JP2001256830A - Resin composition for electric insulation and electric equipment - Google Patents
Resin composition for electric insulation and electric equipmentInfo
- Publication number
- JP2001256830A JP2001256830A JP2000070756A JP2000070756A JP2001256830A JP 2001256830 A JP2001256830 A JP 2001256830A JP 2000070756 A JP2000070756 A JP 2000070756A JP 2000070756 A JP2000070756 A JP 2000070756A JP 2001256830 A JP2001256830 A JP 2001256830A
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- unsaturated polyester
- parts
- electrical insulation
- electric
- 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.)
- Granted
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 43
- 238000009413 insulation Methods 0.000 title claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 46
- 238000010292 electrical insulation Methods 0.000 claims abstract description 23
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 23
- 229920006337 unsaturated polyester resin Polymers 0.000 claims abstract description 21
- 239000002245 particle Substances 0.000 claims abstract description 19
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000007822 coupling agent Substances 0.000 claims abstract description 11
- 235000012239 silicon dioxide Nutrition 0.000 claims description 22
- 239000011256 inorganic filler Substances 0.000 abstract description 11
- 229910003475 inorganic filler Inorganic materials 0.000 abstract description 11
- 238000004062 sedimentation Methods 0.000 abstract description 6
- 239000000805 composite resin Substances 0.000 abstract 1
- 229920006305 unsaturated polyester Polymers 0.000 description 17
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 16
- 239000002966 varnish Substances 0.000 description 15
- 150000007519 polyprotic acids Polymers 0.000 description 13
- 230000017525 heat dissipation Effects 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 8
- 150000005846 sugar alcohols Polymers 0.000 description 8
- 238000005470 impregnation Methods 0.000 description 7
- 230000009974 thixotropic effect Effects 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000004342 Benzoyl peroxide Substances 0.000 description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- MCCIMQKMMBVWHO-UHFFFAOYSA-N octadecanoic acid;titanium Chemical compound [Ti].CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O MCCIMQKMMBVWHO-UHFFFAOYSA-N 0.000 description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000006482 condensation reaction Methods 0.000 description 4
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- -1 allyl ethers Chemical class 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-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
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-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
- 150000008064 anhydrides Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical group CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 150000002432 hydroperoxides Chemical class 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 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
- 230000005855 radiation Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003784 tall oil Substances 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
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
- 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 1
- UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 description 1
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical group CCCCOOCCCC PAOHAQSLJSMLAT-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
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- VEZIVCLKHHASBQ-UHFFFAOYSA-M 2-ethylhexanoate propan-2-olate titanium(4+) Chemical compound [Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].CCCCC(CC)C([O-])=O VEZIVCLKHHASBQ-UHFFFAOYSA-M 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- XYFRHHAYSXIKGH-UHFFFAOYSA-N 3-(5-methoxy-2-methoxycarbonyl-1h-indol-3-yl)prop-2-enoic acid Chemical compound C1=C(OC)C=C2C(C=CC(O)=O)=C(C(=O)OC)NC2=C1 XYFRHHAYSXIKGH-UHFFFAOYSA-N 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 102100033040 Carbonic anhydrase 12 Human genes 0.000 description 1
- 102100033029 Carbonic anhydrase-related protein 11 Human genes 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 101000867855 Homo sapiens Carbonic anhydrase 12 Proteins 0.000 description 1
- 101000867841 Homo sapiens Carbonic anhydrase-related protein 11 Proteins 0.000 description 1
- 101001075218 Homo sapiens Gastrokine-1 Proteins 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- XQOAKYYZMDCSIA-UHFFFAOYSA-N O1OO1 Chemical class O1OO1 XQOAKYYZMDCSIA-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- NBICYCZLCAMSBG-UHFFFAOYSA-L [Co+2].CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O Chemical compound [Co+2].CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O NBICYCZLCAMSBG-UHFFFAOYSA-L 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- TVEKLSSKEBGNMA-UHFFFAOYSA-M butan-1-olate 2-butoxycarbonylbenzoate titanium(4+) Chemical compound CCCCOC(=O)c1ccccc1C(=O)O[Ti](OCCCC)(OCCCC)OCCCC TVEKLSSKEBGNMA-UHFFFAOYSA-M 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking 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
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 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
- SGGOJYZMTYGPCH-UHFFFAOYSA-L manganese(2+);naphthalene-2-carboxylate Chemical compound [Mn+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 SGGOJYZMTYGPCH-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000010998 test method Methods 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
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Insulating Of Coils (AREA)
- Inorganic Insulating Materials (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、電気絶縁用樹脂組
成物及び電気機器に関し、さらに詳しくは不飽和ポリエ
ステル樹脂と無機充填剤の混合物を主成分とする、モー
タ、トランスなどの電気機器用コイルの熱放射性を向上
させる電気絶縁用樹脂組成物及びこの電気絶縁用樹脂組
成物を用いて電気絶縁処理されてなる電気機器に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition for electric insulation and electric equipment, and more particularly to a coil for electric equipment such as a motor and a transformer, which is mainly composed of a mixture of an unsaturated polyester resin and an inorganic filler. TECHNICAL FIELD The present invention relates to a resin composition for electrical insulation that improves the heat radiation property of an electric device, and to an electrical device that is subjected to an electrical insulation treatment using the resin composition for electrical insulation.
【0002】[0002]
【従来の技術】モータ、トランス等の電気機器は、鉄コ
アの固着又は防錆、コイルの絶縁又は固着等を目的とし
て、電気絶縁用樹脂組成物で処理されている。電気絶縁
用樹脂組成物としては、硬化性、空乾性、固着性、電気
絶縁性、経済性などのバランスに優れた不飽和ポリエス
テル樹脂の組成物が広く用いられている。2. Description of the Related Art Electric devices such as motors and transformers are treated with a resin composition for electric insulation for the purpose of fixing or rustproofing an iron core, insulating or fixing a coil, and the like. As the resin composition for electrical insulation, an unsaturated polyester resin composition excellent in balance among curability, air-drying property, sticking property, electrical insulation property, economy and the like is widely used.
【0003】近年の電気機器は、小型・軽量化、高出力
化が進んだため、蓄熱温度がより高くなっている。特
に、電子レンジ、インバータエアコンなどの電気機器に
用いられる変圧器やリアクトルコイルは、運転時に過大
な負荷により発生した熱が放散されずに蓄熱され、電気
機器の温度が上昇する傾向があるため、使用される各材
料は、より耐熱性が高いものが求められるようになって
きた。そこで、樹脂組成物の熱伝導率を上げると共に、
コイルへの樹脂組成物の含浸性を向上させ、電気機器の
熱放散性を向上させるために、大気雰囲気中への熱放散
性を向上させた樹脂組成物が求められる。また、電気機
器の構成部材が同じ場合、そのような樹脂組成物を用い
ることにより、電気機器の信頼性向上に寄与できる。[0003] In recent years, electric appliances have been increasing in heat storage temperature due to progress in miniaturization, weight reduction and high output. In particular, transformers and reactor coils used in electric equipment such as microwave ovens and inverter air conditioners tend to store heat without dissipating heat generated by an excessive load during operation and increase the temperature of the electric equipment, Each of the materials used has been required to have higher heat resistance. Therefore, while increasing the thermal conductivity of the resin composition,
In order to improve the impregnation property of the resin composition into the coil and the heat dissipation property of the electric device, a resin composition having improved heat dissipation property in the air atmosphere is required. Further, when the constituent members of the electric device are the same, use of such a resin composition can contribute to improvement in reliability of the electric device.
【0004】以上より、熱伝導率を高めると共に、電気
機器への含浸性を良好にするために、不飽和ポリエステ
ル樹脂に無機充填剤を添加させて得られる無機充填剤混
合不飽和ポリエステル樹脂が用いられてきた。しかし、
不飽和ポリエステル樹脂に無機充填剤を混合すると、経
日放置により、混合していた無機充填剤が沈降し、不飽
和ポリエステル樹脂と無機充填剤が分離してしまう。更
に、不飽和ポリエステル樹脂と無機充填剤の混合比のバ
ラツキによって、電気機器の放熱性、耐クラック性が問
題となる場合があった。[0004] As described above, in order to increase the thermal conductivity and improve the impregnation property of electric equipment, an unsaturated polyester resin mixed with an unsaturated polyester resin obtained by adding an inorganic filler to an unsaturated polyester resin is used. I have been. But,
When the inorganic filler is mixed with the unsaturated polyester resin, the mixed inorganic filler sediments due to standing over time, and the unsaturated polyester resin and the inorganic filler are separated. Furthermore, the heat dissipation and crack resistance of electric equipment may become a problem due to the variation in the mixing ratio between the unsaturated polyester resin and the inorganic filler.
【0005】電気絶縁用樹脂組成物中の無機充填剤の量
が多くなると、粘度及び揺変度が高くなり電気機器への
含浸性が低下し熱放散性が低下すると共に、硬化物皮膜
が厚くなり、クラックが発生し易くなる問題があり、ま
た、電気絶縁用樹脂組成物中の無機充填剤の量が少なく
なると、含浸性は良好であるが、樹脂の熱伝導率が低下
するため、電気機器の放熱性が低下する問題があった。[0005] When the amount of the inorganic filler in the resin composition for electrical insulation is increased, the viscosity and the degree of thixotropicity are increased, the impregnating property to electric equipment is reduced, the heat dissipation is reduced, and the cured product film becomes thick. In addition, there is a problem that cracks are easily generated, and when the amount of the inorganic filler in the resin composition for electrical insulation is small, impregnation is good, but the thermal conductivity of the resin is reduced, so that There is a problem that the heat radiation of the device is reduced.
【0006】[0006]
【発明が解決しようとする課題】電気絶縁用樹脂組成物
において、近年の要求性能を満足すべく、低粘度且つ低
揺変度で、熱伝導率が高く、更に経日放置による無機充
填剤の沈降速度をかなり遅くさせた電気絶縁用樹脂組成
物が要求されるようになった。SUMMARY OF THE INVENTION In order to satisfy recent performance requirements, an electric insulating resin composition has a low viscosity, a low thixotropic degree, a high thermal conductivity, and an inorganic filler obtained by leaving it for days. There has been a demand for a resin composition for electrical insulation whose sedimentation speed has been considerably reduced.
【0007】本発明は、低粘度且つ低揺変度で電気機器
への含浸性が良好で、熱伝導率が高く、電気機器の運転
時に発生する熱を放散し易くすることができ、更に経日
放置による無機充填剤の沈降速度をかなり遅くさせた電
気絶縁用樹脂組成物及びこの電気絶縁用樹脂組成物を用
いて電気絶縁処理されてなる電気機器を提供するもので
ある。[0007] The present invention has a low viscosity, a low volatility, a good impregnating property to electric equipment, a high thermal conductivity, and can easily dissipate heat generated during operation of electric equipment. An object of the present invention is to provide a resin composition for electrical insulation in which the sedimentation rate of an inorganic filler caused by standing for a day is considerably slowed down, and an electrical device which is subjected to an electrical insulation treatment using the resin composition for electrical insulation.
【0008】[0008]
【課題を解決するための手段】本発明者らは鋭意検討の
結果、不飽和ポリエステル樹脂に平均粒径0.5〜5μ
mの二酸化ケイ素及びチタネート系カップリング剤を混
合させることによって、従来の不飽和ポリエステル樹脂
に平均粒径5μmを超える二酸化ケイ素及びチタネート
系カップリング剤を混合させた場合よりも、二酸化ケイ
素の沈降速度を遅くできるため、樹脂組成物の経日放置
後も、電気機器への含浸性が良好のため、運転時の電気
機器の熱放散性が良好となり、電気機器の温度上昇を低
減できることを見出した。Means for Solving the Problems As a result of intensive studies, the present inventors have found that an unsaturated polyester resin has an average particle size of 0.5 to 5 μm.
m of silicon dioxide and a titanate-based coupling agent, the sedimentation rate of silicon dioxide is higher than that of a case where a conventional unsaturated polyester resin is mixed with silicon dioxide and a titanate-based coupling agent having an average particle size of more than 5 μm. It has been found that, even after leaving the resin composition for days, the impregnating property of the electric device is good, so that the heat dissipation of the electric device during operation is good, and the temperature rise of the electric device can be reduced. .
【0009】本発明は、(A)不飽和ポリエステル樹
脂、(B)平均粒径0.5〜5μmの二酸化ケイ素及び
(C)チタネート系カップリング剤を含有してなる電気
絶縁用樹脂組成物に関する。The present invention relates to an electrically insulating resin composition comprising (A) an unsaturated polyester resin, (B) silicon dioxide having an average particle size of 0.5 to 5 μm, and (C) a titanate coupling agent. .
【0010】また本発明は、前記電気絶縁処理用樹脂組
成物を用いて絶縁処理されてなる電気機器に関する。[0010] The present invention also relates to an electric device which is insulated by using the resin composition for electric insulation treatment.
【0011】[0011]
【発明の実施の形態】本発明に用いられる(A)成分で
ある不飽和ポリエステル樹脂としては、通常、不飽和ポ
リエステル及び架橋性単量体を含有するものが好適に用
いられる。不飽和ポリエステルとしては、通常、不飽和
多塩基酸及び飽和多塩基酸からなる多塩基酸成分と多価
アルコール成分とを脱水縮合反応させ、さらに必要に応
じて変性成分を反応させて得られるものが用いられる。
変性成分の反応は、多塩基酸成分と多価アルコール成分
との脱水縮合反応と同時に行ってもよいし、多塩基酸成
分又は多価アルコール成分の一部と変性成分とを反応さ
せた後、反応生成物を加えて残りの多塩基酸成分及び多
価アルコール成分の脱水縮合反応を行ってもよい。BEST MODE FOR CARRYING OUT THE INVENTION As the unsaturated polyester resin which is the component (A) used in the present invention, a resin containing an unsaturated polyester and a crosslinkable monomer is usually suitably used. As the unsaturated polyester, usually, a polyester obtained by subjecting a polybasic acid component composed of an unsaturated polybasic acid and a saturated polybasic acid to a dehydration condensation reaction with a polyhydric alcohol component, and further reacting a modified component as necessary. Is used.
The reaction of the denaturing component may be performed simultaneously with the dehydration condensation reaction between the polybasic acid component and the polyhydric alcohol component, or after reacting a part of the polybasic acid component or the polyhydric alcohol component with the denaturing component, The dehydration condensation reaction of the remaining polybasic acid component and polyhydric alcohol component may be performed by adding the reaction product.
【0012】不飽和多塩基酸としては、例えばマレイン
酸、無水マレイン酸、フマル酸等の不飽和二塩基酸及び
これらの無水物等の反応性誘導体などが挙げられ、これ
らの内1種若しくは2種以上を使用することができる。
飽和多塩基酸としては、例えば、フタル酸、無水フタル
酸、イソフタル酸、テレフタル酸、テトラヒドロフタル
酸、テトラヒドロ無水フタル酸、ヘキサヒドロフタル
酸、ヘキサヒドロ無水フタル酸、アジピン酸、セバチン
酸等の芳香族カルボン酸、飽和酸、これらの無水物等の
反応性誘導体、大豆油脂肪酸、アマニ油脂肪酸、トール
油脂肪酸等の植物油脂肪酸などが挙げられ、これらの内
1種若しくは2種以上を使用することができる。The unsaturated polybasic acids include, for example, unsaturated dibasic acids such as maleic acid, maleic anhydride and fumaric acid, and reactive derivatives such as anhydrides thereof. More than one species can be used.
Examples of the saturated polybasic acid include aromatic acids such as phthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid, tetrahydrophthalic acid, tetrahydrophthalic anhydride, hexahydrophthalic acid, hexahydrophthalic anhydride, adipic acid, and sebacic acid. Examples thereof include carboxylic acids, saturated acids, reactive derivatives such as anhydrides thereof, and vegetable oil fatty acids such as soybean oil fatty acids, linseed oil fatty acids, and tall oil fatty acids, and one or more of these may be used. it can.
【0013】不飽和多塩基酸の使用量は、多塩基酸成分
の総モル数に対して30〜80モル%とすることが好ま
しく、50〜70モル%とすることがより好ましい。不
飽和多塩基酸の量が30モル%未満であると、硬化性が
低下する傾向があり、80モル%を超えると、安定性が
悪くなる傾向がある。The amount of the unsaturated polybasic acid used is preferably 30 to 80 mol%, more preferably 50 to 70 mol%, based on the total number of moles of the polybasic acid component. If the amount of the unsaturated polybasic acid is less than 30 mol%, the curability tends to decrease, and if it exceeds 80 mol%, the stability tends to deteriorate.
【0014】多価アルコール成分としては、例えばプロ
ピレングリコール、エチレングリコール、ジプロピレン
グリコール、ジエチレングリコール、1,3−ブタンジ
オール、ネオペンチルグリコール等の二価アルコール、
グリセリン、トリメチロールプロパン、ペンタエリスリ
トール等の三価以上の多価アルコールなどが挙げられ、
これらの内1種若しくは2種以上を使用することができ
る。Examples of the polyhydric alcohol component include dihydric alcohols such as propylene glycol, ethylene glycol, dipropylene glycol, diethylene glycol, 1,3-butanediol, and neopentyl glycol.
Glycerin, trimethylolpropane, trihydric or higher polyhydric alcohols such as pentaerythritol, and the like,
One or more of these can be used.
【0015】多価アルコール成分の使用量は、多塩基酸
成分1当量あたり、1.00〜1.30当量とすること
が好ましく、1.05〜1.15当量とすることがより
好ましい。多価アルコール成分の使用量が多塩基酸成分
1当量あたり1.00当量未満及び1.30当量を超え
ると、不飽和ポリエステルが高分子量とならず、十分な
強度の樹脂組成物を得られなくなる傾向がある。The amount of the polyhydric alcohol component used is preferably 1.00 to 1.30 equivalents, more preferably 1.05 to 1.15 equivalents, per equivalent of the polybasic acid component. When the use amount of the polyhydric alcohol component is less than 1.00 equivalent or more than 1.30 equivalent per equivalent of the polybasic acid component, the unsaturated polyester does not have a high molecular weight, and a resin composition having sufficient strength cannot be obtained. Tend.
【0016】変性成分としては、例えばアマニ油、大豆
油、トール油、脱水ヒマシ油、ヤシ油、ジシクロペンタ
ジエン、シクロペンタジエン等を挙げることができ、こ
れらの内1種若しくは2種以上を使用することができ
る。Examples of the modified components include linseed oil, soybean oil, tall oil, dehydrated castor oil, coconut oil, dicyclopentadiene, cyclopentadiene, and the like. One or more of these are used. be able to.
【0017】不飽和ポリエステルとしては、数平均分子
量(ゲルパーミエーションクロマトグラフィーにより測
定し、標準ポリスチレンの検量線を用いて換算した値)
が100〜100,000であるものを用いることが好
ましく、1,000〜50,000であるものを用いる
ことがより好ましい。また、酸価が10〜25であるこ
とが好ましい。As the unsaturated polyester, a number average molecular weight (measured by gel permeation chromatography and converted using a standard polystyrene calibration curve)
Is preferably 100 to 100,000, and more preferably 1,000 to 50,000. Further, the acid value is preferably from 10 to 25.
【0018】架橋性単量体としては、例えばスチレン、
ビニルトルエン、α−メチルスチレン、ターシャリーブ
チルスチレン、ジビニルベンゼン等の芳香族ビニル化合
物、アクリル酸メチル、メタクリル酸メチル、アクリル
酸エチル、メタクリル酸エチル、2−ヒドロキシエチル
メタクリレート等の各種アクリル酸エステル及び/又は
メタクリル酸エステル、ジアリルフタレート等の各種ア
リルエステル、各種アリルエーテルなどが挙げられる。
これらの架橋性単量体は、1種単独で用いてもよいし、
2種以上を併用してもよい。Examples of the crosslinkable monomer include styrene,
Vinyl toluene, α-methylstyrene, tertiary butylstyrene, aromatic vinyl compounds such as divinylbenzene, various acrylates such as methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, 2-hydroxyethyl methacrylate and And / or various allyl esters such as methacrylic acid ester and diallyl phthalate, and various allyl ethers.
These crosslinkable monomers may be used alone,
Two or more kinds may be used in combination.
【0019】架橋性単量体の使用量は、不飽和ポリエス
テル25〜60重量部に対して、好ましくは75〜40
重量部、より好ましくは不飽和ポリエステル35〜50
重量部に対して65〜50重量部の範囲とされる。ただ
し、不飽和ポリエステルと架橋性単量体との総量は、1
00重量部とされる。The amount of the crosslinking monomer used is preferably 75 to 40 parts by weight based on 25 to 60 parts by weight of the unsaturated polyester.
Parts by weight, more preferably 35 to 50 unsaturated polyester
The range is 65 to 50 parts by weight with respect to parts by weight. However, the total amount of the unsaturated polyester and the crosslinkable monomer is 1
00 parts by weight.
【0020】本発明に用いられる(B)成分である二酸
化ケイ素の平均粒径は0.5〜5μmであり、好ましく
は1〜4μm、より好ましくは2〜3μmである。二酸
化ケイ素の平均粒径が5μmを超えると、経日放置とと
もに、二酸化ケイ素が沈降し易くなり、トランス運転時
の温度上昇が大きくなり、0.5μm未満であると、揺
変度が高くなり、コイルへの含浸性が低下してしまう。
なお、平均粒径は、粒度分布測定装置((株)島津製作
所製)を用いて測定することができる。The average particle size of the silicon dioxide as the component (B) used in the present invention is 0.5 to 5 μm, preferably 1 to 4 μm, more preferably 2 to 3 μm. When the average particle size of silicon dioxide exceeds 5 μm, with standing for days, silicon dioxide is likely to settle, the temperature rise during the operation of the transformer becomes large, and when it is less than 0.5 μm, the degree of thixotropic becomes high, The impregnating property of the coil is reduced.
The average particle size can be measured using a particle size distribution measuring device (manufactured by Shimadzu Corporation).
【0021】平均粒径0.5〜5μmの二酸化ケイ素
(B)は、電気機器を運転するときの放熱性を向上させ
ることを主な目的として配合される。放熱性の観点から
は、配合量が多い程よいが、この配合量が多くなると電
気絶縁用樹脂組成物の粘度及び揺変度が高くなり、含浸
性が低下する傾向がある。このことから、不飽和ポリエ
ステル樹脂(A)100重量部に対して、平均粒径0.
5〜5μmの二酸化ケイ素(B)の量は、通常10〜1
00重量部とし、好ましくは25〜82重量部、より好
ましくは43〜66重量部とする。平均粒径0.5〜5
μmの二酸化ケイ素(B)の配合量が10重量部未満で
あると熱伝導性が低くなり放熱性が低下する傾向があ
る。[0021] Silicon dioxide (B) having an average particle size of 0.5 to 5 µm is blended mainly for the purpose of improving heat dissipation when operating electric equipment. From the viewpoint of heat dissipation, the larger the amount, the better. However, the higher the amount, the higher the viscosity and thixotropic degree of the resin composition for electrical insulation, and the lower the impregnation. For this reason, the average particle size of 0.1 part by weight based on 100 parts by weight of the unsaturated polyester resin (A)
The amount of silicon dioxide (B) of 5 to 5 μm is usually 10 to 1
00 parts by weight, preferably 25 to 82 parts by weight, more preferably 43 to 66 parts by weight. Average particle size 0.5-5
If the amount of the silicon dioxide (B) of less than 10 μm is less than 10 parts by weight, the thermal conductivity tends to be low and the heat dissipation tends to be low.
【0022】本発明に用いられる(C)成分のチタネー
ト系カップリング剤は、平均粒径0.5〜5μmの二酸
化ケイ素(B)の添加により高くなる樹脂組成物の粘度
及び揺変度の低下を目的に配合される。粘度及び揺変度
の低下の観点からは、チタネート系カップリング剤
(C)の配合量が多いほど樹脂組成物の粘度及び揺変度
は低下するが、この配合量が多くなると粘度が低くなり
すぎて、二酸化ケイ素の沈降が速くなり、二酸化ケイ素
が分離する傾向がある。また、配合量が少なすぎると粘
度及び揺変度の低下に効果がない。The titanate-based coupling agent (C) used in the present invention has a resin composition having an average particle diameter of 0.5 to 5 μm. It is blended for the purpose. From the viewpoint of decreasing the viscosity and thixotropic degree, the viscosity and thixotropic degree of the resin composition decrease as the amount of the titanate-based coupling agent (C) increases, but the viscosity decreases as the amount increases. Too fast, the sedimentation of the silicon dioxide is faster and the silicon dioxide tends to separate. On the other hand, if the amount is too small, there is no effect on lowering the viscosity and thixotropic degree.
【0023】このことから、チタネート系カップリング
剤(C)の配合量としては、不飽和ポリエステル樹脂
(A)100重量部に対して、0.01〜1.0重量部
の範囲が好ましく、特に0.02〜0.2重量部の範囲
がより好ましい。Accordingly, the amount of the titanate-based coupling agent (C) is preferably in the range of 0.01 to 1.0 part by weight based on 100 parts by weight of the unsaturated polyester resin (A). A range of 0.02 to 0.2 parts by weight is more preferable.
【0024】チタネート系カップリング剤としては、チ
タニウムステアレート、ジ−i−プロキシチタンジイソ
ステアレート、(2−n−ブトキシカルボニルベンゾイ
ルオキシ)トリブトキシチタン、2−エチルヘキサノイ
ルオキシトリ(2−プロポキシ)チタン(いずれも日本
曹達株式会社製)等が挙げられ、1種又は2種以上を用
いることができる。Examples of titanate coupling agents include titanium stearate, di-i-proxytitanium diisostearate, (2-n-butoxycarbonylbenzoyloxy) tributoxytitanium, and 2-ethylhexanoyloxytri (2- Propoxy) titanium (both manufactured by Nippon Soda Co., Ltd.) and the like, and one or more kinds can be used.
【0025】本発明になる電気絶縁用樹脂組成物には、
さらに、必要に応じ、不飽和ポリエステル樹脂の硬化剤
を配合することができる。硬化剤としては、不飽和ポリ
エステル樹脂の硬化剤として通常用いられるものであれ
ば特に制限なく使用することができ、例えばベンゾイル
パーオキサイド、アセチルパーオキサイド等のアシルパ
ーオキサイド、ターシャリブチルパーオキサイド、キュ
メンヒドロパーオキサイド等のヒドロパーオキサイド、
メチルエチルケトンパーオキサイド、シクロヘキサノン
パーオキサイド等のケトンパーオキサイド、ジターシャ
リブチルパーオキサイド、ジクミルパーオキサイド等の
ジアルキルパーオキサイド、ターシャリブチルパーオキ
シアセテート等のオキシパーオキサイドなどを用いるこ
とができる。硬化剤の添加量としては、(A)成分、
(B)成分、(C)成分の総量100重量部に対して
0.3〜5重量部が好ましく、0.5〜1重量部がより
好ましい。The resin composition for electrical insulation according to the present invention includes:
Further, a curing agent for the unsaturated polyester resin can be blended if necessary. As the curing agent, any one can be used without particular limitation as long as it is generally used as a curing agent for an unsaturated polyester resin.Examples include acyl peroxides such as benzoyl peroxide and acetyl peroxide, tertiary butyl peroxide, and cumene. Hydroperoxides such as hydroperoxides,
Ketone peroxides such as methyl ethyl ketone peroxide and cyclohexanone peroxide, dialkyl peroxides such as di-tert-butyl peroxide and dicumyl peroxide, and oxyperoxides such as tert-butyl peroxy acetate can be used. As the addition amount of the curing agent, the component (A)
The amount is preferably from 0.3 to 5 parts by weight, more preferably from 0.5 to 1 part by weight, based on 100 parts by weight of the total of the components (B) and (C).
【0026】また、必要に応じて促進剤及び重合禁止剤
を添加することもできる。促進剤、重合禁止剤として
も、不飽和ポリエステル樹脂の硬化に通常用いられるも
のであれば特に制限なく使用することができる。例え
ば、促進剤としては、ナフテン酸マンガン、ナフテン酸
鉛、ナフテン酸コバルト、オクテン酸コバルト等を用い
ることができる。重合禁止剤としては、例えば、ハイド
ロキノン、ターシャリブチルカテコール、p−ベンゾキ
ノン等のキノン類を用いることができる。If necessary, an accelerator and a polymerization inhibitor can be added. The accelerator and polymerization inhibitor can be used without any particular limitation as long as they are generally used for curing the unsaturated polyester resin. For example, manganese naphthenate, lead naphthenate, cobalt naphthenate, cobalt octenoate, and the like can be used as the accelerator. As the polymerization inhibitor, for example, quinones such as hydroquinone, tert-butylcatechol, and p-benzoquinone can be used.
【0027】本発明の樹脂組成物はエアコン用ファン、
扇風機、洗たく機等のコンデンサーモータ、テレビ、ス
テレオ、コンパクトディスクプレーヤー等の電源トラン
ス等の電気機器の絶縁処理に適用される。[0027] The resin composition of the present invention comprises a fan for an air conditioner,
It is applied to the insulation treatment of electric equipment such as condenser motors such as electric fans and washing machines, and power transformers such as televisions, stereos and compact disc players.
【0028】[0028]
【実施例】以下実施例により本発明を説明するが、本発
明はこれによって制限されるものではない。なお、下記
例中の部は、重量部を意味する。EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited by these examples. In addition, the part in the following examples means a weight part.
【0029】製造例1 不飽和ポリエステル(a−1)
の合成 無水マレイン酸784部、テレフタル酸166部、イソ
フタル酸166部、ジエチレングリコール847部、エ
チレングリコール186部を反応釜に仕込み、窒素ガス
気流中で200〜220℃に昇温させ、次に、ジシクロ
ペンタジエン528部を添加し、以下、常法により脱水
縮合反応させ、酸価が20となったところで冷却した。
得られた不飽和ポリエステルの数平均分子量は35,0
00であった。Production Example 1 Unsaturated polyester (a-1)
784 parts of maleic anhydride, 166 parts of terephthalic acid, 166 parts of isophthalic acid, 847 parts of diethylene glycol, and 186 parts of ethylene glycol were charged into a reaction vessel, and the temperature was raised to 200 to 220 ° C. in a stream of nitrogen gas. After adding 528 parts of cyclopentadiene, a dehydration-condensation reaction was carried out by a conventional method. When the acid value reached 20, the mixture was cooled.
The resulting unsaturated polyester had a number average molecular weight of 35.0.
00.
【0030】実施例1 不飽和ポリエステル(a−1)45部、スチレン35
部、平均粒径2μmの二酸化ケイ素40部、チタニウム
ステアレート0.10部及び硬化剤として不飽和ポリエ
ステルとスチレンの総量に対して1.0重量%のベンゾ
イルパーオキサイドを撹拌混合して電気絶縁用樹脂組成
物のワニスを調製した。Example 1 45 parts of unsaturated polyester (a-1), styrene 35
Parts, 40 parts of silicon dioxide having an average particle size of 2 μm, 0.10 parts of titanium stearate, and 1.0% by weight of benzoyl peroxide, based on the total amount of unsaturated polyester and styrene, as a curing agent, and mixed by stirring. A varnish of the resin composition was prepared.
【0031】実施例2 不飽和ポリエステル(a−1)45部、スチレン35
部、平均粒径4μmの二酸化ケイ素40部、チタニウム
ステアレート0.10部及び硬化剤として不飽和ポリエ
ステルとスチレンの総量に対して1.0重量%のベンゾ
イルパーオキサイドを撹拌混合して電気絶縁用樹脂組成
物のワニスを調製した。Example 2 45 parts of unsaturated polyester (a-1), 35 parts of styrene
Parts, 40 parts of silicon dioxide having an average particle size of 4 μm, 0.10 parts of titanium stearate, and 1.0% by weight of benzoyl peroxide, based on the total amount of unsaturated polyester and styrene, as a curing agent were mixed with stirring for electrical insulation. A varnish of the resin composition was prepared.
【0032】比較例1 不飽和ポリエステル(a−1)45部、スチレン35
部、平均粒径8μmの二酸化ケイ素40部、チタニウム
ステアレート0.10部及び硬化剤として不飽和ポリエ
ステルとスチレンの総量に対して1.0重量%のベンゾ
イルパーオキサイドを撹拌混合して電気絶縁用樹脂組成
物のワニスを調製した。Comparative Example 1 45 parts of unsaturated polyester (a-1), styrene 35
Parts, 40 parts of silicon dioxide having an average particle size of 8 μm, 0.10 parts of titanium stearate, and 1.0% by weight of benzoyl peroxide based on the total amount of unsaturated polyester and styrene as a curing agent, and mixed by stirring. A varnish of the resin composition was prepared.
【0033】比較例2 不飽和ポリエステル(a−1)45部、スチレン35
部、平均粒径10μmの二酸化ケイ素40部、チタニウ
ムステアレート0.10部及び硬化剤として不飽和ポリ
エステルとスチレンの総量に対して1.0重量%のベン
ゾイルパーオキサイドを撹拌混合して電気絶縁用樹脂組
成物のワニスを調製した。Comparative Example 2 Unsaturated polyester (a-1) 45 parts, styrene 35
Parts, 40 parts of silicon dioxide having an average particle diameter of 10 μm, 0.10 parts of titanium stearate, and 1.0% by weight of benzoyl peroxide based on the total amount of unsaturated polyester and styrene as a curing agent, and mixed by stirring. A varnish of the resin composition was prepared.
【0034】得られた電気絶縁用樹脂組成物のワニスに
ついて、電気絶縁用樹脂組成物のワニスを調製直後を初
期とし、初期と40℃10日放置後について、ワニス粘
度、揺変度、二酸化ケイ素の沈降性、熱伝導率及びこの
電気絶縁用樹脂組成物のワニスを用いて電気絶縁処理し
たトランスの運転時の温度上昇と含浸性を調べた。その
結果を表1に示す。Regarding the varnish of the obtained resin composition for electric insulation, the varnish viscosity, degree of thixotropicity, silicon dioxide and the varnish of the resin composition for electric insulation were initially set immediately after the preparation of the varnish and left after standing at 40 ° C. for 10 days. Of the transformer, and the temperature rise and impregnation during the operation of the transformer electrically insulated using the varnish of the resin composition for electrical insulation were examined. Table 1 shows the results.
【0035】なお、これら特性の試験方法は、以下の通
りである。 ワニス粘度、揺変度:JIS C 2105に準じて測
定した。 二酸化ケイ素の沈降性:直径18mmの試験管中にワニ
スを100mmの高さまで入れ、23℃で20日間放置
し、上部に発生するクリアー層部分の高さを測定した。 熱伝導率:直径50mm、厚さ10mmの円盤状の金型
内に電気絶縁用樹脂組成物のワニスを注型し、温度15
0℃で3時間硬化させて試験片を作製し、熱伝導率測定
装置(ダイナテック株式会社製、シーマテック(商品
名))を用いて測定した。 運転時温度上昇:コア寸法が83mm×80mm×50
mmのトランスのコア内部に温度センサーを付け、電気
絶縁用樹脂組成物のワニスを、室温、133hPaの減
圧下に注入し、温度160℃で3時間硬化させた。冷却
後、トランスの温度を測定し、100Vの電圧を2時間
印加した後の温度を再び測定し、電圧印加前後の温度差
から、温度上昇を求めた。また、含浸性については、二
次側コイルを切断し、コイル断面のエナメル線間を実体
顕微鏡で観察し、樹脂組成物の含浸状態を評価した。The test methods for these characteristics are as follows. Varnish viscosity, thixotropic degree: Measured according to JIS C 2105. Precipitation of silicon dioxide: The varnish was placed in a test tube having a diameter of 18 mm up to a height of 100 mm, left at 23 ° C. for 20 days, and the height of a clear layer formed on the top was measured. Thermal conductivity: A varnish of the resin composition for electrical insulation was cast into a disk-shaped mold having a diameter of 50 mm and a thickness of 10 mm, and the temperature was adjusted to 15 ° C.
The test piece was prepared by curing at 0 ° C. for 3 hours, and the test piece was measured using a thermal conductivity measuring device (Cymatec (trade name) manufactured by Dynatech Co., Ltd.). Temperature rise during operation: Core dimensions 83 mm x 80 mm x 50
A temperature sensor was attached to the inside of the core of the transformer of mm, and a varnish of the resin composition for electric insulation was injected at room temperature under a reduced pressure of 133 hPa, and cured at 160 ° C. for 3 hours. After cooling, the temperature of the transformer was measured, the temperature after applying a voltage of 100 V for 2 hours was measured again, and the temperature rise was determined from the temperature difference before and after the voltage was applied. Regarding the impregnating property, the secondary coil was cut, the space between the enameled wires on the coil cross section was observed with a stereoscopic microscope, and the impregnation state of the resin composition was evaluated.
【0036】[0036]
【表1】 表1からわかるように、本発明の実施例の電気絶縁用樹
脂組成物のワニスは、不飽和ポリエステル樹脂に平均粒
径0.5〜5μmの二酸化ケイ素及びチタネート系カッ
プリング剤を混合することによって、二酸化ケイ素の沈
降速度を遅くできるため、ワニスの経日放置後も、電気
機器への含浸性が良好である。従って運転時の電気機器
の熱放散性が良好であり、電気機器の温度上昇を低減で
きる。[Table 1] As can be seen from Table 1, the varnish of the resin composition for electrical insulation according to the example of the present invention is obtained by mixing an unsaturated polyester resin with silicon dioxide having an average particle size of 0.5 to 5 μm and a titanate coupling agent. In addition, since the sedimentation speed of silicon dioxide can be reduced, the impregnating property of electrical equipment is good even after the varnish is left for days. Therefore, the heat dissipation of the electric device during operation is good, and the temperature rise of the electric device can be reduced.
【0037】[0037]
【発明の効果】本発明になる電気絶縁用樹脂組成物は、
電気機器に含浸させて絶縁処理することによって、熱放
散性に優れた電気機器の製造が可能となると共に、樹脂
組成物の経日放置後も、電気機器への含浸性が良好のた
め、運転時の電気機器の熱放散性が良好であり、電気機
器の温度上昇を低減できる。The resin composition for electrical insulation according to the present invention comprises:
By impregnating and insulating the electrical equipment, it is possible to manufacture electrical equipment with excellent heat dissipation, and even after the resin composition has been left for days, the impregnation property of the electrical equipment is good. The heat dissipation of the electric device at the time is good, and the temperature rise of the electric device can be reduced.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) H01F 5/06 H01F 5/06 R 27/32 27/32 A Fターム(参考) 4J002 CF221 DJ006 EC077 EG047 FA086 FD016 FD147 5E044 AC01 AC04 5G303 AA08 AB20 BA12 CA09 CA11 CD03 5G305 AA03 AA12 AB23 BA09 BA15 CA12 CB04 CB14 CC02 CD06 CD08 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) H01F 5/06 H01F 5/06 R 27/32 27/32 A F term (Reference) 4J002 CF221 DJ006 EC077 EG047 FA086 FD016 FD147 5E044 AC01 AC04 5G303 AA08 AB20 BA12 CA09 CA11 CD03 5G305 AA03 AA12 AB23 BA09 BA15 CA12 CB04 CB14 CC02 CD06 CD08
Claims (3)
平均粒径0.5〜5μmの二酸化ケイ素及び(C)チタ
ネート系カップリング剤を含有してなる電気絶縁用樹脂
組成物。1. An unsaturated polyester resin (A), (B)
A resin composition for electrical insulation, comprising silicon dioxide having an average particle size of 0.5 to 5 μm and (C) a titanate coupling agent.
量部、(B)平均粒径0.5〜5μmの二酸化ケイ素1
0〜100重量部及び(C)チタネート系カップリング
剤0.01〜1.0重量部を含有してなる電気絶縁用樹
脂組成物。2. Silicon dioxide 1 having (A) 100 parts by weight of an unsaturated polyester resin and (B) an average particle size of 0.5 to 5 μm.
A resin composition for electrical insulation comprising 0 to 100 parts by weight and (C) 0.01 to 1.0 part by weight of a titanate coupling agent.
組成物を用いて電気絶縁処理されてなる電気機器。3. An electric device which is subjected to an electric insulation treatment using the resin composition for electric insulation according to claim 1 or 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000070756A JP4590675B2 (en) | 2000-03-14 | 2000-03-14 | Resin composition for electrical insulation and electrical equipment |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000070756A JP4590675B2 (en) | 2000-03-14 | 2000-03-14 | Resin composition for electrical insulation and electrical equipment |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2001256830A true JP2001256830A (en) | 2001-09-21 |
| JP4590675B2 JP4590675B2 (en) | 2010-12-01 |
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ID=18589440
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|---|---|---|---|
| JP2000070756A Expired - Fee Related JP4590675B2 (en) | 2000-03-14 | 2000-03-14 | Resin composition for electrical insulation and electrical equipment |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020513464A (en) * | 2016-12-13 | 2020-05-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | Solid polymer highly durable surface material |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04345640A (en) * | 1991-05-23 | 1992-12-01 | Hitachi Ltd | Thermosetting resin composition for high-voltage coil casting, molded coils and panels formed by casting and curing with the composition |
| JP2001152003A (en) * | 1999-11-24 | 2001-06-05 | Hitachi Chem Co Ltd | Resin composition for electric insulation |
-
2000
- 2000-03-14 JP JP2000070756A patent/JP4590675B2/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04345640A (en) * | 1991-05-23 | 1992-12-01 | Hitachi Ltd | Thermosetting resin composition for high-voltage coil casting, molded coils and panels formed by casting and curing with the composition |
| JP2001152003A (en) * | 1999-11-24 | 2001-06-05 | Hitachi Chem Co Ltd | Resin composition for electric insulation |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020513464A (en) * | 2016-12-13 | 2020-05-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | Solid polymer highly durable surface material |
| JP7096821B2 (en) | 2016-12-13 | 2022-07-06 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Solid polymer Highly durable surface material |
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|---|---|
| JP4590675B2 (en) | 2010-12-01 |
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