BE1012882A5 - Melange stabilisant pour matieres organiques, composition le contenant et son procede d'utilisation. - Google Patents
Melange stabilisant pour matieres organiques, composition le contenant et son procede d'utilisation. Download PDFInfo
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- BE1012882A5 BE1012882A5 BE9800927A BE9800927A BE1012882A5 BE 1012882 A5 BE1012882 A5 BE 1012882A5 BE 9800927 A BE9800927 A BE 9800927A BE 9800927 A BE9800927 A BE 9800927A BE 1012882 A5 BE1012882 A5 BE 1012882A5
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- 239000000203 mixture Substances 0.000 title claims abstract description 82
- 239000011368 organic material Substances 0.000 title claims abstract description 26
- 238000000034 method Methods 0.000 title claims description 7
- 239000003381 stabilizer Substances 0.000 title abstract description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 182
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims abstract description 50
- 229910001701 hydrotalcite Inorganic materials 0.000 claims abstract description 50
- 229960001545 hydrotalcite Drugs 0.000 claims abstract description 50
- 230000000087 stabilizing effect Effects 0.000 claims abstract description 48
- 150000001412 amines Chemical class 0.000 claims abstract description 31
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims abstract description 21
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 10
- 239000011707 mineral Substances 0.000 claims abstract description 10
- 230000015556 catabolic process Effects 0.000 claims abstract description 7
- 238000006731 degradation reaction Methods 0.000 claims abstract description 7
- 159000000003 magnesium salts Chemical class 0.000 claims abstract description 7
- 230000003647 oxidation Effects 0.000 claims abstract description 7
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 7
- 229920000098 polyolefin Polymers 0.000 claims abstract description 7
- -1 amine compound Chemical class 0.000 claims description 186
- 239000011777 magnesium Substances 0.000 claims description 146
- 239000011701 zinc Substances 0.000 claims description 94
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 82
- 229910052739 hydrogen Inorganic materials 0.000 claims description 59
- 239000001257 hydrogen Substances 0.000 claims description 51
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 38
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 35
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims description 33
- JYYOBHFYCIDXHH-UHFFFAOYSA-N carbonic acid;hydrate Chemical compound O.OC(O)=O JYYOBHFYCIDXHH-UHFFFAOYSA-N 0.000 claims description 32
- 239000000049 pigment Substances 0.000 claims description 28
- 229920000642 polymer Polymers 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 23
- 239000004743 Polypropylene Substances 0.000 claims description 19
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 18
- 239000010459 dolomite Substances 0.000 claims description 18
- 229910000514 dolomite Inorganic materials 0.000 claims description 18
- 239000006096 absorbing agent Substances 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 239000000460 chlorine Substances 0.000 claims description 17
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 15
- 229920001155 polypropylene Polymers 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 239000000047 product Substances 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 10
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 claims description 9
- 239000011787 zinc oxide Substances 0.000 claims description 9
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 235000010755 mineral Nutrition 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 229920001059 synthetic polymer Polymers 0.000 claims description 7
- 239000004408 titanium dioxide Substances 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 6
- 159000000007 calcium salts Chemical class 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical group OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 claims description 4
- 229920000768 polyamine Polymers 0.000 claims description 4
- HWRLEEPNFJNTOP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-yl)phenol Chemical compound OC1=CC=CC=C1C1=NC=NC=N1 HWRLEEPNFJNTOP-UHFFFAOYSA-N 0.000 claims description 3
- 239000005711 Benzoic acid Substances 0.000 claims description 3
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 claims description 3
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 claims description 3
- 235000010233 benzoic acid Nutrition 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 claims description 3
- 239000013067 intermediate product Substances 0.000 claims description 3
- 229920005606 polypropylene copolymer Polymers 0.000 claims description 3
- GDESWOTWNNGOMW-UHFFFAOYSA-N resorcinol monobenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 GDESWOTWNNGOMW-UHFFFAOYSA-N 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 claims description 2
- ULVDMKRXBIKOMK-UHFFFAOYSA-N 4,5,6,7-tetrachloro-2,3-dihydroisoindol-1-one Chemical compound ClC1=C(Cl)C(Cl)=C2CNC(=O)C2=C1Cl ULVDMKRXBIKOMK-UHFFFAOYSA-N 0.000 claims description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 2
- 150000004056 anthraquinones Chemical class 0.000 claims description 2
- 229910052980 cadmium sulfide Inorganic materials 0.000 claims description 2
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 claims description 2
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 2
- 238000010348 incorporation Methods 0.000 claims description 2
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 claims description 2
- 229910000464 lead oxide Inorganic materials 0.000 claims description 2
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 claims description 2
- RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical compound C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 claims description 2
- 229910017053 inorganic salt Inorganic materials 0.000 claims 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 229910052753 mercury Inorganic materials 0.000 claims 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims 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 claims 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims 1
- 150000003751 zinc Chemical class 0.000 abstract description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 44
- 229920001577 copolymer Polymers 0.000 description 38
- 150000003254 radicals Chemical class 0.000 description 27
- 229910052757 nitrogen Inorganic materials 0.000 description 23
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 20
- 239000000654 additive Substances 0.000 description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 17
- 125000002947 alkylene group Chemical group 0.000 description 17
- 125000001931 aliphatic group Chemical group 0.000 description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 16
- 239000007983 Tris buffer Substances 0.000 description 15
- 238000002835 absorbance Methods 0.000 description 14
- 239000002253 acid Substances 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 14
- 150000002431 hydrogen Chemical class 0.000 description 14
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 12
- 239000004952 Polyamide Substances 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
- 150000002148 esters Chemical group 0.000 description 12
- 229920002647 polyamide Polymers 0.000 description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 11
- 125000000753 cycloalkyl group Chemical group 0.000 description 11
- 230000006641 stabilisation Effects 0.000 description 11
- 238000011105 stabilization Methods 0.000 description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
- 239000005977 Ethylene Substances 0.000 description 10
- 125000003342 alkenyl group Chemical group 0.000 description 10
- 229920001684 low density polyethylene Polymers 0.000 description 10
- 239000004702 low-density polyethylene Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000011575 calcium Substances 0.000 description 9
- 229920001903 high density polyethylene Polymers 0.000 description 9
- 239000004700 high-density polyethylene Substances 0.000 description 9
- 229920002857 polybutadiene Polymers 0.000 description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 8
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 8
- 239000005062 Polybutadiene Substances 0.000 description 8
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 8
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- 239000005416 organic matter Substances 0.000 description 8
- 239000004417 polycarbonate Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 230000002195 synergetic effect Effects 0.000 description 8
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 8
- 239000001052 yellow pigment Substances 0.000 description 8
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 7
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 7
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 7
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
- 125000003710 aryl alkyl group Chemical group 0.000 description 7
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 7
- 150000001993 dienes Chemical class 0.000 description 7
- 229920006324 polyoxymethylene Polymers 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 6
- 239000012860 organic pigment Substances 0.000 description 6
- 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 6
- 239000004800 polyvinyl chloride Substances 0.000 description 6
- 229920000915 polyvinyl chloride Polymers 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 5
- 125000002252 acyl group Chemical group 0.000 description 5
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- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 5
- 239000012964 benzotriazole Substances 0.000 description 5
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- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 5
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- 238000006116 polymerization reaction Methods 0.000 description 5
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 4
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 4
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- CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
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- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 4
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- 238000007906 compression Methods 0.000 description 4
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- 239000008187 granular material Substances 0.000 description 4
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
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- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
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- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
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- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229940098697 zinc laurate Drugs 0.000 description 1
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- 235000007680 β-tocopherol Nutrition 0.000 description 1
- 239000011590 β-tocopherol Substances 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/30—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing heterocyclic ring with at least one nitrogen atom as ring member
-
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP97811018 | 1997-12-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE1012882A5 true BE1012882A5 (fr) | 2001-05-08 |
Family
ID=8230545
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE9800927A BE1012882A5 (fr) | 1997-12-23 | 1998-12-23 | Melange stabilisant pour matieres organiques, composition le contenant et son procede d'utilisation. |
Country Status (10)
| Country | Link |
|---|---|
| US (3) | US20020013390A1 (enExample) |
| JP (2) | JP4950372B2 (enExample) |
| BE (1) | BE1012882A5 (enExample) |
| CA (1) | CA2256800C (enExample) |
| DE (1) | DE19859096A1 (enExample) |
| ES (1) | ES2155364B1 (enExample) |
| FR (1) | FR2772773B1 (enExample) |
| GB (1) | GB2332678B (enExample) |
| IT (1) | IT1304793B1 (enExample) |
| NL (1) | NL1010890C2 (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020016390A1 (en) | 1997-12-23 | 2002-02-07 | Francois Gugumus | Stabilizer mixtures |
| GB2347427B (en) * | 1997-12-23 | 2001-07-18 | Ciba Sc Holding Ag | Stabilizer mixtures comprising a sterically hindered amine |
| US20030191239A1 (en) * | 2000-05-31 | 2003-10-09 | Francois Gugumus | Stabilizer mixtures |
| US6828364B2 (en) * | 2000-07-14 | 2004-12-07 | Ciba Specialty Chemicals Corporation | Stabilizer mixtures |
| DE10123732A1 (de) * | 2001-05-15 | 2002-11-21 | Basf Ag | Stabilisierte Metallocen-Polyolefine |
| DE10152228A1 (de) * | 2001-10-20 | 2003-05-08 | Clariant Gmbh | Mischungen aus Wachsen und Polymeradditiven |
| ZA200301683B (en) | 2002-03-04 | 2004-09-06 | Ciba Sc Holding Ag | Synergistic combinations of UV absorbers for pigmented polyolefins. |
| US20030225191A1 (en) * | 2002-04-12 | 2003-12-04 | Francois Gugumus | Stabilizer mixtures |
| US20060014862A1 (en) * | 2004-07-15 | 2006-01-19 | Dzikowicz Robert T | Vulcanizing latex compounds without the use of metal oxide activators or a zinc based accelerator |
| EP1897914A4 (en) * | 2005-06-29 | 2008-07-02 | Adeka Corp | RESIN ADDITIVE COMPOSITION AND RESIN COMPOSITION |
| ES2373109T3 (es) * | 2006-05-30 | 2012-01-31 | Borealis Technology Oy | Un compuesto que contiene silicio como inhibidor de la corrosión en composiciones poliolefínicas. |
| US8748518B2 (en) * | 2007-05-25 | 2014-06-10 | Clariant Finance (Bvi) Limited | Stabilization of polycarbonates |
| US8822575B2 (en) | 2007-08-28 | 2014-09-02 | Basf Se | Stabilizer mixture |
| JP5651918B2 (ja) | 2007-12-21 | 2015-01-14 | 住友化学株式会社 | ポリプロピレン系樹脂組成物及び成形体 |
| JP5487611B2 (ja) | 2007-12-21 | 2014-05-07 | 住友化学株式会社 | ポリプロピレン系樹脂組成物及びそれからなる成形体 |
| WO2009080427A1 (de) * | 2007-12-21 | 2009-07-02 | Basf Se | Verfahren zur herstellung von uv-absorbierenden hybridmaterialien |
| DE102009041841A1 (de) | 2008-12-17 | 2010-07-08 | Huhtamaki Forchheim Zweigniederlassung Der Huhtamaki Deutschland Gmbh & Co. Kg | UV- und Licht-Schutzfolie |
| CN101838428A (zh) * | 2010-03-15 | 2010-09-22 | 湖北工业大学 | 聚氯乙烯用环保无毒固体有机锡热稳定剂及其制造方法 |
| US9045615B2 (en) * | 2011-08-24 | 2015-06-02 | Fina Technology, Inc. | Metal carboxylate additives for thermoplastics |
| EP2840112B1 (en) * | 2013-08-21 | 2019-04-10 | Baerlocher GmbH | Stabilized polymer compositions and methods of making same |
| KR102242620B1 (ko) * | 2013-11-26 | 2021-04-21 | 가부시키가이샤 아데카 | 광안정제 조성물 및 그 수지 조성물 |
| US10246563B2 (en) | 2015-03-30 | 2019-04-02 | Adeka Corporation | Photostabilizer master batch and method for manufacturing same |
| US10077410B2 (en) | 2016-07-13 | 2018-09-18 | Chevron Oronite Company Llc | Synergistic lubricating oil composition containing mixture of antioxidants |
| JP6859660B2 (ja) * | 2016-10-28 | 2021-04-14 | Toto株式会社 | 樹脂材料および成形体 |
| WO2018221610A1 (ja) * | 2017-06-02 | 2018-12-06 | 凸版印刷株式会社 | 樹脂成型体、積層体及び化粧シート |
| SG11201912421SA (en) * | 2017-07-06 | 2020-01-30 | Basf Se | A polyethylene pipe |
| CN111684042A (zh) | 2018-02-02 | 2020-09-18 | 株式会社Adeka | 稳定剂组合物、含有其的氯乙烯系树脂组合物及其成型体 |
| CN110713638B (zh) * | 2018-07-11 | 2020-12-11 | 北京化工大学 | 一种水滑石/环氧天然橡胶/丁苯橡胶复合材料及制备方法 |
| US11661531B2 (en) | 2019-01-31 | 2023-05-30 | Synthomer Adhesives Technology LLC | Hygiene adhesives comprising low volatile tackifier compositions |
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| EP0290386A2 (de) * | 1987-05-05 | 1988-11-09 | Ciba-Geigy Ag | Stabilisierung von organischen Polymeren gegen Lichtabbau |
| EP0290388A2 (en) * | 1987-05-05 | 1988-11-09 | Ciba-Geigy Ag | Polyethylene stabilizer compositions comprising compounds with piperidine groups and metal compounds |
| EP0344321A1 (en) * | 1987-10-20 | 1989-12-06 | Ferro Corporation | Synthetic resin composition |
| EP0421933A1 (de) * | 1989-10-06 | 1991-04-10 | Ciba-Geigy Ag | Stabilisierte chlorhaltige Polymerzusammensetzungen |
| EP0661341A1 (en) * | 1993-12-27 | 1995-07-05 | MITSUI TOATSU CHEMICALS, Inc. | Filled polypropylene composition containing zinc salts of fatty acids |
| EP0690094A1 (en) * | 1994-06-27 | 1996-01-03 | Ciba-Geigy Ag | Polyolefin or olefin copolymer films having improved light stabilitiy and pesticide resistance |
| GB2293827A (en) * | 1994-10-06 | 1996-04-10 | Sandoz Ltd | Stabilizer composition for polymers |
| EP0768336A2 (de) * | 1995-10-13 | 1997-04-16 | Ciba SC Holding AG | Stabilisatorkombinationen für chlorhaltige Polymere |
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1998
- 1998-12-16 GB GB9827567A patent/GB2332678B/en not_active Expired - Lifetime
- 1998-12-21 DE DE19859096A patent/DE19859096A1/de not_active Ceased
- 1998-12-21 ES ES009802650A patent/ES2155364B1/es not_active Expired - Fee Related
- 1998-12-21 CA CA002256800A patent/CA2256800C/en not_active Expired - Lifetime
- 1998-12-22 IT IT1998MI002776A patent/IT1304793B1/it active
- 1998-12-22 JP JP37631698A patent/JP4950372B2/ja not_active Expired - Lifetime
- 1998-12-22 FR FR9816204A patent/FR2772773B1/fr not_active Expired - Lifetime
- 1998-12-23 BE BE9800927A patent/BE1012882A5/fr not_active IP Right Cessation
- 1998-12-23 NL NL1010890A patent/NL1010890C2/xx not_active IP Right Cessation
-
2001
- 2001-03-19 US US09/811,960 patent/US20020013390A1/en not_active Abandoned
-
2002
- 2002-02-28 US US10/085,221 patent/US20030013784A1/en not_active Abandoned
-
2004
- 2004-08-09 US US10/914,704 patent/US7169835B2/en not_active Expired - Lifetime
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2009
- 2009-03-24 JP JP2009072522A patent/JP4726969B2/ja not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0290391A2 (de) * | 1987-05-05 | 1988-11-09 | Ciba-Geigy Ag | Gegen Lichtschädigung stabilisierte Polyolefine |
| EP0290386A2 (de) * | 1987-05-05 | 1988-11-09 | Ciba-Geigy Ag | Stabilisierung von organischen Polymeren gegen Lichtabbau |
| EP0290388A2 (en) * | 1987-05-05 | 1988-11-09 | Ciba-Geigy Ag | Polyethylene stabilizer compositions comprising compounds with piperidine groups and metal compounds |
| EP0344321A1 (en) * | 1987-10-20 | 1989-12-06 | Ferro Corporation | Synthetic resin composition |
| EP0421933A1 (de) * | 1989-10-06 | 1991-04-10 | Ciba-Geigy Ag | Stabilisierte chlorhaltige Polymerzusammensetzungen |
| EP0661341A1 (en) * | 1993-12-27 | 1995-07-05 | MITSUI TOATSU CHEMICALS, Inc. | Filled polypropylene composition containing zinc salts of fatty acids |
| EP0690094A1 (en) * | 1994-06-27 | 1996-01-03 | Ciba-Geigy Ag | Polyolefin or olefin copolymer films having improved light stabilitiy and pesticide resistance |
| GB2293827A (en) * | 1994-10-06 | 1996-04-10 | Sandoz Ltd | Stabilizer composition for polymers |
| EP0768336A2 (de) * | 1995-10-13 | 1997-04-16 | Ciba SC Holding AG | Stabilisatorkombinationen für chlorhaltige Polymere |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2332678A (en) | 1999-06-30 |
| NL1010890C2 (nl) | 1999-08-02 |
| JP2009132943A (ja) | 2009-06-18 |
| ITMI982776A1 (it) | 2000-06-22 |
| FR2772773B1 (fr) | 2006-01-27 |
| JPH11255957A (ja) | 1999-09-21 |
| NL1010890A1 (nl) | 1999-06-24 |
| US20020013390A1 (en) | 2002-01-31 |
| DE19859096A1 (de) | 1999-06-24 |
| US7169835B2 (en) | 2007-01-30 |
| JP4726969B2 (ja) | 2011-07-20 |
| ES2155364B1 (es) | 2002-07-01 |
| ES2155364A1 (es) | 2001-05-01 |
| US20030013784A1 (en) | 2003-01-16 |
| IT1304793B1 (it) | 2001-03-29 |
| GB9827567D0 (en) | 1999-02-10 |
| JP4950372B2 (ja) | 2012-06-13 |
| GB2332678B (en) | 2000-09-27 |
| US20050006628A1 (en) | 2005-01-13 |
| FR2772773A1 (fr) | 1999-06-25 |
| CA2256800C (en) | 2008-08-26 |
| CA2256800A1 (en) | 1999-06-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK | Patent expired because of reaching the maximum lifetime of a patent |
Effective date: 20181223 |