JPH0617454B2 - Flexible epoxy resin powder composition - Google Patents
Flexible epoxy resin powder compositionInfo
- Publication number
- JPH0617454B2 JPH0617454B2 JP63013626A JP1362688A JPH0617454B2 JP H0617454 B2 JPH0617454 B2 JP H0617454B2 JP 63013626 A JP63013626 A JP 63013626A JP 1362688 A JP1362688 A JP 1362688A JP H0617454 B2 JPH0617454 B2 JP H0617454B2
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- weight
- resin powder
- powder composition
- coating
- 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.)
- Expired - Lifetime
Links
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- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
- Organic Insulating Materials (AREA)
- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、交流電源用フィルムコンデンサ及び保安機能
を持つフィルムコンデンサ等に用いるエポキシ樹脂粉体
組成物に関し、過電圧下での充放電処理を行っても破壊
しない可撓性を有する塗膜を提供し得るエポキシ樹脂粉
体組成物に関するものである。TECHNICAL FIELD The present invention relates to an epoxy resin powder composition used for a film capacitor for an AC power supply, a film capacitor having a safety function, etc., and is subjected to charge / discharge treatment under overvoltage. The present invention relates to an epoxy resin powder composition capable of providing a coating film having flexibility that does not break even when it is used.
エポキシ樹脂粉体塗料は、特性面において、優れた接着
性、耐薬品性、熱安定性、機械的性質、絶縁性を有し、
作業面においては、無公害、省資源、省エネルギー化で
きる事から、電気絶縁材料など多方面に用いられてい
る。Epoxy resin powder coating has excellent adhesion, chemical resistance, thermal stability, mechanical properties, and insulation in terms of characteristics.
In terms of work, it is used in various fields such as electrical insulating materials because it is pollution free, resource saving and energy saving.
フィルムコンデンサに用いられているエポキシ樹脂粉体
塗料は、 一般的に硬い塗膜を形成し、機械的強度、耐湿性を満足
するものである。Epoxy resin powder coatings used for film capacitors generally form a hard coating film and satisfy mechanical strength and moisture resistance.
ところで、交流電源用フィルムコンデンサ及び保安機能
付きフィルムコンデンサは、時として過電圧がかかった
時に、外装被覆材料が膨張し、破壊して絶縁不良を起こ
すという危険がある。By the way, in the film capacitor for AC power supply and the film capacitor with a safety function, there is a risk that the exterior coating material sometimes expands and breaks when an overvoltage is applied to cause insulation failure.
この現象はJIS C4908「電気機器用コンデンサ」あ
るいは米国UL(Underwriter's Laboratories Inc.)141
4「Across-The-Line-CAPACITORS(交流電源コンデン
サ)」のDischarge Testとして規格されているものであ
る。This phenomenon is caused by JIS C4908 "Capacitors for electrical equipment" or US UL (Underwriter's Laboratories Inc.) 141
4 It is standardized as the Discharge Test of "Across-The-Line-CAPACITORS".
従来は、この種のフィルムコンデンサにも硬い塗膜を形
成するエポキシ樹脂粉体塗料が用いられていた。Conventionally, an epoxy resin powder coating which forms a hard coating film has also been used for this type of film capacitor.
それは、塗膜が充放電試験において、電極部の剥離をま
ねかなければ、破壊しても差しつかえなかったためであ
る。This is because, in the charge / discharge test, the coating film could be destroyed even if it was broken unless the electrode portion was peeled off.
しかし、蛍光灯、洗濯機、冷蔵庫などの家庭電気製品に
用いた時に、破壊し、発火するという事故が発生してい
る事より、外装被覆材料も破壊しない事が求められるよ
うになった。However, when it is used in household electric appliances such as fluorescent lamps, washing machines, and refrigerators, it has been destroyed and ignited. Therefore, it has been required that the exterior coating material should not be destroyed.
従来のエポキシ樹脂粉体塗料では過電圧の充放電試験に
より、外装被覆材料が破壊し、絶縁不良が発生するとい
う問題を避けることができなかったが、本発明者はこれ
を防止するため研究した結果、塗膜に可撓性を与える事
により、塗膜が充放電試験によるフィルムコンデンサの
膨張、収縮のストレスを吸収して破壊しないとの知見を
得、種々研究を進めて本発明を完成するに至ったもので
ある。With the conventional epoxy resin powder coating, the problem that the outer coating material is destroyed by the overvoltage charge / discharge test and the insulation failure is unavoidable, but the present inventors have studied to prevent this. In order to complete the present invention, we have obtained the knowledge that by giving flexibility to the coating film, the coating film does not break by absorbing the stress of expansion and contraction of the film capacitor due to the charge-discharge test, and it does not break. It has come.
本発明は、エポキシ樹脂が全体の70重量%以上であ
り、そのエポキシ樹脂の10〜30重量%がダイマー酸
変性エポキシ樹脂であり、エポキシ樹脂100重量部に
対し、酸無水物基2個以上、あるいは酸無水物基1個以
上とカルボキシル基1個以上有する酸無水物化合物を7
〜20重量部含む事を特徴とする可撓性エポキシ樹脂粉
体組成物に係るものである。In the present invention, the epoxy resin is 70% by weight or more of the whole, 10 to 30% by weight of the epoxy resin is a dimer acid-modified epoxy resin, and 100 parts by weight of the epoxy resin, 2 or more acid anhydride groups, Alternatively, an acid anhydride compound having at least one acid anhydride group and at least one carboxyl group may be used.
To 20 parts by weight of the flexible epoxy resin powder composition.
本発明で使用されるエポキシ樹脂は組成物全体の70重
量%以上である事が必須であり、70%未満では硬化物
に充分な可撓性が得られ難くなる。It is essential that the epoxy resin used in the present invention accounts for 70% by weight or more of the total composition, and if it is less than 70%, it becomes difficult to obtain sufficient flexibility in the cured product.
本発明で使用されるダイマー酸変性エポキシ樹脂の市販
品としては、例えば、エポトートYD−172(東都化
成(株)製、商品名)があげられる。ダイマー酸変性エ
ポキシ樹脂はエポキシ樹脂全体の10〜30重量%、好
ましくは15〜25重量%の範囲で混合して使用され
る。Examples of commercially available dimer acid-modified epoxy resin used in the present invention include Epotote YD-172 (trade name, manufactured by Toto Kasei Co., Ltd.). The dimer acid-modified epoxy resin is used by mixing in the range of 10 to 30% by weight, preferably 15 to 25% by weight, based on the whole epoxy resin.
ダイマー酸変性エポキシ樹脂を添加した場合には、得ら
れる樹脂硬化物の特性の中で特に可撓性が改善される。When the dimer acid-modified epoxy resin is added, flexibility is particularly improved among the properties of the resulting resin cured product.
ここで言うダイマー酸とは、リノール酸、リノレン酸、
オレイン酸の様な長鎖の脂肪酸の2量体であり、分子的
に長鎖部分の伸縮性が良好である。この化合物の末端部
にエポキシ基を導入する事によりダイマー酸変性エポキ
シ樹脂を得る事ができる。Dimer acid here means linoleic acid, linolenic acid,
It is a dimer of a long-chain fatty acid such as oleic acid, and has a molecularly good stretchability in the long-chain portion. A dimer acid-modified epoxy resin can be obtained by introducing an epoxy group into the terminal portion of this compound.
ダイマー酸変性エポキシ樹脂が硬化する際に、硬化物の
分子網に組み込まれた場合、硬化物自体の伸縮性、すな
わち可撓性が改善される事となる。When the dimer acid-modified epoxy resin is incorporated into the molecular network of the cured product when cured, the stretchability of the cured product itself, that is, flexibility is improved.
換言すれば、塗料として使用されると硬化物としての塗
膜がゴムのような良好な可撓性を有することが可能とな
る。In other words, when used as a paint, the coating film as a cured product can have good flexibility like rubber.
上記添加量が10重量%未満ではその効果が不十分であ
り、30重量%以上では融点が低下して保存中にブロッ
キング現象が生じ、塗装の際に粉体の流動性不良や塗装
むらを生じたり、使用が全く困難になる恐れもある。If the addition amount is less than 10% by weight, the effect is insufficient, and if it is 30% by weight or more, the melting point is lowered and a blocking phenomenon occurs during storage, resulting in poor fluidity of powder and uneven coating during coating. Or, it may be difficult to use.
本発明におけるダイマー酸変性エポキシ樹脂を除くエポ
キシ当量が1000以上の場合には、該エポキシ樹脂
は、エポキシ樹脂系塗料の特性である絶縁性、耐食性、
耐薬品性を付与する成分である。When the epoxy equivalent excluding the dimer acid-modified epoxy resin according to the present invention is 1000 or more, the epoxy resin has insulating properties, corrosion resistance, and
It is a component that imparts chemical resistance.
上記特性を満足させるエポキシ樹脂は、通常ビスフェノ
ールA型エポキシ樹脂あるいはノボラック型エポキシ樹
脂であり、各種グレードのものが単独あるいは混合して
用いられるが、平均してエポキシ樹脂当量が600〜1
000の範囲のものが好ましい。The epoxy resin satisfying the above characteristics is usually a bisphenol A type epoxy resin or a novolac type epoxy resin, and various grades are used alone or as a mixture, and the epoxy resin equivalent is 600 to 1 on average.
The range of 000 is preferable.
エポキシ当量が600未満の場合、該エポキシ樹脂の融
点が低いので、保存中にブロッキング現象が生じ、塗装
の際に粉の流動性不良を起こしたり、塗装むらを生じた
り、あるいは使用が全く困難になる恐れもある。また、
エポキシ当量が1000以上の場合には、該エポキシ樹
脂の融点が高いので、フィルムコンデンサ塗装の際に、
フィルムの融点以上の高温に加熱しなければならず、さ
もないと付着量が少なく、効率的な塗装作業が困難とな
る。When the epoxy equivalent is less than 600, since the melting point of the epoxy resin is low, a blocking phenomenon occurs during storage, which causes poor fluidity of powder during coating, uneven coating, or makes it completely difficult to use. There is also a fear of becoming. Also,
When the epoxy equivalent is 1000 or more, the melting point of the epoxy resin is high, so when coating the film capacitor,
It must be heated to a temperature higher than the melting point of the film, otherwise the amount of adhesion will be small and efficient painting will be difficult.
ノボラック型エポキシ樹脂はオルソクレゾール型エポキ
シ樹脂あるいはノボラック型エポキシ樹脂をいい、ダイ
マー酸変性エポキシ樹脂を除くエポキシ樹脂全体の20
重量%以下で使用するのが好ましい。ノボラック型エポ
キシ樹脂は耐湿性向上のために使用するものであるが、
通常20重量%を超えると塗膜がもろくなる傾向が強く
なり好ましくない。The novolac type epoxy resin is an ortho-cresol type epoxy resin or a novolac type epoxy resin.
It is preferably used in an amount of not more than wt%. The novolac type epoxy resin is used to improve the moisture resistance,
Usually, if it exceeds 20% by weight, the coating tends to become brittle, which is not preferable.
本発明で使用される硬化剤は、分子内に酸無水物基を2
個以上、あるいは酸無水物基を1個以上とカルボキシル
基を1個以上有する酸無水物硬化剤であり、例えば、無
水トリメリット酸、無水ピロメリット酸、エチレングリ
コールビストリメリテート、グリセロールトリストリメ
リテートなどがあげられる。上記酸無水物硬化剤は、分
子内に硬化に関与すると考えられる酸無水物基を2個以
上あるいは酸無水物基を1個以上とカルボキシル基を1
個以上有する事が必要である。これ以下の場合では、塗
膜化した時のフィルムコンデンサの耐湿性が不十分とな
り好ましくない。The curing agent used in the present invention has 2 acid anhydride groups in the molecule.
Or more, or an acid anhydride curing agent having one or more acid anhydride groups and one or more carboxyl groups, and examples thereof include trimellitic anhydride, pyromellitic dianhydride, ethylene glycol bis trimellitate, glycerol tris trimellitate. Tate etc. can be given. The above acid anhydride curing agent has two or more acid anhydride groups or one or more acid anhydride groups and one carboxyl group which are considered to be involved in curing in the molecule.
It is necessary to have more than one. If it is less than this, the moisture resistance of the film capacitor when formed into a coating film is insufficient, which is not preferable.
耐湿性は、塗膜を形成している高分子構造と相関がある
と考えられており、分子網が密になると向上する傾向が
ある。従って硬化網の拠点となる硬化剤は、官能基が多
いほど耐湿性には好ましいのである。Moisture resistance is considered to be correlated with the polymer structure forming the coating film, and tends to improve as the molecular network becomes denser. Therefore, it is preferable that the curing agent that serves as the base of the curing network has more functional groups for moisture resistance.
何れの上記硬化剤を使用する場合も、エポキシ樹脂10
0重量部に対して、7〜20重量部、特に9〜18重量
部が好ましい。この際7重量部未満では、硬化速度が著
しく低下し、硬化不足状態におちいるため、硬化物の機
械強度不足となり、可撓性が小さくもろい傾向を示し好
ましくない。When any of the above curing agents is used, the epoxy resin 10
With respect to 0 parts by weight, 7 to 20 parts by weight, particularly 9 to 18 parts by weight are preferable. At this time, if it is less than 7 parts by weight, the curing rate is remarkably reduced and the cured product is in an insufficiently cured state, so that the mechanical strength of the cured product becomes insufficient, and the flexibility tends to be small and brittle, which is not preferable.
20重量部より多くなると、保存性が悪くなり、場合に
よっては塗装時の溶融状態が良好でなくなるための平滑
性不足をまねく恐れがある。If the amount is more than 20 parts by weight, the storability is deteriorated, and in some cases, the molten state at the time of coating is not good, which may lead to lack of smoothness.
本発明のエポキシ樹脂粉体組成物は、前述した如き成分
を配合する事によって得られるが、シリカ、炭酸カルシ
ウム、硫酸バリウム、アルミナ粉、タルク、クレーの如
き各種充填剤、二酸化チタン、酸化亜鉛、酸化鉄、グラ
ファイトの如き顔料、流れ調整剤等の添加剤、ゲル化時
間及び硬化時間調整用にアミン類、イミダゾール誘導
体、等を可撓性に悪影響を及ぼさない範囲で添加する事
も出来る。The epoxy resin powder composition of the present invention can be obtained by mixing the components as described above, and various fillers such as silica, calcium carbonate, barium sulfate, alumina powder, talc and clay, titanium dioxide, zinc oxide, It is also possible to add pigments such as iron oxide and graphite, additives such as flow control agents, amines and imidazole derivatives for adjusting the gelation time and the curing time within a range that does not adversely affect flexibility.
本発明のエポキシ樹脂粉体組成物を予熱したフィルムコ
ンデンサに流動浸漬法の如き手段によって塗装を施して
得られる塗膜は、コンデンサの信頼性がすぐれているこ
とはもとより、充放電を繰り返しても、破壊あるいはひ
びも生じる事はなく、安全性向上に対して極めて効果が
大きい。The coating film obtained by applying a coating to a film capacitor preheated with the epoxy resin powder composition of the present invention by means such as a fluidized dipping method has excellent reliability of the capacitor, and even after repeated charging and discharging. It does not break or crack and is extremely effective in improving safety.
以下に本発明の実施例を示す。 Examples of the present invention will be shown below.
実施例1〜6 第1表に示す割合で各成分を配合し、ヘンシェルミキサ
ーにて予備混合後、2軸押出機にて混練してエポキシ樹
脂組成物とした。次に該組成物を粉砕して目的のエポキ
シ樹脂粉体組成物を得た。Examples 1 to 6 The components were blended in the proportions shown in Table 1, preliminarily mixed with a Henschel mixer, and then kneaded with a twin-screw extruder to give epoxy resin compositions. Next, the composition was pulverized to obtain an intended epoxy resin powder composition.
但し、第1表中のダイマー酸変性エポキシ樹脂は東都化
成(株)製YD−172(エポキシ当量約650)であ
り、クレゾールノボラック型エポキシ樹脂は日本化薬
(株)製EOCN−102S(エポキシ当量約220)
である。However, the dimer acid-modified epoxy resin in Table 1 is YD-172 (epoxy equivalent of about 650) manufactured by Tohto Kasei Co., Ltd., and the cresol novolac type epoxy resin is EOCN-102S (epoxy equivalent of Nippon Kayaku Co., Ltd.). 220)
Is.
比較例1〜6 第1表に示した配合で実施例と同様な操作によってエポ
キシ樹脂粉体組成物を得た。Comparative Examples 1 to 6 Epoxy resin powder compositions were obtained with the formulations shown in Table 1 by the same operations as in the examples.
以上の粉体組成物について、以下のようにして塗膜の充
放電試験を行った。With respect to the above powder composition, a charging / discharging test of the coating film was performed as follows.
塗膜の充放電試験方法 フィルムコンデンサを100℃に予熱して流動浸漬法に
て各エポキシ樹脂粉体塗料を膜厚500μmに塗装した
後、100℃の雰囲気中で2時間加熱し、次いで室温ま
で冷却した。得られた塗膜の状態をJIS C4908の保
安性試験に準じて調べた。Coating film charge / discharge test method After preheating the film capacitor to 100 ° C and applying each epoxy resin powder coating material to a film thickness of 500 μm by the fluid immersion method, heat it in the atmosphere of 100 ° C for 2 hours and then to room temperature. Cooled. The state of the obtained coating film was examined according to the safety test of JIS C4908.
判定は次のようにして行った。The judgment was performed as follows.
○:クラックが全く生じない。◯: No cracks occur.
×:クラックが生じた。X: A crack was generated.
フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 H01B 3/40 F 9059−5G H01G 4/18 327 Z 8019−5E Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location H01B 3/40 F 9059-5G H01G 4/18 327 Z 8019-5E
Claims (1)
り、そのエポキシ樹脂の10〜30重量%がダイマー酸
変性エポキシ樹脂であり、エポキシ樹脂100重量部に
対し、酸無水物基を2個以上、あるいは酸無水物基1個
以上とカルボキシル基1個以上有する酸無水物硬化剤を
7〜20重量部含む事を特徴とする可撓性エポキシ樹脂
粉体組成物。1. Epoxy resin accounts for 70% by weight or more of the whole, 10 to 30% by weight of the epoxy resin is a dimer acid-modified epoxy resin, and two acid anhydride groups are added to 100 parts by weight of the epoxy resin. A flexible epoxy resin powder composition comprising the above or 7 to 20 parts by weight of an acid anhydride curing agent having at least one acid anhydride group and at least one carboxyl group.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63013626A JPH0617454B2 (en) | 1988-01-26 | 1988-01-26 | Flexible epoxy resin powder composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63013626A JPH0617454B2 (en) | 1988-01-26 | 1988-01-26 | Flexible epoxy resin powder composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01190724A JPH01190724A (en) | 1989-07-31 |
JPH0617454B2 true JPH0617454B2 (en) | 1994-03-09 |
Family
ID=11838445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63013626A Expired - Lifetime JPH0617454B2 (en) | 1988-01-26 | 1988-01-26 | Flexible epoxy resin powder composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0617454B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW291492B (en) * | 1994-06-23 | 1996-11-21 | Kansai Paint Co Ltd | |
US20140349109A1 (en) * | 2011-12-07 | 2014-11-27 | State of Oregon acting by and through the State Board of Higher Education of behalf of Oregon | Pressure sensitive adhesives based on carboxylic acids and epoxides |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58187465A (en) * | 1982-04-28 | 1983-11-01 | Asahi Chem Ind Co Ltd | Epoxy resin composition for powder paint having flexibility |
-
1988
- 1988-01-26 JP JP63013626A patent/JPH0617454B2/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
垣内弘編「新エポキシ樹脂」(昭60−5−10)昭晃堂P.276−277,P.594 |
Also Published As
Publication number | Publication date |
---|---|
JPH01190724A (en) | 1989-07-31 |
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