JP2007317633A - Resin composition for insulating electric apparatus, and electric apparatus - Google Patents

Resin composition for insulating electric apparatus, and electric apparatus Download PDF

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JP2007317633A
JP2007317633A JP2006257070A JP2006257070A JP2007317633A JP 2007317633 A JP2007317633 A JP 2007317633A JP 2006257070 A JP2006257070 A JP 2006257070A JP 2006257070 A JP2006257070 A JP 2006257070A JP 2007317633 A JP2007317633 A JP 2007317633A
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resin composition
insulating
electrical equipment
unsaturated
electric apparatus
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Isao Umagami
伊三雄 馬上
Manabu Okada
学 岡田
Yasuhiro Obata
康裕 小幡
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Showa Denko Materials Co Ltd
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Hitachi Chemical Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a resin composition for insulating an electric apparatus capable of reducing the dripping thereof from a coil after a dripping treatment, having an excellent impregnation property, hardly adhering to a core, and resultantly capable of reducing the dripping quantity thereof; and an electric apparatus composed by executing an electric insulation treatment by using the resin composition for insulating an electric apparatus. <P>SOLUTION: Viscosity at 90°C of this resin composition for insulating an electric apparatus is 10-1,000 mPa s. The resin composition for insulating an electric apparatus is formed of a reactive monomer containing unsaturated polyester, styrene and vinyltoluene. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、電気機器絶縁用樹脂組成物及び電気機器に関し、特に、ツイストペアの寿命評価において、20000hの耐熱温度が155℃以上のモータ、トランス等の電気機器の処理方法に好適に用いられる電気機器絶縁用樹脂組成物及びこの電気機器絶縁用樹脂組成物を用いて電気絶縁処理してなる電気機器に関する。   TECHNICAL FIELD The present invention relates to a resin composition for insulating an electric device and an electric device, and in particular, an electric device suitably used in a method for treating an electric device such as a motor or a transformer having a heat resistant temperature of 20000 h at 155 ° C. or higher in the life evaluation of a twisted pair. The present invention relates to an insulating resin composition and an electric device obtained by performing an electric insulation treatment using the electric device insulating resin composition.

モータ、トランス等の電気機器は、鉄コアの固着又は防錆、コイルの絶縁若しくは固着等を目的として、電気機器絶縁用樹脂組成物で処理されている。電気機器絶縁用樹脂組成物としては、固着性、硬化性、電気絶縁性等のバランスに優れた不飽和ポリエステル樹脂組成物が広く用いられている(例えば、特許文献1参照)。
特開2002−367432号公報
Electric devices such as motors and transformers are treated with a resin composition for insulating electric devices for the purpose of fixing or preventing rusting of iron cores and insulating or fixing coils. As resin compositions for insulating electrical equipment, unsaturated polyester resin compositions having an excellent balance of adhesion, curability, electrical insulation and the like are widely used (see, for example, Patent Document 1).
JP 2002-367432 A

近年の電気機器は、小型・軽量化、高出力化が進んだため、実機スロット内の電線が占有する割合(占積率)が高くなる傾向があり、スロット内の空隙が減少し、電気機器絶縁用樹脂組成物がスロットの中へ含浸し難くなってきている。   In recent years, electrical equipment has become smaller, lighter, and has higher output, so the proportion occupied by the wires in the actual machine slot (space factor) tends to increase, and the gap in the slot decreases, resulting in electrical equipment. It has become difficult to impregnate the insulating resin composition into the slot.

特に、ドリップ処理では、予熱後の未だ熱い実機コイルへ電気機器絶縁用樹脂組成物を滴下しても、電気機器へ滴下した後に電気機器絶縁用樹脂組成物の温度が上昇して粘度が低下するため、電気機器絶縁用樹脂組成物が直ぐに垂れてしまい、満足する含浸性が得られず、さらに垂れた電気機器絶縁用樹脂組成物がコアへ付着してしまうことにより、コアに付着した電気機器絶縁用樹脂組成物を剥がし取る作業が生じ、生産性が低下してしまう事があった。   In particular, in the drip treatment, even if the resin composition for insulating an electric device is dropped on the still hot coil after preheating, the temperature of the resin composition for insulating the electric device rises and drops in viscosity after dropping on the electric device. For this reason, the resin composition for insulating an electric device immediately sags, a satisfactory impregnation property cannot be obtained, and the sagging resin composition for insulating an electric device adheres to the core, so that the electric device attached to the core The work which peels off the resin composition for insulation arises, and productivity may fall.

また、含浸性の向上を目指し、電気機器絶縁用樹脂組成物の滴下量を増やして滴下するが、電気機器絶縁用樹脂組成物がまた直ぐに垂れてしまい、満足する含浸性が得られず、さらに、垂れた電気機器絶縁用樹脂組成物が更にコアへ付着してしまうという悪循環が生じ、生産性が低下していた。   In addition, aiming to improve the impregnation property, the amount of the resin composition for electrical equipment insulation is increased and dropped, but the resin composition for electrical equipment insulation sags immediately and a satisfactory impregnation property cannot be obtained. As a result, a vicious cycle occurred in which the dripping resin composition for insulating electrical equipment was further adhered to the core, and the productivity was lowered.

本発明の目的は、電気機器絶縁用樹脂組成物が滴下処理後に電気機器の予熱によって高温にさらされ温度上昇に伴って粘度が下がり垂れ易くなってしまうため、高温でさらされる温度での電気機器絶縁用樹脂組成物の粘度範囲を規定する事によって、滴下処理後に電気機器絶縁用樹脂組成物がコイルから垂れ落ちを少なく、含浸性が良好で、且つ、コアへの付着が少なく、結果として、電気機器絶縁用樹脂組成物の滴下量を低減できる電気機器絶縁用樹脂組成物及びこの電気機器絶縁用樹脂組成物を用いて電気絶縁処理してなる電気機器を提供することにある。   The object of the present invention is that the resin composition for electrical equipment insulation is exposed to a high temperature by preheating of the electrical equipment after the dropping treatment, and the viscosity is likely to drop as the temperature rises. By prescribing the viscosity range of the insulating resin composition, the resin composition for electrical equipment insulation is less likely to drip from the coil after the dropping treatment, the impregnation is good, and the adhesion to the core is small. An object of the present invention is to provide an electric device insulating resin composition capable of reducing the dripping amount of the electric device insulating resin composition and an electric device obtained by electric insulation treatment using the electric device insulating resin composition.

本発明者らは鋭意検討の結果、高温でさらされる温度での電気機器絶縁用樹脂組成物の粘度範囲を規定する事によって、滴下処理後に電気機器絶縁用樹脂組成物がコイルから垂れ落ちを少なく、含浸性が良好で、且つ、コアへの付着が少なく、結果として、電気機器絶縁用樹脂組成物の滴下量を低減できることを見出した。   As a result of intensive studies, the present inventors have prescribed the viscosity range of the resin composition for insulating electrical equipment at a temperature exposed to a high temperature, so that the resin composition for insulating electrical equipment is less likely to drip from the coil after the dripping treatment. The present inventors have found that the impregnation property is good and the adhesion to the core is small, and as a result, the dripping amount of the resin composition for electrical equipment insulation can be reduced.

本発明は、90℃における粘度が10〜1000mPa・sである電気機器絶縁用樹脂組成物に関する。
また、本発明は、不飽和ポリエステル樹脂と、スチレン又はビニルトルエンを含む反応性モノマーとを含有する上記の電気機器絶縁用樹脂組成物に関する。
また、本発明は、MW35又はMW81の電線に該電気機器絶縁用樹脂組成物を塗布、硬化させて得られる導線を用いて作製されたツイストペアの寿命評価において、20000hの耐熱温度が155℃以上である上記の電気機器絶縁用樹脂組成物に関する。
また、本発明は、記載の電気機器絶縁用樹脂組成物を用い、ドリップ処理方法によって電気絶縁処理してなる電気機器に関する。
The present invention relates to a resin composition for insulating electrical equipment having a viscosity at 90 ° C. of 10 to 1000 mPa · s.
Moreover, this invention relates to said resin composition for electric equipment insulation containing unsaturated polyester resin and the reactive monomer containing styrene or vinyl toluene.
Further, in the life evaluation of a twisted pair produced by using a conductive wire obtained by applying and curing the resin composition for insulating an electric device to an MW35 or MW81 electric wire, the present invention has a heat resistant temperature of 20000 h of 155 ° C. or higher. The present invention relates to a certain resin composition for insulating electrical equipment.
Moreover, this invention relates to the electric equipment formed by electrically insulating-processing by the drip processing method using the resin composition for electrical equipment insulation described.

本発明になる電気機器絶縁用樹脂組成物は、高温にさらされる温度での電気機器絶縁用樹脂組成物の粘度範囲が一定範囲に規定されている。従って、絶縁処理時の滴下処理後の電気機器絶縁用樹脂組成物のコイルからの垂れ落ちが少なく、含浸性が良好で、且つ、コアへの付着が少なく、結果として、電気機器絶縁用樹脂組成物の滴下量を低減でき、コアに付着した電気機器絶縁用樹脂組成物の削り取り作業が削減できる。
また、この電気機器絶縁用樹脂組成物は高温における固着性にも優れ、これを用いて電気絶縁処理された電気機器は工業的に極めて優れる。
In the resin composition for insulating electrical equipment according to the present invention, the viscosity range of the resin composition for insulating electrical equipment at a temperature exposed to a high temperature is defined as a certain range. Accordingly, the resin composition for insulating electrical equipment after the dripping treatment at the time of the insulation treatment has less dripping from the coil, good impregnation, and less adhesion to the core. As a result, the resin composition for insulating electrical equipment The amount of dripping can be reduced, and the scraping work of the resin composition for insulating electrical equipment attached to the core can be reduced.
In addition, this resin composition for insulating electrical equipment is excellent in adhesion at high temperatures, and electrical equipment that is electrically insulated using this composition is extremely excellent industrially.

本発明の電気機器絶縁用樹脂組成物は、コア汚染を低減し、良好な含浸性を得る点から、90℃における粘度が10〜1000mPa・sであり、20〜300mPa・sであることが好ましく、30〜200mPa・sであることがより好まく、100〜200mPa・sであることがさらに好ましい。90℃における粘度が10mPa・s未満であると電気機器の必要部位へ滴下したワニスが垂れ易くなってコアなど他の部位へ付着し易くなる傾向があり、1000mPa・sを超えると浸透性が悪くなり含浸性が低下する傾向がある。   The resin composition for insulating electrical equipment of the present invention has a viscosity at 90 ° C. of 10 to 1000 mPa · s and preferably 20 to 300 mPa · s from the viewpoint of reducing core contamination and obtaining good impregnation properties. 30 to 200 mPa · s is more preferable, and 100 to 200 mPa · s is more preferable. When the viscosity at 90 ° C. is less than 10 mPa · s, the varnish dripped onto the necessary part of the electric device tends to sag and tends to adhere to other parts such as the core, and when it exceeds 1000 mPa · s, the permeability is poor. Therefore, the impregnation property tends to decrease.

本発明において、電気機器絶縁用樹脂組成物は、特に制限は無く、例えば、エポキシ樹脂、不飽和ポリエステル樹脂、変性不飽和エポキシエステル樹脂、ポリウレタン、フェノール樹脂、メラミン樹脂、ユリア樹脂、アルキド樹脂等の熱硬化性樹脂を含有するものが挙げられる。これらの熱硬化性樹脂は、単独で用いても、複数を組合せて用いても良い。   In the present invention, the resin composition for insulating electrical equipment is not particularly limited, and examples thereof include epoxy resins, unsaturated polyester resins, modified unsaturated epoxy ester resins, polyurethanes, phenol resins, melamine resins, urea resins, alkyd resins, and the like. The thing containing a thermosetting resin is mentioned. These thermosetting resins may be used alone or in combination.

上記各種の熱硬化性樹脂のうち、変性不飽和エポキシエステル樹脂の例としては、エポキシ化合物とα,β−不飽和一塩基酸とを反応させて不飽和エポキシエステル樹脂とし、次いでさらに不飽和酸無水物を反応させて得られるものが挙げられる。この変性不飽和エポキシエステル樹脂の合成に用いられるエポキシ化合物は、一分子内にエポキシ基を1個以上有するものでば特に制限は無く、単独で用いても2種以上を併用しても良い。例えば、ビスフェノールA型エポキシ樹脂、ビスフェノールF型エポキシ樹脂、ブロム化ビスフェノールA型エポキシ樹脂、ノボラック型エポキシ樹脂等がある。特に、一分子内にエポキシ基を2個以上有するものが好ましい。   Among the various thermosetting resins described above, examples of the modified unsaturated epoxy ester resin include an epoxy compound and an α, β-unsaturated monobasic acid reacted to form an unsaturated epoxy ester resin, and then further an unsaturated acid. The thing obtained by making an anhydride react is mentioned. The epoxy compound used for the synthesis of the modified unsaturated epoxy ester resin is not particularly limited as long as it has one or more epoxy groups in one molecule, and may be used alone or in combination of two or more. For example, there are bisphenol A type epoxy resin, bisphenol F type epoxy resin, brominated bisphenol A type epoxy resin, novolac type epoxy resin and the like. In particular, those having two or more epoxy groups in one molecule are preferable.

上記の変性不飽和エポキシエステル樹脂の合成に用いられるα,β−不飽和一塩基酸には特に制限は無く、単独で用いても2種以上を併用しても良い。例えば、アクリル酸、メタクリル酸、桂皮酸、クロトン酸等がある。α,β−不飽和一塩基酸は、カルボキシル基/エポキシ基の当量比が好ましくは0.5〜1.9となるように、より好ましくは0.8〜1.3となるように用いられる。   The α, β-unsaturated monobasic acid used for the synthesis of the modified unsaturated epoxy ester resin is not particularly limited, and may be used alone or in combination of two or more. For example, there are acrylic acid, methacrylic acid, cinnamic acid, crotonic acid and the like. The α, β-unsaturated monobasic acid is used so that the equivalent ratio of carboxyl group / epoxy group is preferably 0.5 to 1.9, more preferably 0.8 to 1.3. .

上記の変性不飽和エポキシエステル樹脂は、エポキシ化合物とα,β−不飽和一塩基酸とを反応させて不飽和エポキシエステル樹脂とした後、更に不飽和酸無水物を反応させることにより、得られる。不飽和酸無水物は、不飽和エポキシエステル樹脂のヒドロキシル基と反応させるために用いられ、その不飽和酸無水物としては、無水マレイン酸無水物、無水イタコン酸無水物、無水シトラコン酸無水物等の不飽和ジカルボン酸無水物などを用いることができる。
不飽和酸無水物は、前記不飽和エポキシエステル樹脂の合成原料であるエポキシ化合物のエポキシ基に対して2〜40モル%に相当する割合で使用されることが好ましく、20〜30モル%に相当する割合で使用されることがより好ましい。不飽和酸無水物の使用量がこの範囲以外では変性不飽和エポキシエステル樹脂の貯藏安定性が悪く、ゲル化し易くなる。
The modified unsaturated epoxy ester resin is obtained by reacting an epoxy compound with an α, β-unsaturated monobasic acid to obtain an unsaturated epoxy ester resin, and further reacting with an unsaturated acid anhydride. . Unsaturated acid anhydride is used to react with hydroxyl group of unsaturated epoxy ester resin, and as unsaturated acid anhydride, maleic anhydride, itaconic anhydride, citraconic anhydride, etc. Unsaturated dicarboxylic acid anhydrides and the like can be used.
The unsaturated acid anhydride is preferably used in a proportion corresponding to 2 to 40 mol% with respect to the epoxy group of the epoxy compound which is a raw material for synthesis of the unsaturated epoxy ester resin, and corresponds to 20 to 30 mol%. More preferably, it is used in a proportion of If the amount of the unsaturated acid anhydride used is outside this range, the storage stability of the modified unsaturated epoxy ester resin is poor and gelation tends to occur.

エポキシ化合物とα,β−不飽和一塩基酸との反応、及び、不飽和エポキシエステル樹脂と不飽和酸無水物との反応には、通常、付加反応触媒として、塩化亜鉛、塩化リチウム等のハロゲン化物、ジメチルサルファイト、メチルフェニルサルファイト等のサルファイト類、ジメチルスルホキサイド、メチルスルホキサイド、メチルエチルスルホキサイド等のスルホキサイド類、N,N−ジメチルアニリン、ピリジン、トリエチルアミン、ベンジルジメチルアミン、ヘキサメチレンジアミン等の3級アミン及びその塩基酸又は臭酸塩、テトラメチルアンモニウムクロライド、トリメチルドデシルベンジルアンモニウムクロライド等の4級アンモニウム塩、パラトルエンスルホン酸などのスルホン酸類、エチルメルカプタン、プロピルメルカプタン等のメルカプタン類などが用いられる。付加反応触媒の配合量は、エポキシ化合物、α,β−不飽和一塩基酸及び不飽和酸無水物の総量100重量部に対して、0.05〜2重量部が好ましく、0.1〜1.0重量部がさらに好ましい。   In the reaction between an epoxy compound and an α, β-unsaturated monobasic acid, and the reaction between an unsaturated epoxy ester resin and an unsaturated acid anhydride, a halogen such as zinc chloride or lithium chloride is usually used as an addition reaction catalyst. , Sulfites such as dimethyl sulfite and methylphenyl sulfite, sulfoxides such as dimethyl sulfoxide, methyl sulfoxide, methylethyl sulfoxide, N, N-dimethylaniline, pyridine, triethylamine, benzyldimethylamine , Tertiary amines such as hexamethylenediamine and its basic acids or bromoacid salts, quaternary ammonium salts such as tetramethylammonium chloride, trimethyldodecylbenzylammonium chloride, sulfonic acids such as paratoluenesulfonic acid, ethyl mercaptan, propyl mercaptan Mercaptans such as are used. The compounding amount of the addition reaction catalyst is preferably 0.05 to 2 parts by weight with respect to 100 parts by weight of the total amount of the epoxy compound, α, β-unsaturated monobasic acid and unsaturated acid anhydride, and 0.1 to 1 More preferred is 0.0 part by weight.

エポキシ化合物とα,β−不飽和一塩基酸との反応、得られた不飽和エポキシエステル樹脂と不飽和酸無水物との反応は、従来からの常法に従い、合成することができる。例えば、エポキシ化合物とα,β−不飽和一塩基酸とを反応させた後、合成された不飽和エポキシエステル樹脂を含む反応混合物中に不飽和酸無水物を添加し、不飽和エポキシエステル樹脂のヒドロキシル基と不飽和酸無水物とを反応させてもよい。   The reaction between the epoxy compound and the α, β-unsaturated monobasic acid, and the reaction between the obtained unsaturated epoxy ester resin and the unsaturated acid anhydride can be synthesized according to conventional methods. For example, after reacting an epoxy compound with an α, β-unsaturated monobasic acid, an unsaturated acid anhydride is added to the reaction mixture containing the synthesized unsaturated epoxy ester resin, and the unsaturated epoxy ester resin A hydroxyl group and an unsaturated acid anhydride may be reacted.

変性不飽和エポキシエステル樹脂(A)は、数平均分子量(ゲルパーミエーションクロマトグラフィー法により測定し、標準ポリスチレン検量線を用いて換算した値、以下も同じ)が500〜5000であることが好ましく、1000〜2000であることがより好ましい。500未満では、樹脂混合物の硬化性及び硬化物特性が極端に劣ることがあり、5000を超えると粘度が高すぎ作業性が悪化する傾向がある。   The modified unsaturated epoxy ester resin (A) preferably has a number average molecular weight (measured by gel permeation chromatography and converted using a standard polystyrene calibration curve, the same applies hereinafter) of 500 to 5000, More preferably, it is 1000-2000. If it is less than 500, the curability and cured product properties of the resin mixture may be extremely inferior, and if it exceeds 5000, the viscosity tends to be too high and the workability tends to deteriorate.

上記の熱硬化性樹脂は、反応性モノマーとともに用いることが好ましい。上記の変性不飽和エポキシエステル樹脂との組み合わせに適した反応性モノマーとしては、通常、ビニルモノマー等、分子内に不飽和基を有する化合物が好ましく、例えば、スチレン、ビニルトルエン、ジビニルベンゼン、α−メチルスチレン等のスチレン誘導体、アクリル酸メチル、アクリル酸エチル等のアクリル酸類、メタクリル酸メチル、メタクリル酸エチル等のメタクリル酸類があり、スチレン、ビニルトルエンが好ましく用いられる。反応性モノマーは、一種単独で用いてもよいし、二種以上を併用してもよい。   The thermosetting resin is preferably used together with a reactive monomer. As a reactive monomer suitable for the combination with the above-mentioned modified unsaturated epoxy ester resin, a compound having an unsaturated group in the molecule such as a vinyl monomer is usually preferable. For example, styrene, vinyl toluene, divinylbenzene, α- There are styrene derivatives such as methylstyrene, acrylic acids such as methyl acrylate and ethyl acrylate, and methacrylic acids such as methyl methacrylate and ethyl methacrylate, and styrene and vinyltoluene are preferably used. A reactive monomer may be used individually by 1 type, and may use 2 or more types together.

本発明の電気機器絶縁用樹脂組成物は、さらに、脂肪酸アミドを含有していてもよい。
脂肪酸アミドについても特に制限は無く、単独で用いても2種以上併用しても良い。脂肪酸アミドは、直鎖脂肪酸アミドであっても分岐脂肪酸アミドであってもよく、また、飽和脂肪酸アミドであっても不飽和脂肪酸アミドであってもよい。好ましい脂肪酸アミドとしては、例えば、オレイン酸アミド、ステアリン酸アミド等のモノアミド、エチレン・ビス・ステアリン酸アミド、エチレン・ビス・オレイン酸アミド等のビスアミドがある。市販品としては例えばT−380、T−550F、T−1700、T−650F(いずれも伊藤製油製)、ダイヤミッドKH、ダイヤミッドH、ZHH、PXH(いずれも日本化成製)等がある。
The resin composition for insulating electrical equipment of the present invention may further contain a fatty acid amide.
The fatty acid amide is not particularly limited, and may be used alone or in combination of two or more. The fatty acid amide may be a linear fatty acid amide or a branched fatty acid amide, and may be a saturated fatty acid amide or an unsaturated fatty acid amide. Preferred fatty acid amides include monoamides such as oleic acid amide and stearic acid amide, and bisamides such as ethylene bis stearic acid amide and ethylene bis oleic acid amide. Examples of commercially available products include T-380, T-550F, T-1700, T-650F (all manufactured by Ito Oil), Diamond KH, Diamond H, ZHH, and PXH (all manufactured by Nippon Kasei).

本発明の電気機器絶縁用樹脂組成物が変性不飽和エポキシエステル樹脂、反応性モノマー及び脂肪酸アミドを含有する場合、変性不飽和エポキシエステル樹脂10〜95重量部、反応性モノマー10〜95重量部及び脂肪酸アミド0.01〜30重量部を含有することが好ましい。変性不飽和エポキシエステル樹脂の量は、より好ましくは40〜70重量部、さらに好ましくは45〜60重量部である。変性不飽和エポキシエステル樹脂の量が10重量部未満では、反応性が極端に低下する傾向があり、95重量部を超えると、粘度が極端に高くなり、作業性が低下する傾向がある。反応性モノマーの量は、より好ましくは30〜60重量部、さらに好ましくは40〜55重量部である。反応性モノマーの量が10重量部未満では、粘度が極端に高くなり、作業性が低下する傾向があり、95重量部を超えると、反応性が極端に低下する傾向がある。脂肪酸アミドの量は、より好ましくは0.05〜20重量部であり、さらに好ましくは0.1〜10重量部である。脂肪酸アミド(C)の量が0.1重量部未満であると、電気機器絶縁用樹脂組成物の粘度が低くなり、垂れによる汚染や含浸不足を生じる傾向があり、30重量部を超えると、含浸性が低下する傾向がある。   When the resin composition for insulating electrical equipment of the present invention contains a modified unsaturated epoxy ester resin, a reactive monomer and a fatty acid amide, 10 to 95 parts by weight of a modified unsaturated epoxy ester resin, 10 to 95 parts by weight of a reactive monomer and It is preferable to contain 0.01-30 weight part of fatty acid amides. The amount of the modified unsaturated epoxy ester resin is more preferably 40 to 70 parts by weight, still more preferably 45 to 60 parts by weight. When the amount of the modified unsaturated epoxy ester resin is less than 10 parts by weight, the reactivity tends to be extremely lowered, and when it exceeds 95 parts by weight, the viscosity becomes extremely high and the workability tends to be lowered. The amount of the reactive monomer is more preferably 30 to 60 parts by weight, still more preferably 40 to 55 parts by weight. When the amount of the reactive monomer is less than 10 parts by weight, the viscosity tends to be extremely high and the workability tends to be lowered, and when it exceeds 95 parts by weight, the reactivity tends to be extremely lowered. The amount of fatty acid amide is more preferably 0.05 to 20 parts by weight, still more preferably 0.1 to 10 parts by weight. When the amount of the fatty acid amide (C) is less than 0.1 parts by weight, the viscosity of the resin composition for insulating electrical equipment tends to be low, and there is a tendency to cause contamination due to dripping or insufficient impregnation. There is a tendency for the impregnation property to decrease.

本発明の電気機器絶縁用樹脂組成物には、必要に応じて硬化剤を配合してもよい。硬化剤としては特に制限はないが、不飽和ポリエステル樹脂、変性不飽和エポキシエステル樹脂などの不飽和樹脂には、有機過酸化物が好ましく用いられる。有機過酸化物としては、例えばベンゾインパーオキサイド、ターシャリブチルパーオキシベンゾエート、メチルエチルケトンパーオキサイド、シクロヘキサノンパーオキサイド、ジターシャリブチルパーオキサイド、ジクミルパーオキサイド等が用いられる。   You may mix | blend a hardening | curing agent with the resin composition for electric equipment insulation of this invention as needed. Although there is no restriction | limiting in particular as a hardening | curing agent, An organic peroxide is preferably used for unsaturated resins, such as unsaturated polyester resin and modified | denatured unsaturated epoxy ester resin. Examples of the organic peroxide include benzoin peroxide, tertiary butyl peroxybenzoate, methyl ethyl ketone peroxide, cyclohexanone peroxide, ditertiary butyl peroxide, dicumyl peroxide and the like.

硬化剤の添加量としては、熱硬化性樹脂、反応性モノマー、脂肪酸アミドの総量100重量部に対して0.5〜3.0重量部が好ましく、1.0〜2.0重量部がより好ましい。   As addition amount of a hardening | curing agent, 0.5-3.0 weight part is preferable with respect to 100 weight part of total amounts of a thermosetting resin, a reactive monomer, and fatty acid amide, and 1.0-2.0 weight part is more. preferable.

また、必要に応じて硬化促進剤及び重合禁止剤を添加することもできる。硬化促進剤としては、例えば不飽和ポリエステル樹脂、変性不飽和エポキシエステル樹脂などの不飽和樹脂には、ナフテン酸マンガン、ナフテン酸鉛、ナフテン酸コバルト、オクテン酸コバルト等が用いられる。重合禁止剤としては、例えばハイドロキノン、ターシャリブチルカテコール、p−ベンゾキノン等のキノン類が用いられる。   Moreover, a hardening accelerator and a polymerization inhibitor can also be added as needed. As the curing accelerator, for example, manganese naphthenate, lead naphthenate, cobalt naphthenate, cobalt octenoate and the like are used for unsaturated resins such as unsaturated polyester resins and modified unsaturated epoxy ester resins. As the polymerization inhibitor, for example, quinones such as hydroquinone, tertiary butyl catechol and p-benzoquinone are used.

硬化促進剤の添加量は、熱硬化性樹脂、反応性モノマー、脂肪酸アミドの総量100重量部に対して0.01〜3.0重量部が好ましく、0.2〜2.0重量部がより好ましい。重合禁止剤の添加量は、熱硬化性樹脂、反応性モノマー、脂肪酸アミドの総量100重量部に対して0.001〜0.1重量部が好ましく、0.004〜0.05重量部がより好ましい。   The addition amount of the curing accelerator is preferably 0.01 to 3.0 parts by weight, more preferably 0.2 to 2.0 parts by weight with respect to 100 parts by weight of the total amount of the thermosetting resin, reactive monomer, and fatty acid amide. preferable. The addition amount of the polymerization inhibitor is preferably 0.001 to 0.1 parts by weight, more preferably 0.004 to 0.05 parts by weight with respect to 100 parts by weight of the total amount of the thermosetting resin, reactive monomer, and fatty acid amide. preferable.

本発明の電気機器絶縁用樹脂組成物は、さらに、二酸化珪素、窒化アルミニウム、タルク等のフィラーを含有していてもよい。フィラーは一種単独で用いても、複数を組合せて用いても良い。これらフィラーは電気機器を運転するときの放熱性を向上させることを主な目的として配合されるものであり、使用する場合、その配合量は、熱硬化性樹脂、反応性モノマー、脂肪酸アミドの総量100重量部あたり、0.001〜10重量部とすることが好ましく、0.1〜5重量部とすることがより好ましい。フィラーの配合量が多すぎると、電気機器絶縁用樹脂組成物の粘度及び揺変度が高くなり、含浸性が低下することがある。フィラーは、平均粒径が50μm以下が好ましく、20μm以下がより好ましい。また、これらフィラーとしては、その表面をオクチルシラン、ジメチルジクロロシラン、ジメチルシリコーンオイル又はヘキサメチルジシラザン等を用いて化学処理を行ない、表面を疎水性にした疎水性フィラーを単独で、又は、表面未処理のフィラーと組合わせて用いると、フィラーの分散性が向上して好ましい。疎水性フィラーは、粒径が500nm以下であることが好ましい。   The resin composition for insulating electrical equipment of the present invention may further contain a filler such as silicon dioxide, aluminum nitride, and talc. A filler may be used individually by 1 type, or may be used in combination of multiple. These fillers are blended mainly for the purpose of improving heat dissipation when operating electrical equipment. When used, the blending amount is the total amount of thermosetting resin, reactive monomer, and fatty acid amide. It is preferable to set it as 0.001-10 weight part per 100 weight part, and it is more preferable to set it as 0.1-5 weight part. When there are too many compounding quantities of a filler, the viscosity of the resin composition for electrical equipment insulation and the degree of fluctuation may become high, and impregnation property may fall. The filler preferably has an average particle size of 50 μm or less, more preferably 20 μm or less. In addition, as these fillers, the surface is subjected to chemical treatment using octylsilane, dimethyldichlorosilane, dimethylsilicone oil, hexamethyldisilazane, etc., and the surface is made hydrophobic filler alone or on the surface. When used in combination with an untreated filler, the dispersibility of the filler is improved, which is preferable. The hydrophobic filler preferably has a particle size of 500 nm or less.

本発明の電気機器絶縁用樹脂組成物は、エアコン用ファン、扇風機、洗濯機等のコンデンサーモートル、電気ドリルなどのアマチュア、テレビ、ステレオ、コンパクトディスクプレーヤー等電源トランス等の電気機器の絶縁処理に適用される。特に、本発明の電気機器絶縁用樹脂組成物は高温での固着性にも優れることから、この樹脂組成物をMW35又はMW81の電線に塗布、硬化させて、得られる導線を用いてツイストペアを作製した場合、ツイストペアの寿命評価において、20000hの耐熱温度が155℃以上であるものを得ることも可能である。なお、この寿命評価は、UL−1446に準拠して行なわれる。   The resin composition for insulating electric equipment of the present invention is applied to insulation treatment of electric equipment such as power transformers such as condenser motors such as air conditioner fans, electric fans and washing machines, amateurs such as electric drills, televisions, stereos and compact disc players. Is done. In particular, since the resin composition for insulating electrical equipment of the present invention is also excellent in adhesion at high temperatures, this resin composition is applied to an MW35 or MW81 wire and cured, and a twisted pair is produced using the resulting conductive wire. In this case, it is possible to obtain a product having a heat resistant temperature of 20000 h at 155 ° C. or higher in the life evaluation of the twisted pair. This life evaluation is performed in accordance with UL-1446.

本発明の電気機器絶縁用樹脂組成物を用いて電気機器を絶縁処理する方法としては、例えば、電気機器絶縁用樹脂組成物を、電気機器自体、又は電気機器の部品に塗布、含浸又は充填した後、通常、100〜200℃、好ましくは120〜150℃で加熱することにより、電気機器絶縁用樹脂組成物を硬化させる。加熱時間は、通常、0.2〜3.0時間である。特に、本発明の電気機器絶縁用樹脂組成物は、絶縁処理時の高熱にさらされたときの粘度低下が少ないため、ドリップ処理に特に好適に用いることができる。   Examples of a method for insulating an electric device using the resin composition for insulating an electric device of the present invention include, for example, applying, impregnating, or filling the electric device insulating resin composition to the electric device itself or parts of the electric device. Then, the resin composition for electrical equipment insulation is normally hardened by heating at 100-200 degreeC, Preferably it is 120-150 degreeC. The heating time is usually 0.2 to 3.0 hours. In particular, the resin composition for insulating electrical equipment according to the present invention is particularly suitable for drip treatment because of a small decrease in viscosity when exposed to high heat during insulation treatment.

以下、実施例により本発明を説明する。なお、下記の各材料の後の部は、重量部を意味する。
製造例1〔変性不飽和エポキシエステル樹脂(A−1)の合成〕
4,4′−イソプロピリデンジフェノールのジグリシジルエーテル(シェル化学(株)製、商品名:EP−828、エポキシ当量188)376部、メタクリル酸172部、ベンジルジメチルアミン2部及びハイドロキノン0.05部を反応釜に仕込み、115℃で10時間反応させ、樹脂酸価が8となった所で、無水マレイン酸25部を仕込み、115℃で2時間反応させ、酸価が20となったところで冷却した。得られた変性不飽和エポキシエステル樹脂の数平均分子量は、1450であった。
Hereinafter, the present invention will be described by way of examples. In addition, the back part of each following material means a weight part.
Production Example 1 [Synthesis of Modified Unsaturated Epoxy Ester Resin (A-1)]
Diglycidyl ether of 4,4′-isopropylidene diphenol (manufactured by Shell Chemical Co., Ltd., trade name: EP-828, epoxy equivalent 188), 376 parts, 172 parts of methacrylic acid, 2 parts of benzyldimethylamine and 0.05 of hydroquinone Part was charged in a reaction kettle and reacted at 115 ° C. for 10 hours. When the resin acid value reached 8, 25 parts of maleic anhydride was charged and reacted at 115 ° C. for 2 hours. Cooled down. The number average molecular weight of the obtained modified unsaturated epoxy ester resin was 1450.

実施例1
変性不飽和エポキシエステル樹脂(A−1)50部、スチレン50部、T−550F(脂肪酸アミド)5部、ナフテン酸コバルト0.3部及びターシャリブチルパーオキシベンゾエート1.0部を撹拌混合して電気機器絶縁用樹脂組成物を調製した。
Example 1
50 parts of modified unsaturated epoxy ester resin (A-1), 50 parts of styrene, 5 parts of T-550F (fatty acid amide), 0.3 part of cobalt naphthenate and 1.0 part of tertiary butyl peroxybenzoate are mixed with stirring. Thus, a resin composition for insulating electrical equipment was prepared.

実施例2
変性不飽和エポキシエステル樹脂(A−1)50部、スチレン50部、T−550F(脂肪酸アミド)2部、一次粒子の平均粒径が500nm以下の疎水性二酸化ケイ素0.8部、ナフテン酸コバルト0.3部及びターシャリブチルパーオキシベンゾエート1.0部を撹拌混合して電気機器絶縁用樹脂組成物を調製した。
Example 2
50 parts of modified unsaturated epoxy ester resin (A-1), 50 parts of styrene, 2 parts of T-550F (fatty acid amide), 0.8 part of hydrophobic silicon dioxide having an average primary particle size of 500 nm or less, cobalt naphthenate 0.3 parts and 1.0 part of tertiary butyl peroxybenzoate were stirred and mixed to prepare a resin composition for electrical equipment insulation.

比較例1
変性不飽和エポキシエステル樹脂(A−1)50部、スチレン50部、ナフテン酸コバルト0.3部及びターシャリブチルパーオキシベンゾエート1.0部を撹拌混合して電気機器絶縁用樹脂組成物を調製した。
Comparative Example 1
50 parts of the modified unsaturated epoxy ester resin (A-1), 50 parts of styrene, 0.3 part of cobalt naphthenate and 1.0 part of tertiary butyl peroxybenzoate are mixed with stirring to prepare a resin composition for electrical equipment insulation. did.

尚、粘度、ヘリカルコイル接着力の試験方法は、JIS C 2105に準じて測定を行った。コア汚染及びステータコイルの含浸性は以下の試験方法に準じて評価を行った。
(1)粘度
JIS C 2105
(2)ヘリカルコイル接着力(電線は直径0.9mm(φ)AI/EIWを使用)
JIS C 2105
なお、ヘリカルコイル接着力を測定するにあたっては、電気絶縁用樹脂組成物の硬化は、130℃において1時間加熱することにより行なった。
(3)コア汚染の試験方法は、図1及び図2に示すステータコイル1(Φ200mm、質量10kg)(図1中、(a)はステータコイル1の概略正面図、図1(b)はその概略側面図、図2は、図1のステータコイル1のコア2のY−Y概略断面図である。)を用い、回転速度15回転/分とし、ステータコイルのコア2の表面温度が90℃の時にコイル3エンドの(1)リード線4有り側の外側、(2)リード線4有り側の内側、(3)リード線4無し側の外側、(4)リード線4無し側の内側の合計四ヶ所(図1)にノズル5を配置し、所定のワニスを20分間に合計300ml滴下し、滴下終了後、回転を続行しながら150℃の乾燥機へ投入し、1h後に乾燥機から取り出して、コア部に付着したワニスの付着の有無を目視で調査した。
(4)含浸性の試験方法は、コア汚染の試験方法でワニス処理したステータコイル1のコア2をコア積み厚の半分の部位で輪切り状に切断し、スロット6内の空隙に対して含浸したワニスの割合を目視で評価した。
スロット6内の空隙に対して含浸したワニスの割合が70%以上を良好とし、50%未満を含浸不足とした。
(5)ツイストペアの耐熱寿命温度は、電線(直径0.9mm(φ)AI/EIW)を用いて、UL−1446に準じて試験を行ない、20000時間後の耐熱寿命温度を得た。
In addition, the test method of a viscosity and a helical coil adhesive force measured according to JISC2105. The core contamination and the impregnation property of the stator coil were evaluated according to the following test methods.
(1) Viscosity JIS C 2105
(2) Helical coil adhesive strength (electric wire uses diameter 0.9mm (φ) AI / EIW)
JIS C 2105
In measuring the adhesive strength of the helical coil, the resin composition for electrical insulation was cured by heating at 130 ° C. for 1 hour.
(3) The test method for core contamination is the stator coil 1 (Φ200 mm, mass 10 kg) shown in FIGS. 1 and 2 (in FIG. 1, (a) is a schematic front view of the stator coil 1, and FIG. 2 is a schematic Y-Y cross-sectional view of the core 2 of the stator coil 1 of FIG. 1. The surface temperature of the stator coil core 2 is 90.degree. (1) outside the lead wire 4 side of the coil 3 end, (2) inside the lead wire 4 side, (3) outside the lead wire 4 side, (4) inside the lead wire 4 side. Nozzles 5 are arranged at a total of four locations (Fig. 1), and a total of 300 ml of predetermined varnish is dripped for 20 minutes. After completion of the dripping, it is put into a dryer at 150 ° C while continuing to rotate, and taken out from the dryer after 1 hour. Visual inspection of varnish adhering to the core It was.
(4) In the impregnation test method, the core 2 of the stator coil 1 varnished by the core contamination test method was cut into a ring shape at a half of the core stack thickness, and impregnated into the voids in the slot 6. The proportion of varnish was visually evaluated.
The ratio of the varnish impregnated with respect to the voids in the slot 6 was 70% or more, and less than 50% was insufficient.
(5) The heat resistant life temperature of the twisted pair was tested according to UL-1446 using an electric wire (diameter 0.9 mm (φ) AI / EIW), and the heat resistant life temperature after 20000 hours was obtained.

Figure 2007317633
Figure 2007317633

表1に示されるように、実施例1及び2で得られた電気機器絶縁用樹脂組成物は、90℃での粘度が適正範囲内であるため、コア汚染が発生し難く、含浸性が良好である。
これに対して、比較例1で得られた電気機器絶縁用樹脂組成物は、90℃での粘度が適正範囲よりも低く、コア汚染が発生してしまい、含浸不足となっている。
As shown in Table 1, since the resin composition for electrical equipment insulation obtained in Examples 1 and 2 has a viscosity at 90 ° C. within an appropriate range, the core contamination hardly occurs and the impregnation property is good. It is.
On the other hand, the resin composition for insulating electrical equipment obtained in Comparative Example 1 has a viscosity at 90 ° C. lower than the appropriate range, causing core contamination and insufficient impregnation.

(a)はコア汚染の試験方法に用いられるステータコイルの概略正面図であり、(b)はその概略側面図である。。(A) is a schematic front view of the stator coil used for the test method of a core contamination, (b) is the schematic side view. . 図1のステータコイルのコアの概略Y−Y断面図である。FIG. 2 is a schematic YY sectional view of a core of the stator coil in FIG. 1.

符号の説明Explanation of symbols

1 ステータコイル
2 コア
3 コイル
4 リード線
5 ノズル
6 スロット
1 Stator Coil 2 Core 3 Coil 4 Lead Wire 5 Nozzle 6 Slot

Claims (4)

90℃における粘度が10〜1000mPa・sである電気機器絶縁用樹脂組成物。   A resin composition for insulating electrical equipment having a viscosity at 90 ° C. of 10 to 1000 mPa · s. 不飽和ポリエステル樹脂と、スチレン又はビニルトルエンを含む反応性モノマーとを含有する請求項1記載の電気機器絶縁用樹脂組成物。   The resin composition for electrical equipment insulation according to claim 1, comprising an unsaturated polyester resin and a reactive monomer containing styrene or vinyltoluene. MW35又はMW81の電線に該電気機器絶縁用樹脂組成物を塗布、硬化させて得られる導線を用いて作製されたツイストペアの寿命評価において、20000hの耐熱温度が155℃以上である請求項1又は2記載の電気機器絶縁用樹脂組成物。   The heat resistance temperature of 20000h is 155 ° C or higher in a life evaluation of a twisted pair produced using a conductive wire obtained by applying and curing the resin composition for electrical equipment insulation to an electric wire of MW35 or MW81. The resin composition for electrical equipment insulation as described. 請求項1〜3いずれかに記載の電気機器絶縁用樹脂組成物を用い、ドリップ処理方法によって電気絶縁処理してなる電気機器。   The electrical equipment formed by using the resin composition for electrical equipment insulation in any one of Claims 1-3, and carrying out an electrical insulation process by the drip processing method.
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JP2012188533A (en) * 2011-03-10 2012-10-04 Hitachi Chemical Co Ltd Thixotropic liquid insulating varnish, and electric apparatus insulating material and electric motor using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012188533A (en) * 2011-03-10 2012-10-04 Hitachi Chemical Co Ltd Thixotropic liquid insulating varnish, and electric apparatus insulating material and electric motor using the same

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