JP2011159793A - Winding coil component manufacturing method - Google Patents

Winding coil component manufacturing method Download PDF

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JP2011159793A
JP2011159793A JP2010020118A JP2010020118A JP2011159793A JP 2011159793 A JP2011159793 A JP 2011159793A JP 2010020118 A JP2010020118 A JP 2010020118A JP 2010020118 A JP2010020118 A JP 2010020118A JP 2011159793 A JP2011159793 A JP 2011159793A
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coil component
winding
solvent
resin composition
resin
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Nobuyuki Kinami
信之 木南
Yoshiki Yuya
義樹 油谷
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Murata Manufacturing Co Ltd
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Murata Manufacturing Co Ltd
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<P>PROBLEM TO BE SOLVED: To provide a winding coil component manufacturing method for readily coping with the change in the size and the shape of a winding coil component which is to be a product, and efficiently manufacturing the winding coil component having exterior resin. <P>SOLUTION: For manufacturing the winding coil component includes the exterior resin 5, arranged to coat a winding wire 4 wound around the winding core portion of a magnetic core 3 having the winding core portion 1 and a pair of flanges 2a, 2b, arranged on both sides of the winding core portion, when the winding coil component is manufactured, a resin composition is prepared which contains an epoxy resin, acid anhydride, and microcapsule-type imidazole based latent hardener; and then after a solvent which has a polar group is added to the resin composition, the resin composition with the solvent added thereto is applied between a pair of flanges so as to coat the winding wire wound around the winding core portion, and hardened, the exterior resin is formed. As the solvent that has the polar group, at least one kind is used that is selected from among a group constituted of aromatic hydrocarbons, ester, alcoholic, ether, and ketone systems. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

本発明は、巻線コイル部品の製造方法に関し、詳しくは、巻芯部と、その両端側に配設された一対の鍔部とを有する磁性コアの、巻芯部に巻回された巻線を覆うように、一対の鍔部間に配設された外装樹脂を備えた巻線コイル部品の製造方法に関する。   The present invention relates to a method of manufacturing a wound coil component, and more specifically, a winding of a magnetic core having a winding core and a pair of flanges disposed on both ends thereof, wound around the winding core. The present invention relates to a method for manufacturing a wound coil component including an exterior resin disposed between a pair of flanges.

巻線コイル部品の一つに、例えば、図4に示すように、巻芯部51とその両端側に配設された一対の鍔部52a,52bを有する磁性コア53と、この磁性コア53の巻芯部51に巻回された巻線54と、巻芯部51に巻回された巻線54を覆うように、一対の鍔部52a,52b間に充填された外装樹脂55と、巻線の両端部が電気的に接続される外部電極56a,56bとを備えた巻線コイル部品がある。   For example, as shown in FIG. 4, a magnetic core 53 having a winding core portion 51 and a pair of flange portions 52 a and 52 b disposed on both ends thereof, A winding 54 wound around the core 51, an exterior resin 55 filled between the pair of flanges 52a and 52b so as to cover the winding 54 wound around the core 51, and the winding There is a wound coil component provided with external electrodes 56a and 56b to which both ends thereof are electrically connected.

そして、このような巻線コイル部品において、外装樹脂として、ガラス転移温度が−20℃以下、より好ましくは、ガラス転移温度が−50℃以下の、磁性粉含有樹脂を塗布して硬化させることにより形成された外装樹脂を備えた巻線コイル部品(面実装コイル部品)が提案されている(特許文献1参照)。
そして、この巻線コイル部品のように、ガラス転移温度が−20℃以下、より好ましくは−50℃以下の磁性粉含有外装樹脂を用いるようにした場合、ヒートサイクル試験における鍔の割れの発生を防止し、使用温度環境の変化が激しい用途に好適なコイル部品が得られるとされている。
In such a wound coil component, by applying and curing a magnetic powder-containing resin having a glass transition temperature of −20 ° C. or lower, more preferably −50 ° C. or lower, as the exterior resin. A wound coil component (surface-mounted coil component) having a formed exterior resin has been proposed (see Patent Document 1).
And when this magnetic coil containing exterior resin whose glass transition temperature is -20 degrees C or less, More preferably, -50 degrees C or less is used like this winding coil component, generation | occurrence | production of the crack of the flaw in a heat cycle test It is said that a coil component suitable for an application in which the temperature environment of use is prevented and the usage temperature environment changes drastically is obtained.

また、金属粉末を55重量%以上含む樹脂混和物、あるいは1〜40重量%のフィラーを含む該樹脂混和物を塗布して硬化させることにより形成された外装樹脂を備えた巻線コイル部品が提案されている(特許文献2参照)。
そして、この巻線コイル部品によれば、ヒートショックなどの環境負荷試験後の信頼性を確保することができるとされている。
Also proposed is a wound coil component having an exterior resin formed by applying and curing a resin mixture containing 55% by weight or more of metal powder or a resin mixture containing 1 to 40% by weight of filler. (See Patent Document 2).
And according to this winding coil component, it is supposed that the reliability after environmental load tests, such as a heat shock, can be ensured.

特開2005−210055号公報Japanese Patent Laid-Open No. 2005-210055 特開2008−300653号公報JP 2008-300653 A

特許文献1のように、外装樹脂として、ガラス転移温度が低い磁性粉含有樹脂を用いた場合、外装樹脂の柔軟性が高くなるため、温度変化に対する対応性が向上するとともに、種々のサイズや形状の巻線型コイル部品に使用することが可能になり、汎用性も向上する。しかしながら、硬化後の外装樹脂が柔らかすぎて、磁性コアの機械的な強度を補って、信頼性を向上させる効果が不十分になるという問題点がある。   As in Patent Document 1, when a magnetic powder-containing resin having a low glass transition temperature is used as the exterior resin, the flexibility of the exterior resin increases, so that the response to temperature changes is improved, and various sizes and shapes are available. It can be used for the wire-wound type coil parts, and versatility is improved. However, there is a problem that the package resin after curing is too soft, and the effect of improving the reliability by supplementing the mechanical strength of the magnetic core becomes insufficient.

一方、特許文献2のように、樹脂中に金属粉末等の充填剤(他に、シリカ粉末やフィラー)を含有させるようにした場合、補強効果は向上するが、巻線コイル部品のサイズや形状が異なると、充填剤の含有量を適切な量に調整することが必要になる。そのため、製品のサイズや形状が変わると、そのたびに充填剤を適切な割合で含有する樹脂組成物を用意しなければならなくなり、生産性の低下やコストの増大を招くという問題点がある。   On the other hand, when the filler (such as silica powder or filler) such as metal powder is contained in the resin as in Patent Document 2, the reinforcing effect is improved, but the size and shape of the wound coil component are improved. Is different, it is necessary to adjust the filler content to an appropriate amount. For this reason, whenever the size or shape of the product changes, a resin composition containing a filler in an appropriate ratio must be prepared each time, which causes a problem of reducing productivity and increasing cost.

本発明は、上記課題を解決するものであり、製品となる巻線コイル部品のサイズや形状の変化に対応することが容易で、外装樹脂を備えた巻線コイル部品を効率よく製造することが可能な巻線コイル部品の製造方法を提供することを目的とする。   The present invention solves the above-mentioned problems, and can easily cope with changes in the size and shape of a wound coil component as a product, and can efficiently manufacture a wound coil component including an exterior resin. It is an object of the present invention to provide a method for manufacturing a possible wound coil component.

上記課題を解決するため、本発明の巻線コイル部品の製造方法は、
巻芯部とその両端側に配設された一対の鍔部とを有する磁性コアと、
前記磁性コアの前記巻芯部に巻回された巻線と、
前記巻芯部に巻回された巻線を覆うように、前記一対の鍔部間に充填された外装樹脂と
を備えた巻線コイル部品の製造方法であって、
エポキシ樹脂と、酸無水物と、マイクロカプセル型イミダゾール系潜在性硬化剤とを含む樹脂組成物を準備する工程と、
前記樹脂組成物に極性基を有する溶剤を添加する工程と、
前記溶剤を添加した樹脂組成物を、前記巻芯部に巻回された巻線を覆うように前記一対の鍔部間に付与する工程と
を備えていることを特徴としている。
In order to solve the above problems, a method for manufacturing a wound coil component according to the present invention includes:
A magnetic core having a winding core and a pair of flanges disposed on both ends thereof;
A winding wound around the core portion of the magnetic core;
A method of manufacturing a wound coil component comprising: an exterior resin filled between the pair of flanges so as to cover the winding wound around the winding core part,
Preparing a resin composition comprising an epoxy resin, an acid anhydride, and a microcapsule type imidazole-based latent curing agent;
Adding a solvent having a polar group to the resin composition;
And a step of applying the resin composition to which the solvent is added between the pair of flanges so as to cover the winding wound around the core part.

前記溶剤としては、芳香族炭化水素系、エステル系、アルコール系、エーテル系、およびケトン系からなる群より選ばれる少なくとも一種を用いることが望ましい。   As the solvent, it is desirable to use at least one selected from the group consisting of aromatic hydrocarbons, esters, alcohols, ethers, and ketones.

前記溶剤の添加量は3重量%以上とすることが望ましく、また、25重量%未満とすることが望ましい。   The amount of the solvent added is desirably 3% by weight or more, and desirably less than 25% by weight.

本発明の巻線コイル部品の製造方法では、エポキシ樹脂と、酸無水物と、マイクロカプセル型イミダゾール系潜在性硬化剤とを含む樹脂組成物を用意しておき、この樹脂組成物に、極性基を有する溶剤を、製品となる巻線コイル部品のサイズや形状に応じた量だけ添加して、巻芯部に巻回された巻線を覆うように一対の鍔部間に付与して硬化させることにより、適切な磁性コア補強効果を有する外装樹脂を備えた巻線コイル部品を効率よく製造することが可能になる。
すなわち、本発明の巻線コイル部品の製造方法においては、添加する溶剤の量に幅を持たせることができるため、その量を調整することにより、硬化後の外装樹脂の特性(Tg、弾性率、残留応力)を制御して、信頼性の高い巻線コイル部品を得ることが可能になる。
In the method for manufacturing a wound coil component of the present invention, a resin composition containing an epoxy resin, an acid anhydride, and a microcapsule-type imidazole-based latent curing agent is prepared, and the resin composition includes a polar group. Is added in an amount corresponding to the size and shape of the wound coil component that is the product, and is applied between the pair of collars so as to cover the winding wound around the winding core, and is cured. As a result, it is possible to efficiently manufacture the wound coil component including the exterior resin having an appropriate magnetic core reinforcing effect.
That is, in the method of manufacturing a wound coil component according to the present invention, the amount of the solvent to be added can be widened. Therefore, by adjusting the amount, the characteristics (Tg, elastic modulus) of the cured exterior resin can be adjusted. , Residual stress) can be controlled to obtain a highly reliable wound coil component.

本発明においては、樹脂組成物を磁性コアに塗布(付与)する前に極性基を有する溶剤を添加することにより、マイクロカプセル型イミダゾール系潜在性硬化剤を構成する、イミダゾールを覆うカプセルが侵され(膨潤し)、カプセルに覆われていたイミダゾール系硬化剤が露出して主材(エポキシ樹脂)と接触し、硬化剤としての機能を発現する。そして、イミダゾール粒子の表層において主剤(エポキシ樹脂)との硬化反応が進行することにより、熱に対して安定な新たなカプセルが形成される。この新たなカプセルの形成により、硬化剤であるイミダゾールの硬化能が不活性化され、樹脂の硬化が抑制されることになる。そして、磁性コアに塗布(付与)された樹脂組成物が硬化することにより形成される硬化塗膜(外装樹脂)の低Tg化、低弾性化が達成され、適度な柔軟性が付与される。その結果、外装樹脂の残留応力に起因する、磁性コアの割れや欠けなどの発生を防止することができる。   In the present invention, by adding a solvent having a polar group before applying (giving) the resin composition to the magnetic core, the capsule covering the imidazole constituting the microcapsule type imidazole-based latent curing agent is eroded. (Swells), the imidazole-based curing agent covered with the capsule is exposed and comes into contact with the main material (epoxy resin), and functions as a curing agent. And the new capsule stable with respect to a heat | fever is formed by the hardening reaction with a main ingredient (epoxy resin) progressing in the surface layer of an imidazole particle. By forming this new capsule, the curing ability of imidazole, which is a curing agent, is inactivated, and the curing of the resin is suppressed. Then, the cured coating film (exterior resin) formed by curing (resining) the resin composition applied (given) to the magnetic core achieves low Tg and low elasticity, and imparts appropriate flexibility. As a result, it is possible to prevent the magnetic core from being cracked or chipped due to the residual stress of the exterior resin.

また硬化能の不活性化の程度は、極性基を有する溶剤の添加量に依存するため、溶剤の添加量によって外装樹脂の物性(硬化塗膜の物性)を制御することが可能になる。したがって、溶剤の添加量を調整するのみで、樹脂組成の配合調整を必要とすることなく、磁性コアのサイズや形状に応じた硬化塗膜の物性制御を行うことが可能になり、1種類の樹脂組成物を用意しておくだけで、簡便に外装樹脂を備えた種々の巻線コイル部品を効率よく製造することができる。   In addition, since the degree of inactivation of the curing ability depends on the addition amount of the solvent having a polar group, the physical property of the exterior resin (the physical property of the cured coating film) can be controlled by the addition amount of the solvent. Therefore, it is possible to control the physical properties of the cured coating film according to the size and shape of the magnetic core without adjusting the composition of the resin composition only by adjusting the addition amount of the solvent. By simply preparing the resin composition, various wound coil components including the exterior resin can be easily and efficiently manufactured.

なお、本発明における、「マイクロカプセル型イミダゾール系潜在性硬化剤」は、イミダゾール系の硬化剤が、イソシアナート化合物、エポキシ化合物、ポリアシド、ポリフェニレンオキシド、ポリアセタール、ポリアリレート、ポリエステル、ポリカーボネート、ポリエーテルイシド、ポリイシド、ポリスルホン、ポリエーテルスルホン、ポリアリルスルホンのうち少なくとも1種からなるカプセル内に保持されているような硬化剤である。イミダゾール系の硬化剤としては、2−メチルイミダゾール、2−エチル−4−メチルイミダゾール、2−ウンデシルイミダゾール、2−ヘプタデシルイミダゾール、2−フェニルイミダゾール、1−アミノエチル−2−メチルイミダゾール、1−(2−ヒドロキシ−3−フェノキシプロピル)−2−メチルイミダゾール、1−(2−ヒドロキシ−3−フェノキシプロピル)−2−エチル−4−メチルイミダゾール、1−(2−ヒドロキシ−3−ブトキシプロピル)−2−メチルイミダゾール、1−(2−ヒドロキシ−3−ブトキシプロピル)−2−エチル−4−メチルイミダゾールが挙げられる。特に、2−メチルイミダゾール、2−ウンデシルイミダゾール、2−ヘプタデシルイミダゾール、2−フェニルイミダゾールが低温硬化性と貯蔵安定性の両立の観点から好ましく、2−メチルイミダゾールが最も好ましい。   In the present invention, the “microcapsule type imidazole-based latent curing agent” refers to an imidazole-based curing agent that is an isocyanate compound, an epoxy compound, a polyacid, a polyphenylene oxide, a polyacetal, a polyarylate, a polyester, a polycarbonate, a polyether ether. It is a curing agent that is held in a capsule composed of at least one of side, polyicid, polysulfone, polyethersulfone, and polyallylsulfone. Examples of imidazole curing agents include 2-methylimidazole, 2-ethyl-4-methylimidazole, 2-undecylimidazole, 2-heptadecylimidazole, 2-phenylimidazole, 1-aminoethyl-2-methylimidazole, 1 -(2-hydroxy-3-phenoxypropyl) -2-methylimidazole, 1- (2-hydroxy-3-phenoxypropyl) -2-ethyl-4-methylimidazole, 1- (2-hydroxy-3-butoxypropyl) ) -2-methylimidazole, 1- (2-hydroxy-3-butoxypropyl) -2-ethyl-4-methylimidazole. In particular, 2-methylimidazole, 2-undecylimidazole, 2-heptadecylimidazole, and 2-phenylimidazole are preferable from the viewpoint of achieving both low-temperature curability and storage stability, and 2-methylimidazole is most preferable.

また、本発明において、極性基を有する溶剤とは、電気陰性度の大きい、酸素や窒素を含む原子団である、極性官能基を分子内に含む溶剤を意味する概念である。極性基としては、例えば、たとえば、−OH,C=O,−COOH,−NH2,−NO2,−NH3 +,−CNなどが例示される。 In the present invention, the solvent having a polar group is a concept that means a solvent having a polar functional group in the molecule, which is an atomic group containing oxygen and nitrogen having a high electronegativity. Examples of the polar group include —OH, C═O, —COOH, —NH 2 , —NO 2 , —NH 3 + , —CN, and the like.

なお、本発明において用いられる樹脂組成物は、エポキシ樹脂、酸無水物、マイクロカプセル型イミダゾール系潜在性硬化剤の他に、巻線コイル部品の特性を改善するための添加物、例えば、金属や、無機酸化物などのフィラーなどを含んでいてもよい。   The resin composition used in the present invention includes an epoxy resin, an acid anhydride, a microcapsule type imidazole-based latent curing agent, an additive for improving the properties of the wound coil component, such as a metal or In addition, a filler such as an inorganic oxide may be included.

なお、本発明においては、樹脂組成物に添加すべき、極性基を有する溶剤として、芳香族炭化水素系、エステル系、アルコール系、エーテル系、およびケトン系からなる群より選ばれる少なくとも一種を用いることにより、確実に外装樹脂の物性(硬化塗膜の物性)を制御することが可能になり、本発明をより実効あらしめることができる。   In the present invention, as the solvent having a polar group to be added to the resin composition, at least one selected from the group consisting of aromatic hydrocarbons, esters, alcohols, ethers, and ketones is used. As a result, the physical properties of the exterior resin (the physical properties of the cured coating film) can be reliably controlled, and the present invention can be made more effective.

そして、上で挙げた溶剤の中でも、特に、アルコール系、エーテル系、ケトン系の溶剤は、極性基が強く、さらに確実に外装樹脂の物性(硬化塗膜の物性)を制御することが可能になる。   Among the solvents listed above, especially alcohol-based, ether-based, and ketone-based solvents have strong polar groups, and can more reliably control the physical properties of the exterior resin (the physical properties of the cured coating film). Become.

また、本発明においては、上記極性基を有する溶剤の、溶剤添加後における樹脂組成物全体に占める割合を3重量%以上となるようにすることにより、磁性コア割れの発生率を0にすることができる。   In the present invention, the rate of occurrence of magnetic core cracks is set to 0 by making the proportion of the solvent having the polar group in the resin composition after addition of the solvent 3% by weight or more. Can do.

また、上記極性基を有する溶剤の、溶剤添加後における樹脂組成物全体に占める割合が25重量%以上になると、本来樹脂組成物に含まれるマイクロカプセル型イミダゾール系潜在性硬化剤を構成するカプセルが侵される(膨潤する)度合いが大きくなる一方、その後の新しいカプセルの形成が進みすぎて、外装樹脂の硬化不足が生じ、それに起因する磁性コア補強効果の不足を生じる場合がある。 そのため、極性基を有する溶剤の添加量は25重量%未満とすることが望ましい。   Moreover, when the ratio of the solvent having the polar group to the entire resin composition after the addition of the solvent is 25% by weight or more, the capsule that originally constitutes the microcapsule type imidazole-based latent curing agent contained in the resin composition is obtained. While the degree of erosion (swelling) increases, the subsequent formation of new capsules may proceed excessively, resulting in insufficient curing of the exterior resin, resulting in insufficient magnetic core reinforcing effect. Therefore, the amount of the solvent having a polar group is desirably less than 25% by weight.

本発明の実施例において用意した、外装樹脂を配設する前の段階の巻線コイル部品素子を示す正面断面図である。It is front sectional drawing which shows the winding coil component element of the stage before arrange | positioning exterior resin prepared in the Example of this invention. 発明の実施例において用意した、外装樹脂を配設する前の段階の巻線コイル部品素子を示す平面図である。It is a top view which shows the winding coil component element of the stage before arrange | positioning exterior resin prepared in the Example of invention. 本発明の実施例にかかる方法により製造した巻線コイル部品を示す正面断面図である。It is front sectional drawing which shows the winding coil components manufactured by the method concerning the Example of this invention. 従来の、外装樹脂を備えた巻線コイル部品を示す正面断面図である。It is front sectional drawing which shows the conventional winding coil component provided with exterior resin.

以下に本発明の実施の形態を示して、本発明の特徴とするところをさらに詳しく説明する。   Embodiments of the present invention will be described below to describe the features of the present invention in more detail.

<実施例1>
[1]樹脂組成物の作製
まず、以下の各原料を秤取し、混合することにより、極性基を有する溶剤を添加する前の段階の樹脂組成物を作製した。
(a)脂肪族系ポリグリシジルエーテル12g
(b)酸無水物16g
(c)シラン系カップリング剤1g
(d)シリカ70g
(e)マイクロカプセル型イミダゾール系潜在性硬化剤1g
<Example 1>
[1] Preparation of Resin Composition First, the following raw materials were weighed and mixed to prepare a resin composition at a stage before adding a solvent having a polar group.
(a) Aliphatic polyglycidyl ether 12g
(b) Acid anhydride 16g
(c) Silane coupling agent 1g
(d) 70 g of silica
(e) 1 g of microcapsule type imidazole-based latent curing agent

それから、溶剤を含まない樹脂組成物に、極性基を有する溶剤としてブチルセロソルブを、樹脂組成物全体に占める割合が3重量%となるように添加して、極性基を有する溶剤を含む樹脂組成物を作製した。   Then, butyl cellosolve as a solvent having a polar group is added to a resin composition not containing a solvent so that the proportion of the total resin composition is 3% by weight, and a resin composition containing the solvent having a polar group is obtained. Produced.

[2]外装樹脂を備えた巻線コイル部品の作製
この実施例では、樹脂組成物を塗布する対象である巻線コイル部品素子として、図1および図2に示すように、巻芯部1と、その両端側に配設された一対の鍔部2a,2bとを有する磁性コア3と、この磁性コア3の巻芯部1に巻回された、表面が絶縁被覆された巻線4と、巻線4の両端部が電気的に接続される外部電極6a,6bを備えた巻線コイル部品素子(外装樹脂を配設する前の巻線コイル部品)A1を用意した。
なお、この巻線コイル部品素子A1を構成する磁性コア3は、寸法が、長さL=3.2mm、幅W=2.5mm、高さT=1.7mmのものである。
[2] Production of wound coil component provided with exterior resin In this example, as shown in FIG. 1 and FIG. 2, as the wound coil component element to which the resin composition is applied, A magnetic core 3 having a pair of flange portions 2a and 2b disposed on both ends thereof, and a winding 4 wound around the core portion 1 of the magnetic core 3 and having an insulating coating on the surface, A winding coil component element (winding coil component before disposing the exterior resin) A1 provided with external electrodes 6a and 6b to which both ends of the winding 4 are electrically connected was prepared.
The magnetic core 3 constituting the coiled coil component element A1 has dimensions of length L = 3.2 mm, width W = 2.5 mm, and height T = 1.7 mm.

そして、図3に示すように、この巻線コイル部品素子A1の、巻芯部1に巻回された巻線4を覆うように、磁性コア3の一対の鍔部2a,2b間に、極性基を有する溶剤を添加した樹脂組成物5aを、ディスペンサ塗布機を用いて塗布、充填した。   Then, as shown in FIG. 3, the polarity of the winding coil component element A1 between the pair of flange portions 2a and 2b of the magnetic core 3 is covered so as to cover the winding 4 wound around the core portion 1. The resin composition 5a to which a solvent having a group was added was applied and filled using a dispenser applicator.

そして、樹脂組成物5aが塗布、充填された巻線コイル部品素子A1を、90℃、30分の条件で熱処理して樹脂組成物5aを乾燥させた後、150℃、60分の条件で熱処理して硬化させることにより、図1に示すように、外装樹脂5を備えた巻線コイル部品Aを製造した。   The wound coil component element A1 coated and filled with the resin composition 5a is heat-treated at 90 ° C. for 30 minutes to dry the resin composition 5a, and then heat-treated at 150 ° C. for 60 minutes. Then, as shown in FIG. 1, a wound coil component A provided with the exterior resin 5 was manufactured.

[3]特性評価のための樹脂硬化膜の作製
また、極性基を有する溶剤を添加した樹脂組成物を硬化させることにより得られる、外装樹脂となる硬化樹脂の特性を評価するため、磁性コアに塗布した樹脂組成物と同じ樹脂、すなわち、溶剤としてブチルセルソルブを3重量%添加した樹脂組成物を塗布して、上記[2]で説明した条件と同じ条件(乾燥条件:90℃、30分、硬化条件:150℃、60分)で乾燥、硬化させることにより、幅10mm、長さ50mm、厚さ0.5mmの樹脂硬化膜を作製した。
[3] Preparation of cured resin film for characteristic evaluation In addition, in order to evaluate the characteristics of a cured resin to be an exterior resin obtained by curing a resin composition to which a solvent having a polar group is added, The same resin as the applied resin composition, that is, a resin composition added with 3% by weight of butyl cellosolve as a solvent was applied, and the same conditions as described in the above [2] (drying conditions: 90 ° C., 30 minutes) Curing conditions: 150 ° C., 60 minutes) were dried and cured to produce a cured resin film having a width of 10 mm, a length of 50 mm, and a thickness of 0.5 mm.

[4]特性の測定および評価
(1)ガラス転移点(Tg)の測定
ガラス転移点(Tg)は、上記[3]に説明した方法で作製した樹脂硬化膜を試料として、動的粘弾性装置(SII社製 DMS110)を用いて、昇温速度10℃/minで測定した。そして、tanδのピーク位置をガラス転移温度(Tg)とした。
なお、樹脂硬化膜(外装樹脂)のTgの値としては、通常70℃以下であることが望ましい。
[4] Measurement and evaluation of characteristics
(1) Measurement of glass transition point (Tg) The glass transition point (Tg) was measured using a dynamic viscoelastic device (DMS110 manufactured by SII) using the cured resin film prepared by the method described in [3] above as a sample. The measurement was performed at a temperature rising rate of 10 ° C./min. The peak position of tan δ was defined as the glass transition temperature (Tg).
The Tg value of the cured resin film (exterior resin) is usually desirably 70 ° C. or lower.

(2)弾性率
弾性率は、上記[3]において説明した方法で作製した樹脂硬化膜を試料として、万能試験機(オリエンテック社製テンシロンUCT−IT)を用いて、JIS K7171に準拠して測定した。
なお、樹脂硬化膜(外装樹脂)の弾性率は、通常8000MPa未満であることが望ましい。
(2) Elastic modulus The elastic modulus is based on JIS K7171 using a universal testing machine (Tensilon UCT-IT manufactured by Orientec Co., Ltd.) using a cured resin film prepared by the method described in [3] above as a sample. It was measured.
The elastic modulus of the cured resin film (exterior resin) is usually desirably less than 8000 MPa.

(3)磁性コアの割れ発生率
上記[2]において説明した方法で作製した巻線コイル部品Aの外観観察および断面観察によって、磁性コアの割れの発生状態(割れの発生率)を調べた。
(3) Crack generation rate of magnetic core The occurrence state of cracks in the magnetic core (breakage rate of cracks) was examined by observing the appearance and cross section of the wound coil component A manufactured by the method described in [2] above.

(4)巻線コイル部品の強度
上記[2]の方法で作製した巻線コイル部品を、テーピング部品連用のテープ(リールに巻き取られるテープ)の収納部に収納して、テーピング部品連を製造する工程での、テープへの巻線コイル部品の収納時における巻線コイル部品の割れ、欠けの有無を調べて、巻線コイル部品の強度を評価した。
上記のようにして調べた特性を表1に示す。なお、表1では、テーピング部品連を製造する工程での割れ、欠けの認められないものを、巻線コイル部品の強度が良であるとした。
(4) Strength of coiled coil parts The coiled coil parts produced by the above method [2] are housed in the taped part continuous tape (tape wound around the reel) storage part to produce a series of taped parts. The strength of the winding coil component was evaluated by examining whether or not the winding coil component was cracked or chipped when the winding coil component was stored in the tape.
The characteristics examined as described above are shown in Table 1. In Table 1, the strength of the wound coil component was determined to be good if no cracks or chips were observed in the process of manufacturing the taping component series.

<実施例2>
上記実施例1では、極性基を有する溶剤としてブチルセルソルブを3重量%添加した樹脂組成物を用いたが、この実施例2では、ブチルセロソルブの添加量を7重量%とした。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 2>
In Example 1 above, a resin composition to which 3% by weight of butyl cellosolve was added as a solvent having a polar group was used. In Example 2, the amount of butyl cellosolve added was 7% by weight. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.

<実施例3>
上記実施例1では、極性基を有する溶剤としてブチルセルソルブを3重量%添加した樹脂組成物を用いたが、この実施例3では、ブチルセロソルブの添加量を10重量%とした。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 3>
In Example 1 above, a resin composition to which 3% by weight of butyl cellosolve was added as a solvent having a polar group was used, but in Example 3, the amount of butyl cellosolve added was 10% by weight. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.

<実施例4>
上記実施例1では、極性基を有する溶剤としてブチルセルソルブを3重量%添加した樹脂組成物を用いたが、この実施例4では、ブチルセロソルブの添加量を15重量%とした。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 4>
In Example 1, the resin composition to which 3% by weight of butyl cellosolve was added as a solvent having a polar group was used. In Example 4, the amount of butyl cellosolve added was 15% by weight. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.

<実施例5>
上記実施例1では、極性基を有する溶剤としてブチルセルソルブを3重量%添加した樹脂組成物を用いたが、この実施例5では、ブチルセロソルブの添加量を20重量%とした。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 5>
In Example 1 above, a resin composition to which 3% by weight of butyl cellosolve was added as a solvent having a polar group was used. In Example 5, the amount of butyl cellosolve added was 20% by weight. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.

<実施例6>
この実施例6では、上記実施例1で用いたブチルセルソルブに代えて、極性基を有する溶媒としてカルビトールを用い、その添加量を3重量%とした。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 6>
In Example 6, instead of butyl cellosolve used in Example 1 above, carbitol was used as a solvent having a polar group, and the amount added was 3% by weight. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.

<実施例7>
この実施例7では、上記実施例1で用いたブチルセルソルブに代えて、極性基を有する溶媒としてメチルエチルケトンを用い、その添加量を3重量%とした。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 7>
In this Example 7, instead of the butyl cellosolve used in Example 1 above, methyl ethyl ketone was used as a solvent having a polar group, and the amount added was 3% by weight. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.

<実施例8>
この実施例8では、磁性コアの寸法を、長さL=4.0mm、幅W=4.0mm、高さT=2.0mm(実施例1では、長さL=3.2mm、幅W=2.5mm、高さT=1.7mm)としたことを除いて、上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 8>
In Example 8, the dimensions of the magnetic core are as follows: length L = 4.0 mm, width W = 4.0 mm, height T = 2.0 mm (in Example 1, length L = 3.2 mm, width W = 2.5 mm, height T = 1.7 mm), a sample was prepared under the same conditions as in Example 1, and the characteristics were evaluated in the same manner as in Example 1.

<実施例9>
この実施例9では、磁性コアの寸法を、長さL=2.0mm、幅W=2.0mm、高さT=1.5mm(実施例1では、長さL=3.2mm、幅W=2.5mm、高さT=1.7mm)としたことを除いて、上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Example 9>
In Example 9, the dimensions of the magnetic core are as follows: length L = 2.0 mm, width W = 2.0 mm, height T = 1.5 mm (in Example 1, length L = 3.2 mm, width W = 2.5 mm, height T = 1.7 mm), a sample was prepared under the same conditions as in Example 1, and the characteristics were evaluated in the same manner as in Example 1.

<比較例1>
上記実施例1ではブチルセルソルブを3重量%添加した樹脂組成物を用いたが、この比較例1では、ブチルセロソルブを添加しない樹脂組成物(ブチルセルソルブ0重量%)を用いた。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
<Comparative Example 1>
In Example 1, a resin composition to which 3% by weight of butyl cellosolve was added was used. In Comparative Example 1, a resin composition to which butyl cellosolve was not added (butyl cellosolve 0% by weight) was used. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.

<比較例2>
上記実施例1ではブチルセルソルブを3重量%添加した樹脂組成物を用いたが、この比較例2では、ブチルセロソルブに代えて、極性基を有していないヘキサンを3重量%の割合で添加した樹脂組成物(ブチルセルソルブ0重量%)を用いた。それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価した。
上記の各実施例および比較例において調べた特性を表1に併せて示す。
<Comparative example 2>
In Example 1 above, a resin composition to which 3% by weight of butyl cellosolve was added was used. In Comparative Example 2, hexane having no polar group was added at a rate of 3% by weight in place of butyl cellosolve. A resin composition (butyl cellosolve 0% by weight) was used. Other than that, the sample was produced on the same conditions as the case of the said Example 1, and the characteristic was evaluated by the same method as the case of the said Example 1. FIG.
The characteristics examined in each of the above examples and comparative examples are also shown in Table 1.

Figure 2011159793
Figure 2011159793

表1に示すように、本発明の要件を備えた実施例1〜9の場合、ガラス転移点(Tg)、弾性率、磁性コアの割れ発生率、および巻線コイル部品の強度について、良好な結果が得られることが確認された。   As shown in Table 1, in the case of Examples 1 to 9 having the requirements of the present invention, the glass transition point (Tg), the elastic modulus, the crack occurrence rate of the magnetic core, and the strength of the wound coil component are good. It was confirmed that a result was obtained.

また、表1には示していないが、極性基を有する溶剤として、ブチルセロソルブの添加量を1重量%とし、それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価したところ、作製された巻線コイル部品において、磁性コアの割れが少し発生した(発生率<10%)。なお、巻線コイル部品をテープの収納部に収納してテーピング部品連を製造する工程での不良は発生しなかった。   Although not shown in Table 1, as a solvent having a polar group, a sample was prepared under the same conditions as in Example 1 except that the addition amount of butyl cellosolve was 1% by weight. When the characteristics were evaluated by the same method as in, a few cracks occurred in the magnetic core in the produced wound coil component (incidence rate <10%). It should be noted that no defect occurred in the process of manufacturing the taping component series by storing the coiled coil component in the tape storage part.

また、表1には示していないが、極性基を有する溶剤として、ブチルセルソルブの添加量を25重量%とし、それ以外は上記実施例1の場合と同じ条件で試料を作製し、上記実施例1の場合と同じ方法で特性を評価したところ、巻線コイル部品をテープの収納部に収納してテーピング部品連を製造する工程で少し不良が発生した。ただし、作製された巻線コイル部品において、磁性コアの割れの発生は認められなかった。   Although not shown in Table 1, as a solvent having a polar group, a sample was prepared under the same conditions as in Example 1 except that the addition amount of butyl cellosolve was 25% by weight. When the characteristics were evaluated by the same method as in Example 1, a little defect occurred in the process of manufacturing the taping component series by storing the wound coil component in the tape storage portion. However, in the manufactured wound coil component, no cracking of the magnetic core was observed.

この結果および上記表1に示した結果から、通常は、極性基を有する溶剤の添加量は3重量%以上、25重量%未満であることが望ましいと考えられる。
ただし、極性基を有する溶剤の極性の強さなどによっては(すなわち、用いる溶剤の種類によっては)、溶剤の添加量を3重量%未満としたり、25重量%以上としたりすることが望ましい場合もあり得るものと推測される。
From these results and the results shown in Table 1 above, it is usually considered that the amount of the solvent having a polar group added is desirably 3% by weight or more and less than 25% by weight.
However, depending on the polarity of the solvent having a polar group (that is, depending on the type of solvent used), it may be desirable to add the solvent to less than 3% by weight or 25% by weight or more. Presumed to be possible.

これに対し、極性基を有する溶剤を添加していない樹脂組成物を用いた比較例1では、硬化塗膜(外装樹脂)のガラス転移温度(Tg)が高く、弾性率も大きいため、作製された巻線コイル部品において、磁性コアの割れの発生が高い割合で認められた。   On the other hand, in Comparative Example 1 using a resin composition to which a solvent having a polar group was not added, the cured coating film (exterior resin) had a high glass transition temperature (Tg) and a large elastic modulus. In the wound coil parts, the occurrence of cracks in the magnetic core was observed at a high rate.

また、溶剤として、極性基を有さないヘキサンを添加した比較例2の場合も、硬化塗膜(外装樹脂)のガラス転移温度(Tg)が高く、弾性率も大きいため、作製された巻線コイル部品において、磁性コアの割れの発生が高い割合で認められた。   In the case of Comparative Example 2 in which hexane not having a polar group was added as a solvent, the cured coating film (exterior resin) had a high glass transition temperature (Tg) and a large elastic modulus. In coil parts, the occurrence of cracks in the magnetic core was observed at a high rate.

以上の結果から、本発明によれば、溶剤の添加量を調整するだけで、樹脂組成の配合調整をすることなく、磁性コアのサイズ、形状に応じた硬化塗膜の物性制御が可能になること、すなわち、同一樹脂組成で簡便に種々の巻線コイル部品に対応できることがわかる。   From the above results, according to the present invention, it is possible to control the physical properties of the cured coating film according to the size and shape of the magnetic core, without adjusting the blending of the resin composition, only by adjusting the addition amount of the solvent. That is, it turns out that it can respond easily to various winding coil components with the same resin composition.

なお、上記実施例では、樹脂組成物が金属粉末や特性改善用のフィラーなどを含んでいない場合を例にとって説明したが、樹脂組成物として、本発明の硬化を損なわない範囲で、金属粉末や特性改善用のフィラーなどを含むものを用いることも可能である。   In the above examples, the case where the resin composition does not contain a metal powder or a filler for improving characteristics has been described as an example. However, as a resin composition, the metal powder or It is also possible to use a material containing a filler for improving characteristics.

本発明は、さらにその他の点においても上記実施例に限定されるものではなく、磁性コアの形状や巻線の巻回数、樹脂組成物を構成する原料の種類や配合割合、溶剤の種類などに関し、発明の範囲内において、種々の応用、変形を加えることが可能である。   The present invention is not limited to the above examples in other points as well, and relates to the shape of the magnetic core, the number of turns of the winding, the type and blending ratio of raw materials constituting the resin composition, the type of solvent, etc. Various applications and modifications can be made within the scope of the invention.

1 巻芯部
2a,2b 鍔部
3 磁性コア
4 巻線
5 外装樹脂
5a 樹脂組成物
6a,6b 外部電極
A1 巻線コイル部品素子
A 巻線コイル部品
DESCRIPTION OF SYMBOLS 1 Core part 2a, 2b Eaves part 3 Magnetic core 4 Winding 5 Exterior resin 5a Resin composition 6a, 6b External electrode A1 Winding coil component element A Winding coil component

Claims (4)

巻芯部とその両端側に配設された一対の鍔部とを有する磁性コアと、
前記磁性コアの前記巻芯部に巻回された巻線と、
前記巻芯部に巻回された巻線を覆うように、前記一対の鍔部間に充填された外装樹脂と
を備えた巻線コイル部品の製造方法であって、
エポキシ樹脂と、酸無水物と、マイクロカプセル型イミダゾール系潜在性硬化剤とを含む樹脂組成物を準備する工程と、
前記樹脂組成物に極性基を有する溶剤を添加する工程と、
前記溶剤を添加した樹脂組成物を、前記巻芯部に巻回された巻線を覆うように前記一対の鍔部間に付与する工程と
を備えていることを特徴とする巻線コイル部品の製造方法。
A magnetic core having a winding core and a pair of flanges disposed on both ends thereof;
A winding wound around the core portion of the magnetic core;
A method of manufacturing a wound coil component comprising: an exterior resin filled between the pair of flanges so as to cover the winding wound around the winding core part,
Preparing a resin composition comprising an epoxy resin, an acid anhydride, and a microcapsule type imidazole-based latent curing agent;
Adding a solvent having a polar group to the resin composition;
Applying the resin composition to which the solvent is added between the pair of brim parts so as to cover the winding wound around the core part. Production method.
前記溶剤は、芳香族炭化水素系、エステル系、アルコール系、エーテル系、およびケトン系からなる群より選ばれる少なくとも一種であることを特徴とする請求項1記載の巻線コイル部品の製造方法。   2. The method for manufacturing a wound coil component according to claim 1, wherein the solvent is at least one selected from the group consisting of aromatic hydrocarbons, esters, alcohols, ethers, and ketones. 前記溶剤の添加量は3重量%以上であることを特徴とする請求項1記載の巻線コイル部品の製造方法。   2. The method of manufacturing a wound coil component according to claim 1, wherein the amount of the solvent added is 3% by weight or more. 前記溶剤の添加量は25重量%未満であることを特徴とする請求項1記載の巻線コイル部品の製造方法。   2. The method of manufacturing a wound coil component according to claim 1, wherein the amount of the solvent added is less than 25% by weight.
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WO2013146251A1 (en) * 2012-03-29 2013-10-03 株式会社村田製作所 Coil component
JP7363726B2 (en) 2020-09-18 2023-10-18 株式会社村田製作所 Wire-wound inductor parts

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JP2004331728A (en) * 2003-05-01 2004-11-25 Nippon Steel Chem Co Ltd Adhesive film for covering electronic component
JP2008038111A (en) * 2006-08-10 2008-02-21 Nippon Steel Chem Co Ltd Film-shaped adhesive and method for producing semiconductor package using the same
JP2008300653A (en) * 2007-05-31 2008-12-11 Nec Tokin Corp Coil component

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JPH11345733A (en) * 1998-05-29 1999-12-14 Toshiba Corp Manufacture for electrically insulated coil
JP2004331728A (en) * 2003-05-01 2004-11-25 Nippon Steel Chem Co Ltd Adhesive film for covering electronic component
JP2008038111A (en) * 2006-08-10 2008-02-21 Nippon Steel Chem Co Ltd Film-shaped adhesive and method for producing semiconductor package using the same
JP2008300653A (en) * 2007-05-31 2008-12-11 Nec Tokin Corp Coil component

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Publication number Priority date Publication date Assignee Title
WO2013146251A1 (en) * 2012-03-29 2013-10-03 株式会社村田製作所 Coil component
JP5668860B2 (en) * 2012-03-29 2015-02-12 株式会社村田製作所 Coil parts
JPWO2013146251A1 (en) * 2012-03-29 2015-12-10 株式会社村田製作所 Coil parts
US9318255B2 (en) 2012-03-29 2016-04-19 Murata Manufacturing Co., Ltd. Coil component
JP7363726B2 (en) 2020-09-18 2023-10-18 株式会社村田製作所 Wire-wound inductor parts

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