JP5278164B2 - Ignition coil parts - Google Patents
Ignition coil parts Download PDFInfo
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- JP5278164B2 JP5278164B2 JP2009125453A JP2009125453A JP5278164B2 JP 5278164 B2 JP5278164 B2 JP 5278164B2 JP 2009125453 A JP2009125453 A JP 2009125453A JP 2009125453 A JP2009125453 A JP 2009125453A JP 5278164 B2 JP5278164 B2 JP 5278164B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- polyphenylene ether
- resin composition
- weight
- styrene
- 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.)
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- 229920005989 resin Polymers 0.000 claims abstract description 110
- 239000011347 resin Substances 0.000 claims abstract description 110
- 229920001955 polyphenylene ether Polymers 0.000 claims abstract description 59
- 239000011342 resin composition Substances 0.000 claims abstract description 52
- 230000015556 catabolic process Effects 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 17
- 238000010998 test method Methods 0.000 claims abstract description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 57
- 239000003365 glass fiber Substances 0.000 claims description 11
- 239000011256 inorganic filler Substances 0.000 claims description 9
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 9
- 239000001023 inorganic pigment Substances 0.000 claims description 9
- 238000009413 insulation Methods 0.000 claims description 7
- 239000010445 mica Substances 0.000 claims description 5
- 229910052618 mica group Inorganic materials 0.000 claims description 5
- 239000000454 talc Substances 0.000 claims description 4
- 229910052623 talc Inorganic materials 0.000 claims description 4
- 239000010456 wollastonite Substances 0.000 claims description 4
- 229910052882 wollastonite Inorganic materials 0.000 claims description 4
- 239000000306 component Substances 0.000 claims description 2
- 238000000465 moulding Methods 0.000 abstract description 18
- -1 poly (2,6-dimethyl-1,4-phenylene) Polymers 0.000 description 31
- 229920001577 copolymer Polymers 0.000 description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- 239000012760 heat stabilizer Substances 0.000 description 12
- 238000002156 mixing Methods 0.000 description 12
- 238000004898 kneading Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 9
- 239000000178 monomer Substances 0.000 description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 238000013329 compounding Methods 0.000 description 5
- 229920005669 high impact polystyrene Polymers 0.000 description 5
- 239000004797 high-impact polystyrene Substances 0.000 description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 5
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 4
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 239000006259 organic additive Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 229920005992 thermoplastic resin Polymers 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 229920000265 Polyparaphenylene Polymers 0.000 description 3
- 239000005083 Zinc sulfide Substances 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- 229910052984 zinc sulfide Inorganic materials 0.000 description 3
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- FRCLQKLLFQYUJJ-UHFFFAOYSA-N P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1C(C)(C)C)C)C(C)(C)C Chemical compound P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1C(C)(C)C)C)C(C)(C)C FRCLQKLLFQYUJJ-UHFFFAOYSA-N 0.000 description 2
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 2
- CGRTZESQZZGAAU-UHFFFAOYSA-N [2-[3-[1-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]-2-methylpropan-2-yl]-2,4,8,10-tetraoxaspiro[5.5]undecan-9-yl]-2-methylpropyl] 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCC(C)(C)C2OCC3(CO2)COC(OC3)C(C)(C)COC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 CGRTZESQZZGAAU-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- FEODVXCWZVOEIR-UHFFFAOYSA-N (2,4-ditert-butylphenyl) octyl hydrogen phosphite Chemical compound CCCCCCCCOP(O)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C FEODVXCWZVOEIR-UHFFFAOYSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
- GJDRKHHGPHLVNI-UHFFFAOYSA-N 2,6-ditert-butyl-4-(diethoxyphosphorylmethyl)phenol Chemical compound CCOP(=O)(OCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 GJDRKHHGPHLVNI-UHFFFAOYSA-N 0.000 description 1
- QQOMQLYQAXGHSU-UHFFFAOYSA-N 236TMPh Natural products CC1=CC=C(C)C(O)=C1C QQOMQLYQAXGHSU-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 1
- OMIHGPLIXGGMJB-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]hepta-1,3,5-triene Chemical group C1=CC=C2OC2=C1 OMIHGPLIXGGMJB-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- MXFVKYNQQHVOQP-UHFFFAOYSA-N C(CCCCCCC)P(O)(O)OC1=CC=C(C=C1C(C)(C)C)C(C)(C)C Chemical compound C(CCCCCCC)P(O)(O)OC1=CC=C(C=C1C(C)(C)C)C(C)(C)C MXFVKYNQQHVOQP-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- GIATZHZBSIMOEE-UHFFFAOYSA-N P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C Chemical compound P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C GIATZHZBSIMOEE-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 229920010524 Syndiotactic polystyrene Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes 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
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- UELGRCOBOPRCQU-UHFFFAOYSA-N biphenylene;hydroxyphosphanyloxyphosphinous acid Chemical compound OPOPO.C1=CC=C2C3=CC=CC=C3C2=C1 UELGRCOBOPRCQU-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920012128 methyl methacrylate acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008188 pellet Substances 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
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006350 polyacrylonitrile resin Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
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- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- Manufacture Of Macromolecular Shaped Articles (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
本発明は、イグニッションコイル用部品に関する。詳しくは、絶縁破壊強度が著しく高い高絶縁性ポリフェニレンエーテル系樹脂成形品よりなるイグニッションコイル用部品に関する。 The present invention relates to an ignition coil component . More particularly, to a ignition coil component dielectric breakdown strength is significantly more high have high insulation polyphenylene ether resin molded article.
ポリフェニレンエーテル系樹脂は、耐熱性、電気特性、耐酸性、耐アルカリ性等に優れ、しかも低比重、低吸水性である等の優れた特性を有する樹脂であるが、溶融粘度が高いために成形加工性に劣り、耐衝撃性も劣るという欠点を有している。そこで、ポリフェニレンエーテル系樹脂は、通常、その成形加工性や耐衝撃性の改良を目的として、各種の樹脂を配合した樹脂組成物として用いられており、配合樹脂として、スチレン系樹脂を用いたものが提供されている。 Polyphenylene ether resins are excellent in heat resistance, electrical properties, acid resistance, alkali resistance, etc., and have excellent properties such as low specific gravity and low water absorption. It has the disadvantages that it is inferior in impact and impact resistance. Therefore, polyphenylene ether resins are usually used as resin compositions containing various resins for the purpose of improving molding processability and impact resistance, and styrene resins are used as compounded resins. Is provided.
このようなポリフェニレンエーテル系樹脂/スチレン系樹脂組成物は、ポリフェニレンエーテル系樹脂のもつ電気特性、高耐熱性の特性を生かして、イグニッションコイル等の電気部品のコイルボビンの芯材等の成形材料として利用されている。
本出願人は、このようなイグニッションコイル用ポリフェニレンエーテル系樹脂組成物として、先に(A)ポリフェニレンエーテル系樹脂40〜90重量%と(B)スチレン系樹脂60〜10重量%の合計100重量部に対し、(C)強化充填材5〜50重量部、及び(D)フッ素樹脂0.1〜2重量部配合してなるイグニッションコイル部品用強化ポリフェニレンエーテル系樹脂組成物に係る発明を特許出願した(特許文献1)。
Such a polyphenylene ether resin / styrene resin composition is used as a molding material for the core material of a coil bobbin of an electrical component such as an ignition coil by taking advantage of the electrical characteristics and high heat resistance characteristics of the polyphenylene ether resin. Has been.
The present applicant, as such a polyphenylene ether-based resin composition for an ignition coil, previously has a total of 100 parts by weight of (A) 40-90% by weight of a polyphenylene ether-based resin and (B) 60-10% by weight of a styrene-based resin. In contrast, (C) 5-50 parts by weight of reinforcing filler and (D) 0.1-2 parts by weight of fluororesin compounded for an invention related to a reinforced polyphenylene ether-based resin composition for ignition coil parts have been applied for a patent. (Patent Document 1).
電気部品、特にイグニッションコイル部品にあっては、高耐熱性、高機械的強度であることの他、絶縁破壊特性に優れることが必要とされ、特に絶縁破壊強度については、より一層の改善が望まれている。
しかしながら、特許文献1のポリフェニレンエーテル系樹脂組成物等をはじめ、従来提供されているポリフェニレンエーテル系樹脂組成物の絶縁破壊強度(IEC60243に準拠)は、高くても40kV/mmであり、更なる絶縁破壊強度の向上が望まれている。
Electrical parts, especially ignition coil parts, are required to have high heat resistance and high mechanical strength, as well as excellent dielectric breakdown characteristics. In particular, further improvement in dielectric breakdown strength is desired. It is rare.
However, the dielectric breakdown strength (based on IEC60243) of the polyphenylene ether-based resin composition conventionally provided including the polyphenylene ether-based resin composition of Patent Document 1 is 40 kV / mm at the highest, and further insulation Improvement in fracture strength is desired.
本発明は上記従来の実状に鑑みてなされたものであって、絶縁破壊強度が著しく高い高絶縁性ポリフェニレンエーテル系樹脂成形品よりなるイグニッションコイル用部品を提供することを目的とする。 The present invention has been made in view of the above-described conventional situation, and an object of the present invention is to provide an ignition coil component made of a highly insulating polyphenylene ether-based resin molded product having a remarkably high dielectric breakdown strength.
本発明者らは上記課題を解決すべく鋭意検討を重ねた結果、機械的強度や耐熱性の向上、更には着色を目的として、通常、ポリフェニレンエーテル系樹脂組成物に配合されるガラス繊維や酸化チタン等の無機成分の配合量を少量とすることにより、或いはこれらの無機成分を全く配合しないことにより、従来にない著しく絶縁破壊強度の高いポリフェニレンエーテル系樹脂成形品を実現することができることを見出した。 As a result of intensive studies to solve the above-mentioned problems, the present inventors usually improved the mechanical strength and heat resistance, and further, for the purpose of coloring, glass fibers and oxidation compounds that are usually blended in polyphenylene ether-based resin compositions. It has been found that a polyphenylene ether-based resin molded article with significantly high dielectric breakdown strength can be realized by reducing the blending amount of inorganic components such as titanium or by not blending these inorganic components at all. It was.
本発明はこのような知見に基づいて達成されたものであって、以下を要旨とする。 The present invention has been achieved based on such findings, and the gist thereof is as follows.
[1] 樹脂成分として少なくともポリフェニレンエーテル系樹脂とスチレン系樹脂とを含み、該樹脂成分以外の成分として、ガラス繊維、マイカ、タルク、及びワラストナイトよりなる群から選ばれる1種以上の無機充填材と、無機顔料とを含む樹脂組成物からなり、該樹脂成分中のポリフェニレンエーテル系樹脂の含有量が40〜90重量%でスチレン系樹脂の含有量が60〜10重量%であり、該樹脂組成物中の該無機充填材の含有量が30重量%以下で、該無機顔料の含有量が2.5重量%以下である樹脂成形品であって、IEC60243に準拠して、下記試験条件で測定された絶縁破壊強度が85kV/mm以上である高絶縁性ポリフェニレンエーテル系樹脂成形品よりなるイグニッションコイル用部品。
<試験条件>
電極:φ25mm円柱/φ25mm円柱
試料厚み:0.5mm
試験方法:短時間法
試験温度:23℃
[1] see contains at least a polyphenylene ether resin and a styrene resin as the resin component, as a component other than the resin component, glass fibers, mica, talc, and one or more inorganic selected from the group consisting of wollastonite and fillers, inorganic pigments and Ri Do from including the resin composition, the content of the styrene resin content of the polyphenylene ether resin of the resin component is at 40 to 90% by weight is 60 to 10 wt% , the content of the resin composition inorganic filler is 30 wt% or less, a content of the inorganic pigment is 2.5 wt% or less der Ru resin molded article, in conformity with IEC 60243, the measured dielectric breakdown strength high insulation polyphenylene ether component ignition coil made of resin molded article Ru der least 85 kV / mm by the following test conditions.
<Test conditions>
Electrode: φ25 mm cylinder / φ25 mm cylinder Sample thickness: 0.5 mm
Test method: Short-time method Test temperature: 23 ° C
本発明の高絶縁性ポリフェニレンエーテル系樹脂成形品は、絶縁破壊強度(IEC60243に準拠)が85kV/mmと著しく高く、高電圧下における絶縁性に優れる。本発明の高絶縁性ポリフェニレンエーテル系樹脂成形品に用いる樹脂組成物は、樹脂組成物の配合成分及び、その配合量の調整により、このような著しく高い絶縁破壊強度を実現するものであり、絶縁破壊強度の向上のための特別な配合材料や特別な手段、特殊な設備を必要とせず、工業的に極めて有利である。 The highly insulative polyphenylene ether resin molded product of the present invention has an extremely high dielectric breakdown strength (based on IEC60243) of 85 kV / mm, and is excellent in insulation under high voltage. The resin composition used for the highly insulating polyphenylene ether-based resin molded article of the present invention realizes such a high dielectric breakdown strength by adjusting the blending component of the resin composition and the blending amount thereof. It does not require special compounding materials, special means, or special equipment for improving fracture strength, and is extremely advantageous industrially.
このような本発明の高絶縁性ポリフェニレンエーテル系樹脂成形品は、高電圧下における高い絶縁性が要求されるイグニッションコイル部品として有用である。 Such highly insulating polyphenylene ether resin molded article of the present invention is useful as an ignition coil unit products high insulation property at high voltages are required.
以下に本発明の実施の形態を詳細に説明する。 Hereinafter, embodiments of the present invention will be described in detail.
[ポリフェニレンエーテル系樹脂組成物]
本発明の樹脂成形品に用いるポリフェニレンエーテル系樹脂組成物(以下、「本発明のポリフェニレンエーテル系樹脂組成物」と称す場合がある。)は、樹脂成分として少なくともポリフェニレンエーテル系樹脂とスチレン系樹脂を含み、当該樹脂組成物からなる樹脂成形品の絶縁破壊強度(IEC60243に準拠)が85kV/mm以上であることを特徴とする。
[Polyphenylene ether resin composition]
Polyphenylene ether-based resin composition used for the resin molded article of the present invention (hereinafter sometimes referred to as "polyphenylene ether-based resin composition of the present invention".) Is less and also the port polyphenylene ether resin as a resin component The dielectric breakdown strength (based on IEC60243) of a resin molded product comprising the styrene resin and comprising the resin composition is 85 kV / mm or more.
{ポリフェニレンエーテル系樹脂}
本発明に用いられるポリフェニレンエーテル系樹脂は、下記一般式(1)で示されるフェニレンエーテルユニットを主鎖に持つ重合体であって、ホモポリマーであってもコポリマーであってもよい。
{Polyphenylene ether resin}
The polyphenylene ether resin used in the present invention is a polymer having a phenylene ether unit represented by the following general formula (1) in the main chain, and may be a homopolymer or a copolymer.
(式中、2つのR1は、それぞれ独立して、水素原子又は炭素数1〜3のアルキル基を表し、2つのR2は、それぞれ独立して、水素原子又は炭素数1〜3のアルキル基を表す。ただし、2つのR1が共に水素原子になることはない。) (In the formula, two R 1 s each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, and two R 2 s each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms. Represents a group, but two R 1 s are not hydrogen atoms.)
ホモポリマーとしては、例えば、ポリ(2,6−ジメチル−1,4−フェニレン)エーテル、ポリ(2,6−ジエチル−1,4−フェニレン)エーテル、ポリ(2,6−ジプロピル−1,4−フェニレン)エーテル、ポリ(2−メチル−6−エチル−1,4−フェニレン)エーテル、ポリ(2−メチル−6−プロピル−1,4−フェニレン)エーテル等の2,6−ジアルキルフェニレンエーテルの重合体が挙げられ、コポリマーとしては、各種2,6−ジアルキルフェノール/2,3,6−トリアルキルフェノール共重合体が挙げられる。
本発明に使用されるポリフェニレンエーテル系樹脂としては、特に、ポリ(2,6−ジメチル−1,4−フェニレン)エーテル、2,6−ジメチルフェノール/2,3,6−トリメチルフェノール共重合体が好ましい。
Examples of the homopolymer include poly (2,6-dimethyl-1,4-phenylene) ether, poly (2,6-diethyl-1,4-phenylene) ether, and poly (2,6-dipropyl-1,4). -Phenylene) ether, poly (2-methyl-6-ethyl-1,4-phenylene) ether, poly (2-methyl-6-propyl-1,4-phenylene) ether and the like of 2,6-dialkylphenylene ether Examples of the copolymer include various 2,6-dialkylphenol / 2,3,6-trialkylphenol copolymers.
Examples of the polyphenylene ether resin used in the present invention include poly (2,6-dimethyl-1,4-phenylene) ether and 2,6-dimethylphenol / 2,3,6-trimethylphenol copolymer. preferable.
また、本発明で使用されるポリフェニレンエーテル系樹脂は、クロロホルム中、温度30℃で測定した固有粘度が0.2〜0.8dl/gであるものが好ましく、0.2〜0.7dl/gのものがより好ましく、0.25〜0.6dl/gのものが特に好ましい。固有粘度を0.2dl/g以上とすることにより、樹脂組成物の機械的強度の低下を防ぐことができ、0.8dl/g以下とすることにより、樹脂流動性が良好となり、成形加工が容易となる。なお、固有粘度の異なる2種以上のポリフェニレンエーテル系樹脂を混合して、この固有粘度の範囲としてもよい。 The polyphenylene ether resin used in the present invention preferably has an intrinsic viscosity of 0.2 to 0.8 dl / g measured in chloroform at a temperature of 30 ° C., and preferably 0.2 to 0.7 dl / g. Are more preferable, and those of 0.25 to 0.6 dl / g are particularly preferable. By setting the intrinsic viscosity to 0.2 dl / g or more, the mechanical strength of the resin composition can be prevented from being lowered. By setting the intrinsic viscosity to 0.8 dl / g or less, the resin fluidity is improved and the molding process is improved. It becomes easy. In addition, it is good also as a range of this intrinsic viscosity by mixing 2 or more types of polyphenylene ether-type resin from which intrinsic viscosity differs.
本発明に使用されるポリフェニレンエーテル系樹脂の製造法は、特に限定されるものではなく、公知の方法に従って、例えば、2,6−ジメチルフェノール等のモノマーをアミン銅触媒の存在下、酸化重合することにより製造することができ、その際、反応条件を選択することにより、固有粘度を所望の範囲に制御することができる。固有粘度の制御は、重合温度、重合時間、触媒量等の条件を選択することにより達成できる。 The method for producing the polyphenylene ether-based resin used in the present invention is not particularly limited. For example, a monomer such as 2,6-dimethylphenol is oxidatively polymerized in the presence of an amine copper catalyst according to a known method. In this case, the intrinsic viscosity can be controlled within a desired range by selecting reaction conditions. Control of intrinsic viscosity can be achieved by selecting conditions such as polymerization temperature, polymerization time, and catalyst amount.
本発明において、ポリフェニレンエーテル系樹脂は1種を単独で用いても良く、2種以上を混合して用いても良い。 In the present invention, the polyphenylene ether resins may be used alone or in combination of two or more.
{スチレン系樹脂}
本発明に用いられるスチレン系樹脂としては、スチレン系単量体の重合体、スチレン系単量体と他の共重合可能な単量体との共重合体及びスチレン系グラフト共重合体等が挙げられる。
{Styrene resin}
Examples of the styrene resin used in the present invention include a styrene monomer polymer, a copolymer of a styrene monomer and another copolymerizable monomer, and a styrene graft copolymer. It is done.
スチレン系単量体としては、例えば、スチレン、α−メチルスチレン、p−メチルスチレン等が挙げられ、これらの中でも、スチレンが好ましい。
スチレン系単量体と共重合可能な単量体としては、例えば、アクリロニトリル、メタクリロニトリル等のシアン化ビニル単量体、アクリル酸メチル、アクリル酸エチル、アクリル酸プロピル、メタクリル酸メチル、メタクリル酸エチル等の(メタ)アクリル酸アルキルエステル、マレイミド、N−フェニルマレイミド等が挙げられ、これらの中でも、シアン化ビニル単量体、(メタ)アクリル酸アルキルエステルが好ましい。
Examples of the styrenic monomer include styrene, α-methylstyrene, p-methylstyrene, and among these, styrene is preferable.
Examples of the monomer copolymerizable with the styrenic monomer include vinyl cyanide monomers such as acrylonitrile and methacrylonitrile, methyl acrylate, ethyl acrylate, propyl acrylate, methyl methacrylate, and methacrylic acid. Examples include (meth) acrylic acid alkyl esters such as ethyl, maleimide, N-phenylmaleimide, and the like. Among these, vinyl cyanide monomers and (meth) acrylic acid alkyl esters are preferable.
スチレン系単量体の重合体としては、例えば、ポリスチレン樹脂等が、スチレン系単量体と他の共重合可能な単量体との共重合体としては、例えば、スチレン・ブタジエン・スチレン共重合体(SBS樹脂)、水添スチレン・ブタジエン・スチレン共重合体(SEBS)、水添スチレン・イソプレン・スチレン共重合体(SEPS)、耐衝撃性ポリスチレン(HIPS)、アクリロニトリル・スチレン共重合体(AS樹脂)、アクリロニトリル・ブタジエン・スチレン共重合体(ABS樹脂)、メチルメタクリレート・ブタジエン・スチレン共重合体(MBS樹脂)、メチルメタクリレート・アクリロニトリル・ブタジエン・スチレン共重合体(MABS樹脂)、アクリロニトリル・アクリルゴム・スチレン共重合体(AAS樹脂)、アクリロニトリル・エチレンプロピレン系ゴム・スチレン共重合体(AES樹脂)、スチレン・IPN型ゴム共重合体等が挙げられる。さらにシンジオタクティクポリスチレン等のように立体規則性を有するものであってもよい。
これらの中でも、ポリスチレン(PS)、耐衝撃性ポリスチレン(HIPS)が好ましい。
Examples of the styrene monomer polymer include polystyrene resins, and examples of the copolymer of the styrene monomer and other copolymerizable monomers include styrene / butadiene / styrene copolymer. Polymer (SBS resin), hydrogenated styrene / butadiene / styrene copolymer (SEBS), hydrogenated styrene / isoprene / styrene copolymer (SEPS), high impact polystyrene (HIPS), acrylonitrile / styrene copolymer (AS) Resin), acrylonitrile / butadiene / styrene copolymer (ABS resin), methyl methacrylate / butadiene / styrene copolymer (MBS resin), methyl methacrylate / acrylonitrile / butadiene / styrene copolymer (MABS resin), acrylonitrile / acrylic rubber・ Styrene copolymer (AAS resin), acrylic Nitrile-ethylene propylene rubber-styrene copolymer (AES resin), styrene · IPN type rubber copolymer, and the like. Further, it may have stereoregularity such as syndiotactic polystyrene.
Among these, polystyrene (PS) and impact-resistant polystyrene (HIPS) are preferable.
このようなスチレン系樹脂の製造方法としては、乳化重合法、溶液重合法、懸濁重合法あるいは塊状重合法等の公知の方法が挙げられる。 Examples of the method for producing such a styrene resin include known methods such as an emulsion polymerization method, a solution polymerization method, a suspension polymerization method, and a bulk polymerization method.
本発明において、スチレン系樹脂は1種を単独で用いても良く、2種以上を混合して用いても良い。 In the present invention, the styrene resin may be used alone or in combination of two or more.
{樹脂成分}
本発明のポリフェニレンエーテル系樹脂組成物の樹脂成分は、ポリフェニレンエーテル系樹脂40〜90重量%、好ましくは45〜80重量%、特に好ましくは50〜80重量%と、スチレン系樹脂60〜10重量%、好ましくは55〜20重量%、特に好ましくは50〜20重量%とを含むものである。樹脂成分中のポリフェニレンエーテル系樹脂を40重量%以上とすることにより、荷重撓み温度や機械的強度を優れたものとすることができ、ポリフェニレンエーテル系樹脂を90重量%以下とすることにより、樹脂組成物の流動性を良好に保ち成形加工が容易となるため、成形時の樹脂滞留劣化を起こすことなく、得られる成形品の性能を優れたものとすることができる。
{Resin component}
The resin component of the polyphenylene ether-based resin composition of the present invention, port polyphenylene ether resin 40 to 90 wt%, good Mashiku 45 to 80 wt%, particularly preferably 50 to 80 wt%, scan styrene resin 60 to 10 wt%, good Mashiku is 55-20% by weight, particularly preferably those containing a 50-20% by weight. By making the polyphenylene ether resin in the resin component 40% by weight or more, the load deflection temperature and mechanical strength can be made excellent. By making the polyphenylene ether resin 90% by weight or less, the resin Since the fluidity of the composition is kept good and the molding process becomes easy, the performance of the obtained molded product can be made excellent without causing resin retention deterioration during molding.
なお、本発明のポリフェニレンエーテル系樹脂組成物には、本発明の効果を損なわない範囲において、ポリフェニレンエーテル系樹脂及びスチレン系樹脂以外のその他の樹脂を配合することができる。その他の樹脂としては、例えば、フッ素樹脂、ポリアミド樹脂、ポリエステル樹脂、ポリフェニレンサルファイド樹脂、液晶ポリエステル樹脂、ポリカーボネート樹脂、ポリアセタール樹脂、ポリアクリロニトリル樹脂、アクリル樹脂、ポリエチレン樹脂、ポリプロピレン樹脂、エチレン−プロピレン共重合体等のオレフィン系樹脂等の熱可塑性樹脂や、エポキシ樹脂、メラミン樹脂、シリコーン樹脂等の熱硬化性樹脂等が挙げられる。これらの熱可塑性樹脂及び熱硬化性樹脂は、2種以上を組み合わせて使用することもできる。これらのその他の樹脂の配合量は、樹脂成分中の50重量%以下であることが好ましく、45重量%以下であることがさらに好ましい。 In addition, in the polyphenylene ether-type resin composition of this invention, in addition to the range which does not impair the effect of this invention, other resins other than a polyphenylene ether-type resin and a styrene resin can be mix | blended. Examples of other resins include fluorine resin, polyamide resin, polyester resin, polyphenylene sulfide resin, liquid crystal polyester resin, polycarbonate resin, polyacetal resin, polyacrylonitrile resin, acrylic resin, polyethylene resin, polypropylene resin, and ethylene-propylene copolymer. And thermoplastic resins such as olefin-based resins, and thermosetting resins such as epoxy resins, melamine resins, and silicone resins. These thermoplastic resins and thermosetting resins can be used in combination of two or more. The blending amount of these other resins is preferably 50% by weight or less, more preferably 45% by weight or less in the resin component.
本発明においては、樹脂組成物溶融混練時に目やにが発生する可能性がある場合は、その目やにを低減する目的で、上記のポリフェニレンエーテル系樹脂及びスチレン系樹脂以外のその他の樹脂の中でも、フッ素系樹脂を配合することが効果的である。
フッ素樹脂としては、例えば、ポリテトラフルオロエチレン、テトラフルオロエチレン・パーフルオロアルキルビニルエーテル共重合体、テトラフルオロエチレン・ヘキサフルオロプロピレン共重合体、フッ化ビニリデン等のフッ素化ポリオレフィン等が挙げられ、好ましくはポリテトラフルオロエチレン、テトラフルオロエチレン・ヘキサフルオロプロピレン共重合体である。
In the present invention, if there is a possibility that eyes may occur during melt-kneading of the resin composition, among other resins other than the above polyphenylene ether resins and styrene resins, a fluorine-based resin may be used for the purpose of reducing the eyes and eyes. It is effective to blend a resin.
Examples of the fluororesin include polytetrafluoroethylene, tetrafluoroethylene / perfluoroalkyl vinyl ether copolymer, tetrafluoroethylene / hexafluoropropylene copolymer, fluorinated polyolefin such as vinylidene fluoride, and the like. Polytetrafluoroethylene, tetrafluoroethylene / hexafluoropropylene copolymer.
フッ素樹脂は、温度350℃おける溶融粘度が、1.0×102〜1.0×1015Pa・sのものが好ましく、1.0×103〜1.0×1014Pa・sのものがより好ましく、1.0×1010〜1.0×1012Pa・sのものが特に好ましい。溶融粘度を1.0×102Pa・s以上とすることにより、目やに防止効果を十分発揮することができ、1.0×1015Pa・s以下とすることにより、樹脂組成物の流動性を良好に保つことができる。 The fluororesin preferably has a melt viscosity at a temperature of 350 ° C. of 1.0 × 10 2 to 1.0 × 10 15 Pa · s, 1.0 × 10 3 to 1.0 × 10 14 Pa · s. It is more preferred, particularly preferably from 1.0 × 10 10 ~1.0 × 10 12 Pa · s. By setting the melt viscosity to 1.0 × 10 2 Pa · s or more, a sufficient prevention effect can be exhibited, and by setting the melt viscosity to 1.0 × 10 15 Pa · s or less, the fluidity of the resin composition. Can be kept good.
フッ素樹脂の含有量は、樹脂成分中の0.1〜2重量%であることが好ましく、0.1〜1.5重量部であることがより好ましい。フッ素樹脂の含有量を0.1重量%以上とすることにより、目やに防止能を十分に発揮することができ、2重量%以下とすることにより、樹脂組成物製造時の押出安定性を良好に保ち、機械的強度の著しい低下を抑止することができる。 It is preferable that content of a fluororesin is 0.1 to 2 weight% in a resin component, and it is more preferable that it is 0.1 to 1.5 weight part. By making the content of the fluororesin 0.1% by weight or more, the protective ability can be sufficiently exhibited, and by making it 2% by weight or less, the extrusion stability during the production of the resin composition is improved. It is possible to maintain and suppress a significant decrease in mechanical strength.
{樹脂成分含有量}
本発明のポリフェニレンエーテル系樹脂組成物は、上述の樹脂成分の含有量が70重量%以上、特に75重量%以上であることが好ましい。樹脂組成物中の他の配合成分の種類によっても異なるが、樹脂組成物中の樹脂成分含有量が70重量%未満では、高い絶縁破壊強度を実現し得ない場合がある。
{Resin component content}
In the polyphenylene ether resin composition of the present invention, the content of the above-mentioned resin component is preferably 70% by weight or more, particularly preferably 75% by weight or more. Although depending on the type of other compounding components in the resin composition, if the resin component content in the resin composition is less than 70% by weight, high dielectric breakdown strength may not be achieved.
即ち、本発明は、従来、機械的強度の向上のため必須成分として配合されていたガラス繊維や酸化チタン等の無機成分を、あえて配合せずに或いはその配合量を従来の一般的な配合量よりも少ないものとして、組成物中の樹脂成分含有量を70重量%以上、特に75重量%以上と、従来にない多量配合とすることにより、絶縁破壊強度が格段に向上することを見出すことにより達成されたものであり、絶縁破壊強度85kV/mm以上の本発明の高絶縁性ポリフェニレンエーテル系樹脂成形品を実現するための一手段として、組成物中の樹脂成分含有量を70重量%以上、特に75重量%以上とすることは重要である。 That is, the present invention does not dare to blend inorganic components such as glass fiber and titanium oxide, which were conventionally blended as essential components for improving the mechanical strength, or the blending amount thereof is a conventional general blending amount. By finding that the resin component content in the composition is 70% by weight or more, particularly 75% by weight or more, and by adding a large amount unprecedented, the dielectric breakdown strength is significantly improved. As one means for realizing the highly insulating polyphenylene ether-based resin molded product of the present invention having a dielectric breakdown strength of 85 kV / mm or more, the resin component content in the composition is 70% by weight or more. In particular, it is important to set it to 75% by weight or more.
{樹脂成分以外の配合成分}
<好ましくない配合成分>
本発明のポリフェニレンエーテル系樹脂組成物にあっては、通常、ポリフェニレンエーテル系樹脂組成物に配合される成分であっても、得られる成形品の絶縁破壊強度85kV/mm以上を満たすためには、配合量を制限すべき、好ましくない配合成分が存在し、例えば、次のような配合成分については、その含有量を低く抑えるか或いは非含有とすることが好ましい。
{Composition ingredients other than resin ingredients}
<Unfavorable ingredients>
In the polyphenylene ether-based resin composition of the present invention, in order to satisfy the dielectric breakdown strength of 85 kV / mm or more of the obtained molded product, even if it is a component that is usually blended in the polyphenylene ether-based resin composition, There are unfavorable compounding components that should limit the compounding amount. For example, the following compounding components are preferably kept low or not contained.
(無機充填材)
通常、ポリフェニレンエーテル系樹脂組成物には、その機械的強度及び寸法安定性の向上のために、ガラス繊維、マイカ、タルク、ワラストナイト、ガラスフレーク、ガラスビーズ、ミルドファイバー、アルミナ繊維、炭素繊維、アラミド繊維、酸化チタン、酸化マグネシウム、炭酸カルシウム、硫酸バリウム、窒化硼素、チタン酸カリウィスカー等の無機充填材が配合されるが、本発明において、絶縁破壊強度85kV/mm以上を実現するためには、これらの無機充填材の樹脂組成物中の含有量(2種以上含む場合にはその合計の含有量)は、30重量%以下、好ましくは20重量%以下とする。本発明の樹脂組成物はこれらの無機充填材のうち、特にガラス繊維、マイカ、タルク、ワラストナイトについてはその合計で20重量%以下とするか、含まないことが好ましい。無機充填材の含有量が樹脂組成物中の30重量%を超える場合は、所望の絶縁破壊強度が得られない場合がある。
(Inorganic filler)
Usually, polyphenylene ether-based resin compositions have glass fibers, mica, talc, wollastonite, glass flakes, glass beads, milled fibers, alumina fibers, carbon fibers in order to improve their mechanical strength and dimensional stability. Inorganic fillers such as aramid fiber, titanium oxide, magnesium oxide, calcium carbonate, barium sulfate, boron nitride, and potassium titanate are blended. In the present invention, in order to achieve a dielectric breakdown strength of 85 kV / mm or more. the content of the resin composition of the inorganic filler (amount of the total in the case of containing two or more) is 30 wt% or less, preferably shall be the 20 wt% or less. Among these inorganic fillers, the resin composition of the present invention is preferably 20% by weight or less in total, particularly for glass fiber, mica, talc and wollastonite. When content of an inorganic filler exceeds 30 weight% in a resin composition, desired dielectric breakdown strength may not be obtained.
(無機顔料)
ポリフェニレンエーテル系樹脂組成物には、着色のために、酸化チタン等の酸化物、硫化亜鉛等の硫化物、硫酸バリウム等の硫酸塩、カーボンブラック等の無機顔料が配合される場合があるが、本発明において、絶縁破壊強度85kV/mm以上を実現するためには、これらの無機顔料の樹脂組成物中の含有量(2種以上含む場合にはその合計の含有量)は、2.5重量%以下、好ましくは2.2重量%以下とする。本発明の樹脂組成物はこれらの無機顔料のうち、特に酸化チタン、硫化亜鉛、カーボンブラックについては合計で2.5重量%以下とすることが好ましい。
(Inorganic pigment)
The polyphenylene ether-based resin composition may be mixed with an oxide such as titanium oxide, a sulfide such as zinc sulfide, a sulfate such as barium sulfate, or an inorganic pigment such as carbon black for coloring. In the present invention, in order to achieve a dielectric breakdown strength of 85 kV / mm or more, the content of these inorganic pigments in the resin composition (when two or more types are included, the total content thereof) is 2.5 weights. % or less, preferably shall be the 2.2 wt% or less. Among these inorganic pigments, the resin composition of the present invention is preferably 2.5% by weight or less in particular for titanium oxide, zinc sulfide, and carbon black.
<好ましい配合成分>
本発明のポリフェニレンエーテル系樹脂組成物にあっては、ポリフェニレンエーテル系樹脂組成物に通常配合される成分のうち、上記以外の成分、特に有機成分については、通常の配合量で使用することが可能であり、特に以下の成分については、本発明の目的を損なわない範囲で組成物中に含有させることができる。
<Preferred ingredients>
In the polyphenylene ether-based resin composition of the present invention, among the components usually blended in the polyphenylene ether-based resin composition, components other than the above, particularly organic components, can be used in usual blending amounts. In particular, the following components can be contained in the composition as long as the object of the present invention is not impaired.
(熱安定剤)
本発明においては、樹脂組成物の製造及び成形工程における溶融混練時や高温雰囲気で使用時の熱安定性を向上させる目的で、ヒンダードフェノール系化合物、リン系化合物等の熱安定剤を配合することが好ましい。
(Heat stabilizer)
In the present invention, a heat stabilizer such as a hindered phenol compound or a phosphorus compound is blended for the purpose of improving the heat stability during melt kneading in the production and molding process of the resin composition or when used in a high temperature atmosphere. It is preferable.
熱安定剤としてのヒンダードフェノール系化合物の具体例としては、n−オクタデシル−3−(3’,5’−ジ−t−ブチル−4’−ヒドロキシフェニル)プロピオネート、1,6−ヘキサンジオール−ビス〔3−(3’,5’−ジ−t−ブチル−4’−ヒドロキシフェニル)プロピオネート〕、ペンタエリスリトール−テトラキス〔3−(3’,5’−ジ−t−ブチル−4’−ヒドロキシフェニル)プロピオネート〕、2,6−ジ−t−ブチル−4−メチルフェノール、3,9−ビス〔1,1−ジメチル−2−{β−(3−t−ブチル−4−ヒドロキシ−5−メチルフェニル)プロピオニルオキシ}エチル〕−2,4,8,10−テトラオキサスピロ〔5,5〕ウンデカン、トリエチレングリコール−ビス〔3−(3−t−ブチル−5−メチル−4−ヒドロキシフェニル)プロピオネート〕、3,5−ジ−t−ブチル−4−ヒドロキシベンジルホスホネート−ジエチルエステル、1,3,5−トリメチル−2,4,6−トリス(3’,5’−ジ−t−ブチル−4’−ヒドロキシベンジル)ベンゼン、2,2−チオ−ジエチレンビス〔3−(3’,5’−ジ−t−ブチル−4’−ヒドロキシフェニル)プロピオネート〕、トリス−(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)−イソシアヌレート、N,N’−ヘキサメチレンビス(3,5−ジ−t−ブチル−4−ヒドロキシ−ヒドロシンナマイド)等が挙げられる。これらの中で、n−オクタデシル−3−(3’,5’−ジ−t−ブチル−4’−ヒドロキシフェニル)プロピオネート、1,6−ヘキサンジオール−ビス〔3−(3’,5’−t−ブチル−4’−ヒドロキシフェニル)プロピオネート〕、2,6−ジ−t−ブチル−4−メチルフェノール、3,9−ビス〔1,1−ジメチル−2−{β−(3−t−ブチル−4−ヒドロキシ−5−メチルフェニル)プロピオニルオキシ}エチル〕−2,4,8,10−テトラオキサスピロ〔5,5〕ウンデカンが好ましい。 Specific examples of the hindered phenol compound as the heat stabilizer include n-octadecyl-3- (3 ′, 5′-di-t-butyl-4′-hydroxyphenyl) propionate, 1,6-hexanediol- Bis [3- (3 ′, 5′-di-t-butyl-4′-hydroxyphenyl) propionate], pentaerythritol-tetrakis [3- (3 ′, 5′-di-t-butyl-4′-hydroxy Phenyl) propionate], 2,6-di-t-butyl-4-methylphenol, 3,9-bis [1,1-dimethyl-2- {β- (3-t-butyl-4-hydroxy-5- Methylphenyl) propionyloxy} ethyl] -2,4,8,10-tetraoxaspiro [5,5] undecane, triethylene glycol-bis [3- (3-tert-butyl-5-methyl) 4-hydroxyphenyl) propionate], 3,5-di-t-butyl-4-hydroxybenzylphosphonate-diethyl ester, 1,3,5-trimethyl-2,4,6-tris (3 ′, 5 ′ -Di-t-butyl-4'-hydroxybenzyl) benzene, 2,2-thio-diethylenebis [3- (3 ', 5'-di-t-butyl-4'-hydroxyphenyl) propionate], tris- (3,5-di-t-butyl-4-hydroxybenzyl) -isocyanurate, N, N′-hexamethylenebis (3,5-di-t-butyl-4-hydroxy-hydrocinnamide) and the like. It is done. Among these, n-octadecyl-3- (3 ′, 5′-di-t-butyl-4′-hydroxyphenyl) propionate, 1,6-hexanediol-bis [3- (3 ′, 5′- t-butyl-4′-hydroxyphenyl) propionate], 2,6-di-t-butyl-4-methylphenol, 3,9-bis [1,1-dimethyl-2- {β- (3-t- Butyl-4-hydroxy-5-methylphenyl) propionyloxy} ethyl] -2,4,8,10-tetraoxaspiro [5,5] undecane is preferred.
熱安定剤としてのリン系化合物としては、例えば、ホスホナイト化合物、ホスファイト化合物を用いることが好ましい。 As the phosphorus compound as the heat stabilizer, for example, phosphonite compounds and phosphite compounds are preferably used.
ホスホナイト化合物としては、例えば、テトラキス(2,4−ジ−t−ブチルフェニル)−4,4’−ビフェニレンジホスホナイト、テトラキス(2,5−ジ−t−ブチルフェニル)−4,4’−ビフェニレンジホスホナイト、テトラキス(2,3,4−トリメチルフェニル)−4,4’−ビフェニレンジホスホナイト、テトラキス(2,3−ジメチル−5−エチルフェニル)−4,4’−ビフェニレンジホスホナイト、テトラキス(2,6−ジ−t−ブチル−5−エチルフェニル)−4,4’−ビフェニレンジホスホナイト、テトラキス(2,3,4−トリブチルフェニル)−4,4’−ビフェニレンジホスホナイト、テトラキス(2,4,6−トリ−t−ブチルフェニル)−4,4’−ビフェニレンジホスホナイト等が挙げられ、中でも、テトラキス(2,4−ジ−t−ブチルフェニル)−4,4’−ビフェニレンジホスホナイトが好ましい。 Examples of the phosphonite compound include tetrakis (2,4-di-t-butylphenyl) -4,4′-biphenylenediphosphonite, tetrakis (2,5-di-t-butylphenyl) -4,4′-. Biphenylene diphosphonite, tetrakis (2,3,4-trimethylphenyl) -4,4'-biphenylene diphosphonite, tetrakis (2,3-dimethyl-5-ethylphenyl) -4,4'-biphenylene diphosphonite Tetrakis (2,6-di-t-butyl-5-ethylphenyl) -4,4'-biphenylenediphosphonite, tetrakis (2,3,4-tributylphenyl) -4,4'-biphenylenediphosphonite , Tetrakis (2,4,6-tri-t-butylphenyl) -4,4′-biphenylenediphosphonite, among others Tetrakis (2,4-di -t- butyl-phenyl) -4,4'-biphenylene phosphonite are preferred.
ホスファイト化合物としては、例えば、トリス(2,4−ジ−t−ブチルフェニル)ホスファイト、ビス(2,4−ジ−t−ブチルフェニル)ペンタエリスリトール−ジ−ホスファイト、ビス(2,6−ジ−t−ブチル−4−メチルフェニル)ペンタエリスリトール−ジ−ホスファイト、2,2−メチレンビス(4,6−ジ−t−ブチルフェニル)オクチルホスファイト、4,4’−ブチリデン−ビス−(3−メチル−6−t−ブチルフェニル−ジ−トリデシル)ホスファイト、1,1,3−トリス(2−メチル−4−ジトリデシルホスファイト−5−t−ブチル−フェニル)ブタン、トリス(ノニルフェニル)ホスファイト、4,4’−イソプロピリデンビス(フェニル−ジアルキルホスファイト)等が挙げられ、中でも、トリス(2,4−ジ−t−ブチルフェニル)ホスファイト、2,2−メチレンビス(4,6−ジ−t−ブチルフェニル)オクチルホスファイト、ビス(2,6−ジ−t−ブチル−4−メチルフェニル)ペンタエリスリトール−ジ−ホスファイト等が好ましい。 Examples of the phosphite compound include tris (2,4-di-t-butylphenyl) phosphite, bis (2,4-di-t-butylphenyl) pentaerythritol-di-phosphite, and bis (2,6 -Di-t-butyl-4-methylphenyl) pentaerythritol-di-phosphite, 2,2-methylenebis (4,6-di-t-butylphenyl) octyl phosphite, 4,4'-butylidene-bis- (3-methyl-6-tert-butylphenyl-di-tridecyl) phosphite, 1,1,3-tris (2-methyl-4-ditridecyl phosphite-5-tert-butyl-phenyl) butane, tris ( Nonylphenyl) phosphite, 4,4′-isopropylidenebis (phenyl-dialkyl phosphite), etc., among which tris (2,4 Di-t-butylphenyl) phosphite, 2,2-methylenebis (4,6-di-t-butylphenyl) octylphosphite, bis (2,6-di-t-butyl-4-methylphenyl) pentaerythritol -Di-phosphite and the like are preferred.
これらの熱安定剤は、1種を単独で用いても良く、2種以上を混合して用いても良い。 These heat stabilizers may be used alone or in a combination of two or more.
熱安定剤の配合量は、樹脂成分100重量部に対し、好ましくは0.01〜5重量部、より好ましくは0.05〜3重量部、さらに好ましくは0.05〜2重量部であって、樹脂組成物中の含有量として2重量%以下、特に1.5重量%以下とすることが好ましい。熱安定剤の配合量を上記下限以上とすることにより、熱安定剤としての効果を十分に発揮させることができ、上記上限以下とすることにより機械的強度の低下や成形時のモールドデボジット発生を抑止することができる。また、組成物中の熱安定剤の配合量を上記下限以上とすることにより、絶縁破壊強度85kV/mm以上の達成が容易となる。 The blending amount of the heat stabilizer is preferably 0.01 to 5 parts by weight, more preferably 0.05 to 3 parts by weight, still more preferably 0.05 to 2 parts by weight with respect to 100 parts by weight of the resin component. The content in the resin composition is preferably 2% by weight or less, particularly preferably 1.5% by weight or less. By making the blending amount of the heat stabilizer more than the above lower limit, the effect as a heat stabilizer can be sufficiently exerted, and by making the amount less than the above upper limit, the mechanical strength is reduced and the mold devoid occurs at the time of molding. Can be deterred. In addition, by setting the blending amount of the heat stabilizer in the composition to the above lower limit or more, it becomes easy to achieve a dielectric breakdown strength of 85 kV / mm or more.
なお、熱安定剤としては、従来、酸化亜鉛が用いられる場合もあるが、本発明において、絶縁破壊強度85kV/mm以上の実現のために、酸化亜鉛は樹脂組成物中の含有量として0.3重量%以下とすることが好ましく、特に酸化亜鉛は非含有とすることが好ましい。 In addition, although zinc oxide may be conventionally used as the heat stabilizer, in the present invention, zinc oxide is contained in the resin composition in an amount of 0.00 to achieve a dielectric breakdown strength of 85 kV / mm or more. The content is preferably 3% by weight or less, and particularly preferably zinc oxide is not contained.
(その他の有機系添加剤)
本発明の樹脂組成物には、本発明の趣旨を逸脱しない範囲内において、上記成分のほか必要に応じて公知の有機系樹脂添加剤等を配合することもできる。このような添加剤としては、例えば、染料、酸化防止剤、離型剤、紫外線吸収剤、触媒失活剤、滑剤、帯電防止剤、色調改良剤、発泡剤、可塑剤、難燃剤、難燃助剤、耐衝撃改良剤等の有機系添加剤が挙げられる。これら他の有機系添加剤は、1種又は2種以上配合することができる。これらのその他の有機系添加剤は、その合計で樹脂組成物中に20重量%以下とすることが、絶縁破壊強度を高める上で好ましい。
(Other organic additives)
In the resin composition of the present invention, a known organic resin additive or the like can be blended as necessary in addition to the above components within the range not departing from the gist of the present invention. Examples of such additives include dyes, antioxidants, mold release agents, ultraviolet absorbers, catalyst deactivators, lubricants, antistatic agents, color tone improvers, foaming agents, plasticizers, flame retardants, and flame retardants. Organic additives such as auxiliaries and impact resistance improvers can be mentioned. These other organic additives can be used alone or in combination of two or more. The total of these other organic additives is preferably 20% by weight or less in the resin composition in terms of increasing the dielectric breakdown strength.
{製造方法}
本発明のポリフェニレンエーテル系樹脂組成物の製造方法は、特定の方法に限定されるものではないが、好ましくは溶融混練によるものであり、熱可塑性樹脂について一般に実用化されている混練方法が適用できる。例えば、ポリフェニレンエーテル系樹脂、スチレン系樹脂、熱安定剤、及び必要に応じて用いられるその他の成分等を、ヘンシェルミキサー、リボンブレンダー、V型ブレンダー等により均一に混合した後、一軸又は多軸混練押出機、ロール、バンバリーミキサー、ラボプラストミル(ブラベンダー)等で混練することができる。各成分は混練機に一括でフィードしても、順次フィードしてもよく、各成分から選ばれた2種以上の成分を予め混合したものを用いてもよい。
{Production method}
The production method of the polyphenylene ether-based resin composition of the present invention is not limited to a specific method, but is preferably by melt-kneading, and a kneading method generally put to practical use for thermoplastic resins can be applied. . For example, polyphenylene ether resin, styrene resin, heat stabilizer, and other components used as necessary are uniformly mixed with a Henschel mixer, ribbon blender, V-type blender, etc., and then uniaxial or multiaxial kneading It can be kneaded with an extruder, a roll, a Banbury mixer, a lab plast mill (Brabender) or the like. Each component may be fed all at once to the kneader, or may be fed sequentially, or a mixture of two or more components selected from each component may be used.
混練温度と混練時間は、望まれる樹脂組成物や混練機の種類等の条件により、任意に選ぶことができるが、通常、混練温度は200〜350℃、好ましくは220〜320℃、混練時間は20分以下が好ましい。この温度が高過ぎると、ポリフェニレンエーテル系樹脂やスチレン系樹脂の熱劣化が問題となり、成形品の物性の低下や外観不良を生じることがある。また、200℃以上の温度で混練することにより、樹脂組成物を十分に混練することができ、無機充填材や無機顔料等の無機成分を配合する場合は、これらの成分の分散不良による物性の低下や着色むらを抑制することができる。 The kneading temperature and kneading time can be arbitrarily selected according to conditions such as the desired resin composition and the type of kneading machine. 20 minutes or less is preferable. When this temperature is too high, thermal deterioration of the polyphenylene ether resin or styrene resin becomes a problem, and the physical properties of the molded product may be deteriorated or the appearance may be deteriorated. Further, by kneading at a temperature of 200 ° C. or higher, the resin composition can be sufficiently kneaded. When an inorganic component such as an inorganic filler or an inorganic pigment is blended, the physical properties due to poor dispersion of these components can be obtained. Reduction and uneven coloring can be suppressed.
{成形方法}
本発明のポリフェニレンエーテル系樹脂組成物は、熱可塑性樹脂について一般に用いられている成形法、すなわち射出成形、射出圧縮成形、中空成形、押出成形、シート成形、熱成形、回転成形、積層成形、プレス成形等の各種成形法によって成形することができる。特に好ましい成形方法は、流動性の観点から、射出成形法である。射出成形にあたっては、樹脂温度を、例えば、270〜320℃にコントロールするのが好ましい。
{Molding method}
The polyphenylene ether-based resin composition of the present invention is a molding method generally used for thermoplastic resins, that is, injection molding, injection compression molding, hollow molding, extrusion molding, sheet molding, thermoforming, rotational molding, laminate molding, press It can be molded by various molding methods such as molding. A particularly preferable molding method is an injection molding method from the viewpoint of fluidity. In the injection molding, the resin temperature is preferably controlled to 270 to 320 ° C., for example.
[高絶縁性ポリフェニレンエーテル系樹脂成形品]
本発明の高絶縁性ポリフェニレンエーテル系樹脂成形品は、上記に詳説した樹脂組成物からなる成形品であって、その絶縁破壊強度(IEC60243に準拠)が85kV/mm以上であることを特徴とする。
[Highly insulating polyphenylene ether resin molded product]
The highly insulating polyphenylene ether-based resin molded article of the present invention is a molded article made of the resin composition detailed above, and has a dielectric breakdown strength (based on IEC60243) of 85 kV / mm or more. .
{絶縁破壊強度}
本発明のポリフェニレンエーテル系樹脂組成物からなる樹脂成形品の絶縁破壊強度は、IEC60243に準拠して、下記試験条件で測定された絶縁破壊強度である。
{Dielectric breakdown strength}
The dielectric breakdown strength of the resin molded article made of the polyphenylene ether-based resin composition of the present invention is a dielectric breakdown strength measured under the following test conditions in accordance with IEC60243.
<試験条件>
電極:φ25mm円柱/φ25mm円柱
試料厚み:0.5mm
試験方法:短時間法
試験温度:23℃
<Test conditions>
Electrode: φ25 mm cylinder / φ25 mm cylinder Sample thickness: 0.5 mm
Test method: Short-time method Test temperature: 23 ° C
試験には、例えば、ヤマヨ試験器(有)製 絶縁破壊試験装置「YST−243−100RHO」を使用することができる。この絶縁破壊強度は好ましくは90kV/mm以上であり、高い程好ましいが、ポリフェニレンエーテル系樹脂組成物としての絶縁性の限界として、通常、絶縁破壊強度の上限は110kV/mmである。 For the test, for example, a dielectric breakdown test device “YST-243-100RHO” manufactured by Yamayo Tester Co., Ltd. can be used. The dielectric breakdown strength is preferably 90 kV / mm or higher, and is preferably as high as possible. However, the upper limit of the dielectric breakdown strength is usually 110 kV / mm as the limit of insulation as the polyphenylene ether-based resin composition.
本発明のポリフェニレンエーテル系樹脂成形品は、著しく高い絶縁破壊強度を有し、耐熱性にも優れているため、高い絶縁性が要求されるイグニッションコイル用部品として有用である。 Polyphenylene ether resin molded article of the present invention has a significantly higher breakdown strength and excellent in heat resistance, is useful as a component for an ignition coil high have insulating properties are required.
以下、本発明を実施例によりさらに詳細に説明するが、本発明はその要旨を超えない限り以下の実施例に限定されるものではない。 EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to a following example, unless the summary is exceeded.
以下の実施例及び比較例の各樹脂組成物の調製に用いた原材料は次の通りである。 The raw materials used for the preparation of the resin compositions of the following examples and comparative examples are as follows.
ポリフェニレンエーテル系樹脂(PPE):ポリ(2,6−ジメチル−1,4−フェニレン)エーテル、三菱エンジニアリングプラスチックス(株)製「商品名:PX100L」、クロロホルム中で測定した30℃の固有粘度0.47dl/g Polyphenylene ether resin (PPE): Poly (2,6-dimethyl-1,4-phenylene) ether, “trade name: PX100L” manufactured by Mitsubishi Engineering Plastics Co., Ltd., intrinsic viscosity at 30 ° C. measured in chloroform 0 .47 dl / g
スチレン系樹脂1:ハイインパクトポリスチレン(HIPS)、PSジャパン社製「商品名:HT478」、分子量Mw200,000、MFR3.0g/10分 Styrene resin 1: high impact polystyrene (HIPS), “trade name: HT478” manufactured by PS Japan, molecular weight Mw 200,000, MFR 3.0 g / 10 min
スチレン系樹脂2:ポリスチレン(GPPS)、PSジャパン社製「商品名:HF77」、分子量Mw222,000、MFR8.0g/10分 Styrene resin 2: Polystyrene (GPPS), “trade name: HF77” manufactured by PS Japan, molecular weight Mw 222,000, MFR 8.0 g / 10 min
ガラス繊維:旭ファイバーグラス社製「商品名:CS03JA404」 Glass fiber: “Asahi Fiber Glass” “Product name: CS03JA404”
マイカ:山口雲母工業所社製「商品名:A−21B」 Mica: “Product name: A-21B” manufactured by Yamaguchi Mica Industry Co., Ltd.
熱安定剤1:リン系酸化防止剤(テトラキス(2,4−ジ−t−ブチルフェニル)−4,4’−ビフェニレンジホスホナイト)クラリアントジャパン社製「商品名:サンドスタブP−EPQ」
熱安定剤2:ヒンダードフェノール系老化防止剤(2,6−ジ−t−ブチル−4−メチルフェノール)住友化学社製「商品名:スミライザーBHT」
Thermal stabilizer 1: Phosphorus antioxidant (tetrakis (2,4-di-t-butylphenyl) -4,4′-biphenylenediphosphonite) “Clear name: Sandstub P-EPQ” manufactured by Clariant Japan
Heat stabilizer 2: Hindered phenol-based anti-aging agent (2,6-di-t-butyl-4-methylphenol) “Product name: Sumilyzer BHT” manufactured by Sumitomo Chemical Co., Ltd.
カーボンブラック:レジノカラー工業社製「商品名:BLACK−SBF M8800」
酸化チタン:Millennium Inorganic Chemicals社製「商品名:TiONA RCL−69」
硫化亜鉛:SACHTLEBEN社製「商品名:サクトリスHD」
Carbon black: “Product name: BLACK-SBF M8800” manufactured by Resino Color Industry Co., Ltd.
Titanium oxide: “Product name: TiONA RCL-69” manufactured by Millennium Inorganic Chemicals
Zinc sulfide: “Product name: Sacritus HD” manufactured by SACHTLEBEN
[実施例8〜9、参考例1〜7及び比較例1〜11]
表1及び2に示す割合で原材料を秤量し、ガラス繊維(ガラス繊維を用いた場合)を除く原材料をタンブラーミキサーにて均一に混合した後、得られた原材料混合物にさらにガラス繊維(ガラス繊維を用いた場合)を加え、タンブラーにて均一に混合した。得られた原材料混合物は、二軸押出機(池貝社製「PCM30」、スクリュー径30mm、L/D=42)を用いて、シリンダー設定温度280℃、スクリュー回転数400rpmの条件にて溶融混練しペレット化した。混練に際し、上記混合した原材料は、ホッパーに一括して投入した。
[Examples 8 to 9 , Reference Examples 1 to 7 and Comparative Examples 1 to 11]
The raw materials are weighed at the ratios shown in Tables 1 and 2, and the raw materials excluding glass fibers (when glass fibers are used) are uniformly mixed with a tumbler mixer, and then glass fibers (glass fibers are added to the obtained raw material mixture). (When used) and added uniformly with a tumbler. The obtained raw material mixture was melt-kneaded using a twin-screw extruder (“PCM30” manufactured by Ikegai Co., Ltd., screw diameter 30 mm, L / D = 42) under the conditions of a cylinder set temperature of 280 ° C. and a screw rotation speed of 400 rpm. Pelletized. During the kneading, the mixed raw materials were put into a hopper all at once.
得られた樹脂組成物のペレットを120℃で4時間乾燥後、住友重機械工業社製SG125型射出成形機により、金型設定温度90℃、シリンダー設定温度300℃、射出圧力98MPa、成形サイクル40秒で下記評価用試験片を成形し、以下の(1),(2)の試験を実施した。
評価結果を表1及び2に示す。
The obtained pellets of the resin composition were dried at 120 ° C. for 4 hours, and then the mold setting temperature was 90 ° C., the cylinder setting temperature was 300 ° C., the injection pressure was 98 MPa, and the molding cycle was 40 using a SG125 type injection molding machine manufactured by Sumitomo Heavy Industries, Ltd. The following test specimens for evaluation were molded in seconds, and the following tests (1) and (2) were performed.
The evaluation results are shown in Tables 1 and 2.
[評価方法]
(1)絶縁破壊強度:IEC60243に準じて以下の試験条件で行った。
<試験条件>
電極:φ25mm円柱/φ25mm円柱
試料厚み:0.5mm
試験方法:短時間法
試験温度:23℃
[Evaluation method]
(1) Dielectric breakdown strength: It was performed under the following test conditions in accordance with IEC60243.
<Test conditions>
Electrode: φ25 mm cylinder / φ25 mm cylinder Sample thickness: 0.5 mm
Test method: Short-time method Test temperature: 23 ° C
(2)荷重撓み温度:負荷1.80MPaで、ISO75に準じて行った。 (2) Load deflection temperature: It was performed according to ISO75 with a load of 1.80 MPa.
Claims (1)
該樹脂成分以外の成分として、ガラス繊維、マイカ、タルク、及びワラストナイトよりなる群から選ばれる1種以上の無機充填材と、無機顔料とを含む樹脂組成物からなり、
該樹脂成分中のポリフェニレンエーテル系樹脂の含有量が40〜90重量%でスチレン系樹脂の含有量が60〜10重量%であり、
該樹脂組成物中の該無機充填材の含有量が30重量%以下で、該無機顔料の含有量が2.5重量%以下である樹脂成形品であって、IEC60243に準拠して、下記試験条件で測定された絶縁破壊強度が85kV/mm以上である高絶縁性ポリフェニレンエーテル系樹脂成形品よりなるイグニッションコイル用部品。
<試験条件>
電極:φ25mm円柱/φ25mm円柱
試料厚み:0.5mm
試験方法:短時間法
試験温度:23℃ Look containing at least a polyphenylene ether resin and a styrene resin as the resin component,
As components other than the resin component, glass fibers, mica, talc and the one or more inorganic fillers selected from the group consisting of wollastonite, Ri Do an inorganic pigment from including the resin composition,
The content of polyphenylene ether resin in the resin component is 40 to 90% by weight and the content of styrene resin is 60 to 10% by weight,
In the content of the inorganic filler in the resin composition is 30 wt% or less, a content of the inorganic pigment is 2.5 wt% or less der Ru resin molded article, in conformity with IEC 60243, the following the measured dielectric breakdown strength high insulation polyphenylene ether component ignition coil made of resin molded article Ru der least 85 kV / mm at test conditions.
<Test conditions>
Electrode: φ25 mm cylinder / φ25 mm cylinder Sample thickness: 0.5 mm
Test method: Short-time method Test temperature: 23 ° C
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