JPH04146980A - Coating composition for electronic part - Google Patents

Coating composition for electronic part

Info

Publication number
JPH04146980A
JPH04146980A JP27178990A JP27178990A JPH04146980A JP H04146980 A JPH04146980 A JP H04146980A JP 27178990 A JP27178990 A JP 27178990A JP 27178990 A JP27178990 A JP 27178990A JP H04146980 A JPH04146980 A JP H04146980A
Authority
JP
Japan
Prior art keywords
epoxy resin
resistance
dihydrazide
weight
parts
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.)
Granted
Application number
JP27178990A
Other languages
Japanese (ja)
Other versions
JPH0791506B2 (en
Inventor
Hiroshi Miyake
啓史 三宅
Tatsuya Toyoshima
豊島 達也
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.)
NOF Corp
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Nippon Oil and Fats 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 Matsushita Electric Industrial Co Ltd, Nippon Oil and Fats Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP2271789A priority Critical patent/JPH0791506B2/en
Publication of JPH04146980A publication Critical patent/JPH04146980A/en
Publication of JPH0791506B2 publication Critical patent/JPH0791506B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To improve the solder resistance, insulation resistance, moisture resistance, heat resistance and durability of a cured coating film and storage stability as a one-pack type by compounding an epoxy resin, a specified dihydrazide compd. and an inorg. extender pigment. CONSTITUTION:The title compsn. is obtd. by compounding 100 pts.wt. epoxy resin which is pref. a bisphenol A type epoxy resin and/or a cresol novolak type epoxy resin, 10-60 pts.wt. dihydrazide compd. contg. 70wt.% or more aliph. dihydrazide compd. of the formula (wherein n is 8-10) which is a curing agent for the epoxy resin, 60-150 pts.wt. inorg. extender pigment consisting of an inorg. filler and, if necessary, a coloring pigment, an anti-sag agent, a (non)- reactive diluent, a flame-retardant, etc.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は電子部品の絶縁防湿保護に適した塗料組成物に
関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a coating composition suitable for the insulation and moisture-proof protection of electronic components.

〔従来の技術〕[Conventional technology]

エポキシ樹脂は、電気絶縁性、耐湿性、機械的および熱
的特性などにすぐれており、たとえば表面に抵抗体とし
ての炭素皮膜や金属皮膜を有する固定抵抗器などの各種
電子部品の絶縁防湿保護用として広く使用されている。
Epoxy resin has excellent electrical insulation, moisture resistance, mechanical and thermal properties, and is used for insulation and moisture-proof protection of various electronic components such as fixed resistors that have a carbon film or metal film on the surface as a resistor. It is widely used as

この種の用途にエポキシ樹脂を使用する場合、エポキシ
樹脂と適当な硬化剤とを組み合せて、硬化させるという
方法がとられるが、ここで用いる硬化剤としては、たと
えばポリアミン、酸無水物、フェノール、イミダゾール
、ジシアンジアミド、三弗化はう素のアミン錯体、ジヒ
ドラジドなどが知られている。
When using an epoxy resin for this type of application, a method is used in which the epoxy resin and an appropriate curing agent are combined and cured. Examples of curing agents used here include polyamines, acid anhydrides, phenols, Imidazole, dicyandiamide, amine complex of fluorine trifluoride, dihydrazide, etc. are known.

しかし、ポリアミン、酸無水物、フェノールは、エポキ
シ樹脂と混合すると室温でも硬化反応が進むため、可使
時間が制限される。このため、実際には、エポキシ樹脂
と硬化剤とを別容器に保管して、使用直前に両者を必要
量だけ混合する、いわゆる二液型として取り扱う必要が
あり、作業上面倒であり、またこのように混合させたも
のの使用残りはゲル化して使用不能となるため、経済的
にも不利である。
However, when polyamines, acid anhydrides, and phenols are mixed with epoxy resins, curing reactions proceed even at room temperature, which limits their pot life. For this reason, in reality, it is necessary to store the epoxy resin and the curing agent in separate containers, and to handle them as a two-component type, by mixing only the required amounts of both immediately before use, which is cumbersome and difficult to handle. The remainder of the mixture becomes gelled and becomes unusable, which is economically disadvantageous.

これに対し、イミダゾール、ジシアンジアミド、三弗化
はう素のアミン錯体、ジヒドラジドには、上記欠点がな
く、−液量の塗料として十分に取り扱うことができる。
On the other hand, imidazole, dicyandiamide, amine complexes of fluorine trifluoride, and dihydrazide do not have the above-mentioned drawbacks and can be adequately handled as a -liquid coating material.

しかるに、これら硬化剤のうち、イミダゾール、ジシア
ンジアミドは硬化塗膜の耐湿性に劣り、また三弗化はう
素のアミン錯体は加熱硬化時にアミンガスを発生して塗
膜を変色させるという欠点がある。
However, among these curing agents, imidazole and dicyandiamide have the disadvantage that the cured coating film has poor moisture resistance, and the amine complex of boron trifluoride generates amine gas during heat curing, causing discoloration of the coating film.

このことから、現状では、ジヒドラジドが、液量の塗料
として取り扱えて、かつ上記耐湿性や変色などの問題の
ない最も好適な硬化剤として、賞用されている。このよ
うなジヒドラジドとしては、特開昭60−127702
号公報に、芳香族系のジカルボン酸ジヒドラジドや、複
素環を有する2、4−ジヒドラジン−6−アルキルアミ
ノトリアジンなどが示されている。
For this reason, dihydrazide is currently being used as the most suitable curing agent that can be handled as a liquid paint and does not have the above-mentioned problems such as moisture resistance and discoloration. As such dihydrazide, Japanese Patent Application Laid-Open No. 60-127702
The publication discloses aromatic dicarboxylic acid dihydrazide, 2,4-dihydrazine-6-alkylaminotriazine having a heterocycle, and the like.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかるに、上記公知のジヒドラジドは、上述の如き長所
はあるものの、硬化塗膜の耐ハンダ性に劣り、ハンダ浴
への浸漬後に硬化塗膜にクラックが発生して、電子部品
が前記固定抵抗器の場合、上記クラックの発生で抵抗値
が大きく増大するという問題があった。
However, although the above-mentioned known dihydrazides have the above-mentioned advantages, the cured coating film is inferior in solder resistance, and cracks occur in the cured coating film after being immersed in a solder bath, causing electronic components to be damaged by the fixed resistor. In this case, there was a problem in that the resistance value greatly increased due to the occurrence of the above-mentioned cracks.

本発明は、このような従来技術の問題点を克服し、併せ
て近年特に家電製品や電子機器などに対して厳しく要求
されている他の各種特性をも満足する電子部品用塗料組
成物を提供することを目的としている。
The present invention provides a coating composition for electronic components that overcomes the problems of the prior art and also satisfies various other properties that have been strictly required in recent years, especially for home appliances and electronic devices. It is intended to.

すなわち、本発明の目的は、硬化塗膜の耐ハンダ性にす
ぐれ、また塗膜本来の耐絶縁性、耐湿性、耐熱性、耐久
性(冷・熱サイクル性)などの特性をも満足するエポキ
シ樹脂組成物であって、かつこの組成物が一液型として
良好な貯蔵安定性を有すると共に、硬化時には所定の加
熱温度で速やかに硬化できるような電子部品用塗料組成
物を捉供することにある。
That is, the object of the present invention is to develop an epoxy resin that has excellent solder resistance in a cured coating film, and also satisfies the properties inherent in the coating film, such as insulation resistance, moisture resistance, heat resistance, and durability (cold/thermal cycling resistance). An object of the present invention is to provide a coating composition for electronic parts which is a resin composition, which has good storage stability as a one-component type, and which can be rapidly cured at a predetermined heating temperature when curing. .

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

本発明者らは、上記の目的を達成するために鋭意研究を
重ねた結果、エポキシ樹脂の硬化剤として脂肪族系の特
定のジヒドラジド化合物を用いたときに、前記の要求特
性をすべて満足する電子部品用塗料組成物が得られるこ
とを見い出し、本発明を完成した。
As a result of extensive research to achieve the above object, the present inventors have found that when a specific aliphatic dihydrazide compound is used as a curing agent for epoxy resin, an electronic It was discovered that a coating composition for parts can be obtained, and the present invention was completed.

すなわち、本発明は、つぎの1M1〜(e)三成分;(
alエポキシ樹脂 山)一般式(I); (式中、nは8〜10の実数である) で表される脂肪族系のジヒドラジド化合物を70重量%
以上含有するジヒドラジド化合物 (C)無機体質顔料 を必須成分とし、かつ上記+a)成分のエポキシ樹脂1
00重量部に対して(b)成分のジヒドラジド化合物が
10〜60重量部、(C)成分の無機体質顔料が60〜
15011量部であることを特徴とする電子部品用塗料
組成物に係るものである。
That is, the present invention provides the following three components 1M1 to (e);
al epoxy resin) 70% by weight of an aliphatic dihydrazide compound represented by general formula (I); (wherein n is a real number from 8 to 10)
The dihydrazide compound (C) containing the above inorganic extender pigment as an essential component, and the epoxy resin 1 of the above +a) component
00 parts by weight, the dihydrazide compound as the component (b) is 10 to 60 parts by weight, and the inorganic extender pigment as the component (C) is 60 to 60 parts by weight.
The present invention relates to a coating composition for electronic components, characterized in that the amount is 15,011 parts.

〔発明の構成・作用〕[Structure and operation of the invention]

本発明に用いられる(a)成分の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、タレゾールノボラ
ック型エポキシ樹脂、ビスフェノールF型エポキシ樹脂
、脂環式エポキシ樹脂、フェノールノボラック型エポキ
シ樹脂、有機二塩基酸のジグリシジルエステル、ヒダン
トイン環を有するエポキシ樹脂などが挙げられる。
The epoxy resin of component (a) used in the present invention includes bisphenol A epoxy resin, Talesol novolak epoxy resin, bisphenol F epoxy resin, alicyclic epoxy resin, phenol novolak epoxy resin, organic dibasic acid diglycidyl esters, epoxy resins having a hydantoin ring, and the like.

これらのエポキシ樹脂の中から、その一種または二種以
上が用いられるが、特に好ましくは、ビスフェノールA
型エポキシ樹脂(エポキシ当量300以下)および/ま
たはタレゾールノボラック型エポキシ樹脂を用いるのが
よい。
One or more of these epoxy resins can be used, but bisphenol A is particularly preferred.
It is preferable to use a type epoxy resin (epoxy equivalent: 300 or less) and/or a Talesol novolac type epoxy resin.

本発明番こおいて上記のエポキシ樹脂の硬化剤として使
用する…)成分のジヒドラジド化合物としては、つぎの
一般式(I): Hz N HN C(CHzト。CNHNH,・・・ 
(7)(式中、nは8〜10の実数である) で表される脂肪族系のジヒドラジド化合物、つまリセバ
シン酸および/またはドデカンジカルボン酸のジヒドラ
ジド化合物が用いられる。
In the present invention, the dihydrazide compound used as a curing agent for the above-mentioned epoxy resin has the following general formula (I): Hz NHNH, .
An aliphatic dihydrazide compound represented by (7) (wherein n is a real number of 8 to 10), that is, a dihydrazide compound of risebacic acid and/or dodecanedicarboxylic acid, is used.

ここで、一般式中のnが7以下となる、たとえばしゆう
酸、コハク酸、マロン酸、アジピン酸などの脂肪族ジカ
ルボン酸のジヒドラジド化合物では、塗膜の耐湿性が悪
くなる。一般式中のnが11以上となる脂肪族ジカルボ
ン酸のジヒドラジド化合物では、耐熱性が悪く、また市
販品として入手しがたく、実用的でない。
Here, in dihydrazide compounds of aliphatic dicarboxylic acids such as oxalic acid, succinic acid, malonic acid, and adipic acid, in which n in the general formula is 7 or less, the moisture resistance of the coating film becomes poor. Dihydrazide compounds of aliphatic dicarboxylic acids in which n in the general formula is 11 or more have poor heat resistance and are difficult to obtain as commercial products, making them impractical.

本発明では、上述のように、一般式中のnが8〜10で
ある脂肪族系の特定のジヒドラジド化合物を用いること
を特徴とするが、この化合物の使用量が(bl成分のジ
ヒドラジド化合物全体の70重量%以上、好ましくは7
5重量%以上であれば、本発明の前記目的は達成される
。この場合、残り30重量%以下のジヒドラジド化合物
は、一般式中のnが7以下あるいは11以上となる上記
脂肪族系のジヒドラジド化合物であってもよいし、従来
公知の前記芳香族系のジカルボン酸ジヒドラジドなどで
あってもよい。
As mentioned above, the present invention is characterized by using a specific aliphatic dihydrazide compound in which n in the general formula is 8 to 10. 70% by weight or more, preferably 7% by weight of
If the amount is 5% by weight or more, the above object of the present invention can be achieved. In this case, the remaining 30% by weight or less of the dihydrazide compound may be the above-mentioned aliphatic dihydrazide compound in which n in the general formula is 7 or below or 11 or above, or the above-mentioned conventionally known aromatic dicarboxylic acid. Dihydrazide and the like may also be used.

本発明に使用される(cl成分の無機体質顔料は、塗料
組成物を電子部品に塗布する際の垂れをなくし、また塗
膜の耐久性(冷・熱サイクル性)、耐湿性や、その他機
械的強度などを保持させるために必要不可欠な成分であ
って、電子部品封止材料などに用いられる公知の無機質
フィラー、たとえばシリカ(粒度5〜50μm)、アル
ミナ、水和アルミナ、水和マグネシウム、タルク、マイ
カ、炭酸カルシウム、硫酸バリウム、炭酸バリウム、ジ
ルコニア、窒化珪素、窒化ホウ素、窒化アルミニウム、
クレイなどが用いられる。
The inorganic extender pigment (cl component) used in the present invention eliminates dripping when applying the paint composition to electronic parts, and also improves the durability (cold/thermal cycle resistance), moisture resistance, and other mechanical properties of the paint film. Known inorganic fillers that are essential for maintaining physical strength and are used in electronic component sealing materials, such as silica (particle size 5 to 50 μm), alumina, hydrated alumina, hydrated magnesium, and talc. , mica, calcium carbonate, barium sulfate, barium carbonate, zirconia, silicon nitride, boron nitride, aluminum nitride,
Clay etc. are used.

本発明において、上記伸)〜rc+三成分の混合割合と
しては、(81成分100重量部に対して、(bl成分
が10〜60重量部、好ましくは25〜50重量部で、
tc+成分が60〜150重量部、好ましくは70〜1
20M量部である。
In the present invention, the mixing ratio of the above-mentioned elongation) to rc+ three components is 10 to 60 parts by weight, preferably 25 to 50 parts by weight of the BL component to 100 parts by weight of the 81 components,
tc+ component is 60-150 parts by weight, preferably 70-1
The amount is 20M parts.

(b)成分が10重量部未満となると、本発明の効果が
得られに<<、特に硬化性や塗膜の耐湿性、耐ハンダ性
などの特性が損なわれ、また60重量部を超えても、そ
れ以上の性能の向上は期待できず、コスト的に不利とな
る。さらに、(C1成分が60重量部未満となると、塗
料の垂れ防止や塗膜の耐久性(冷・熱サイクル性)、耐
湿性などの向上効果が得られず、また150重量部を超
えると、塗膜の耐湿性や機械的強度などの低下を引き起
こす結果となる。
If component (b) is less than 10 parts by weight, the effects of the present invention may not be obtained, and properties such as curability, moisture resistance, and solder resistance of the coating film may be impaired, and if it exceeds 60 parts by weight, However, no further improvement in performance can be expected, and it is disadvantageous in terms of cost. Furthermore, if the C1 component is less than 60 parts by weight, it will not be possible to prevent paint from dripping, improve the durability of the paint film (cold/thermal cycling properties), and moisture resistance, and if it exceeds 150 parts by weight, This results in a decrease in the moisture resistance and mechanical strength of the coating film.

本発明の塗料組成物は、以上のfat〜(C)三成分を
必須成分として用いるほか、必要に応して一般の塗料に
使用されている着色顔料(たとえば二酸化チタン、カー
ボンブラック、弁柄、黄色酸化鉄などの無機着色顔料や
各種の有機着色顔料)、レオロジーコントロール用の各
種型れ止め剤(たとえば粒度1.0μm以下の微粉シリ
カ、有機ベントナイトなど)、レヘリング剤、消泡剤、
カップリング剤などを使用してもよい。
The coating composition of the present invention uses the above three components fat to (C) as essential components, and if necessary, coloring pigments used in general coatings (such as titanium dioxide, carbon black, Bengara, Inorganic coloring pigments such as yellow iron oxide and various organic coloring pigments), various anti-moulding agents for rheology control (for example, fine powder silica with a particle size of 1.0 μm or less, organic bentonite, etc.), leveling agents, antifoaming agents,
A coupling agent or the like may also be used.

また、各種の非反応性希釈剤(ジオクチルフタレート、
ジブチルフタレ−1・などの可塑剤)、反応性希釈剤(
フェニルグリシジルエーテル、プチルグルンジルユーテ
ルなどの前記ta)成分のエポキシ樹脂よりも低分子量
でかつ低粘度のエポキシ基含有化合物など)、有機溶剤
、難燃性を付与するための公知の難燃剤(ブロム化エポ
キシ樹脂、リン酸エステル類、三酸化アンチモンなど)
も使用可能である。
In addition, various non-reactive diluents (dioctyl phthalate,
plasticizers such as dibutyl phthalate-1), reactive diluents (
epoxy group-containing compounds having a lower molecular weight and lower viscosity than the epoxy resin of component ta), such as phenyl glycidyl ether and butylgrundyle ether), organic solvents, and known flame retardants for imparting flame retardance (bromine, etc.); epoxy resins, phosphate esters, antimony trioxide, etc.)
is also available.

さらに、硬化温度の低下や硬化時間の短縮のために、硬
化触媒として、イミダゾール、三級アミン、カルボン酸
、クロロフェニル−1,1−N−ジメチル尿素、有機金
属化合物の塩などを使用してもよく、これらの中でも特
にイミダゾール、有機金属化合物の塩が好ましく用いら
れる。
Furthermore, in order to lower the curing temperature and shorten the curing time, imidazole, tertiary amines, carboxylic acids, chlorophenyl-1,1-N-dimethylurea, salts of organometallic compounds, etc. may be used as curing catalysts. Among these, imidazole and salts of organometallic compounds are particularly preferably used.

本発明の電子部品用塗料組成物は、一般に、以上の構成
成分を適宜の手段で均一に混合したー液型塗料として取
り扱われるが、この混合後の安定性にすくれており、た
とえば40℃下で1ケ月といった長期間の貯蔵中に粘度
が急激に増大したり、ゲル化するといった支障は起こら
ない。
The coating composition for electronic parts of the present invention is generally treated as a liquid coating composition in which the above-mentioned components are uniformly mixed by an appropriate means. During storage for a long period of time, such as one month, problems such as rapid increase in viscosity or gelation do not occur.

本発明の電子部品用塗料組成物は、上記各成分の均−混
合後に、固定抵抗器などの電子部品の表面に、常法によ
り塗布乾燥したのち、通常160〜180℃で1〜10
分という短時間の条件で加熱硬化させることにより、塗
布時に垂れなどの問題を生じることな(、厚さが通常2
0〜2.000μmとなるピンホールやクラックのない
外観の良好な硬化塗膜を形成することができる。
The coating composition for electronic components of the present invention is prepared by uniformly mixing the above-mentioned components, applying it to the surface of an electronic component such as a fixed resistor by a conventional method, and drying it.
By heating and curing in a short time of 2 minutes, problems such as dripping do not occur during application (the thickness is usually 2 minutes).
A cured coating film with a diameter of 0 to 2.000 μm and a good appearance without pinholes or cracks can be formed.

この硬化塗膜は、上記良好な外観に加えて、耐絶縁性、
耐湿性、耐熱性、耐久性(冷・熱サイクル性)などにす
ぐれ、しかも耐ハンダ性も良好で、ハンダ浴浸漬後に硬
化塗膜にクラックが発生してくるといった問題がなく、
固定抵抗器などの電子部品の絶縁防湿保護用として非常
に良好な性能を発揮する。
In addition to the above-mentioned good appearance, this cured coating film has insulation resistance and
It has excellent moisture resistance, heat resistance, durability (cold/thermal cycling), etc., and also has good solder resistance, and there are no problems such as cracks occurring in the cured coating after immersion in a solder bath.
It exhibits very good performance as insulation and moisture-proof protection for electronic components such as fixed resistors.

〔発明の効果〕〔Effect of the invention〕

以上のように、本発明の(al〜(C1三成分を必須と
した電子部品用塗料組成物によれば、貯蔵安定性の良好
な一液型塗料として取り扱えると共に、硬化時には所定
の加熱温度で速やかに硬化でき、しかもこの硬化塗膜の
耐ハンダ性やその他耐絶縁性、耐湿性、耐熱性、耐久性
(冷・熱サイクル性)などをすべて満足させることがで
きる。
As described above, according to the coating composition for electronic components of the present invention, which includes the three components (al to It can be cured quickly, and the cured coating film can satisfy all of the requirements such as solder resistance, insulation resistance, moisture resistance, heat resistance, and durability (cold/heat cycle resistance).

〔実施例〕〔Example〕

以下、実施例および比較例によって、本発明を具体的に
説明する。ただし、実施例は本発明を限定するものでは
ない。
Hereinafter, the present invention will be specifically explained with reference to Examples and Comparative Examples. However, the examples are not intended to limit the invention.

実施例1〜6および比較例1〜6 第1表の配合に基づいて、エポキシ樹脂、ジヒドラジド
化合物、無機体質顔料およびその他の成分を予め混合し
、この混合物を3本型ローラーを60℃に加熱しながら
粒度4oμmに分散混練して、実施例および比較例合わ
せて、12種類の電子部品用塗料組成物を調製した。
Examples 1 to 6 and Comparative Examples 1 to 6 Based on the formulations in Table 1, the epoxy resin, dihydrazide compound, inorganic extender pigment, and other components were mixed in advance, and the mixture was heated to 60°C using a three-roller. The mixture was dispersed and kneaded to a particle size of 4 μm to prepare 12 types of coating compositions for electronic components including Examples and Comparative Examples.

上記の各電子部品用塗料組成物を試料塗料として、下記
の7種の試験を行った。その結果は、後記の第2表に示
されるとおりであった。
The following seven types of tests were conducted using each of the above-mentioned electronic component coating compositions as sample coatings. The results were as shown in Table 2 below.

(1)貯蔵安定性 深さ80n、断面直径60鶴のガラスビンに、70fl
の深さまで試料塗料を入れて密閉し、40℃の恒温器中
に30日間静置して、初期と試験後との粘度をリオンビ
スコテスター(20℃;単位ポイズ)によって測定した
。試験後の粘度が初期の粘度の1.5倍以下のときを合
格とした。
(1) Storage stability: 70fl in a glass bottle with a depth of 80n and a cross-sectional diameter of 60mm.
A sample paint was poured into the container to a depth of 1,000 degrees Celsius, the container was sealed, and left to stand for 30 days in a constant temperature chamber at 40° C., and the initial and post-test viscosities were measured using a Rion Visco tester (20° C.; unit: poise). When the viscosity after the test was 1.5 times or less of the initial viscosity, it was considered to be passed.

(2)塗装作業性と外観 1/4W型IMΩの炭素皮膜固定抵抗器に、25℃に調
整した試料塗料を塗布し、170℃で10分加熱して硬
化させた。塗布時に垂れがなく、硬化塗膜の厚さが最低
200μm以上で外観にピンホールやクラックのないと
きを合格とした。
(2) Painting workability and appearance A sample paint adjusted to 25°C was applied to a 1/4W type IMΩ carbon film fixed resistor and cured by heating at 170°C for 10 minutes. The test was passed if there was no sagging during application, the thickness of the cured film was at least 200 μm or more, and there were no pinholes or cracks in appearance.

(3)耐湿性 試験(2)で塗装した抵抗器を、85℃、85%相対温
度の雰囲気中で、250 VDCで1.5時間通電後、
0.5時間無通電を1サイクルとして、250サイクル
の試験を行った。初期と試験後との抵抗値を測定して、
初期の抵抗値に対する試験後の抵抗値の変化率が±5%
以内であるときを合格とした。
(3) Moisture resistance test The resistor coated in (2) was energized at 250 VDC for 1.5 hours in an atmosphere of 85°C and 85% relative temperature.
A test was conducted for 250 cycles, with 0.5 hours of no current being applied as one cycle. Measure the resistance value at the initial stage and after the test,
The change rate of the resistance value after the test with respect to the initial resistance value is ±5%
If it was within the range, it was considered a pass.

(4)耐熱性 試験(2)で塗装した抵抗器を、155℃に調整したオ
ーブン中に1,000時間静置した。試験後、外観にク
ラックがなく、初期の抵抗値に対する試験後の抵抗値の
変化率が±1%以内であるときを合格とした。
(4) Heat Resistance Test The resistor coated in (2) was left standing in an oven adjusted to 155°C for 1,000 hours. After the test, if there were no cracks in the appearance and the rate of change in the resistance value after the test with respect to the initial resistance value was within ±1%, it was judged as passing.

(5)耐久性(冷・熱サイクル性) 試験(2)で塗装した抵抗器を、125℃×30分、2
5℃×10分、−55℃×30分の温度変化を1サイク
ルとして、5サイクルの試験を行った。
(5) Durability (cold/thermal cycling) The resistor coated in test (2) was heated at 125°C for 30 minutes for 2
Five cycles of the test were conducted, with temperature changes of 5° C. x 10 minutes and -55° C. x 30 minutes as one cycle.

試験後、外観にクラックがなく、初期の抵抗値に対する
試験後の抵抗値の変化率が±1%以内であるときを合格
とした。
After the test, if there were no cracks in the appearance and the rate of change in the resistance value after the test with respect to the initial resistance value was within ±1%, it was judged as passing.

(6)耐絶縁性 試験(2)で塗装した抵抗器を、直角の金属製■フロッ
クの内側に、両端がはみださないように置き、■ブロッ
クとリード線の間に500Vの直流電圧を2分間印加し
て、抵抗値を測定した。10,000MΩ以上を合格と
した。
(6) Insulation resistance test Place the resistor painted in (2) inside the right-angled metal flock so that both ends do not protrude, and apply 500V DC voltage between the block and the lead wire. was applied for 2 minutes and the resistance value was measured. A value of 10,000MΩ or more was considered to be a pass.

(7)耐ハンダ性 試験(2)で塗装した抵抗器を、沸騰水中で5分間煮沸
したのち、280℃のハンダ浴に10秒間浸漬した。試
験後、外観にクラックがなく、初期の抵抗値に対する試
験後の抵抗値の変化率が±5%以内であるときを合格と
した。
(7) Solder resistance test The resistor coated in (2) was boiled in boiling water for 5 minutes and then immersed in a 280°C solder bath for 10 seconds. After the test, if there were no cracks in the appearance and the rate of change in the resistance value after the test with respect to the initial resistance value was within ±5%, it was judged as passing.

上記の第2表の結果から明らかなように、本発明に係る
実施例1〜6の塗料組成物は、いずれの試験項目共、良
好な結果を示し、特に耐湿性や耐ハンダ性が良好で、電
子部品用塗料に対する要求特性を十分に満たしている。
As is clear from the results in Table 2 above, the coating compositions of Examples 1 to 6 according to the present invention showed good results in all test items, and in particular had good moisture resistance and solder resistance. , fully meets the required characteristics for paints for electronic parts.

これに対し、比較例1〜6の塗料組成物は、いずれかの
項目において不合格であり、特に耐湿性や耐ハンダ性に
劣り、電子部品用塗料に対する要求特性を満たしていな
い。なお、比較例4の塗料組成物は、硬化不十分であっ
たため、その後の塗膜性能試験は行わなかった。
On the other hand, the coating compositions of Comparative Examples 1 to 6 failed in any of the items, and were particularly poor in moisture resistance and solder resistance, and did not meet the required characteristics for coatings for electronic components. In addition, since the coating composition of Comparative Example 4 was insufficiently cured, subsequent coating film performance tests were not conducted.

代 理 人teenager Reason Man

Claims (1)

【特許請求の範囲】[Claims] (1) つぎの(a)〜(c)三成分; (a) エポキシ樹脂 (b) 一般式( I ); ▲数式、化学式、表等があります▼…( I ) (式中、nは8〜10の実数である) で表される脂肪族系のジヒドラジド化合物 を70重量%以上含有するジヒドラジド化 合物。 (c) 無機体質顔料 を必須成分とし、かつ上記(a)成分のエポキシ樹脂1
00重量部に対して(b)成分のジヒドラジド化合物が
10〜60重量部、(c)成分の無機体質顔料が60〜
150重量部であることを特徴とする電子部品用塗料組
成物。
(1) The following three components (a) to (c); (a) Epoxy resin (b) General formula (I); ▲There are numerical formulas, chemical formulas, tables, etc.▼...(I) (In the formula, n is 8 A dihydrazide compound containing 70% by weight or more of an aliphatic dihydrazide compound represented by: (c) Epoxy resin 1 containing an inorganic extender pigment as an essential component and the above component (a)
00 parts by weight, the dihydrazide compound as the component (b) is 10 to 60 parts by weight, and the inorganic extender pigment as the component (c) is 60 to 60 parts by weight.
A coating composition for electronic parts, characterized in that the content is 150 parts by weight.
JP2271789A 1990-10-09 1990-10-09 Coating composition for electronic parts Expired - Fee Related JPH0791506B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2271789A JPH0791506B2 (en) 1990-10-09 1990-10-09 Coating composition for electronic parts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2271789A JPH0791506B2 (en) 1990-10-09 1990-10-09 Coating composition for electronic parts

Publications (2)

Publication Number Publication Date
JPH04146980A true JPH04146980A (en) 1992-05-20
JPH0791506B2 JPH0791506B2 (en) 1995-10-04

Family

ID=17504876

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2271789A Expired - Fee Related JPH0791506B2 (en) 1990-10-09 1990-10-09 Coating composition for electronic parts

Country Status (1)

Country Link
JP (1) JPH0791506B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11286647A (en) * 1998-04-03 1999-10-19 Matsushita Electric Ind Co Ltd Coating material for fixed resistor

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57145121A (en) * 1981-03-05 1982-09-08 Dainippon Jushi Kenkyusho:Kk Epoxy resin composition containing dibasic acid dihydrazide as curing agent
JPS5949224A (en) * 1982-09-14 1984-03-21 Hitachi Chem Co Ltd Epoxy resin composition
JPS6020927A (en) * 1983-07-15 1985-02-02 Hitachi Chem Co Ltd One-pack epoxy resin composition
JPS6055025A (en) * 1983-09-06 1985-03-29 Toshiba Corp Epoxy resin composition
JPS60177018A (en) * 1984-02-23 1985-09-11 Matsushita Electric Works Ltd Epoxy resin composition
JPS6112724A (en) * 1984-06-27 1986-01-21 Toshiba Corp Epoxy resin composition
JPS6136318A (en) * 1984-07-30 1986-02-21 Hitachi Chem Co Ltd Epoxy resin composition

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57145121A (en) * 1981-03-05 1982-09-08 Dainippon Jushi Kenkyusho:Kk Epoxy resin composition containing dibasic acid dihydrazide as curing agent
JPS5949224A (en) * 1982-09-14 1984-03-21 Hitachi Chem Co Ltd Epoxy resin composition
JPS6020927A (en) * 1983-07-15 1985-02-02 Hitachi Chem Co Ltd One-pack epoxy resin composition
JPS6055025A (en) * 1983-09-06 1985-03-29 Toshiba Corp Epoxy resin composition
JPS60177018A (en) * 1984-02-23 1985-09-11 Matsushita Electric Works Ltd Epoxy resin composition
JPS6112724A (en) * 1984-06-27 1986-01-21 Toshiba Corp Epoxy resin composition
JPS6136318A (en) * 1984-07-30 1986-02-21 Hitachi Chem Co Ltd Epoxy resin composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11286647A (en) * 1998-04-03 1999-10-19 Matsushita Electric Ind Co Ltd Coating material for fixed resistor

Also Published As

Publication number Publication date
JPH0791506B2 (en) 1995-10-04

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