SK284469B6 - Synergické zmesi stabilizátorov, kompozície, ktoré ich obsahujú a ich použitie na stabilizáciu organických materiálov - Google Patents

Synergické zmesi stabilizátorov, kompozície, ktoré ich obsahujú a ich použitie na stabilizáciu organických materiálov Download PDF

Info

Publication number: SK284469B6
Authority: SK; Slovakia
Prior art keywords: group; compound; tert; carbon atoms; component
Prior art date: 1995-01-23

Application number

SK88-96A

Other languages

English (en)

Slovak (sk)

Other versions

SK8896A3 (en

Inventor

Fran�Ois Gugumus

Original Assignee

Ciba Specialty Chemicals Holding Inc.

Priority date (The priority date 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 date listed.)

1995-01-23

Filing date

1996-01-22

Publication date

2005-04-01

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=8221688&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK284469(B6) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1996-01-22 Application filed by Ciba Specialty Chemicals Holding Inc. filed Critical Ciba Specialty Chemicals Holding Inc.

1997-03-05 Publication of SK8896A3 publication Critical patent/SK8896A3/sk

2005-04-01 Publication of SK284469B6 publication Critical patent/SK284469B6/sk

Links

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LRUUZFQPCUFYPV-UHFFFAOYSA-N n-dodecyldodecan-1-imine oxide Chemical compound CCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCC LRUUZFQPCUFYPV-UHFFFAOYSA-N 0.000 description 1
GBMIPYGHTZRCRH-UHFFFAOYSA-N n-ethylethanimine oxide Chemical compound CC[N+]([O-])=CC GBMIPYGHTZRCRH-UHFFFAOYSA-N 0.000 description 1
DBCWENWKZARTGU-UHFFFAOYSA-N n-heptadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+]([O-])CCCCCCCCCCCCCCCCC DBCWENWKZARTGU-UHFFFAOYSA-N 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
GCDJFNYVSDFWDB-UHFFFAOYSA-N n-hexadecylhexadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCC GCDJFNYVSDFWDB-UHFFFAOYSA-N 0.000 description 1
FHAFFFSIDLDWQA-UHFFFAOYSA-N n-hexadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+]([O-])CCCCCCCCCCCCCCCC FHAFFFSIDLDWQA-UHFFFAOYSA-N 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
LVZUNTGFCXNQAF-UHFFFAOYSA-N n-nonyl-n-phenylaniline Chemical class C=1C=CC=CC=1N(CCCCCCCCC)C1=CC=CC=C1 LVZUNTGFCXNQAF-UHFFFAOYSA-N 0.000 description 1
ZXGDIORKSOYRMQ-UHFFFAOYSA-N n-octadecylheptadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCCC ZXGDIORKSOYRMQ-UHFFFAOYSA-N 0.000 description 1
MCMMSXFAWOGWQE-UHFFFAOYSA-N n-octadecylhexadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCC MCMMSXFAWOGWQE-UHFFFAOYSA-N 0.000 description 1
HORBOHJHQGXXOR-UHFFFAOYSA-N n-octadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCCCC HORBOHJHQGXXOR-UHFFFAOYSA-N 0.000 description 1
QXJGVICBAANVMZ-UHFFFAOYSA-N n-octyloctan-1-imine oxide Chemical compound CCCCCCCC[N+]([O-])=CCCCCCCC QXJGVICBAANVMZ-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
CVVFFUKULYKOJR-UHFFFAOYSA-N n-phenyl-4-propan-2-yloxyaniline Chemical compound C1=CC(OC(C)C)=CC=C1NC1=CC=CC=C1 CVVFFUKULYKOJR-UHFFFAOYSA-N 0.000 description 1
NYLGUNUDTDWXQE-UHFFFAOYSA-N n-phenyl-n-prop-2-enylaniline Chemical compound C=1C=CC=CC=1N(CC=C)C1=CC=CC=C1 NYLGUNUDTDWXQE-UHFFFAOYSA-N 0.000 description 1
SLYJXPKHTZCZOG-UHFFFAOYSA-N n-tetradecyltetradecan-1-imine oxide Chemical compound CCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCC SLYJXPKHTZCZOG-UHFFFAOYSA-N 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
229930014626 natural product Natural products 0.000 description 1
150000002816 nickel compounds Chemical class 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
IXVLEAZXSJJKFR-UHFFFAOYSA-N octadecyl 2-[(4-hydroxy-3,5-dimethylphenyl)methylsulfanyl]acetate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CSCC1=CC(C)=C(O)C(C)=C1 IXVLEAZXSJJKFR-UHFFFAOYSA-N 0.000 description 1
RNVAPPWJCZTWQL-UHFFFAOYSA-N octadecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 RNVAPPWJCZTWQL-UHFFFAOYSA-N 0.000 description 1
125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 1
XQAABEDPVQWFPN-UHFFFAOYSA-N octyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=CC=CC3=N2)=C1O XQAABEDPVQWFPN-UHFFFAOYSA-N 0.000 description 1
DMFXLIFZVRXRRR-UHFFFAOYSA-N octyl 3-[3-tert-butyl-5-(5-chlorobenzotriazol-2-yl)-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O DMFXLIFZVRXRRR-UHFFFAOYSA-N 0.000 description 1
NTTIENRNNNJCHQ-UHFFFAOYSA-N octyl n-(3,5-ditert-butyl-4-hydroxyphenyl)carbamate Chemical compound CCCCCCCCOC(=O)NC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NTTIENRNNNJCHQ-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229950000688 phenothiazine Drugs 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
ZPNJBTBYIHBSIG-UHFFFAOYSA-N phenyl-(2,2,6,6-tetramethylpiperidin-4-yl)methanone Chemical compound C1C(C)(C)NC(C)(C)CC1C(=O)C1=CC=CC=C1 ZPNJBTBYIHBSIG-UHFFFAOYSA-N 0.000 description 1
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
239000011990 phillips catalyst Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
239000012994 photoredox catalyst Substances 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001627 poly(4-methyl styrene) Polymers 0.000 description 1
229920001084 poly(chloroprene) Polymers 0.000 description 1
229920003055 poly(ester-imide) Polymers 0.000 description 1
229920001643 poly(ether ketone) Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002492 poly(sulfone) Polymers 0.000 description 1
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
229920003251 poly(α-methylstyrene) Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920002312 polyamide-imide Polymers 0.000 description 1
229920002480 polybenzimidazole Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920006393 polyether sulfone Polymers 0.000 description 1
229920001601 polyetherimide Polymers 0.000 description 1
229940068886 polyethylene glycol 300 Drugs 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920000069 polyphenylene sulfide Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
239000006254 rheological additive Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
239000005060 rubber Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000565 sealant Substances 0.000 description 1
229940116351 sebacate Drugs 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
235000010234 sodium benzoate Nutrition 0.000 description 1
239000004299 sodium benzoate Substances 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
IJRHDFLHUATAOS-DPMBMXLASA-M sodium ricinoleate Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O IJRHDFLHUATAOS-DPMBMXLASA-M 0.000 description 1
229940074404 sodium succinate Drugs 0.000 description 1
ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000009987 spinning Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229920006132 styrene block copolymer Polymers 0.000 description 1
239000011115 styrene butadiene Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 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
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
229960000984 tocofersolan Drugs 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
235000019149 tocopherols Nutrition 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
125000005591 trimellitate group Chemical group 0.000 description 1
CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920006337 unsaturated polyester resin Polymers 0.000 description 1
125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
229920001866 very low density polyethylene Polymers 0.000 description 1
235000019154 vitamin C Nutrition 0.000 description 1
239000011718 vitamin C Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003751 zinc Chemical class 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
239000002076 α-tocopherol Substances 0.000 description 1
235000004835 α-tocopherol Nutrition 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
239000002446 δ-tocopherol Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/35—Heterocyclic compounds having nitrogen in the ring having also oxygen in the ring
- C08K5/353—Five-membered rings

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)
Plural Heterocyclic Compounds (AREA)

SK88-96A 1995-01-23 1996-01-22 Synergické zmesi stabilizátorov, kompozície, ktoré ich obsahujú a ich použitie na stabilizáciu organických materiálov SK284469B6 (sk)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP95810042		1995-01-23

Publications (2)

Publication Number	Publication Date
SK8896A3 SK8896A3 (en)	1997-03-05
SK284469B6 true SK284469B6 (sk)	2005-04-01

Family

ID=8221688

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK88-96A SK284469B6 (sk)	1995-01-23	1996-01-22	Synergické zmesi stabilizátorov, kompozície, ktoré ich obsahujú a ich použitie na stabilizáciu organických materiálov

Country Status (13)

Country	Link
US (3)	US6015849A (ja)
EP (1)	EP0723990B1 (ja)
JP (1)	JP3975410B2 (ja)
KR (1)	KR100378236B1 (ja)
CN (1)	CN1082066C (ja)
BR (1)	BR9600195A (ja)
CA (1)	CA2167660C (ja)
DE (1)	DE59611198D1 (ja)
ES (1)	ES2236728T3 (ja)
MX (1)	MXPA96000326A (ja)
SK (1)	SK284469B6 (ja)
TW (1)	TW357174B (ja)
ZA (1)	ZA96476B (ja)

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TW358820B (en) *	1995-04-11	1999-05-21	Ciba Sc Holding Ag	Synergistic stabilizer mixture
TW464670B (en) *	1996-08-07	2001-11-21	Ciba Sc Holding Ag	Stabilizer mixtures containing a hindered amine
US5807635A (en) *	1997-01-24	1998-09-15	Union Carbide Chemicals & Plastics Technology Corporation	Telephone cables
DE19820157B4 (de) *	1997-05-13	2010-04-08	Clariant Produkte (Deutschland) Gmbh	Neue Verbindungen auf Basis von Polyalkyl-1-oxa-diazaspirodecan-Verbindungen
US6353042B1 (en)	1997-07-24	2002-03-05	Evergreen Solar, Inc.	UV-light stabilization additive package for solar cell module and laminated glass applications
CN1280576A (zh) *	1997-12-08	2001-01-17	Cytec技术有限公司	吗啉代封端的受阻胺取代的氨基三嗪和其作为光稳定剂的应用
DE19804910A1 (de) *	1998-02-07	1999-08-12	Clariant Gmbh	Polyolefin-Formmasse zur Herstellung von kalandrierten Folien/Platten
ITMI980366A1 (it)	1998-02-25	1999-08-25	Ciba Spec Chem Spa	Preparazione di eteri amminici stericamente impediti
IL133922A (en)	1999-02-01	2005-03-20	Ciba Sc Holding Ag	Compositions comprising polyolefins produced by polymerization over a metallocene catalyst and a stabilizer mixture and a method for stabilizing said polyolefins
US6946517B2 (en) *	1999-08-17	2005-09-20	Ciba Specialty Chemicals Corporation	Stabilizer mixtures
DE10004158A1 (de)	2000-02-01	2001-08-02	Basf Ag	Stabilisatorzusammensetzung
KR100727524B1 (ko)	2000-02-22	2007-06-14	시바 스폐셜티 케미칼스 홀딩 인코포레이티드	폴리올레핀용 안정화제 혼합물
GB2378952B (en) *	2000-05-31	2004-04-21	Ciba Sc Holding Ag	Stabiliser mixtures
DE10196264T1 (de) *	2000-05-31	2003-05-15	Ciba Sc Holding Ag	Stabilisatorgemische
TW572952B (en) *	2000-05-31	2004-01-21	Ciba Sc Holding Ag	Stabilizer mixtures
DE10196267T1 (de) *	2000-05-31	2003-05-15	Ciba Sc Holding Ag	Stabilisatorgemische
ITMI20012085A1 (it)	2000-10-17	2003-04-09	Ciba Sc Holding Ag	Polpropilene metallocene stabilizzato
US20030225191A1 (en) *	2002-04-12	2003-12-04	Francois Gugumus	Stabilizer mixtures
MXPA06005663A (es) *	2003-11-21	2006-08-17	Ciba Sc Holding Ag	Poliestireno pigmentado firme a la intemperie.
US20080070146A1 (en) *	2006-09-15	2008-03-20	Cabot Corporation	Hydrophobic-treated metal oxide
EP3143082B1 (en) *	2014-05-15	2020-11-18	Basf Se	Highly effective stabilizer
CN106589514B (zh) *	2015-10-20	2020-03-24	天罡新材料（廊坊）股份有限公司	一种光稳定剂组合物母粒及其制备方法和应用
CN110724331B (zh) *	2018-07-16	2022-04-08	中国石油化工股份有限公司	适用于高速加工的电缆护套用聚乙烯组合物及其制备方法
CN110724334B (zh) *	2018-07-16	2022-04-08	中国石油化工股份有限公司	具有优异耐慢速裂纹增长性能的耐热聚乙烯组合物及其制备方法
CN110724332B (zh) *	2018-07-16	2022-04-08	中国石油化工股份有限公司	综合性能优异的双壁波纹管用聚乙烯组合物及其制备方法
EP3786242A1 (en) *	2019-08-27	2021-03-03	Nitto Belgium N.V	Pressure-sensitive adhesive sheet with improved weatherability
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1996
- 1996-01-13 TW TW085100385A patent/TW357174B/zh not_active IP Right Cessation
- 1996-01-15 EP EP19960810031 patent/EP0723990B1/de not_active Revoked
- 1996-01-15 DE DE59611198T patent/DE59611198D1/de not_active Expired - Lifetime
- 1996-01-15 ES ES96810031T patent/ES2236728T3/es not_active Expired - Lifetime
- 1996-01-19 CA CA002167660A patent/CA2167660C/en not_active Expired - Lifetime
- 1996-01-22 ZA ZA96476A patent/ZA96476B/xx unknown
- 1996-01-22 SK SK88-96A patent/SK284469B6/sk not_active IP Right Cessation
- 1996-01-23 JP JP02855796A patent/JP3975410B2/ja not_active Expired - Lifetime
- 1996-01-23 KR KR1019960001330A patent/KR100378236B1/ko not_active IP Right Cessation
- 1996-01-23 CN CN96100663A patent/CN1082066C/zh not_active Expired - Lifetime
- 1996-01-23 MX MXPA96000326A patent/MXPA96000326A/es active IP Right Grant
- 1996-01-23 BR BR9600195A patent/BR9600195A/pt not_active IP Right Cessation
1997
- 1997-04-21 US US08/858,191 patent/US6015849A/en not_active Expired - Lifetime
1999
- 1999-03-24 US US09/275,859 patent/US6380286B1/en not_active Expired - Lifetime
2002
- 2002-02-22 US US10/081,291 patent/US7884147B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
TW357174B (en)	1999-05-01
ZA96476B (en)	1996-07-23
JPH08239511A (ja)	1996-09-17
SK8896A3 (en)	1997-03-05
CA2167660A1 (en)	1996-07-24
CN1082066C (zh)	2002-04-03
EP0723990B1 (de)	2005-02-23
EP0723990A1 (de)	1996-07-31
BR9600195A (pt)	1997-10-07
CN1137541A (zh)	1996-12-11
US6380286B1 (en)	2002-04-30
KR960029430A (ko)	1996-08-17
US6015849A (en)	2000-01-18
JP3975410B2 (ja)	2007-09-12
KR100378236B1 (ko)	2003-06-11
CA2167660C (en)	2007-06-19
ES2236728T3 (es)	2005-07-16
DE59611198D1 (de)	2005-03-31
MXPA96000326A (es)	2005-04-19
US7884147B2 (en)	2011-02-08
US20020120042A1 (en)	2002-08-29

Publication	Publication Date	Title
SK284469B6 (sk)	2005-04-01	Synergické zmesi stabilizátorov, kompozície, ktoré ich obsahujú a ich použitie na stabilizáciu organických materiálov
SK281600B6 (sk)	2001-05-10	Synergické zmesi stabilizátorov, prostriedky, ktoré ich obsahujú a ich použitie na stabilizáciu organických materiálov
JP4114177B2 (ja)	2008-07-09	相乗安定剤混合物
SK283984B6 (sk)	2004-06-08	Zmes blokových oligomérov obsahujúca 2,2,6,6-tetrametyl-4- piperidylové skupiny, spôsob jej prípravy, kompozícia stabilizovaná touto zmesou a spôsob stabilizácie organického materiálu použitím tejto zmesi
SK285104B6 (sk)	2006-06-01	Synergická stabilizátorová zmes, kompozícia s jej obsahom a spôsob stabilizácie organického materiálu
SK284174B6 (sk)	2004-10-05	Synergická zmes stabilizátorov, kompozícia obsahujúca túto zmes a organický materiál a použitie tejto zmesi
US5616780A (en)	1997-04-01	Bisphenol ester derivatives
BE1011448A3 (fr)	1999-09-07	Melange stabilisant, composition le contenant et procede l'utilisant pour stabiliser une polyolefine.
JPH11193381A (ja)	1999-07-21	有機材料のための安定剤混合物
JPH0931456A (ja)	1997-02-04	相乗的安定剤混合物
FR2809740A1 (fr)	2001-12-07	Melanges de stabilisants
KR100786241B1 (ko)	2007-12-17	안정화제 혼합물
KR100452336B1 (ko)	2004-12-23	2,4-디메틸-6-s-알킬페놀과입체장애페놀로구성된상승작용혼합물
KR19980018297A (ko)	1998-06-05	안정화제 혼합물
KR100705557B1 (ko)	2007-04-10	안정화제 혼합물
SK138995A3 (en)	1996-07-03	2,2,6,6-tetramethylpiperidine derivatives and their use as stabilizer of organic materials against effect of the light, heat and oxidation
US6328912B1 (en)	2001-12-11	Tetramethylpiperidyl-containing polysiloxane or polyamine/cyanuric cl/tetramethyl-4-piperidylamine stabilizer
EP0835873A1 (en)	1998-04-15	Mixtures of trisubstituted and tetrasubstituted polyalkylpiperidinylaminotriazine tetraamine compounds
KR19980032710A (ko)	1998-07-25	삼치환 및 사치환 폴리알킬피페리디닐아미노트리아진 테트라아민 화합물의 혼합물

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2016-03-01	MK4A	Expiry of patent	Expiry date: 20160122