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JPS6227490B2 - - Google Patents
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JPS6227490B2 - - Google Patents

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Publication number
JPS6227490B2
JPS6227490B2 JP56020213A JP2021381A JPS6227490B2 JP S6227490 B2 JPS6227490 B2 JP S6227490B2 JP 56020213 A JP56020213 A JP 56020213A JP 2021381 A JP2021381 A JP 2021381A JP S6227490 B2 JPS6227490 B2 JP S6227490B2
Authority
JP
Japan
Prior art keywords
resin
fbt
properties
dielectric
comparative examples
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
Application number
JP56020213A
Other languages
Japanese (ja)
Other versions
JPS57134919A (en
Inventor
Tetsuo Tajima
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP56020213A priority Critical patent/JPS57134919A/en
Publication of JPS57134919A publication Critical patent/JPS57134919A/en
Publication of JPS6227490B2 publication Critical patent/JPS6227490B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/302Polyurethanes or polythiourethanes; Polyurea or polythiourea

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Insulating Of Coils (AREA)
  • Coils Or Transformers For Communication (AREA)
  • Organic Insulating Materials (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

本発明は、ポリブタゞ゚ン系暹脂組成物を甚い
お絶瞁凊理するこずによるフラむバツクトラン
ス、特にボビン、ダむオヌド、コむル、フオヌカ
ス抵抗、コンデンサヌ、ケヌスを䞀䜓化したフラ
むバツクトランスの補造法に関するものである。 テレビ受像機甚フラむバツクトランス
FBTは、䟋えば耇数個の仕切り壁を有するプ
ラスチツクボビンに分割巻きした次コむル、
぀以䞊のガラスモヌルドダむオヌドを配線しなが
ら、次コむルず類䌌の分割巻きを行な぀た次
コむル、フオヌカス電圧調節甚の抵抗、゚ポキシ
レゞンモヌルドコンデンサヌ、ケヌスなどの郚品
で構成されおおり、これらを泚圢レゞンで絶瞁凊
理するこずによ぀お完成品ずなる。 䞊蚘のようなFBTを絶瞁凊理する堎合、その
各構成郚品の熱膚匵係数には倧きな差があるた
め、泚圢レゞンを加熱硬化埌、冷华する時に、あ
るいは枩床サむクルが加わ぀た堎合、郚品ず泚圢
レゞンずの間に耇雑な応力が発生し、クラツクや
はく離が生じる。 FBTの各構成郚品には高電圧が印加されるた
め、これらのクラツクやはく離が原因ずな぀おコ
ロナ攟電などを生じ、FBTが絶瞁砎壊する。 埓来、熱硬化性゚ポキシレゞンや䞍飜和ポリ゚
ステルレゞン、シリコヌンゎムなどの絶瞁材料が
泚圢レゞンずしお䜿甚されおいる。それは、これ
らのレゞンが機械特性や絶瞁特性に優れおいるた
めであり、たたシリコヌンゎムに぀いおはこれら
のレゞンずは党く異な぀たゎム匟性䜓ではあるけ
れども、難燃性や誘電特性に優れおいるためであ
る。 しかしながら、゚ポキシレゞンや䞍飜和ポリ゚
ステルレゞンは、機械特性に優れおいるけれど
も、ヒヌトシペツクに察しお匱く、急激な枩床倉
化によ぀おたびたびクラツクが発生し補品の信頌
性に欠ける。たた、加熱硬化時にレゞンが収瞮を
起こし、内郚に応力が残぀たたゝで硬化する。こ
れが硬化歪ず蚀われるものである。この傟向は、
特に䞍飜和ポリ゚ステルレゞンに匷く、倧きな問
題の䞀぀ずな぀おいる。これらの解決策ずしおレ
ゞンに可ずう性を䞎えるこずがしばしばずられお
いるが、レゞンに可ずう性を付䞎するこずは、誘
電特性の悪化を招き絶瞁材料ずしお臎呜的な堎合
がある。シリコヌンゎムは、誘電率、誘電正接の
䜎い材料であり、可ずう性にも優れおいるなど絶
瞁材料ずしおは優れた特性を有しおいるものの、
䞀般にはコストが高く、か぀透湿性が倧きいなど
の理由により甚途が制玄されおいる。䞀方、りレ
タン系絶瞁材料ずしおポリ゚ステル系、ポリ゚ヌ
テル系、ひたし油系の材料が存圚するが、いずれ
も耐氎性が悪く、絶瞁材料ずしおの䜿甚䞊充分な
胜力がないうえ、誘電特性も悪く、難燃性は有す
るもののFBTには䜿甚されおいない。たた、特
殊なりレタン系絶瞁材料ずしおポリブタゞ゚ン系
の材料が存圚し、これは耐氎性、誘電特性が䞊蚘
りレタンに比范しお優れおいるが、りレタン系絶
瞁材料は䞀般にむ゜シアネヌト成分のポリオヌル
成分に察する反応性が他の材料に比べ高すぎるた
め、可䜿時間が短かく䞡成分の混合液の粘床が急
激に䞊昇するため、コむル間ぞのレゞンの含浞性
が䞍充分ずなり、FBTの絶瞁砎壊を招く欠点が
あ぀た。䜆し、マスクドむ゜シアネヌトは垞枩で
は䜎反応性ではあるが、反応枩床が高過ぎるこず
ず、ボむド発生、誘電特性䜎䞋などのために甚い
るこずができない。 本発明の目的ずするずころは、䞊蚘した埓来技
術の欠点をなくし、硬化させたレゞン組成物の可
ずう性が優れ、たた、それずFBT構成郚品ずの
接着性、レゞンの耐氎性、誘電特性、難燃性が良
奜であり、さらにレゞンが適床に䜎反応性で可䜿
時間が長く、コむル間ぞの含浞性が良奜なポリブ
タゞ゚ン系暹脂組成物でFBTのボビン、ダむオ
ヌド、コむル、フオヌカス抵抗、コンデンサヌ、
ケヌスを同時に絶瞁凊理しおFBTを補造する方
法を提䟛するにある。 䞊蚘目的を達成するために発明者は、ポリブタ
ゞ゚ン系暹脂組成物を皮々怜蚎した結果、 (ã‚€) 分子䞡末端に氎酞基を有する液状ポリブタゞ
゚ンホモポリマヌ、あるいは分子䞡末端に氎酞
基を有する液状スチレンブタゞ゚ンコポリマ
ヌ、あるいは分子䞡末端に氎酞基を有する液状
アクリロニトリルブタゞ゚ンコポリマヌ、たた
はそれらの混合物、 (ロ) 短鎖ゞオヌルおよび又は短鎖トリオヌル、 (ハ) 以䞋に瀺す化孊匏のむ゜シアネヌト、 䜆し、〜10、〜10、〜10 (ニ) 氎和アルミナ、 (ホ) 赀燐粉末、 からなるポリブタゞ゚ン系暹脂組成物で、FBT
のボビン、ダむオヌド、コむル、フオヌカス抵
抗、コンデンサヌ、ケヌスを同時に絶瞁凊理する
こずによりはじめお達成できるこずを明らかにし
た。 すなわち、本発明は䞊蚘ポリブタゞ゚ン系暹脂
組成物で䞊蚘の各構成郚品を同時に絶瞁凊理しお
FBTを補造するこずを特城ずし、これによ぀お
埗られたFBTは、硬化させたレゞン組成物が可
ずう性に優れ、それずFBT構成郚品ずの接着
性、レゞン硬化物の耐氎性、誘電特性、難燃性が
良奜であり、䞔぀レゞン液状物は適床に䜎反応性
で可䜿時間が長く、コむル間ぞの含浞性が良奜で
あるためFBTの耐電圧特性が優れ信頌性の高い
ものずなる。 次に本発明で䜿甚する材料に぀いお説明する。
ポリオヌルの䞀成分である液状ポリブタゞ゚ン
は、分子量500〜10000で分子䞡末端に氎酞基を有
するポリブタゞ゚ンホモポリマヌ、スチレンブタ
ゞ゚ンコポリマ、アクリロニトリルブタゞ゚ンコ
ポリマヌのいずれの液状ポリブタゞ゚ンでも有効
である。これらは、たずえば−45HT、−
45M、CS−15、CN−15なる商品名で出光石油化
å­Š(æ ª)より垂販されおいる。 残りのポリオヌル成分で架橋剀でもある短鎖ゞ
オヌルおよび短鎖トリオヌルずしおは、以䞋のも
のがある。 −゚チル−・−ヘキサンゞオヌル、ブタ
ンゞオヌル、・−ビス−ヒドロキシプロ
ピルアニリンなどの短鎖ゞオヌル、・・
−ヘキサントリオヌル、グリセリンなどの短鎖ト
リオヌルである。これらは単独たたは混合しお甚
いる。ポリブタゞ゚ンポリオヌルのみであれば硬
床が軟かくお特に高枩時の物理特性がそこなわ
れ、あたり倚く加えるず硬くなりすぎるので、ポ
リオヌル成分ずしお〜30重量97〜70重量
はポリブタゞ゚ンポリオヌル配合するこずが望
たしい。 む゜シアネヌトずしおは、以䞋に瀺す化孊匏の
ものが反応速床が適床に遅く、可䜿時間が長い点
で良く、配合量は䞊蚘皮のポリオヌル成分の掻
性氎玠圓量に察しお0.6〜1.3圓量の割合が特性
飜和の点で望たしい。 䞊匏の、、は〜10、〜10、
〜10のものが奜たしく、、、はよ
り小さいず反応性が高くなり過ぎ含浞䞍良ずな
り、10より倧きいず反応性が䜎すぎるため硬化䞍
良が生じ機械特性、電気特性が䞍充分ずなる。 氎和アルミナずしおは、Al2O3・3H2Oなる化孊
匏で瀺されるものであれば良く、䞀般垂販品が充
分䜿甚できる。このものは難燃性に効果がある。
その配合量は、䞊蚘皮のポリオヌル成分の合蚈
量100重量郚に察しお40〜150重量郚が有効であ
る。すなわち、40重量郚未満のもの難燃効果が少
なく、150重量郚を越えるものは誘電率、誘電正
接が悪化するほか、粘床䞊昇による䜜業性の䜎䞋
をきたす。 赀燐粉末は難燃性を䞎えるのに効果のあるもの
であるが、特に氎和アルミナず䜵甚した堎合に盞
乗効果により優れた難燃性を瀺す。これを配合す
るこずにより、氎和アルミナの配合量を所定の量
たで䜎枛でき、誘電率、誘電正接を悪化させるこ
ずなく難燃性を䞎えるこずができる。その配合量
は、䞊蚘皮のポリオヌル成分の合蚈量100重量
郚に察しお10重量郚以䞊が効果があり、さらに奜
たしくは10〜30重量郚である。 すなわち、10重量郚未満のものは難燃効果が少
なく、30重量郚を越えおもその効果は倉わらなか
぀た。その他さらに必芁に応じお粘床調敎剀ずし
お、゚ステル類、オむル類炭化氎玠オむルやハ
ロゲン化オむル、゚ポキシ化脂肪酞などを配合
しおも良い。たた、特性向䞊のために、必芁に応
じ他の無機充おん剀、シランカツプリング剀、消
泡剀、着色剀などを添加するこずが出来る。 次に、諞特性の枬定方法を述べる。 (1) レゞン硬化物の可ずう性軟銅補字圢ワツ
シダ内埄mm、倖埄22mm、厚さmm、切蟌み
幅mmをレゞン組成物䞭に埋め蟌んだ詊隓片
レゞン硬化物の肉厚mmを、䞊限枩床を100
℃䞀定ずし、䞋限枩床を40℃よりサむクル
各枩床時間ず぀保持毎に10℃ず぀枩床を
䞋げながらヒヌトシペツク詊隓を行ない、詊隓
片にクラツクが発生した時の枩床を10個の詊隓
片に぀いお求め、その平均倀をクラツク発生枩
床ずし可ずう性の優劣の目安ずした。すなわ
ち、クラツク発生枩床の䜎い方のレゞンが可ず
う性に優れおいる。 (2) 接着性アルミニりム棒盎埄11.3mmφ、接
着面積cm2に12mm×12mm×mmのポリブチレ
ンテレフタレヌトPBT板をはさみ、アル
ミニりム棒ずPBT板ずの間の接着局玄50Ό
にレゞン組成物を付着、加熱硬化しお詊隓片ず
した。匕匵り詊隓埌に砎断面を芳察し、いずれ
の詊隓片もレゞンずPBT板ずの間がはく離す
るこずを確かめた。枬定倀は、25℃での枬定倀
10個の平均倀ずした。 (3) 耐氎性JIS K6911に準じ、個の詊料に぀
いお23℃、24時間埌におけるレゞン硬化物の吞
氎率を枬定し、その平均倀を耐氎性の目
安ずした。吞氎率の䜎い方のレゞンは耐氎性に
優れおいる。 (4) 誘電特性JIS K6911に準じ、90℃、10KHz
で求めた。個の詊料に぀いお、ずもに誘電率
が以䞋、誘電正接が以䞋のものを
「」、それ以倖のものを「」ずした。 (5) 可䜿時間40℃におけるレゞンの粘床が倍
になるたでの時間。個の詊料の平均倀で瀺し
た。 (6) 高枩時の物理特性機械特性をJIS K6301に
準じ90℃で求めた。個の詊料に぀いお、ずも
に匕匵匷床50Kgcm2以䞊、䌞び200以䞊のも
のを「」、それ以倖のものを「」ずした。 (7) 難燃性UL94芏栌に準じ、1/16むンチ厚み
のテストピヌスで求めた。UL94V−に合栌
するものを「−」ずし、䞍合栌のものを
「燃焌」ずした。 (8) 含浞性コむル巻線間ぞのレゞンの含浞性
は、レゞンを泚圢硬化したFBTのコむル巻線
郚分を切断しお、断面を50倍皋床の顕埮鏡で芳
察し、コむル〜コむル間に含浞しおいるレゞン
のコむル間面積に察する割合を調べた。95以
䞊を合栌ずした。なお、レゞンの硬化条件はす
べお60℃3h100℃2hずした。以䞋、本発
明を実斜䟋により詳述する。 実斜䟋  第衚の実斜䟋No.1〜10、比范䟋No.1〜10に
瀺すレゞン組成物でクラツク発生枩床、接着性、
吞氎率、誘電特性、可䜿時間、高枩時の機械特
性、難燃性を枬定したずころ第衚の結果を埗
た。FBT甚泚圢レゞンは、そのクラツク発生枩
床が−50℃より䜎くなければ䜿甚できない。実斜
䟋No.1〜10は−70℃より䜎く、比范䟋もNo.2ず
No.4を陀いお−70℃より䜎く、可ずう性ずいう
面からは満足できる。しかし、短鎖ゞオヌルの配
合割合が倚い比范䟋No.2ずNo.4は、硬くなりす
ぎクラツチ発生枩床が−20℃ず高く、可ずう性は
劣぀おおりFBTには䜿甚できない。接着性に぀
いお芋るず、実斜䟋、比范䟋ずもに100Kgcm2よ
り高く満足できる。 たた吞氎率も、実斜䟋、比范䟋ずもに100Kg
cm2より高く満足できる。 レゞンの誘電特性の面から芋るず、氎和アルミ
ナの配合量の倚い比范䟋No.6を陀いお実斜䟋、
比范䟋ずもに良奜であり満足できる。 FBTレゞンずしおは、コむル巻線間ぞのレゞ
ンの含浞が必須である。そのためには、グリコヌ
ル成分ずむ゜シアネヌト成分を混合した埌の反応
性が適床に䜎いこずが重芁である。その目安ずし
お可䜿時間を甚い、これが長い方が䜎反応性であ
るず蚀える。実積から芋るず可䜿時間は40℃で少
なくずも時間を越える必芁がある。本発明のむ
゜シアネヌトを甚いない比范䟋No.9、No.10はず
もに可䜿時間が時間より短かいものであ぀た。 しかし、本発明のむ゜シアネヌトを甚いた実斜
䟋、他の比范䟋は、ずもに時間より長く良奜な
ものであ぀た。高枩時の機械特性では、短鎖ゞオ
ヌルを党く含たない比范䟋No.1ずNo.3が䞍良で
あ぀た。しかし、短鎖ゞオヌルを含む実斜䟋、䞊
蚘以倖の比范䟋はずもに良奜であ぀た。 たた、難燃性もFBTには重芁な特性であり、
レゞンではUL94V−に合栌したものしか甚い
るこずが出来ない。氎和アルミナの配合量が少な
い比范䟋No.5、赀燐配合量の少ない比范䟋No.7
は、ずもに難燃性の点で䞍合栌であ぀た。しか
し、氎和アルミナ、赀燐をずもに必芁量配合した
実斜䟋、䞊蚘以倖の比范䟋は、ずもに難燃性を満
足した。なお、比范䟋No.8は、赀燐を必芁量以
䞊に過剰に配合したもので特に難燃性は䜎䞋しな
か぀たが、過剰量は無駄なものであ぀た。 以䞊の特性をすべお満足できるレゞン組成物は
実斜䟋No.1〜10である。
The present invention relates to a method for manufacturing a flyback transformer by insulating a polybutadiene resin composition, particularly a flyback transformer in which a bobbin, a diode, a coil, a focus resistor, a capacitor, and a case are integrated. A flyback transformer (FBT) for a television receiver, for example, consists of a primary coil, 1
It consists of parts such as a secondary coil with split winding similar to the primary coil, a resistor for focus voltage adjustment, an epoxy resin molded capacitor, and a case, while wiring three or more glass molded diodes. The finished product is made by insulating it with cast resin. When insulating FBT as described above, there are large differences in the coefficient of thermal expansion of each of its component parts. Complex stress is generated between the mold and the resin, resulting in cracks and peeling. Since high voltage is applied to each component of the FBT, cracks and peeling of these components can cause corona discharge, leading to dielectric breakdown of the FBT. Conventionally, insulating materials such as thermosetting epoxy resin, unsaturated polyester resin, and silicone rubber have been used as casting resins. This is because these resins have excellent mechanical and insulating properties, and although silicone rubber is a completely different rubber elastic body from these resins, it has excellent flame retardant and dielectric properties. It is. However, although epoxy resins and unsaturated polyester resins have excellent mechanical properties, they are sensitive to heat shock and often crack due to rapid temperature changes, resulting in a lack of product reliability. Additionally, the resin contracts during heating and curing, and the resin hardens while stress remains inside. This is called hardening strain. This trend is
It is particularly strong against unsaturated polyester resins, which has become a major problem. As a solution to these problems, it is often taken to impart flexibility to the resin, but imparting flexibility to the resin may lead to deterioration of the dielectric properties, which may be fatal as an insulating material. Silicone rubber is a material with a low dielectric constant and dielectric loss tangent, and has excellent properties as an insulating material, such as excellent flexibility.
In general, its use is limited due to high cost and high moisture permeability. On the other hand, polyester-based, polyether-based, and castor oil-based materials exist as urethane-based insulating materials, but all of them have poor water resistance and do not have sufficient ability to be used as insulating materials, have poor dielectric properties, and are flame retardant. Although it has sex, it is not used in FBT. In addition, there is a polybutadiene-based material as a special urethane-based insulating material, which has superior water resistance and dielectric properties compared to the above-mentioned urethane, but urethane-based insulating materials generally have a high reactivity with the polyol component of the isocyanate component. is too high compared to other materials, the pot life is short, and the viscosity of the mixture of both components increases rapidly, resulting in insufficient resin impregnation between the coils, leading to dielectric breakdown of the FBT. It was hot. However, although masked isocyanate has low reactivity at room temperature, it cannot be used because the reaction temperature is too high, voids occur, and dielectric properties deteriorate. The purpose of the present invention is to eliminate the above-mentioned drawbacks of the prior art, to provide a cured resin composition with excellent flexibility, and to improve the adhesion between it and FBT components, the water resistance and dielectric properties of the resin, and to improve the flexibility of the cured resin composition. FBT bobbins, diodes, coils, focus resistors, and capacitors are made of polybutadiene resin compositions that have good flame retardancy, have moderately low reactivity, have a long pot life, and have good impregnation properties between coils. ,
The purpose of the present invention is to provide a method for manufacturing an FBT by simultaneously insulating the case. In order to achieve the above object, the inventor investigated various polybutadiene resin compositions and found that (a) a liquid polybutadiene homopolymer having hydroxyl groups at both ends of the molecule, or a liquid styrene-butadiene copolymer having hydroxyl groups at both ends of the molecule; Alternatively, a liquid acrylonitrile butadiene copolymer having hydroxyl groups at both ends of the molecule, or a mixture thereof; (b) a short chain diol and/or a short chain triol; (c) an isocyanate having the chemical formula shown below; However, l = 2 to 10, m = 2 to 10, n = 2 to 10 (d) hydrated alumina, (e) red phosphorus powder.
It was revealed that this can only be achieved by insulating the bobbin, diode, coil, focus resistor, capacitor, and case at the same time. That is, the present invention simultaneously insulates each of the above components with the above polybutadiene resin composition.
FBT is characterized in that the cured resin composition of FBT obtained by this process has excellent flexibility, adhesion between it and FBT components, water resistance of the cured resin, and dielectric properties. , has good flame retardancy, and the resin liquid has moderately low reactivity, has a long pot life, and has good impregnation properties between coils, so FBT has excellent withstand voltage characteristics and is highly reliable. Become. Next, materials used in the present invention will be explained.
The liquid polybutadiene, which is one component of the polyol, is effective in any of the following liquid polybutadienes: a polybutadiene homopolymer, a styrene-butadiene copolymer, and an acrylonitrile-butadiene copolymer, each having a molecular weight of 500 to 10,000 and having hydroxyl groups at both ends of the molecule. These are, for example, R-45HT, R-
It is commercially available from Idemitsu Petrochemical Co., Ltd. under the trade names 45M, CS-15, and CN-15. The remaining polyol components and short chain diols and short chain triols which are also crosslinking agents include the following. Short chain diols such as 2-ethyl-1,3-hexanediol, butanediol, N,N-bis(2-hydroxypropyl)aniline, 1,2,6
- Short chain triols such as hexanetriol and glycerin. These may be used alone or in combination. If only polybutadiene polyol is used, it will have a soft hardness and its physical properties, especially at high temperatures, will be impaired, and if too much is added, it will become too hard, so 3-30% by weight (97-70% by weight) should be added as a polyol component.
It is desirable to incorporate polybutadiene polyol). As the isocyanate, those with the chemical formula shown below are good because the reaction rate is moderately slow and the pot life is long, and the blending amount is 0.6 to 1.3 equivalents per equivalent of active hydrogen of the above two types of polyol components. is desirable in terms of characteristic saturation. In the above formula, l, m, and n are l = 2 to 10, m = 2 to 10,
It is preferable that n = 2 to 10. If l, m, and n are smaller than 2, the reactivity will be too high, resulting in poor impregnation, and if larger than 10, the reactivity will be too low, resulting in poor curing, resulting in poor mechanical and electrical properties. It becomes insufficient. The hydrated alumina may be one having the chemical formula Al 2 O 3 .3H 2 O, and commercially available products can be used. This material has flame retardant properties.
The effective blending amount is 40 to 150 parts by weight based on 100 parts by weight of the total amount of the above two types of polyol components. That is, if it is less than 40 parts by weight, the flame retardant effect will be low, and if it exceeds 150 parts by weight, the dielectric constant and dielectric loss tangent will deteriorate, and workability will decrease due to increased viscosity. Red phosphorus powder is effective in providing flame retardancy, particularly when used in combination with hydrated alumina, which exhibits excellent flame retardancy due to a synergistic effect. By blending this, the blending amount of hydrated alumina can be reduced to a predetermined amount, and flame retardance can be imparted without deteriorating the dielectric constant and dielectric loss tangent. The blending amount is preferably 10 parts by weight or more, more preferably 10 to 30 parts by weight, based on 100 parts by weight of the two types of polyol components in total. That is, if the amount was less than 10 parts by weight, the flame retardant effect was small, and even if it exceeded 30 parts by weight, the effect did not change. In addition, esters, oils (hydrocarbon oils and halogenated oils), epoxidized fatty acids, and the like may be added as viscosity modifiers, if necessary. Further, in order to improve the properties, other inorganic fillers, silane coupling agents, antifoaming agents, coloring agents, etc. can be added as necessary. Next, methods for measuring various characteristics will be described. (1) Flexibility of cured resin product: Test piece with a C-shaped annealed copper washer (inner diameter 8 mm, outer diameter 22 mm, thickness 5 mm, cut width 2 mm) embedded in a resin composition (wall thickness of cured resin product 7 mm) ), the upper limit temperature is 100
A heat shock test was carried out with the lower limit temperature kept at a constant temperature of 40°C and the temperature was lowered by 10°C every cycle (each temperature was held for 2 hours), and the temperature at which a crack occurred in the test piece was measured for 10 tests. The average value was taken as the crack generation temperature and used as a measure of flexibility. That is, the resin with a lower crack generation temperature has excellent flexibility. (2) Adhesion: A 12 mm x 12 mm x 3 mm polybutylene terephthalate (PBT) plate is sandwiched between an aluminum rod (diameter 11.3 mmφ, adhesive area 1 cm 2 ), and the adhesive layer between the aluminum rod and the PBT plate is approximately 50 ÎŒm.
A resin composition was applied to the sample and cured by heating to obtain a test piece. After the tensile test, the fracture surface was observed and it was confirmed that the resin and PBT plate peeled off in all test pieces. Measured values are measured at 25℃
The average value of 10 values was taken as the average value. (3) Water resistance: According to JIS K6911, the water absorption rate (%) of the cured resin product was measured for three samples at 23°C after 24 hours, and the average value was used as a guideline for water resistance. Resins with lower water absorption have excellent water resistance. (4) Dielectric properties: According to JIS K6911, 90℃, 10KHz
I asked for it. For the three samples, those with a dielectric constant of 4 or less and a dielectric loss tangent of 2% or less were rated "O", and the other samples were rated "X". (5) Pot life: The time it takes for the viscosity of the resin to double at 40℃. The average value of three samples is shown. (6) Physical properties at high temperatures: Mechanical properties were determined at 90°C according to JIS K6301. Of the five samples, those with a tensile strength of 50 kg/cm 2 or more and an elongation of 200% or more were rated "O", and the others were rated "X". (7) Flame retardancy: Measured using a 1/16 inch thick test piece in accordance with the UL94 standard. Those that passed UL94V-O were designated as "V-O", and those that failed were designated as "combustion". (8) Impregnability: The impregnability of the resin between the coil windings can be determined by cutting the coil winding part of FBT that has been cast and cured with resin, and observing the cross section with a microscope at about 50x magnification. The ratio of the resin impregnated to the area between the coils was investigated. A score of 95% or higher was considered a pass. The curing conditions for all resins were 60°C/3 hours + 100°C/2 hours. Hereinafter, the present invention will be explained in detail with reference to Examples. Example 1 The crack occurrence temperature, adhesion,
The water absorption rate, dielectric properties, pot life, mechanical properties at high temperatures, and flame retardancy were measured, and the results shown in Table 2 were obtained. FBT casting resin cannot be used unless its crack generation temperature is lower than -50°C. Examples Nos. 1 to 10 are lower than -70℃, and comparative examples are also lower than No. 2.
Except for No. 4, the temperature was lower than -70℃, which is satisfactory from the standpoint of flexibility. However, Comparative Examples No. 2 and No. 4, which have a high blending ratio of short-chain diols, are too hard, have a high clutch generation temperature of -20°C, and have poor flexibility, so they cannot be used for FBT. Looking at the adhesion properties, both the Examples and Comparative Examples are satisfactory, being higher than 100 Kg/cm 2 . In addition, the water absorption rate was 100Kg/
cm 2 higher and more satisfying. From the perspective of the dielectric properties of the resin, Examples
Both comparative examples are good and satisfactory. For FBT resin, it is essential to impregnate the space between the coil windings with resin. For this purpose, it is important that the reactivity after mixing the glycol component and the isocyanate component is appropriately low. The pot life is used as a guideline; the longer the pot life, the lower the reactivity. Based on actual results, the pot life should be at least 5 hours at 40°C. Comparative Examples No. 9 and No. 10, which did not use the isocyanate of the present invention, both had a pot life of less than 1 hour. However, both Examples using the isocyanate of the present invention and other comparative examples were good for longer than 5 hours. In terms of mechanical properties at high temperatures, Comparative Examples No. 1 and No. 3, which did not contain any short chain diol, were poor. However, both Examples containing short chain diols and Comparative Examples other than those mentioned above were good. Flame retardancy is also an important property for FBT.
Only resins that pass UL94V-O can be used. Comparative example No. 5 with a small amount of hydrated alumina, Comparative example No. 7 with a small amount of red phosphorus
Both failed in terms of flame retardancy. However, both Examples and Comparative Examples other than those mentioned above, in which the required amounts of hydrated alumina and red phosphorus were blended, both satisfied flame retardancy. In Comparative Example No. 8, red phosphorus was added in excess of the necessary amount, and although the flame retardance did not particularly deteriorate, the excess amount was wasteful. Resin compositions that can satisfy all of the above characteristics are Examples Nos. 1 to 10.

【衚】【table】

【衚】【table】

【衚】【table】

【衚】 実斜䟋  10mmHg枛圧容噚に、図瀺したように次ボビ
ン、次ボビン、ダむオヌド、次コむル
、次コむル、フオヌカス抵抗、コンデン
サをケヌス内に収玍したFBTを眮き、第
衚実斜䟋No.1〜10、比范䟋No.1〜、、10に
瀺すレゞン組成物を流し蟌み垞圧に戻した埌、所
定の条件で硬化した。泚圢硬化埌のFBTの断面
図を瀺した。図䞭は泚圢レゞンである。 比范䟋No.1、No.3を甚いたFBTは高枩動䜜な
どの取扱い䜜業䞭にレゞン硬化物の砎断が生じ、
動䜜詊隓で絶瞁砎壊した。 比范䟋No.2、No.4を甚いたFBTは、100℃2h
ず−50℃2hの冷熱サむクルを20サむクル䞎え
た埌コア付近にクラツクが生じ、動䜜詊隓で絶瞁
砎壊した。 比范䟋No.5、No.7を甚いたFBTは、電取法の
燃焌詊隓で䞍合栌であ぀た。 比范䟋No.6を甚いたFBTは、レゞンの誘電特
性が悪く、動䜜時に絶瞁砎壊した。 比范䟋No.9、No.10を甚いたFBTは、レゞンの
可䜿時間が短かく、反応性が高いため、コむル巻
線間ぞのレゞンの含浞性が著しく悪く動䜜時に絶
瞁砎壊した。 䞀方、第衚実斜䟋No.1〜10のレゞン組成物
を甚いたFBTは、䜕らの異垞も認められなか぀
た。 以䞊述べたように、本発明にかかるポリブタゞ
゚ン系暹脂組成物は適床に䜎反応性で可䜿時間が
長くFBTコむル間ぞの含浞性が良奜であり、䞔
぀硬化させたレゞン組成物の可ずう性、接着性だ
けでなく、レゞンの耐氎性、誘電特性、難燃性が
著しく向䞊するため、埗られたFBTは耐電圧特
性、誘電特性、難燃性および信頌性の高いものず
なる。それ故工業的䟡倀は倧きい。
[Table] Example 2 In a 10 mmHg vacuum container, the primary bobbin 2, secondary bobbin 3, diode 4, primary coil 5, secondary coil 6, focus resistor 7, and capacitor 8 are housed in the case 9 as shown. Place the FBT that was
The resin compositions shown in Examples Nos. 1 to 10 and Comparative Examples Nos. 1 to 7, 9, and 10 in the table were poured, returned to normal pressure, and then cured under predetermined conditions. A cross-sectional view of the FBT after casting and hardening is shown. 9 in the figure is a cast resin. FBT using Comparative Examples No. 1 and No. 3 suffered from breakage of the cured resin during handling operations such as high-temperature operation.
Dielectric breakdown occurred during the operation test. FBT using Comparative Examples No. 2 and No. 4 was conducted at 100℃/2h.
After 20 cycles of heating and cooling at -50°C for 2 hours, a crack appeared near the core, and dielectric breakdown occurred during an operation test. The FBTs using Comparative Examples No. 5 and No. 7 failed the combustion test according to the Electricity Control Law. In the FBT using Comparative Example No. 6, the dielectric properties of the resin were poor and dielectric breakdown occurred during operation. In the FBTs using Comparative Examples No. 9 and No. 10, the pot life of the resin was short and the reactivity was high, so the impregnation of the resin between the coil windings was extremely poor and dielectric breakdown occurred during operation. On the other hand, no abnormality was observed in FBT using the resin compositions of Examples Nos. 1 to 10 in Table 1. As described above, the polybutadiene resin composition according to the present invention has moderately low reactivity, has a long pot life, and has good impregnability between FBT coils, and has a high flexibility of the cured resin composition. , not only the adhesive properties but also the water resistance, dielectric properties, and flame retardance of the resin are significantly improved, so the obtained FBT has high withstand voltage properties, dielectric properties, flame retardance, and reliability. Therefore, it has great industrial value.

【図面の簡単な説明】[Brief explanation of the drawing]

図はフラむバツクトランスの断面を衚わす。   泚圢レゞン、  次ボビン、  
次ボビン、  ダむオヌド、  次コむ
ル、  次コむル、  フオヌカス抵抗、
  コンデンサヌ、  ケヌス。
The figure shows a cross section of a flyback transformer. 1... Casting resin, 2... Primary bobbin, 3...
Secondary bobbin, 4... diode, 5... primary coil, 6... secondary coil, 7... focus resistor,
8... Capacitor, 9... Case.

Claims (1)

【特蚱請求の範囲】  (ã‚€) 分子䞡末端に氎酞基を有する液状ポリブ
タゞ゚ンホモポリマヌ、あるいは分子䞡末端に
氎酞基を有する液状スチレンブタゞ゚ンコポリ
マヌ、あるいは分子䞡末端に氎酞基を有する液
状アクリロニトリルブタゞ゚ンコポリマヌ、た
たはそれらの混合物、 (ロ) 短鎖ゞオヌルおよび又は短鎖トリオヌル、 (ハ) 以䞋に瀺す化孊匏のむ゜シアネヌト、 䜆し、〜10、〜10、〜10 (ニ) 氎和アルミナ、 (ホ) 赀燐粉末、 からなるポリブタゞ゚ン系暹脂組成物で絶瞁凊理
するこずを特城ずするフラむバツクトランスの補
造法。
[Scope of Claims] 1 (a) Liquid polybutadiene homopolymer having hydroxyl groups at both molecular ends, liquid styrene-butadiene copolymer having hydroxyl groups at both molecular ends, liquid acrylonitrile butadiene copolymer having hydroxyl groups at both molecular ends, or the like. (b) a short-chain diol and/or a short-chain triol; (c) an isocyanate having the chemical formula shown below; However, l = 2 to 10, m = 2 to 10, n = 2 to 10 (d) hydrated alumina, (e) red phosphorus powder. Manufacturing method of back transformer.
JP56020213A 1981-02-16 1981-02-16 Fabrication of fly-back transformer Granted JPS57134919A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56020213A JPS57134919A (en) 1981-02-16 1981-02-16 Fabrication of fly-back transformer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56020213A JPS57134919A (en) 1981-02-16 1981-02-16 Fabrication of fly-back transformer

Publications (2)

Publication Number Publication Date
JPS57134919A JPS57134919A (en) 1982-08-20
JPS6227490B2 true JPS6227490B2 (en) 1987-06-15

Family

ID=12020878

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56020213A Granted JPS57134919A (en) 1981-02-16 1981-02-16 Fabrication of fly-back transformer

Country Status (1)

Country Link
JP (1) JPS57134919A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07255433A (en) * 1994-03-26 1995-10-09 Techno Torasuto Kyodo Kumiai Dehydrated raw laver disentangling machine and bulk dried laver production unit using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07255433A (en) * 1994-03-26 1995-10-09 Techno Torasuto Kyodo Kumiai Dehydrated raw laver disentangling machine and bulk dried laver production unit using the same

Also Published As

Publication number Publication date
JPS57134919A (en) 1982-08-20

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