JPS5974168A - Film formation - Google Patents

Film formation

Info

Publication number
JPS5974168A
JPS5974168A JP18501382A JP18501382A JPS5974168A JP S5974168 A JPS5974168 A JP S5974168A JP 18501382 A JP18501382 A JP 18501382A JP 18501382 A JP18501382 A JP 18501382A JP S5974168 A JPS5974168 A JP S5974168A
Authority
JP
Japan
Prior art keywords
latex
film
liq
polymer
carboxylic acid
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
JP18501382A
Other languages
Japanese (ja)
Inventor
Kunihito Sakai
酒井 国人
Akinobu Tamaoki
玉置 明信
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.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric 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 Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP18501382A priority Critical patent/JPS5974168A/en
Publication of JPS5974168A publication Critical patent/JPS5974168A/en
Pending legal-status Critical Current

Links

Landscapes

  • Paints Or Removers (AREA)
  • Insulating Of Coils (AREA)
  • Insulating Bodies (AREA)
  • Manufacture Of Motors, Generators (AREA)

Abstract

PURPOSE:To form films without run-off of impregnated resins, by a process wherein an aq. polymer liq. is applied to yield films, which are immersed in a vapor or liq. of carboxylic acid to cure the polymer for preventive measures against run-off of impregnated resins used for insulation. CONSTITUTION:As means for forming films and sealing for preventive measures against run-off of flowable liqs. (impregnated resins) used for insulation of electric equipment or electronic components, an aq. polymer liq. (e.g., a water-base liq. comprising natural or synthetic rubber particles dispersed in water) are applied. Latexes such as acrylate latex are used as said aq. liq. Then, to change the hydrogen ion concn. of the coating film, the film is immersed in vapor or liq. of carboxylic acids to form a coating film by curing of the polymer, such as rubber coagulation or quickly oxidizable film formation. The drawing shows the state at which a latex 6 held to a stator 1 is being cured in acetic acid vapor.

Description

【発明の詳細な説明】 本発明は電気機器などの絶縁を目的として含浸された液
状樹脂が経時変化するとともに外部に流出することを防
止する手段として、高分子の水性液たとえば天然ゴムま
たは合成ゴム粒子が水に分散した水性液(以下、ラテッ
クスという)を塗布後、塗布膜をカルボン酸蒸気中また
はカルボン酸の液中に浸漬し、ゴムの凝集または速酸化
性皮膜の形成(以下、両者とも硬化という)を、液状樹
脂の表面層全体に生せしめる方法に閃する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a means for preventing a liquid resin impregnated for the purpose of insulating electrical equipment from changing over time and leaking out to the outside. After applying an aqueous liquid in which particles are dispersed in water (hereinafter referred to as latex), the coated film is immersed in carboxylic acid vapor or carboxylic acid liquid to prevent rubber agglomeration or formation of a fast-oxidizing film (hereinafter referred to as both). The idea was to make the entire surface layer of the liquid resin undergo hardening.

一般に電動機、モールド変圧器、発電機などは絶縁を目
的として液状の樹脂を含浸または塗布して硬化させてい
る。
Generally, electric motors, molded transformers, generators, etc. are impregnated or coated with liquid resin and then cured for the purpose of insulation.

たとえば、電動機の絶縁処理について詳細に説明する。For example, insulation treatment for electric motors will be explained in detail.

エナメル線などを複数本束ねたコイル表面にマイカやガ
ラステープなどの絶縁材料をテーピング作柴により数回
まきつける。そのままでは機械強度や絶縁特性が不足す
るため、低粘度の熱硬化性含浸樹脂(以下、含浸樹脂と
いう)を真空および加圧の条件下でマイカやガラステー
プなどの内部まで含浸させる。
Insulating material such as mica or glass tape is wrapped several times on the surface of a coil made by bundling multiple enameled wires using taping techniques. Since mechanical strength and insulation properties are insufficient if left as is, low-viscosity thermosetting impregnating resin (hereinafter referred to as impregnating resin) is impregnated into the inside of mica, glass tape, etc. under vacuum and pressurized conditions.

含浸後、含浸樹脂を硬化させるために全体を100〜1
50°Cに加熱する。ところがその加熱工程において一
旦含浸された含浸樹脂が硬化するまでに外部に流出し、
マ・rカまたはガラステープなどの内部が空胴になり、
機械強度や絶縁性能が低下するなどの問題が生ずる。す
なわち含浸樹脂はマイカやガラステープなどをまきつけ
た非常に小さい間”K<’&通って内部まで含浸される
必要があるため低粘度のものが要求され、電動機用含浸
樹脂の粘度は200ops以下のものが多い。
After impregnation, the whole is heated to 100-1 to harden the impregnated resin.
Heat to 50°C. However, during the heating process, the impregnated resin flows out before it hardens.
The inside of the camera or glass tape becomes hollow,
Problems such as decreased mechanical strength and insulation performance arise. In other words, the impregnated resin needs to be impregnated to the inside through a very small space covered with mica or glass tape, so it is required to have a low viscosity, and the viscosity of the impregnated resin for electric motors is 200 ops or less. There are many things.

一方、含浸樹脂として熱硬化性樹脂が一般に用いられる
から、含浸後に加熱硬化される必要があり、全体が10
0〜150°0に加熱される。加熱により含浸樹脂の温
度があがり、粘度が低下する。粘度が低下するとマイカ
やガラステープ内部に一旦含浸された樹脂も簡単に外部
に流出して、内部が空胴になる。
On the other hand, since a thermosetting resin is generally used as the impregnating resin, it must be heated and hardened after impregnation, and the entire
Heated from 0 to 150°0. Heating increases the temperature of the impregnated resin and reduces its viscosity. When the viscosity decreases, the resin that has once been impregnated inside the mica or glass tape easily flows out, leaving a void inside.

前記問題点を解決するため、含浸後すみやかに全体を回
転させながら硬化する方法が行なわれている。しかしそ
の方法は加熱炉中で回転させる装置が必要なこと、一度
に多社のものを回転させにくいこと、回転できない構造
のものがあることおよび重量物は回転させるために動力
費が高くなることなどの欠点な有する。
In order to solve the above-mentioned problems, a method has been used in which the entire material is cured while being rotated immediately after impregnation. However, this method requires a device to rotate it in a heating furnace, it is difficult to rotate items from multiple manufacturers at once, some items have structures that cannot be rotated, and the power costs are high to rotate heavy items. It has disadvantages such as.

本発明者らは前記の従来法の欠点を改善するため鋭意研
究を行なった結果、本発明に到達した。
The present inventors conducted extensive research to improve the drawbacks of the conventional methods described above, and as a result, they arrived at the present invention.

に皮膜形成および封止を行なう手段として、高分子の水
性液の水素イオン濃度を変化させることまたは高分子の
水性液に陽イオンを加えることにより高分子を硬化させ
ることを特徴とする皮膜形成法に関する。すなわち従来
とは全く異なる手段による含浸後の含浸樹脂流出防止法
として、ラテックスの水素イオン濃度(以下、pHとい
う)を変化させるまたはラテックスに陽イオンを加える
とラテックスが硬化することを利用し、含浸後または含
浸前のコイル表面などにラテックスを浸漬法またはスプ
レー法などにより付着させ、そののちカルボン酸たとえ
ば酢酸の蒸気中またはi 中ニ浸漬することにより表面
のラテックスをわずか5秒間以内で硬化せしめ、含浸樹
脂が流出しない皮膜を形成する方法に閃する。
A film forming method characterized by curing the polymer by changing the hydrogen ion concentration of the aqueous polymer liquid or adding cations to the polymer aqueous liquid as a means for forming and sealing the polymer. Regarding. In other words, as a method to prevent the impregnated resin from flowing out after impregnation using a completely different method than conventional methods, the impregnating method takes advantage of the fact that latex hardens when the hydrogen ion concentration (hereinafter referred to as pH) of latex is changed or cations are added to latex. Latex is applied to the surface of the coil after or before impregnation by a dipping method or a spray method, and then the latex on the surface is hardened within just 5 seconds by immersing it in the vapor of a carboxylic acid such as acetic acid or in i. I was inspired by a method to form a film that prevents the impregnated resin from flowing out.

本発明に用いられる高分子としてはアクリレート系、ア
クリロニトリル−ブタジェン系またはスチレン−ブタジ
ェン系など一般に水性液として用いうる高分子があげら
れる。
Examples of the polymers used in the present invention include acrylate-based, acrylonitrile-butadiene-based, and styrene-butadiene-based polymers that can generally be used as aqueous liquids.

本発明に用いられる高分子の水性液として、前記高分子
のエマルジョンまたはラテックスなどの通常の水性液が
ある。
The aqueous polymeric liquid used in the present invention includes conventional aqueous liquids such as emulsions or latexes of the aforementioned polymers.

本発明に用いられる高分子の水性液のpHを変化させる
ためのカルボン酸として、ギ酸、酢酸、プロピオン酸、
酪酸またはカプロン酸など通常用いられる一塩基性カル
ボン酸があげられ、前記高分子の水性液に加えられる陽
イオンとしてNaOl、C&C12、AIO13などか
ら生ずる陽イオンがあげられる。
Examples of carboxylic acids for changing the pH of the aqueous polymer liquid used in the present invention include formic acid, acetic acid, propionic acid,
Commonly used monobasic carboxylic acids such as butyric acid or caproic acid may be cited, and cations added to the aqueous polymer solution may include cations generated from NaOl, C&C12, AIO13, and the like.

本発明のカルボン酸により高分子の水性液を硬化させる
方法として、高分子の水性液をカルボン酸蒸気中を通す
またはカルボン酸液中に浸漬させるなどの方法がある。
As a method for curing an aqueous polymeric liquid with the carboxylic acid of the present invention, there are methods such as passing the aqueous polymeric liquid through carboxylic acid vapor or immersing it in a carboxylic acid liquid.

高分子の水性液たとえばラテックスがカルボン酸と接触
すると前記ラテックスのpHが酸性側に変化するため、
通常の化学反応ではえられないような5秒以内という高
速度で表面が硬化し、皮膜を形成する。皮膜が形成した
のち加熱炉で含浸樹脂を硬化させる。加熱によりコイル
中に含浸した含浸樹脂の粘度が低下するが、表面にラテ
ックスの皮膜があるため外部に流出することなく硬化さ
せうる。硬化後、ラテックスの皮膜が製品に障害となる
ばあいには、ラテックスに接着性がないため簡単に皮膜
を除去しうる。
When an aqueous polymeric liquid such as latex comes into contact with carboxylic acid, the pH of the latex changes to the acidic side.
The surface hardens at a high speed of less than 5 seconds, which cannot be achieved with normal chemical reactions, forming a film. After the film is formed, the impregnated resin is cured in a heating furnace. Although the viscosity of the impregnated resin impregnated into the coil decreases due to heating, since there is a latex film on the surface, it can be cured without flowing out. If the latex film becomes a hindrance to the product after curing, it can be easily removed since latex has no adhesive properties.

ラテックスを高速硬化させる方法として、ラテックスの
pHを酸性側に変化させる以外に下記の方法も用いうる
。すなわち、ラテックスは陰イオン系乳化剤を用いてい
るため陰イオンに対しては比較的安定であるが、反対に
陽イオンが混入したばあいにはラテックス粒子の界面へ
対イオン(陽イオン)の吸着がおこり、電気二重層が対
イオンの吸着により圧縮され、ラテックス粒子同士のポ
テンシャル障害が小さくなり、ラテックスが硬化される
ことが知られている。たとえばNap/ % OaO/
2、Al(1’/3などの水溶液とラテックスを接触さ
せると速硬化性の皮膜が形成され、前記pHを変化させ
たばあいと同様に高速度で硬化されうる。
In addition to changing the pH of the latex to the acidic side, the following method can also be used to rapidly cure the latex. In other words, because latex uses an anionic emulsifier, it is relatively stable against anions, but on the other hand, when cations are mixed in, counterions (cations) are adsorbed to the interface of latex particles. It is known that the electric double layer is compressed by the adsorption of counterions, the potential disturbance between latex particles is reduced, and the latex is hardened. For example, Nap/% OaO/
2. When the latex is brought into contact with an aqueous solution such as Al (1'/3), a fast-curing film is formed, and it can be cured at a high speed similarly to when the pH is changed.

本発明において、高分子の水性液たとえばラテックスな
どを電動機などに含浸樹脂を含浸させたものの表面に塗
布する方法として浸漬法またはスプレー法など通常の方
法が用いられる。
In the present invention, a conventional method such as a dipping method or a spray method is used to apply an aqueous polymeric liquid such as latex to the surface of an electric motor or the like impregnated with an impregnating resin.

つぎに実施例および比較例をあげて本発明の詳細な説明
するが、本発明はかかる実施例のみに限定されるもので
はない。
EXAMPLES Next, the present invention will be described in detail with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.

実施例1 小型電動機固定子(以下、固定子という)(1)を25
80% 120分間、1mmH,にて含浸樹脂(4)に
浸漬シてコイル(3)に含浸樹脂(4)を含浸させた。
Example 1 Small electric motor stator (hereinafter referred to as stator) (1)
80% The coil (3) was impregnated with the impregnating resin (4) by immersing it in the impregnating resin (4) for 120 minutes at 1 mmH.

含浸後取出し、第6図のごとくラテックス(6)(二ポ
ール4850、日本ゼオン■製)の中に25°Cで約1
0秒間浸漬したのち取出し、ただちに第4図に示すよう
に25°Cの酢酸(7)の蒸気(10)中に入れた。ラ
テックス(6)は酢酸(7)の蒸蜘0)に接触すること
により、ラテックス(6)のpHが酢性側に変化して、
5秒以内と通常の化学反応ではえられないような高速度
で硬化し、皮膜を形成した。皮膜形成後加熱炉で含浸樹
脂(4)を100°C×60分間熱硬化させた。熱硬化
時にコイすることなく熱硬化させることができた。
After impregnation, take it out and put it in latex (6) (Nipole 4850, Nippon Zeon ■) at 25°C for about 1 hour as shown in Figure 6.
After being immersed for 0 seconds, it was taken out and immediately placed in acetic acid (7) vapor (10) at 25°C as shown in FIG. When the latex (6) comes into contact with the vapor of acetic acid (7), the pH of the latex (6) changes to the acetic acid side.
It cured within 5 seconds, a high speed that cannot be achieved with normal chemical reactions, and formed a film. After the film was formed, the impregnated resin (4) was thermally cured at 100°C for 60 minutes in a heating furnace. It was possible to heat cure without curling during heat curing.

第1表に熱硬化後の固定子(1)への含浸樹脂(4)の
付着量を示す。
Table 1 shows the amount of the impregnated resin (4) adhered to the stator (1) after thermosetting.

第1表からラテックス皮膜を有するばあい、含浸樹脂付
着量が多く、熱硬化中に流出しにくいことがわかる。
From Table 1, it can be seen that when a latex film is provided, the amount of impregnated resin deposited is large and it is difficult to flow out during heat curing.

第   1    表 比較例1 ラテックス(6)への浸漬および皮膜形成をしないこと
以外は実施例1と同様にして固定子(1)を含浸樹脂(
4)に浸漬してコイル(3)に含浸樹脂(4)を含浸さ
せ、含浸後取出し、加熱炉で熱硬化させた。
Table 1 Comparative Example 1 The stator (1) was prepared in the same manner as in Example 1 except that the latex (6) was not dipped and the film was not formed.
4) to impregnate the coil (3) with the impregnating resin (4), and after impregnation, it was taken out and thermally hardened in a heating furnace.

第1表に熱硬化後の固定子(1)への含が樹脂(4)の
付着量を示す。
Table 1 shows the amount of adhesive resin (4) adhered to the stator (1) after thermosetting.

実施例2 皮膜形成用ラテックスとラテックスを硬化させるための
カルボン酸とを第2表に示すように組合せ、第5図に示
すように25mm X 50mmのガラス板(9)上に
1.の各種ラテックス(以下特記しない限り日本ゼオン
■製)(6)を滴下し、相当する各種カルボン酸の蒸気
に20°aXS秒間接触させ、形成した皮膜の厚さを測
定した。
Example 2 A latex for forming a film and a carboxylic acid for curing the latex were combined as shown in Table 2, and as shown in FIG. 5, 1. Various types of latex (manufactured by Nippon Zeon ■ unless otherwise specified) (6) were dropped onto the surface of the sample and brought into contact with the corresponding vapors of various carboxylic acids for 20° aXS seconds, and the thickness of the formed film was measured.

第2表にその結果を示す。Table 2 shows the results.

第    2    表 第2表から用いたラテックスとカルボン酸とのいずれの
組合せにおいても短時間で皮膜が形成されることがわか
る。
Table 2 It can be seen from Table 2 that a film is formed in a short time in any combination of latex and carboxylic acid used.

実施例3 第2表に示すラテックスとカルボン酸との組合せを用い
て、実施例2と同様にガラス板(9)上に1゜の各種ラ
テックス(6)を滴下したのち相当する各種カルボン酸
溶液中に2oc1:I×5秒間浸漬し、形成した皮膜の
厚さを測定した。
Example 3 Using the combinations of latex and carboxylic acid shown in Table 2, various latexes (6) at 1° were dropped onto a glass plate (9) in the same manner as in Example 2, and then the corresponding various carboxylic acid solutions were added. The thickness of the formed film was measured by immersing it in 2oc1:I×5 seconds.

第6表にその結果を示す。Table 6 shows the results.

第    6    表 第6表からカルボン酸溶液中に浸漬しても蒸気に接触さ
せたばあいと同様に短時間で皮膜が形成されることがわ
かる。
Table 6 It can be seen from Table 6 that a film is formed in a short time even when immersed in a carboxylic acid solution, similar to when brought into contact with steam.

実施例4 第2表の試料番号4のラテックスとカルボン酸との組合
せを用いたばあいの皮膜形成に対する温度、カルボン酸
との接触時間の影響について、実施例2と同様にして測
定した。
Example 4 The influence of temperature and contact time with carboxylic acid on film formation when using the combination of latex and carboxylic acid of Sample No. 4 in Table 2 was measured in the same manner as in Example 2.

その結果を第4表に示す。The results are shown in Table 4.

第    4    表 第4表から皮膜形成は一5°Oという低温においても充
分性なわれ、0°Cから40°Cまでの範囲の温度にお
いては5秒または60秒の接触時間でそれぞれ0.21
mmから1.30mmまでの速硬化皮膜が形成されるこ
とがわかる。
Table 4 From Table 4, it can be seen that film formation is sufficient even at temperatures as low as -5°C, and at temperatures ranging from 0°C to 40°C, a contact time of 5 seconds or 60 seconds results in a film formation of 0.21°C, respectively.
It can be seen that a fast-curing film with a thickness of 1.30 mm to 1.30 mm was formed.

また低温においても皮膜を形成しうるため、冷却するこ
とによりコイル(3)に含浸させた含浸樹脂(4)の粘
度を上昇させ、流出しに<<シてから皮膜を形成させう
るという利点もある。
In addition, since a film can be formed even at low temperatures, the viscosity of the impregnated resin (4) impregnated into the coil (3) can be increased by cooling, and the film can be formed after it has flowed out. be.

【図面の簡単な説明】[Brief explanation of the drawing]

第1〜4図は本発明の工程を順次説明するための説明図
であって、第1図は固定子の斜視図、第2図は固定子に
含浸樹脂を含浸させている状態を示す説明図、第6図は
含浸樹脂を含浸させた固定子をラテックス中に浸漬させ
ている状態を示す説明図、第4図は固定子に付着したラ
テックスを酢酸蒸気中で硬化させている状態を示す説明
図であり、第5図は皮膜形成のために、ガラス板上にラ
テックスを滴下した状態を示す説明図である。 (図面の主要符号) (1):固定子 (2):積層コア (3):コイル (4):含浸樹脂 (5):容 器 (6)ニラテックス (8):仕切板 第1 図 3′ 第2図 手続補正書(自発)   5・ 6゜ 11゛許庁長宮殿 と 1 °If f’lの表示    ′4馴p(i昭57
−485013号2 ブこ明の名称 皮膜形成法 :(を山II  を 1−ると 代表者片由仁へ部 4代理人 名 493− 補正の対象 (1)明細書の「発明の詳細な説明」の欄補正の内容 (1)明細書2頁18行の「速醸化性」を「速硬化性」
補正する。 以  上
Figures 1 to 4 are explanatory diagrams for sequentially explaining the steps of the present invention, in which Figure 1 is a perspective view of a stator, and Figure 2 is an explanation showing a state in which the stator is impregnated with impregnating resin. Figure 6 is an explanatory diagram showing a state in which a stator impregnated with impregnated resin is immersed in latex, and Figure 4 shows a state in which latex attached to the stator is hardened in acetic acid vapor. FIG. 5 is an explanatory diagram showing a state in which latex is dropped onto a glass plate to form a film. (Main symbols in the drawing) (1): Stator (2): Laminated core (3): Coil (4): Impregnated resin (5): Container (6) Nilatex (8): Partition plate 1 Figure 3 ' Figure 2 Procedural Amendment (Voluntary) 5.6゜11゛Indication of Governor's Palace and 1°If f'l
- No. 485013 No. 2 Bukomei's name Film forming method: (Mountain II 1- and Representative Kata Yuhito Part 4 Name of agent 493- Subject of amendment (1) Detailed description of the invention in the specification Contents of column amendment (1) “Fast brewing property” on page 2, line 18 of the specification was changed to “fast curing property”
to correct. that's all

Claims (5)

【特許請求の範囲】[Claims] (1)電気機器、電子部品の電気絶縁を目的とする流動
性液体(含浸樹脂)の流出防止のために皮膜形成および
封止を行なう手段として、高分子の水性液の水素イオン
濃度を変化させることまたは高分子の水性液に陽イオン
を加えることにより高分子を硬化させることを特徴とす
る皮膜形成法。
(1) Changing the hydrogen ion concentration of an aqueous polymeric liquid as a means of film formation and sealing to prevent the leakage of a fluid liquid (impregnated resin) intended for electrical insulation of electrical equipment and electronic components. A film forming method characterized by curing the polymer by adding cations to the aqueous liquid of the polymer.
(2)電気機器、電子部品の電気絶縁を目的とする流動
性液体(含浸樹脂)の流出防止のために皮膜形成および
封止を行なう手段に用いる前記高分子の水性液として、
エマルジョンを用いることヲ%徴とする特許請求の範囲
第(1)項記載の皮膜形成法。
(2) The aqueous polymeric liquid used as a means for forming and sealing a film to prevent leakage of a fluid liquid (impregnated resin) for the purpose of electrical insulation of electrical equipment and electronic parts;
A film forming method according to claim (1), characterized in that an emulsion is used.
(3)前記電気絶縁を目的とする流動性液体の流出防止
手段に用いる前記高分子の水性液としてラテックスを用
いることを特徴とする特許請求の範囲第(1)項記載の
皮膜形成法。
(3) The method for forming a film according to claim (1), characterized in that latex is used as the aqueous polymeric liquid used in the means for preventing outflow of the fluid liquid for the purpose of electrical insulation.
(4)前記ラテックスとしてアクリレート系ラテックス
、アクリロニトリル−ブタジェン系ラテックスまたはス
チレン−ブタジェン系ラテックスを用い、硬化手段とし
てカルボン酸を用いることを特徴とする特許請求の範囲
第(1)項または第(3)項記載の皮膜形成法。
(4) Claims (1) or (3) characterized in that acrylate latex, acrylonitrile-butadiene latex, or styrene-butadiene latex is used as the latex, and carboxylic acid is used as the curing means. Film forming method described in section.
(5)前記カルボン酸として1塩基性カルボン酸を用い
ることを特徴とする特許請求の範囲第(4)項記載の皮
膜形成法。
(5) The film forming method according to claim (4), characterized in that a monobasic carboxylic acid is used as the carboxylic acid.
JP18501382A 1982-10-19 1982-10-19 Film formation Pending JPS5974168A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18501382A JPS5974168A (en) 1982-10-19 1982-10-19 Film formation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18501382A JPS5974168A (en) 1982-10-19 1982-10-19 Film formation

Publications (1)

Publication Number Publication Date
JPS5974168A true JPS5974168A (en) 1984-04-26

Family

ID=16163239

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18501382A Pending JPS5974168A (en) 1982-10-19 1982-10-19 Film formation

Country Status (1)

Country Link
JP (1) JPS5974168A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102664499A (en) * 2012-04-26 2012-09-12 哈尔滨电机厂有限责任公司 Preparation method of low resistance anti-corona material for vacuum pressure impregnation(VPI) insulation system

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102664499A (en) * 2012-04-26 2012-09-12 哈尔滨电机厂有限责任公司 Preparation method of low resistance anti-corona material for vacuum pressure impregnation(VPI) insulation system

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