Patent Application
20220177694
The present invention relates to a resin composition for forming a magnetic member and a method for manufacturing a magnetic member.
So far, various developments have been conducted in magnetic members. As a technique of this kind, for example, a technique disclosed in Patent Document 1 is known. Patent Document 1 discloses that, in production of a dust magnetic core stator obtained by compacting, joining, and solidifying magnetic powder, single-crystal iron powder is used as the magnetic powder (claim 1 and the like of Patent Document 1).
[Patent Document 1] Japanese Unexamined Patent Publication No. 2004-282832
However, as a result of studies, the present inventor has found that, in the magnetic member disclosed in Patent Document 1, there is room for improvement in terms of magnetic characteristics.
It has been known that magnetic particles include crystalline magnetic powder and amorphous magnetic powder. For example, in a case of a magnetic core, since the amorphous magnetic powder has better iron loss characteristics, attempts have been made to use the amorphous magnetic powder.
In such an attempt, in a case of producing a magnetic member such as a dust core, usually, a powder molding method (pressing method) has been used (see Patent Document 1 and the like). This powder molding method requires high pressure and high temperature during molding.
However, in a case where high pressure and high temperature are applied, amorphous material (noncrystalline) in the magnetic powder may undergo structural change and crystallize, resulting in an increase in core loss. As a result, the iron loss characteristics due to the amorphous magnetic powder may not be sufficiently obtained.
As a result of further studies based on such circumstances, the present inventor has found that, by using a transfer molding method instead of the powder molding method, a magnetic core can be produced under relatively low pressure and low temperature molding conditions, so that the iron loss characteristics due to the amorphous magnetic powder can be sufficiently obtained.
As a result of further diligent studies based on such findings, the present inventor has found that, by utilizing low-pressure and low-temperature transfer molding using a binder resin such as a thermosetting resin, excellent magnetic characteristics such as iron loss can be exhibited in a magnetic member using a resin composition for forming a magnetic member, which includes iron-based amorphous particles, thereby completing the present invention.
According to the present invention, a resin composition for forming a magnetic member, which is used for a transfer molding, including a thermosetting resin and iron-based particles, in which the iron-based particles include iron-based amorphous particles, is provided.
In addition, according to the present invention, a method for manufacturing a magnetic member, which includes injecting a molten product of the above-described resin composition for forming a magnetic member into a mold using a transfer molding apparatus and curing the molten product to obtain a magnetic member, is provided.
According to the present invention, a resin composition for forming a magnetic member having excellent magnetic characteristics and a method for manufacturing a magnetic member using the same are provided.
Hereinafter, embodiments of the present invention will be described with reference to the drawings. In all drawings, the same constituents are designated by the same reference numerals, and description thereof will not be repeated. In addition, the drawings are schematic views and do not match the actual dimensional ratio.
In the present specification, a term “abbreviation” means to include a range in consideration of manufacturing tolerances, assembly variations, and the like, unless otherwise specified explicitly.
In the present specification, a notation “a to b” in a description of a numerical range means a or more and b or less unless otherwise specified. For example, “1 to 5% by mass” means “1% by mass or more and 5% by mass or less”.
In a notation of a group (atomic group) in the present specification, a notation which does not indicate whether it is substituted or unsubstituted includes both those having no substituent and those having a substituent. For example, an “alkyl group” includes not only an alkyl group having no substituent (unsubstituted alkyl group) but also an alkyl group having a substituent (substituted alkyl group).
Unless otherwise specified, a term “organic group” in the present specification means an atomic group obtained by removing one or more hydrogen atoms from an organic compound. For example, a “monovalent organic group” represents an atomic group obtained by removing one hydrogen atom from any organic compound.
The outline of the resin composition for forming a magnetic member according to the present embodiment will be described.
The resin composition for forming a magnetic member according to the present embodiment is a resin composition used for transfer molding, and is a resin composition used for forming a magnetic member. This resin composition includes a thermosetting resin and iron-based particles. The iron-based particles included in the resin composition include iron-based amorphous particles.
According to the findings of the present inventor, since molding can be performed under relatively low pressure and low temperature conditions by using transfer molding, in a magnetic member formed by using a resin composition for forming a magnetic member including iron-based amorphous particles, magnetic characteristics such as iron loss and relative magnetic permeability can be improved.
Although the detailed mechanism is not clear, it is considered that, in contrast to the phenomenon that an amorphous component (noncrystalline) in the iron-based particles changes its structure into crystals at high temperature and high pressure, such as powder treatment, amorphous structural changes can be suppressed by using transfer molding under low pressure and low temperature conditions. Therefore, sufficient magnetic characteristics such as iron loss and relative magnetic permeability due to the amorphous magnetic powder can be obtained.
In addition, by using the resin composition according to the present embodiment, it is possible to realize a magnetic member having low thermal expansion even at room temperature or high temperature. Such a magnetic member can also be adopted to use in a high temperature environment.
The magnetic member according to the present embodiment can be used for various applications, and can be suitably used, for example, as a magnetic component in an electric/electronic device. More specifically, it is preferable to be used as a magnetic core of a coil or the like.
<Resin Composition>
Components which can be included in the resin composition according to the present embodiment will be described.
The resin composition includes a thermosetting resin and a magnetic powder.
(Thermosetting Resin)
Examples of the thermosetting resin include an epoxy resin, a phenol resin, a polyimide resin, a bismaleimide resin, a urea resin, a melamine resin, a polyurethane resin, a cyanate ester resin, a silicone resin, an oxetane resin (oxetane compound), a (meth)acrylate resin, an unsaturated polyester resin, a diallyl phthalate resin, and a benzoxazine resin. These may be used alone or in combination of two or more thereof. From the viewpoint of heat resistance, for example, an epoxy resin may be used.
(Epoxy Resin)
The resin composition according to the present embodiment may include an epoxy resin.
The epoxy resin may be any resin as long as it includes an epoxy group. Examples of the epoxy resin include bisphenol-type epoxy resins such as a bisphenol A-type epoxy resin, a bisphenol F-type epoxy resin, a tetramethyl bisphenol F-type epoxy resin, a bisphenol S-type epoxy resin, a bisphenol E-type epoxy resin, a bisphenol M-type epoxy resin, a bisphenol P-type epoxy resin, and a bisphenol Z-type epoxy resin; novolac-type epoxy resins such as a phenol novolac-type epoxy resin and a cresol novolac-type epoxy resin; and epoxy resins such as a biphenyl-type epoxy resin, a biphenyl aralkyl-type epoxy resin, an arylalkylene-type epoxy resin, a naphthalene-type epoxy resin, an anthracene-type epoxy resin, a phenoxy-type epoxy resin, a dicyclopentadiene-type epoxy resin, a norbornene-type epoxy resin, an adamantane-type epoxy resin, a fluorene-type epoxy resin, and a trisphenylmethane-type epoxy resin.
The epoxy resin may be semi-cured (solid) at room temperature (25° C.)
The epoxy resin may include a polyfunctional epoxy resin having three or more epoxy groups in a molecule and/or a low-viscosity epoxy resin having an ICI viscosity at 150° C. of 0.1 to 50 mPa·s.
In particular, it is preferable that the epoxy resin includes at least one selected from the group consisting of an epoxy resin including a trisphenylmethane structure as an example of the polyfunctional epoxy resin and an epoxy resin including a bisphenol structure as an example of the low-viscosity epoxy resin. It is considered that, due to appropriate rigidity of the structures of these epoxy resins, it is easy to make curing behavior more appropriate, and by extension, moldability can be further improved.
(Epoxy Resin (A1))
The resin composition according to the present embodiment may include an epoxy resin (A1) (also simply referred to as an “epoxy resin (A1)”) having a triarylmethane skeleton.
The “having a triarylmethane skeleton” specifically includes a partial structure in which three of four hydrogen atoms of a methane (CH4) are replaced with aromatic rings. The “aromatic ring” here may be a benzene-based aromatic ring such as a benzene ring or a naphthalene ring, or may be a heteroaromatic ring such as furan, thiophene, pyrrole, pyrazole, imidazole, pyridine, pyridazine, pyrimidine, and pyrazine. In addition, the three aromatic rings may be the same or different from each other.
However, from the viewpoint of cost, the viewpoint of mechanical properties of a molded product (magnetic member), and the like, the aromatic ring is preferably a benzene-based aromatic ring such as a benzene ring or a naphthalene ring. In addition, it is preferable that the three aromatic rings are the same.
The epoxy resin (A1) preferably has a structural unit represented by General Formula (a1). By connecting two or more structural units represented by General Formula (a1), the triarylmethane skeleton (triphenylmethane skeleton) is formed.
By using the epoxy resin having a structural unit represented by General Formula (a1) as the epoxy resin (A1), in particular, it is possible to more reliably obtain an effect of good heat resistance in a case of forming a magnetic member.
In General Formula (a1),
in a case of a plurality of R11's, the plurality of R11's each independently represent a monovalent substituent,
in a case of a plurality of R12's, the plurality of R12's each independently represent a monovalent substituent,
i represents an integer of 0 to 3, and
j represents an integer of 0 to 4.
Examples of the monovalent substituent in R11 and R12 include a monovalent organic group, a halogen atom, a hydroxy group, and a cyano group.
Examples of the monovalent organic group include an alkyl group, an alkenyl group, an alkynyl group, an alkylidene group, an aryl group, an aralkyl group, an alkaryl group, a cycloalkyl group, an alkoxy group, a heterocyclic group, and a carboxyl group. The number of carbon atoms in the monovalent organic group is, for example, 1 to 30, preferably 1 to 20, more preferably 1 to 10, and still more preferably 1 to 6.
Examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a neopentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, and a decyl group.
Examples of the alkenyl group include an allyl group, a pentenyl group, and a vinyl group.
Examples of the alkynyl group include an ethynyl group.
Examples of the alkylidene group include a methylidene group and an ethylidene group.
Examples of the aryl group include a tolyl group, a xylyl group, a phenyl group, a naphthyl group, and an anthracenyl group.
Examples of the aralkyl group include a benzyl group and a phenethyl group.
Examples of the alkaryl group include a tolyl group and a xylyl group.
Examples of the cycloalkyl group include an adamantyl group, a cyclopentyl group, a cyclohexyl group, and a cyclooctyl group.
Examples of the alkoxy group include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, a s-butoxy group, an isobutoxy group, a t-butoxy group, an n-pentyloxy group, an neopentyloxy group, and an n-hexyloxy group.
Examples of the heterocyclic group include an epoxy group and an oxetanyl group.
i and j are each independently preferably 0 to 2 and more preferably 0 or 1.
In one aspect, both i and j are 0. That is, as the one aspect, all benzene rings in General Formula (a1) do not have a substituent other than the specified glycidyloxy group as a monovalent substituent.
The number average molecular weight of the epoxy resin (A1) is not particularly limited, but is typically approximately 200 to 700. Usually, the number average molecular weight can be obtained as a standard polystyrene-equivalent value by gel permeation chromatography (GPC).
(Epoxy Resin (A2))
The resin composition according to the present embodiment may include at least one epoxy resin (A2) (also simply referred to as an “epoxy resin (A2)”) selected from the group consisting of an epoxy resin having a structural unit represented by General Formula (a2-1) and a bisphenol-type epoxy resin having a structure represented by General Formula (a2-2).
In General Formula (a2-1),
Cy represents a divalent organic group including an alicyclic structure,
in a case of a plurality of R21's, the plurality of R21's each independently represent a monovalent substituent, and
l represents an integer of 0 to 3.
In General Formula (a2-2),
two R's each independently represent a hydrogen atom or a methyl group,
in a case of a plurality of R22's, the plurality of R22's each independently represent a monovalent substituent,
in a case of a plurality of R23's, the plurality of R23's each independently represent a monovalent substituent, and
p and q each independently represent an integer of 0 to 4.
The alicyclic structure included in Cy of General Formula (a2-1) is not particularly limited, and may be a monocyclic structure or a polycyclic structure. From the viewpoint of appropriate viscosity at the time of melting and mechanical properties of the obtained magnetic member, it is preferable to include a polycyclic structure.
The number of carbon atoms in Cy is typically 5 to 20, preferably 6 to 18 and more preferably 6 to 15.
Examples of an alicyclic ring include monocyclic alicyclic rings (3- to 15-membered ring, preferably 5- or 6-membered cycloalkane ring) such as a cyclopentane ring, a cyclohexane ring, a cyclooctane ring, and a cyclododecane ring.
In addition, examples thereof also include polycyclic alicyclic rings (bridged carbon rings) such as a decalin ring (perhydronaphthalene ring), a perhydroindene ring (bicyclo[4.3.0]nonane ring), a perhydroanthracene ring, a perhydrofluorene ring, a perhydrophenanthrene ring, a perhydroacenaphthene ring, a perhydrophenalene ring, a norbornane ring (bicyclo[2.2.1]heptane ring), an isobornane ring, an adamantane ring, a bicyclo[3.3.0]octane ring, a tricyclo[5.2.1.02,6]decane ring, and a tricyclo [6.2.1.02,7]undecane ring. The term “polycyclic” preferably means approximately 2 to 4 rings.
For example, Cy can be a divalent group obtained by removing two hydrogen atoms from these monocyclic or polycyclic alicyclic rings.
The alicyclic structure included in Cy may or may not have a substituent. For example, one or more hydrogen atoms in the alicyclic structure may be replaced with any substituent. Examples of the substituent include those described as the monovalent substituent of R11 and R12 in General Formula (a1).
In addition, Cy may include a carbonyl structure (═O) or the like.
In addition, Cy may be the alicyclic structure itself, or may have the alicyclic structure and other structures. For example, the alicyclic structure may be directly bonded to a benzene ring (by a single bond), or may be bonded to a benzene ring through any linking group.
More specifically, the latter case can be expressed as -Cy′-L- in the -Cy- portion of General Formula (a2-1). Here, Cy′ is an alicyclic ring (specific examples thereof include the above-described monocyclic or polycyclic alicyclic rings), and L is a divalent linking group. Examples of the divalent linking group of L include an alkylene group (for example, having 1 to 6 carbon atoms), a cycloalkylene group, an ether group, a carbonyl group, an ester group, and a group in which two or more of these are linked.
Specific examples of the monovalent substituent of R21 in General Formula (a2-1) include the same as those described as the monovalent substituent of R11 and R12 in General Formula (a1).
In General Formula (a2-1), l is preferably 0 to 2 and more preferably 0 or 1.
In one aspect, l is 0. That is, as the one aspect, the benzene ring in General Formula (a2-1) does not have a substituent other than the specified glycidyloxy group as a monovalent substituent.
Specific examples of the monovalent substituent of R22 and R23 in General Formula (a2-2) include the same as those described as the monovalent substituent of R11 and R12 in General Formula (a1). Here, as the monovalent substituent of R22 and R23, an alkyl group is preferable, a linear or branched alkyl group having 1 to 6 carbon atoms is more preferable, and a methyl group is particularly preferable.
p and q in General Formula (a2-2) are each independently preferably 0 to 3 and more preferably 0 to 2.
From the viewpoint of appropriate fluidity at the time of melting, and the like, in a case where two R's are methyl groups, p and q are preferably 0, and in a case where two R's are hydrogen atoms, p and q are preferably 1 or 2.
The number average molecular weight (standard polystyrene-equivalent value measured by GPC) of the epoxy resin having the structural unit represented by General Formula (a2-1) is not particularly limited, but is, for example, 200 to 400.
An epoxy resin including a biphenyl structure is specifically an epoxy resin including a structure in which two benzene rings are linked by a single bond. The benzene ring here may or may not have a substituent.
Specifically, the epoxy resin including a biphenyl structure has a partial structure represented by General Formula (BP).
In General Formula (BP),
in a case of a plurality of Ra's or Rb's, the plurality of Ra's or Rb's are each independently a monovalent organic group, a hydroxyl group, or a halogen atom,
r and s are each independently 0 to 4, and
* represents that it is linked to another atomic group.
Specific examples of the monovalent organic group of Ra and Rb include those listed as a monovalent organic group of R1, R2, and R3 in General Formula (AM) described later.
r and s are each independently preferably 0 to 2 and more preferably 0 or 1. In one aspect, both r and s are 0.
More specifically, the epoxy resin including a biphenyl structure has a structural unit represented by General Formula (BP1).
In General Formula (BP1),
definitions and specific aspects of Ra and Rb are the same as those of General Formula (BP),
definitions and preferred ranges of r and s are the same as those of General Formula (BP),
in a case of a plurality of Rc's, the plurality of Rc's are each independently a monovalent organic group, a hydroxyl group, or a halogen atom, and
t is an integer of 0 to 3.
Specific examples of the monovalent organic group of Rc include those listed as a monovalent organic group of R1, R2, and R3 in General Formula (AM) described later.
t is preferably 0 to 2 and more preferably 0 or 1.
The resin composition according to the present embodiment may include an epoxy resin having a low ICI viscosity at 150° C. as the epoxy resin.
The resin composition may include an epoxy resin having an ICI viscosity at 150° C. of more preferably 0.1 to 50 mPa·s, still more preferably 0.5 to 45 mPa·s, and particularly preferably 1 to 40 mPa·s. The epoxy resin (A2) is used as an epoxy resin having an ICI viscosity in such a numerical range. These may be used alone or in combination of two or more thereof.
By using an epoxy resin having a low ICI viscosity, fluidity of the resin composition can be improved, and as a result, a resin composition suitable for transfer molding can be provided.
As an ICI viscosity measuring device, an ICI cone-plate viscometer from MST Engineering, Ltd. and the like can be used.
The molecular weight (number average molecular weight) of the epoxy resin is not particularly limited, but is, for example, 100 to 3,000, preferably 100 to 2,000 and more preferably approximately 100 to 1,000.
The resin composition according to the present embodiment may include only one type of the epoxy resin, or may include two or more types of the epoxy resin. In addition, epoxy resins of the same type, which have different weight average molecular weights, may be used in combination.
The amount of the epoxy resin in the resin composition is, for example, 0.1 to 20% by mass, preferably 0.5 to 10% by mass based on the entire resin composition.
In addition, the content of the epoxy resin is, for example, 1 to 30% by volume, preferably 5 to 25% by volume based on the entire resin composition.
By appropriately adjusting the amount ratio of the epoxy resin (A1) and the epoxy resin (A2), heat resistance, moldability, and blocking resistance can be achieved at a higher level.
Specifically, in a case where the number of moles of the epoxy group included in the epoxy resin (A1) is defined as M1 and the number of moles of the epoxy group included in the epoxy resin (A2) is defined as M2, the value of M1/M2 is preferably 0.5 to 1.5, more preferably 0.6 to 1.4, and still more preferably 0.8 to 1.2.
The value of M1/M2 can be obtained by a molar calculation from the molecular weights and epoxy equivalents of the epoxy resin (A1) and the epoxy resin (A2).
In addition, in a case where the resin composition includes the polyfunctional epoxy resin and the bisphenol-type epoxy resin, in the above-described M1/M2, M1 may be the number of moles of the epoxy group included in the polyfunctional epoxy resin and M2 may be the number of moles of the epoxy group included in the bisphenol-type epoxy resin.
The total amount of the epoxy resin (A1) and the epoxy resin (A2) in the resin composition is, for example, 0.1 to 20% by mass, preferably 0.5 to 10% by mass based on the entire resin composition.
The total amount of the epoxy resin (A1) and the epoxy resin (A2) in the resin composition is, for example, 1 to 30% by volume, preferably 5 to 25% by volume based on the entire resin composition.
By setting such a numerical range, the moldability can be further improved, and mechanical properties or magnetic characteristics of the obtained cured product (magnetic member) can be further improved.
The resin composition according to the present embodiment may include a curing agent. The curing agent is not particularly limited as long as it reacts with the thermosetting resin. In a case where the epoxy resin is used as the thermosetting resin, for example, a phenol resin or an aromatic diamine may be used as the curing agent.
(Phenol-Based Curing Agent)
The resin composition according to the present embodiment may include a phenol-based curing agent.
The phenol-based curing agent is not particularly limited as long as it includes a phenolic hydroxy group and can react with the epoxy resin (A1) and/or the epoxy resin (A2). The phenol-based curing agent may be a low molecular weight substance or a polymer.
The resin composition according to the present embodiment may include the epoxy resin (A1) having a triarylmethane skeleton, at least one epoxy resin (A2) selected from the group consisting of an epoxy resin having a structural unit represented by General Formula (a2-1) described above and an epoxy resin having a structure represented by General Formula (a2-2) described above, and a phenol-based curing agent (B).
The phenol-based curing agent preferably includes any skeleton selected from the group consisting of a biphenyl skeleton and a novolac skeleton. In a case where the phenol-based curing agent includes any of these skeletons, heat resistance of the magnetic member can be particularly enhanced.
The “biphenyl skeleton” refers to a skeleton in which two benzene rings are linked through a single bond. More specifically, the “biphenyl skeleton” is a skeleton represented by General Formula (BP).
In General Formula (BP),
in a case of a plurality of R1's or R2's, the plurality of R1's or R2's each independently represent a monovalent substituent,
r and s are each independently 0 to 4, and
* represents that it is linked to another atomic group.
Specific examples of the monovalent substituent of R1 and R2 include the same as those described as the monovalent substituent of R11 and R12 in General Formula (a1).
r and s are each independently preferably 0 to 2 and more preferably 0 or 1. In one aspect, both r and s are 0.
Specific examples of the phenol-based curing agent having a biphenyl skeleton include those having a structural unit represented by General Formula (BP1).
In General Formula (BP1),
definitions and specific examples of R1 and R2 are the same as those of General Formula (BP),
definitions and preferred ranges of rand s are the same as those of General Formula (BP),
in a case of a plurality of R3's, the plurality of R3's each independently represent a monovalent substituent, and
t is an integer of 0 to 3.
Specific examples of the monovalent substituent of R3 include the same as those described as the monovalent substituent of R11 and R12 in General Formula (a1).
t is preferably 0 to 2 and more preferably 0 or 1.
Specific examples of the phenol-based curing agent having a novolac skeleton include those having a structural unit represented by General Formula (N).
In General Formula (N),
R4 represents a monovalent substituent, and
u represents an integer of 0 to 3.
Specific examples of the monovalent substituent of R4 include the same as those described as the monovalent substituent of R11 and R12 in General Formula (a1).
u is preferably 0 to 2, more preferably 0 or 1, and still more preferably 0.
In a case where the phenol-based curing agent is a polymer or an oligomer, the number average molecular weight (standard polystyrene-equivalent value measured by GPC) of the phenol-based curing agent is not particularly limited, but is, for example, approximately 200 to 800.
The content of the phenol-based curing agent in the resin composition is, for example, 0.1 to 20% by mass, preferably 0.5 to 10% by mass based on the entire resin composition.
In addition, the content of the phenol-based curing agent in the resin composition is, for example, 1 to 30% by volume, preferably 5 to 25% by volume based on the entire resin composition.
By appropriately adjusting the amount of the phenol-based curing agent, the moldability can be further improved, and mechanical properties or magnetic characteristics of the obtained cured product (magnetic member) can be improved.
(Aromatic Diamine)
The resin composition according to the present embodiment may include an aromatic diamine.
As the aromatic diamine, any compound having one or more aromatic ring structures and two amino groups (—NH2) in one molecule can be used without particular limitation. As the aromatic diamine, a compound having a structure in which the amino group is directly linked to the aromatic ring.
The reason why both moldability and heat resistance can be improved by a resin composition including an epoxy resin, an aromatic diamine, and magnetic particles is not entirely clear, but it is presumed that (1) appropriate fluidity can be obtained by appropriate reaction rate between the epoxy group of the epoxy resin and the amino group of the aromatic diamine and (2) after the molten resin composition is cured, a glass transition temperature rises due to a crosslinked structure of the epoxy resin-aromatic diamine and a rigid aromatic ring skeleton of the aromatic diamine itself (thermal motion of molecules in the cured product is restricted) are involved.
The present invention is not limited by this presumption.
The melting point can be used as a reference in a case of selecting the aromatic diamine. By using an aromatic diamine having an appropriate melting point, the aromatic diamine is appropriately melted during kneading and molding of the resin composition. As a result, the fluidity can be improved. In addition, since the resin composition can be kneaded more uniformly, it is considered that the heat resistance and mechanical characteristics (strength and the like) of the finally obtained cured product (magnetic member) can be improved.
Specifically, the melting point of the aromatic diamine is preferably 160° C. or lower, more preferably 150° C. or lower, and still more preferably 140° C. or lower.
The lower limit value of the melting point of the aromatic diamine is not particularly limited, but is, for example, 60° C. or higher, preferably 70° C. or higher, and more preferably 80° C. or higher.
In a case where a commercially available product is used as the aromatic diamine, a catalog value can be adopted for the melting point.
Incidentally, the aromatic diamine is preferably a solid at normal temperature (25° C.) and not a liquid. In addition, the resin composition according to the present embodiment may include an amine compound other than the aromatic diamine, but the amine compound is also preferably a solid at normal temperature (25° C.) and not a liquid.
The resin composition according to the present embodiment is typically prepared in a form of granules or tablets. From the viewpoint of ease of preparation, handleability of the resin composition in a form of granules or tablets, which is obtained by the preparation, and the like, the aromatic diamine (and in some cases, the amine compound other than the aromatic diamine) is preferably solid at normal temperature.
The resin composition preferably includes a compound represented by General Formula (AM) as the aromatic diamine.
In General Formula (AM),
in a case of a plurality of X's, the plurality of X's are each independently any group selected from the group consisting of a single bond, a linear or branched alkylene group, an ether group, a carbonyl group, an ester group, and a group in which two or more of these are linked,
Y is any group selected from the group consisting of a single bond, a linear or branched alkylene group, an ether group, a carbonyl group, an ester group, and a group in which two or more of these are linked,
in a case of a plurality of R1's, R2's, or R3's, the plurality of R1's, R2's, or R3's are each independently a monovalent organic group, a hydroxyl group, or a halogen atom,
k, l, and m are each independently an integer of 0 to 4, and
n is an integer of 0 or more.
As the linear or branched alkylene group of X and Y, those having 1 to 6 carbon atoms are preferable, and those having 1 to 3 carbon atoms are more preferable.
In a case where a part or all of X and Y are branched alkylene groups, the skeleton of the aromatic diamine can be appropriately rigid. This is considered to be related to the appropriateness of the above-described “melting point”. In addition, in a case where the skeleton of the aromatic diamine is appropriately rigid, it is considered that effects of further improving the heat resistance of the cured product (magnetic member) and improving the mechanical strength can also be obtained.
Examples of the monovalent organic group of R1, R2, and R3 include an alkyl group, an alkenyl group, an alkynyl group, an alkylidene group, an aryl group, an aralkyl group, an alkaryl group, a cycloalkyl group, an alkoxy group, a heterocyclic group, and a carboxyl group.
Examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a neopentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, and a decyl group.
Examples of the alkenyl group include an allyl group, a pentenyl group, and a vinyl group.
Examples of the alkynyl group include an ethynyl group.
Examples of the alkylidene group include a methylidene group and an ethylidene group.
Examples of the aryl group include a tolyl group, a xylyl group, a phenyl group, a naphthyl group, and an anthracenyl group.
Examples of the aralkyl group include a benzyl group and a phenethyl group.
Examples of the alkaryl group include a tolyl group and a xylyl group.
Examples of the cycloalkyl group include an adamantyl group, a cyclopentyl group, a cyclohexyl group, and a cyclooctyl group.
Examples of the alkoxy group include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, a s-butoxy group, an isobutoxy group, a t-butoxy group, an n-pentyloxy group, an neopentyloxy group, and an n-hexyloxy group.
Examples of the heterocyclic group include an epoxy group and an oxetanyl group.
The total number of carbon atoms in the monovalent organic group of R1, R2, and R3 is, for example, 1 to 30, preferably 1 to 20, more preferably 1 to 10, and particularly preferably 1 to 6.
k, l, m are each independently preferably an integer of 0 or 1.
In one aspect, k, l, and m are all 0. That is, as the one aspect, all benzene rings in General Formula (AM) are not substituted with an atomic group other than the amino group.
n is preferably 0 to 3 and more preferably 0 to 2.
Specific examples of the aromatic diamine are shown below. The aromatic diamine is not limited to the following. In addition, as a matter of course, examples thereof also include 1,3-bis[1-(4-aminophenyl)-1-methylethyl]benzene, 2,2′-bis[4-(4-aminophenoxy)phenyl]propane, and 1,3-bis(4-aminophenoxy)benzene, which are used in Examples described later.
As the aromatic diamine, a commercially available product may be used. The aromatic diamine can be obtained from, for example, SEIKA CORPORATION., MITSUI FINE CHEMICAL Inc., FUJIFILM Wako Pure Chemical Corporation, and the like.
The resin composition according to the present embodiment may include only one type of the aromatic diamine, or may include two or more types of the aromatic diamine.
The amount of the aromatic diamine in the resin composition is, for example, 0.1 to 20% by mass, preferably 0.5 to 10% by mass based on the entire resin composition.
In addition, the content of the aromatic diamine in the resin composition is, for example, 1 to 30% by volume, preferably 5 to 25% by volume based on the entire resin composition. By setting such a numerical range, it is possible to improve moldability and mechanical properties.
The amount of the aromatic diamine in the composition is preferably adjusted appropriately in relation to the epoxy resin.
Specifically, the ratio of the number of moles of the epoxy group in the epoxy resin to the number of moles of the amino group in the aromatic diamine (that is, the number of moles of the epoxy group of the epoxy resin/the number of moles of the amino group in the aromatic diamine) is preferably 1 to 3, more preferably 1.5 to 2.5, and still more preferably 1.7 to 2.3.
One amino group (—NH2) can react with two epoxy groups. Therefore, it is considered that, by adjusting the amount ratio of the epoxy resin and the aromatic diamine such that the above-described ratio is around 2, the crosslinked structure of the amino group and the epoxy group during curing can be denser. Then, it is considered that the glass transition temperature of the cured product (magnetic member) can be increased to enhance the heat resistance.
The above-described ratio can be obtained by calculating from the epoxy equivalent or epoxy value of the epoxy resin included in the composition, the molecular weight of the epoxy resin (these are usually listed in the epoxy resin catalog), the molecular weight of the aromatic diamine, and the like.
(Magnetic Particles)
The resin composition according to the present embodiment includes magnetic particles.
As the magnetic particles, any particles can be used as long as the molded product produced by using the resin composition according to the present embodiment exhibits magnetism.
The magnetic particles preferably include one or two or more elements selected from the group consisting of Fe, Cr, Co, Ni, Ag, and Mn. By selecting any of these magnetic particles, the magnetic characteristics can be further enhanced.
In particular, the magnetic characteristics can be further enhanced by using particles including 85% by mass or more of Fe as the magnetic particles.
In the present embodiment, the magnetic particles include iron-based particles.
The iron-based particles refer to particles including an iron atom as a main component (content mass of the iron atom is the largest in the chemical composition), and more specifically, refer to an iron alloy having the largest content mass of the iron atom in the chemical composition.
The iron-based particles may include iron-based amorphous particles or may be composed of only iron-based amorphous particles. However, the iron-based particles may include iron-based amorphous particles and iron-based crystal particles. In addition, as the iron-based particles, those having one kind of chemical composition may be used, or two or more kinds having different chemical compositions may be used in combination.
The iron-based amorphous particles may have an amorphous phase inside the particles, or may be partially or wholly composed of an amorphous phase.
In the iron-based amorphous particles, the amorphous phase with respect to all phases in one particle may be, for example, 80% or more, preferably 90% or more, and more preferably 100% on a volume basis.
More specifically, as the iron-based particles, particles (soft magnetic iron-high-content particles) exhibiting soft magnetism and having an iron atom (Fe) content of 85% by mass or more can be used. The soft magnetism refers to ferromagnetism having a small coercive force, and generally, ferromagnetism having a coercive force of 800 A/m or less is referred to as soft magnetism.
Examples of a constituent material of such particles include a metal-containing material having an iron content of 85% by mass or more as a constituent element. Such a metal material having a high iron content as a constituent element exhibits soft magnetism in which magnetic characteristics such as magnetic permeability and magnetic flux density are relatively good. Therefore, a resin composition capable of exhibiting good magnetic characteristics in a case of being molded can be obtained.
Examples of a form of the metal-containing material include simple substances, solid solutions, eutectic crystals, and alloys such as an intermetallic compound. By using the particles composed of such a metal material, it is possible to obtain a resin composition having excellent magnetic characteristics derived from iron, that is, magnetic characteristics such as high magnetic permeability and high magnetic flux density.
In addition, the above-described metal-containing material may contain an element other than iron as a constituent element. Elements of the element other than iron include B, C, N, O, Al, Si, P, S, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Cd, In, and Sn, and one kind of these may be used or two or more kinds of these may be used in combination.
Specific examples of the above-described metal-containing material include pure iron, silicon steel, iron-cobalt alloy, iron-nickel alloy, iron-chromium alloy, iron-aluminum alloy, carbonyl iron, stainless steel, and a composite material containing one or two or more of these. From the viewpoint of availability, carbonyl iron can be preferably used.
In the above description, the iron-based particles have been mainly described, but certainly, the magnetic particles may be other particles. For example, the magnetic particles may be magnetic particles including Ni-based soft magnetic particles, Co-based soft magnetic particles, and the like.
In addition, the magnetic particles may be surface-treated. For example, the surface may be treated with a coupling agent or treated with plasma. By such a surface treatment, it is possible to bond a functional group to the surface of the magnetic particles. The functional group can cover a part or all of the surface of these particles.
As such a functional group, a functional group represented by the General Formula (1) can be used.
*—O—X—R (1)
[in the formula, R represents an organic group, X is Si, Ti, Al, or Zr, and * is one of atoms constituting the magnetic particle]
For example, the above-described functional group is preferably a residue formed by a surface treatment with a known coupling agent such as a silane-based coupling agent, a titanium-based coupling agent, an aluminum-based coupling agent, and a zirconium-based coupling agent, or a residue of a coupling agent selected from the group consisting of a silane-based coupling agent and a titanium-based coupling agent. As a result, in a case where the magnetic particles are blended with the resin composition to obtain a resin composition, fluidity thereof can be further enhanced.
In a case where the surface is treated with a coupling agent, examples thereof include a method of immersing the magnetic particles in a diluted solution of the coupling agent and a method of directly spraying the coupling agent to the magnetic particles.
The amount of the coupling agent used is, for example, preferably 0.01 to 1 part by mass and more preferably 0.05 to 0.5 part by mass with respect to 100 parts by mass of the magnetic particles.
Examples of a solvent for reacting the coupling agent with the magnetic particles include methanol, ethanol, and isopropyl alcohol. In addition, the amount of the coupling agent used in this case is preferably 0.1 to 2 parts by mass and more preferably 0.5 to 1.5 parts by mass with respect to 100 parts by mass of the solvent.
The reaction time (for example, immersion time in the diluted solution) between the coupling agent and the magnetic particles is preferably 1 to 24 hours.
In addition, in a case where the functional group as described above is bonded, plasma treatment may be performed in advance as a part of the surface treatment on the magnetic particles. For example, by performing oxygen plasma treatment, OH groups are generated on the surface of the magnetic particles, and a bonding between the magnetic particles and the residue of the coupling agent through oxygen atoms is easy. As a result, the functional group can be bonded more firmly.
The plasma treatment here is preferably oxygen plasma treatment. As a result, the OH group can be efficiently modified on the surface of the magnetic particles.
The pressure of the oxygen plasma treatment is not particularly limited, but is preferably 100 to 200 Pa and more preferably 120 to 180 Pa.
The flow rate of processing gas in the oxygen plasma treatment is not particularly limited, but is preferably 1000 to 5000 mL/min and more preferably 2000 to 4000 mL/min.
The output of the oxygen plasma treatment is not particularly limited, but is preferably 100 to 500 W and more preferably 200 to 400 W.
The treatment time of the oxygen plasma treatment is appropriately set according to the above-described various conditions, but is preferably 5 to 60 minutes and more preferably 10 to 40 minutes.
In addition, argon plasma treatment may be further performed before the oxygen plasma treatment is performed. As a result, an active site for modifying the OH group can be formed on the surface of the magnetic particles, so that the modification of the OH group can be performed more efficiently.
The pressure of the argon plasma treatment is not particularly limited, but is preferably 10 to 100 Pa and more preferably 15 to 80 Pa.
The flow rate of processing gas in the argon plasma treatment is not particularly limited, but is preferably 10 to 100 mL/min and more preferably 20 to 80 mL/min.
The output of the argon plasma treatment is preferably 100 to 500 W and more preferably 200 to 400 W.
The treatment time of the argon plasma treatment is preferably 5 to 60 minutes and more preferably 10 to 40 minutes.
The fact that the magnetic particles and the residue of the coupling agent are bonded through an oxygen atom can be confirmed by, for example, a Fourier transform infrared spectrophotometer.
In addition, the surface treatment as described above may be applied to all particles included in the resin composition, or may be applied to only some of the particles.
In addition, another coating treatment may be applied to a base of the surface treatment described above. Examples of such a coating treatment include a resin coating of a silicone resin, a phosphoric acid coating, and a silica coating. By applying such a coating treatment, insulating property of the magnetic particles can be further enhanced. Such a coating treatment may be applied as needed or may be omitted. This coating treatment may be applied alone, not as a base of the surface treatment described above.
From another point of view, the magnetic particles preferably have a shape close to a perfect circle (true sphere). It is considered that this reduces friction between the particles and further enhances the fluidity.
Specifically, “circularity” defined below is determined for any 10 or more (preferably 50 or more) magnetic particles, and an average circularity obtained by averaging the values is preferably 0.60 or more and more preferably 0.75 or more.
Definition of circularity: when a contour of the magnetic particles is observed with a scanning electron microscope, in a case where an isoarea equivalent circle diameter obtained from the contour is defined as Req and a radius of a circle circumscribing the contour is defined as Rc, a value of Req/Rc.
In addition, a median diameter D50 (average particle diameter) of the iron-based particles on a volume basis is, for example, 0.1 μm to 100 μm or less, preferably 0.5 to 75 μm, more preferably 0.75 to 65 μm, and still more preferably 1 to 60 μm. By appropriately adjusting the particle diameter (median diameter), it is possible to further improve the fluidity during molding and improve magnetic performance. The average particle diameter of the iron-based amorphous particles may also be within the above-described numerical range of the average particle diameter of the iron-based particles.
From the viewpoint of good fluidity and improvement of magnetic performance due to high filling, it is preferable to appropriately adjust the particle diameter of the magnetic particles.
The resin composition according to the present embodiment may include two or more types of the iron-based particles having different average particle diameters. As a result, it is possible to increase filling of the iron-based particles, and enhance the magnetic characteristics and mechanical strength.
In addition, the resin composition according to the present embodiment may include two or more types of iron-based amorphous particles having different average particle diameters. As a result, the magnetic characteristics can be further improved. For example, ferrous amorphous particles having a D50 of 30 μm or more and 100 μm or less and ferric amorphous particles having a D50 of 1 μm or more and less than 30 μm may be used in combination.
The median diameter D50 can be obtained by, for example, a laser diffraction/scattering type particle diameter distribution measuring device. Specifically, a particle diameter distribution curve is obtained by measuring the magnetic particles in a dry manner with a particle diameter distribution measuring device “LA-950” manufactured by HORIBA, Ltd., and the D50 can be obtained by analyzing this distribution curve.
The content of the iron-based particles in the resin composition is preferably 85% by mass or more, more preferably 90% by mass or more, and still more preferably 93% by mass or more based on the entire resin composition. From the viewpoint of practically ensuring the fluidity of the resin composition, the upper limit of the content of the iron-based particles in the resin composition is, for example, 99% by mass or less. By sufficiently increasing the content of the iron-based particles, magnetic performance (magnetic permeability, iron loss, and the like) can be improved.
The content of the iron-based amorphous particles in the resin composition is, for example, 65% by mass or more, preferably 70% by mass or more, more preferably 85% by mass or more, and still more preferably 90% by mass or more with respect to 100% by mass of the iron-based particles. By sufficiently increasing the content of the iron-based amorphous particles, magnetic performance (magnetic permeability, iron loss, and the like) can be further improved. On the other hand, the upper limit of the content of the iron-based amorphous particles in the resin composition is not particularly limited, but may be, for example, 100% by mass or less or 99% by mass or less. Moldability is improved.
In addition, on a volume basis, the content of the magnetic particles in the resin composition is preferably 60% by volume or more, more preferably 70% by volume or more, and still more preferably 80% by volume or more based on the entire resin composition. From the viewpoint of practically ensuring the fluidity of the resin composition, the upper limit of the content is, for example, 95% by volume or less.
The resin composition according to the present embodiment may include any component other than the epoxy resin, the aromatic diamine, and the magnetic particles. Hereinafter, optional components will be described.
(Mold Release Agent)
The resin composition according to the present embodiment may include a mold release agent. As a result, releasability of the resin composition during molding can be improved.
Examples of the mold release agent include natural waxes such as carnauba wax, synthetic waxes such as montanic acid ester wax and polyethylene oxide wax, higher fatty acids such as zinc stearate and metal salts thereof, and paraffin. These may be used alone or in combination of two or more thereof.
In a case where a mold release agent is used, the content thereof is preferably 0.01 to 3% by mass and more preferably 0.05 to 2% by mass based on the entire resin composition. As a result, the effect of improving the releasability can be surely obtained.
(Curing Catalyst)
The resin composition according to the present embodiment may include a curing catalyst. As a result, curability of the resin composition can be improved.
As the curing catalyst, any catalyst can be used as long as it promotes curing reaction of the epoxy resin. For example, a known epoxy curing catalyst can be used.
Specific examples thereof include phosphorus atom-containing compounds such as organic phosphine, a tetra-substituted phosphonium compound, a phosphobetaine compound, an adduct of phosphine compound and quinone compound, and an adduct of phosphonium compound and silane compound; imidazoles (imidazole-based curing catalyst) such as 2-methylimidazole; and nitrogen atom-containing compounds such as amidines and tertiary amines, for example, 1,8-diazabicyclo[5.4.0]undecene-7 and benzyldimethylamine, and quaternary salts of amidine or amine.
In a case where a curing catalyst is used, only one type may be used, or two or more types may be used.
In a case where a curing catalyst is used, the content thereof is preferably 0.01 to 1% by mass and more preferably 0.05 to 0.8% by mass with respect to the entire resin composition. By setting such a numerical range, the effect of sufficiently improving the curability can be obtained.
(Non-Magnetic Particles)
From the viewpoint of adjusting the fluidity and the like, the resin composition according to the present embodiment may include non-magnetic particles exhibiting non-magnetism. As the non-magnetic particles, for example, particles having a cumulative 50% value (D50) of 3 μm or less in the particle diameter distribution curve can be used. In addition, in the present specification, non-magnetism refers to having no ferromagnetism.
In a case where the resin composition includes non-magnetic particles, the resin composition exhibits higher fluidity during molding, and exudation of the resin composition during molding is suppressed. Therefore, the moldability of the resin composition is better, and filling property and uniformity of the magnetic particles can be further improved. Accordingly, the magnetic characteristics of the cured product (magnetic member) can be improved.
In addition, by suppressing the exudation of the resin composition, generation of resin burrs and the like during molding is suppressed. In addition, it is possible to prevent the component balance of the resin composition from being disturbed due to the exudation and the mechanical properties of the molded product from being deteriorated. Therefore, a molded product with few molding defects can be obtained.
Examples of a constituent material of the non-magnetic particles include ceramic materials and glass materials. Among these, those including a ceramic material are preferably used. Since such non-magnetic particles have a high affinity with a thermosetting resin, the fluidity of the resin composition can be maintained.
Examples of the ceramic material include oxide-based ceramic materials such as silica, alumina, zirconia, titania, magnesia, and calcia, nitride-based ceramic materials such as silicon nitride and aluminum nitride, and carbide-based ceramic materials such as silicon carbide and boron carbide.
In addition, the ceramic material preferably includes silica in particular. Silica has a high affinity with a thermosetting resin and a high insulating property, and is therefore useful as a constituent particle of the non-magnetic particles.
The true specific gravity of the constituent material of the non-magnetic particles is preferably 1.0 to 6.0, more preferably 1.2 to 5.0, and still more preferably 1.5 to 4.5. Since such non-magnetic particles have a small specific gravity, the non-magnetic particles easily flow together with the molten product of the resin composition. Therefore, in a case where the molten product of the resin composition flows toward gaps of a molding mold during molding, the non-magnetic particles easily flow together with the molten product. As a result, the gap is closed by the non-magnetic particles, and exudation from the gap can be suppressed more reliably. The “gap” here includes, for example, a gap (clearance) between a plunger and a cylinder of a transfer molding machine.
The cumulative 50% value of the non-magnetic particles in the volume-based particle diameter distribution curve is not particularly limited, but is typically 3 μm or less, preferably 0.1 to 2.8 μm, and more preferably 0.5 to 2.5 μm. This particle diameter is a particle diameter which is preferable for preventing the above-described “exudation” and in which the non-magnetic particles easily flow together with the molten product of the resin composition.
In addition, the cumulative 50% value of the non-magnetic particles in the volume-based particle diameter distribution curve is preferably 3 μm or less and smaller than the D50 of the magnetic particles, but the difference therebetween is more preferably 5 μm or more, still more preferably 10 to 100 μm, and particularly preferably 15 to 60 μm.
The average circularity (this definition is the same as that in the magnetic particles) of the non-magnetic particles included in the non-magnetic particles is not particularly limited, but is preferably 0.50 to 1 and more preferably 0.75 to 1. In a case where the circularity is within this range, the fluidity of the resin composition can be ensured by utilizing rolling of the non-magnetic particles themselves, while the non-magnetic particles are likely to be clogged in the gaps and the like and it is easy to suppress exudation of the thermosetting resin. That is, it is possible to achieve both the fluidity of the resin composition and the suppression of the exudation of the thermosetting resin.
In a case where non-magnetic particles are used, the amount thereof is preferably 0.5 to 10% by mass and more preferably 1 to 5% by mass based on the entire resin composition. As a result, a resin composition having higher fluidity and capable of more reliably suppressing exudation can be obtained.
(Thermoplastic Resin)
From the viewpoint of adjusting fluidity and moldability, the resin composition according to the present embodiment may include a thermoplastic resin.
Examples of the thermoplastic resin include acrylic resins, polyamide resins (for example, nylon and the like), thermoplastic urethane resins, polyolefin resins (for example, polyethylene, polypropylene, and the like), polycarbonates, polyester resins (for example, polyethylene terephthalate, polybutylene terephthalate, and the like), polyacetals, polyphenylene sulfides, polyether ether ketones, liquid crystal polymers, fluororesins (for example, polytetrafluoroethylene, polyvinylidene fluoride, and the like), modified polyphenylene ethers, polysulfones, polyether sulfones, polyarylates, polyamideimides, polyether imides, and thermoplastic polyimides.
In a case where a thermoplastic resin is used, one type may be used alone, or two or more different types may be used in combination. In addition, two or more resins of the same type, which have different weight average molecular weights, may be used in combination. In addition, a certain resin and its prepolymer may be used in combination.
Ina case where a thermoplastic resin is used, the amount thereof is preferably 0.1 to 20% by mass and more preferably 0.5 to 10% by mass based on the entire resin composition. As a result, it is considered that the effect of adjusting the fluidity and moldability can be sufficiently obtained.
(Other Components)
The resin composition according to the present embodiment may include a component other than the above-described components. For example, the resin composition according to the present embodiment may include a low stress agent, a coupling agent, an adhesion aid, a coloring agent, an antioxidant, an anticorrosion, a dye, a pigment, a flame retardant, and the like.
Examples of the low stress agent include silicone compounds such as a polybutadiene compound, an acrylonitrile butadiene copolymer compound, a silicone oil, and a silicone rubber. In a case where a low stress agent is used, only one type may be used, or two or more types may be used in combination.
As the coupling agent, the above-described coupling agent used for the surface treatment of the magnetic particles can be used. Examples thereof include a silane-based coupling agent, a titanium-based coupling agent, a zirconia-based coupling agent, and an aluminum-based coupling agent. In a case where a coupling agent is used, only one type may be used, or two or more types may be used in combination.
The minimum melt viscosity of the resin composition, which is measured in a range of 80° C. to 250° C., is, for example, 50 Pa·s or more and 500 Pa·s or less, preferably 60 Pa·s or more and 450 Pa·s or less, and preferably 70 Pa·s or more and 400 Pa·s or less. By setting the melt viscosity to the above-described upper limit value or less, the fluidity can be enhanced and excellent moldability can be realized. In addition, by setting the melt viscosity to the above-described lower limit value or more, it is possible to suppress occurrence of resin leakage from the mold during transfer molding, and it is possible to suppress precipitation of the magnetic powder in the resin composition during transfer molding.
The temperature at which the melt viscosity of the resin composition is minimum, which is measured in a range of 80° C. to 250° C., is, for example, within a range of 100° C. or higher and 150° C. or lower, preferably 105° C. or higher and 145° C. or lower, and more preferably 110° C. or higher and 140° C. or lower. Within such a range, it is possible to appropriately control the viscosity during transfer molding.
The average linear expansion coefficient α1 of the cured product of the resin composition in a range of 50° C. to 70° C. is, for example, 30 ppm/° C. or less, preferably 28 ppm/° C. or less, and more preferably 16 ppm/° C. or less. As a result, it is possible to improve dimensional stability in an environment near room temperature. The lower limit value of the above-described average linear expansion coefficient α1 is not particularly limited, but may be 1 ppm/° C. or more.
The average linear expansion coefficient α2 of the cured product of the resin composition in a range of 270° C. to 290° C. is, for example, 20 ppm/° C. or more and 80 ppm/° C. or less, preferably 22 ppm/° C. or more and 75 ppm/° C. or less, and more preferably 25 ppm/° C. or more and 47 ppm/° C. or less. By setting the average linear expansion coefficient α2 to the above-described upper limit value or less, dimensional stability in a high temperature environment can be improved.
(Properties of resin composition, manufacturing method, and the like)
The resin composition according to the present embodiment may be solid at room temperature of 25° C.
The properties of the resin composition according to the present embodiment can be powdery, granular, tablet, or the like.
The resin composition according to the present embodiment can be produced by, for example, (1) mixing each component using a mixer, (2) kneading the mixture at approximately 120° C. for approximately 5 minutes using a roll to obtain a kneaded product, and (3) cooling and then pulverizing the obtained kneaded product (from the above, a powdery resin composition can be obtained).
As necessary, the powdery resin composition may be tableted into granules or tablets. As a result, a resin composition suitable for resin molding such as transfer molding can be obtained. In addition, by solidifying the resin composition at room temperature (25° C.), it is possible to further improve transportability and storability.
<Method for Manufacturing Magnetic Member>
The resin composition according to the present embodiment is molded into a desired shape by, for example, a transfer molding method.
A magnetic member can be obtained by injecting a molten product of the above-described resin composition into a mold using a transfer molding apparatus, and curing the molten product. The molded product can be suitably used, for example, as a magnetic component in an electric/electronic device. More specifically, the molded product is preferably used as a magnetic core of a coil (also called a reactor or an inductor depending on the application or purpose).
The transfer molding can be performed by appropriately using a known transfer molding apparatus. Specifically, first, a preheated resin composition is placed in a heating chamber, which is also called a transfer chamber, and melted to obtain a molten product. Thereafter, the molten product is poured into a mold with a plunger and held as it is to cure the molten product. As a result, a desired molded product can be obtained.
From the viewpoint of controllability of dimensions of the molded product, improvement of degree of freedom in shape, and the like, the transfer molding is preferable as compared with other molding methods.
Various conditions in the transfer molding can be set optionally. For example, the preheating temperature can be appropriately adjusted to 60° C. to 100° C., the heating temperature for melting can be appropriately adjusted to 150° C. to 250° C., the mold temperature can be appropriately adjusted to 150° C. to 200° C., and the pressure at which the molten product of the resin composition is injected into the mold can be appropriately adjusted between 1 to 20 MPa.
<Magnetic Member and Coil>
A magnetic member formed by the resin composition according to the present embodiment (magnetic member formed by curing the resin composition according to the present embodiment) and a coil including the magnetic member as a magnetic core or an exterior member will be described.
(First Aspect)
As shown in
From the viewpoint of ensuring insulation of these, the coil 100 may have a structure in which an insulator (not shown) is interposed between the winding 10 and the magnetic core 20.
In the coil 100, the winding 10 and the magnetic core 20 may be sealed by an exterior member 30 (sealing member). For example, the winding 10 and the magnetic core 20 are housed in a housing (case), a liquid resin is introduced therein, and the liquid resin is cured as necessary, so that the exterior member 30 may be formed around the winding 10 and the magnetic core 20. In this case, the winding 10 may have a drawing portion (not shown) in which an end portion of the winding is pulled out to an outside of the exterior member 30.
The winding 10 is usually formed by winding a winding having an insulating coating on the surface of a metal wire. The metal wire preferably has high conductivity, and copper and copper alloys can be preferably used. In addition, as the insulating coating, a coating such as enamel can be used. Examples of a cross-sectional shape of the winding include a circular shape, a rectangular shape, and a hexagonal shape.
On the other hand, a cross-sectional shape of the magnetic core 20 is not particularly limited, but for example, in cross-sectional view, the cross-sectional shape may be a circular shape or a polygonal shape such as a quadrangle or a hexagon. Since the magnetic core 20 is composed of, for example, a transfer molded product of the resin composition according to the present embodiment, it is possible to have a desired shape.
According to the cured product of the resin composition according to the present embodiment, the magnetic core 20 having excellent moldability and magnetic characteristics can be realized. That is, the coil 100 provided with the magnetic core 20 is expected to have good mass production suitability and a small iron loss. In addition, since the magnetic core 20 having excellent mechanical properties can be realized, it is possible to improve durability, reliability, and manufacturing stability of the coil 100. Therefore, the coil 100 can be used as a reactor for a booster circuit or a large current.
(Second Aspect)
As an aspect different from the above-described coil, an outline of a coil (inductor) including an exterior member composed of a cured product of the resin composition according to the present embodiment will be described with reference to
As shown in
From the viewpoint of ensuring insulation of these, the coil 100B may have a structure in which an insulator (not shown) is interposed between the winding 10B and the magnetic core 20B.
In the coil 100B, the winding 10B and the magnetic core 20B are sealed by an exterior member 30B (sealing member). For example, by placing the magnetic core 20B filled in the winding 10B in a mold, and molding the mold by transfer molding or the like using the resin composition according to the present embodiment, the resin composition can be cured to form the exterior member 30B around the winding 10B and the magnetic core 20B. In this case, the winding 10B may have a drawing portion (not shown) in which an end portion of the winding is pulled out to an outside of the exterior member 30B.
The winding 10B is usually formed by winding a conducting wire having an insulating coating on the surface of a metal wire. The metal wire preferably has high conductivity, and copper and copper alloys can be preferably used. In addition, as the insulating coating, a coating such as enamel can be used. Examples of a cross-sectional shape of the winding 10B include a circular shape, a rectangular shape, and a hexagonal shape.
On the other hand, a cross-sectional shape of the magnetic core 20B is not particularly limited, but for example, in cross-sectional view, the cross-sectional shape may be a circular shape or a polygonal shape such as a quadrangle or a hexagon. As the magnetic core 20B, for example, a powder iron core composed of a magnetic powder and a binder can be used.
According to the cured product of the resin composition according to the present embodiment, the exterior member 30B having excellent moldability and magnetic characteristics can be realized, so that low magnetic loss is expected in the coil 100B provided with the magnetic core 20B. In addition, since the exterior member 30B having excellent mechanical properties can be realized, it is possible to improve durability, reliability, and manufacturing stability of the coil 100B.
(Third Aspect)
As still another aspect, an outline of an integrated inductor including a magnetic core composed of a cured product of the resin composition according to the present embodiment and an exterior member will be described with reference to
As shown in
As a method for manufacturing the integrated inductor 100C, for example, the winding 10C is placed in a mold, and mold molding such as transfer molding is performed using the resin composition according to the present embodiment. As a result, the resin composition can be cured to integrally form the magnetic core 20C filled in the winding 10C and the exterior member 30C around these. In this case, the winding 10C may have a drawing portion (not shown) in which an end portion of the winding is pulled out to an outside of the exterior member 30C.
The winding 10C is usually formed by winding a conducting wire having an insulating coating on the surface of a metal wire. The metal wire preferably has high conductivity, and copper and copper alloys can be preferably used. In addition, as the insulating coating, a coating such as enamel can be used. Examples of a cross-sectional shape of the winding 10C include a circular shape, a rectangular shape, and a hexagonal shape.
On the other hand, a cross-sectional shape of the magnetic core 20C is not particularly limited, but for example, in cross-sectional view, the cross-sectional shape may be a circular shape or a polygonal shape such as a quadrangle or a hexagon. Since the magnetic core 20C is composed of a transfer molded product of the resin composition according to the present embodiment, it is possible to have a desired shape.
According to the cured product of the resin composition according to the present embodiment, the magnetic core 20C and exterior member 30C, which have excellent moldability and magnetic characteristics, can be realized, so that low magnetic loss is expected in the integrated inductor 100C having these. In addition, since the exterior member 30C having excellent mechanical properties can be realized, it is possible to improve durability, reliability, and manufacturing stability of the integrated inductor 100C. Therefore, the integrated inductor 100C can be used as an inductor for a booster circuit or a large current.
The embodiments of the present invention have been described above, but these are examples of the present invention and various configurations other than the above can be adopted. In addition, the present invention is not limited to the above-described embodiments, and modifications, improvements, and the like within the range in which the object of the present invention can be achieved are included in the present invention.
Hereinafter, the present invention will be described in detail with reference to Examples, but the present invention is not limited to the description of Examples.
<Preparation of Resin Composition>
For each Examples, a resin composition was prepared as follows. First, each component shown in Table 1 was prepared in a stated amount and mixed using a mixer. Next, the resulting mixture was roll-kneaded. Thereafter, the mixture was cooled, pulverized, and tableted. From the above, a tablet-shaped resin composition was obtained.
The amount of each component shown in Table 1 is part by mass.
Specifically, raw material components shown in Table 1 are as follows.
(Epoxy Resin)
(Phenol-Based Curing Agent)
(Aromatic diamine)
(Mold Release Agent)
(Curing Catalyst)
(Magnetic Particles)
<Performance Evaluation>
The following evaluations were carried out for each resin composition.
(Average linear expansion coefficient α1 (50° C. to 70° C.) and average linear expansion coefficient α2 (270° C. to 290° C.))
The obtained resin composition was injection-molded using a low-pressure transfer molding machine (“KTS-30” manufactured by KOHTAKI Corporation) at a mold temperature of 175° C., an injection pressure of 9.8 MPa, and a curing time of 120 seconds to obtain a molded product of 15 mm×4 mm×4 mm. Next, the obtained molded product was post-cured at 175° C. for 4 hours to produce a test piece. With regard to the obtained test piece, using a thermomechanical analyzer (manufactured by Seiko Instruments Inc., TMA100), a glass transition temperature (° C.), an average linear expansion coefficient α1 (ppm/° C.) at 50° C. to 70° C., and an average linear expansion coefficient α2 (ppm/° C.) at 270° C. to 290° C. were measured under the conditions of a measurement temperature range of 0° C. to 400° C., a heating rate of 5° C./min.
(Relative Magnetic Permeability)
The resin composition was injection-molded using a low-pressure transfer molding machine (“KTS-30” manufactured by KOHTAKI Corporation) at a mold temperature of 175° C., an injection pressure of 9.8 MPa, and a curing time of 120 seconds to obtain a columnar molded product having a diameter of 16 mmΦ and a height of 32 mm. Next, the obtained molded product was post-cured at 175° C. for 4 hours to produce a test piece for evaluating relative magnetic permeability. With regard to the obtained columnar molded product, using a DC/AC magnetization characteristic test device (“MTR-1488” manufactured by Metron Giken Co., Ltd.), a B—H initial magnetization curve was measured in a range of H=0 to 100 kA/m, a value of H=5 kA/m of the B—H initial magnetization curve was defined as the relative magnetic permeability.
(Iron Loss (50 Mt, 50 Khz))
The obtained resin composition was injection-molded using a low-pressure transfer molding machine (“KTS-30” manufactured by KOHTAKI Corporation) at a mold temperature of 175° C., an injection pressure of 9.8 MPa, and a curing time of 120 seconds to obtain a ring-shaped molded product having an outer diameter of 27 mmΦ, an inner diameter of 15 mmΦ, and a thickness of 3 mm. Next, the obtained molded product was post-cured at 175° C. for 4 hours to produce a ring-shaped test piece. With regard to the obtained ring-shaped test piece, using a BH curve tracer, a hysteresis loss Wh (kW/m3) and an eddy current loss We (kW/m3) at an excitation magnetic flux density Bm: 50 mT and a measurement frequency: 50 kHz were measured, and the hysteresis loss Wh+ the eddy current loss We was calculated as the iron loss (kW/m3).
Compositions and evaluation results of each resin composition are listed in the table below.
(Minimum Melt Viscosity)
With regard to the resin composition of Example 1, using a rheometer (“HAAKEMARS III” manufactured by Thermo Fisher Scientific Inc.), a melt viscosity (Pa·s) at 80° C. to 250° C. was measured under the conditions of a heating rate 10° C./min and a frequency of 1 Hz. As a result, the minimum melt viscosity of Example 1 was 152 Pa·s at 128° C.
As shown in Table 1, in the evaluation using the resin compositions of Examples 1 to 4, the iron loss was reduced as compared with that of Comparative Examples 1 and 2. That is, it was shown that the magnetic characteristics of the magnetic members formed by using the resin compositions of Examples 1 to 4 are high. In addition, in the evaluation using the resin compositions of Examples 1 to 3, the relative magnetic permeability was higher than that of Example 4.
On the other hand, Examples 1 to 4 had a smaller average linear expansion coefficient α1 at 50° C. to 70° C. and a smaller average linear expansion coefficient α2 at 270° C. to 290° C. than those of Comparative Examples 1 and 2. Therefore, it was shown that the magnetic members formed by using the resin compositions of Examples 1 to 4 had low thermal expansion and could be preferably used under room temperature and high temperature conditions.
Priority is claimed on Japanese Patent Application No. 2019-079786, filed Apr. 19, 2019, the disclosure of which is incorporated herein by reference.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-079786 | Apr 2019 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2020/015870 | 4/8/2020 | WO | 00 |
