JPH0356558A - Resin composition for electrical insulating treatment, electrical insulating treatment and stator coil - Google Patents
Resin composition for electrical insulating treatment, electrical insulating treatment and stator coilInfo
- Publication number
- JPH0356558A JPH0356558A JP19339189A JP19339189A JPH0356558A JP H0356558 A JPH0356558 A JP H0356558A JP 19339189 A JP19339189 A JP 19339189A JP 19339189 A JP19339189 A JP 19339189A JP H0356558 A JPH0356558 A JP H0356558A
- Authority
- JP
- Japan
- Prior art keywords
- coil
- stator coil
- parts
- resin composition
- electrical insulating
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は絶縁処理用樹脂組成物、家庭電器機類等に用い
られる絶縁処理されたステータコイルの絶縁処理方法お
よび絶縁処理されたステータコイルに関する.
〔従来の技術〕
従来、ステータコイルの絶縁処理方法としては、(1)
コイルエンド部を糸で結束し、0.l〜3ポアズ程度の
液状ワニスにステータ.コイル全体を含浸する方法、(
2)コイル部分のみにワニスを滴下含浸する方法、(3
)コイル部分のみに粉末ワニスを用いて加熱硬化する方
法、(4)コンパウンドを用いてステータコイル全体を
モールドする方法などが採用されている.
前記液状ワニスを用いる方法は、材料費が安く、ワニス
処理工程の自動化が容易であるが、硬化時にワニスが流
出しやすく、硬化後のコイルエンド部のワニス付着量が
少なくなり、振動や衝撃によって絶縁性が低下し、高湿
度下での絶縁性に劣る欠点がある。また使用するワニス
自身の難燃性が不足するという問題があった。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a resin composition for insulation treatment, a method for insulation treatment of an insulated stator coil used in home appliances, etc., and an insulation treated stator coil. .. [Conventional technology] Conventionally, methods for insulation treatment of stator coils include (1)
Bind the coil end with thread and tie it to 0. Stator coated with liquid varnish of about 1 to 3 poise. How to impregnate the entire coil, (
2) Method of dripping and impregnating only the coil part with varnish, (3
) A method in which powder varnish is used to heat and harden only the coil portion, and (4) a method in which the entire stator coil is molded using a compound. The method using liquid varnish has low material costs and the varnish treatment process is easy to automate; however, the varnish tends to flow out during curing, the amount of varnish adhered to the coil end after curing is small, and it is susceptible to vibration and impact. The disadvantage is that the insulation properties are lower and the insulation properties are poor under high humidity. Another problem was that the varnish used itself lacked flame retardancy.
粉末ワニスを用いる方法は、コイルエンド部の結束処理
を省略することができ、絶縁処理工程の自動化が可能で
あるが、コイル内部への粉末ワニスの含漫性が劣るため
、高湿度下の絶縁性に劣る欠点がある。また使用する粉
末ワニス自身の難燃性が不足し、また燃焼時の発煙量が
多く、有害戒分の発生が多いなどの問題があった。The method using powder varnish can omit the bundling process of the coil ends and automate the insulation treatment process, but since the powder varnish does not contain the inside of the coil, it is difficult to insulate under high humidity. There are disadvantages that are inferior to gender. Further, there were other problems such as the powder varnish used itself lacked flame retardancy, produced a large amount of smoke when burned, and generated a large amount of harmful substances.
コンパウンドを用いてステータコイル全体をモールドす
る方法は、モータの静音化や耐湿性の向上には効果があ
るが、絶縁処理の自動化が困難であり、材料費が比較的
割高となる。またコンバウンド自身の難燃性に劣るなど
の問題があった。The method of molding the entire stator coil using a compound is effective in making the motor quieter and improving moisture resistance, but it is difficult to automate the insulation process and the material cost is relatively high. In addition, there were other problems such as the inferior flame retardancy of Conbound itself.
特に近年、モータにおいては、従来以上の製品の安全性
(難燃性の向上)、静音化(固着力の向上)および低価
格化(絶縁処理工程の合理化、処理時間の短縮化)が強
く望まれている.〔発明が解決しようとする課題〕
本発明の目的は、前記従来技術の問題点を解決し、モー
タの難燃化、静音化および耐湿劣化に対する高信頼性を
図ることができ、ステータコイルのコイルエンド部の糸
による結束の省略により絶縁処理工程を短縮することが
できる絶縁処理用樹脂組底物、ステータコイルの絶縁処
理方法および絶縁処理されたステータコイルを提供する
ことにある。Particularly in recent years, there has been a strong demand for motors to be safer (improved flame retardancy), quieter (improved adhesion), and lower in price (rationalized insulation treatment process, shorter processing time). It is rare. [Problems to be Solved by the Invention] An object of the present invention is to solve the problems of the prior art described above, to make the motor flame retardant, quiet, and highly reliable against moisture deterioration, and to improve the coil of the stator coil. It is an object of the present invention to provide a resin assembly for insulation treatment, a method for insulation treatment of a stator coil, and an insulation treatment treated stator coil, which can shorten the insulation treatment process by omitting binding with threads at the end portions.
本発明は、熱または光と熱により硬化する不飽和ポリエ
ステル樹脂100重量部、水酸化アルミニウム100〜
200重量部およびシリカ粉末O.1〜3重量部を含有
してなる絶縁処理用樹脂組成物、この絶縁処理用樹脂組
成物に、コイルエンド部を糸で結束しないステータコイ
ルの一方のコイルエンド部を含浸した後、該ステータコ
イルを反転して他方のコイルエンド部を前記絶縁処理用
樹脂組成物に含浸し、次いで両コイルエンド部が含浸さ
れたステータコイルを反転させながら熱または光と熱に
より硬化させるステータコイルの絶縁処理方法およびこ
の絶縁処理方法で処理されたステータコイルに関する.
本発明に用いられる不飽和ポリエステル樹脂としては、
熱または光と熱により硬化するものであれば特に制限は
なく、例えば不飽和ポリエステル、反応性不飽和結合を
有するエボキシエステルなどに、架橋性単量体および過
酸化物を含有させて得られる。また必要に応じて光増感
剤、促進剤、重合禁止剤等を用いることができる.
前記不飽和ポリエステルは、酸或分とアルコール或分ま
たは酸或分、アルコール或分および変性成分から合威さ
れる。酸戒分としては、マレイン酸、無水マレイン酸、
フマル酸、イタコン酸、シトラコン酸等の不飽和酸、フ
タル酸、無水フタル酸、イソフタル酸、テレフタル酸、
テトラヒドロ無水フタル酸、アジピン酸等の飽和酸、大
豆油、トール油、ヤシ油、ヒマシ油等の植物油脂肪酸な
どが用いられる。アルコール戒分としては、エチレング
リコール、プロピレングリコール、ジエチレングリコー
ル、ジプロピレングリコール、ブタンジオール、ネオベ
ンチルグリコール、グリセリン、トリメチロールプロパ
ン、ペンタエリスリト−ルなどが用いられる。また変性
戒分としては、ジシクロペンタジエン、シクロペンタジ
エンおよびこれらの誘導体などが用いられる。The present invention consists of 100 parts by weight of an unsaturated polyester resin that is cured by heat or light and heat, and 100 parts by weight of aluminum hydroxide.
200 parts by weight and silica powder O. A resin composition for insulation treatment containing 1 to 3 parts by weight, one coil end portion of a stator coil whose coil end portions are not bound with thread is impregnated with this resin composition for insulation treatment, and then the stator coil A method for insulation treatment of a stator coil, in which the other coil end is impregnated with the resin composition for insulation treatment, and then the stator coil with both coil end portions impregnated is cured by heat or light and heat while being reversed. and stator coils treated with this insulation treatment method. The unsaturated polyester resin used in the present invention includes:
There is no particular restriction as long as it can be cured by heat or light and heat, and can be obtained by, for example, unsaturated polyester, epoxy ester having a reactive unsaturated bond, etc., containing a crosslinkable monomer and a peroxide. Additionally, photosensitizers, accelerators, polymerization inhibitors, etc. can be used as necessary. The unsaturated polyester is synthesized from an acid component and an alcohol component, or an acid component, an alcohol component, and a modifying component. As acid compounds, maleic acid, maleic anhydride,
Unsaturated acids such as fumaric acid, itaconic acid, citraconic acid, phthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid,
Saturated acids such as tetrahydrophthalic anhydride and adipic acid, vegetable oil fatty acids such as soybean oil, tall oil, coconut oil, and castor oil are used. Examples of the alcohol used include ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, butanediol, neobentyl glycol, glycerin, trimethylolpropane, and pentaerythritol. Further, as the modified component, dicyclopentadiene, cyclopentadiene and derivatives thereof are used.
反応性不飽和結合を有するエボキシエステルは、1分子
中にl個以上のエポキシ基をもつエポキシ樹脂と不飽和
結合を有する酸或分から合威される.エポキシ樹脂とし
てはビスフェノールA型エボキシ樹脂が好ましく、エピ
コート828、1001,1004 (シェル化学社製
)などが挙げられる。不飽和結合を有する酸或分として
は、アクリル酸、メタクリル酸、無水マレイン酸などが
使用できる。An epoxy ester having a reactive unsaturated bond is synthesized from an epoxy resin having one or more epoxy groups in one molecule and an acid having an unsaturated bond. As the epoxy resin, bisphenol A type epoxy resins are preferred, such as Epicote 828, 1001, and 1004 (manufactured by Shell Chemical Co., Ltd.). Acrylic acid, methacrylic acid, maleic anhydride, etc. can be used as the acid having an unsaturated bond.
前記架橋性単量体としては、スチレン、ビニルトルエン
、α−メチルスチレン、ターシャリープチルスチレン、
ジビニルベンゼン、各種アクリル酸エステル、各種メタ
クリル酸エステル、ジアリルフタレートなどが用いられ
る。Examples of the crosslinkable monomer include styrene, vinyltoluene, α-methylstyrene, tertiarybutylstyrene,
Divinylbenzene, various acrylic esters, various methacrylic esters, diallyl phthalate, etc. are used.
また過酸化物としては、ペンゾイルバーオキサイド、ア
セチルパーオキサイドなどのアシルパーオキサイド、タ
ーシャリープチルヒドロパーオキサイド、キュメンヒド
ロパーオキサイドなどのヒドロパーオキサイド、メチル
エチルケトンバーオキサイド、シクロヘキサノンパーオ
キサイドなどのケトンバーオキサイド、ジターシャリー
プチルパーオキサイド、ジクミルバーオキサイドなどの
ジアルキルパーオキサイドなどが用いられる。その添加
量は、不飽和ポリエステルおよび架橋性単量体の総量に
対して0. 5〜3重景%の範囲であることが好ましい
。Peroxides include acyl peroxides such as penzoyl peroxide and acetyl peroxide, hydroperoxides such as tertiary butyl hydroperoxide and cumene hydroperoxide, ketone peroxides such as methyl ethyl ketone peroxide and cyclohexanone peroxide, Dialkyl peroxides such as ditertiary butyl peroxide and dicumyl peroxide are used. The amount added is 0.0% based on the total amount of unsaturated polyester and crosslinkable monomer. It is preferably in the range of 5-3%.
必要に応じて用いられる光増感剤としては、ベンゾイン
エチルエーテル、ペンゾインイソプロビルエーテルなど
のベンゾインエーテル類、アセトフェノン、2.2−ジ
メトキシ−2−フエニルアセトフェノンなどのアセトフ
ェノン類、ペンゾインー箋ヒラーケトン類、ペンゾイン
チオエーテル類、アントラキノン類などが用いられる。Examples of photosensitizers used as necessary include benzoin ethers such as benzoin ethyl ether and penzoin isopropyl ether, acetophenones such as acetophenone and 2,2-dimethoxy-2-phenylacetophenone, and penzoin-Hiller's ketone. , penzointhioethers, anthraquinones, etc. are used.
その添加量は、不飽和ポリエステルおよび架橋性単量体
の総量に対して0. 1〜3重量%の範囲であることが
好ましい。The amount added is 0.0% based on the total amount of unsaturated polyester and crosslinkable monomer. It is preferably in the range of 1 to 3% by weight.
また促進剤としては、ナフテン酸マンガン、ナフテン酸
亜鉛、ナフテン酸コバルト、オクテン酸コバルト等の金
属石鹸やアミン類が用いられる。Further, as the accelerator, metal soaps and amines such as manganese naphthenate, zinc naphthenate, cobalt naphthenate, and cobalt octenoate are used.
重合禁止剤としては、ハイドロキノン、ターシャリープ
チル力テコール、p−ペンゾキノン、2,5−ジターシ
ャリープチルハイドロキノンなどが用いられる。As the polymerization inhibitor, hydroquinone, tertiarybutylhydroquinone, p-penzoquinone, 2,5-ditertiarybutylhydroquinone, etc. are used.
本発明に用いられる水酸化アルミニウムには特に制限は
ないが、Af (OH).またはAl!Os・3H,O
の含有量が99%以上、真比重が2.0〜3. 0であ
り、5μm以下の粒度分布をもち、かつ吸着水分量が0
. 5%以下のものが好ましい。該水酸化アルミニウム
としては、市販品である昭和電工社製商品名ハイジライ
トや住友化学社製、日本軽金属社製などから市販される
粒アルミナが好ましく用いられる.水酸化アルミニウム
の使用量は、不飽和ポリエステル樹脂100重量部に対
し100〜200重量部である=この使用量が100重
量部未満では難燃性を向上させることができず、またコ
イルへのワニス付着量が少なくなる。Aluminum hydroxide used in the present invention is not particularly limited, but Af (OH). Or Al! Os・3H,O
The content is 99% or more, and the true specific gravity is 2.0 to 3. 0, has a particle size distribution of 5 μm or less, and has an adsorbed moisture content of 0.
.. The content is preferably 5% or less. As the aluminum hydroxide, commercially available products such as Higilite (trade name) manufactured by Showa Denko Co., Ltd., and granular alumina commercially available from Sumitomo Chemical Co., Ltd., Nippon Light Metal Co., Ltd., etc. are preferably used. The amount of aluminum hydroxide used is 100 to 200 parts by weight per 100 parts by weight of the unsaturated polyester resin. If this amount is less than 100 parts by weight, the flame retardance cannot be improved, and the varnish on the coil The amount of adhesion decreases.
また200重量部を超えると粘度が高くなり、コイル内
部への含漫性が低下する.
本発明に用いられるシリカ粉末にも特に制限はないが、
エロジール(日本アエロジール社製)等の微粉末シリカ
が好ましい.この使用量は、不飽和ポリエステル樹脂1
00重量部に対し0.1〜3重量部である。該使用量が
0.1重量部未満では水酸化アルミニウムの沈降が大き
く、均一な組成物が得られず、また3重量部を超えると
粘度が高く、揺変性も大きくなり、コイル内部への含漫
性が低下する。Moreover, if it exceeds 200 parts by weight, the viscosity becomes high and the ability to contain it inside the coil decreases. There are no particular restrictions on the silica powder used in the present invention, but
Finely powdered silica such as Erogil (manufactured by Nippon Aerosil Co., Ltd.) is preferred. This usage amount is 1 part of unsaturated polyester resin.
The amount is 0.1 to 3 parts by weight per 00 parts by weight. If the amount used is less than 0.1 parts by weight, precipitation of aluminum hydroxide will be large, making it impossible to obtain a uniform composition, and if it exceeds 3 parts by weight, the viscosity will be high, the thixotropy will be large, and the content inside the coil will be increased. Manifestability decreases.
本発明の絶縁処理用樹脂&Il或物は、前記不飽和ポリ
エステル樹脂、水酸化アルξニウムおよびシリカ粉末を
高速攪拌機などで混合して得られる。The insulation treatment resin &Il of the present invention is obtained by mixing the unsaturated polyester resin, aluminum hydroxide, and silica powder using a high-speed stirrer or the like.
本発明において、ステータコイルの絶縁処理は前記絶縁
処理用樹脂組成物を用いて例えば次のようにして行われ
る。In the present invention, the insulation treatment of the stator coil is performed, for example, as follows using the resin composition for insulation treatment.
まずコイルエンド部を糸で結束しないステータコイルを
、あらかじめ通電加熱法または高周波誘導加熱法を用い
て高速昇温させることか好ましい。次いでこのステータ
コイルの一方のコイルエンド部を絶縁処理用樹脂組成物
にスロット面まで浸漬含浸し、その後、ステータコイル
を絶縁処理用組成物から引き上げて反転し、他方のコイ
ルエンド部を同様に絶縁処理用樹脂組成物に浸漬含浸し
て引上げる。次にこのステータコイルを硬化炉中で両コ
イルエンド部が交互に上下となるように反転させながら
熱または光と熱により硬化する。First, it is preferable to heat the stator coil, whose coil end portions are not bound with thread, in advance at high speed using an electrical heating method or a high frequency induction heating method. Next, one coil end of this stator coil is immersed in an insulation treatment resin composition up to the slot surface, and then the stator coil is lifted out of the insulation treatment composition and turned over, and the other coil end is similarly insulated. It is immersed in a treatment resin composition and then pulled up. Next, this stator coil is cured by heat or light and heat while being turned over in a curing furnace so that both coil end portions are alternately placed vertically.
硬化炉中での反転は、時間の間隔をおいて行われる。Inversion in the curing oven takes place at time intervals.
光硬化には、紫外線が用いられ、熱硬化には紫外線、高
周波などが用いられる。Ultraviolet rays are used for photocuring, and ultraviolet rays, high frequency waves, etc. are used for thermosetting.
以上のように、水酸化アルミニウムを高充填した液状の
不飽和ポリエステル樹脂組成物にコイルエンド部を、上
記のように反転してワニス浸漬処理し、かつ上記のよう
に反転させて硬化させることにより、コイルエンド部の
糸による結束が省略できるとともに、ワニス付着量を多
くすることができ、かつコイル内部への含漫性のよいス
テータコイルを製作することが可能となる。As described above, by inverting the coil end portion as described above and immersing it in varnish in a liquid unsaturated polyester resin composition highly filled with aluminum hydroxide, and then inverting and curing as described above. In addition, it is possible to omit the need for binding the coil end portions with threads, increase the amount of varnish deposited, and manufacture a stator coil that has good impurity inside the coil.
以下、本発明を実施例により詳しく説明する。 Hereinafter, the present invention will be explained in detail with reference to Examples.
なお、例中、部とあるのは重量部を意味する。In addition, in the examples, parts mean parts by weight.
実施例1
1)絶縁処理用樹脂組成物の製造
プロピレングリコール532Lエチレングリコール24
8部、無水マレイン酸441部、無水フタル酸150部
およびハイドロキノン0. 4部を4つ口フラスコに仕
込み、窒素ガス吹込み下で180゜Cに1. 5時間保
ち、次いで220℃で反応を続け、酸価l8.0の不飽
和ポリエステルAを得た.この不飽和ポリエステルA5
5部、スチレンモノマ45部、ナフテン酸マンガン0.
2部、ペンゾイルパーオキサイド1.5部、ハイジライ
トH−32(昭和電工社製、水酸化アルミニウム)11
0部およびエロジール380(日本アエロジール社製、
微粉未シリカ)1部を高速撹拌機を用いて混合し、樹脂
組成物(A)を得た。Example 1 1) Production of resin composition for insulation treatment Propylene glycol 532L Ethylene glycol 24
8 parts, 441 parts of maleic anhydride, 150 parts of phthalic anhydride, and 0.8 parts of hydroquinone. 4 parts were placed in a 4-necked flask and heated to 180°C for 1.5 hours under nitrogen gas blowing. The mixture was kept for 5 hours, and then the reaction was continued at 220°C to obtain unsaturated polyester A with an acid value of 18.0. This unsaturated polyester A5
5 parts, 45 parts of styrene monomer, 0.5 parts of manganese naphthenate.
2 parts, 1.5 parts of penzoyl peroxide, Hygilite H-32 (manufactured by Showa Denko, aluminum hydroxide) 11
0 part and Erogil 380 (manufactured by Nippon Aerosil Co., Ltd.,
1 part of fine powder (non-silica) was mixed using a high-speed stirrer to obtain a resin composition (A).
2)ステータコイルの絶縁処理
コイルエンド部を糸で結束しないステータコイル(定格
1 0 0 V,出力100W,:17寸法l1Omm
X 1 1 0mmX4 0ma+、直径0. 6 m
mのポリエステルエナメル銅線使用)に通電し、コイル
温度を100゜Cまで昇温しで予熱を行った。このコイ
ルを空冷し、コイルの表面温度が80゜Cとなったとき
に、一方のコイルエンド部をスロット面まで樹脂組成物
(A)に浸漬含浸し、約30秒間保持した。次にこのス
テータコイルを引上げ、直ちに反転し、他方のコイルエ
ンド部をスロット面まで樹脂組成物(A)に浸漬含浸し
、約30秒間保持した。次いで、ステータコイルを引上
げ、直ちに反転して遠赤外線硬化炉(l35゜C)で加
熱硬化した。硬化開始後、2分後ついで3分後にステー
タコイルを反転して樹脂付着量の均一化を図り、その後
、この状態を保ちなから135゜Cで25分間加熱硬化
し、ステータコイルを絶縁処理した。2) Insulating the stator coil Stator coil without binding the coil end with thread (Rating: 100 V, output: 100 W, 17 dimensions: 10 mm)
X110mmX40ma+, diameter 0. 6 m
The coil temperature was raised to 100°C to perform preheating. This coil was air-cooled, and when the surface temperature of the coil reached 80° C., one end of the coil was immersed in the resin composition (A) up to the slot surface and held for about 30 seconds. Next, this stator coil was pulled up, immediately reversed, and the other end of the coil was dipped and impregnated with the resin composition (A) up to the slot surface, and maintained for about 30 seconds. Next, the stator coil was pulled up, immediately turned over, and heated and cured in a far-infrared curing oven (135°C). After 2 minutes and then 3 minutes after the start of curing, the stator coil was reversed to make the amount of resin adhered uniform, and then, while maintaining this state, it was heated and cured at 135°C for 25 minutes, and the stator coil was insulated. .
実施例2
1)絶縁処理用樹脂組成物の製造
実施例1で得られた不飽和ポリエステルA55部、スチ
レンモノマ45部、ナフテン酸マンガン0.2部、ペン
ゾイルバーオキサイド1. 0部、ベンゾインエチルエ
ーテル1.0部、ハイジライトH一32(昭和電工社製
、水酸化アルξニウム)110部およびエロジール38
0(日本アエロジール社製、微粉末シリカ)0.7部を
高速撹拌機を用いて混合し、樹脂組成物(B)を得た。Example 2 1) Production of resin composition for insulation treatment 55 parts of unsaturated polyester A obtained in Example 1, 45 parts of styrene monomer, 0.2 part of manganese naphthenate, 1.0 parts of penzoyl peroxide. 0 parts, benzoin ethyl ether 1.0 parts, Hygilite H-32 (manufactured by Showa Denko, aluminum ξnium hydroxide) 110 parts and Erosil 38
0 (manufactured by Nippon Aerosil Co., Ltd., fine powder silica) was mixed using a high-speed stirrer to obtain a resin composition (B).
2)ステータコイルの絶縁処理
実施例1で用いたステータコイルと同型のステータコイ
ルを用いて通電し、コイル温度を1oo゜Cまで昇温し
て予熱を行った。このコイルを空冷し、コイルの表面温
度が80゜Cとなったときに、一方のコイルエンド部を
スロット面まで樹脂組成物(B)に浸漬含浸し、約30
秒間保持した。次にこのステータコイルを引上げ、直ち
に反転し、他方のコイルエンド部をスロット面まで樹脂
組底物(B)に浸漬含浸し、約30秒間保持した。その
後ステータコイルを引上げ、直ちに反転し、オーク社製
高圧水銀ランプを用いて25cmの距離から2分間紫外
線照射した。次いでこのステータコイルを反転し、同様
にして2分間紫外線照射して表面を硬化させた後、13
5゜Cの高周波誘導加熱炉で15分加熱し、ステータコ
イルを絶縁処理した。2) Stator Coil Insulation Treatment A stator coil of the same type as the stator coil used in Example 1 was energized and the coil temperature was raised to 100°C to perform preheating. This coil was air-cooled, and when the surface temperature of the coil reached 80°C, one end of the coil was immersed in the resin composition (B) up to the slot surface, and the coil was soaked for about 30°C.
held for seconds. Next, this stator coil was pulled up and immediately reversed, and the other end of the coil was immersed and impregnated in the resin assembly (B) up to the slot surface, and held for about 30 seconds. Thereafter, the stator coil was pulled up, immediately reversed, and ultraviolet rays were irradiated for 2 minutes from a distance of 25 cm using a high-pressure mercury lamp manufactured by Oak. Next, this stator coil was turned over and similarly irradiated with ultraviolet rays for 2 minutes to harden the surface.
The stator coil was insulated by heating in a high frequency induction heating furnace at 5°C for 15 minutes.
比較例l
実施例1で得られた不飽和ポリエステルA55部、スチ
レンモノマ45部、ナフテン酸マンガン0. 2部およ
びペンゾイルバーオキサイド1. 5部を混合撹拌し、
樹脂組底物(C)を得た。Comparative Example 1 55 parts of the unsaturated polyester A obtained in Example 1, 45 parts of styrene monomer, 0.5 parts of manganese naphthenate. 2 parts and penzoyl peroxide 1. Mix and stir 5 parts,
A resin composite sole (C) was obtained.
次に実施例1で用いたステータコイルと同型のステータ
コイルを用いて通電し、コイル温度を100゜Cまで昇
温しで予熱した。このコイルを空冷し、コイル表面温度
が50゜Cとなったときにコイル全体を樹脂組成物(C
)にステータコイル全体を浸漬含浸し、30秒保持した
。その後このコイルを引上げ、室温下で約10分余滴滴
下を行い、135゜Cの遠赤外線硬化炉で30分間加熱
硬化した。Next, a stator coil of the same type as that used in Example 1 was energized, and the coil temperature was raised to 100°C to preheat it. This coil is air-cooled, and when the coil surface temperature reaches 50°C, the entire coil is coated with a resin composition (C
), the entire stator coil was dipped and impregnated and held for 30 seconds. Thereafter, this coil was pulled up, and dropwise addition was continued for approximately 10 minutes at room temperature, followed by heat curing for 30 minutes in a far-infrared curing oven at 135°C.
比較例2
■)粉末塗料の製造
エピコー}1007 (シェル化学製)100部、2,
4−ジアミノー6−〔2−メチルイミダゾ−ルー(1)
〕一エチルトリアジン(2MZ−AZINE、四国化或
工業社製)2部、エロジール200(日本アエロジール
社製、微粉未シリカ)0.5部、炭酸カルシウムシルバ
ーW(白石工業社製)50部およびモダクロ(モンサン
ト社製界面活性剤、アクリル共重合体)1部を乾式混合
した後、90゜Cで溶融混練した.冷却後、ミルで微粉
砕し、180amの篩で振って通過したものを粉末塗料
(D)とした.
2)ステータコイルの絶縁処理
実施例lで用いたステータコイルと同型のステータコイ
ルを通電加熱して160゜Cとした後、片側のコイルエ
ンド部に粉末塗料(D)を塗装し、1 6 0 ”Cで
5分保持して硬化した.次いでもう一方のコイルエンド
部に粉末塗料を塗装し、160゜Cで5分保持して硬化
し、ステータコイルを絶縁処理した.
く試験例〉
実施例l、2および比較例1、2で得られたステータコ
イルについて、ステータコイル表面の硬化性、
難燃性およびモータの耐湿寿命を測定し、その結果を第
1表に示した。Comparative Example 2 ■) Manufacture of powder coating Epicor} 1007 (manufactured by Shell Chemical) 100 parts, 2,
4-diamino-6-[2-methylimidazole (1)
] 2 parts of monoethyl triazine (2MZ-AZINE, manufactured by Shikoku Kakogyo Co., Ltd.), 0.5 parts of Erogil 200 (manufactured by Nippon Aerosil Co., Ltd., finely powdered non-silica), 50 parts of Calcium Carbonate Silver W (manufactured by Shiraishi Kogyo Co., Ltd.), and Modaclo (Surfactant manufactured by Monsanto Co., Ltd., acrylic copolymer) 1 part were dry mixed and then melt-kneaded at 90°C. After cooling, it was pulverized in a mill and passed through a 180-am sieve, which was used as a powder coating (D). 2) Stator coil insulation treatment A stator coil of the same type as the stator coil used in Example 1 was electrically heated to 160°C, and one end of the coil was coated with powder paint (D). It was cured by holding at 160°C for 5 minutes.Then, the other coil end was coated with powder paint, and it was cured by holding at 160℃ for 5 minutes, and the stator coil was insulated. For the stator coils obtained in Comparative Examples 1 and 2 and Comparative Examples 1 and 2, the hardenability and flame retardance of the stator coil surface and the moisture resistance life of the motor were measured, and the results are shown in Table 1.
第
■
表
*l:コアを指触で評価し、粘着がない状態を○とした
。Table 1 *l: The core was evaluated by finger touch, and a state of no adhesion was rated as ○.
*2:ステータコイルに付属しているプロテクターを取
り除き、IOOV印加して通電予熱を続け、レヤーショ
ートを起こさせた場合の発火状態で試験した。*2: The protector attached to the stator coil was removed, and IOOV was applied to continue energization preheating, causing a layer short circuit.
*3:60゜C−95%RH(相対湿度)中で600■
印加し、絶縁破壊に到るまでの時間を測定した。*3: 600cm in 60°C-95%RH (relative humidity)
was applied, and the time until dielectric breakdown occurred was measured.
以上の結果から、本実施例のステータコイルは、従来の
方法で得られたステータコイルに比べ、難燃性および耐
湿寿命に優れることが示された。From the above results, it was shown that the stator coil of this example has superior flame retardancy and moisture resistance life compared to stator coils obtained by conventional methods.
本発明の絶縁処理用樹脂組成物は、難燃性に優れ、これ
によって絶縁処理されたステニタコイルの燃焼試験によ
る発火に到るまでの時間および発炎時間を改善すること
ができる。また本発明の製造法によれば、ステータコイ
ルのコイルエンド部の糸による結束を省略でき、また液
状の樹脂組威物を用いるため、処理工程の自動化が容易
である.また本発明の製造法で得られるステータコイル
は、ワニス付着量が多く、コイル内部への含漫性に優れ
、耐湿寿命特性に優れる。The resin composition for insulation treatment of the present invention has excellent flame retardancy, and as a result, it is possible to improve the time required to reach ignition and the flame ignition time in a combustion test of an insulated stenitor coil. Furthermore, according to the manufacturing method of the present invention, it is possible to omit binding the coil ends of the stator coils with threads, and since a liquid resin composite is used, automation of the processing process is easy. Furthermore, the stator coil obtained by the manufacturing method of the present invention has a large amount of varnish deposited, has excellent impregnation into the inside of the coil, and has excellent moisture resistance and life characteristics.
Claims (3)
樹脂100重量部、水酸化アルミニウム100〜200
重量部およびシリカ粉末0.1〜3重量部を含有してな
る絶縁処理用樹脂組成物。1. 100 parts by weight of unsaturated polyester resin that cures with heat or light and heat, 100-200 parts of aluminum hydroxide
A resin composition for insulation treatment, comprising parts by weight and 0.1 to 3 parts by weight of silica powder.
ンド部を糸で結束しないステータコイルの一方のコイル
エンド部を含浸した後、該ステータコイルを反転して他
方のコイルエンド部を上記絶縁処理用樹脂組成物に含浸
し、次いで両コイルエンド部が含浸されたステータコイ
ルを反転させながら熱または光と熱により硬化させるこ
とを特徴とするステータコイルの絶縁処理方法。2. After impregnating one coil end portion of a stator coil whose coil end portions are not bound with thread with the resin composition for insulation treatment according to claim 1, the stator coil is reversed and the other coil end portion is subjected to the insulation treatment as described above. 1. A method for insulating a stator coil, the method comprising: impregnating the stator coil with a resin composition, and then curing the stator coil with heat or light and heat while inverting the stator coil with both coil end portions impregnated.
コイル。3. A stator coil treated by the insulation treatment method according to claim 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19339189A JPH0699623B2 (en) | 1989-07-26 | 1989-07-26 | Insulation treatment resin composition, insulation treatment method and stator coil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19339189A JPH0699623B2 (en) | 1989-07-26 | 1989-07-26 | Insulation treatment resin composition, insulation treatment method and stator coil |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0356558A true JPH0356558A (en) | 1991-03-12 |
| JPH0699623B2 JPH0699623B2 (en) | 1994-12-07 |
Family
ID=16307160
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19339189A Expired - Fee Related JPH0699623B2 (en) | 1989-07-26 | 1989-07-26 | Insulation treatment resin composition, insulation treatment method and stator coil |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0699623B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0718356A3 (en) * | 1994-12-19 | 1998-05-27 | Mitsubishi Denki Kabushiki Kaisha | Complex compound and switch containing it |
| JP2002348452A (en) * | 2001-05-25 | 2002-12-04 | Hitachi Chem Co Ltd | Resin composition for electrical insulation |
| JP2003224019A (en) * | 2002-01-28 | 2003-08-08 | Matsushita Electric Works Ltd | Resin impregnated coil and method of manufacturing resin impregnated coil |
-
1989
- 1989-07-26 JP JP19339189A patent/JPH0699623B2/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0718356A3 (en) * | 1994-12-19 | 1998-05-27 | Mitsubishi Denki Kabushiki Kaisha | Complex compound and switch containing it |
| US6361848B1 (en) | 1994-12-19 | 2002-03-26 | Mitsubishi Denki Kabushiki Kaisha | Organic and inorganic complex compound and switch using same |
| US6414067B2 (en) | 1994-12-19 | 2002-07-02 | Mitsubishi Denki Kabushiki Kaisha | Organic and inorganic complex compound and switch using same |
| JP2002348452A (en) * | 2001-05-25 | 2002-12-04 | Hitachi Chem Co Ltd | Resin composition for electrical insulation |
| JP2003224019A (en) * | 2002-01-28 | 2003-08-08 | Matsushita Electric Works Ltd | Resin impregnated coil and method of manufacturing resin impregnated coil |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0699623B2 (en) | 1994-12-07 |
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