DE2660746C2 - Verwendung von Stabilisatorensystemen aus Triarylphosphiten und Phenolen - Google Patents
Verwendung von Stabilisatorensystemen aus Triarylphosphiten und PhenolenInfo
- Publication number
- DE2660746C2 DE2660746C2 DE2660746A DE2660746A DE2660746C2 DE 2660746 C2 DE2660746 C2 DE 2660746C2 DE 2660746 A DE2660746 A DE 2660746A DE 2660746 A DE2660746 A DE 2660746A DE 2660746 C2 DE2660746 C2 DE 2660746C2
- Authority
- DE
- Germany
- Prior art keywords
- tert
- butyl
- bis
- acid
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 title claims description 11
- 239000003381 stabilizer Substances 0.000 title description 17
- 150000002989 phenols Chemical class 0.000 title description 6
- -1 polyethylene Polymers 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 14
- 229920000098 polyolefin Polymers 0.000 claims description 10
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 7
- 239000004743 Polypropylene Substances 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 6
- 239000002530 phenolic antioxidant Substances 0.000 claims description 6
- 229920001155 polypropylene Polymers 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229920001519 homopolymer Polymers 0.000 claims description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 229920002367 Polyisobutene Polymers 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- 150000002815 nickel Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 2
- BGCSUUSPRCDKBQ-UHFFFAOYSA-N 2,4,8,10-tetraoxaspiro[5.5]undecane Chemical compound C1OCOCC21COCOC2 BGCSUUSPRCDKBQ-UHFFFAOYSA-N 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 2
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical class NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 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 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000006078 metal deactivator Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- YEYCMBWKTZNPDH-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) benzoate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C1=CC=CC=C1 YEYCMBWKTZNPDH-UHFFFAOYSA-N 0.000 description 1
- KJYSXRBJOSZLEL-UHFFFAOYSA-N (2,4-ditert-butylphenyl) 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 KJYSXRBJOSZLEL-UHFFFAOYSA-N 0.000 description 1
- HQEPZWYPQQKFLU-UHFFFAOYSA-N (2,6-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC(O)=C1C(=O)C1=CC=CC=C1 HQEPZWYPQQKFLU-UHFFFAOYSA-N 0.000 description 1
- ATLWFAZCZPSXII-UHFFFAOYSA-N (2-octylphenyl) 2-hydroxybenzoate Chemical compound CCCCCCCCC1=CC=CC=C1OC(=O)C1=CC=CC=C1O ATLWFAZCZPSXII-UHFFFAOYSA-N 0.000 description 1
- ARVUDIQYNJVQIW-UHFFFAOYSA-N (4-dodecoxy-2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(OCCCCCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 ARVUDIQYNJVQIW-UHFFFAOYSA-N 0.000 description 1
- GOZHNJTXLALKRL-UHFFFAOYSA-N (5-benzoyl-2,4-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(O)=C(C(=O)C=2C=CC=CC=2)C=C1C(=O)C1=CC=CC=C1 GOZHNJTXLALKRL-UHFFFAOYSA-N 0.000 description 1
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- VNQNXQYZMPJLQX-UHFFFAOYSA-N 1,3,5-tris[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CN2C(N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(=O)N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C2=O)=O)=C1 VNQNXQYZMPJLQX-UHFFFAOYSA-N 0.000 description 1
- VMDYMJSKWCVEEB-UHFFFAOYSA-N 1-[3,5-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyl]-1,3,5-triazinan-1-yl]-3-(3,5-ditert-butyl-4-hydroxyphenyl)propan-1-one Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)N2CN(CN(C2)C(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 VMDYMJSKWCVEEB-UHFFFAOYSA-N 0.000 description 1
- VETPHHXZEJAYOB-UHFFFAOYSA-N 1-n,4-n-dinaphthalen-2-ylbenzene-1,4-diamine Chemical compound C1=CC=CC2=CC(NC=3C=CC(NC=4C=C5C=CC=CC5=CC=4)=CC=3)=CC=C21 VETPHHXZEJAYOB-UHFFFAOYSA-N 0.000 description 1
- ZRMMVODKVLXCBB-UHFFFAOYSA-N 1-n-cyclohexyl-4-n-phenylbenzene-1,4-diamine Chemical compound C1CCCCC1NC(C=C1)=CC=C1NC1=CC=CC=C1 ZRMMVODKVLXCBB-UHFFFAOYSA-N 0.000 description 1
- WGCOJSGVXOMWKK-UHFFFAOYSA-N 10-(2,2-diphenylhydrazinyl)-10-oxodecanoic acid Chemical compound C1(=CC=CC=C1)N(NC(CCCCCCCCC(=O)O)=O)C1=CC=CC=C1 WGCOJSGVXOMWKK-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- AFTBJQDQENGCPC-UHFFFAOYSA-N 2,5-ditert-butyl-4-methylphenol Chemical compound CC1=CC(C(C)(C)C)=C(O)C=C1C(C)(C)C AFTBJQDQENGCPC-UHFFFAOYSA-N 0.000 description 1
- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 1
- SCXYLTWTWUGEAA-UHFFFAOYSA-N 2,6-ditert-butyl-4-(methoxymethyl)phenol Chemical compound COCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SCXYLTWTWUGEAA-UHFFFAOYSA-N 0.000 description 1
- QHPKIUDQDCWRKO-UHFFFAOYSA-N 2,6-ditert-butyl-4-[2-(3,5-ditert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 QHPKIUDQDCWRKO-UHFFFAOYSA-N 0.000 description 1
- FTIQNMPDOJXJJN-UHFFFAOYSA-N 2-(3-dodecylsulfanylbutyl)-4,6-dimethylphenol Chemical compound CCCCCCCCCCCCSC(C)CCC1=CC(C)=CC(C)=C1O FTIQNMPDOJXJJN-UHFFFAOYSA-N 0.000 description 1
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical class OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 description 1
- XBXUJQFRMLQPCG-UHFFFAOYSA-N 2-[12-hydroxyimino-23-(2-hydroxy-4-methylphenyl)tricosyl]-5-methylphenol Chemical compound OC1=CC(C)=CC=C1CCCCCCCCCCCC(=NO)CCCCCCCCCCCC1=CC=C(C)C=C1O XBXUJQFRMLQPCG-UHFFFAOYSA-N 0.000 description 1
- HHPDFYDITNAMAM-UHFFFAOYSA-N 2-[cyclohexyl(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(CCO)C1CCCCC1 HHPDFYDITNAMAM-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- OMCYEZUIYGPHDJ-UHFFFAOYSA-N 2-hydroxy-N-[(2-hydroxyphenyl)methylideneamino]benzamide Chemical compound OC1=CC=CC=C1C=NNC(=O)C1=CC=CC=C1O OMCYEZUIYGPHDJ-UHFFFAOYSA-N 0.000 description 1
- WBJWXIQDBDZMAW-UHFFFAOYSA-N 2-hydroxynaphthalene-1-carbonyl chloride Chemical compound C1=CC=CC2=C(C(Cl)=O)C(O)=CC=C21 WBJWXIQDBDZMAW-UHFFFAOYSA-N 0.000 description 1
- JJBOJSJSDIRUGY-UHFFFAOYSA-N 2-tert-butyl-4-[2-(5-tert-butyl-4-hydroxy-2-methylphenyl)-4-dodecylsulfanylbutan-2-yl]-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)(CCSCCCCCCCCCCCC)C1=CC(C(C)(C)C)=C(O)C=C1C JJBOJSJSDIRUGY-UHFFFAOYSA-N 0.000 description 1
- ABVIEQXJRPFGKY-UHFFFAOYSA-N 2-tert-butyl-4-[2-(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)(CC)C1=CC(C(C)(C)C)=C(O)C=C1C ABVIEQXJRPFGKY-UHFFFAOYSA-N 0.000 description 1
- GPNYZBKIGXGYNU-UHFFFAOYSA-N 2-tert-butyl-6-[(3-tert-butyl-5-ethyl-2-hydroxyphenyl)methyl]-4-ethylphenol Chemical compound CC(C)(C)C1=CC(CC)=CC(CC=2C(=C(C=C(CC)C=2)C(C)(C)C)O)=C1O GPNYZBKIGXGYNU-UHFFFAOYSA-N 0.000 description 1
- HCILJBJJZALOAL-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)-n'-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyl]propanehydrazide Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 HCILJBJJZALOAL-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 1
- FKIOYBLZUCCLTL-UHFFFAOYSA-N 4-butyl-2-tert-butyl-5-methylphenol Chemical compound CCCCC1=CC(C(C)(C)C)=C(O)C=C1C FKIOYBLZUCCLTL-UHFFFAOYSA-N 0.000 description 1
- XFMUCDRJXZLSNE-UHFFFAOYSA-N 4-methoxy-2,6-dimethylaniline Chemical compound COC1=CC(C)=C(N)C(C)=C1 XFMUCDRJXZLSNE-UHFFFAOYSA-N 0.000 description 1
- KDVYCTOWXSLNNI-UHFFFAOYSA-N 4-t-Butylbenzoic acid Chemical compound CC(C)(C)C1=CC=C(C(O)=O)C=C1 KDVYCTOWXSLNNI-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OUBMGJOQLXMSNT-UHFFFAOYSA-N N-isopropyl-N'-phenyl-p-phenylenediamine Chemical compound C1=CC(NC(C)C)=CC=C1NC1=CC=CC=C1 OUBMGJOQLXMSNT-UHFFFAOYSA-N 0.000 description 1
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- UOJYYXATTMQQNA-UHFFFAOYSA-N Proxan Chemical compound CC(C)OC(S)=S UOJYYXATTMQQNA-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XIBVYPPJCGNOEO-UHFFFAOYSA-N [3-(2-hydroxy-4-octoxybenzoyl)phenyl]-(2-hydroxy-4-octoxyphenyl)methanone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC(C(=O)C=2C(=CC(OCCCCCCCC)=CC=2)O)=C1 XIBVYPPJCGNOEO-UHFFFAOYSA-N 0.000 description 1
- SAMOITCGMRRXJU-UHFFFAOYSA-N [3-(2-hydroxybenzoyl)phenyl]-(2-hydroxyphenyl)methanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC(C(=O)C=2C(=CC=CC=2)O)=C1 SAMOITCGMRRXJU-UHFFFAOYSA-N 0.000 description 1
- HHFMFWAFQGUGOB-UHFFFAOYSA-N [5-(4-tert-butylbenzoyl)-2,4-dihydroxyphenyl]-(4-tert-butylphenyl)methanone Chemical compound C1=CC(C(C)(C)C)=CC=C1C(=O)C1=CC(C(=O)C=2C=CC(=CC=2)C(C)(C)C)=C(O)C=C1O HHFMFWAFQGUGOB-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- PYHXGXCGESYPCW-UHFFFAOYSA-N alpha-phenylbenzeneacetic acid Natural products C=1C=CC=CC=1C(C(=O)O)C1=CC=CC=C1 PYHXGXCGESYPCW-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000005001 aminoaryl group Chemical group 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 1
- 229940116224 behenate Drugs 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- UTTHLMXOSUFZCQ-UHFFFAOYSA-N benzene-1,3-dicarbohydrazide Chemical compound NNC(=O)C1=CC=CC(C(=O)NN)=C1 UTTHLMXOSUFZCQ-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- MJPRWNNXQTWWLY-UHFFFAOYSA-N dioctadecyl 2,2-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioate Chemical compound C=1C(C(C)(C)C)=C(O)C(C(C)(C)C)=CC=1CC(C(=O)OCCCCCCCCCCCCCCCCCC)(C(=O)OCCCCCCCCCCCCCCCCCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 MJPRWNNXQTWWLY-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000006289 hydroxybenzyl group Chemical group 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- YIMHRDBSVCPJOV-UHFFFAOYSA-N n'-(2-ethoxyphenyl)-n-(2-ethylphenyl)oxamide Chemical compound CCOC1=CC=CC=C1NC(=O)C(=O)NC1=CC=CC=C1CC YIMHRDBSVCPJOV-UHFFFAOYSA-N 0.000 description 1
- FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 description 1
- XAROSYDTKRFVLL-UHFFFAOYSA-N n-butan-2-yl-4-ethoxyaniline Chemical compound CCOC1=CC=C(NC(C)CC)C=C1 XAROSYDTKRFVLL-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- GZNRISJLOXVOSH-UHFFFAOYSA-N n-phenylaniline;propan-2-one Chemical compound CC(C)=O.C=1C=CC=CC=1NC1=CC=CC=C1 GZNRISJLOXVOSH-UHFFFAOYSA-N 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- WBHHMMIMDMUBKC-QJWNTBNXSA-M ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O WBHHMMIMDMUBKC-QJWNTBNXSA-M 0.000 description 1
- 229940066675 ricinoleate Drugs 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- HBYRZSMDBQVSHO-UHFFFAOYSA-N tris(2-tert-butyl-4-methylphenyl) phosphite Chemical compound CC(C)(C)C1=CC(C)=CC=C1OP(OC=1C(=CC(C)=CC=1)C(C)(C)C)OC1=CC=C(C)C=C1C(C)(C)C HBYRZSMDBQVSHO-UHFFFAOYSA-N 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
- C07F9/145—Esters of phosphorous acids with hydroxyaryl compounds
-
- 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
- C08K5/13—Phenols; Phenolates
-
- 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
- C08K5/52—Phosphorus bound to oxygen only
-
- 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
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C08K5/526—Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Description
2,2'-Methylenbis-(6-tert.butyl-4-methy!phenol),
2,2'-Methylenbis-(6-tert.butyl-4-äthyIphenol),
2,2'-Methylenbis-[4-methyl-6-(ir-methylcyclohexyl)-phenol],
l,l-Bis(5-tert.butyI-4-hyclroxy-2-methylphenyl)-butan,
2,2-Bis-(5-tert.butyl-4-hydroxy-2-methyIphenyl)-butan,
2,2-Bis-(3,5-di-tert.butyl-4-hydroxyphenyl)-propan,
l,l,3-Tris-(5-tert.butyl-4-hydroxy-2-methylphenyl)-butan,
2,2-Bis-(5-tert.butyl-4-hydroxy-2-methylphenyl)-4-n-dodecylmercapto-butan,
l,l,5,5-Tetra-(5-tert.butyl-4-hydroxy-2-methy!phenyl)-pentan,
Äthylcnglykolbis-[3,3-bis-(3'-tert.butyl-4'-hydroxyphenyl)-butyrat],
l,l-Bis-(3,5-dimethyl-2-hydroxyphenyl)-3-(n-dodecylthio)-butan oder
4,4'-Thiobis-(6-lert.butyl-3-methylphenoI).
2,2-Bis-(3,5-di-tert.butyl-4-hydroxybenzyl)-malonsäuredioctadecylester,
l,3,5-Tris-(3,5-di-tert.butyl-4-hydroxybenzyl)-isocyanurat oder
S^-Di-tert.butyM-hydroxybenzyl-phosphonsäurediäthylester.
l,3,5-Tris-(3,5-di-tert.butyI-4-hydroxyphenyl-propionyl)-hexahydro-s-triazin,
N,N'-Di-(3,5-di-tert.butyl-4-hydroxyphenyl-propionyl)-hexamethylendiarnin.
3,9-Bis-[l, I-dimethyl^t.^S-di-lcrt.butyM-hydroxyphenyD-äthylJ^^.SJO-tetraoxaspiro-IS.SJundecan.
2,6-Di-tert.-butyl-4-methyI-phenoI,
N,N'-Di-2-naphthyl-p-phenylendiamin, Ν,Ν'-Di-sec.butyl-p-phenylendiamin,
o-Äthoxy^^^-trimethyl-l^-dihydrochinolin, o-Dodecyl^^^-trimethyl-l^-dihydrochinolin,
N-Phenyl-N'-isopropyl-p-phenylendiamin, N.N'-Di-sec.octyl-p-phenylendiaminr,
N-Phenyl-N'-sec.octyl-p-phenylendiamin, N,N'-Di(?.4-d;inethylpentyl)-p-phenylendiamin,
N^N'-Dimrthyl-r^N'-dKsec.octyD-p-phenylendiamin, 2,6-Dimethyl-4-methoxyanilin,
Beim Einsatz dieser Gruppe ist mit Verfärbungserscheinungen zu rechnen.
S'-or-Methylbenzyl-S'-methyl-, S'-a-Methylbenzyl-S'-methyl-S-chlor-, 4'-Hydroxy-, 4'-Meihoxy-,
4'-Octoxy-, 3',5'-Di-tert.amyl-, 3'-MethyI-5'-carbomethoxyäthyl-, S-Chlor^'^'-di
6-Äthy!-, 6-Heptadecyl-, 6-Undecyl-Derivat.
4,2\4'-Trihydroxy-, 2'-Hydroxy-4,4'-dimethoxy-Derivat.
Bcnzoylresorcin, 3,5-Di-tert.butyl-4-hydroxybenzoesäure-2,4-di-tert.butylphenylester oder
-octadecylester oder ^-methyM.o-di-tert.butylester.
a-Carbomethoxy-zimtsäuremethylester,
N-0S-Carbomethoxyvinyl)-2-methyl-indolin.
4-Benzoyloxy-2,2,6,6-tetramethylpiperidin,
4-Stearoylü\y-2,2,6.6-tetramethy !piperidin,
Bis-(2,2,6.6-methylpiperidyl)-sebacat,
3-n-Octy!-7,7,9,9-telramethyl-l,3,8-triaza-spiro[4,5]-decan-2,4-dion.
4,4'-Di-oetyloxy-oxanilid,
2,2'-Di-octyloxy-5,5'-di-tert.butyl-oxanilid,
2,2'-Di-dodecyloxy-5,5'-di-tert.butyI-oxanilid,
2-Äthoxy-2'-äthyl-oxanilid,
N,N'-Bis-(3-dimethylaminopropyl)-oxalamid,
2-Äthoxy-5-tert.butyl-2'-äthyl-oxanilid
Metalldesaktivatoren, wie z.B.
4-tcrt.Butylbenzoesäure. Adipinsäure, Diphenylessigsäure.
Claims (1)
- Patentansprüche:
1. Verwendung von symmetrischen Triaiylphosphiten der allgemeinen Formel IworinR1 und R2 tertButyl sind, R3 Wasserstoff ist,in Kombination mit phenolischen Antioxidantien zum Stabilisieren von Polyolefinen, ausgenommen die Verwendung von symmetrischen Triarylphosphiten und phenolischen Antioxidantien zum Stabilisieren von Homopolymeren aus der Gruppe Polyäthylen, das gegebenenfalls vernetzt sein kann, Polypropylen, Polyisobutylen, Polyrnethylbüien-i, Polyir.ethyipenten-l sowie Mischungen der genannten Homopoiymeren und Copolymere aus den genannten Homopolymeren zugrundeliegenden Monomeren, bei der man als Triarylphosphit a) eine Verbindung der allgemeinen Formel I
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH215575A CH613466A5 (en) | 1975-02-20 | 1975-02-20 | Stabiliser system for polyolefins, comprising a symmetrical triaryl phosphite and a phenolic antioxidant |
CH1223175 | 1975-09-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2660746C2 true DE2660746C2 (de) | 1986-07-03 |
DE2660746C3 DE2660746C3 (de) | 1993-07-15 |
Family
ID=25689664
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19762606358 Expired DE2606358C3 (de) | 1975-02-20 | 1976-02-18 | Verwendung von stabilisatorensystemen aus triarylphosphiten und phenolen |
DE19762660746 Expired - Lifetime DE2660746C3 (de) | 1975-02-20 | 1976-02-18 | Verwendung von stabilisatorensystemen aus triarylphosphiten und phenolen |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19762606358 Expired DE2606358C3 (de) | 1975-02-20 | 1976-02-18 | Verwendung von stabilisatorensystemen aus triarylphosphiten und phenolen |
Country Status (13)
Country | Link |
---|---|
US (1) | US4290941A (de) |
JP (1) | JPS565417B2 (de) |
AU (1) | AU498192B2 (de) |
BR (1) | BR7601007A (de) |
CA (1) | CA1078991A (de) |
DE (2) | DE2606358C3 (de) |
ES (1) | ES445315A1 (de) |
FR (1) | FR2301558A1 (de) |
GB (1) | GB1490938A (de) |
HK (1) | HK44680A (de) |
IT (1) | IT1062063B (de) |
NL (1) | NL191566C (de) |
SE (1) | SE423634B (de) |
Families Citing this family (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2393829A1 (fr) * | 1977-06-07 | 1979-01-05 | Solvay | Procede pour l'extrusion de compositions a base de polymeres d'alpha-olefines |
DE2860898D1 (en) * | 1977-08-08 | 1981-11-05 | Ciba Geigy Ag | Process for the preparation of triarylphosphites |
DE2929993A1 (de) * | 1978-07-27 | 1980-02-07 | Ciba Geigy Ag | Neue stabilisatoren |
JPS5552347A (en) * | 1978-10-12 | 1980-04-16 | Adeka Argus Chem Co Ltd | Stabilized polyphenylene oxide resin composition |
CA1118140A (en) * | 1979-01-11 | 1982-02-09 | William E. Horn, Jr. | Stabilized olefin polymers |
DE2921616A1 (de) * | 1979-05-28 | 1980-12-11 | Basf Ag | Verwendung einer speziellen polyolefin-formmasse zum herstellen von folien nach dem folienblasverfahren |
DE2921648A1 (de) * | 1979-05-28 | 1980-12-11 | Basf Ag | Verwendung einer speziellen polyolefin-formmasse zum herstellen von folien nach dem folienblasverfahren |
DE2940548A1 (de) * | 1979-10-06 | 1981-04-16 | Hoechst Ag, 6000 Frankfurt | Kristallisiertes tris-(2-tert.-butylphenyl)-phosphit und verfahren zu seiner herstellung |
JPS573842A (en) * | 1980-06-10 | 1982-01-09 | Sumitomo Chem Co Ltd | Stabilized polyolefin composition |
DE3029176C2 (de) * | 1980-08-01 | 1995-02-02 | Hoechst Ag | Migrationsfeste, polymere, aromatische Phosphite |
US4384062A (en) * | 1980-10-01 | 1983-05-17 | Uniroyal, Inc. | Hydrolytically stable diphosphites useful as antioxidants |
JPS57143351A (en) * | 1981-03-02 | 1982-09-04 | Tokuyama Soda Co Ltd | Thermoplastic resin composition |
JPS57179234A (en) * | 1981-04-28 | 1982-11-04 | Nippon Chibagaigii Kk | Radiation resistant polyolefin composition |
US4755546A (en) * | 1981-05-11 | 1988-07-05 | Borg-Warner Chemicals, Inc. | Stabilized olefin polymers |
JPS57200455A (en) * | 1981-06-05 | 1982-12-08 | Tokuyama Soda Co Ltd | Thermoplastic resin composition |
CA1190692A (en) * | 1982-02-09 | 1985-07-16 | Du Pont Canada Inc. | Polyethylene compositions for rotational moulding processes |
DE3408948C2 (de) * | 1983-03-21 | 1995-07-27 | Sandoz Ag | 4-Amino-polyalkylpiperidinverbindungen |
JPS61113631A (ja) * | 1984-11-07 | 1986-05-31 | Adeka Argus Chem Co Ltd | ポリオレフイン樹脂組成物 |
JPH0759652B2 (ja) * | 1985-08-07 | 1995-06-28 | 住友化学工業株式会社 | ポリオレフイン樹脂組成物 |
JPS6286036A (ja) * | 1985-10-12 | 1987-04-20 | Sumitomo Chem Co Ltd | ポリオレフイン組成物 |
DE3688241T2 (de) * | 1985-11-29 | 1993-09-16 | Ge Specialty Chem | Stabilisatorgemische auf phosphitbasis. |
CA1326094C (en) * | 1986-12-11 | 1994-01-11 | Thomas Max Chucta | Polyolefins stabilized against oxidative degradation with mixtures of aralkyl-substituted diarylamines and sterically hindered phosphites |
US4888369A (en) * | 1987-01-21 | 1989-12-19 | Himont Incorporated | Polypropylene composition resistant to high energy radiation, and radiation sterilized articles therefrom |
GB8710171D0 (en) * | 1987-04-29 | 1987-06-03 | Shell Int Research | Copolymer composition |
US4814367A (en) * | 1987-07-30 | 1989-03-21 | Argus Chemical Corporation | Stabilizing high density polyethylene containing chromium catalyst residues with 2,2'-ethylidene-bis(4,6-di-t-butylphenol), a solid polyol having five to six carbon atoms, and a tris(alkylaryl) phosphite |
IT1215943B (it) * | 1988-02-24 | 1990-02-22 | Enichem Sintesi | Composizione stabilizzante per polimeri organici. |
ES2032649T3 (es) | 1988-12-21 | 1993-02-16 | Hoechst Aktiengesellschaft | Procedimiento para preparar derivados organicos fosforados del 2,4-di-t-butilfenol, los compuestos de 4,4'-dihalogenomagnesio de bifenilo, y la utilizacion de los derivados organicos fosforados para estabilizar materiales sinteticos, especialmente en masas de moldeo poliolefinas |
FR2647800A1 (fr) * | 1989-05-31 | 1990-12-07 | Organo Synthese Ste Fse | Phosphite de tris(ditertiobutyl-2,4 phenyle) presentant des proprietes physiques ameliorees |
IT1231769B (it) * | 1989-08-02 | 1991-12-21 | Himont Inc | Procedimento per la stabilizzazione di poliolefine e prodotti da esso ottenuti. |
MY106664A (en) * | 1990-02-27 | 1995-07-31 | Mitsui Chemicals Inc | Ethylene-pentene-1 copolymer, process for the preparation of the same, and ethylene/pentene-1 copolymer composition. |
GB2252324A (en) * | 1990-12-20 | 1992-08-05 | Bp Chem Int Ltd | Stabilizer composition |
TW254955B (de) * | 1992-09-25 | 1995-08-21 | Ciba Geigy | |
DE4240694A1 (de) * | 1992-12-03 | 1994-06-09 | Basf Ag | Verfahren zur Stabilisierung von Polyethylengrieß |
BE1007888A3 (fr) * | 1993-12-27 | 1995-11-14 | Solvay | Procede continu de greffage d'une polyolefine, les polyolefines greffees obtenues au moyen de ce procede. |
ES2164131T3 (es) | 1994-12-27 | 2002-02-16 | Solvay | Composicion de polimero de etileno. |
EP0734031B1 (de) * | 1995-03-24 | 2004-06-09 | TDK Corporation | Vielschichtvaristor |
EP0781803A1 (de) | 1995-12-29 | 1997-07-02 | General Electric Company | Stabilisierte thermoplastische Polymerzusammensetzung |
US6613823B1 (en) * | 1998-10-21 | 2003-09-02 | Phillips Petroleum Company | Phosphite additives in polyolefins |
BE1012638A3 (fr) | 1999-04-29 | 2001-01-09 | Solvay | Compositions de polyolefines, procede pour leur preparation et utilisation de celles-ci. |
JP4833436B2 (ja) * | 2001-05-17 | 2011-12-07 | 東洋ゴム工業株式会社 | タイヤコード被覆用ゴム組成物 |
CN1302058C (zh) * | 2002-05-27 | 2007-02-28 | 大湖化学公司欧洲分公司 | 稳定化的聚丙烯 |
US20060128849A1 (en) * | 2003-06-19 | 2006-06-15 | Franco Sartori | Olefin polymers with stabilisers and polyolefin fibres produced therefrom |
US7157511B2 (en) * | 2003-11-21 | 2007-01-02 | Chevron Phillipschemical Company Lp | Phosphite additives in polyolefins |
CN101331185B (zh) * | 2005-12-14 | 2012-09-05 | 巴塞尔聚烯烃意大利有限责任公司 | 用于生产含乙烯-乙烯醇共聚物的聚烯烃模制品的方法 |
US7888414B2 (en) † | 2006-06-20 | 2011-02-15 | Chemtura Corporation | Liquid phosphite blends as stabilizers |
US8183311B2 (en) * | 2006-06-20 | 2012-05-22 | Chemtura Corporation | Liquid phosphite composition derived from cresols |
US8815990B2 (en) | 2009-04-24 | 2014-08-26 | Sumitomo Chemical Company, Limited | Stabilizer composition |
CN102686662B (zh) | 2009-12-22 | 2015-11-25 | 巴塞尔聚烯烃意大利有限责任公司 | 用于膜的聚烯烃组合物 |
WO2011129396A1 (ja) | 2010-04-14 | 2011-10-20 | 住友化学株式会社 | 熱可塑性ポリマー組成物および安定剤組成物 |
US20130035427A1 (en) | 2010-04-14 | 2013-02-07 | Sumitomo Chemical Company, Limited | Thermoplastic polymer composition and processing stabiliser |
EP2559735A1 (de) | 2010-04-14 | 2013-02-20 | Sumitomo Chemical Company Limited | Thermoplastische polymerzusammensetzung und verarbeitungsstabilisator dafür |
JP2012107182A (ja) * | 2010-05-12 | 2012-06-07 | Sumitomo Chemical Co Ltd | 熱可塑性ポリマー組成物 |
JP5712070B2 (ja) * | 2010-06-28 | 2015-05-07 | 住友化学株式会社 | 熱可塑性ポリマー組成物および加工安定化剤 |
TW201204775A (en) * | 2010-06-28 | 2012-02-01 | Sumitomo Chemical Co | Thermoplastic polymer composition and process stabilizing agent |
JP5712069B2 (ja) * | 2010-06-28 | 2015-05-07 | 住友化学株式会社 | 熱可塑性ポリマー組成物および加工安定化剤 |
JP5712068B2 (ja) * | 2010-06-28 | 2015-05-07 | 住友化学株式会社 | 熱可塑性ポリマー組成物および加工安定化剤 |
JP5781807B2 (ja) * | 2010-06-29 | 2015-09-24 | 住友化学株式会社 | 熱可塑性ポリマー組成物 |
EP3591001A1 (de) * | 2014-11-20 | 2020-01-08 | Cytec Industries Inc. | Stabilisatorzusammensetzungen und verfahren zur verwendung davon zum schutz organischer materialien vor uv-licht und thermischem abbau |
JP6578117B2 (ja) * | 2015-03-27 | 2019-09-18 | ホーユー株式会社 | エアゾール容器用吐出具 |
GB201812145D0 (en) | 2018-07-25 | 2018-09-05 | Addivant Switzerland Gmbh | Composition |
GB2591482A (en) | 2020-01-29 | 2021-08-04 | Si Group Switzerland Chaa Gmbh | Non-dust blend |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3558554A (en) * | 1966-06-09 | 1971-01-26 | Yoshitomi Pharmaceutical | Oxidatively stable polyolefin composition |
DE1593946A1 (de) * | 1966-05-11 | 1971-02-25 | Nat Polychemicals Inc | Verfaerbungsinhibierung von Alkylphenol-Produkten |
Family Cites Families (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1065170B (de) * | 1956-01-20 | 1959-09-10 | Petrochemicals Limited, London | Verfahren zur Stabilisierung von Polyolefinen oder Mischpolymerisaten aus niedermolekularen Olefinen |
US2915496A (en) * | 1957-05-20 | 1959-12-01 | Gen Tire & Rubber Co | Stability of polyether glycol urethane products |
US2997454A (en) * | 1959-05-18 | 1961-08-22 | Argus Chem | Polyvinyl chloride stabilizer combinations of phosphorus acid with triphosphites andheavy metal salts |
BE595794A (de) | 1959-09-02 | |||
DE1183504B (de) * | 1960-04-11 | 1964-12-17 | Ethyl Corp | Verwendung von synergistisch wirkenden Gemischen aus Phosphitestern und Methylenbisphenolen zum Stabilisieren von Motorentreibstoffen, Schmiermitteln und hoehermolekularen oder polymeren Kohlenwasserstoffen gegen Autoxydation in der Waerme |
US3115465A (en) * | 1960-04-11 | 1963-12-24 | Ethyl Corp | Stabilized compositions of matter |
US3039993A (en) * | 1960-05-10 | 1962-06-19 | Weston Chemical Corp | Polyethylene stabilizers |
US3080338A (en) * | 1960-06-15 | 1963-03-05 | Texas Us Chem Co | Diene rubbers stabilized with organic phosphites and phenols |
NL274762A (de) * | 1961-02-15 | |||
GB1078772A (en) * | 1963-07-15 | 1967-08-09 | Union Carbide Corp | Anti-oxidants |
NL130435C (de) * | 1963-08-30 | |||
US3364169A (en) * | 1963-12-16 | 1968-01-16 | Allied Chem | Polyolefin stabilizer composition |
US3330887A (en) * | 1964-05-28 | 1967-07-11 | Firestone Tire & Rubber Co | Reaction product of an alkylated phenol and a phosphate and process for making same |
DE1224925B (de) * | 1964-10-03 | 1966-09-15 | Hoechst Ag | Verfahren zum Stabilisieren von fluessigen AEthylenpolymerisaten |
US3305520A (en) * | 1965-04-06 | 1967-02-21 | Bayer Ag | Polycarbonates stabilized by phosphites |
US3489702A (en) * | 1965-05-28 | 1970-01-13 | Argus Chem | Enhancement of resistance of ethylene sulfide polymers to heat deterioration |
US3412064A (en) * | 1965-11-08 | 1968-11-19 | Uniroyal Inc | Olefin polymer composition |
US3409587A (en) * | 1966-08-05 | 1968-11-05 | Phillips Petroleum Co | Antioxidant system for polyolefins |
NL133660C (de) | 1965-12-27 | |||
FR1545567A (fr) * | 1965-12-27 | 1968-11-15 | Phillips Petroleum Co | Procédé de stabilisation de polymères de 1-oléfines, système stabilisateur phénolique et polymères stabilisés ainsi obtenus |
US3533989A (en) * | 1967-03-15 | 1970-10-13 | Exxon Research Engineering Co | Phosphite antioxidants in polyolefins |
US3554964A (en) | 1967-10-19 | 1971-01-12 | Goodyear Tire & Rubber | Stabilization systems for polymers |
US3677965A (en) * | 1967-12-29 | 1972-07-18 | Geigy Chem Corp | Alkylhydroxyphenyl polyamides as antioxidants |
US3531483A (en) * | 1968-10-25 | 1970-09-29 | Goodrich Co B F | Hydroxyphenylalkyleneyl isocyanurates |
US3595936A (en) * | 1969-04-29 | 1971-07-27 | Allied Chem | Filament comprising a polymer blend of polyester and polyamide containing an organic phosphorus compound and a sterically hindered phenolic compound |
GB1307281A (en) * | 1970-02-13 | 1973-02-14 | Ici Ltd | Rubber-polyester compositions |
US3661825A (en) | 1970-04-21 | 1972-05-09 | Goodyear Tire & Rubber | Stabilization systems for polymers |
US3658743A (en) * | 1970-04-30 | 1972-04-25 | Uniroyal Inc | Stabilization of unsaturated hydrocarbon elastomers by synergistic combination of a phenolic compound an organic sulfide or thioester and an epoxide or phosphite ester |
JPS5142617B2 (de) * | 1971-11-12 | 1976-11-17 | ||
GB1392365A (en) * | 1971-11-29 | 1975-04-30 | Weston Chemical Corp | Friable distearyl pentaerythitol diphosphite |
DE2300348A1 (de) * | 1972-01-19 | 1973-07-26 | M & T Chemicals Inc | Stabilisator fuer halogenhaltige flammhemmende mittel |
JPS5230172B2 (de) * | 1973-06-23 | 1977-08-06 | ||
JPS5021041A (de) * | 1973-06-25 | 1975-03-06 | ||
DE2334163A1 (de) * | 1973-07-05 | 1975-01-30 | Bayer Ag | Nicht verfaerbende stabilisierungsmittel |
US3886114A (en) * | 1973-08-24 | 1975-05-27 | Vanderbilt Co R T | Synergistic antioxidant combination |
SE7500057L (de) * | 1974-01-21 | 1975-07-22 | Ciba Geigy Ag |
-
1976
- 1976-02-18 CA CA246,043A patent/CA1078991A/en not_active Expired
- 1976-02-18 DE DE19762606358 patent/DE2606358C3/de not_active Expired
- 1976-02-18 GB GB6460/76A patent/GB1490938A/en not_active Expired
- 1976-02-18 NL NL7601652A patent/NL191566C/xx not_active IP Right Cessation
- 1976-02-18 BR BR7601007A patent/BR7601007A/pt unknown
- 1976-02-18 DE DE19762660746 patent/DE2660746C3/de not_active Expired - Lifetime
- 1976-02-19 AU AU11235/76A patent/AU498192B2/en not_active Expired
- 1976-02-19 IT IT20345/76A patent/IT1062063B/it active
- 1976-02-19 ES ES445315A patent/ES445315A1/es not_active Expired
- 1976-02-19 FR FR7604556A patent/FR2301558A1/fr active Granted
- 1976-02-19 SE SE7601955A patent/SE423634B/xx unknown
- 1976-02-20 JP JP1780976A patent/JPS565417B2/ja not_active Expired
-
1979
- 1979-08-24 US US06/069,480 patent/US4290941A/en not_active Expired - Lifetime
-
1980
- 1980-08-21 HK HK446/80A patent/HK44680A/xx unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1593946A1 (de) * | 1966-05-11 | 1971-02-25 | Nat Polychemicals Inc | Verfaerbungsinhibierung von Alkylphenol-Produkten |
US3558554A (en) * | 1966-06-09 | 1971-01-26 | Yoshitomi Pharmaceutical | Oxidatively stable polyolefin composition |
Also Published As
Publication number | Publication date |
---|---|
JPS51109050A (de) | 1976-09-27 |
JPS565417B2 (de) | 1981-02-04 |
DE2606358C3 (de) | 1986-12-04 |
NL7601652A (nl) | 1976-08-24 |
NL191566C (nl) | 1995-09-19 |
AU498192B2 (en) | 1979-02-15 |
SE7601955L (sv) | 1976-08-23 |
BR7601007A (pt) | 1976-09-14 |
CA1078991A (en) | 1980-06-03 |
SE423634B (sv) | 1982-05-17 |
GB1490938A (en) | 1977-11-02 |
DE2660746C3 (de) | 1993-07-15 |
IT1062063B (it) | 1983-06-25 |
AU1123576A (en) | 1977-08-25 |
NL191566B (nl) | 1995-05-16 |
FR2301558A1 (fr) | 1976-09-17 |
ES445315A1 (es) | 1984-05-01 |
US4290941A (en) | 1981-09-22 |
FR2301558B1 (de) | 1979-02-02 |
HK44680A (en) | 1980-08-29 |
DE2606358A1 (de) | 1976-09-02 |
DE2606358C2 (de) | 1982-12-30 |
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