JP2522432B2 - High voltage transformer manufacturing method - Google Patents
High voltage transformer manufacturing methodInfo
- Publication number
- JP2522432B2 JP2522432B2 JP2070858A JP7085890A JP2522432B2 JP 2522432 B2 JP2522432 B2 JP 2522432B2 JP 2070858 A JP2070858 A JP 2070858A JP 7085890 A JP7085890 A JP 7085890A JP 2522432 B2 JP2522432 B2 JP 2522432B2
- Authority
- JP
- Japan
- Prior art keywords
- filler
- epoxy resin
- resin composition
- voltage transformer
- average particle
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000003822 epoxy resin Substances 0.000 claims description 44
- 229920000647 polyepoxide Polymers 0.000 claims description 44
- 239000000945 filler Substances 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 35
- 239000002245 particle Substances 0.000 claims description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000005470 impregnation Methods 0.000 description 16
- 239000000047 product Substances 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- -1 amine compound Chemical class 0.000 description 7
- 150000008065 acid anhydrides Chemical class 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 238000004382 potting Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- AJKNNUJQFALRIK-UHFFFAOYSA-N 1,2,3-trifluorobenzene Chemical compound FC1=CC=CC(F)=C1F AJKNNUJQFALRIK-UHFFFAOYSA-N 0.000 description 1
- OQZDJLFNMXRJHZ-UHFFFAOYSA-N 1-benzyl-2-ethylimidazole Chemical compound CCC1=NC=CN1CC1=CC=CC=C1 OQZDJLFNMXRJHZ-UHFFFAOYSA-N 0.000 description 1
- NBNGHXWJFSMASY-UHFFFAOYSA-N 2,3,4-tris(dimethylamino)phenol Chemical compound CN(C)C1=CC=C(O)C(N(C)C)=C1N(C)C NBNGHXWJFSMASY-UHFFFAOYSA-N 0.000 description 1
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 1
- NXIFLHKNGSUALF-UHFFFAOYSA-N 2-[(2,3-dibromo-4-methylphenoxy)methyl]oxirane Chemical compound BrC1=C(Br)C(C)=CC=C1OCC1OC1 NXIFLHKNGSUALF-UHFFFAOYSA-N 0.000 description 1
- FDZMLNCJBYFJBH-UHFFFAOYSA-N 2-[(2,3-dibromophenoxy)methyl]oxirane Chemical compound BrC1=CC=CC(OCC2OC2)=C1Br FDZMLNCJBYFJBH-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 description 1
- MWSKJDNQKGCKPA-UHFFFAOYSA-N 6-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1CC(C)=CC2C(=O)OC(=O)C12 MWSKJDNQKGCKPA-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910002026 crystalline silica Inorganic materials 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VYKXQOYUCMREIS-UHFFFAOYSA-N methylhexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21C VYKXQOYUCMREIS-UHFFFAOYSA-N 0.000 description 1
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N methylimidazole Natural products CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
Landscapes
- Insulating Of Coils (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は高圧トランスの製造方法に関し、さらに詳し
くは熱伝導率に優れ、耐クラック性が大幅に改善され
た、電気機器として好適な高圧トランスの製造方法に関
する。Description: TECHNICAL FIELD The present invention relates to a method for manufacturing a high-voltage transformer, and more particularly, to a high-voltage transformer having excellent thermal conductivity and greatly improved crack resistance, which is suitable as an electric device. Manufacturing method.
従来、高圧トランスの製造方法としては、プラスチッ
クケースにコイルや回路部品等をセットし、エポキシ樹
脂と無機フィラーとの均一混合物に、酸無水物および硬
化促進剤またはアミン化合物を混合したエポキシ樹脂組
成物を常圧または真空下で注入して硬化するポッティン
グ法が知られている。Conventionally, as a method of manufacturing a high-voltage transformer, an epoxy resin composition in which a coil, a circuit component and the like are set in a plastic case, and an acid anhydride and a curing accelerator or an amine compound are mixed in a uniform mixture of an epoxy resin and an inorganic filler. There is known a potting method of injecting and curing under normal pressure or vacuum.
しかし、この方法では混合時の粘度および注入作業性
の面から混合する無機フィラーの添加量に限界があり、
例えば、重量比でフィラー1.0に対するエポキシ樹脂組
成物の使用割合は0.4が限度である。このため製品価格
が高くなる欠点がある。またエポキシ樹脂組成物が硬化
する際に体積収縮を生じるため、硬化物にクラックが生
じ、内蔵されているコイルおよび部品やケースに剥離や
クラックが発生し易く、また熱伝導率が悪いために電気
機器の温度が高くなり、使用する温度が制限されるなど
の問題がある。さらにエポキシ樹脂組成物と無機フィラ
ーを混合して真空下で脱泡した後に注入作業を行うた
め、エポキシ樹脂組成物の硬化時間の長いものを使用す
る必要があり、注入後の硬化時間も長くなり、作業工程
の合理化、省エネルギー化に限界がある。However, in this method, there is a limit to the amount of the inorganic filler to be mixed in terms of viscosity during mixing and injection workability,
For example, the weight ratio of the epoxy resin composition to the filler of 1.0 is limited to 0.4. Therefore, there is a drawback that the product price becomes high. In addition, since volume contraction occurs when the epoxy resin composition cures, cracks occur in the cured product, peeling and cracking easily occur in the built-in coil and parts or case, and the thermal conductivity is poor There is a problem that the temperature of the equipment becomes high and the temperature to be used is limited. Furthermore, since the injection work is performed after the epoxy resin composition and the inorganic filler are mixed and defoamed under vacuum, it is necessary to use one having a long curing time of the epoxy resin composition, and the curing time after injection also becomes long. There is a limit to the rationalization of work processes and energy saving.
本発明の目的は、前記従来技術の欠点をなくし、硬化
性、耐クラック性および熱伝導率に優れた高圧トランス
の製造方法を提供することにある。An object of the present invention is to eliminate the above-mentioned drawbacks of the prior art and to provide a method of manufacturing a high-voltage transformer excellent in curability, crack resistance and thermal conductivity.
本発明は、高圧トランス用部品が収納されたケース内
に、平均粒子径100μm以上のフィラーを充填した後、
エポキシ樹脂および硬化剤を含むエポキシ樹脂組成物ま
たはエポキシ樹脂、硬化剤および平均粒子径50μm以下
のフィラーを含むエポキシ樹脂組成物を注入し、硬化さ
せることを特徴とする高圧トランスの製造方法に関す
る。The present invention, after filling a filler having an average particle size of 100 μm or more in a case in which parts for a high-voltage transformer are stored,
The present invention relates to a method for producing a high-voltage transformer, which comprises injecting and curing an epoxy resin composition containing an epoxy resin and a curing agent or an epoxy resin composition containing an epoxy resin, a curing agent and a filler having an average particle size of 50 μm or less.
本発明に用いられる平均粒子径が100μm以上のフィ
ラー(以下、フィラー(A)という)は、エポキシ樹脂
組成物が注入される前にコイルや部品が収納されたケー
ス内に充填される。好ましい平均粒子径は200〜2000μ
mである。該平均粒子径は、JIS Z 2602−1976によ
って測定される。該平均粒子径が100μm未満では粒子
が細かく粒子と粒子の空隙が小さいため、エポキシ樹脂
組成物を注入した際に未含浸部が残り、熱伝導性が低下
し、また絶縁性が損なわれる。また部品間にフィラー
(A)が不均一に充填されるため、トランス全体の線膨
張係数が不均一となり、ヒートサイクル時にコイルや部
品の周辺に剥離やクラックが発生する。The filler having an average particle size of 100 μm or more (hereinafter referred to as filler (A)) used in the present invention is filled in the case in which the coil and the parts are housed before the epoxy resin composition is injected. Preferred average particle size is 200-2000μ
m. The average particle diameter is measured according to JIS Z 2602-1976. If the average particle size is less than 100 μm, the particles are fine and the voids between the particles are small, so that when the epoxy resin composition is injected, unimpregnated parts remain, the thermal conductivity decreases, and the insulating property is impaired. Further, since the filler (A) is unevenly filled between the parts, the linear expansion coefficient of the entire transformer becomes non-uniform, and peeling or cracks occur around the coil and the parts during the heat cycle.
フィラー(A)の種類には特に制限はなく、例えば硅
砂、シリカ、アルミナ、クレーマイカ、ガラスビーズ等
が用いられる。この市販品としては、パールサンド4
号、パールサンド6号、三河硅砂V−3(トウチュウ社
製商品名)、モランダム−A(昭和電工社製)、GB−A
G、GB−AC、GB−B(東芝バロティーニ社製)等が挙げ
られる。これらは併用して用いることもできる。The type of the filler (A) is not particularly limited and, for example, silica sand, silica, alumina, clay mica, glass beads and the like are used. This commercial product is Pearl Sand 4
No., Pearl Sand No. 6, Mikawa Sisand V-3 (trade name of Tochu Co., Ltd.), Morundum-A (Showa Denko KK), GB-A
G, GB-AC, GB-B (manufactured by Toshiba Ballotini) and the like can be mentioned. These can be used in combination.
本発明に用いられる平均粒子径が50μm以下のフィラ
ー(以下、フィラー(B)という)は、エポキシ樹脂組
成物に混合して用いられる。好ましい平均粒子径は5〜
20μmである。該平均粒子径は、セディグラフ(MICROM
ERI−TICS社製)を用いて測定される。該平均粒子径が5
0μmを超えると、エポキシ樹脂組成物の保管中の際に
フィラー(B)の沈降が早く、目的とするエポキシ樹脂
組成物が得られない。またエポキシ樹脂組成物をフィラ
ー(A)上に注入した際に未い含浸部分が残り、熱伝導
性が低下し、絶縁性が損なわれる。さらに部品間にフィ
ラー(B)が不均一に充填されるため、トランス全体の
線膨脹係数が不均一となり、ヒートサイクル時にコイル
や部品の周辺に剥離、クラックが発生する。The filler having an average particle diameter of 50 μm or less (hereinafter referred to as filler (B)) used in the present invention is used by mixing with the epoxy resin composition. A preferable average particle size is 5
20 μm. The average particle size is calculated based on the sedigraph (MICROM
ERI-TICS). The average particle size is 5
When it exceeds 0 μm, the filler (B) precipitates quickly during storage of the epoxy resin composition, and the desired epoxy resin composition cannot be obtained. Moreover, when the epoxy resin composition is injected onto the filler (A), unimpregnated portions remain, the thermal conductivity is lowered, and the insulating property is impaired. Furthermore, since the filler (B) is unevenly filled between the parts, the linear expansion coefficient of the entire transformer becomes non-uniform, and peeling and cracks occur around the coil and parts during the heat cycle.
フィラー(B)としては、例えば結晶シリカ、溶融シ
リカ、水和アルミナ、酸化アルミナ、タルク、炭酸カル
シウム、マイカ、ガラスビーズ、水酸化マグネシウム、
クレー等が用いられる。この市販品としてはCRT−AA、C
RT−D、RD−8(龍森社製)、C−303H、C−315H、C
−308(住友化学社製)、SL−700(竹原化学社製)等が
挙げられる。これらは併用して用いることもできる。Examples of the filler (B) include crystalline silica, fused silica, hydrated alumina, alumina oxide, talc, calcium carbonate, mica, glass beads, magnesium hydroxide,
Clay or the like is used. This commercially available product is CRT-AA, C
RT-D, RD-8 (manufactured by Tatsumori), C-303H, C-315H, C
Examples include −308 (Sumitomo Chemical Co., Ltd.) and SL-700 (Takehara Chemical Co., Ltd.). These can be used in combination.
本発明に用いられるエポキシ樹脂は、1分子中に少な
くとも1個のエポキシ基を有するものであり、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、ビスフェノールAD型エポキシ樹脂、多価ア
ルコールのポリグリシジルエステルなどを用いることが
できる。これらの樹脂としては特に制限はないが、常温
で液状のものが好ましく、市販品しては、エピコート82
8(シェル化学社製商品名)、GY−260(チバガイギー社
製商品名)、DER−331(ダウケミカル社製商品名)等が
挙げられる。これらは併用して用いることもできる。The epoxy resin used in the present invention has at least one epoxy group in one molecule. For example, bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol AD type epoxy resin, polyglycidyl polyhydric alcohol. Esters and the like can be used. Although these resins are not particularly limited, those which are liquid at room temperature are preferable, and commercially available products are Epicoat 82
8 (Shell Chemical Co., Ltd. trade name), GY-260 (Ciba Geigy Co., Ltd. trade name), DER-331 (Dow Chemical Co., Ltd. trade name) and the like. These can be used in combination.
本発明に用いられる硬化剤としては、酸無水物および
硬化促進剤、またはアミン化合物が用いられる。As the curing agent used in the present invention, an acid anhydride, a curing accelerator, or an amine compound is used.
上記酸無水物としては特に制限はないが、常温で液体
のものが好ましく、例えばメチルテトラヒドロ無水フタ
ル酸、メチルヘキサヒドロ無水フタル酸、メチルエンド
メチレン無水フタル酸、ドデセニル無水フタル酸等が用
いられる。市販品としてはHN−2200(日立化成社製商品
名)、QH−200(日本ゼオン社製商品名)等が挙げられ
る。これらは併用して用いることもできる。該酸無水物
の配合量は、エポキシ樹脂100重量部に対して50〜150重
量部が好ましい。The above-mentioned acid anhydride is not particularly limited, but those which are liquid at room temperature are preferable, and for example, methyltetrahydrophthalic anhydride, methylhexahydrophthalic anhydride, methylendomethylenephthalic acid, dodecenylphthalic anhydride and the like are used. Examples of commercially available products include HN-2200 (trade name, manufactured by Hitachi Chemical Co., Ltd.) and QH-200 (trade name, manufactured by Nippon Zeon Co., Ltd.). These can be used in combination. The amount of the acid anhydride is preferably 50 to 150 parts by weight based on 100 parts by weight of the epoxy resin.
上記酸無水物の硬化促進剤としては、例えば2−エチ
ル−4−メチルイミダゾール、1−シアノエチル−4−
メチルイミダゾール、1−ベンジル−2−エチルイミダ
ゾール等のイミダゾールおよびその誘導体、トリスジメ
チルアミノフェノール、ベンジンメチルアミン等の第3
級アミン類などが用いられる。市販品としては2E4MZ
(四国化成社製商品名)、BDMA(花王社製商品名)等が
挙げられる。該硬化促進剤の配合量は、酸無水物100重
量部当たり0.1〜5.0重量部が好ましい。Examples of the acid anhydride curing accelerator include 2-ethyl-4-methylimidazole and 1-cyanoethyl-4-
Imidazole and its derivatives such as methylimidazole and 1-benzyl-2-ethylimidazole, and tertiary such as trisdimethylaminophenol and benzinemethylamine
Primary amines and the like are used. 2E4MZ as a commercial product
(Trade name manufactured by Shikoku Kasei), BDMA (trade name manufactured by Kao), and the like. The compounding amount of the curing accelerator is preferably 0.1 to 5.0 parts by weight per 100 parts by weight of the acid anhydride.
上記アミン化合物としては、芳香族ポリアミンとその
変性物、脂肪族ポリアミンとその変性物が挙げられ、例
えばジアミノジフェニルメタンとエポキシ樹脂の付加物
等が用いられる。市販品としてはEH−520(旭電化社製
商品名)、EH−551(アデカ社製商品名)、アンカミン2
007(アンカーケミカル社製)等が挙げられる。これら
は併用して用いることもできる。該アミノ化合物の配合
量は、エポキシ樹脂100重量部に対して5〜50重量部が
好ましい。Examples of the amine compound include aromatic polyamines and modified products thereof, and aliphatic polyamines and modified products thereof. For example, an addition product of diaminodiphenylmethane and an epoxy resin is used. As commercial products, EH-520 (product name manufactured by Asahi Denka Co., Ltd.), EH-551 (product name manufactured by ADEKA Co., Ltd.), Ancamine 2
007 (manufactured by Anchor Chemical Co.) and the like. These can be used in combination. The content of the amino compound is preferably 5 to 50 parts by weight with respect to 100 parts by weight of the epoxy resin.
エポキシ樹脂および硬化剤を含むエポキシ樹脂組成物
またはこれにフィラー(B)を含むエポキシ樹脂組成物
には、必要に応じて赤リン、ヘキサブロモベンゼン、ジ
ブロモフェニルグリシジルエーテル、ジブロモクレジル
グリシジルエーテル、三酸化アンチモン等の難燃剤、ベ
ンガラ、酸化第2鉄、カーボン、チタンホワイト等の着
色剤、シラン系カップリング剤、シリコーン剤等の消泡
剤、モノグリシジルエーテル、ジグリシジルエーテル等
の希釈剤などを配合させることができる。In the epoxy resin composition containing the epoxy resin and the curing agent or the epoxy resin composition containing the filler (B) therein, red phosphorus, hexabromobenzene, dibromophenyl glycidyl ether, dibromocresyl glycidyl ether, and ternary trifluorobenzene may be added, if necessary. Flame retardants such as antimony oxide, red iron oxide, ferric oxide, carbon, coloring agents such as titanium white, silane coupling agents, defoaming agents such as silicone agents, diluents such as monoglycidyl ether, diglycidyl ether, etc. It can be mixed.
本発明で得られる高圧トランスとしては、例えばプラ
スチックまたは金属ケースに電子部品、電気部品を収納
したトランス、ソレノイドコイル、電磁クラッチ、安定
器、イグナイター、イグニッション、レギュレーター等
の電気機器、セラミック基板、プリント基板等の回路板
を内蔵した電気機器などが挙げられる。The high-voltage transformer obtained in the present invention includes, for example, a transformer in which electronic parts and electric parts are housed in a plastic or metal case, an electric device such as a solenoid coil, an electromagnetic clutch, a ballast, an igniter, an ignition, a regulator, a ceramic substrate, and a printed circuit board. Examples include electric equipment having a built-in circuit board such as.
以下、本発明を実施例により説明する。下記例中の
「部」は、重量部を意味する。Hereinafter, the present invention will be described with reference to examples. "Parts" in the following examples means parts by weight.
(1)フィラー(A)の平均粒子径:JIS Z 2602−19
76「鋳物砂の粒度分布試験方法」に準じて粒度分布を測
定し、累積重量%が50重量%の粒子径を平均粒子径とし
た。(1) Average particle size of filler (A): JIS Z 2602-19
The particle size distribution was measured according to 76 “Method for testing particle size distribution of foundry sand”, and the particle size with a cumulative weight% of 50% by weight was taken as the average particle size.
(2)フィラー(B)の平均粒子径:セディグラフ5000
ET(島津製作所社製)を用い、スタート粒子径を50μm
としてヘキサメタリン酸ソーダ0.1重量%の水溶液にフ
ィラー(B)を約8重量%の濃度で加え、予備分散とし
て超音波洗浄を20分間行い、粒度分布を測定し、累積重
量%が50重量%の粒子径を平均粒子径とした (3)モデル含浸率:直径50mmのポリエチレン製ビーカ
にフィラー(A)を加振しながら充填後、秤量してフィ
ラー(A)の重量(W0g)を求める。次にエポキシ樹脂
組成物を注入し、10mmHgの減圧下で10分間放置し、常
圧、80℃/3時間で硬化させる。次いでポリエチレン製ビ
ーカから硬化物を取出し、下部のエポキシ樹脂組成物が
含浸されず硬化物から分離されるフィラー(A)の重量
(W1g)を求め、次式からモデル含浸性を算出した。(2) Average particle diameter of filler (B): Cedigraph 5000
ET (manufactured by Shimadzu Corporation) is used and the start particle size is 50 μm.
As a filler (B) at a concentration of about 8% by weight to an aqueous solution of 0.1% by weight sodium hexametaphosphate, ultrasonic cleaning is performed for 20 minutes as a preliminary dispersion, and the particle size distribution is measured. (3) Model impregnation rate: A polyethylene beaker having a diameter of 50 mm is filled while vibrating the filler (A) and then weighed to obtain the weight (W 0 g) of the filler (A). Next, the epoxy resin composition is injected and left under reduced pressure of 10 mmHg for 10 minutes, and cured at 80 ° C. for 3 hours at normal pressure. Then, the cured product was taken out from the polyethylene beaker, the weight (W 1 g) of the filler (A) separated from the cured product without impregnating the lower epoxy resin composition was calculated, and the model impregnation property was calculated from the following formula.
モデル含浸率は、エポキシ樹脂組成物がフィラー
(A)中に含浸した割合を求めるものであり、未含浸部
のフィラー(A)が少なければモデル含浸率が高くな
り、含浸性に優れることを示す。 The model impregnation rate is obtained by determining the rate of the epoxy resin composition impregnated in the filler (A). If the filler (A) in the non-impregnated portion is small, the model impregnation rate is high and the impregnation property is excellent. .
(4)熱伝導率:直径50mmのポリエチレン製ビーカにフ
ィラー(A)を加振しながら充填する。次にエポキシ樹
脂組成物を注入し、10mmHgの減圧下で10分間放置し、常
圧、80℃で3時間で硬化させ、直径50mm、厚さ10mmの円
板状の試験片を作成し、熱伝導率測定器(ダイナテック
社製)で熱伝導率(cal/cm・sec・℃)を求めた。(4) Thermal conductivity: Fill a polyethylene beaker with a diameter of 50 mm while vibrating the filler (A). Next, inject the epoxy resin composition, leave it under a reduced pressure of 10 mmHg for 10 minutes, and cure at atmospheric pressure and 80 ° C. for 3 hours to prepare a disc-shaped test piece with a diameter of 50 mm and a thickness of 10 mm, and heat it. The thermal conductivity (cal / cm · sec · ° C) was determined with a conductivity meter (Dynatech).
(5)耐クラック性:(3)と同じ方法で注型して試験
片を作製し、JIS C 2105「電気絶縁用無溶剤液状レ
ジン試験方法」の耐クラック性試験に準じて試験した。
クラック試験片は5個とし、所定の冷熱サイクルを行
い、サイクルごとにクラック発生の有無を確認し、最初
にクラックが発生したサイクル数を記載した。(5) Crack resistance: A test piece was prepared by casting in the same manner as in (3), and the test piece was tested according to the crack resistance test of JIS C 2105 “Testing method for solvent-free liquid resin for electrical insulation”.
The number of crack test pieces was five, and a predetermined cooling / heating cycle was performed. The presence or absence of cracks was confirmed for each cycle, and the number of cycles in which cracks occurred first was described.
(6)線膨脹係数:熱伝導率の測定試験片を用いて5mm
×5mm×2mmの試験片を切り出し、TMA熱物理試験機(理
学電気社製)を用いて線膨脹係数(℃-1)を求めた。(6) Coefficient of linear expansion: 5 mm using a test piece for measuring thermal conductivity
A test piece of × 5 mm × 2 mm was cut out, and the coefficient of linear expansion (° C. −1 ) was determined using a TMA thermophysical tester (manufactured by Rigaku Corporation).
(7)モデルトランスへの含浸性:変性ポリフェニレン
オキサイド製のボビン(10スリット)に、直線0.05mmの
ウレタン線を各250ターン巻きつけたコイルと抵抗等の
部品を、ボビンと同一材質のケースに収納したモデルト
ランスを100℃で1時間乾燥した後、これにフィラー
(A)に加振しながら充填する。次にエポキシ樹脂組成
物を注入し、10mmHgの減圧下で10分間放置し、常圧に戻
して80℃で3時間で硬化させる。次いでモデルトランス
を切断し、コイルおよび部品間隙への含浸状態と、フィ
ラー(A)に対するエポキシ樹脂組成物の含浸状態につ
いて次のように観察した。(7) Impregnation into model transformer: A coil made of modified polyphenylene oxide bobbin (10 slits) wound with 250 mm of urethane wire for each 250 turns and parts such as resistors are placed in a case made of the same material as the bobbin. The stored model transformer is dried at 100 ° C. for 1 hour and then filled into the filler (A) while vibrating. Next, the epoxy resin composition is injected, left for 10 minutes under a reduced pressure of 10 mmHg, returned to normal pressure and cured at 80 ° C. for 3 hours. Then, the model transformer was cut, and the state of impregnation into the coil and the gap between the components and the state of impregnation of the epoxy resin composition into the filler (A) were observed as follows.
○:エポキシ樹脂組成物がコイルおよび部品の間隙に含
浸し、かつフィラー(A)にエポキシ樹脂組成物が含浸
している。◯: The gap between the coil and the component was impregnated with the epoxy resin composition, and the filler (A) was impregnated with the epoxy resin composition.
△:コイルおよび部品の間隙またはフィラー(A)にエ
ポキシ樹脂組成物が含浸していない。Δ: The gap between the coil and the part or the filler (A) is not impregnated with the epoxy resin composition.
×:コイルおよび部品の間隙およびフィラー(A)にエ
ポキシ樹脂組成物が含浸していない。X: The epoxy resin composition is not impregnated into the gap between the coil and the part and the filler (A).
なお、実施例および比較例で用いたフィラー(A)と
フィラー(B)の商品名(製造会社)、組成および平均
粒子径を第1表に示した。Table 1 shows the trade names (manufacturing companies), compositions, and average particle diameters of the filler (A) and the filler (B) used in Examples and Comparative Examples.
実施例1〜3 第2表に示す配合のフィラー(A)とフィラー(B)
を含まないエポキシ樹脂組成物を用いて上記の試験方法
により試験片を作製し、各特性を調べた。その結果を第
2表に示したが、いずれの場合もモデル含浸性およびモ
デルトランスへの含浸性は良好であり、熱伝導率も高
く、線膨脹係数も小さく、また耐クラック性も良好であ
った。 Examples 1 to 3 Filler (A) and filler (B) having the composition shown in Table 2
A test piece was prepared by the above-described test method using an epoxy resin composition not containing, and each property was examined. The results are shown in Table 2. In all cases, the model impregnation property and the model transformer impregnation property were good, the thermal conductivity was high, the linear expansion coefficient was small, and the crack resistance was also good. It was
実施例4〜6 第2表に示す配合のフィラー(A)とフィラー(B)
を含むエポキシ樹脂組成物を用いて上記の試験方法によ
り試験片を作製し、各特性を調べた。その結果を第2表
に示したが、いずれの場合もモデル含浸性およびモデル
トランスへの含浸性は良好であり、熱伝導率も高く、線
膨脹係数も小さく、また耐クラック性も良好であった。Examples 4 to 6 Filler (A) and filler (B) having the composition shown in Table 2
Using the epoxy resin composition containing, a test piece was prepared by the above-mentioned test method, and each property was examined. The results are shown in Table 2. In all cases, the model impregnation property and the model transformer impregnation property were good, the thermal conductivity was high, the linear expansion coefficient was small, and the crack resistance was also good. It was
比較例1 実施例4において、フィラー(A)を用いなかった以
外は実施例4と同様にして試験片を作製し、その特性を
調べた。その結果を第2表に示したが、熱伝導率が小さ
く、耐クラック性に劣り、また線膨脹係数も大きかっ
た。Comparative Example 1 A test piece was prepared in the same manner as in Example 4 except that the filler (A) was not used, and the characteristics thereof were examined. The results are shown in Table 2. The thermal conductivity was low, the crack resistance was poor, and the linear expansion coefficient was also high.
比較例2 比較例1において、フィラー(B)としてH−32の使
用量を350gとした以外は比較例1と同様にして試験片を
作製し、その特性を調べた。その結果を第2表に示した
が、モデルトランスでのコイルおよび部品間隙への含浸
性に劣った。Comparative Example 2 A test piece was prepared in the same manner as in Comparative Example 1 except that the amount of H-32 used as the filler (B) was changed to 350 g, and the characteristics thereof were examined. The results are shown in Table 2, but the impregnability of the coil and the component gap in the model transformer was poor.
比較例3 実施例4において、フィラー(B)としてEC−H(平
均粒子径:150μm)を用いた以外は実施例4と同様にし
て試験片を作製し、その特性を調べた。その結果を第2
表に示したが、モデル含浸性およびモデルトランスの含
浸性に劣り、線膨脹係数のバラツキが大きく、また耐ク
ラック性に劣った。Comparative Example 3 A test piece was prepared in the same manner as in Example 4 except that EC-H (average particle size: 150 μm) was used as the filler (B), and its characteristics were examined. The result is the second
As shown in the table, the model impregnation property and the model transformer impregnation property were inferior, the coefficient of linear expansion varied greatly, and the crack resistance was inferior.
比較例4 実施例6において、フィラー(A)としてEC−40(平
均粒子径:40μm)を用いた以外は実施例6と動揺にし
て試験片を作製し、その特性を調べた。その結果を第2
表に示したが、モデル含浸性およびモデルトランスの含
浸性に劣り、線膨脹係数のバラツキが大きく、また耐ク
ラック性に劣った。Comparative Example 4 A test piece was prepared by shaking with Example 6 except that EC-40 (average particle size: 40 μm) was used as the filler (A), and its characteristics were examined. The result is the second
As shown in the table, the model impregnation property and the model transformer impregnation property were inferior, the coefficient of linear expansion varied greatly, and the crack resistance was inferior.
〔発明の効果〕 本発明の製造方法によれば、ケース内のフィラー
(A)にエポキシ樹脂組成物が均一に充分に含浸され、
硬化物には気泡がなく、部品、素子、基板などとよく密
着した高圧トランスが得られる。この含浸性および密着
性は、従来のポッティング法、すなわちエポキシ樹脂組
成物とフィラーとをあらかじめ混合した後にケース内に
注入して硬化する方法による場合とほとんど差がないも
のである。また本発明の方法によれば、フィラーの総量
を多くできるため、トータルコストの低減が可能であ
り、また硬化時の硬化収縮が小さく、硬化物の熱伝導率
およびヒートサイクル時のクラック性が向上し、高圧ト
ランスの性能が大幅に向上する。 EFFECT OF THE INVENTION According to the production method of the present invention, the filler (A) in the case is uniformly and sufficiently impregnated with the epoxy resin composition,
There are no bubbles in the cured product, and a high-voltage transformer can be obtained that is in close contact with parts, elements, substrates, etc. The impregnating property and the adhesiveness are almost the same as those obtained by the conventional potting method, that is, the method in which the epoxy resin composition and the filler are mixed in advance and then injected into the case and cured. Further, according to the method of the present invention, since the total amount of filler can be increased, the total cost can be reduced, the curing shrinkage during curing is small, and the thermal conductivity of the cured product and the cracking property during the heat cycle are improved. However, the performance of the high voltage transformer is significantly improved.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 岡田 泰典 茨城県日立市東町4丁目13番1号 日立 化成工業株式会社山崎工場内 (56)参考文献 特開 昭54−3264(JP,A) 特開 昭54−3289(JP,A) 特開 昭54−66451(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yasunori Okada 4-13-1, Higashimachi, Hitachi City, Ibaraki Prefecture Hitachi Chemical Co., Ltd. Yamazaki Plant (56) References JP-A-54-3264 (JP, A) Special Features Kai 54-3289 (JP, A) JP 54-66451 (JP, A)
Claims (1)
に、平均粒子径100μm以上のフィラーを充填した後、
エポキシ樹脂および硬化剤を含むエポキシ樹脂組成物ま
たはエポキシ樹脂、硬化剤および平均粒子径50μm以下
のフィラーを含むエポキシ樹脂組成物を注入し、硬化さ
せることを特徴とする高圧トランスの製造方法。1. A case in which high-voltage transformer parts are housed is filled with a filler having an average particle size of 100 μm or more,
A method for producing a high-voltage transformer, which comprises injecting and curing an epoxy resin composition containing an epoxy resin and a curing agent or an epoxy resin composition containing an epoxy resin, a curing agent and a filler having an average particle diameter of 50 μm or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2070858A JP2522432B2 (en) | 1990-03-20 | 1990-03-20 | High voltage transformer manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2070858A JP2522432B2 (en) | 1990-03-20 | 1990-03-20 | High voltage transformer manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03270207A JPH03270207A (en) | 1991-12-02 |
| JP2522432B2 true JP2522432B2 (en) | 1996-08-07 |
Family
ID=13443683
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2070858A Expired - Lifetime JP2522432B2 (en) | 1990-03-20 | 1990-03-20 | High voltage transformer manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2522432B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4577759B2 (en) * | 2004-07-09 | 2010-11-10 | Necトーキン株式会社 | Magnetic core and wire ring parts using the same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS543264A (en) * | 1977-06-09 | 1979-01-11 | Denki Onkyo Co Ltd | Method of molding parts for high voltage circuit |
-
1990
- 1990-03-20 JP JP2070858A patent/JP2522432B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03270207A (en) | 1991-12-02 |
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