JPH02148512A - Electrical equipment - Google Patents
Electrical equipmentInfo
- Publication number
- JPH02148512A JPH02148512A JP29959788A JP29959788A JPH02148512A JP H02148512 A JPH02148512 A JP H02148512A JP 29959788 A JP29959788 A JP 29959788A JP 29959788 A JP29959788 A JP 29959788A JP H02148512 A JPH02148512 A JP H02148512A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- curing
- weight
- unsaturated polyester
- organic acid
- 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.)
- Pending
Links
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- 229920006305 unsaturated polyester Polymers 0.000 claims abstract description 16
- 239000000178 monomer Substances 0.000 claims abstract description 14
- -1 acrylic ester Chemical class 0.000 claims abstract description 11
- 150000007524 organic acids Chemical class 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 10
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 7
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 claims abstract description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000011701 zinc Substances 0.000 claims abstract description 6
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 6
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- 239000011342 resin composition Substances 0.000 claims description 16
- 239000010941 cobalt Substances 0.000 claims description 6
- 229910017052 cobalt Inorganic materials 0.000 claims description 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 6
- 229910052748 manganese Inorganic materials 0.000 claims description 5
- 239000011572 manganese Substances 0.000 claims description 5
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 229920005989 resin Polymers 0.000 abstract description 3
- 239000011347 resin Substances 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 abstract description 2
- MZZUATUOLXMCEY-UHFFFAOYSA-N cobalt manganese Chemical compound [Mn].[Co] MZZUATUOLXMCEY-UHFFFAOYSA-N 0.000 abstract 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 44
- 238000001723 curing Methods 0.000 description 22
- 235000019645 odor Nutrition 0.000 description 13
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 238000005470 impregnation Methods 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 229920006337 unsaturated polyester resin Polymers 0.000 description 3
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 2
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 2
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- HGDULKQRXBSKHL-UHFFFAOYSA-N 1,1-bis(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(CC)(OC(=O)C(C)=C)OC(=O)C(C)=C HGDULKQRXBSKHL-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical compound OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- BJEMXPVDXFSROA-UHFFFAOYSA-N 3-butylbenzene-1,2-diol Chemical group CCCCC1=CC=CC(O)=C1O BJEMXPVDXFSROA-UHFFFAOYSA-N 0.000 description 1
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical class [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical class [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical class [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- OIAUFEASXQPCFE-UHFFFAOYSA-N formaldehyde;1,3-xylene Chemical compound O=C.CC1=CC=CC(C)=C1 OIAUFEASXQPCFE-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Chemical class 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[発明の目的]
(産業上の利用分野)
本発明は、硬化後の刺激性臭気が少なく、低温度、短時
間で硬化可能な不飽和ポリエステル樹脂組成物によって
絶縁処理が施された電気機器に関する。Detailed Description of the Invention [Objective of the Invention] (Industrial Field of Application) The present invention provides insulation treatment using an unsaturated polyester resin composition that has little irritating odor after curing and can be cured at low temperatures and in a short time. Regarding electrical equipment that has been given.
(従来の技術)
不飽和ポリエステル樹脂組成物は、機械的、電気的、熱
的な特性、作業性、価格などの点で比較的バランスがと
れているため、各分野に広く使用されている。 特に電
気機器の絶縁用として、作業性が優れているため、コイ
ル含浸や注形用などに多く使用されている。 この電気
機器用樹脂組成物は、不飽和ポリエステルに架橋性単量
体、硬化触媒を混合してラジカル重合開始剤で硬化反応
を進めるが、ラジカルを励起させるには熱硬化あるいは
紫外線硬化の方法がある。一般には、硬化触媒としてコ
バルト又はマンガンの有機酸金属塩、架橋性単量体とし
てスチレンが使用されている。 ところで近年、製造工
程の省力化やスピードアップの見地から、樹脂をより低
温で、かつ短時間で硬化させることが要求されている。(Prior Art) Unsaturated polyester resin compositions are relatively well-balanced in terms of mechanical, electrical, thermal properties, workability, price, etc., and are therefore widely used in various fields. It is particularly used for insulating electrical equipment, and because of its excellent workability, it is often used for coil impregnation and casting. This resin composition for electrical equipment is made by mixing unsaturated polyester with a crosslinking monomer and a curing catalyst, and then proceeding with the curing reaction using a radical polymerization initiator, but heat curing or ultraviolet curing is required to excite the radicals. be. Generally, an organic acid metal salt of cobalt or manganese is used as a curing catalyst, and styrene is used as a crosslinking monomer. Incidentally, in recent years, from the standpoint of saving labor and speeding up the manufacturing process, there has been a demand for curing resins at lower temperatures and in shorter times.
しかし、上記従来の不飽和ポリエステル樹脂組成物を低
温で短時間の硬化を行う場合、硬化物には未反応のスチ
レンが残留し易く、その臭気が問題となるこ、とが多か
った。 特に扇風機、換気扇、エアーコンディショナー
等のステーターコイルを処理した時、臭気がなくなるま
で硬化させるには、少なくとも120℃以上の硬化温度
で約20〜30分間以上の硬化時間を必要とし、それよ
り短時間の処理や低温度の処理では残存臭気が実用上問
題となっていた。However, when the above-mentioned conventional unsaturated polyester resin compositions are cured at low temperatures for a short time, unreacted styrene tends to remain in the cured product, and its odor often becomes a problem. In particular, when treating stator coils of electric fans, ventilation fans, air conditioners, etc., curing time of approximately 20 to 30 minutes or more at a curing temperature of at least 120°C is required to cure the odor until it disappears, or a shorter period of time. Residual odor has been a practical problem during processing and low-temperature processing.
(発明が解決しようとする課題)
本発明は、上記の事情に鑑みてなされ、低温度、短時間
の絶縁処理をしたものであっても、刺激性臭気の発生が
少ない電気機器を提供するものである。(Problems to be Solved by the Invention) The present invention has been made in view of the above circumstances, and provides an electrical device that generates little irritating odor even when subjected to low temperature and short time insulation treatment. It is.
[発明の構成コ
(課題を解決するための手段)
本発明者らは、上記の目的を達成するために鋭意検討を
行った結果、架橋性単量体として、スチレンと、アクリ
ル酸エステル又はメタクリル酸エステルとを併用すると
ともに、硬化触媒としても、コバルト又はマンガンの有
機酸金属塩と鉛、亜鉛、錫の有機酸金属塩とを併用する
ことによって、スチレンの共重合性を高め、上記目的を
達成できることを見いだして本発明を完成したものであ
る。[Constitution of the Invention (Means for Solving the Problems) As a result of intensive studies to achieve the above object, the present inventors found that styrene, acrylic ester or methacrylate as crosslinkable monomers By using cobalt or manganese organic acid metal salts and organic acid metal salts of lead, zinc, and tin together as curing catalysts, the copolymerizability of styrene can be increased and the above objective can be achieved. The present invention was completed by discovering what can be achieved.
すなわち、本発明は、
不飽和ポリエステル70〜30重量部と、アクリル酸エ
ステル又はメタクリル酸エステルを3〜50重量%含む
架橋性単量体30〜70重量部と、硬化触媒としてコバ
ルト又はマンガンの有機酸金属塩及び鉛、亜鉛又は鍋の
有機酸金属塩とを含む樹脂組成物を処理硬化させてなる
ことを特徴とする電気機器である。That is, the present invention comprises 70 to 30 parts by weight of an unsaturated polyester, 30 to 70 parts by weight of a crosslinkable monomer containing 3 to 50% by weight of an acrylic ester or a methacrylic ester, and an organic compound of cobalt or manganese as a curing catalyst. The present invention is an electrical device characterized by being formed by processing and curing a resin composition containing an acid metal salt and an organic acid metal salt of lead, zinc, or a pot.
本発明に用いる不飽和ポリエステルは、−mに使用され
ている不飽和ポリエステルと変らないもので、酸成分と
アルコール成分、必要に応じて変性成分を150〜22
0℃で反応させて得られるもので、特に制限はない。The unsaturated polyester used in the present invention is the same as the unsaturated polyester used in -m, and has an acid component, an alcohol component, and if necessary a modifying component of 150 to 22%.
It is obtained by reacting at 0°C, and there are no particular restrictions.
酸成分としては、マレイン酸、無水マレイン酸、フマー
ル酸などの不飽和酸、フタル酸、イソフタール酸、テレ
フタール酸、テトラヒドロフタール酸、無水フタール酸
、無水テトラヒドロフタール酸、アジピン酸などの飽和
酸、及びアマニ油、大豆油などの植物から得られる脂肪
酸等が挙げられ、これらは単独又は2g!以上混合して
使用することができる。Acid components include unsaturated acids such as maleic acid, maleic anhydride, and fumaric acid, and saturated acids such as phthalic acid, isophthalic acid, terephthalic acid, tetrahydrophthalic acid, phthalic anhydride, tetrahydrophthalic anhydride, and adipic acid. , and fatty acids obtained from plants such as linseed oil and soybean oil, which can be used alone or in amounts of 2g! The above can be used in combination.
アルコール成分としては、エチレングリコール、プロピ
レングリコール、ジプロピレングリコール、ジエチレン
グリコール、ネオペンチルグリコール、グリセリン、1
.3−ブタンジオール等が挙げられ、これらは単独又は
2種以上混合して使用することができる。Alcohol components include ethylene glycol, propylene glycol, dipropylene glycol, diethylene glycol, neopentyl glycol, glycerin,
.. Examples include 3-butanediol, and these can be used alone or in a mixture of two or more.
また変性成分としては、アマニ油、大豆油、トール油、
キシレンホルムアルデヒド樹脂、ジシクロペンタジェン
などが挙げられ、これらは単独又は2種以上混合して使
用することができる。Modified ingredients include linseed oil, soybean oil, tall oil,
Examples include xylene formaldehyde resin and dicyclopentadiene, and these can be used alone or in a mixture of two or more.
本発明に用いる架橋性単量体としては、スチレンとアク
リル酸エステル又はメタクリル酸エステルである。 具
体的な化合物として、スチレン、2−ヒドロキシアクリ
レート、2−ヒドロキシメタクリレート、2−ヒドロキ
シプロピルアクリレート、2−ヒドロキシプロピルメタ
クリレート、ステアリルアクリレート、ステアリルメタ
クリレート、ラウリルアクリレート、ラウリルメタクリ
レート、トリメチロールプロパントリアクリレート、ト
リメチロールプロパントリメタクリレート等が挙げられ
、これらは単独又は2種以、上混合して使用することが
できる。 そしてアクリル酸エステル又はメタクリル酸
エステルは、架橋性単量体に対し3〜50f!量%含有
するものである。 含有量が3重量%未満ではスチレン
との高い共重合性が得られず、また50重量%を超える
と樹脂組成物の粘度が増大し、かつ経済的でなく望まし
くない、 より好ましくは10〜30重量%である。The crosslinking monomer used in the present invention is styrene and acrylic ester or methacrylic ester. Specific compounds include styrene, 2-hydroxyacrylate, 2-hydroxymethacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, stearyl acrylate, stearyl methacrylate, lauryl acrylate, lauryl methacrylate, trimethylolpropane triacrylate, and trimethylol. Examples include propane trimethacrylate, and these can be used alone or in a mixture of two or more. And the acrylic ester or methacrylic ester is 3 to 50 f! relative to the crosslinkable monomer! % content. If the content is less than 3% by weight, high copolymerizability with styrene cannot be obtained, and if it exceeds 50% by weight, the viscosity of the resin composition increases, which is uneconomical and undesirable. More preferably 10 to 30% by weight. Weight%.
不飽和ポリエステルと架橋性単量体の配合割合は、不飽
和ポリエステル70〜30重量部に対し、架橋性単量体
30〜70重量部配合することが望ましい。The blending ratio of the unsaturated polyester and the crosslinkable monomer is preferably 30 to 70 parts by weight of the crosslinkable monomer to 70 to 30 parts by weight of the unsaturated polyester.
架橋性単量体が30重量部未溝では粘度が増大し流動性
が悪くなるので好ましくない、 また70重量部を超え
ると硬化性が低下し、かつ脆くなるので好ましくない。If the amount of the crosslinking monomer is 30 parts by weight without grooves, the viscosity increases and fluidity deteriorates, which is undesirable. If it exceeds 70 parts by weight, the curability decreases and the product becomes brittle, which is not preferred.
本発明に用いる硬化触媒としては、コバルト又はマンガ
ンの有機酸金属塩と鉛、便船又は錫等の有′R1!!金
属塩とを併用する。 金属塩を構成する有機酸は、ナフ
テン酸、オクトエ酸などが例示される。 これらの金属
塩の他にカルシウム、鉄、ジルコニウム、アルミニウム
、チタン等の金属塩を使用することができる。 鉛、亜
鉛又は錫の配合割合は組成物全体に対し、金属分として
o、 oos〜0.2重量%配合することが望ましい、
配合量がo、oos重量%未溝では十分な硬化性が得
られず好ましくない、 また0、2重量%を超えると表
面粘着が生じたり、樹脂組成物に濁りが生じたりして好
ましくない、 より好ましくは金属分0.01〜0.1
重量%の範囲内である。The curing catalyst used in the present invention includes an organic acid metal salt of cobalt or manganese, lead, tin, etc. ! Use in combination with metal salts. Examples of the organic acid constituting the metal salt include naphthenic acid and octoic acid. In addition to these metal salts, metal salts of calcium, iron, zirconium, aluminum, titanium, etc. can be used. The blending ratio of lead, zinc or tin is preferably o, oos to 0.2% by weight as a metal content based on the entire composition.
If the blending amount is o or oos wt % without grooves, sufficient curability cannot be obtained, which is not preferable, and if it exceeds 0.2 wt %, surface adhesion may occur or the resin composition may become cloudy, which is not preferable. More preferably metal content 0.01-0.1
Within the range of % by weight.
本発明に用いる樹脂組成物は、不飽和ポリエステル、架
橋性単量体、硬化触媒を含むが、この組成物に硬化剤及
び重合禁止剤その池を加えて硬化させることができる。The resin composition used in the present invention contains an unsaturated polyester, a crosslinkable monomer, and a curing catalyst, and can be cured by adding a curing agent and a polymerization inhibitor to this composition.
硬化剤としては、ベンゾイルパーオキサイド、アセチ
ルパーオキサイドなどのアシルパーオキサイド、ターシ
ャリ−ブチルパーオキサイドなどのヒドロパーオキサイ
ド、メチルエチルケトンなどのケトンパーオキサイド等
の有機過酸化物が挙げられる。 硬化剤の添加量は一般
的に樹脂組成物に対して0,5〜3重量%の範囲内であ
る。 また、使用される重合禁止剤としては、ハイドロ
キノン、パラターシャリ−ブチルカテコール、ピロガロ
ール等のキノン類、その他一般に使用されているものが
挙げられる。 こうして得られた樹脂組成物は処理硬化
、つまりコイル含浸や注形などの処理をして電気機器を
製造することができる。Examples of the curing agent include organic peroxides such as acyl peroxides such as benzoyl peroxide and acetyl peroxide, hydroperoxides such as tertiary-butyl peroxide, and ketone peroxides such as methyl ethyl ketone. The amount of curing agent added is generally within the range of 0.5 to 3% by weight based on the resin composition. Examples of the polymerization inhibitor used include quinones such as hydroquinone, paratertiary butylcatechol, and pyrogallol, and other commonly used ones. The resin composition thus obtained can be cured, that is, processed by coil impregnation, casting, etc., to produce electrical equipment.
電気機器の含浸方法としては、通常用いられる浸漬法や
滴下含浸法等が用いられ、製造工程の省力化の見地から
滴下含浸法が多く採用されている。As a method for impregnating electrical equipment, the commonly used dipping method, drip impregnation method, etc. are used, and the drip impregnation method is often adopted from the viewpoint of labor saving in the manufacturing process.
(作用)
本発明の電気機器は、特定の樹脂組成物を用いることに
よって効果が得られる。 すなわち、架橋性単量体とし
て、アクリル酸エステル又はメタクリル酸エステルを用
いてスチレン量を置換減少させてスチレンの共重合性を
向上させ硬化後の刺激性臭気を減少させることができる
。 また硬化触媒としてコバルト又はマンガンの有機酸
金属塩と鉛、亜鉛又は錫の有機酸金属塩とを併用するこ
とによって適正なスチレンとの共重合性及び硬化性が得
られ、低温度・短時間処理が可能となる。(Function) The electric device of the present invention can obtain effects by using a specific resin composition. That is, the amount of styrene can be reduced by substitution using an acrylic ester or a methacrylic ester as a crosslinkable monomer to improve the copolymerizability of styrene and reduce the irritating odor after curing. In addition, by using an organic acid metal salt of cobalt or manganese and an organic acid metal salt of lead, zinc, or tin as a curing catalyst, appropriate copolymerizability and curing with styrene can be obtained, and low temperature and short time processing can be achieved. becomes possible.
(実施例)
次に本発明を実施例によって説明するが、本発明はこれ
らの実施例によって限定されるものではない、 以下の
実施例および比較例において1部」とは「重量部」を意
味する。(Example) Next, the present invention will be explained by Examples, but the present invention is not limited by these Examples. In the following Examples and Comparative Examples, "1 part" means "part by weight". do.
実施例 1
無水マレイン酸76.2部、イソフタールf12153
.3部、テトラハイドロ無水フタール酸37.0部、お
よびプロピレングリコール182部を 150〜220
℃で反応させて、酸価21の不飽和ポリエステルを合成
した。 この不飽和ポリエステル100部にハイドロキ
ノン0.06部、スチレン77部、および2−しドロキ
シメタクリルレート21部を加えて溶解し、その後ナフ
テン酸コバルト6%溶液0.1部、およびナフテン酸亜
鉛6%溶液0.8部を加えて攪拌均一に混合して樹脂組
成物を得な、 この樹脂組成物100部に硬化剤のt−
ブチルパーオキシオクトエート 1部を添加混合して、
扇風機用ステーターコイルに、滴下時のコイル温度90
℃1滴下量20g。Example 1 76.2 parts of maleic anhydride, isophthal f12153
.. 3 parts, 37.0 parts of tetrahydrophthalic anhydride, and 182 parts of propylene glycol.
The reaction was carried out at 0.degree. C. to synthesize an unsaturated polyester having an acid value of 21. 0.06 parts of hydroquinone, 77 parts of styrene, and 21 parts of 2-hydroxymethacrylate were added and dissolved in 100 parts of this unsaturated polyester, and then 0.1 part of a 6% solution of cobalt naphthenate and 6 parts of zinc naphthenate were added. Add 0.8 parts of % solution and stir to mix uniformly to obtain a resin composition. To 100 parts of this resin composition, add t-
Add and mix 1 part of butyl peroxyoctoate,
Coil temperature 90 when dripping onto stator coil for electric fan
℃1 drop amount 20g.
硬化温度110℃、硬化時間10分の条件で滴下含浸処
理を行った。 この滴下含浸処理後のステーターコイル
を室温まで冷却後、内容積41のブリキ製缶に封入し、
120℃で1時間加熱させ、その缶内の気中スチレンガ
ス濃度を検知管法で測定した結果、約50ppraと極
めて低い値であった。 このステーターコイルで組み立
てた扇風機を、気積約23m2(6畳の部屋)の密室で
1時間稼動試験を行った後の室内には、スチレンその他
の悪臭は全くなかった。Drop impregnation treatment was performed under the conditions of a curing temperature of 110° C. and a curing time of 10 minutes. After cooling the stator coil after this drip impregnation treatment to room temperature, it is sealed in a tin can with an internal volume of 41,
The can was heated at 120° C. for 1 hour, and the concentration of styrene gas in the air inside the can was measured using the detection tube method, and the result was an extremely low value of about 50 ppra. After conducting an operation test for an hour in a closed room with an air volume of approximately 23m2 (6 tatami room) using an electric fan assembled with this stator coil, there was no styrene or other bad odor in the room.
比較例 1
実施例1で合成した不飽和ポリエステル100部に、ハ
イドロキノン0.06部、およびスチレン100部を混
合溶解し、ナフテン酸コバルト6%溶液0.1部を添加
混合して樹脂組成物を得た。 この樹脂組成物100部
に過酸化物のt−ブチルパーオキシオクトエート 1部
を混合して実施例1と同様に滴下含浸処理を行い、スチ
レンガス濃度の測定を行ったところ280ppI!と高
く、また密室での稼動試験後の室内の空気はスチレンの
刺激臭気が強く、その他の臭気も強かっな。Comparative Example 1 0.06 parts of hydroquinone and 100 parts of styrene were mixed and dissolved in 100 parts of the unsaturated polyester synthesized in Example 1, and 0.1 part of a 6% cobalt naphthenate solution was added and mixed to form a resin composition. Obtained. 1 part of the peroxide t-butyl peroxyoctoate was mixed with 100 parts of this resin composition and subjected to dropwise impregnation treatment in the same manner as in Example 1, and the styrene gas concentration was measured and found to be 280 ppI! Moreover, after the operation test in a closed room, the air inside the room had a strong pungent odor of styrene and other odors.
実施例 2
無水マレイン酸81.8部、無水フタール酸98.8部
、アジピン11924.3部、およびジエチレングリコ
ール211.7部を150〜220℃で反応させて、酸
価23の不飽和ポリエステルを合成した。 この不飽和
ポリエステル100部に、ハイドロキノン0.06部を
加え、スチレン80部、2−しドロキシメタクリレート
13部、および2−ヒドロキシプロピルメタクリレート
6部を加えて溶解し、ナフテン酸コバルト6%溶液0.
1部、およびナフテン酸!915%溶液0.4部を添加
混合して樹脂組成物を得た。 実施例1と同様にしてス
テーターコイルの滴下含浸処理を行い、スチレンガス濃
度を測定したところ58pantと極めて低い値であっ
た。 また実施例1と同様にして密室における1時間稼
動試験後の室内には、スチレンその他の悪臭は全くなか
った。Example 2 81.8 parts of maleic anhydride, 98.8 parts of phthalic anhydride, 11924.3 parts of adipine, and 211.7 parts of diethylene glycol were reacted at 150 to 220°C to synthesize an unsaturated polyester with an acid value of 23. did. To 100 parts of this unsaturated polyester, 0.06 parts of hydroquinone was added, 80 parts of styrene, 13 parts of 2-hydroxymethacrylate, and 6 parts of 2-hydroxypropyl methacrylate were added and dissolved. ..
1 part, and naphthenic acid! A resin composition was obtained by adding and mixing 0.4 part of a 915% solution. The stator coil was subjected to drip impregnation treatment in the same manner as in Example 1, and the styrene gas concentration was measured and found to be an extremely low value of 58 pant. Further, in the same manner as in Example 1, there was no styrene or other bad odor in the room after the 1 hour operation test in a closed room.
比較例 2
実施例2の不飽和ポリエステル100部に、ハイドロキ
ノン0.06部、およびスチレン100部とを混合溶解
し、ナフテン酸コバルト6%溶液0.1部を添加混合し
て樹脂組成物を得た。 この組成物100部に、硬化剤
のt−ブチルパーオキシオクトエ−ト 1部を添加混合
して、実施例1と同様にして滴下含浸処理を行い、スチ
レンガス濃度を測定したところ270pp1Mと高く、
密室での稼動試験後の室内の空気はスチレン刺激臭気が
強く、その池の悪臭も強かった。Comparative Example 2 0.06 parts of hydroquinone and 100 parts of styrene were mixed and dissolved in 100 parts of the unsaturated polyester of Example 2, and 0.1 part of a 6% cobalt naphthenate solution was added and mixed to obtain a resin composition. Ta. To 100 parts of this composition, 1 part of t-butyl peroxyoctoate as a hardening agent was added and mixed, and dropwise impregnation treatment was performed in the same manner as in Example 1. The styrene gas concentration was measured and was as high as 270 pp1M. ,
After the operation test in a closed room, the air in the room had a strong styrene odor, and the pond had a strong odor as well.
[発明の効果]
以上の説明から明らかなように、本発明の電気機器は、
硬化後の刺激性臭気が少なく、低温度、短時間処理が可
能な硬化性の優れた樹脂組成物を用いたことによって、
安全で、製造工程の省力化、スピードアップを図ること
ができるものである。[Effects of the Invention] As is clear from the above explanation, the electrical equipment of the present invention has the following effects:
By using a resin composition with excellent curability that has little irritating odor after curing and can be processed at low temperatures and in a short time,
It is safe and can save labor and speed up the manufacturing process.
特許出願人 東芝ケミカル株式会社Patent applicant: Toshiba Chemical Corporation
Claims (1)
酸エステル又はメタクリル酸エステルを3〜50重量%
含む架橋性単量体30〜70重量部と、硬化触媒として
コバルト又はマンガンの有機酸金属塩及び鉛、亜鉛又は
錫の有機酸金属塩とを含む樹脂組成物を処理硬化させて
なることを特徴とする電気機器。1 70-30 parts by weight of unsaturated polyester and 3-50% by weight of acrylic ester or methacrylic ester
30 to 70 parts by weight of a crosslinkable monomer, and a resin composition containing an organic acid metal salt of cobalt or manganese and an organic acid metal salt of lead, zinc or tin as a curing catalyst. and electrical equipment.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29959788A JPH02148512A (en) | 1988-11-29 | 1988-11-29 | Electrical equipment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29959788A JPH02148512A (en) | 1988-11-29 | 1988-11-29 | Electrical equipment |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02148512A true JPH02148512A (en) | 1990-06-07 |
Family
ID=17874697
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29959788A Pending JPH02148512A (en) | 1988-11-29 | 1988-11-29 | Electrical equipment |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02148512A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002184239A (en) * | 2000-12-18 | 2002-06-28 | Asahi Denka Kogyo Kk | Coating material composition for coil wire |
JP2002332317A (en) * | 2001-05-10 | 2002-11-22 | Hitachi Chem Co Ltd | Thermosetting resin composition and method for manufacturing coil by using the same |
JP2005285424A (en) * | 2004-03-29 | 2005-10-13 | Kyocera Chemical Corp | High moisture resistance electrical insulating resin composition |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5964665A (en) * | 1982-10-04 | 1984-04-12 | Matsushita Electric Works Ltd | Unsaturated polyester resin varnish |
JPS6070712A (en) * | 1983-09-27 | 1985-04-22 | Toshiba Chem Corp | Resin composite material for insulation of transformer |
JPS61115966A (en) * | 1984-11-12 | 1986-06-03 | Toshiba Chem Corp | Electrical insulating varnish |
-
1988
- 1988-11-29 JP JP29959788A patent/JPH02148512A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5964665A (en) * | 1982-10-04 | 1984-04-12 | Matsushita Electric Works Ltd | Unsaturated polyester resin varnish |
JPS6070712A (en) * | 1983-09-27 | 1985-04-22 | Toshiba Chem Corp | Resin composite material for insulation of transformer |
JPS61115966A (en) * | 1984-11-12 | 1986-06-03 | Toshiba Chem Corp | Electrical insulating varnish |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002184239A (en) * | 2000-12-18 | 2002-06-28 | Asahi Denka Kogyo Kk | Coating material composition for coil wire |
JP2002332317A (en) * | 2001-05-10 | 2002-11-22 | Hitachi Chem Co Ltd | Thermosetting resin composition and method for manufacturing coil by using the same |
JP2005285424A (en) * | 2004-03-29 | 2005-10-13 | Kyocera Chemical Corp | High moisture resistance electrical insulating resin composition |
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