JPS6245784B2 - - Google Patents
Info
- Publication number
- JPS6245784B2 JPS6245784B2 JP4187580A JP4187580A JPS6245784B2 JP S6245784 B2 JPS6245784 B2 JP S6245784B2 JP 4187580 A JP4187580 A JP 4187580A JP 4187580 A JP4187580 A JP 4187580A JP S6245784 B2 JPS6245784 B2 JP S6245784B2
- Authority
- JP
- Japan
- Prior art keywords
- thermosetting resin
- temperature
- foaming
- armature
- armature winding
- 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
Links
- 229920005989 resin Polymers 0.000 claims description 29
- 239000011347 resin Substances 0.000 claims description 29
- 229920001187 thermosetting polymer Polymers 0.000 claims description 24
- 238000004804 winding Methods 0.000 claims description 22
- 238000005187 foaming Methods 0.000 claims description 15
- 238000006116 polymerization reaction Methods 0.000 claims description 13
- 239000004088 foaming agent Substances 0.000 claims description 11
- 239000003094 microcapsule Substances 0.000 claims description 11
- 239000003999 initiator Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000011342 resin composition Substances 0.000 description 7
- 229920006305 unsaturated polyester Polymers 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000004641 Diallyl-phthalate Substances 0.000 description 4
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000003505 polymerization initiator Substances 0.000 description 4
- -1 that is Chemical class 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000006082 mold release agent Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000004005 microsphere Substances 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000001721 transfer moulding Methods 0.000 description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 2
- ROLAGNYPWIVYTG-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethanamine;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1CC(N)C1=CC=C(OC)C=C1 ROLAGNYPWIVYTG-UHFFFAOYSA-N 0.000 description 1
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02K—DYNAMO-ELECTRIC MACHINES
- H02K15/00—Processes or apparatus specially adapted for manufacturing, assembling, maintaining or repairing of dynamo-electric machines
- H02K15/12—Impregnating, moulding insulation, heating or drying of windings, stators, rotors or machines
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Power Engineering (AREA)
- Insulation, Fastening Of Motor, Generator Windings (AREA)
- Manufacture Of Motors, Generators (AREA)
- Dc Machiner (AREA)
Description
本発明は熱硬化性樹脂の加熱硬化により、少な
くとも電機子巻線部分を一体的に剛体化した無鉄
心電機子の製造方法に関する。
電機子巻線は電線を所定数巻装して、ワニス等
の結着剤により、その支持鉄心と共に一体的に固
着して剛体化を図るのが一般である。しかし無鉄
心電機子の如く支持鉄心のない電機子巻線の場合
は何等かの方法で電機子巻線自身の一体的剛体化
を図らなければならない。特に数ワツトから数百
ワツトまでの比較的大形の無鉄心電機子としての
電機子巻線の場合は一体的剛体化に要求される特
性も高度であり、高温における強度、寸法安定
性、耐熱衝撃性、電気絶縁性、長時間にわたる耐
熱劣化性に応えられる一体的剛体化が要求され
る。従つて上記無鉄心電機子の少なくとも電機子
巻線部分には無機質充填剤を通常50%以上含む熱
硬化性樹脂成形材料による移送成形を適用し、更
に電機子巻線の一部表面にプリプレグ硬化層を設
けることによる複合効果を利用した無鉄心電機子
が実用化されていた。
上記数ワツトから数百ワツトの比較的大形の無
鉄心電機子はモータとして、その応答性が早い利
点を生かして、インクリメンタル動作を行なわせ
るものが多く、パルスモータでは追従できない分
野へ使われる例が多い。すなわち磁気デイスク、
フアクシミリ、自動溶接機、工業ロボツト、工作
機械等の分野である。しかしこれ等の機器の高性
能化や高精度化の背景から、一段と制御応答性を
高めたモータ、すなわち低慣性無鉄心電機子の出
現が望まれていた。
本発明は上記要請に鑑みてなされたもので、熱
硬化性樹脂の加熱硬化により、少なくとも電機子
巻線部分を一体的剛体化する無鉄心電機子の低慣
性化を目的とした製造方法に関するものである。
すなわち金型内で少なくとも電機子巻線部分に
熱硬化性樹脂、発泡剤或いはこれを包んだ微細カ
プセルおよび発泡開始剤を充填し、前記発泡剤ま
たはそれを包んだ微細カプセルの膨張最低温度ま
たはわずかに低い温度で発泡開始剤を分解せし
め、前記熱硬化性樹脂の重合温度より低い温度で
発泡せしめるとともに、速やかに前記熱硬化性樹
脂を重合せしめて、前記熱硬化性樹脂の内部から
の発泡圧力によつて熱硬化性樹脂を型内に完全充
填せしめることを特徴とするものである。
以下本発明を更に詳細に説明する。
本発明で対象とする無鉄心電機子は数ワツトか
ら数百ワツトに至るモータとして使用されるもの
であつて、巻線式の無鉄心電機子であれば偏平状
であつても、或いはカツプ状であつても差支えな
い。また電線を所定数巻装し、所定形状に賦形さ
れていない未整形の電機子巻線であつても、整形
された電機子巻線であつても差支えない。
また本発明の製造方法において熱硬化性樹脂は
室温で固形或いはパテ状のものでも差支えない
が、固形のものは移送成形、パテ状のものでは圧
縮成形を採ることが望ましい。
本発明で用いる熱硬化性樹脂とは基本樹脂と、
これを硬化し得る化合物、或いは重合開始剤、発
泡剤、充填剤及び必要に応じて加える繊維、離型
剤、着色剤からなり、好ましくは、発泡倍率1.5
〜2.5倍の発泡性樹脂組成物をいうが、更に無鉄
心電機子の電機子巻線の一部表面に有機質或いは
無機質繊維からなる織布もしくは不織布、或いは
それ等を基材としたプリプレグ体を適宜用いてサ
ンドイツチ状複合体の表面材としてもよく、或い
は電機子巻線片側表面だけプリプレグ硬化層を配
する構成のものとしても差支えない。
本発明で用いる熱硬化性樹脂、即ち基本樹脂と
これを硬化し得る化合物或いは重合開始剤、発泡
剤、充填剤及び必要に応じて加える繊維質、離型
剤、着色剤からなる発泡性熱硬化性樹脂組成物に
ついて以下に説明する。
基本樹脂とは不飽和ポリエステル、ジアリルフ
タレート、ウレタン、フエノール、エポキシ、ユ
リアなどであり、中でも不飽和ポリエステル、ジ
アリルフタレートが好ましい。本発明で使用する
不飽和ポリエステルとは、α、β不飽和カルボン
酸又はこれ等と飽和ジカルボン酸、更には飽和、
不飽和モノカルボン酸を含む有機酸類とアルコー
ル類、即ちグリコール類、多価アルコール類及び
一価アルコール類とのエステル化反応により得ら
れる不飽和ポリエステルを、これと重合可能な架
橋単量体に溶解したもので、通常少量の重合禁止
剤を含み、更に所望ならば低収縮剤としてポリス
チレン、ポリエチレン、ポリメタクリル酸メチル
及び共重合体、ポリ塩化ビニル、ポリカプロラク
トン飽和ポリエステルを含有するものを言う。ま
たジアリルフタレートとはジアリルオルソフタレ
ート、ジアリルイソフタレート、テトラブロモジ
アリルフタレート、テトラクロロジアリルフタレ
ートなどのプレポリマー及びそれ等の共重合体で
単量体を含み、更に所望ならばブタジエン、ウレ
タン等のゴム或いはポリスチレン等の熱可塑性樹
脂を含むものを言う。
硬化剤または重合開始剤とは上記基本樹脂の場
合には有機過酸化物、例えばベンゾイルパーオキ
サイド、メチルエチルケトンパーオキサイド等が
あり、促進剤としてはコバルトナフテネート、コ
バルトオクトエート等の金属塩、トリエタノール
アミン、ジエチルアニリン等のアミン類等が任意
に使用される。
発泡剤としては、例えばジニトロソペンタメチ
レンテトラミン、アゾジカルボンアミド、トルエ
ンスルホニルヒドラジド、アゾイソブチルニトリ
ルなどの加熱時ガスを発生する物質、或いはアク
リルニトリル−塩化ビニリデン共重合体、ポリス
チレン、ポリα−メチルスチレン、ポリイソブチ
レン等の微細カプセル中に前記加熱時ガスを発生
させる物質もしくはプロパン、ペンタン、ヘキサ
ン、ヘプタン、石油エーテル、ジクロルペンタン
シクロペンタジエンの如き微細カプセル物質を溶
解させない脂肪族及び環状脂肪族炭化水素を発泡
剤として含浸させたものを言う。
この外、炭酸カルシウム、水和アルミナ、シリ
カ等の充填剤、ガラス、ビニロン等の繊維、ステ
アリン酸亜鉛、ステアリン酸カルシウム等の離型
剤、酸化チタン、フタロシアンブルーなどの着色
剤を適宜必要に応じて用いる。
上記発泡性熱硬化性樹脂組成物の重合硬化は通
常発熱を伴う。発熱しながら重合硬化により粘度
上昇し、ついには硬化に至る。比較的低温で重合
が開始される場合でも、重合が開始されれば通常
かなりの高温度まで温度が上昇するが、その時点
では粘度の上昇も著しく、発泡性熱硬化樹脂組成
物は発泡せず、金型内で完全充填するに至らな
い。従つて重合初期のまだ粘度が低い間に発泡剤
或いはそれを包んだ微細カプセルが膨張する温度
に達する必要があり、電機子巻線一体的剛体化温
度が発泡剤或いはそれを包んだ微細カプセルが膨
張する最低温度以下、或いはその温度に近い温度
の場合は熱伝導の時間遅れから、内部が発泡剤或
いはそれを包んだ微細カプセルの膨張温度に達す
るのは重合開始後の重合熱によるものとなり、す
でに粘度上昇が著しく、硬化物の発泡倍率が少な
くなり、所望の無鉄心電機子は得られない。即ち
重合熱によらずに系の内部まで発泡剤或いはそれ
を包んだ微細カプセルの膨張温度以上に温度上昇
するためには電機子一体的剛体化温度を発泡温度
よりも高くする必要がある。
重合開始前に金型内で発泡剤或いはそれらを包
んだ微細カプセルを膨張させた場合、その状態で
長時間放置すると、発泡した気泡或いはマイクロ
バルーンが再び溶融樹脂や架橋単量体などにより
破壊されることがある。従つて金型内で電機子巻
線を埋め込んだ時点で速やかに重合して粘度が上
昇し、硬化することが望ましく、粘度がある程度
上昇しさえすれば気泡或いはマイクロバルーンが
破壊されても空隙は小さなセルとして残存するこ
とになり、所望の低慣性無鉄心電機子が得られる
のである。従つて基本樹脂を硬化し得る化合物、
或いは重合開始剤は少なくとも発泡剤或いはそれ
を包んだ微細カプセルが膨張し得る最低温度より
やや低目か、同程度の温度で分解する開始剤が好
ましい。
以下実施例を示す。
実施例 1
φ0.25の自己融着層を有する絶縁電線を50回巻
回した単コイルを23個偏平状に整列した電機子巻
線群と整流子から成る電機子巻線を用意した。
またアクリルニトリル−塩化ビニリデン共重合
物微細カプセル中にイソブタンを包含したマイク
ロスフエアーを用いて下記組成の発泡性熱硬化性
樹脂組成物を得た。
不飽和ポリエステル 70重量部
スチレン 80重量部
マイクロスフエアー 3.5重量部
過酸化ベンゾイル 1重量部
炭酸カルシウム 150重量部
ステアリン酸亜鉛 2重量部
以上をニーダで混合したのち10gを、予め金型
内に装填ずみの電機子巻線の中央部分に載置し、
The present invention relates to a method of manufacturing a coreless armature in which at least the armature winding portion is made integrally rigid by heating and curing a thermosetting resin. Generally, the armature winding is made into a rigid body by wrapping a predetermined number of electric wires around it and fixing it together with the supporting core using a binder such as varnish. However, in the case of an armature winding without a supporting core, such as a coreless armature, the armature winding itself must be made integrally rigid by some method. In particular, in the case of armature windings used as relatively large coreless armatures ranging from several watts to several hundred watts, the properties required for integral rigidity are sophisticated, such as strength at high temperatures, dimensional stability, and heat resistance. An integrated rigid body that can meet impact resistance, electrical insulation properties, and long-term heat deterioration resistance is required. Therefore, transfer molding is applied to at least the armature winding portion of the above-mentioned coreless armature using a thermosetting resin molding material that usually contains 50% or more of an inorganic filler, and prepreg hardening is further applied to a part of the surface of the armature winding. Iron-free armatures that utilize the combined effect of providing layers have been put into practical use. The relatively large coreless armatures mentioned above, ranging from a few watts to several hundred watts, are often used as motors to perform incremental motion by taking advantage of their quick response, and are used in fields that cannot be followed by pulse motors. There are many. i.e. magnetic disk,
These fields include facsimiles, automatic welding machines, industrial robots, and machine tools. However, as the performance and precision of these devices have increased, there has been a desire for a motor with even higher control responsiveness, that is, a low-inertia iron-core armature. The present invention has been made in view of the above-mentioned demands, and relates to a manufacturing method for the purpose of lowering the inertia of a coreless armature in which at least the armature winding portion is made into an integral rigid body by heating and curing a thermosetting resin. It is. That is, in a mold, at least the armature winding portion is filled with a thermosetting resin, a foaming agent, or microcapsules encasing the same, and a foaming initiator, and the foaming agent or the microcapsules encasing it are filled with the lowest expansion temperature or slightly below. The foaming initiator is decomposed at a low temperature to cause foaming to occur at a temperature lower than the polymerization temperature of the thermosetting resin, and the thermosetting resin is quickly polymerized to reduce the foaming pressure from inside the thermosetting resin. This method is characterized by completely filling the mold with the thermosetting resin. The present invention will be explained in more detail below. The iron core armature that is the object of the present invention is used in motors ranging from several watts to several hundred watts, and if it is a wire-wound type iron core armature, it can be flat or cup-shaped. There is no problem even if it is. Further, the armature winding may be an unshaped armature winding in which a predetermined number of electric wires are wound and not shaped into a predetermined shape, or a shaped armature winding. Further, in the manufacturing method of the present invention, the thermosetting resin may be solid at room temperature or putty-like, but it is preferable to use transfer molding for solid resins and compression molding for putty-like resins. The thermosetting resin used in the present invention is a basic resin,
It consists of a compound capable of curing this, or a polymerization initiator, a foaming agent, a filler, and fibers added as necessary, a mold release agent, and a coloring agent, preferably with a foaming ratio of 1.5.
It refers to a foamable resin composition of ~2.5 times the size of the foamed resin composition, and in addition, a woven or nonwoven fabric made of organic or inorganic fibers, or a prepreg body based on these, is added to a part of the surface of the armature winding of the iron-core armature. It may be used as a surface material for a sandwich-like composite body by using it as appropriate, or it may be configured such that a cured prepreg layer is provided only on one surface of the armature winding. The thermosetting resin used in the present invention, that is, a foaming thermosetting resin consisting of a basic resin, a compound capable of curing it, a polymerization initiator, a foaming agent, a filler, and optionally added fibers, a mold release agent, and a coloring agent. The resin composition will be explained below. The basic resin includes unsaturated polyester, diallyl phthalate, urethane, phenol, epoxy, urea, etc., and among them, unsaturated polyester and diallyl phthalate are preferred. The unsaturated polyester used in the present invention refers to α, β unsaturated carboxylic acids or these and saturated dicarboxylic acids, further saturated,
An unsaturated polyester obtained by an esterification reaction between organic acids including unsaturated monocarboxylic acids and alcohols, that is, glycols, polyhydric alcohols, and monohydric alcohols, is dissolved in a crosslinking monomer that can be polymerized with the unsaturated polyester. It usually contains a small amount of polymerization inhibitor and, if desired, contains polystyrene, polyethylene, polymethyl methacrylate and copolymers, polyvinyl chloride, polycaprolactone saturated polyester as low shrinkage agents. Furthermore, diallyl phthalate is a prepolymer such as diallyl orthophthalate, diallyl isophthalate, tetrabromo diallyl phthalate, tetrachlorodiallyl phthalate, or a copolymer thereof, and contains monomers such as butadiene, urethane, etc., if desired. Alternatively, it refers to a material containing thermoplastic resin such as polystyrene. Curing agents or polymerization initiators include organic peroxides such as benzoyl peroxide, methyl ethyl ketone peroxide, etc. in the case of the above basic resins, and metal salts such as cobalt naphthenate, cobalt octoate, and triethanol as accelerators. Amines, amines such as diethylaniline, etc. are optionally used. Examples of the blowing agent include substances that generate gas when heated, such as dinitrosopentamethylenetetramine, azodicarbonamide, toluenesulfonylhydrazide, and azoisobutylnitrile, or acrylonitrile-vinylidene chloride copolymer, polystyrene, and polyα-methylstyrene. , substances that generate gas when heated in the fine capsules such as polyisobutylene, or aliphatic and cycloaliphatic hydrocarbons that do not dissolve the fine capsule substances such as propane, pentane, hexane, heptane, petroleum ether, dichloropentane cyclopentadiene, etc. is impregnated with foaming agent. In addition, fillers such as calcium carbonate, hydrated alumina, and silica, fibers such as glass and vinylon, mold release agents such as zinc stearate and calcium stearate, and colorants such as titanium oxide and phthalocyan blue are added as appropriate. used. Polymerization and curing of the foamable thermosetting resin composition is usually accompanied by heat generation. The viscosity increases due to polymerization and curing while generating heat, and finally hardening occurs. Even when polymerization starts at a relatively low temperature, the temperature usually rises to a fairly high temperature once polymerization has started, but at that point the viscosity increases significantly and the foamable thermosetting resin composition does not foam. , the mold is not completely filled. Therefore, it is necessary for the blowing agent or the microcapsules surrounding it to reach a temperature at which it expands while the viscosity is still low at the beginning of polymerization. If the temperature is below the minimum expansion temperature or close to that temperature, due to the time delay in heat conduction, the expansion temperature of the foaming agent or the microcapsules enclosing it will be reached by the polymerization heat after polymerization starts. The viscosity has already increased significantly, the foaming ratio of the cured product has decreased, and the desired iron-free armature cannot be obtained. That is, in order to raise the temperature to the inside of the system above the expansion temperature of the foaming agent or the microcapsules surrounding it without using polymerization heat, it is necessary to make the armature-integral rigidity temperature higher than the foaming temperature. If the foaming agent or the microcapsules enclosing them are expanded in the mold before polymerization starts, if left in that state for a long time, the foamed bubbles or microballoons may be destroyed again by the molten resin or crosslinked monomer. Sometimes. Therefore, it is desirable that the armature winding is quickly polymerized, its viscosity increases, and hardened when it is embedded in the mold.As long as the viscosity increases to a certain extent, even if the bubbles or microballoons are destroyed, there will be no voids. It remains as a small cell, and the desired low inertia coreless armature can be obtained. Compounds capable of curing the basic resin,
Alternatively, the polymerization initiator is preferably an initiator that decomposes at a temperature that is slightly lower than or approximately the same as the lowest temperature at which the blowing agent or the microcapsules enclosing it can expand. Examples are shown below. Example 1 An armature winding consisting of a commutator and an armature winding group in which 23 single coils of insulated wire having a self-bonding layer of φ0.25 were wound 50 times and arranged in a flat shape was prepared. Further, a foamable thermosetting resin composition having the following composition was obtained using microspheres containing isobutane in microcapsules of acrylonitrile-vinylidene chloride copolymer. Unsaturated polyester 70 parts by weight Styrene 80 parts by weight Microsphere 3.5 parts by weight Benzoyl peroxide 1 part by weight Calcium carbonate 150 parts by weight Zinc stearate 2 parts by weight After mixing the above in a kneader, 10 g was loaded into the mold in advance. Place it in the center of the armature winding of
【表】
尚、上例の電機子巻線重量は52.9g、整流子は
24.5gであり、実施例で用いた発泡性樹脂組成物
の発泡倍率は1.9〜2.2倍のものである。
第1表から明らかなように本発明実施例は従来
の無鉄心電機子に対し総重量で18〜20%もの軽量
化を達成した。即ちモータとして18〜20%もの低
慣性化を達成し、極めて制御応答性の優れた動作
を行なうものとなる。
更に電機子巻線、電機子軸、整流子を一体化す
る熱硬化性樹脂硬化物中にセルまたはバルーンを
多数包含する構造の無鉄心電機子であるため、セ
ル或いはバルーンが吸音機能を果し、結果として
モータ騒音の低減への効果も大きい。
また、本発明によれば、発泡剤またはそれを包
んだ微細カプセルの膨張最低温度またはわずかに
低い温度で発泡開始剤を分解せしめ、熱硬化性樹
脂の重合温度より低い温度で発泡せしめるととも
に、速やかに熱硬化性樹脂を重合せしめるから、
熱硬化性樹脂を型内に完全に充填することができ
て、極めて良質の無鉄心電機子を得ることができ
る。[Table] In the above example, the armature winding weight is 52.9g, and the commutator is
The foaming ratio of the foamable resin composition used in the examples is 1.9 to 2.2 times. As is clear from Table 1, the embodiment of the present invention achieved a total weight reduction of 18 to 20% compared to the conventional ironless armature. In other words, the motor achieves a reduction in inertia of 18 to 20% and operates with extremely excellent control response. Furthermore, since it is a coreless armature with a structure that includes many cells or balloons in the thermosetting resin that integrates the armature winding, armature shaft, and commutator, the cells or balloons have a sound absorbing function. As a result, the effect of reducing motor noise is also large. Further, according to the present invention, the foaming initiator is decomposed at the lowest expansion temperature of the foaming agent or the microcapsules enclosing it, or at a slightly lower temperature, and foaming is performed at a temperature lower than the polymerization temperature of the thermosetting resin, and the foaming is rapidly performed. Because thermosetting resin is polymerized with
The mold can be completely filled with the thermosetting resin, and a coreless armature of extremely high quality can be obtained.
Claims (1)
性樹脂および発泡剤またはれを包んだ微細カプセ
ルならびに発泡開始剤を充填し、前記発泡剤また
はそれを包んだ微細カプセルの膨張最低温度また
はそれよりわずかに低い温度で発泡開始剤を分解
せしめ、前記熱硬化性樹脂の重合温度より低い温
度で発泡せしめるとともに、速やかに前記熱硬化
性樹脂を重合せしめて、前記熱硬化性樹脂の内部
からの発泡圧力によつて熱硬化性樹脂を型内に完
全充填せしめる工程を必須としたことを特徴とす
る、前記熱硬化性樹脂を加熱硬化して電機子巻線
を一体的剛体化してなる無鉄心電機子の製造方
法。1. In a mold, at least the armature winding portion is filled with a thermosetting resin, a foaming agent, or microcapsules encasing the same, and a foaming initiator, and the foaming agent or the microcapsules encasing the same are filled with the lowest expansion temperature or lower. The foaming initiator is decomposed at a slightly lower temperature, and the thermosetting resin is foamed at a temperature lower than the polymerization temperature of the thermosetting resin. An ironless core formed by heating and curing the thermosetting resin to make the armature winding an integral rigid body, characterized in that the step of completely filling the mold with the thermosetting resin by using foaming pressure is essential. Method of manufacturing armature.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4187580A JPS56139061A (en) | 1980-03-31 | 1980-03-31 | Manufacture of coreless armature |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4187580A JPS56139061A (en) | 1980-03-31 | 1980-03-31 | Manufacture of coreless armature |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56139061A JPS56139061A (en) | 1981-10-30 |
| JPS6245784B2 true JPS6245784B2 (en) | 1987-09-29 |
Family
ID=12620434
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4187580A Granted JPS56139061A (en) | 1980-03-31 | 1980-03-31 | Manufacture of coreless armature |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS56139061A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102011111806A1 (en) * | 2011-08-27 | 2013-02-28 | Daimler Ag | Component or component group of an electrical machine and method for producing a component or component group of an electrical machine |
| JP7092617B2 (en) * | 2018-08-29 | 2022-06-28 | 日立Astemo株式会社 | Manufacturing method of stator of rotary electric machine |
| WO2026079478A1 (en) * | 2024-10-11 | 2026-04-16 | 大日本印刷株式会社 | Rotary electric machine and method for manufacturing same, and reinforcing member and reinforcing sheet |
-
1980
- 1980-03-31 JP JP4187580A patent/JPS56139061A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56139061A (en) | 1981-10-30 |
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