JPS62252479A - Powder coating composition - Google Patents

Powder coating composition

Info

Publication number
JPS62252479A
JPS62252479A JP9339886A JP9339886A JPS62252479A JP S62252479 A JPS62252479 A JP S62252479A JP 9339886 A JP9339886 A JP 9339886A JP 9339886 A JP9339886 A JP 9339886A JP S62252479 A JPS62252479 A JP S62252479A
Authority
JP
Japan
Prior art keywords
content
epoxy resin
epoxy
powder coating
coating composition
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
JP9339886A
Other languages
Japanese (ja)
Inventor
Masato Kishi
正人 岸
Joji Kuroyanagi
黒柳 錠次
Akihiro Kurasawa
倉沢 明裕
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.)
Tomoegawa Co Ltd
Original Assignee
Tomoegawa Paper Co Ltd
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 Tomoegawa Paper Co Ltd filed Critical Tomoegawa Paper Co Ltd
Priority to JP9339886A priority Critical patent/JPS62252479A/en
Publication of JPS62252479A publication Critical patent/JPS62252479A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a powder coating compsn. which has a high crosslink density, has excellent adhesion, gives a cured coating film which hardly absorbs water, and is suitable for use in coating electrical and electronic components, containing an epoxy resin having a very high epoxy group content and a very low impurity content. CONSTITUTION:An epoxy resin having an epoxy group content of not lower than 90% expressed by the formula (wherein W is an epoxy equivalent in g/eq; A is an alpha-diol content in meq/100g; Cl is a hydrolyzable chlorine content in wt%; and P is a free phenol content in ppm) is prepd. by a two-step method comprising a polyaddition reaction between a low-molecular liquid resin and bisphenol A. The epoxy resin is blended with additives such as a curing agent (e.g., dicyandiamide), a curing accelerator (e.g., an imidazole catalyst), a filler, a pigment, etc., to obtain the desired powder coating compsn.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は電線の絶縁やソレノイPコイルの含浸用等の粉
体塗料用組我物、特にエポキシ樹脂系の粉体塗料組底物
に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a powder coating assembly for insulating electric wires and impregnating solenoid P coils, and particularly to an epoxy resin powder coating assembly.

従来の技術 従来電気絶縁用もしくはコイル類の含浸或いは防湿保護
等に用いられる樹脂にはエポキシ樹脂を初め種々の樹脂
塗料が考えられているが、中でもエポキシ樹脂は電気、
電子部品の絶縁被覆に適し次耐湿性や高温電気特性等を
有するものとして使用されている。
BACKGROUND OF THE INVENTION Conventionally, various resin paints including epoxy resin have been considered as resins used for electrical insulation, impregnation of coils, moisture-proof protection, etc. Among them, epoxy resin is used for electrical,
It is suitable for insulating coatings on electronic parts, and is used because it has moisture resistance and high-temperature electrical properties.

ここに用いられるエポキシ樹脂は特に粉体塗料としたも
のが溶剤を使用しないため健康上も良く、又火災の危険
性もないので公害防止の見地からも好ましいものとして
評価されている。エポキシ拉(脂粉体塗料はビスフェノ
ールA型エポキシ樹脂、ノゼラツク型エポキシ樹脂、脂
環型エポキシ樹脂等のエポキシ樹脂、酸無水物、ポリア
ミン等の硬化剤、第3級アミン、イミダゾール等の硬化
促進剤、充填剤及びその他の添加剤等の材料から構成さ
れ流動浸漬法、静電流動浸漬法等の方法で電気電子部品
に塗装されている。
The epoxy resin used here is particularly good for health since powder coatings do not require the use of solvents, and there is no risk of fire, so they are evaluated as preferable from the standpoint of pollution prevention. Epoxy resin (fat powder coatings include epoxy resins such as bisphenol A type epoxy resin, Nozerak type epoxy resin, and alicyclic type epoxy resin, acid anhydrides, curing agents such as polyamines, curing accelerators such as tertiary amines, imidazole, etc.), It is composed of materials such as fillers and other additives, and is applied to electrical and electronic parts using methods such as fluidized dipping and electrostatic dipping.

発明が解決すべき問題点 しかし最近電気電子部品の高信頼性の動きに伴ない、エ
ポキシ樹脂粉体塗料の耐湿性や被塗被物への高湿接着力
等の向上の要求が一層高まり、これに対応する方策が要
求されているところである。。
Problems to be Solved by the Invention However, with the recent trend toward higher reliability in electrical and electronic components, there has been an increasing demand for improved moisture resistance of epoxy resin powder coatings and high-humidity adhesion to coated objects. Measures to deal with this are required. .

問題点を解決するための手段 本発明はこのような状況に鑑み種々検討の結果なされた
もので、特にビスフェノールに型エポキシ樹脂の構造に
着目し次ことによシ、化学構造的に水分生成可能性の少
なく、かつ優れ次接着力を有するエポキシ樹脂を粉体塗
料としたことにより前記従来の技術の問題点を解決した
ものである。
Means for Solving the Problems The present invention was developed as a result of various studies in view of the above circumstances, and in particular, focused on the structure of bisphenol-type epoxy resins, which are capable of producing water due to their chemical structure. The problems of the prior art described above are solved by using an epoxy resin with low adhesiveness and excellent adhesion as a powder coating.

即ちこの種エポキシ樹脂の末端化学構造は以下の通りで
あるものと考えられる OHOH(meq/工00?] OHOJ        [%] 0Hフリーフェノール (ppm) この構造式から判るようにl”2) 、 (3]及び〔
4〕はH20生成の危険性を有するものであるから[1
)を多くしなければならない。
In other words, the terminal chemical structure of this type of epoxy resin is considered to be as follows: 3] and [
4] has the risk of producing H20, so [1
) must be increased.

ところで現在までに粉体塗料として珀いられているエポ
キシ樹脂の合成法は一段法と呼ばれる方法であり、エポ
キシ樹脂のエポキシ基含有率は約60〜90未満係であ
ることが判っ九。
By the way, the method of synthesizing epoxy resins currently used as powder coatings is a method called a one-step method, and it has been found that the epoxy group content of epoxy resins is about 60 to less than 90%.

ここにエポキシ基含有率は以下の式により7出される。Here, the epoxy group content is calculated by the following formula.

1ooxto3 v::xポキシ当鵞(9/eq) A : α−ジオール(meq/ hoot )Cl:
 加水分解性塩素(wt%) P : フリーフェノール(ppm )本発明者はこの
ような見地からエポキシ基の含有率を90係以上とし次
エポキシ梱脂粉体塗料により前記従来の技術の問題点を
解決したものである。
1ooxto3 v::x poxy (9/eq) A: α-diol (meq/hoot) Cl:
Hydrolyzable chlorine (wt%) P: Free phenol (ppm) From this perspective, the inventor of the present invention solved the problems of the conventional technology by increasing the content of epoxy groups to 90 or more and using an epoxy fat powder paint. This is what I did.

上記における本発明で用いられるエポキシ樹脂は低分子
量の液体樹脂とビスフェノールAとから重付加反応をさ
せる二段法CF’usion法)により合成されるもの
であり、エポキシ含有率が非常に高くなっただけ例えば
α−ジオール等の不純物は少なくなり、接着力特に高温
でのせん断接着力が大となり、かつα−ジオールの水酸
基の数が減少しただけ耐水性が良くなり、過酷なヒート
サイクルによっても塗布面にクラックを生ずることがな
い。
The epoxy resin used in the present invention mentioned above is synthesized by a two-step CF'usion method in which a low molecular weight liquid resin and bisphenol A are subjected to a polyaddition reaction, and has a very high epoxy content. However, the amount of impurities such as α-diol is reduced, the adhesive strength, especially the shear adhesive strength at high temperatures, is increased, and the decrease in the number of hydroxyl groups in α-diol improves water resistance, making it difficult to apply even under severe heat cycles. No cracks will occur on the surface.

具体的にはソレノイドコイルの防湿保護等に使用した場
合、コイルのゼピンを形成しているポリブチレンテレフ
タレート等のポリマーとの接着力が格別優れ、かつ吸水
性の少ない硬化塗膜を得るものである。
Specifically, when used for moisture-proof protection of solenoid coils, it provides a cured coating that has exceptional adhesion to the polymer such as polybutylene terephthalate that forms the coil's zepin, and has low water absorption. .

実施例 以下本発明の実施例及び比較例の粉体塗料を作りソレノ
イドコイルに塗工して130℃、lh4+水中15m1
0回のサイクルテストt−行なった。
Examples Below, powder coatings of Examples and Comparative Examples of the present invention were made and applied to solenoid coils at 130°C and 15ml of lh4 + water.
0 cycle test t- performed.

テストに当っては中心孔を有するポリブチレンテレフタ
レート(PBT ) It!yNビンにソレノイドコイ
ルが巻き付けられたものを用い、その外部から粉体塗料
を塗布したものについて行なった。
For testing, polybutylene terephthalate (PBT) with a central hole was used. A yN bottle with a solenoid coil wound around it was used, and a powder coating was applied from the outside.

実施例1 エポキシ基含有率95%の二段法エポキシ樹脂  10
0重量部(エポトート YD904.東部化故社展)ジ
シアン、ジアミド                 
2 #イミダゾール系触媒             
  ■l(2MZ−A、四国ファインケミカル社製)顔
料 ペンが2                2.5
1(R−550,利根産業社裂) 流動調整剤                    
03I(モダフロー、4ウダーI、そンサント社製]上
記成分をへンシエルミキサーにて乾式混合した後、押出
機により熱溶融混練押出して冷却後粗粉砕、微粉砕して
体積基準積算50%径が35μmの粉体塗料組成物を得
た。
Example 1 Two-step epoxy resin with 95% epoxy group content 10
0 parts by weight (Epotote YD904.Tobu Kaishisha Exhibition) Dicyan, diamide
2 #imidazole catalyst
■l (2MZ-A, manufactured by Shikoku Fine Chemical Co., Ltd.) Pigment Pen 2 2.5
1 (R-550, Tone Sangyo Shari) Flow regulator
03I (Modaflow, 4 Uda I, manufactured by Sonsanto Co., Ltd.) The above ingredients were dry mixed in a Henschel mixer, then hot melt kneaded and extruded using an extruder, cooled, and then coarsely and finely crushed to give a volume-based integrated diameter of 50%. A powder coating composition having a diameter of 35 μm was obtained.

得られた粉体を2枚のPBTテストピースに挾み% t
SO℃30秒、加熱硬化して接着し、一旦冷却した後テ
ンシロンでせん断接着力を測定したところ、20℃の雰
囲気でtiox7.’儒2.125℃でtosK9/備
、150℃で35に9/備2であシ、高温に於ても相当
の接着力を有するものであった。
The obtained powder was sandwiched between two PBT test pieces and the %t
The bond was cured by heating at SO℃ for 30 seconds, and after cooling once, the shear adhesive strength was measured using Tensilon, and it was found that tiox7. It had a tosK9/2 at 2.125°C and 35 to 9/2 at 150°C, and had considerable adhesive strength even at high temperatures.

次に上記により伜られた粉体を流動浸漬法によりソレノ
イドコイルに塗膜厚さが500〜600μmになるよう
に塗着せしめ、130℃、1時間空中放置後15分間水
中に浸漬し、これを100サイクル繰り返したところ、
pBT&ビンとノ剥離や塗布面のクラックの発生がなく
、実用上充分な特性を備えたものであった。
Next, the powder obtained above was applied to a solenoid coil using a fluidized dipping method to a coating thickness of 500 to 600 μm, left in air at 130°C for 1 hour, and then immersed in water for 15 minutes. After repeating 100 cycles,
There was no peeling of pBT or cracks on the coated surface, and the coating had sufficient properties for practical use.

実施例2 実施例1の配合中ジシアンジアミPに代えて。Example 2 In place of dicyandiami P in the formulation of Example 1.

酸無水物系硬化剤である無水トリメリット酸を10重量
部用い次外は全て実施例1と同様にして本発明の粉体塗
料組成物を得次。
A powder coating composition of the present invention was obtained in the same manner as in Example 1 except that 10 parts by weight of trimellitic anhydride, which is an acid anhydride curing agent, was used.

得られた本発明の粉体のPBT・テストピース間のせん
断接着力は20℃の雰囲気でti3に7.’cm2,1
00℃で7 i Kg / cm2.150Cで40に
9/6n2であ凱 高温に於ても相当の接着力を廟する
ものである。
The shear adhesive strength between the PBT and the test piece of the obtained powder of the present invention was 7.5% at ti3 in an atmosphere of 20°C. 'cm2,1
7 i Kg/cm2 at 00°C. 40 to 9/6n2 at 150°C. It exhibits considerable adhesive strength even at high temperatures.

得られ次本発明の粉体を実施例1と同様にして評価した
ところ実用上充分な特性を備えたものであった。
The obtained powder of the present invention was then evaluated in the same manner as in Example 1, and was found to have practically sufficient properties.

比較例 工?キシ含有1[87%の一段法エボキシ樹脂   1
00ii部(エポレート YDO14、東部化成社製)
ジシアンジアミド                 
2 。
Comparative example? One-step epoxy resin containing 1 [87%] 1
Part 00ii (Eporate YDO14, manufactured by Tobu Kasei Co., Ltd.)
Dicyandiamide
2.

イミダゾール系触媒               l
l(2MZ−A、 17c!r5377’(7’yミカ
に社p)顔料 ベンガラ              
   25#(R−550、利根産業社裂〕 流動調整剤                   o
3゜(モダフローパラ/−1,モンサン)JJ[)得ら
れた粉体を実施例1と同様にしてPBT・テストピース
間のせん断接着カfr:測定し次ところ、20Cの雰囲
気では45Kg/備2であったが15(1℃の雰囲気で
は全く接着力を示さなかつ九。
Imidazole catalyst l
l (2MZ-A, 17c!r5377'(7'y Mikanishap) Pigment Red Garla
25# (R-550, Tone Sangyosha Rip) Flow regulator o
3゜(Modaflow Para/-1, Montsan) JJ [) The obtained powder was measured in the same manner as in Example 1, and the shear adhesion fr: between PBT and the test piece was measured. However, it showed no adhesion at all in an atmosphere of 15°C (9°C).

、 更に実施例1と同様にしてソレノイドコイルに塗布
し、加熱サイクル試験を行なったところ、PBT  y
j#ビンとの剥離及び塗布面のクラックが発生し、実用
上支障を来すものであった。
, Furthermore, when it was applied to a solenoid coil in the same manner as in Example 1 and a heating cycle test was performed, PBT y
Peeling from the j# bottle and cracks on the coated surface occurred, which caused problems in practical use.

発明の効果 本発明によればエポキシ樹脂粉体塗料がヱボキせん断接
着力の温度依存性が少なく、吸水性の小さい硬化塗膜を
与えるものである。
Effects of the Invention According to the present invention, the epoxy resin powder coating provides a cured coating film with less temperature dependence of shear adhesive strength and less water absorption.

代理人 弁理士  竹 内   守 手続補正書(自発) 昭和61年6月4日 特許庁長官 宇 賀 道 部 殿 1、事件の表示 昭和61年特許m第93398号 2、発明の名称 粉体塗料組成物 3、補正をする者 事件との関係  特許出願人 住 所 東京都中央区京橋−丁目5番15号名 称  
株式会社 巴用裏紙所 代表者井上貴雄 4、代理人〒101 居 所 東京都千代田区内神田二丁目15番13号南部
ビル 5、補正の対象 明細書の「特許請求の範囲」の欄及び「発明の詳細な説
明」の欄 (1)特許請求の範囲を別紙のとおシ補正する。
Agent Patent Attorney Mamoru Takeuchi Procedural Amendment (Voluntary) June 4, 1986 Director General of the Patent Office Michibe Uga 1, Indication of the Case 1986 Patent M No. 93398 2, Name of the Invention Powder Coating Composition Item 3: Relationship with the case of the person making the amendment Patent applicant address: 5-15 Kyobashi-chome, Chuo-ku, Tokyo Name:
Representative Takao Inoue 4, Tomoe Urashisho Co., Ltd. Address: 101 Address: Nanbu Building 5, 2-15-13 Uchikanda, Chiyoda-ku, Tokyo, "Claims" column of the specification to be amended and "Detailed Description of the Invention" Column (1) Amend the claims by adding a separate sheet.

(2)明細書の8g3頁第2行目に「被塗被物」とある
を「被塗装物」と補正する。
(2) In the second line of page 8g3 of the specification, the phrase "subject to be coated" is amended to read "object to be coated."

(3)  同第4頁第12行目の式の分母にr355J
とあるをr 35.5 Jと補正する。
(3) The denominator of the formula on page 4, line 12 is r355J.
Correct it to r 35.5 J.

(4)同第7頁第3行目に「10回」とあるを「100
回」と補正する。
(4) In the third line of page 7, the phrase “10 times” was replaced with “100 times.”
Correct it to "times".

(5)  同第7頁第3行目に「30秒」とあるをr3
0分」と補正する。
(5) The 3rd line of page 7 says “30 seconds” r3
0 minutes”.

以上 2、特許請求の範囲 下記の式で示されるエポキシ基含有率が90%以上であ
るエポキシ樹脂を含有することを特徴とする粉体塗料組
成物 100XI O’
2. Claims: A powder coating composition 100XI O' characterized by containing an epoxy resin represented by the following formula and having an epoxy group content of 90% or more.

Claims (1)

【特許請求の範囲】 下記の式で示されるエポキシ基含有率が90%以上であ
るエポキシ樹脂を含有することを特徴とする粉体塗料組
成物 エポキシ含有率={(100×10^3/W)/[(1
00×10^3/W)+A+(Cl×10^3/35.
5)+(P×10^−^4/114)]}×100(%
) 但し、w:エポキシ当量(g/eq) A:α−ジオール(meg/100gr) Cl:加水分解酵素 P:フリーフェノール
[Scope of Claims] A powder coating composition characterized by containing an epoxy resin having an epoxy group content of 90% or more represented by the following formula: Epoxy content = {(100×10^3/W )/[(1
00×10^3/W)+A+(Cl×10^3/35.
5)+(P×10^-^4/114)]}×100(%
) However, w: epoxy equivalent (g/eq) A: α-diol (meg/100gr) Cl: hydrolase P: free phenol
JP9339886A 1986-04-24 1986-04-24 Powder coating composition Pending JPS62252479A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9339886A JPS62252479A (en) 1986-04-24 1986-04-24 Powder coating composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9339886A JPS62252479A (en) 1986-04-24 1986-04-24 Powder coating composition

Publications (1)

Publication Number Publication Date
JPS62252479A true JPS62252479A (en) 1987-11-04

Family

ID=14081193

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9339886A Pending JPS62252479A (en) 1986-04-24 1986-04-24 Powder coating composition

Country Status (1)

Country Link
JP (1) JPS62252479A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0678564A2 (en) * 1994-04-22 1995-10-25 Tomoegawa Paper Co. Ltd. Powder coating
JP2020105262A (en) * 2018-12-26 2020-07-09 日鉄ケミカル&マテリアル株式会社 Epoxy resin powder coating

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59152964A (en) * 1983-02-18 1984-08-31 Mitsui Petrochem Ind Ltd Epoxy resin powder coating

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59152964A (en) * 1983-02-18 1984-08-31 Mitsui Petrochem Ind Ltd Epoxy resin powder coating

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0678564A2 (en) * 1994-04-22 1995-10-25 Tomoegawa Paper Co. Ltd. Powder coating
EP0678564A3 (en) * 1994-04-22 1998-02-11 Tomoegawa Paper Co. Ltd. Powder coating
JP2020105262A (en) * 2018-12-26 2020-07-09 日鉄ケミカル&マテリアル株式会社 Epoxy resin powder coating

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