JP2023540431A - 改善された加水分解安定性を有する難燃性ポリマーのための難燃剤および安定剤の組合せ及びその使用 - Google Patents
改善された加水分解安定性を有する難燃性ポリマーのための難燃剤および安定剤の組合せ及びその使用 Download PDFInfo
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- JP2023540431A JP2023540431A JP2023503415A JP2023503415A JP2023540431A JP 2023540431 A JP2023540431 A JP 2023540431A JP 2023503415 A JP2023503415 A JP 2023503415A JP 2023503415 A JP2023503415 A JP 2023503415A JP 2023540431 A JP2023540431 A JP 2023540431A
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 62
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 229920000642 polymer Polymers 0.000 title claims description 47
- 230000003301 hydrolyzing effect Effects 0.000 title abstract description 16
- 239000003381 stabilizer Substances 0.000 title description 29
- 239000000203 mixture Substances 0.000 claims abstract description 78
- -1 carbodiimide compound Chemical class 0.000 claims abstract description 64
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- 239000000314 lubricant Substances 0.000 claims abstract description 20
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical class [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims abstract description 9
- 239000006082 mold release agent Substances 0.000 claims abstract description 6
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims abstract description 6
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000001875 compounds Chemical group 0.000 claims description 68
- 229920000728 polyester Polymers 0.000 claims description 42
- 229920000877 Melamine resin Polymers 0.000 claims description 25
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 24
- 238000000465 moulding Methods 0.000 claims description 22
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 20
- 229920000388 Polyphosphate Polymers 0.000 claims description 19
- 239000001205 polyphosphate Substances 0.000 claims description 19
- 235000011176 polyphosphates Nutrition 0.000 claims description 19
- 239000004416 thermosoftening plastic Substances 0.000 claims description 19
- 239000004952 Polyamide Substances 0.000 claims description 18
- 239000003365 glass fiber Substances 0.000 claims description 18
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- 238000000034 method Methods 0.000 claims description 13
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- 235000011007 phosphoric acid Nutrition 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
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- 239000004814 polyurethane Substances 0.000 claims description 9
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- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 8
- 239000000835 fiber Substances 0.000 claims description 8
- YSRVJVDFHZYRPA-UHFFFAOYSA-N melem Chemical compound NC1=NC(N23)=NC(N)=NC2=NC(N)=NC3=N1 YSRVJVDFHZYRPA-UHFFFAOYSA-N 0.000 claims description 8
- 150000005846 sugar alcohols Polymers 0.000 claims description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- 239000007859 condensation product Substances 0.000 claims description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
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- 125000003118 aryl group Chemical group 0.000 claims description 6
- 238000009833 condensation Methods 0.000 claims description 6
- 230000005494 condensation Effects 0.000 claims description 6
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000000454 talc Substances 0.000 claims description 6
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- 125000001931 aliphatic group Chemical group 0.000 claims description 5
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- 150000001408 amides Chemical class 0.000 claims description 5
- 238000001125 extrusion Methods 0.000 claims description 5
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- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical group NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims description 5
- 150000007974 melamines Chemical class 0.000 claims description 5
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- 229910052725 zinc Inorganic materials 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
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- 150000004668 long chain fatty acids Chemical class 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 4
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 4
- 239000001095 magnesium carbonate Substances 0.000 claims description 4
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 4
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- 239000010453 quartz Substances 0.000 claims description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
- 239000004408 titanium dioxide Substances 0.000 claims description 4
- YZEZMSPGIPTEBA-UHFFFAOYSA-N 2-n-(4,6-diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(NC=2N=C(N)N=C(N)N=2)=N1 YZEZMSPGIPTEBA-UHFFFAOYSA-N 0.000 claims description 3
- 241000219112 Cucumis Species 0.000 claims description 3
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 claims description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 claims description 3
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000000962 organic group Chemical group 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 3
- 150000008301 phosphite esters Chemical class 0.000 claims description 3
- 230000002787 reinforcement Effects 0.000 claims description 3
- 150000004760 silicates Chemical class 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 229910052712 strontium Inorganic materials 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 229920006345 thermoplastic polyamide Polymers 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 2
- QLMGIWHWWWXXME-UHFFFAOYSA-N 2-(3,5-ditert-butyl-4-hydroxyphenyl)acetic acid Chemical compound CC(C)(C)C1=CC(CC(O)=O)=CC(C(C)(C)C)=C1O QLMGIWHWWWXXME-UHFFFAOYSA-N 0.000 claims description 2
- CDMGNVWZXRKJNS-UHFFFAOYSA-N 2-benzylphenol Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1 CDMGNVWZXRKJNS-UHFFFAOYSA-N 0.000 claims description 2
- DBHUTHZPCWZNRW-UHFFFAOYSA-N 3-(3,5-dicyclohexyl-4-hydroxyphenyl)propanoic acid Chemical compound OC=1C(C2CCCCC2)=CC(CCC(=O)O)=CC=1C1CCCCC1 DBHUTHZPCWZNRW-UHFFFAOYSA-N 0.000 claims description 2
- 229930185605 Bisphenol Natural products 0.000 claims description 2
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000000732 arylene group Chemical group 0.000 claims description 2
- 239000003990 capacitor Substances 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
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- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 238000009413 insulation Methods 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004957 naphthylene group Chemical group 0.000 claims description 2
- 150000002829 nitrogen Chemical class 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- WAKMOVBCOYGSDK-UHFFFAOYSA-N phenol;triazine Chemical class C1=CN=NN=C1.OC1=CC=CC=C1 WAKMOVBCOYGSDK-UHFFFAOYSA-N 0.000 claims description 2
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical class OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 claims description 2
- 150000003016 phosphoric acids Chemical class 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
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- FJDLQLIRZFKEKJ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanamide Chemical compound CC(C)(C)C1=CC(CCC(N)=O)=CC(C(C)(C)C)=C1O FJDLQLIRZFKEKJ-UHFFFAOYSA-N 0.000 claims 1
- FLZYQMOKBVFXJS-UHFFFAOYSA-N 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoic acid Chemical compound CC1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O FLZYQMOKBVFXJS-UHFFFAOYSA-N 0.000 claims 1
- DOAJGZPIIASLSO-UHFFFAOYSA-N C=1C=CC=CC=1OP(=O)OCC1=CC=CC=C1 Chemical class C=1C=CC=CC=1OP(=O)OCC1=CC=CC=C1 DOAJGZPIIASLSO-UHFFFAOYSA-N 0.000 claims 1
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- 235000021317 phosphate Nutrition 0.000 claims 1
- XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical class NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 claims 1
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- SKOSORCOJSCFFS-UHFFFAOYSA-K bis(diethoxyphosphoryloxy)alumanyl diethyl phosphate Chemical compound [Al+3].CCOP([O-])(=O)OCC.CCOP([O-])(=O)OCC.CCOP([O-])(=O)OCC SKOSORCOJSCFFS-UHFFFAOYSA-K 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000006085 branching agent Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- PSLLHWNSDFLVDT-UHFFFAOYSA-L calcium dioxidophosphanium Chemical class [Ca+2].[O-][PH2]=O.[O-][PH2]=O PSLLHWNSDFLVDT-UHFFFAOYSA-L 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- UCVPKAZCQPRWAY-UHFFFAOYSA-N dibenzyl benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC=2C=CC=CC=2)C=1C(=O)OCC1=CC=CC=C1 UCVPKAZCQPRWAY-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- KTLIMPGQZDZPSB-UHFFFAOYSA-M diethylphosphinate Chemical compound CCP([O-])(=O)CC KTLIMPGQZDZPSB-UHFFFAOYSA-M 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 1
- GOJNABIZVJCYFL-UHFFFAOYSA-N dimethylphosphinic acid Chemical compound CP(C)(O)=O GOJNABIZVJCYFL-UHFFFAOYSA-N 0.000 description 1
- BEQVQKJCLJBTKZ-UHFFFAOYSA-N diphenylphosphinic acid Chemical compound C=1C=CC=CC=1P(=O)(O)C1=CC=CC=C1 BEQVQKJCLJBTKZ-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- PFBWBEXCUGKYKO-UHFFFAOYSA-N ethene;n-octadecyloctadecan-1-amine Chemical compound C=C.CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC PFBWBEXCUGKYKO-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- NXHKQBCTZHECQF-UHFFFAOYSA-N ethyl(methyl)phosphinic acid Chemical compound CCP(C)(O)=O NXHKQBCTZHECQF-UHFFFAOYSA-N 0.000 description 1
- 239000012765 fibrous filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- RMJCJLHZCBFPDN-UHFFFAOYSA-N methyl(phenyl)phosphinic acid Chemical compound CP(O)(=O)C1=CC=CC=C1 RMJCJLHZCBFPDN-UHFFFAOYSA-N 0.000 description 1
- SZTJCIYEOQYVED-UHFFFAOYSA-N methyl(propyl)phosphinic acid Chemical compound CCCP(C)(O)=O SZTJCIYEOQYVED-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- GWLJTAJEHRYMCA-UHFFFAOYSA-N phospholane Chemical class C1CCPC1 GWLJTAJEHRYMCA-UHFFFAOYSA-N 0.000 description 1
- CZQYVJUCYIRDFR-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical group NC1=NC(N)=NC(N)=N1.NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O CZQYVJUCYIRDFR-UHFFFAOYSA-N 0.000 description 1
- QVJYHZQHDMNONA-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical group OP(O)(O)=O.NC1=NC(N)=NC(N)=N1.NC1=NC(N)=NC(N)=N1 QVJYHZQHDMNONA-UHFFFAOYSA-N 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000004313 potentiometry Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000009757 thermoplastic moulding Methods 0.000 description 1
- 229920006346 thermoplastic polyester elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical class C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical class CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DXZMANYCMVCPIM-UHFFFAOYSA-L zinc;diethylphosphinate Chemical compound [Zn+2].CCP([O-])(=O)CC.CCP([O-])(=O)CC DXZMANYCMVCPIM-UHFFFAOYSA-L 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5313—Phosphinic compounds, e.g. R2=P(:O)OR'
-
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- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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-
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- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
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- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
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- C08K5/00—Use of organic ingredients
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- C08K5/13—Phenols; Phenolates
- C08K5/134—Phenols containing ester groups
-
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34922—Melamine; Derivatives thereof
-
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34928—Salts
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- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5393—Phosphonous compounds, e.g. R—P(OR')2
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Abstract
Description
R1およびR2は、互いに同じかまたは異なり、Hまたは直鎖状または枝分かれしたC1~C6-アルキルおよび/またはアリールであり;
R3は、直鎖状のまたは枝分かれしたC1~C10-アルキレン、C6~C10-アリーレン、-アルキルアリーレンまたは-アリールアルキレンであり;
Mは、H,Mg,Ca,Al,Sb,Sn,Ge,Ti,Fe,Zn,Zr,Ce,Bi,Sr,Mn,Li,Na,Kおよび/またはプロトン化窒素塩基であり;
mは、1~4であり;
nは、1~4であり;および
xは、1~4である。]
- 成分Bとして、0.5重量%~20重量%のポリマー性カルボジイミド化合物またはその混合物、
- 成分Bとして、0.5重量%~20重量%のポリマー性カルボジイミド化合物またはその混合物、
- 成分Cとして、0重量%~20重量%の立体障害性フェノールまたはその混合物、
- 成分Dとして、0重量%~20重量%の有機ホスファイトおよび/または有機ホスホナイトまたはそれらの混合物、
- 成分Eとして、0重量%~50重量%のメラミン塩、メラミンの縮合生成物またはメラミンとリン酸および/または縮合リン酸との反応生成物、またはメラミンの縮合生成物とリン酸および/または縮合リン酸との反応生成物、および/または上記生成物の混合物および/または上記以外の窒素含有難燃剤、
- 成分Fとして、0重量%~90重量%のフィラーまたは補強材またはそれらの混合物、
- 成分Gとして、0重量%~40重量%の潤滑剤および/または離型剤またはそれらの混合物、
- 成分Hとして、0重量%~40重量%の成分A~G以外の添加剤、
を含む混合物に関する、ここで、成分の総重量は100重量%であり、当該混合物は少なくとも成分C、Dおよび/またはGの少なくとも2つならびに成分AおよびBを含む。
R4は、NCOであり、
R5、R6、R7、R8、R9、R10、R11およびR12は、それぞれ独立に、水素、またはC1~C10-アルキル、C6~C12-アリール、C7~C13-アラルキルまたはC7~C13-アルキルアリールの群からの基であり、
gは、0~5の整数であり、
hは、2~100の整数である];
mは、2~5000の整数、好ましくは2~500の整数である、
R3は、-N=C=N基を有する芳香族炭素原子に対して、少なくとも1のオルト位、好ましくは両オルト位に、少なくとも2個の炭素原子を有する脂肪族および/または脂環式置換基、好ましくは少なくとも3個の炭素原子を有する分岐または環状の脂肪族基を有するアリーレン基、好ましくは4,4’-メチレンビス(2,6-ジアルキルフェニル)基である、
R’は、アリール、アラルキル、アリール-NCOまたはアラルキル-NCOである、および、
R’’は、-N=C=N-アリール、-N=C=N-アラルキルまたは-NCOである。]
1)工業後リサイクル物:これは、重縮合または加工における生産廃棄物、例えば、射出成形による加工の場合にはスプルー、射出成形または押出成形による加工の場合にはスタートアップ材料、または押出シートまたはフィルムからのエッジカットオフ材料を含む。
1.使用成分
熱可塑性ポリマー、成分I:
ポリブチレンテレフタレート(PBT):Ultradur(登録商標)4500(BASF、D)
熱可塑性コポリエーテルエステルエラストマー(TPC):
Riteflex(登録商標)655TPC無充填(セラニーズ、ショアーD硬度55)、TPC-55と称される
Riteflex(登録商標)440TPC無充填(セラニーズ、ショアーD硬度40)
ナイロン-6,6:Ultramid(登録商標)A27、BASF
TPU:Elastollan(登録商標)1185、BASF
ジエチルホスフィン酸のアルミニウム塩、以下DEPALと称される。
Stabaxol(登録商標)P、ポリマー性カルボジイミド、融点50~60℃、Lanxess
Stabaxol(登録商標)P100、高分子量カルボジイミド、融点75~85℃、Lanxess
Stabaxol(登録商標)P110、高分子量カルボジイミド、融点60~70℃、Lanxess
Stabaxol(登録商標)PLF、モノマー成分を含まないポリマー性カルボジイミドであるLanxess
Lubio(登録商標)AS3、ポリマー性カルボジイミド、シェーファー・アディティブシステム、AS3と称される
Lubio(登録商標)AS18、高分子量ポリマーカルボジイミド、シェーファー・アディティブシステム、AS18と称される
Irganox(登録商標)1010(ペンタエリスリトールテトラキス(3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート)、BASFから、立体障害性フェノールと称される
Irganox(登録商標)1330(3,3’,3’,5,5’,5’-ヘキサ-tert-ブチル-a,a’,a’-(メシチレン-2,4,6-トリイル)トリ-p-クレゾール)、BASFから、立体障害性フェノールと称される
Irganox(登録商標)245エチレンビス(オキシエチレン)ビス(3-(5-tert-ブチル-4-ヒドロキシ-m-トリル)プロピオネート)、立体障害性フェノールと称される
Melapur(登録商標)MC50(メラミンシアヌレート)、BASFから、MCと称される
Melapur(登録商標)200/70(メラミンポリホスフェート=MPP)、BASF、MPPと称される
Delflam20(メレム)、Delamin,UK、メレムと称される
PPG HP 3610 EC 10 4.5mmガラス繊維
PPG HP 3786 EC 10 4.5mmガラス繊維、日本電気硝子NLから
潤滑剤:Licowax(登録商標)E、モンタンワックス、クラリアントCHから
AralditeGT7072;HuntsmanCHから、エポキシドと称される
LotaderAX8900、Arkemaから、エチレン-メチルアクリレート-グリシジルメタクリレートターポリマーに基づく耐衝撃性改良剤、AX8900と称される
V-2:綿指示材が燃焼滴下物によって着火する。他の基準はV-1に関するとおり。
表2:PBT GF25コンパウンド:新たに射出成形されたものの延伸および気候制御キャビネット(85℃/85%相対湿度、40日間)での保管後および加圧器試験(PCT、121℃、1barg、3日間)の比較;B3は本発明の実施例である。
表6:加水分解安定化を伴うおよび伴わないTPU-V-0コンパウンド。水中85℃で7日間保管後の引張強さ。B10およびB11は本発明の実施例である。
Claims (21)
- - 成分Aとして、5重量%~95重量%の、式(V)のホスフィン酸塩、式(VI)のジホスフィン酸塩、または、それらの2以上のポリマーまたは混合物、
R1およびR2は、互いに同じかまたは異なり、Hまたは直鎖状または枝分かれしたC1~C6-アルキルおよび/またはアリールである、
R3は、直鎖状のまたは枝分かれしたC1~C10-アルキレン、C6~C10-アリーレン、-アルキルアリーレンまたは-アリールアルキレンであり、
Mは、H,Mg,Ca,Al,Sb,Sn,Ge,Ti,Fe,Zn,Zr,Ce,Bi,Sr,Mn,Li,Na,Kおよび/またはプロトン化窒素塩基であり;
mは、1~4であり;
nは、1~4であり;および
xは、1~4である。]
- 成分Bとして、0.5重量%~20重量%のポリマー性カルボジイミド化合物またはその混合物、
- 成分Cとして、0重量%~20重量%の立体障害性フェノールまたはその混合物、
- 成分Dとして、0重量%~20重量%の有機ホスファイトおよび/または有機ホスホナイトまたはそれらの混合物、
- 成分Eとして、0重量%~50重量%のメラミン塩、メラミンの縮合生成物またはメラミンとリン酸および/または縮合リン酸との反応生成物、またはメラミンの縮合生成物とリン酸および/または縮合リン酸との反応生成物、および/または上記生成物の混合物および/または上記以外の窒素含有難燃剤、
- 成分Fとして、0重量%~90重量%のフィラーまたは補強材またはそれらの混合物、
- 成分Gとして、0重量%~40重量%の潤滑剤および/または離型剤またはそれらの混合物、
- 成分Hとして、0重量%~40重量%の成分A~G以外の添加剤、
を含む混合物、
ここで、成分の総重量は100重量%であり、当該混合物は少なくとも成分C、Dおよび/またはGの少なくとも2つならびに成分AおよびBを含む。 - R1およびR2は、互いに同じかまたは異なり、メチル、エチル、n-プロピル、イソプロピル、n-ブチル、tert-ブチル、n-ペンチルおよび/またはフェニルである、請求項1の混合物。
- R3は、メチレン、エチレン、n-プロピレン、イソプロピレン、n-ブチレン、tert-ブチレン、n-ペンチレン、n-オクチレンまたはn-ドデシレン;フェニレンまたはナフチレン;メチルフェニレン、エチルフェニレン、tert-ブチルフェニレン、メチルナフチレン、エチルナフチレンまたはtert-ブチルナフチレン;フェニルメチレン、フェニルエチレン、フェニルプロピレンまたはフェニルブチレンである、請求項1または2の混合物。
- 成分Bの-N=C=N含有ポリマー性コンパウンドは、一般式(II)または(III)のコンパウンドである、請求項1~3の少なくとも1に記載の混合物。
R4は、NCOであり、
R5、R6、R7、R8、R9、R10、R11およびR12は、それぞれ独立に、水素、またはC1~C10-アルキル、C6~C12-アリール、C7~C13-アラルキルまたはC7~C13-アルキルアリールの群からの基であり、
gは、0~5の整数であり、
hは、2~100の整数である];
mは、2~5000の整数、好ましくは2~500の整数である、
R3は、-N=C=N基を有する芳香族炭素原子に対して、少なくとも1のオルト位、好ましくは両オルト位に、少なくとも2個の炭素原子を有する脂肪族および/または脂環式置換基、好ましくは少なくとも3個の炭素原子を有する分岐または環状の脂肪族基を有するアリーレン基、好ましくは4,4’-メチレンビス(2,6-ジアルキルフェニル)基である、
R’は、アリール、アラルキル、アリール-NCOまたはアラルキル-NCOである、および、
R’’は、-N=C=N-アリール、-N=C=N-アラルキルまたは-NCOである。] - 成分Bは、式(IV)または(V)のN=C=N含有化合物を含む、請求項4の混合物。
- 成分Cは、アルキル化モノフェノール、立体障害性アルキルチオメチルフェノール、立体障害性ヒドロキシル化チオジフェニルエーテル、立体障害性アルキリデンビスフェノール、立体障害性ベンジルフェノール、立体障害性ヒドロキシベンジル化マロネート、立体障害性ヒドロキシベンジル芳香族、立体障害性フェノールトリアジンコンパウンド、立体障害性フェノールベンジルホスホネート、N-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)カルバミン酸アルキル、β-(3.5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオン酸と一価または多価アルコールとのエステル、β-(5-tert-ブチル-4-ヒドロキシ-3-メチルフェニル)プロピオン酸と一価または多価アルコールとのエステル、β-(3,5-ジシクロヘキシル-4-ヒドロキシフェニル)プロピオン酸と一価または多価アルコールとのエステル、3,5-ジ-tert-ブチル-4-ヒドロキシフェニル酢酸と一価または多価アルコールとのエステル、β-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオン酸アミドおよびそれらの2以上の混合物からなる群から選択される、請求項1~5の少なくとも1に記載された混合物。
- 成分Dは、一般式P(OR)3の有機ホスファイト、ここでRは一価の有機基である、および、一般式PR’(OR)2の有機ホスホナイト、ここでRおよびR’は一価の有機基である、からなる群から選択される、請求項1~6の少なくとも1に記載された混合物。
- 成分Eは、20以上の平均縮合度を有するメラミンポリホスフェート、メラミンシアヌレート、メラミンホスフェート、ジメラミンホスフェート、メラミンピロホスフェート、メラミンポリホスフェート、メラムポリホスフェート、メレムポリホスフェートおよび/またはメロンポリホスフェートからなる群から選択される、請求項1~7の少なくとも1つに記載された混合物。
- 成分Fは、タルク、雲母、ケイ酸塩、石英、二酸化チタン、珪灰石、カオリン、非晶質シリカ、炭酸マグネシウム、チョーク、長石および/または硫酸バリウムおよび/またはガラス繊維をベースとする鉱物性粒子状フィラーからなる群から選択される、請求項1~8の少なくとも1つに記載された混合物。
- 成分Gは、長鎖脂肪酸、その塩、そのエステル誘導体および/またはアミド誘導体、モンタンワックスおよび/または低分子量ポリエチレンおよび/またはポリプロピレンワックスからなる群から選択される、請求項1~9の少なくとも1つに記載された混合物。
- 請求項1~10の混合物、および、さらなる成分Iとして、熱可塑性ポリマーまたはその混合物、好ましくは熱可塑性ポリエステル、熱可塑性ポリアミド、熱可塑性ポリウレタン、熱可塑性エラストマーポリエステル、熱可塑性エラストマーポリアミドおよび/または熱可塑性エラストマーポリウレタンを含む、組成物。
- 40重量%~94.9重量%の成分I、10重量%~20重量%の成分A、0.3重量%~3重量%の成分B、0重量%~3重量%の成分C、0重量%~10重量%の成分D、0重量%~10重量%の成分E、15重量%~35重量%の成分F、0重量%~2重量%の成分Gおよび0重量%~2重量%の成分Hを含む、ここで、成分の総重量は100重量%であり、成分C、Dおよび/またはGのうち少なくとも2つは存在する、請求項11に記載された組成物。
- 成分Eは、メラミンシアヌレート、メラミンポリホスフェートもしくはメレム、またはこれらの成分の混合物である、請求項11または12に記載された組成物。
- 成分Fは、タルク、雲母、ケイ酸塩、石英、二酸化チタン、珪灰石、カオリン、非晶質シリカ、炭酸マグネシウム、チョーク、長石および/または硫酸バリウムおよび/またはガラス繊維をベースとする鉱物性粒子状フィラーを含む、請求項11~13の少なくとも1つに記載された組成物。
- 成分Fは、ガラス繊維を含む、請求項14に記載された組成物。
- 成分Iは、PBTまたは熱可塑性エラストマーポリエステルを含む、請求項11~15の少なくとも1つに記載された組成物。
- 成分Gは、長鎖脂肪酸、その塩、そのエステル誘導体および/またはアミド誘導体、モンタンワックスおよび/または低分子量ポリエチレンおよび/またはポリプロピレンワックスを含む、請求項11~16の少なくとも1つに記載された組成物。
- 請求項1~17の少なくとも1つに記載された成分A~Iを、溶融押出により、特定の重量割合で混合する、加水分解安定性および難燃性のポリマーコンパウンドの製造方法。
- 請求項11~17の少なくとも1つに記載された加水分解安定性および難燃性のポリマーコンパウンドから作られるファイバー、フィルム、成形品および造形品。
- プラグ、スイッチ、コンデンサ、絶縁システム、ランプソケット、コイルフォーム、ハウジング、制御装置およびその他の物品における、請求項11~17の少なくとも1つに記載の加水分解安定性および難燃性ポリマーコンパウンドから製造されたファイバー、フィルムおよび成形品の使用。
- 家庭、産業、医療、自動車、航空機、船舶、宇宙船、およびその他移動手段、オフィス設備、ならびにその他物品および建造物における、請求項11~17の少なくとも1つに記載の加水分解安定性および難燃性ポリマーコンパウンドから製造されたファイバー、フィルムおよび成形品の使用。
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EP2365028B1 (de) | 2010-03-10 | 2012-10-03 | LANXESS Deutschland GmbH | -N=C=N- enthaltende Verbindungen zur Verhinderung des thermischen Abbaus von Metall-dialkylphosphinat enthaltenden Polyalkylenterephthalaten in der Schmelze |
DE102010053483A1 (de) | 2010-12-04 | 2012-06-06 | Lanxess Deutschland Gmbh | =N=C=N- enthaltende Verbindung zur Verhinderung des thermischen Abbaus in Schmelzen |
CN102190866A (zh) * | 2010-03-10 | 2011-09-21 | 朗盛德国有限责任公司 | 用于在熔融物中防止热降解的包括-n=c=n-的化合物 |
DE102010049968A1 (de) * | 2010-10-28 | 2012-05-03 | Clariant International Ltd. | Flammwidrige Polyestercompounds |
EP2881433B1 (en) | 2012-07-30 | 2018-10-24 | Toray Industries, Inc. | Flame-retardant thermoplastic polyester resin composition and molded article |
MY178814A (en) | 2013-04-25 | 2020-10-20 | Basf Se | Stress-crack-resistant, halogen-free, flame-protected polyester |
DE102016203221A1 (de) * | 2016-02-29 | 2017-08-31 | Clariant Plastics & Coatings Ltd | Flammhemmende Polyamidzusammensetzung |
KR20170128024A (ko) * | 2016-05-13 | 2017-11-22 | 현대자동차주식회사 | 전선용 시스 조성물 및 이를 포함하는 충전 케이블 |
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2020
- 2020-07-30 EP EP20188649.6A patent/EP3945110A1/de not_active Withdrawn
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2021
- 2021-06-25 TW TW110123366A patent/TW202206529A/zh unknown
- 2021-07-15 KR KR1020237007350A patent/KR20230045050A/ko active Search and Examination
- 2021-07-15 CN CN202180060351.XA patent/CN116134083A/zh active Pending
- 2021-07-15 US US18/018,322 patent/US20230279221A1/en active Pending
- 2021-07-15 JP JP2023503415A patent/JP7541179B2/ja active Active
- 2021-07-15 EP EP21745783.7A patent/EP4189005A1/en active Pending
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EP3945110A1 (de) | 2022-02-02 |
TW202206529A (zh) | 2022-02-16 |
CN116134083A (zh) | 2023-05-16 |
JP7541179B2 (ja) | 2024-08-27 |
WO2022023064A1 (en) | 2022-02-03 |
KR20230045050A (ko) | 2023-04-04 |
US20230279221A1 (en) | 2023-09-07 |
EP4189005A1 (en) | 2023-06-07 |
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