JP2000212504A - Coating film for coil - Google Patents

Coating film for coil

Info

Publication number
JP2000212504A
JP2000212504A JP11017603A JP1760399A JP2000212504A JP 2000212504 A JP2000212504 A JP 2000212504A JP 11017603 A JP11017603 A JP 11017603A JP 1760399 A JP1760399 A JP 1760399A JP 2000212504 A JP2000212504 A JP 2000212504A
Authority
JP
Japan
Prior art keywords
epoxy resin
weight
coil
coating film
component
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP11017603A
Other languages
Japanese (ja)
Inventor
Junko Kawada
純子 川田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Somar Corp
Original Assignee
Somar Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Somar Corp filed Critical Somar Corp
Priority to JP11017603A priority Critical patent/JP2000212504A/en
Publication of JP2000212504A publication Critical patent/JP2000212504A/en
Pending legal-status Critical Current

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  • Epoxy Resins (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a coating film for coil coating use having excellent adhesivity and thermal shock resistance, etc., suitable for effectively preventing the damage of a rotor coil of e.g. a power tool motor caused by foreign material. SOLUTION: The objective coating film for coil coating use is produced by curing a composition containing an epoxy component composed of (A) 50-100 wt.% of a bisphenol-type epoxy resin and (B) 0-50 wt.% of a urethane-modified epoxy resin having chelate-forming property and, based on 100 pts.wt. of A+B, (C) 3-15 pts.wt. of a latent curing agent such as dicyandiamide, (D) 0.5-10 pts.wt. of a cure accelerator such as toluenebisdimethylurea, (E) 1-200 pts.wt. of an inorganic filler such as calcium carbonate and (F) 3-10 pts.wt. of a thixotropic agent such as fine silica powder.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明はエポキシ樹脂組成物
の硬化物からなるコイル被覆用塗膜、さらに詳しくは、
特に、一液型で電動工具用モータなどの回転子コイルが
異物による損傷を受けるのを効果的に防止するのに好適
な接着性及び耐熱衝撃性などに優れるコイル被覆用塗膜
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coating film for coil coating comprising a cured product of an epoxy resin composition.
In particular, the present invention relates to a one-pack type coating film for coil coating having excellent adhesiveness and thermal shock resistance suitable for effectively preventing a rotor coil such as a motor for a power tool from being damaged by a foreign substance. .

【0002】[0002]

【従来の技術】従来、電動工具用モータなどの回転子コ
イルが異物による損傷を受けるのを防止する方法として
は、例えば樹脂を含浸できる帯状部材をコイルに巻き付
けた後でコイルに樹脂を含浸させて、帯状部材をコイル
に固着させるとともに、コイルを固める方法や、コイル
への樹脂含浸による型崩れを防止するために、チクソ性
接着剤をコイルに部分的に付着させた後で、コイルに樹
脂を含浸させてコイルを固める方法(いずれも、特開平
8−322178号公報に開示されている方法)などが
知られている。
2. Description of the Related Art Conventionally, as a method for preventing a rotor coil such as a motor for a power tool from being damaged by a foreign substance, for example, a coil is impregnated with a resin after winding a band-like member capable of impregnating the resin. Then, in order to fix the belt-shaped member to the coil, and to prevent the mold from collapsing due to the method of solidifying the coil and the resin impregnation of the coil, the thixotropic adhesive is partially adhered to the coil. And a method of hardening the coil by impregnation (all methods disclosed in Japanese Patent Application Laid-Open No. 8-322178) are known.

【0003】しかしながら、前者の方法においては、帯
状部材は取り扱いにくく、作業性に劣る上、該帯状部材
を巻き付けた後ではコイルに樹脂を十分に含浸させるこ
とが困難であり、その結果、コイルを均質にしっかりと
固めにくいなどの欠点がある。一方、後者の方法におい
ては、チクソ性接着剤とコイルとの接着性が必ずしも十
分ではなく、回転子コイルが回転中に、該チクソ性接着
剤がコイルから脱落しやすいという欠点がある。
However, in the former method, the band-shaped member is difficult to handle, the workability is poor, and it is difficult to sufficiently impregnate the coil with the resin after winding the band-shaped member. There are drawbacks such as difficulty in hardening uniformly. On the other hand, the latter method has a disadvantage that the adhesion between the thixotropic adhesive and the coil is not always sufficient, and that the thixotropic adhesive easily falls off the coil while the rotor coil is rotating.

【0004】[0004]

【発明が解決しようとする課題】本発明は、このような
事情のもとで、特に、電動工具用モータなどの回転子コ
イルが異物による損傷を受けるのを効果的に防止するの
に好適な、接着性及び耐熱衝撃性などに優れるコイル被
覆用塗膜を提供することを目的としてなされたものであ
る。
Under such circumstances, the present invention is particularly suitable for effectively preventing a rotor coil such as a motor for a power tool from being damaged by foreign matter. The object of the present invention is to provide a coil coating film having excellent adhesiveness, thermal shock resistance and the like.

【0005】[0005]

【課題を解決するための手段】本発明者らは、接着性及
び耐熱衝撃性などに優れるコイル被覆用塗膜について鋭
意研究を重ねた結果、ビスフェノール型エポキシ樹脂、
キレート形成能を有するウレタン変性エポキシ樹脂、潜
在性硬化剤、硬化促進剤、無機充填剤及び揺変剤を、そ
れぞれ所定の割合で含有するエポキシ樹脂組成物特に一
液型の硬化物が、前記目的に適合しうることを見出し、
この知見に基づいて本発明を完成するに至った。
Means for Solving the Problems The present inventors have conducted intensive studies on a coating film for coil coating having excellent adhesiveness and thermal shock resistance, and as a result, have found that bisphenol type epoxy resin,
An epoxy resin composition containing a urethane-modified epoxy resin having a chelate-forming ability, a latent curing agent, a curing accelerator, an inorganic filler, and a thixotropic agent at a predetermined ratio, particularly a one-pack type cured product, has the above-mentioned object. Found that it could conform to
Based on this finding, the present invention has been completed.

【0006】すなわち、本発明は、(A)ビスフェノー
ル型エポキシ樹脂50〜100重量%と(B)キレート
形成能を有するウレタン変性エポキシ樹脂0〜50重量
%とからなるエポキシ樹脂成分と、その100重量部当
たり、(C)潜在性硬化剤3〜15重量部、(D)硬化
促進剤0.5〜10重量部、(E)無機充填剤1〜20
0重量部及び(F)揺変剤3〜10重量部を含有する組
成物の硬化物からなるコイル被覆用塗膜を提供するもの
である。
That is, the present invention provides an epoxy resin component comprising (A) 50 to 100% by weight of a bisphenol type epoxy resin and (B) 0 to 50% by weight of a urethane-modified epoxy resin having a chelate-forming ability, and 100% by weight thereof. Per part, (C) 3 to 15 parts by weight of a latent curing agent, (D) 0.5 to 10 parts by weight of a curing accelerator, (E) 1 to 20 parts of an inorganic filler.
An object of the present invention is to provide a coating film for coil coating comprising a cured product of a composition containing 0 parts by weight and (F) 3 to 10 parts by weight of a thixotropic agent.

【0007】[0007]

【発明の実施の形態】本発明のコイル被覆用塗膜は、以
下に説明する各成分を含むエポキシ樹脂組成物の硬化物
からなるものである。上記組成物における(A)成分の
ビスフェノール型エポキシ樹脂としては、例えば、ビス
フェノールA型エポキシ樹脂、ビスフェノールF型エポ
キシ樹脂、ビスフェノールAD型エポキシ樹脂などの中
から任意のものを1種又は2種以上選択して使用するこ
とができる。特にエポキシ当量が170〜300の範囲
にあり、かつ温度25℃における粘度が8,000〜2
0,000センチポイズの液状ビスフェノールA型エポ
キシ樹脂を単独で、又は2種以上組み合わせて用いるの
が好ましい。また、本発明の目的が損なわれない限り、
所望により、ノボラック型エポキシ樹脂やアミノ基を有
する多官能エポキシ樹脂などで、前記ビスフェノール型
エポキシ樹脂を、その50重量%以下で置き換えてもよ
い。さらに、モノグリシジルエーテルなどのエポキシ基
を有する反応性希釈剤を、該ビスフェノール型エポキシ
樹脂に対し、30重量%以下の割合で併用することがで
きる。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The coating film for coil coating of the present invention comprises a cured product of an epoxy resin composition containing the following components. As the bisphenol-type epoxy resin of the component (A) in the above composition, for example, one or more arbitrary ones are selected from bisphenol A-type epoxy resin, bisphenol F-type epoxy resin, bisphenol AD-type epoxy resin and the like. Can be used. In particular, the epoxy equivalent is in the range of 170 to 300, and the viscosity at a temperature of 25 ° C is 8,000 to 2
It is preferable to use a 000 centipoise liquid bisphenol A epoxy resin alone or in combination of two or more. Also, unless the object of the present invention is impaired,
If desired, the bisphenol-type epoxy resin may be replaced with a novolak-type epoxy resin or a polyfunctional epoxy resin having an amino group at 50% by weight or less. Further, a reactive diluent having an epoxy group such as monoglycidyl ether may be used in combination with the bisphenol-type epoxy resin at a ratio of 30% by weight or less.

【0008】一方、(B)成分として、所望により用い
られるキレート形成能を有する液状ウレタン変性エポキ
シ樹脂としては、例えば、トリレンジイソシアネート、
イソホロンジイソシアネート、ジフェニルメタンジイソ
シアネート、ジメチルヘキサメチレンジイソシアネート
などのジイソシアネート化合物に、1分子中に少なくと
も1個のヒドロキシル基を有するビスフェノールA型エ
ポキシ樹脂、ビスフェノールF型エポキシ樹脂などのビ
スフェノール型エポキシ樹脂とを反応させてウレタン変
性エポキシ樹脂を製造する際に、エチレンジアミン四酢
酸などのポリアミノカルボン酸基、縮合リン酸骨格など
を有するポリオールを反応させたものである。
On the other hand, as the component (B), a liquid urethane-modified epoxy resin having a chelate-forming ability which is optionally used includes, for example, tolylene diisocyanate,
By reacting a diisocyanate compound such as isophorone diisocyanate, diphenylmethane diisocyanate, dimethylhexamethylene diisocyanate with a bisphenol-type epoxy resin such as a bisphenol A-type epoxy resin having at least one hydroxyl group in one molecule and a bisphenol F-type epoxy resin. When a urethane-modified epoxy resin is produced, a polyol having a polyaminocarboxylic acid group such as ethylenediaminetetraacetic acid, a condensed phosphoric acid skeleton, or the like is reacted.

【0009】このようなキレート形成能を有するウレタ
ン変性エポキシ樹脂を配合することにより、エポキシ樹
脂組成物の揺変性の経時変化を防止することができる。
このキレート形成能を有するウレタン変性エポキシ樹脂
は単独で用いてもよいし、2種以上を組み合わせて用い
てもよい。
By mixing such a urethane-modified epoxy resin having a chelate-forming ability, it is possible to prevent the thixotropy of the epoxy resin composition from changing over time.
The urethane-modified epoxy resin having chelating ability may be used alone or in combination of two or more.

【0010】本発明においては、前者(A)成分のビス
フェノール型エポキシ樹脂と(B)成分のキレート形成
能を有するウレタン変性エポキシ樹脂との配合割合は、
(A)成分が50〜100重量%で、(B)成分が50
〜0重量%の範囲にあることが必要である。(B)成分
の量が50重量%を超えると塗膜の耐熱性が低下すると
ともに、組成物の粘度が上昇し、取り扱い性が悪くな
る。組成物の揺変性の経時変化や粘度及び塗膜の耐熱性
などを考慮すると、この(A)成分と(B)成分との配
合割合は、(A)成分が60〜80重量%で、(B)成
分が40〜20重量%の範囲にあるのが好ましい。
In the present invention, the mixing ratio of the former (A) component bisphenol type epoxy resin and the (B) component urethane-modified epoxy resin having chelate forming ability is as follows:
The component (A) is 50 to 100% by weight, and the component (B) is 50% by weight.
It must be in the range of 0% by weight. When the amount of the component (B) exceeds 50% by weight, the heat resistance of the coating film decreases, and the viscosity of the composition increases, resulting in poor handleability. In consideration of the time-dependent change in the thixotropic properties of the composition, the viscosity, and the heat resistance of the coating film, the mixing ratio of the component (A) to the component (B) is 60 to 80% by weight of the component (A). Preferably, component B) is in the range of 40 to 20% by weight.

【0011】本発明に係る組成物において、(C)成分
として用いられる潜在性硬化剤としては、例えばジシア
ンジアミド、尿素系化合物、有機酸ヒドラジド系化合
物、ポリアミン塩系化合物、アミンアダクト系化合物な
どの中から任意のものを1種又は2種以上選択して使用
することができるが、取り扱いやすく、かつ入手が容易
な点から、ジシアンジアミドが好適である。
In the composition according to the present invention, examples of the latent curing agent used as the component (C) include dicyandiamide, urea compounds, organic acid hydrazide compounds, polyamine salt compounds, amine adduct compounds and the like. And any one or more of them can be selected and used, but dicyandiamide is preferred because it is easy to handle and easily available.

【0012】この(C)成分の潜在性硬化剤の配合量
は、エポキシ樹脂成分量、すなわち、前者(A)成分と
(B)成分との合計量100重量部に対し、3〜15重
量部の範囲であることが必要である。この量が3重量部
未満では組成物の硬化速度が遅いし、15重量部を超え
ると塗膜が脆くなるおそれがある。硬化速度及び塗膜物
性などを考慮すると、この(C)成分の好ましい配合量
は4〜11重量部の範囲である。
The compounding amount of the latent curing agent of the component (C) is 3 to 15 parts by weight based on the amount of the epoxy resin component, that is, 100 parts by weight of the total of the former component (A) and the component (B). Must be within the range. If the amount is less than 3 parts by weight, the curing speed of the composition is low, and if it exceeds 15 parts by weight, the coating film may be brittle. Considering the curing speed and the physical properties of the coating film, the preferred amount of the component (C) is in the range of 4 to 11 parts by weight.

【0013】本発明に係る組成物において、(D)成分
として用いられる硬化促進剤としては、例えば尿素系化
合物、ホスフィン系化合物、イミダゾール系化合物など
の中から任意のものを1種又は2種以上選択して使用す
ることができるが、組成物の速硬化性及び塗膜の耐熱性
の点から、トルエンビスジメチルウレア及びメチレンジ
フェニルビスジメチルウレアが好ましい。
In the composition according to the present invention, the curing accelerator used as the component (D) is, for example, one or more of urea compounds, phosphine compounds, imidazole compounds and the like. Although it can be selected and used, toluene bisdimethylurea and methylenediphenylbisdimethylurea are preferred from the viewpoint of the rapid curing property of the composition and the heat resistance of the coating film.

【0014】この(D)成分の硬化促進剤の配合量は、
エポキシ樹脂成分量、すなわち、前記(A)成分と
(B)成分との合計量100重量部に対し、0.5〜1
0重量部の範囲であることが必要である。この量が0.
5重量部未満では硬化速度が遅く、かつ塗膜の耐熱性が
不十分となるおそれがあるし、10重量部を超えると組
成物の保存安定性が低下する。硬化速度、塗膜の耐熱性
及び組成物の保存安定性などを考慮すると、この(D)
成分の好ましい配合量は1〜6重量部の範囲である。
The compounding amount of the curing accelerator of the component (D) is as follows:
The amount of the epoxy resin component, that is, 0.5 to 1 based on 100 parts by weight of the total amount of the components (A) and (B)
It must be in the range of 0 parts by weight. If this amount is 0.
If the amount is less than 5 parts by weight, the curing rate may be low and the heat resistance of the coating film may be insufficient. If the amount is more than 10 parts by weight, the storage stability of the composition is reduced. Considering the curing speed, heat resistance of the coating film and storage stability of the composition, this (D)
The preferred amount of the components is in the range of 1 to 6 parts by weight.

【0015】本発明に係る組成物において、(E)成分
として用いられる無機充填剤としては、例えば炭酸カル
シウム、シリカ、アルミナ、水酸化アルミニウム、酸化
マグネシウム、タルク、マイカ、クレーなどの中から、
任意のものを1種又は2種以上選択して使用することが
できるが、経済性及び塗膜の切削性などの取り扱いやす
さの点から、炭酸カルシウムが好適である。この炭酸カ
ルシウムとしては特に制限はなく、沈降性炭酸カルシウ
ム、重質炭酸カルシウム、軽質炭酸カルシウムなど、い
ずれも用いることができる。
In the composition according to the present invention, the inorganic filler used as the component (E) includes, for example, calcium carbonate, silica, alumina, aluminum hydroxide, magnesium oxide, talc, mica, clay and the like.
One or more of them can be selected and used, but calcium carbonate is preferred from the viewpoint of economy and ease of handling such as cutting properties of the coating film. The calcium carbonate is not particularly limited, and any of precipitated calcium carbonate, heavy calcium carbonate, light calcium carbonate and the like can be used.

【0016】この無機充填剤は、組成物の粘度及びディ
スペンサーの吐出性などの点から、平均粒径が、通常
0.5〜35μm、好ましくは1〜10μmの範囲にあ
るものが有利である。この(E)成分の無機充填剤の配
合量は、エポキシ樹脂成分量、すなわち前記(A)成分
と(B)成分との合計量100重量部に対し、1〜20
0重量部の範囲にあることが必要である。この量が1重
量部未満では放熱性、耐熱性及び硬化収縮性などが良好
な塗膜が得らないし、200重量部を超えると組成物の
粘度が高くなり、取り扱い性が悪くなる。塗膜物性及び
組成物の粘度などを考慮すると、この(E)成分の好ま
しい配合量は30〜100重量部の範囲である。
Advantageously, the inorganic filler has an average particle size of usually 0.5 to 35 μm, preferably 1 to 10 μm, in view of the viscosity of the composition and the dischargeability of the dispenser. The compounding amount of the inorganic filler of the component (E) is 1 to 20 with respect to the amount of the epoxy resin component, that is, 100 parts by weight of the total amount of the components (A) and (B).
It must be in the range of 0 parts by weight. If the amount is less than 1 part by weight, a coating film having good heat radiation properties, heat resistance and curing shrinkage properties cannot be obtained, and if it exceeds 200 parts by weight, the viscosity of the composition becomes high and the handleability deteriorates. Considering the properties of the coating film and the viscosity of the composition, the preferred amount of the component (E) is in the range of 30 to 100 parts by weight.

【0017】本発明に係る組成物においては、(F)成
分として用いられる揺変剤としては、例えば微粒子状シ
リカ、微粒子状アルミナ、微粒子状炭酸カルシウムなど
の中から任意のものを1種又は2種以上選択して使用す
ることができるが、組成物のタレ防止能の点から、微粒
子状シリカが好適である。この揺変剤は、タレ防止能の
点から、平均粒径が、通常0.005〜10μm、好ま
しくは0.01〜1μmの範囲にあるものが有利であ
る。
In the composition according to the present invention, the thixotropic agent used as the component (F) may be, for example, one or two kinds of arbitrary ones from among particulate silica, particulate alumina, particulate calcium carbonate and the like. More than one kind can be selected and used, but from the viewpoint of the sagging prevention ability of the composition, particulate silica is preferred. The thixotropic agent has an average particle diameter of usually from 0.005 to 10 μm, preferably from 0.01 to 1 μm, from the viewpoint of anti-sagging ability.

【0018】この(F)成分の揺変剤の配合量は、エポ
キシ樹脂成分量、すなわち(A)成分と(B)成分との
合計量100重量部に対し、3〜10重量部の範囲にあ
ることが必要である。この量が3重量部未満では組成物
のタレ防止性が十分に発揮されないし、10重量部を超
えると組成物の粘度が高くなり、取り扱い性が悪くな
る。組成物のタレ防止性及び粘度を考慮すると、この
(F)成分の好ましい配合量は4〜7重量部の範囲であ
る。
The compounding amount of the thixotropic agent of the component (F) is in the range of 3 to 10 parts by weight based on the amount of the epoxy resin component, that is, 100 parts by weight of the total amount of the components (A) and (B). It is necessary to be. If the amount is less than 3 parts by weight, the composition will not sufficiently exhibit sagging resistance, and if it exceeds 10 parts by weight, the viscosity of the composition will increase and the handleability will deteriorate. Considering the anti-sagging property and the viscosity of the composition, the preferred amount of the component (F) is in the range of 4 to 7 parts by weight.

【0019】本発明に係るエポキシ樹脂組成物には、本
発明の目的が損なわれない範囲で、必要に応じ、従来慣
用されている各種添加剤、例えば、可とう性付与剤、難
燃剤、消泡剤、界面活性剤、着色剤等を配合することが
できる。この組成物の調製方法については特に制限はな
く、前記(A)成分、(B)成分、(C)成分、(D)
成分、(E)成分、(F)成分及び所望により用いられ
る各種添加剤を、それぞれ所定の割合で均質に混合する
ことにより、調製することができる。
The epoxy resin composition according to the present invention may contain, if necessary, various conventional additives such as a flexibility-imparting agent, a flame retardant, a fire-extinguishing agent, as long as the object of the present invention is not impaired. A foaming agent, a surfactant, a coloring agent and the like can be added. The method for preparing this composition is not particularly limited, and the components (A), (B), (C), and (D)
It can be prepared by homogeneously mixing the components, the component (E), the component (F), and various additives used as desired at predetermined ratios.

【0020】本発明のコイル被覆用塗膜は、このように
して調製したエポキシ樹脂組成物の硬化物からなるもの
であり、例えば以下のようにして形成することができ
る。すなわち、電動工具用モータなどの回転子コイルに
コイル含浸用エポキシ樹脂組成物などを含浸させ、その
上からディスペンサーなどを使用してコイル全体が被覆
されるように、本発明に係るエポキシ樹脂組成物を塗布
し、加熱硬化させることにより、所望の塗膜が形成され
る。上記本発明に係るエポキシ樹脂組成物の塗布は、コ
イル含浸用エポキシ樹脂組成物などを加熱硬化させる前
でも後でもどちらでもよい。また、コイル含浸用エポキ
シ樹脂組成物などの種類に特に制限はないが、取り扱い
やすさ及び本発明に係るコイル被覆用エポキシ樹脂組成
物との接着性の点から、このエポキシ樹脂組成物と組成
の類似したもの、例えば、ジシアンジアミド硬化系のエ
ポキシ樹脂組成物が好ましい。一方、従来からコイル含
浸用液状エポキシ樹脂組成物として使用されている酸無
水物硬化系の二液性エポキシ樹脂組成物は、コイル含浸
性には優れるがポットライフが短く、二液性であること
から取り扱いにくく、本発明に係るコイル被覆用エポキ
シ樹脂組成物との接着性が十分でないという問題があ
る。コイル含浸用エポキシ樹脂組成物として、ビスフェ
ノール型エポキシ樹脂、ジシアンジアミド、尿素化合物
などからなるエポキシ樹脂組成物を使用することで、コ
イル含浸用エポキシ樹脂組成物と本発明に係るコイル被
覆用エポキシ樹脂組成物とを同一工程で塗布、硬化で
き、作業工程の簡略化も実現できる。
The coating film for coil coating of the present invention comprises a cured product of the epoxy resin composition thus prepared, and can be formed, for example, as follows. That is, the epoxy resin composition according to the present invention is impregnated into a rotor coil of a motor for a power tool or the like with an epoxy resin composition for coil impregnation or the like, and the entire coil is coated thereon using a dispenser or the like. Is applied and cured by heating to form a desired coating film. The application of the epoxy resin composition according to the present invention may be performed before or after the epoxy resin composition for coil impregnation is cured by heating. The type of the epoxy resin composition for coil impregnation and the like are not particularly limited, but from the viewpoint of ease of handling and adhesiveness with the epoxy resin composition for coil coating according to the present invention, the epoxy resin composition and the Similar ones, for example, dicyandiamide-curable epoxy resin compositions are preferred. On the other hand, an acid anhydride-curable two-part epoxy resin composition conventionally used as a liquid epoxy resin composition for coil impregnation has excellent coil impregnation, but has a short pot life and is two-part. Therefore, there is a problem that the adhesiveness with the epoxy resin composition for coil coating according to the present invention is not sufficient. By using an epoxy resin composition comprising a bisphenol-type epoxy resin, dicyandiamide, a urea compound, or the like as the coil resin epoxy resin composition, the coil resin epoxy resin composition and the coil coating epoxy resin composition according to the present invention are used. Can be applied and cured in the same process, and the working process can be simplified.

【0021】[0021]

【発明の効果】本発明のコイル被覆用塗膜の形成に用い
られるエポキシ樹脂組成物は、適当な揺変性、速硬化
性、保存安定性を有することから、塗布性、作業性、放
熱性などに優れ、コイル全体が被覆されるように塗布し
て使用することができる。形成された塗膜は、コイルと
の接着性、耐熱衝撃性に優れ、回転子コイルの回転中に
異物が衝突しても脱落することがなく、電動工具用モー
タなどの回転子コイルが異物による損傷を受けるのを防
止するのに好適である。
The epoxy resin composition used for forming the coating film for coil coating according to the present invention has appropriate thixotropic properties, fast curing properties, and storage stability. It can be applied and used so as to cover the entire coil. The formed coating film has excellent adhesiveness to the coil and excellent thermal shock resistance, and does not fall off even if a foreign object collides during rotation of the rotor coil. It is suitable for preventing damage.

【0022】[0022]

【実施例】次に、実施例により本発明をさらに詳細に説
明するが、本発明はこれらの例によってなんら限定され
るものではない。なお、組成物、硬化物(150℃、1
時間の条件で硬化)の物性は次に示す方法で評価した。
Next, the present invention will be described in more detail by way of examples, but the present invention is not limited to these examples. The composition and the cured product (150 ° C., 1
The physical properties of (curing under the conditions of time) were evaluated by the following methods.

【0023】(1)粘性 JIS K 6838及びJIS K 7117に準拠
して、回転粘度計を用い、25℃で測定し、作業性を考
慮し、下記の基準で評価した。 ○:100ポイズ以上3000ポイズ未満 ×:100ポイズ未満及び3000ポイズ以上 (2)耐熱性 試料硬化物(15mm×5mm×5mm)をセイコー電
子工業社製熱機械測定(TMA)装置4010にかけて
室温から250℃まで5℃/分で昇温しながら各温度に
おける線膨張係数を求め、線膨張係数が変化する温度を
ガラス転移温度とし、以下の基準で評価した。ガラス転
移温度が120℃以上のものは耐熱性が良好である。 ○:120℃以上 △:100〜120℃未満 ×:100℃未満 (3)接着性 JIS K 6850に準拠し、100mm×25mm
×1.6mmの軟鋼板に試料組成物を12.5mmのシ
ングルオーバーラップになるように塗布し、その上に同
寸法の軟鋼板を圧着し、150℃、1時間の条件で硬化
し、常温雰囲気下に放置し、常温雰囲気下で引張りせん
断接着強度を測定し、以下の基準で評価した。 良好:引張りせん断接着強度が2kgf/mm2以上 (4)硬化性 JIS C 2105に準拠して、150℃の熱板上に
0.4ccの組成物をとり、ゲル化するまでの時間を測
定し、以下の基準により評価した。 良好:ゲル化時間150秒未満 (5)保存安定性 初期粘度と25℃、30日間保管後の組成物の粘度とを
測定し、次の基準により判定した。その値が初期値の2
倍未満であるものは保存安定性が良好である。 ○:初期値の2倍未満 ×:初期値の2倍以上 (6)揺変性 (株)東京計器社製EHD型粘度計を使用し、3゜×R
14のコーンにより、0.5rpm(η1)及び2.5
rpm(η2)の25℃、5分経過後の粘度を求め、
0.5rpmの粘度(η1)を2.5rpmの粘度
(η2)で除した値を計算し、以下の基準で評価した。 ○:η1/η2が1.4以上 ×:η1/η2が1.4未満
(1) Viscosity Measured at 25 ° C. using a rotational viscometer in accordance with JIS K 6838 and JIS K 7117, and evaluated according to the following criteria in consideration of workability. :: 100 poise or more and less than 3000 poise ×: less than 100 poise and 3000 poise or more (2) Heat resistance A cured sample (15 mm × 5 mm × 5 mm) is subjected to a thermomechanical measurement (TMA) device 4010 manufactured by Seiko Denshi Kogyo Co., Ltd. from room temperature to 250 While the temperature was raised to 5 ° C. at a rate of 5 ° C./min, the coefficient of linear expansion at each temperature was determined. Those having a glass transition temperature of 120 ° C. or higher have good heat resistance. :: 120 ° C. or more Δ: 100 to less than 120 ° C. ×: less than 100 ° C. (3) Adhesion 100 mm × 25 mm according to JIS K 6850
A sample composition was applied to a × 1.6 mm mild steel sheet so as to have a single overlap of 12.5 mm, and a mild steel sheet of the same dimensions was pressed thereon, cured at 150 ° C. for 1 hour, and then at room temperature. It was left in an atmosphere, and the tensile shear adhesive strength was measured in a normal temperature atmosphere, and evaluated according to the following criteria. Good: Tensile shear adhesive strength is 2 kgf / mm 2 or more. (4) Curability According to JIS C 2105, 0.4 cc of a composition is placed on a hot plate at 150 ° C., and the time until gelation is measured. Was evaluated according to the following criteria. Good: less than 150 seconds for gelation time (5) Storage stability The initial viscosity and the viscosity of the composition after storage at 25 ° C. for 30 days were measured, and determined according to the following criteria. Its value is the initial value 2
If it is less than twice, the storage stability is good. :: Less than twice the initial value ×: More than twice the initial value (6) Thixotropic 3 ゜ × R using an EHD type viscometer manufactured by Tokyo Keiki Co., Ltd.
With 14 cones, 0.5 rpm (η 1 ) and 2.5 rpm
The viscosity after 5 minutes at 25 ° C. of rpm (η 2 ) was determined,
The value obtained by dividing calculated in viscosity of 0.5 rpm (eta 1) the viscosity of 2.5rpm (η 2), and evaluated according to the following criteria. :: η 1 / η 2 is 1.4 or more ×: η 1 / η 2 is less than 1.4

【0024】また、使用した各成分の具体的な内容を次
に示す。 (1)ビスフェノールA型エポキシ樹脂 油化シェルエポキシ社製,商品名「エピコート82
8」,エポキシ当量187 (2)キレート形成能を有するウレタン変性エポキシ樹
脂 旭電化工業社製,商品名「アデカEPU−78−11」 (3)ジシアンジアミド 油化シェルエポキシ社製,商品名「DICY#15」,
平均粒径7〜10μm (4)メチルテトラヒドロ無水フタル酸 新日本理化社製,商品名「リカシッドMT−500」 (5)メチレンジフェニルビスメチルウレア エイ・シー・アイ・ジャパン社製,商品名「オミキュア
52」 (6)炭酸カルシウム 備北粉化工業社製,商品名「ソフトン1800」,平均
粒径1.25μm (7)微粒子シリカ 日本アエロジル社製,商品名「アエロジルR−20
2」,平均粒径0.014μm
The specific contents of each component used are shown below. (1) Bisphenol A type epoxy resin “Epicoat 82” manufactured by Yuka Shell Epoxy
8 ", epoxy equivalent 187 (2) Urethane-modified epoxy resin capable of forming chelate Asahi Denka Kogyo Co., Ltd., trade name" ADEKA EPU-78-11 "(3) Dicyandiamide Yuka Shell Epoxy Co., Ltd., trade name" DICY # 15 ",
Average particle size: 7 to 10 μm (4) Methyltetrahydrophthalic anhydride manufactured by Shin Nippon Rika Co., Ltd., trade name “Licacid MT-500” (5) Methylene diphenylbismethylurea ACI Japan Co., Ltd., trade name “Omicure” 52 "(6) Calcium carbonate manufactured by Bihoku Powder Chemical Industry Co., Ltd., trade name" Softon 1800 ", average particle size 1.25 [mu] m (7) Fine particle silica manufactured by Nippon Aerosil Co., Ltd., trade name" Aerosil R-20 "
2 ", average particle size 0.014 μm

【0025】実施例1〜5、比較例1〜4 表1及び表2に示す組成のエポキシ樹脂組成物を調製
し、その物性を評価すると共に、硬化物の物性を評価し
た。結果を表1及び表2に示す。
Examples 1 to 5, Comparative Examples 1 to 4 Epoxy resin compositions having the compositions shown in Tables 1 and 2 were prepared, and their physical properties were evaluated, as well as the physical properties of cured products. The results are shown in Tables 1 and 2.

【0026】[0026]

【表1】 [Table 1]

【0027】[0027]

【表2】 [Table 2]

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 (A)ビスフェノール型エポキシ樹脂5
0〜100重量%と(B)キレート形成能を有するウレ
タン変性エポキシ樹脂0〜50重量%とからなるエポキ
シ樹脂成分と、その100重量部当たり、(C)潜在性
硬化剤3〜15重量部、(D)硬化促進剤0.5〜10
重量部、(E)無機充填剤1〜200重量部及び(F)
揺変剤3〜10重量部を含有する組成物の硬化物からな
るコイル被覆用塗膜。
1. A bisphenol type epoxy resin (A)
An epoxy resin component comprising 0 to 100% by weight and (B) 0 to 50% by weight of a urethane-modified epoxy resin capable of forming a chelate, and (C) 3 to 15 parts by weight of a latent curing agent per 100 parts by weight thereof; (D) curing accelerator 0.5 to 10
Parts by weight, (E) 1 to 200 parts by weight of an inorganic filler and (F)
A coil coating film comprising a cured product of a composition containing 3 to 10 parts by weight of a thixotropic agent.
【請求項2】 (D)成分の硬化促進剤がトルエンビス
ジメチルウレア及びメチレンジフェニルビスジメチルウ
レアの中から選ばれる少なくとも1種であるコイル被覆
用塗膜。
2. A coating film for coil coating, wherein the curing accelerator of the component (D) is at least one selected from toluenebisdimethylurea and methylenediphenylbisdimethylurea.
【請求項3】 (E)成分の無機充填剤が炭酸カルシウ
ムである請求項1又は2記載のコイル被覆用塗膜。
3. The coating film for coil coating according to claim 1, wherein the inorganic filler as the component (E) is calcium carbonate.
JP11017603A 1999-01-26 1999-01-26 Coating film for coil Pending JP2000212504A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11017603A JP2000212504A (en) 1999-01-26 1999-01-26 Coating film for coil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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Publications (1)

Publication Number Publication Date
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Family

ID=11948469

Family Applications (1)

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Country Status (1)

Country Link
JP (1) JP2000212504A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005290190A (en) * 2004-03-31 2005-10-20 Tdk Corp Epoxy resin composition, coil body and inductor
JP2007302792A (en) * 2006-05-11 2007-11-22 Kansai Paint Co Ltd Anionic electrodeposition coating composition
US7786214B2 (en) * 2002-05-03 2010-08-31 Sika Technology Ag Composition of epoxy resin, epoxy adduct, urea derivative thixotropic agent and curing agent
US8062468B2 (en) 2005-07-05 2011-11-22 Sika Technology Ag Low-temperature impact resistant thermosetting epoxide resin compositions with solid epoxide resins
US8076424B2 (en) 2003-07-16 2011-12-13 Sika Technology Ag Heat-curable compositions comprising low-temperature impact strength modifiers
JP2012016644A (en) * 2010-07-07 2012-01-26 Meeshikku:Kk Method for using sewage sludge incineration ash
US9221969B2 (en) 2002-12-17 2015-12-29 Sika Technology Ag Thermally hardenable epoxy resin composition having an improved impact resistance at low temperatures

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7786214B2 (en) * 2002-05-03 2010-08-31 Sika Technology Ag Composition of epoxy resin, epoxy adduct, urea derivative thixotropic agent and curing agent
US9221969B2 (en) 2002-12-17 2015-12-29 Sika Technology Ag Thermally hardenable epoxy resin composition having an improved impact resistance at low temperatures
US8076424B2 (en) 2003-07-16 2011-12-13 Sika Technology Ag Heat-curable compositions comprising low-temperature impact strength modifiers
JP2005290190A (en) * 2004-03-31 2005-10-20 Tdk Corp Epoxy resin composition, coil body and inductor
US8062468B2 (en) 2005-07-05 2011-11-22 Sika Technology Ag Low-temperature impact resistant thermosetting epoxide resin compositions with solid epoxide resins
JP2007302792A (en) * 2006-05-11 2007-11-22 Kansai Paint Co Ltd Anionic electrodeposition coating composition
JP2012016644A (en) * 2010-07-07 2012-01-26 Meeshikku:Kk Method for using sewage sludge incineration ash

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