2 5.4 0.6 7.1 --2 # P-2 12,500 400 82.0 5.5 0.5 -- --3 # P-3 10,600 300 72.8 5.7 1.5 7.5 0.5Com-parisonExample1 # P-4 11,000 250 72.0 5.6 -- 7.0 --2 # P-5 12,200 350 81.0 5.7 -- -- --3 # P-6 10,200 300 72.2 5.8 -- 7.2 0.5______________________________________
As is apparent from the results of the Examples and Comparison Examples, the powdery magnetic material containing at least Fe, B, and Ti of the present invention is excellent, particularly in anti-oxidation properties. Furthermore, it has been found that the powdery magnetic material is excellent in orientation in a magnetic field when used in producing a tape, and that a high squareness ratio (Br/Bs) is obtained.
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.

Number	Name	Date
2651105	Neel	Sep 1953
3206338	Miller	Sep 1965
3369886	Metzger	Feb 1968
3535104	Little, Jr.	Oct 1970
3648260	Gyorgy	Mar 1972
3661556	Jolley	May 1972
3663318	Little	May 1972
3679398	Geus	Jul 1972
4096316	Tamai et al.	Jun 1978

Process for production of ferromagnetic powder

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