JPH0211667A - Epoxy resin powder coating composition - Google Patents

Epoxy resin powder coating composition

Info

Publication number
JPH0211667A
JPH0211667A JP15940088A JP15940088A JPH0211667A JP H0211667 A JPH0211667 A JP H0211667A JP 15940088 A JP15940088 A JP 15940088A JP 15940088 A JP15940088 A JP 15940088A JP H0211667 A JPH0211667 A JP H0211667A
Authority
JP
Japan
Prior art keywords
epoxy resin
bisphenol
powder coating
coating composition
curing agent
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
JP15940088A
Other languages
Japanese (ja)
Inventor
Kiyoshi Masuda
増田 喜好
Susumu Hosojima
細島 進
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.)
Sumitomo Bakelite Co Ltd
Sumitomo Durez Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
Sumitomo Durez 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 Sumitomo Bakelite Co Ltd, Sumitomo Durez Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP15940088A priority Critical patent/JPH0211667A/en
Publication of JPH0211667A publication Critical patent/JPH0211667A/en
Pending legal-status Critical Current

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  • Paints Or Removers (AREA)

Abstract

PURPOSE:To obtain the title composition improved in flow and adhesion to substrate without detriment to its electrical properties, etc., by mixing an epoxy resin with a curing agent comprising bisphenol A, a filler, etc. CONSTITUTION:An epoxy resin (a) (e.g., o-cresol novolac epoxy resin) is mixed with a curing agent (b) comprising bisphenol A of a single MW of about 200 in an amount to give an equivalent ratio of the OH groups of component (b) to the epoxy groups of component (a) of 0.5-1.5, desirably, 0.9-1.1, a filler (c) such as an inorganic powder such as CaCO3, silica or Al(OH)3 and, optionally, a coupling agent, a pigment, a cure accelerator, etc., (d).

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、粉体塗料の流れ性が絶大で、かつ素子(被塗
物)との密着性も強靭となるエポキシ樹脂粉体塗ネ4組
成物に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention provides an epoxy resin powder coating material 4 that has excellent flowability and strong adhesion to elements (objects to be coated). The present invention relates to a composition.

〔従来の技術〕[Conventional technology]

エポキシ樹脂粉体塗料の用途は種々である。例えばモー
ターの絶縁、電気、電子部品の絶縁、さらには電線ある
いは各種電気製品のカバー等に実用化されている。
Epoxy resin powder coatings have various uses. For example, it has been put to practical use in motor insulation, electrical and electronic component insulation, and even as covers for electric wires and various electrical products.

従来、これらの↑5)体塗料の構成は、エポキシ樹脂の
一部としてノボラック型エポキシ樹脂を使用したもの、
ノボランク型エポキシ樹脂と硬化剤としてフェノールノ
ボラックを使用したもの、あるいは硬化剤としてTMA
 <無水トリメリット酸)を使用したものなどがあった
Conventionally, these ↑5) body paints used a novolak type epoxy resin as part of the epoxy resin;
Novolank type epoxy resin and phenol novolac as a hardening agent, or TMA as a hardening agent
There were some that used trimellitic anhydride).

これらの粉体塗料は、上記した各種用途に粉体塗装され
、それを焼成する際、溶融時に流れ性を保有するもので
ある。特にモータのコイルの固着剤などに用いられる場
合、従来使われている粉体塗料はその流れ性が小さいた
めにコイル間のすき間に含浸せずコイル表面に被覆層を
形成し放熱効果をさまたげるという問題があり、流れ性
が絶大な粉体塗料が求められていた。
These powder coatings are powder-coated for the various uses mentioned above, and when they are fired, they retain flowability when melted. In particular, when used as a fixing agent for motor coils, conventionally used powder coatings have low flowability, so they do not impregnate the gaps between the coils, forming a coating layer on the coil surface, which hinders heat dissipation. There was a need for a powder coating with excellent flowability.

(発明が解決しようとする課題〕 本発明者らは、硬化溶融時の流れ性が絶大で被塗物との
密着性が強靭な粉体塗料を開発するために種々検討した
結果、エポキシ樹脂、硬化剤、充填剤等からなる粉体塗
料において、硬化剤としてビスフェノール八を含有する
ことにより、電気特性および他の緒特性を劣化させるこ
となく、流れ性、密着性が著しく優れた扮体塗す4組成
物が得られることを見出した。
(Problems to be Solved by the Invention) As a result of various studies conducted by the present inventors in order to develop a powder coating that has excellent flowability during curing and melting and has strong adhesion to the coated object, the inventors have found that epoxy resin, By containing bisphenol 8 as a hardening agent in powder coatings consisting of hardeners, fillers, etc., it is possible to create coatings with extremely excellent flowability and adhesion without deteriorating electrical properties or other properties. It was found that four compositions were obtained.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は、エポキシ樹脂、硬化剤、充填剤等から成り、
硬化剤としてビスフェノールAを含有することを特徴と
するエポキシ樹脂粉体塗料組成物である。
The present invention consists of an epoxy resin, a hardening agent, a filler, etc.
This is an epoxy resin powder coating composition characterized by containing bisphenol A as a curing agent.

エポキシ樹脂としては、ビスフェノールA型エポキシ樹
脂、ノボラックエポキシ樹脂、脂環式エポキシ樹脂等を
用い得るが、本発明ではそれらを限定するものではない
As the epoxy resin, bisphenol A type epoxy resin, novolak epoxy resin, alicyclic epoxy resin, etc. can be used, but the present invention is not limited thereto.

充填剤としては炭酸カルシウム、シリカ、水酸化アルミ
ニウム等の無機物粉末を用いるが、本発明ではそれらを
限定するものではない、またカップリング剤、顔料等は
必要に応じて用いても良い。
Inorganic powders such as calcium carbonate, silica, and aluminum hydroxide are used as fillers, but the present invention is not limited to them. Coupling agents, pigments, etc. may be used as necessary.

本発明によるエポキシ樹脂わ1体塗料はエポキシ樹脂、
ビスフェノールA、硬化促進剤、顔料、その他の添加剤
を押し出し機、ロールなどにより混練、冷却した後希望
する粒度に粉砕して得られる。
The epoxy resin paint according to the present invention includes an epoxy resin,
It is obtained by kneading bisphenol A, a hardening accelerator, a pigment, and other additives using an extruder or roll, cooling, and then pulverizing to a desired particle size.

〔作   用〕[For production]

本た明は硬化剤としてビスフェノール八を用いることに
特徴がある。
This invention is characterized by the use of bisphenol 8 as a curing agent.

硬化剤としてフェノールノボラック樹脂を用いることは
公知の技術であるが、これを用いた粉体塗料は流れ性が
小さい欠点がある。この理由はフェノールノボラック樹
脂は分子量が大きく (平均分子量400〜1000)
 、広い分子量分布をもっているためと考えられる。そ
こで分子量が200で、単一分子量のビスフェノールA
を用いることで始めて大きな流れ性を得ることが出来た
ものである。
Although it is a known technique to use a phenol novolak resin as a curing agent, powder coatings using this resin have a drawback of poor flowability. The reason for this is that phenol novolak resin has a large molecular weight (average molecular weight 400-1000).
This is thought to be due to the wide molecular weight distribution. Therefore, bisphenol A with a molecular weight of 200 and a single molecular weight
It was only by using this that great flowability could be achieved.

硬化剤としてビスフェノールへの配合量は通常エポキシ
樹脂のエポキシ基に対するビスフェノールAの水酸基の
当量比において0.5〜1.5であり、好ましくは0.
9〜1.1である。ビスフェノールへが0.5より少な
いと、流れ性が小さくなり、実用的でない場合もある。
The amount of bisphenol added as a curing agent is usually 0.5 to 1.5, preferably 0.5 to 1.5, based on the equivalent ratio of the hydroxyl group of bisphenol A to the epoxy group of the epoxy resin.
It is 9-1.1. When the amount of bisphenol is less than 0.5, the flowability becomes low and may not be practical.

1.5より多く配合すると密着性が小さくなる(川向が
ある。
If the amount is more than 1.5, the adhesion will decrease (there is a problem).

しかし、本発明者らの検討の結果、ビスフェノールAは
硬化速度が遅いので、工業的には用途が限定されること
が考えられる。それを改良するために、硬化促進剤を併
用するのが好ましい。
However, as a result of studies conducted by the present inventors, bisphenol A has a slow curing speed, so it is thought that its industrial use is limited. In order to improve this, it is preferable to use a curing accelerator in combination.

硬化促進剤のIl類および配合量はゲル化時間、二次転
移点等と流れ性とのバランスを考慮して決める必要があ
るが、実験結果から、通常の場合においては、前記硬化
促進剤の配合割合はエポキシ樹脂に対して15重量%以
下とするのが好ましい。
The type Il of the curing accelerator and its blending amount must be determined by considering the balance between gelation time, secondary transition point, etc., and flowability, but from the experimental results, in normal cases, the curing accelerator The blending ratio is preferably 15% by weight or less based on the epoxy resin.

15重噴筒以上では良好な流れ性が得られないことが多
いからである。
This is because good flowability is often not obtained with 15 or more injection tubes.

硬化促進剤としては例えば、 (11エチレンジアミン、トリエチレンテトラミン等の
脂肪族ポリアミン、モノエタノールアミン、プロパツー
ルアミン等の脂肪族ヒドロキシルアミン、メクフエニレ
ンジアミン、4.4′−ジアミノフェニルメタン等の号
香族アミン、ピペラジン、1−リエチレンジアミン等の
環状構造を有する脂肪族アミン等のアミン化合物、 (2)  フタール酸、マレイン酸、テトラヒドロフク
ール酸、トリメリット酸、アゼライン酸、ベンゾフェノ
ンテトラカルボン酸、アジピン酸等の多価カルボン酸又
はその無水物、 (3)  その他、ジシアンジアミド、カルボン酸、ジ
ヒドラジド、第三級アミン、イミダゾール類等の窒素含
有化合物、及び有機酸金属塩等、がありこれらは限定す
るものではない。
Examples of curing accelerators include (11) aliphatic polyamines such as ethylenediamine and triethylenetetramine, aliphatic hydroxylamines such as monoethanolamine and propatoolamine, mekphenylenediamine, and 4,4'-diaminophenylmethane. Amine compounds such as aliphatic amines having a cyclic structure such as aromatic amines, piperazine, and 1-lyethylenediamine; (2) phthalic acid, maleic acid, tetrahydrofucuric acid, trimellitic acid, azelaic acid, benzophenonetetracarboxylic acid; Polyhydric carboxylic acids such as adipic acid or their anhydrides, (3) Other nitrogen-containing compounds such as dicyandiamide, carboxylic acids, dihydrazides, tertiary amines, imidazoles, and organic acid metal salts, but these are limited. It's not something you do.

〔実 施 例〕〔Example〕

第1表に示す各実施例、各比較例において、それぞれの
組成材料を溶融混練した後、冷却し粉砕し、得られた粉
体塗料の流れ性、密着性を測定した。
In each of the Examples and Comparative Examples shown in Table 1, the respective composition materials were melt-kneaded, cooled and pulverized, and the flowability and adhesion of the resulting powder coatings were measured.

流れ性は13■1φの金型を用いて粉体塗ネ40.5g
を200 kg / cdで圧縮してタブレットを得、
このタブレフトを150℃の電気加熱炉内で表面平滑な
10度傾斜の鉄板上に乗せ、溶融させ、30分後の流れ
た長さを測定した。
Flowability is 13.40.5g powder coated using a 1φ mold.
is compressed at 200 kg/cd to obtain a tablet,
This tablet left was placed on a 10 degree inclined iron plate with a smooth surface in an electric heating furnace at 150° C. to melt it, and the length of flow after 30 minutes was measured.

密着性は、JIS  K6850r引張り剪断接着強さ
試験方法」により、鉄−鉄の接着部分に粉体塗$1o、
3gを挟み、電気加熱炉内テ200℃30分焼成して試
験片を得、この試験片を120℃熱間内で引張剪断接着
強度を試験した。
Adhesion was determined using the JIS K6850r tensile shear adhesive strength test method, with powder coating applied to the iron-to-iron bonded area for $10,000.
A test piece was obtained by sandwiching 3 g of the sample and baking it for 30 minutes at 200°C in an electric heating furnace, and the tensile shear adhesive strength of this test piece was tested at 120°C.

〔発明の効果〕〔Effect of the invention〕

本発明の粉体塗料組成物は、硬化剤としてビスフェノー
ル八を含有しているので流れ性が絶大であり、得られた
塗膜は密着性が著しく優れている。
Since the powder coating composition of the present invention contains bisphenol 8 as a curing agent, it has excellent flowability, and the resulting coating film has extremely excellent adhesion.

このような特長から、粉体塗料として、特にモーフのコ
イル固着用などの大きな流れ性が要求される用途に対し
て極めて好適である。
Because of these features, it is extremely suitable as a powder coating, particularly for applications that require great flowability, such as for fixing Morph coils.

Claims (1)

【特許請求の範囲】[Claims] (1)エポキシ樹脂、硬化剤、充填剤等から成り、硬化
剤としてビスフェノールAを含有することを特徴とする
エポキシ樹脂粉体塗料組成物。
(1) An epoxy resin powder coating composition comprising an epoxy resin, a curing agent, a filler, etc., and containing bisphenol A as the curing agent.
JP15940088A 1988-06-29 1988-06-29 Epoxy resin powder coating composition Pending JPH0211667A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15940088A JPH0211667A (en) 1988-06-29 1988-06-29 Epoxy resin powder coating composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15940088A JPH0211667A (en) 1988-06-29 1988-06-29 Epoxy resin powder coating composition

Publications (1)

Publication Number Publication Date
JPH0211667A true JPH0211667A (en) 1990-01-16

Family

ID=15692945

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15940088A Pending JPH0211667A (en) 1988-06-29 1988-06-29 Epoxy resin powder coating composition

Country Status (1)

Country Link
JP (1) JPH0211667A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002275410A (en) * 2001-03-19 2002-09-25 Sumitomo Bakelite Co Ltd Epoxy resin powder coating composition
KR100988637B1 (en) * 2008-10-29 2010-10-18 김재명 Organic coating composition and construction method thereby

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002275410A (en) * 2001-03-19 2002-09-25 Sumitomo Bakelite Co Ltd Epoxy resin powder coating composition
JP4736213B2 (en) * 2001-03-19 2011-07-27 住友ベークライト株式会社 Epoxy resin powder coating composition
KR100988637B1 (en) * 2008-10-29 2010-10-18 김재명 Organic coating composition and construction method thereby

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