Magnetic powder for magnetic recording medium

Abstract

A magnetic powder for a magnetic recording medium which is a cobalt-adsorbed magnetic iron oxide having a coercive force of 1000 Oe or more and a ratio of a coercive force at -196.degree. C. to a coercive force at room temperature of 3 or less.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a magnetic powder for a magnetic recording medium which has high coercive force.

2. Description of the Prior Art

Iron oxide of .gamma.-Fe.sub.2 O.sub.3 has been usually used as a magnetic powder for a magnetic recording medium. Recently, a chromium tape has been developed. Thus, cobalt or ferrous ion is adsorbed on chromium dioxide or .gamma.-Fe.sub.2 O.sub.3 to impart high coercive force whereby high density recording has been attained. Recently, an alloy type magnetic powder has been developed and the tendency of the development has been further increased.

In general, a cobalt-doped type magnetic powder and a cobalt-adsorbed type magnetic powder have been proposed to give high coercive force. The cobalt-doped type magnetic powder imparts easily high coercive force but is thermally unstable and has inferior printing characteristics. On the other hand, the cobalt-adsorbed type magnetic powder has low coercive force such as up to 1000 Oe.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide a magnetic powder which is thermally stable and has excellent printing characteristics and high coercive force of at least 1000 Oe in a cobalt-adsorbed type.

The foregoing and other objects of the present invention have been attained by providing a magnetic powder for a magnetic recording medium which is a cobalt-adsorbed magnetic iron oxide having a coercive force of 1000 Oe or more and a ratio of a coercive forces at -196.degree. C. to a coercive force at room temperature of 3 or less..

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph showing a relation of a coercive force of the magnetic powder obtained by varying Fe.sup.2+ at a ratio of Fe.sup.2+ /Co.sup.2+ of 1 to 8 in the presence of 6.5 wt.% of a cobalt component in the process of the production;

FIG. 2 is a graph showing a relation of an amount of Fe.sup.2+ to .gamma.-Fe.sub.2 O.sub.3 at a ratio of Fe.sup.2+ /Co.sup.2+ of 3, a coercive force and a saturated magnetic flux density; and

FIG. 3 is a graph showing X ray diffraction of the cobalt-adsorbed magnetic powder.

FIG. 4 is a graph showing a relation of a ratio of Fe.sup.2+ /Co.sup.2+ by weight in the product and a ratio of Fe.sup.2+ /Co.sup.2+ by weight in the process of the production.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

In Co-adsorbed type magnetic powders, a coercive force increases in proportion to ferrous ion content until reaching a certain level of ferrous ion content; however, a coercive force may decrease over said level of ferrous ion content. In view of this fact, a change of a coercive force is measured under variation of ferrous ions at a constant Co content of 6.5 wt.%. The result is shown in FIG. 1.

That is, .gamma.-Fe.sub.2 O.sub.3 is coated with a Co component by adding cobalt ion to .gamma.-Fe.sub.2 O.sub.3 at a ratio of 6 wt.% or more and then, adding a ferrous ion at a ratio of 20 wt.% or more as Fe.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 and at a ratio of Fe.sup.2+ /Co.sup.2+ of 3.0 to 4.5 by weight to obtain Co-adsorbed magnetic iron oxide. A ratio of ferrous salt to Co component as Fe.sup.2+ /Co.sup.2+ in the product is in a range of 2.0 to 3.5 by weight. The ratio relates to a coercive force. When the ratio of Fe.sup.2+ /Co.sup.2+ (the components added to .gamma.-Fe.sub.2 O.sub.3) in the process of the production is in the range of 3 to 4.5, a coercive force is as high as at least 1000 Oe.

The relation of the ratio of Fe.sup.2+ /Co.sup.2+ by weight in the product and a ratio of Fe.sup.2+ /Co.sup.2+ by weight in the process of the production is shown in FIG. 4. The ratio of Fe.sup.2+ /Co.sup.2+ by weight in the product is preferably in a range of 2.0 to 3.5 which corresponds to the ratio of the Fe.sup.2+ /Co.sup.2+ by weight in the process of the production of 3.0 to 4.5.

The most important factor is a ratio of coercive force at -196.degree. C. to a coercive force at room temperature and this should be 3 or less.

In FIG. 2, the full line shows the relation of the ferrous ion content to the coercive force and the saturated magnetic flux density in the case of the ratio of Fe.sup.2+ /Co.sup.2+ of 3 (the components added to .gamma.-Fe.sub.2 O.sub.3). As it is clear from the fact, when the ratio of Fe.sup.2+ /Co.sup.2+ is constant, the coercive force increases depending upon an increase of contents of the cobalt salt and the ferrous salt. There is no critical point in the addition of the ferrous ion. In this case, the residual magnetic flux density is kept constant.

In FIG. 2, the broken line shows the relation of the ferrous ion content to the coercive force and the saturated magnetic flux density in the case of the cobalt content of 6 wt.%.

When the ferrous ion content is 20 wt.%, the coercive force reaches to 1000 Oe. The coercive force decreases when the ferrous ion content is more or less. That is, there is critical point for the ferrous ion content. The residual magnetic flux density increases depending upon an increase of the ferrous ion content.

When the cobalt content based on .gamma.-Fe.sub.2 O.sub.3 is at least 6 wt.% and the ferrous ion content based on .gamma.-Fe.sub.2 O.sub.3 is at least 20 wt.%, the coercive force can be at least 1000 Oe.

In view of FIG. 1 and FIG. 2, it is necessary to add at least 6 wt.% of a cobalt component and at least 20 wt.% of ferrous ion based on .gamma.-Fe.sub.2 O.sub.3 at a ratio of Fe.sup.2+ /Co.sup.2+ of 3 to 4.5.

FIG. 3 shows the result of X-ray diffraction of the Co-adsorbed magnetic powder wherein X-ray intensity on .gamma.-Fe.sub.2 O.sub.3 [211] is upto 20 cps; and a spacing (d) on [220] is changed from 2,950 .ANG. to 2,965 .ANG.. When the content of Fe.sup.2+ is at least 20 wt.%, it is converted into Fe.sub.2 O.sub.4. This fact is confirmed by the X-ray diffraction.

When the magnetic powder is boiled in 1 N-HCl for 2-3 hours to dissolve the surface thereof and X-ray diffraction, magnetic characteristics, a content of Fe.sup.2+ and a surface specific area (BET method) of the resulting seeds are tested. As a result, it is confirmed to be Fe.sub.3 O.sub.4.

The resulting magnetic powder has high coercive force of at least 1000 Oe and can be used for a preparation of an audio cassette tape and a video tape having excellent high frequency characteristics. When the magnetic powder is heat-treated in non-oxidative atmosphere, a magnetic powder having a coercive force of at least 1300 Oe can be obtained. When a cobalt component is adsorbed on the seeds made of Fe.sub.3 O.sub.4 and the product is heat-treated, a content of Fe.sup.2+ is not easily controlled. In the cases of the examples, the content of Fe.sup.2+ is easily controlled to attain a stable coercive force.

Certain examples and references are shown below and the magnetic characteristics of the magnetic powder are shown in Table 1.

The seeds used in the examples and references are as follows: .gamma.-Fe.sub.2 O.sub.3 having an average diameter of 0.35.mu.; a squareness ratio of 8/1; Hc of 350 Oe; and .sigma..sub.s of 74.0 emu/g. Fe.sub.3 O.sub.4 having an average diameter of 0.35.mu.; a squareness ratio of 8/1; Hc of 400 Oe and .sigma..sub.s of 80 emu/g.

The present invention will be further illustrated by certain examples and references which are provided for purposes of illustration only and are not intended to be limiting the present invention.

EXAMPLE 1

Into 40 liters of water, 4000 g. of .gamma.-Fe.sub.2 O.sub.3 was dispersed and 1240 g. of cobalt sulfate (CoSO.sub.4.7H.sub.2 O) was charged and dissolved and then, a solution of 4700 g. of sodium hydroxide in 10 liters of water was added and a solution of 3976 g. of ferrous sulfate in 20 liters of water was added. The resulting slurry was boiled for 180 minutes and the solid component was washed, filtered and dried to obtain a magnetic powder. In this case, 20 wt.% of Fe.sup.2+ and 6.5 wt.% of Co.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 were added at a ratio of Fe.sup.2+ /Co.sup.2+ of 3.0. The cobalt component in the resulting magnetic powder was 4.5 wt.% as Co.sup.2+. The magnetic characteristics of the magnetic powder are as follows:

Hc=1000 Oe; .sigma..sub.s =76.5 emu/g; .sigma..sub.r /.sigma..sub.s =0.52.

EXAMPLE 2

Into 40 liters of water, 4000 g. of .gamma.-Fe.sub.2 O.sub.3 was dispersed and 1430 g. of cobalt sulfate was charged and dissolved and then, a solution of 5964 g. of ferrous sulfate in 20 liters of water was added. The resulting slurry was boiled for 180 minutes and the solid component was washed, filtered and dried to obtain a magnetic powder. In this case, 30 wt.% of Fe.sup.2+ and 7.5 wt.% of Co.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 were added at a ratio of Fe.sup.2+ /Co.sup.2+ of 4.0. The cobalt component in the resulting magnetic powder was 5.1 wt.% as Co.sup.2+. The magnetic characteristics of the magnetic powder are as follows:

Hc=1000 Oe; .sigma..sub.s =76.5 emu/g; .sigma..sub.r /.sigma..sub.s =0.52.

EXAMPLE 3

Into 40 liters of water, 4000 g. of .gamma.-Fe.sub.2 O.sub.3 was dispersed and 1908 g. of cobalt sulfate was charged and dissolved and then, a solution of 6000 g. of sodium hydroxide in 20 liters of water was added and a solution of 7952 g. of ferrous sulfate in 20 liters of water was added. The resulting slurry was boiled for 3 hours and the solid component was washed, filtered and dried to obtain a magnetic powder. In this case, 40 wt.% of Fe.sup.2+ and 10 wt.% of Co.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 were added at a ratio of Fe.sup.2+ /Co.sup.2+ of 4.0. The cobalt component in the resulting magnetic powder was 5.7 wt.% as Co.sup.2+. The magnetic characteristics of the magnetic powder are as follows:

Hc=1150 Oe; .sigma..sub.s =76.5 emu/g; .sigma..sub.r /.sigma..sub.s =0.53.

EXAMPLE 4

Into 40 liters of water, 4000 g. of .gamma.-Fe.sub.2 O.sub.3 was dispersed and 2290 g. of cobalt sulfate was charged and dissolved and then, a solution of 6000 g. of sodium hydroxide in 20 liters of water was added and a solution of 7157 g. of ferrous sulfate in 20 liters of water was added. The resulting slurry was boiled for 180 minutes and the solid component was washed, filtered and dried to obtain a magnetic powder. In this case, 36 wt.% of Fe.sup.2+ and 12 wt.% of Co.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 were added at a ratio of Fe.sup.2+ /Co.sup.2+ of 3.0. The cobalt component in the resulting magnetic powder was 6.3 wt.% as Co. The magnetic characteristics of the magnetic powder are as follows:

Hc=1225 Oe; .sigma..sub.s =76.5 emu/g; .sigma..sub.r /.sigma..sub.s =0.52.

REFERENCE 1

The magnetic powder obtained in Example 2 was heat-treated in nitrogen atmosphere at 350.degree. C. for 60 minutes. The magnetic characteristics of the heat-treated magnetic powder are as follows:

Hc=1300 Oe; .sigma..sub.s =76.0 emu/g; .sigma..sub.r /.sigma..sub.s =0.54.

REFERENCE 2

Into 40 liters of water, 4000 g. of .gamma.-Fe.sub.2 O.sub.3 was dispersed and 1145 g. of cobalt sulfate was charged and dissolved and a solution of 5300 g. of sodium hydroxide in 20 liters of water was added and a solution of 7157 g. of ferrous sulfate in 20 liters of water was added. The resulting slurry was boiled for 180 minutes and the solid component was washed, filtered and dried to obtain a magnetic powder. In this case, 36 wt.% of Fe.sup.2+ and 6 wt.% of Co.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 were added at a ratio of Fe.sup.2+ /Co.sup.2+ of 6.0. The cobalt component in the resulting magnetic powder was 3.8 wt.% as Co.sup.2+. The magnetic characteristics of the magnetic powder are as follows:

Hc=950 Oe; .sigma..sub.s =78.0 emu/g; .sigma..sub.r /.sigma..sub.s =0.51.

REFERENCE 3

Into 40 liters of water, 4000 g. of .gamma.-Fe.sub.2 O.sub.3 was dispersed and 1145 g. of cobalt sulfate was charged and dissolved and then, a solution of 4400 g. of sodium hydroxide in 20 liters of water was added and a solution of 2982 g. of ferrous sulfate in 10 liters of water was added. The resulting slurry was boiled for 180 minutes and the solid component was washed, filtered and dried to obtain a magnetic powder. In this case, 15 wt.% of Fe.sup.2+ and 6 wt.% of Co.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 were added at a ratio of Fe.sup.2+ /Co.sup.2+ of 2.5. The cobalt component in the magnetic powder was 5.0 wt.% as Co.sup.2+. The magnetic characteristics of the magnetic powder are as follows:

Hc=825 Oe; .sigma..sub.s =75 emu/g; .sigma..sub.r /.sigma..sub.s =0.51.

REFERENCE 4

Into 40 liters of water, 4000 g. of Fe.sub.3 O.sub.4 was dispersed and 764 g. of cobalt sulfate was charged and dissolved and then, a solution of 4400 g. of sodium hydroxide in 20 liters of water added. The resulting slurry was boiled for 180 minutes and the solid component was washed, filtered and dried to obtain a magnetic powder. In this case, 4 wt.% of Co.sup.2+ based on Fe.sub.3 O.sub.4 was added. The cobalt component in the magnetic powder was 3.8 wt.% as Co.sup.2+. The magnetic characteristics of the magnetic powder are as follows:

Hc=600 Oe; .sigma..sub.s =76 emu/g; .sigma..sub.r /.sigma..sub.s =0.50.

REFERENCE 5

The magnetic powder obtained in Reference 4 was heat-treated in nitrogen atmosphere at 300.degree. C. for 60 minutes. The cobalt component in magnetic powder was 3.8 wt.% as Co.sup.2+. The magnetic characteristics of the heat-treated magnetic powder are as follows:

Hc=1300 Oe; .sigma..sub.s =76 emu/g; .sigma..sub.r /.sigma..sub.s =0.53.

REFERENCE 6

Into 40 liters of water, 4000 g. of .gamma.-Fe.sub.2 O.sub.3 was dispersed and 572 g. of cobalt sulfate was charged and dissolved and a solution of 4400 g. of sodium hydroxide in 10 liters was added and a solution of 994 g. of ferrous sulfate in 10 liters of water was added. The resulting slurry was boiled for 180 minutes and the solid component was washed, filtered and dried to obtain a magnetic powder. The cobalt component in the resulting magnetic powder was 2.8 wt.% as Co. The magnetic characteristics of the magnetic powder are as follows:

Hc=550 Oe; .sigma..sub.s =emu/g; .sigma..sub.r /.sigma..sub.s =0.5.

REFERENCE 7

The magnetic powder obtained in Reference 6 was heat-treated in nitrogen atmosphere at 400.degree. C. The magnetic characteristics of the resulting magnetic powder are as follows:

Hc=1000 Oe; .sigma..sub.s =73 emu/g; .sigma..sub.r /.sigma..sub.s =0.53. TABLE 1__________________________________________________________________________ Exp. 1 Exp. 2 Exp. 3 Exp. 4 Ref. 1__________________________________________________________________________Type:Co-adsorbed O O O O --Co-doped -- -- -- -- OHeat treatment none none none none OFormulation (wt. %):Seed .gamma.-Fe.sub.2 O.sub.3 O O O O OSeed Fe.sub.3 O.sub.4 -- -- -- -- --Co content 6.5 7.5 10.0 12.0 7.5Fe content 20.0 30.0 40.0 36.0 30.0ratio of Fe.sup.2+ /Co.sup.2+ 3.0/1 4.0/1 4.0/1 3.0/1 4.0/1Magnetic characteristic:Hc 1000 1100 1150 1225 1300.sigma..sub.s 76.5 76.5 76.5 76.5 76.0.sigma..sub.r /.sigma..sub.s 0.52 0.52 0.53 0.52 0.54Temp. characteristic-196.degree. C./room temp.:ratio of Hc 2.2 2.2 2.4 2.3 3.4ratio of .sigma..sub.r 1.34 1.34 1.34 1.35 1.61ratio of .sigma..sub.s 1.03 1.03 1.04 1.02 0.89Product ratio of Fe.sup.2+ /Co.sup.2+ 2.4 2.7 2.8 2.2__________________________________________________________________________ O shows the correspondency TABLE 1'__________________________________________________________________________ Ref. 2 Ref. 3 Ref. 4 Ref. 5 Ref. 6 Ref. 7__________________________________________________________________________Type:Co-adsorbed O O O -- O --Co-doped -- -- -- O -- OHeat Treatment none none none O none OFormulation (wt. %):Seed .gamma.-Fe.sub.2 O.sub.3 O O -- -- O OSeed Fe.sub.3 O.sub.4 -- -- O O -- --Co content 6.0 6.0 4.0 4.0 3.0 3.0Fe content 36.0 15.0 0 0 5.0 5.0ratio of Fe.sup.2+ /Co.sup.2+ 6.0/1 2.5/1 1.7/1 1.7/1Magnetic characteristic:Hc 950 825 600 1300 550 1000.sigma..sub.s 78.0 75.0 76.0 76.0 74.0 73.0.sigma..sub.r /.sigma..sub.s 0.51 0.51 0.50 0.53 0.50 0.53Temp. characteristic-196.degree. C./room temp.:ratio of Hc 2.4 2.0 1.6 3.1 2.3 4.3ratio of .sigma..sub.r 1.35 1.30 1.2 1.81 1.4 1.5ratio of .sigma..sub.s 1.03 1.00 1.06 0.98 1.06 0.93__________________________________________________________________________ O shows the correspondency

Claims

1. A magnetic powder for a magnetic recording medium which is a cobalt-adsorbed magnetic iron oxide comprising .gamma.-Fe.sub.2 O.sub.3, having a coercive force of at least 1000 Oe and a ratio of a coercive force at -196.degree. C. to a coercive force at room temperature of 3 or less, which magnetic powder is obtained by coating said .gamma.-Fe.sub.2 O.sub.3 in dispersion with a cobalt component by adding cobalt ion to .gamma.-Fe.sub.2 O.sub.3 at a ratio of 6 wt. % or more, and then adding ferrous ion at a ratio of 20 wt. % or more as Fe.sup.2+ based on .gamma.-Fe.sub.2 O.sub.3 and at a ratio of said ferrous salt to said cobalt salt of 3.0 to 4.5 by weight so as to adsorb Fe.sup.2+ and Co.sup.2+ in a Fe.sup.2+ /Co.sup.2+ weight ratio of 2.0 to 3.5.