JP2013501094A - ポリヒドロキシポリマーを含む熱老化耐性ポリアミド組成物 - Google Patents
ポリヒドロキシポリマーを含む熱老化耐性ポリアミド組成物 Download PDFInfo
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- JP2013501094A JP2013501094A JP2012522994A JP2012522994A JP2013501094A JP 2013501094 A JP2013501094 A JP 2013501094A JP 2012522994 A JP2012522994 A JP 2012522994A JP 2012522994 A JP2012522994 A JP 2012522994A JP 2013501094 A JP2013501094 A JP 2013501094A
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- poly
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- polyamide
- terephthalamide
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- 239000000203 mixture Substances 0.000 title claims abstract description 127
- 229920002647 polyamide Polymers 0.000 title claims abstract description 100
- 239000004952 Polyamide Substances 0.000 title claims abstract description 99
- 229920000642 polymer Polymers 0.000 title claims abstract description 36
- 230000032683 aging Effects 0.000 title description 14
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 46
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 46
- 238000002844 melting Methods 0.000 claims abstract description 38
- 230000008018 melting Effects 0.000 claims abstract description 38
- 239000003381 stabilizer Substances 0.000 claims abstract description 38
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 16
- 239000012744 reinforcing agent Substances 0.000 claims abstract description 13
- 230000009477 glass transition Effects 0.000 claims abstract description 5
- -1 Aromatic dicarboxylic acids Chemical class 0.000 claims description 73
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 60
- 125000004432 carbon atom Chemical group C* 0.000 claims description 52
- PGGROMGHWHXWJL-UHFFFAOYSA-N 4-(azepane-1-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1CCCCCC1 PGGROMGHWHXWJL-UHFFFAOYSA-N 0.000 claims description 36
- 229920001577 copolymer Polymers 0.000 claims description 26
- LKWSTQPRPRGLDP-UHFFFAOYSA-N 4-(azacycloundecane-1-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1CCCCCCCCCC1 LKWSTQPRPRGLDP-UHFFFAOYSA-N 0.000 claims description 25
- 239000000178 monomer Substances 0.000 claims description 25
- 229920006139 poly(hexamethylene adipamide-co-hexamethylene terephthalamide) Polymers 0.000 claims description 25
- 125000001931 aliphatic group Chemical group 0.000 claims description 23
- 150000004982 aromatic amines Chemical group 0.000 claims description 23
- 229920000933 poly (ε-caprolactam) Polymers 0.000 claims description 23
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 17
- 239000005977 Ethylene Substances 0.000 claims description 17
- HLPFMOOKIBJIQT-UHFFFAOYSA-N 4-(pyrrolidine-1-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1CCCC1 HLPFMOOKIBJIQT-UHFFFAOYSA-N 0.000 claims description 16
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 15
- 150000001412 amines Chemical class 0.000 claims description 15
- 239000003365 glass fiber Substances 0.000 claims description 15
- 150000005846 sugar alcohols Polymers 0.000 claims description 15
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 13
- CELROVGXVNNJCW-UHFFFAOYSA-N 11-aminoundecanamide Chemical compound NCCCCCCCCCCC(N)=O CELROVGXVNNJCW-UHFFFAOYSA-N 0.000 claims description 12
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 12
- 229910052802 copper Inorganic materials 0.000 claims description 12
- 239000010949 copper Substances 0.000 claims description 12
- 150000003951 lactams Chemical class 0.000 claims description 12
- OCBDCKOLSAYNMN-UHFFFAOYSA-N 4-(azacyclotridecane-1-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1CCCCCCCCCCCC1 OCBDCKOLSAYNMN-UHFFFAOYSA-N 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 11
- SNNMLPUQKZGXOJ-UHFFFAOYSA-N 12-aminododecanamide Chemical compound NCCCCCCCCCCCC(N)=O SNNMLPUQKZGXOJ-UHFFFAOYSA-N 0.000 claims description 10
- FQLAJSQGBDYBAL-UHFFFAOYSA-N 3-(azepane-1-carbonyl)benzamide Chemical compound NC(=O)C1=CC=CC(C(=O)N2CCCCCC2)=C1 FQLAJSQGBDYBAL-UHFFFAOYSA-N 0.000 claims description 10
- 150000001408 amides Chemical class 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 238000002411 thermogravimetry Methods 0.000 claims description 9
- 229920003231 aliphatic polyamide Polymers 0.000 claims description 8
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 7
- CSJJNGBTPIRXBE-UHFFFAOYSA-N 6-(azepan-1-yl)-6-oxohexanamide Chemical compound NC(=O)CCCCC(=O)N1CCCCCC1 CSJJNGBTPIRXBE-UHFFFAOYSA-N 0.000 claims description 6
- 239000004953 Aliphatic polyamide Substances 0.000 claims description 6
- 229920000572 Nylon 6/12 Polymers 0.000 claims description 6
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- 150000002989 phenols Chemical class 0.000 claims description 6
- 230000004580 weight loss Effects 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
- 229920006012 semi-aromatic polyamide Polymers 0.000 claims description 5
- 229920006345 thermoplastic polyamide Polymers 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- 229920003023 plastic Polymers 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 239000004711 α-olefin Substances 0.000 claims description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 3
- 101150097440 PADI6 gene Proteins 0.000 claims description 3
- 102100035732 Protein-arginine deiminase type-6 Human genes 0.000 claims description 3
- 239000002826 coolant Substances 0.000 claims description 3
- 239000012745 toughening agent Substances 0.000 claims description 3
- WXBUUJNOVQVTFV-UHFFFAOYSA-N 10-(azacycloundec-1-yl)-10-oxodecanamide Chemical compound NC(=O)CCCCCCCCC(=O)N1CCCCCCCCCC1 WXBUUJNOVQVTFV-UHFFFAOYSA-N 0.000 claims description 2
- MXAOILAHPVJWBS-UHFFFAOYSA-N 10-(azepan-1-yl)-10-oxodecanamide Chemical compound NC(=O)CCCCCCCCC(=O)N1CCCCCC1 MXAOILAHPVJWBS-UHFFFAOYSA-N 0.000 claims description 2
- ZWSFGBDPFXZAHJ-UHFFFAOYSA-N 10-oxo-10-piperidin-1-yldecanamide Chemical compound NC(=O)CCCCCCCCC(=O)N1CCCCC1 ZWSFGBDPFXZAHJ-UHFFFAOYSA-N 0.000 claims description 2
- ANDAQSIUDBVMNP-UHFFFAOYSA-N 12-(azepan-1-yl)-12-oxododecanamide Chemical compound NC(=O)CCCCCCCCCCC(=O)N1CCCCCC1 ANDAQSIUDBVMNP-UHFFFAOYSA-N 0.000 claims description 2
- LFUWLWCAQXSNJN-UHFFFAOYSA-N 15-(azepan-1-yl)-15-oxopentadecanamide Chemical compound NC(=O)CCCCCCCCCCCCCC(=O)N1CCCCCC1 LFUWLWCAQXSNJN-UHFFFAOYSA-N 0.000 claims description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 2
- 239000005909 Kieselgur Substances 0.000 claims description 2
- 229920000393 Nylon 6/6T Polymers 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- VCNTUJWBXWAWEJ-UHFFFAOYSA-J aluminum;sodium;dicarbonate Chemical compound [Na+].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O VCNTUJWBXWAWEJ-UHFFFAOYSA-J 0.000 claims description 2
- 238000001479 atomic absorption spectroscopy Methods 0.000 claims description 2
- 239000011324 bead Substances 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 239000004917 carbon fiber Substances 0.000 claims description 2
- 230000003197 catalytic effect Effects 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 claims description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 2
- 229920000554 ionomer Polymers 0.000 claims description 2
- 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 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000391 magnesium silicate Substances 0.000 claims description 2
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- 235000019792 magnesium silicate Nutrition 0.000 claims description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 2
- 235000019341 magnesium sulphate Nutrition 0.000 claims description 2
- 239000010445 mica Substances 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- AJCDFVKYMIUXCR-UHFFFAOYSA-N oxobarium;oxo(oxoferriooxy)iron Chemical compound [Ba]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O AJCDFVKYMIUXCR-UHFFFAOYSA-N 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- 239000010456 wollastonite Substances 0.000 claims description 2
- 229910052882 wollastonite Inorganic materials 0.000 claims description 2
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 2
- SQFRYRZOLAMMSP-UHFFFAOYSA-N 13-(azepan-1-yl)-13-oxotridecanamide Chemical compound NC(=O)CCCCCCCCCCCC(=O)N1CCCCCC1 SQFRYRZOLAMMSP-UHFFFAOYSA-N 0.000 claims 1
- PHXXJRXZJIMOJM-UHFFFAOYSA-N 2-methylidenedecanediamide Chemical compound NC(=O)CCCCCCCC(=C)C(N)=O PHXXJRXZJIMOJM-UHFFFAOYSA-N 0.000 claims 1
- XZSUTGMNXBMJMJ-UHFFFAOYSA-N CCCCCCCCCC.NC(=O)c1ccc(cc1)C(N)=O Chemical compound CCCCCCCCCC.NC(=O)c1ccc(cc1)C(N)=O XZSUTGMNXBMJMJ-UHFFFAOYSA-N 0.000 claims 1
- LXHHROBUZABRSD-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC.CCCCCCCCCCCC LXHHROBUZABRSD-UHFFFAOYSA-N 0.000 claims 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 claims 1
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- 238000012360 testing method Methods 0.000 description 19
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 18
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- 150000001733 carboxylic acid esters Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
- VDBXLXRWMYNMHL-UHFFFAOYSA-N decanediamide Chemical compound NC(=O)CCCCCCCCC(N)=O VDBXLXRWMYNMHL-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- PXRMLPZQBFWPCV-UHFFFAOYSA-N dioxasilirane Chemical compound O1O[SiH2]1 PXRMLPZQBFWPCV-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- FTZSDHHWPWGCDI-UHFFFAOYSA-N dodecanediamide Chemical compound NC(=O)CCCCCCCCCCC(N)=O FTZSDHHWPWGCDI-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000010102 injection blow moulding Methods 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- FDAKZQLBIFPGSV-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)NC(C)(C)C1 FDAKZQLBIFPGSV-UHFFFAOYSA-N 0.000 description 1
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003386 piperidinyl group Chemical class 0.000 description 1
- 125000005936 piperidyl group Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006131 poly(hexamethylene isophthalamide-co-terephthalamide) Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- UOIBLYKRMCDKBM-UHFFFAOYSA-N prop-1-en-2-ylbenzene;1-(2,2,6,6-tetramethylpiperidin-4-yl)pyrrole-2,5-dione Chemical compound CC(=C)C1=CC=CC=C1.C1C(C)(C)NC(C)(C)CC1N1C(=O)C=CC1=O UOIBLYKRMCDKBM-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 102200015813 rs387906871 Human genes 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- NZNAAUDJKMURFU-UHFFFAOYSA-N tetrakis(2,2,6,6-tetramethylpiperidin-4-yl) butane-1,2,3,4-tetracarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC(C(=O)OC1CC(C)(C)NC(C)(C)C1)C(C(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 NZNAAUDJKMURFU-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 238000003878 thermal aging Methods 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical group 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L29/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
- C08L29/02—Homopolymers or copolymers of unsaturated alcohols
- C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyamides (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22983709P | 2009-07-30 | 2009-07-30 | |
| US61/229,837 | 2009-07-30 | ||
| PCT/US2010/043515 WO2011014548A2 (en) | 2009-07-30 | 2010-07-28 | Heat aging resistant polyamide compositions including polyhydroxy polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013501094A true JP2013501094A (ja) | 2013-01-10 |
| JP2013501094A5 JP2013501094A5 (enExample) | 2015-04-23 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012522994A Pending JP2013501094A (ja) | 2009-07-30 | 2010-07-28 | ポリヒドロキシポリマーを含む熱老化耐性ポリアミド組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20110028621A1 (enExample) |
| EP (1) | EP2459648A2 (enExample) |
| JP (1) | JP2013501094A (enExample) |
| CN (1) | CN102597114B (enExample) |
| BR (1) | BR112012001930A2 (enExample) |
| WO (1) | WO2011014548A2 (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014514405A (ja) * | 2011-04-13 | 2014-06-19 | ローディア オペレーションズ | 安定化されたポリアミド組成物 |
| WO2015046247A1 (ja) | 2013-09-27 | 2015-04-02 | 旭化成ケミカルズ株式会社 | ポリアミド樹脂組成物及び成形品 |
| JP2015105378A (ja) * | 2013-11-28 | 2015-06-08 | ランクセス・ドイチュランド・ゲーエムベーハー | ポリアミド組成物 |
| WO2018216770A1 (ja) * | 2017-05-25 | 2018-11-29 | 東洋紡株式会社 | ガラス繊維強化ポリアミド樹脂組成物 |
| JP2019172805A (ja) * | 2018-03-28 | 2019-10-10 | 旭化成株式会社 | ポリアミド樹脂組成物及び成形品 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2965565B1 (fr) | 2010-10-05 | 2014-05-02 | Rhodia Operations | Composition polyamide thermo-stabilisee |
| US8921460B2 (en) * | 2011-06-21 | 2014-12-30 | E. I. Du Pont De Nemours And Company | Heat-stabilized acrylate elastomer composition and process for its production |
| EP2580285B8 (en) | 2011-06-21 | 2014-02-19 | E. I. Du Pont de Nemours and Company | Process for production of a heat-stabilised polyamide-filled acrylate polymer |
| FR2970970B1 (fr) * | 2011-07-11 | 2015-04-03 | Rhodia Operations | Composition polyamide stabilisee |
| US20130115401A1 (en) | 2011-11-08 | 2013-05-09 | E I Du Pont De Nemouras And Company | Hydrolytic resistant polyamide compositions comprising polyhydroxy polymers |
| WO2013109529A1 (en) | 2012-01-16 | 2013-07-25 | Promerus Llc | Thermo-oxidatively stable, side chain polyether functionalized polynorbornenes for microelectronic and optoelectronic devices and assemblies thereof |
| US20130281589A1 (en) * | 2012-04-23 | 2013-10-24 | E I Du Pont De Nemours And Company | Thermoplastic polyamide composition |
| CN104098889B (zh) * | 2013-04-07 | 2016-06-01 | 杜邦公司 | 含有二氧化钛包覆的云母片的增强聚酰胺组合物 |
| FR3008984B1 (fr) * | 2013-07-24 | 2017-04-28 | Rhodia Operations | Articles obtenus a partir d'une composition polymerique, procede de preparation et utilisations |
| CN106832904A (zh) * | 2017-02-24 | 2017-06-13 | 广州市聚赛龙工程塑料股份有限公司 | 一种无卤阻燃尼龙材料及其制备方法和应用 |
| CN108587139B (zh) * | 2017-07-24 | 2020-10-16 | 中广核俊尔新材料有限公司 | 抗污染的增强尼龙复合材料及其制备方法和在制备卫浴产品中的应用 |
| JP7308818B2 (ja) | 2017-09-28 | 2023-07-14 | デュポン ポリマーズ インコーポレイテッド | 重合方法 |
| WO2019189035A1 (ja) * | 2018-03-28 | 2019-10-03 | 富士フイルム株式会社 | 内視鏡用可撓管、内視鏡型医療機器及び内視鏡用可撓管基材被覆用樹脂組成物 |
| CN115368732A (zh) * | 2022-08-24 | 2022-11-22 | 浙江美亚特精密机械有限公司 | 一种聚酰胺组合物及用其制成滑动和滚动零件的制造方法 |
| CN116554676B (zh) * | 2023-04-28 | 2024-10-29 | 珠海万通特种工程塑料有限公司 | 一种聚酰胺组合物及其制备方法和应用 |
| WO2025049564A1 (en) * | 2023-08-29 | 2025-03-06 | Basf Se | Polyamide molding compositions with improved heat-aging resistance |
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- 2010-07-28 BR BR112012001930A patent/BR112012001930A2/pt not_active IP Right Cessation
- 2010-07-28 CN CN201080043813.9A patent/CN102597114B/zh not_active Expired - Fee Related
- 2010-07-28 WO PCT/US2010/043515 patent/WO2011014548A2/en not_active Ceased
- 2010-07-28 JP JP2012522994A patent/JP2013501094A/ja active Pending
- 2010-07-28 EP EP10738137A patent/EP2459648A2/en not_active Withdrawn
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014514405A (ja) * | 2011-04-13 | 2014-06-19 | ローディア オペレーションズ | 安定化されたポリアミド組成物 |
| WO2015046247A1 (ja) | 2013-09-27 | 2015-04-02 | 旭化成ケミカルズ株式会社 | ポリアミド樹脂組成物及び成形品 |
| JP2015105378A (ja) * | 2013-11-28 | 2015-06-08 | ランクセス・ドイチュランド・ゲーエムベーハー | ポリアミド組成物 |
| WO2018216770A1 (ja) * | 2017-05-25 | 2018-11-29 | 東洋紡株式会社 | ガラス繊維強化ポリアミド樹脂組成物 |
| JP2019172805A (ja) * | 2018-03-28 | 2019-10-10 | 旭化成株式会社 | ポリアミド樹脂組成物及び成形品 |
| JP7074531B2 (ja) | 2018-03-28 | 2022-05-24 | 旭化成株式会社 | ポリアミド樹脂組成物及び成形品 |
Also Published As
| Publication number | Publication date |
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| CN102597114B (zh) | 2015-04-01 |
| CN102597114A (zh) | 2012-07-18 |
| EP2459648A2 (en) | 2012-06-06 |
| WO2011014548A3 (en) | 2011-04-14 |
| WO2011014548A2 (en) | 2011-02-03 |
| BR112012001930A2 (pt) | 2016-03-15 |
| US20110028621A1 (en) | 2011-02-03 |
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