JP4856602B2 - Iron-based soft magnetic powder for dust core and dust core - Google Patents

Description

  The present invention relates to an iron-based soft magnetic powder for dust cores and a dust core particularly excellent in mechanical strength and electrical insulation.

2. Description of the Related Art In recent years, a powder magnetic core obtained by compression-molding soft magnetic powder is being used as an electromagnetic component that is used in an alternating magnetic field and has excellent magnetic characteristics and a high degree of freedom in three-dimensional shape. For example, the following soft magnetic powder is compression-molded for the purpose of low iron loss and high magnetic flux density as a core material (powder magnetic core) for motors and transformers used at a frequency of about 50 kHz or less, and then strained. The thing of the structure which removes and anneals is known (patent document 1). In addition, the soft magnetic powder for a dust core is coated with iron oxide on the surface of pure iron powder for the purpose of excellent compressibility and high insulation properties. The structure is such that at least one insulating layer selected from oxides, carbonates and sulfates is coated, and the surface of this insulating layer is further coated with a silicone resin layer (Patent Document 1).
JP 2006-233295 A

  The conventional dust core performs strain relief annealing at a high temperature in order to reduce hysteresis loss. In addition, in order to suppress the heat insulation at this high temperature, which in turn reduces the electrical insulation and easily reduces the specific resistance, the iron oxide covering the surface of the pure iron powder and the surface of the iron oxide After providing the insulating layer covering the film, there is a problem that the following high-temperature heat treatment must be added. This heat treatment at a high temperature is referred to as a bond strengthening treatment, and heat treatment must be performed at 500 to 1200 ° C. for 20 to 240 minutes in a non-oxidizing atmosphere.

  The present invention solves the above-mentioned problems, and does not add a heat treatment at a high temperature called a bond strengthening process, and has excellent mechanical strength even when molded at a high density, and iron-based soft magnetic powder particles An iron-based soft magnetic powder for dust cores with excellent thermal stability that can effectively insulate the gap and maintain good electrical insulation even after strain relief annealing, and this powder It aims at providing the used powder magnetic core.

In order to achieve the above object, the invention according to claim 1 of the present invention is characterized in that Fe and Co are formed on the surface of an iron-based (excluding Fe-Co alloy and Fe-Ni-Co alloy) soft magnetic powder. An iron-based soft magnetic powder for a dust core, characterized in that a coating film, a phosphoric acid-based chemical conversion film not containing Co, and a silicone resin film are formed in this order. This makes it possible to effectively insulate the iron-based soft magnetic powder particles even when molded at a high density without applying a heat treatment at a high temperature called a bond strengthening treatment. Furthermore, it is possible to realize an iron-based soft magnetic powder for a dust core that is excellent in thermal stability so that electrical insulation can be maintained well even if strain relief annealing is performed. Moreover, since the phosphoric acid-based chemical conversion film does not contain Co, a high specific resistance can be maintained even if the strain relief annealing is performed at a higher temperature.

The invention according to claim 2 is characterized in that, in the invention according to claim 1, the film thickness of the coating made of Fe and Co is 1 to 10 nm. As a result, the degree of freedom of deformation of the iron-based soft magnetic powder can be secured while maintaining the formability of the film made of Fe and Co, so that the density of the powder at the time of molding can be increased and a high magnetic flux density can be realized.

The invention described in claim 3 is characterized in that, in the invention described in claim 1 or 2 , the silicone resin for forming the silicone resin film is a trifunctional methyl silicone resin. Thereby, the handleability of the powder during molding is improved.

The invention according to claim 4 is a dust core obtained by molding the iron-based soft magnetic powder for dust core according to any one of claims 1 to 3 . If such a magnetic core is used at a frequency of about 50 kHz or less, for example, a low iron loss and a high magnetic flux density can be realized as a core material for a motor or transformer, and the performance of the motor or transformer can be improved.

As described above, the present invention provides an iron-based (excluding Fe-Co alloy and Fe-Ni-Co alloy) soft magnetic powder surface, a coating made of Fe and Co, and phosphoric acid not containing Co. Since the chemical conversion coating and the silicone resin coating are formed in this order, the iron-based soft magnetic powder for the dust core is not subjected to heat treatment at a high temperature called bond strengthening treatment, and Even when molded at high density, it has excellent mechanical strength, can effectively insulate between iron-based soft magnetic powder particles, and can maintain good electrical insulation even after strain relief annealing Thus, an iron-based soft magnetic powder for a dust core having excellent thermal stability can be realized. Moreover, since the phosphoric acid-based chemical conversion film does not contain Co, a high specific resistance can be maintained even if the strain relief annealing is performed at a higher temperature.

  Further, since the present invention is a dust core obtained by molding the iron-based soft magnetic powder for a dust core, if such a core is used at a frequency of about 50 kHz or less, for example, a motor or transformer As a core material, it is possible to realize a low iron loss and a high magnetic flux density, thereby improving the performance of a motor and a transformer.

  Hereinafter, the present invention will be described in more detail while illustrating embodiments.

(Configuration of iron-based soft magnetic powder for dust core and dust core using this powder according to the present invention)
An iron-based soft magnetic powder for a dust core according to the present invention has a coating made of Fe and Co on an iron-based (excluding Fe-Co alloy and Fe-Ni-Co alloy) soft magnetic powder surface, An iron-based soft magnetic powder for a dust core, in which a phosphoric acid-based chemical conversion film not containing Co and a silicone resin film are formed in this order. This makes it possible to effectively insulate the iron-based soft magnetic powder particles even when molded at a high density without applying a heat treatment at a high temperature called a bond strengthening treatment. Furthermore, it is possible to realize an iron-based soft magnetic powder for a dust core that is excellent in thermal stability so that electrical insulation can be maintained well even if strain relief annealing is performed. Moreover, since the phosphoric acid-based chemical conversion film does not contain Co, a high specific resistance can be maintained even if the strain relief annealing is performed at a higher temperature.

  Moreover, it is preferable that the film thickness of the film which consists of Fe and Co is 1-10 nm. As a result, the degree of freedom of deformation of the iron-based soft magnetic powder can be secured while maintaining the formability of the film made of Fe and Co, so that the density of the powder at the time of molding can be increased and a high magnetic flux density can be realized. More preferably, the film thickness of the film made of Fe and Co is about 1 to 2 nm.

  Moreover, it is preferable that the silicone resin for forming a silicone resin film is a trifunctional methyl silicone resin. Thereby, the handleability of the powder during molding is improved.

  Hereinafter, the reason for the above configuration will be described in detail.

  The present inventors, in any case, have improved mechanical strength when molded at a high density without heat treatment at a high temperature called a bond strengthening treatment such as the conventional iron-based soft magnetic powder for dust cores. Excellent iron core for powder magnetic cores, which can effectively insulate between iron-based soft magnetic powder particles and has excellent thermal stability that can maintain good electrical insulation even after strain relief annealing We conducted intensive research on whether or not a base soft magnetic powder could be realized. As a result, the following points were found as the most important points. It actively excludes Co as an additive element from the treatment solution for phosphate conversion coating for coating the surface of iron-based soft magnetic powder for dust cores, but instead contains this Co alone. The above problem can be solved by first forming a coating film on the surface of the powder using a cobalt phosphate aqueous solution. The detailed mechanism of why such a configuration can solve the above problem has not yet been elucidated. However, as one mechanism, the film formed using the cobalt phosphate aqueous solution suppresses the aggregation of the phosphate conversion coating that does not contain Co formed thereon, and as a result, this phosphate conversion coating It is considered that tearing (physical destruction) is suppressed, mechanical strength is excellent, and electrical insulation can be maintained well.

  The present invention is described in detail below.

  The iron-based soft magnetic powder is a ferromagnetic metal powder, and specific examples include pure iron powder, iron-based alloy powder (Fe-A1 alloy, Fe-Si alloy, Sendust, Permalloy, etc.) and amorphous powder. Can be mentioned. Such a soft magnetic powder can be produced, for example, by reducing it into fine particles by the atomizing method, reducing it, and then pulverizing it. In such a production method, a soft magnetic powder having a particle size distribution evaluated by the sieving method and having a cumulative particle size distribution of 50% and a particle size of about 20 to 250 μm is obtained. In the present invention, the average particle size is 50 to 50 μm. Those having a thickness of about 150 μm are preferably used.

In the present invention, a coating containing Co as a main component is first formed on the soft magnetic powder. The coating containing Co as a main component is obtained by adding an aqueous solution of cobalt phosphate {Co ₃ (PO ₄ ) ₂ or Co ₃ (PO ₄ ) ₂ · 8H ₂ O} to the soft magnetic powder to form a V-type mixer. It is obtained by mixing for 30 minutes or more and then drying in the air for 30 minutes. The Co concentration in this case is 0.005 to 0.1% by mass in 100% by mass of the soft magnetic powder. Thereby, the film thickness of the film containing Co as a main component (finally, the film that becomes a mixed layer of Fe and Co) is set to 1 nm to 10 nm. This is because if the film thickness is less than 1 nm, a sufficient effect of improving the specific resistance cannot be obtained when the strain relief annealing temperature is 450 ° C. or higher, and it is difficult to form the film itself. On the other hand, if the thickness exceeds 10 nm, a hard shell is formed, the powder cannot be deformed and the density is hardly increased, and it is difficult to increase the thickness of the coating itself. Preferably, it is about 1-2 nm.

Next, a phosphoric acid-based chemical conversion film is formed on the soft magnetic powder on which the film containing Co as a main component is formed. This phosphoric acid-based chemical conversion film is a glassy film formed by chemical conversion treatment with a treatment liquid containing orthophosphoric acid (H ₃ PO ₄ ) as a main component. In the present invention, the phosphate conversion coating film may contain one or more elements selected from the group consisting of Na, S, Mg, B and W in addition to P. Two or more of these elements may be used in combination. The addition amount of these elements is as follows: P is 0.005 to 1% by mass, Na is 0.002 to 0.6% by mass, and S is 0.001 to 0.2% in 100% by mass of the soft magnetic powder. Mass%, Mg is 0.001 to 0.5 mass%, B is 0.001 to 0.5 mass%, and W is preferably 0.011 to 0.5 mass%. However, Co is not included. In addition, the film thickness adjustment of a phosphoric acid type | system | group chemical conversion film adjusts the ratio of the process liquid with respect to soft-magnetic powder (If a ratio is doubled, thickness will double), or the dilution rate of a process liquid is adjusted. (If the magnification is halved, the film thickness is doubled.) The phosphoric acid-based chemical conversion film is prepared by mixing a treatment liquid adjusted to a predetermined amount and soft magnetic powder using a known mixer, ball mill, kneader, V-type mixer, granulator, etc., and in the atmosphere, under reduced pressure, or vacuum Under drying at 150-250 ° C. In the present invention, a very important point is that in the subsequent step, it is necessary to perform a heat treatment at 500 to 1200 ° C. for 20 to 240 minutes in a non-oxidizing atmosphere referred to as a bond strengthening treatment as in the prior art. It is not.

Next, a silicone resin film is further formed on the surface of the soft magnetic powder covered with the phosphoric acid-based chemical conversion film. At the end of the crosslinking / curing reaction of the silicone resin (at the time of molding the green compact), the powders are firmly bonded to each other, so that the mechanical strength is increased. In addition, an Si—O bond having excellent heat resistance is formed to provide an insulating film having excellent thermal stability. As a silicone resin, since the powder is sticky when the curing is slow and the handling property after film formation is poor, the trifunctionality is higher than the bifunctional D unit (R ₂ SiX ₂ : X is a hydrolyzable group). It is preferable to have a large number of T units (RSiX ₃ : X is the same as described above). However, if a large amount of tetrafunctional Q units (SiX ₄ : X is the same as described above) is contained, the powder simultaneously binds strongly at the time of preliminary curing, and the subsequent molding process cannot be performed. It is not preferable. Accordingly, a silicone resin having a T unit of 60 mol% or more is preferable, a silicone resin having 80 mol% or more is more preferable, and a silicone resin having all T units is most preferable.

  Further, as the silicone resin, a methylphenyl silicone resin in which R is a methyl group or a phenyl group is generally used, and it is considered that the heat resistance is higher when waiting for more phenyl groups, but this is intended in the present invention. In such a high temperature heat treatment, the presence of the phenyl group was not so effective. It is thought that the bulkiness of the phenyl group may disturb the delicate glassy network structure and reduce the thermal stability and the compound formation inhibitory effect with iron. Therefore, in the present invention, it is preferable to use a methylphenyl silicone resin having a methyl group of 50 mol% or more (for example, KR255, KR311, etc. manufactured by Shin-Etsu Chemical Co., Ltd.), and 70 mol% or more (for example, manufactured by Shin-Etsu Chemical Co., Ltd. KR300, etc.) are more preferable, and methyl silicone resins that do not wait for phenyl groups at all (for example, KR251, KR400, KR22OL, KR242A, KR240, KR500, KC89, etc., manufactured by Shin-Etsu Chemical Co., Ltd.) are most preferable. In addition, about the ratio and functionality of the methyl group of a silicone resin, and a phenyl group, it can analyze by FT-IR etc.

  The adhesion amount of the silicone resin coating is adjusted to be 0.05 to 0.3% by mass when the total of the soft magnetic powder on which the phosphoric acid-based chemical conversion coating is formed and the silicone resin coating is 100% by mass. It is preferable. If the amount is less than 0.05% by mass, the insulating property is inferior and the electric resistance is lowered. However, if the amount is more than 0.3% by mass, it is difficult to achieve high density of the molded body.

  The silicone resin coating can be formed by dissolving a silicone resin in alcohols, petroleum-based organic solvents such as toluene and xylene, and mixing the solution and soft magnetic powder to volatilize the organic solvent. The film forming conditions are not particularly limited, but the resin solution prepared so that the solid content is about 2 to 10% by mass is added to 100 parts by mass of the soft magnetic powder on which the phosphoric acid-based chemical conversion film is formed. On the other hand, about 0.5 to 10 parts by mass may be added, mixed and dried. If the amount is less than 0.5 parts by mass, mixing may take time or the coating film may become non-uniform. On the other hand, if it exceeds 10 parts by mass, drying may take time or drying may be insufficient. The resin solution may be appropriately heated. The same mixer as described above can be used.

  In the drying step, it is desirable to sufficiently evaporate the organic solvent by heating to a temperature at which the organic solvent used volatilizes and below the curing temperature of the silicone resin. A specific drying temperature is preferably about 60 to 80 ° C. in the case of the alcohols and petroleum organic solvents described above. After drying, it is preferable to pass through a sieve having a predetermined opening in order to remove aggregated lumps.

  In addition, the film thickness adjustment of a silicone resin film can respond | correspond by adjusting the ratio of the resin solid content with respect to a soft-magnetic powder (If a ratio is doubled, thickness will double).

  Next, it is recommended to pre-cure the dried silicone resin film. The pre-curing is a process for terminating the softening process at the time of curing the silicone resin film in a powder state. By this pre-curing treatment, the flowability of the soft magnetic powder can be ensured during warm forming (about 100 to 250 ° C.). As a specific method, a method of heating a soft magnetic powder having a silicone resin coating formed in the vicinity of the curing temperature of the silicone resin for a short time is simple, but a method using a drug (curing agent) can also be used. is there. The difference between pre-curing and curing (complete curing that is not preliminary) is that the pre-curing process can be easily crushed without completely solidifying the powder, whereas In the high temperature heat curing process to be performed, the resin is cured and the powders are bonded and solidified. The strength of the molded body is improved by the complete curing treatment.

As mentioned above, after pre-curing the silicone resin, it can be crushed to obtain a powder with excellent fluidity, which can be poured into the mold during sand compaction like sand. become able to. If it is not pre-cured, for example, powders may adhere to each other during warm molding, and it may be difficult to charge the mold in a short time. In practical operation, the improvement of handling is very significant. It has also been found that the specific resistance of the resulting dust core is greatly improved by pre-curing. The reason for this is not clear, but it is thought that this is because the adhesiveness with the soft magnetic powder during curing increases.

  When pre-curing is performed by a short-time heating method, the heat treatment is preferably performed at 100 to 200 ° C. for 5 to 100 minutes. 10-30 minutes is more preferable at 130-170 degreeC. Even after the preliminary curing, as described above, it is preferable to pass through a sieve.

The iron-based soft magnetic powder for dust core of the present invention may further contain a lubricant. The action of this lubricant can reduce the frictional resistance between the soft magnetic powder during compression molding of the powder for the powder magnetic core, or between the soft magnetic powder and the inner wall of the molding die, and it can reduce the mold galling and heat generation during molding. Can be prevented. In order to effectively exhibit such an effect, it is preferable that the lubricant is contained in an amount of 0.2% by mass or more in the total amount of the powder. However, if the amount of lubricant increases, it is against the densification of the green compact, so it is preferable to keep it at 0.8% by mass or less. Further, when compression molding is performed, a lubricant is applied to the inner wall surface of the mold and then molded (mold lubrication molding), and the amount of lubricant may be less than 0.2% by mass.

  As the lubricant, conventionally known ones may be used. Specifically, metal stearate powder such as zinc stearate, lithium stearate, calcium stearate, and paraffin, wax, natural or synthetic resin derivatives. Etc.

  The iron-based soft magnetic powder for dust core of the present invention is used for the production of a core material (dust core) used at a frequency of about 50 kHz or less, such as for motors and transformers. In order to manufacture this powder magnetic core, first, the powder is compression molded. The compression molding method is not particularly limited, and a conventionally known method can be employed.

A suitable condition for compression molding is a surface pressure of 490 MPa to 1960 MPa, more preferably 790 MPa to 1180 MPa. In particular, when compression molding is performed under conditions of 980 MPa or more, a dust core having a density of 7.50 g / cm ³ or more can be easily obtained, and a dust core having high strength and good magnetic properties (magnetic flux density) can be obtained. preferable. The molding temperature can be either room temperature molding or warm molding (100 to 250 ° C.). It is preferable to perform warm molding by mold lubrication molding because a high-strength powder magnetic core can be obtained.

  After molding, heat treatment is performed at a high temperature to reduce the hysteresis loss of the dust core. The heat treatment temperature at this time is preferably 400 ° C. or higher, and it is desirable to perform the heat treatment at a higher temperature (specifically, 500 ° C. to 600 ° C. is preferable) if there is no deterioration in specific resistance. The heat treatment atmosphere is not particularly limited as long as it does not contain oxygen, but is preferably an inert gas atmosphere such as nitrogen. The heat treatment time is not particularly limited as long as the specific resistance does not deteriorate, but is preferably 20 minutes or more, and more preferably 30 minutes or more.

  Hereinafter, the present invention will be described in detail based on examples. However, the following examples are not intended to limit the present invention, and all modifications made without departing from the spirit of the preceding and following descriptions are included in the technical scope of the present invention. Unless otherwise specified, “part” means “part by mass” and “%” means “% by mass”.

(Effect of the first coating of iron-based soft magnetic powder (coating composed of Fe and Co))
A pure iron powder (manufactured by Kobe Steel; Atmel 300NH; average particle size of 80 to 100 μm) was used as the iron-based soft magnetic powder, and a coating containing Co as a main component was first formed. Specifically, water: 1000 _parts, by mixing Co _{3 (PO 4)} 2 30 parts, further treatment liquid 200g diluted 10-fold, was added to the pure iron powder 1000g through a sieve having a mesh opening 300μm Then, after mixing for 30 minutes or more using a V-type mixer, it was dried in the air for 30 minutes and passed through a sieve having an opening of 300 μm. The film formed under these conditions was composed of Fe and Co, and the film thickness was 7 nm.

  Next, a phosphoric acid-based chemical conversion film (however, Co is not included) was formed on the pure iron powder on which the film containing Co as a main component was formed. The composition of the treatment liquid for forming the phosphoric acid-based chemical conversion film (stock solution before 10-fold dilution) was as follows (in addition, the additive elements in the phosphoric acid-based chemical conversion film formed thereby were designated as No. 1 in Table 1). 1-25). However, the phosphorus concentration in this case was 0.07% by mass in 100% by mass of pure iron powder. For comparison, a treatment liquid (diluted 10 times) for forming a phosphoric acid-based chemical conversion film in which Co is directly added to pure iron powder on which the Co-based film is not formed on the surface in advance. The composition of the previous stock solution is also shown below (and the additive elements in the phosphoric acid-based chemical conversion film formed thereby are shown in Nos. 26 to 50 in Table 2).

No. Treatment liquid used in 1 to 5: water: 1000 parts, H ₃ PO ₄ : 193 parts Treatment liquid used in 6 to 10: water: 1000 parts, H ₃ PO ₄ : 193 parts, MgO: 31 parts, H ₃ BO ₃ : 30 parts Treatment liquid used in 11-15 ... water: 1000 _parts, H ₃ PO 4: 193 parts, MgO: 31 _parts, H 3 _BO 3: 30 _{parts, H 3 PW l2 O 40 ·} nH 2 0: 150 parts No. Treatment liquid used in 16 to 20: water: 1000 parts, H ₃ PO ₄ : 193 parts, MgO: 31 parts, H ₃ BO ₃ : 30 parts, SiO ₂ · 12WO ₃ · 26H ₂ 0: 150 parts Treatment liquid used in 21 to 25: water: 1000 parts, Na ₂ HPO ₄ : 88.5 parts, H ₃ PO ₄ : 181 parts, H ₂ SO ₄ : 61 parts Treatment liquid used in Nos. 26 to 30: Water: 1000 parts, H ₃ PO ₄ : 193 parts, Co ₃ (PO ₄ ) ₂ : 30 parts Treatment liquid used in 31 to 35: water: 1000 parts, H ₃ PO ₄ : 193 parts, MgO: 31 parts, H ₃ BO ₃ : 30 parts, Co ₃ (PO ₄ ) ₂ : 30 parts Treatment liquid used in 36 to 40 ... water: 1000 _parts, H ₃ PO 4: 193 parts, MgO: 31 _parts, H 3 _BO 3: 30 _{parts, H 3 PW l2 O 40 ·} nH 2 0: 150 parts, Co _{3 (PO 4)} 2: 30 parts No. Treatment liquid used in 41 to 45: water: 1000 parts, H ₃ PO ₄ : 193 parts, MgO: 31 parts, H ₃ BO ₃ : 30 parts, SiO ₂ · 12WO ₃ · 26H ₂ 0: 150 parts, Co _{3 (PO 4)} 2: 30 parts No. Treatment liquid used in 46 to 50: Water: 1000 parts, Na ₂ HPO ₄ : 88.5 parts, H ₃ PO ₄ : 181 parts, H ₂ SO ₄ : 61 parts, Co ₃ (PO ₄ ) ₂ : 30 parts

  Next, a silicone resin “KR220L” manufactured by Shin-Etsu Chemical Co., Ltd. was dissolved in toluene to prepare a resin solution having a solid content concentration of 4.8%. The resin solution was mixed with the above-mentioned sample no. It added and mixed so that resin solid content might be 0.1 mass% with respect to each 1-50 pure iron powder. This was heated in an oven furnace at 75 ° C. for 30 minutes in the atmosphere, dried to form a silicone resin film, and then passed through a sieve with a predetermined opening.

  Subsequently, the sample No. 1 was coated with the silicone resin film. Each 1-50 pure iron powder was pre-cured in air at 150 ° C. for 30 minutes. Thereafter, compacting using a mold as described below was performed.

Next, after the zinc stearate was dispersed in alcohol and applied to the surface of the mold, the pre-curing treatment was completed. 1 to 50 pure iron powders were placed in the above molds and press molded at room temperature at a surface pressure of 980 MPa. The dimensions of the pressed toroidal compact after the press molding are outer diameter φ45 mm × inner diameter φ33 mm × height 5 mm, and the density is 7.5 g / cm ³ . Then, these compacting bodies were heat-processed (annealing) which hold | maintained at 400 degreeC-600 degreeC for 30 minutes in nitrogen atmosphere, and was furnace-cooled after that. The heating rate was about 5 ° C./min. The specific resistances of the toroidal shaped compacts thus obtained (corresponding to the above sample Nos. 1 to 50) were measured by the four-terminal method (measurement results are shown in Tables 1 and 2, respectively). )

  For example, a core material (a powder magnetic core) for a motor or transformer used at about 50 kHz or less is required to realize both a low iron loss and a high magnetic flux density. For this purpose, it is first necessary to form a high density in order to satisfy a high magnetic flux density, in which case the mechanical strength is also excellent, and the pure iron powder particles must be effectively insulated. In order to reduce the iron loss, the hysteresis loss must be reduced. For this purpose, stress relief annealing is performed (the higher the stress relief annealing, the greater the effect of reducing hysteresis loss), but the thermal stability is such that electrical insulation can be maintained well even after this heat treatment. Therefore, there is a need for a pure iron powder for a dust core that is excellent in resistance (a decrease in resistivity is suppressed even when subjected to high-temperature heat treatment). This is because, if the specific resistance is remarkably lowered, for example, eddy current loss becomes extremely large when used at about 50 kHz, and low iron loss cannot be realized. This results in a decrease in the performance of the motor and transformer. As described above, it is extremely important to suppress a decrease in specific resistance after the stress relief annealing performed at a higher temperature. From such a viewpoint, the measurement results of the specific resistance shown in Tables 1 and 2 will be considered.

  For example, the examples in Table 1 (Sample Nos. 1 to 5; Co is not added as an additive element in the phosphoric acid-based chemical conversion coating. However, Co is present in the lower layer coating) and the comparative examples in Table 2 (Sample No. .26-30: Co as an additive element in the phosphoric acid-based chemical conversion coating film, but there is no lower layer coating itself. ) Also has a higher specific resistance. Moreover, the effect becomes more remarkable as the heat treatment temperature is higher. This tendency is similar to other examples (samples Nos. 6 to 10, Nos. 11 to 15, Nos. 16 to 20, Nos. 21 to 25) and comparative examples (samples Nos. 31 to 35, Nos. 36 to 40). , No. 41 to 45, No. 46 to 50), and the same result. Moreover, an Example (sample No. 21-25) has a relatively high specific resistance in all the Examples. In particular, the specific resistance is high when the heat treatment temperature is 600 ° C.

  The phosphoric acid-based chemical conversion film may inevitably contain some Co, but it is desirable that it does not contain Co. Thereby, a high specific resistance can be maintained even if the strain relief annealing is performed at a higher temperature.

  These results show that after removing Co from the additive element in the phosphoric acid-based chemical conversion film and adding it separately as a single element in the treatment liquid for forming the coating underneath it, after high-temperature heat treatment (strain relief annealing) It shows that a decrease in specific resistance can be suppressed. In order to produce these effects, a heat treatment at a high temperature called a bond strengthening treatment is additionally applied after the formation of the first layer coating and the second layer coating on the surface of pure iron powder as in the conventional example. The biggest advantage is that it is no longer necessary.

Claims (4)

An iron-based (excluding Fe-Co alloy and Fe-Ni-Co alloy) soft magnetic powder surface, a coating made of Fe and Co, a phosphate-based chemical conversion coating not containing Co , a silicone resin coating, Are formed in this order, an iron-based soft magnetic powder for a dust core. The iron-based soft magnetic powder for a dust core according to claim 1, wherein the film made of Fe and Co has a thickness of 1 to 10 nm. Silicone resins for forming the silicone resin coating film, trifunctional dust core for iron-based soft magnetic powder according to claim 1 or 2, characterized in that the methyl silicone resin. A dust core obtained by molding the iron-based soft magnetic powder for dust core according to any one of claims 1 to 3 .