SU539537A3 - Стабилизированна композици на основе синтетического полимера - Google Patents
Стабилизированна композици на основе синтетического полимераInfo
- Publication number
- SU539537A3 SU539537A3 SU2021234A SU2021234A SU539537A3 SU 539537 A3 SU539537 A3 SU 539537A3 SU 2021234 A SU2021234 A SU 2021234A SU 2021234 A SU2021234 A SU 2021234A SU 539537 A3 SU539537 A3 SU 539537A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- group
- tetramethylpiperidine
- formula
- alkylene
- substituted
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 18
- 229920001059 synthetic polymer Polymers 0.000 title claims description 12
- -1 1-substituted piperidine Chemical class 0.000 claims description 27
- 125000002947 alkylene group Chemical group 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 claims description 2
- 125000004450 alkenylene group Chemical group 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 125000006839 xylylene group Chemical group 0.000 claims description 2
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical group [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 claims 2
- 241001122767 Theaceae Species 0.000 claims 1
- 230000006378 damage Effects 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 description 25
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 20
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 230000032683 aging Effects 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 238000012360 testing method Methods 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 3
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920002292 Nylon 6 Polymers 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 150000001993 dienes Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- OBPPFQMNVVRUAO-UHFFFAOYSA-N ethyl 2-(2,2,6,6-tetramethylpiperidin-1-yl)acetate Chemical compound CCOC(=O)CN1C(C)(C)CCCC1(C)C OBPPFQMNVVRUAO-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- XHRZKYNDTBJUEQ-SOFGYWHQSA-N (e)-1-(2,2,6,6-tetramethylpiperidin-1-yl)but-2-en-1-one Chemical compound C\C=C\C(=O)N1C(C)(C)CCCC1(C)C XHRZKYNDTBJUEQ-SOFGYWHQSA-N 0.000 description 1
- YAXWOADCWUUUNX-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidine Chemical compound CC1CCCN(C)C1(C)C YAXWOADCWUUUNX-UHFFFAOYSA-N 0.000 description 1
- XSSNQTNFUAJWMT-UHFFFAOYSA-N 1-(2,2,6,6-tetramethylpiperidin-1-yl)ethanone Chemical compound CC(=O)N1C(C)(C)CCCC1(C)C XSSNQTNFUAJWMT-UHFFFAOYSA-N 0.000 description 1
- BEQRAXVKXWIKMR-UHFFFAOYSA-N 1-(2,2,6,6-tetramethylpiperidin-1-yl)prop-2-en-1-one Chemical compound CC1(C)CCCC(C)(C)N1C(=O)C=C BEQRAXVKXWIKMR-UHFFFAOYSA-N 0.000 description 1
- VHBKAFDIYYVORD-UHFFFAOYSA-N 1-(2,2,6,6-tetramethylpiperidin-1-yl)propan-2-yl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC(C)CN1C(C)(C)CCCC1(C)C VHBKAFDIYYVORD-UHFFFAOYSA-N 0.000 description 1
- PUJOWDGGIRODQT-UHFFFAOYSA-N 1-[(2-chlorophenyl)methyl]-2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1CC1=CC=CC=C1Cl PUJOWDGGIRODQT-UHFFFAOYSA-N 0.000 description 1
- BSSPSGCZOKGRCX-UHFFFAOYSA-N 1-benzyl-2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1CC1=CC=CC=C1 BSSPSGCZOKGRCX-UHFFFAOYSA-N 0.000 description 1
- ITGFCLVROZZDJT-UHFFFAOYSA-N 1-but-2-enyl-2,2,6,6-tetramethylpiperidine Chemical compound CC=CCN1C(C)(C)CCCC1(C)C ITGFCLVROZZDJT-UHFFFAOYSA-N 0.000 description 1
- WRBGFIRROIPTIY-UHFFFAOYSA-N 1-butyl-2,2,6,6-tetramethylpiperidine Chemical compound CCCCN1C(C)(C)CCCC1(C)C WRBGFIRROIPTIY-UHFFFAOYSA-N 0.000 description 1
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 1
- KAPBNXIQDUKTCP-UHFFFAOYSA-N 1-phenyl-2-(2,2,6,6-tetramethylpiperidin-1-yl)ethanol Chemical compound CC1(C)CCCC(C)(C)N1CC(O)C1=CC=CC=C1 KAPBNXIQDUKTCP-UHFFFAOYSA-N 0.000 description 1
- PZXHNHXMZKDXTL-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-(1-phenylethyl)piperidine Chemical compound CC1(N(C(CCC1)(C)C)C(C)C1=CC=CC=C1)C PZXHNHXMZKDXTL-UHFFFAOYSA-N 0.000 description 1
- GMFQINLKUNDHCB-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-(oxiran-2-ylmethyl)piperidine Chemical compound CC1(C)CCCC(C)(C)N1CC1OC1 GMFQINLKUNDHCB-UHFFFAOYSA-N 0.000 description 1
- OMLMFUBBKXQDET-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-[2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl]piperidine Chemical compound CC1(C)CCCC(C)(C)N1CCN1C(C)(C)CCCC1(C)C OMLMFUBBKXQDET-UHFFFAOYSA-N 0.000 description 1
- NHSGQBQHUYRABY-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-[4-(2,2,6,6-tetramethylpiperidin-1-yl)butyl]piperidine Chemical compound CC1(C)CCCC(C)(C)N1CCCCN1C(C)(C)CCCC1(C)C NHSGQBQHUYRABY-UHFFFAOYSA-N 0.000 description 1
- FEBRPUJWZOLULO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-[6-(2,2,6,6-tetramethylpiperidin-1-yl)hexyl]piperidine Chemical compound CC1(C)CCCC(C)(C)N1CCCCCCN1C(C)(C)CCCC1(C)C FEBRPUJWZOLULO-UHFFFAOYSA-N 0.000 description 1
- MBXDYHRKWHUIOF-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-octadecylpiperidine Chemical compound CCCCCCCCCCCCCCCCCCN1C(C)(C)CCCC1(C)C MBXDYHRKWHUIOF-UHFFFAOYSA-N 0.000 description 1
- LWHAUSHVSZUAER-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-propylpiperidine Chemical compound CCCN1C(C)(C)CCCC1(C)C LWHAUSHVSZUAER-UHFFFAOYSA-N 0.000 description 1
- SIVAGBOXYFFQPU-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine-1-carbaldehyde Chemical compound CC1(C)CCCC(C)(C)N1C=O SIVAGBOXYFFQPU-UHFFFAOYSA-N 0.000 description 1
- MWKUBKNHFINRGO-UHFFFAOYSA-N 2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl 2-hydroxybenzoate Chemical compound CC1(C)CCCC(C)(C)N1CCOC(=O)C1=CC=CC=C1O MWKUBKNHFINRGO-UHFFFAOYSA-N 0.000 description 1
- FSUROEPUYUTDQO-UHFFFAOYSA-N 2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl 2-phenylacetate Chemical compound CC1(C)CCCC(C)(C)N1CCOC(=O)CC1=CC=CC=C1 FSUROEPUYUTDQO-UHFFFAOYSA-N 0.000 description 1
- QKSBECREOWGKFX-UHFFFAOYSA-N 2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl acetate Chemical compound CC(=O)OCCN1C(C)(C)CCCC1(C)C QKSBECREOWGKFX-UHFFFAOYSA-N 0.000 description 1
- IQBUACMFVVBEAH-UHFFFAOYSA-N 2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl prop-2-enoate Chemical compound CC1(C)CCCC(C)(C)N1CCOC(=O)C=C IQBUACMFVVBEAH-UHFFFAOYSA-N 0.000 description 1
- ICUNCZXNMBKXNM-UHFFFAOYSA-N 2-[2-(2,2,6,6-tetramethylpiperidin-1-yl)acetyl]oxyethyl 2-(2,2,6,6-tetramethylpiperidin-1-yl)acetate Chemical compound CC1(C)CCCC(C)(C)N1CC(=O)OCCOC(=O)CN1C(C)(C)CCCC1(C)C ICUNCZXNMBKXNM-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- CXHQNZYCISJOSX-UHFFFAOYSA-N 6-[2-(2,2,6,6-tetramethylpiperidin-1-yl)acetyl]oxyhexyl 2-(2,2,6,6-tetramethylpiperidin-1-yl)acetate Chemical compound CC1(C)CCCC(C)(C)N1CC(=O)OCCCCCCOC(=O)CN1C(C)(C)CCCC1(C)C CXHQNZYCISJOSX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- YARBAQDFPQCZRA-UHFFFAOYSA-N [1-phenyl-2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl] acetate Chemical compound C=1C=CC=CC=1C(OC(=O)C)CN1C(C)(C)CCCC1(C)C YARBAQDFPQCZRA-UHFFFAOYSA-N 0.000 description 1
- BCDJPYNQDWNMGG-UHFFFAOYSA-N [1-phenyl-2-(2,2,6,6-tetramethylpiperidin-1-yl)ethyl] benzoate Chemical compound CC1(C)CCCC(C)(C)N1CC(C=1C=CC=CC=1)OC(=O)C1=CC=CC=C1 BCDJPYNQDWNMGG-UHFFFAOYSA-N 0.000 description 1
- QJGUWXIZESKRPV-UHFFFAOYSA-N [4-[2-(2,2,6,6-tetramethylpiperidin-1-yl)acetyl]oxyphenyl] 2-(2,2,6,6-tetramethylpiperidin-1-yl)acetate Chemical compound CC1(C)CCCC(C)(C)N1CC(=O)OC(C=C1)=CC=C1OC(=O)CN1C(C)(C)CCCC1(C)C QJGUWXIZESKRPV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- GOISUXCUYBZRRV-UHFFFAOYSA-N benzyl 2-(2,2,6,6-tetramethylpiperidin-1-yl)acetate Chemical compound CC1(C)CCCC(C)(C)N1CC(=O)OCC1=CC=CC=C1 GOISUXCUYBZRRV-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- SEQBORCPDVJFHT-UHFFFAOYSA-N methyl 2,2,6,6-tetramethylpiperidine-1-carboxylate Chemical compound COC(=O)N1C(C)(C)CCCC1(C)C SEQBORCPDVJFHT-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- PZVYRKRYNKEYTJ-UHFFFAOYSA-N octyl 2,2,6,6-tetramethylpiperidine-1-carboxylate Chemical compound CCCCCCCCOC(=O)N1C(C)(C)CCCC1(C)C PZVYRKRYNKEYTJ-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940070891 pyridium Drugs 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004383 yellowing Methods 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
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- 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
- C08K5/132—Phenols containing keto groups, e.g. benzophenones
-
- 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
- C08K5/20—Carboxylic acid amides
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Hydrogenated Pyridines (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH575373 | 1973-04-19 | ||
| JP1112874A JPS5634036B2 (enExample) | 1974-01-26 | 1974-01-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU539537A3 true SU539537A3 (ru) | 1976-12-15 |
Family
ID=25698322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU2021234A SU539537A3 (ru) | 1973-04-19 | 1974-04-19 | Стабилизированна композици на основе синтетического полимера |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US3975357A (enExample) |
| AT (1) | AT328745B (enExample) |
| AU (1) | AU477237B2 (enExample) |
| BE (1) | BE813922A (enExample) |
| BR (1) | BR7403130D0 (enExample) |
| DD (1) | DD110505A5 (enExample) |
| FR (1) | FR2226437B1 (enExample) |
| GB (1) | GB1440864A (enExample) |
| IL (1) | IL44629A (enExample) |
| IT (1) | IT1009485B (enExample) |
| LU (1) | LU69904A1 (enExample) |
| NL (1) | NL7405373A (enExample) |
| SE (1) | SE7405216L (enExample) |
| SU (1) | SU539537A3 (enExample) |
| ZA (1) | ZA742467B (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE412071B (sv) * | 1975-03-21 | 1980-02-18 | Montefibre Spa | Stabiliserade polyolefinbaserade polymerkompositioner och motsvarande stabilisator |
| GB1496844A (en) * | 1975-05-28 | 1978-01-05 | Ciba Geigy Ag | Stabilization of polymers |
| JPS53101380A (en) * | 1977-01-14 | 1978-09-04 | Sankyo Co Ltd | Piperidine derivatives |
| JPS5578033A (en) * | 1978-12-08 | 1980-06-12 | Adeka Argus Chem Co Ltd | Stabilized synthetic resin composition |
| CA1118139A (en) * | 1979-01-15 | 1982-02-09 | Elyse M. Bullock | Light-stable polypropylene compositions |
| IT1110826B (it) * | 1979-02-01 | 1986-01-06 | Montedison Spa | N-alchil-piperidin derivati dell'acido idrossi-benzil malonico e loro impiego come stabilizzanti per polimeri |
| US4315848A (en) * | 1979-05-10 | 1982-02-16 | Ciba-Geigy Corporation | 2-[2-Hydroxy-3,5-di-(α,α-dimethylbenzyl)-phenyl]-2H-benzotriazole and stabilized compositions |
| JPS57136567A (en) * | 1981-02-17 | 1982-08-23 | Adeka Argus Chem Co Ltd | N-2-hydroxy-3-substituted piperidine compound |
| DE3212336C1 (de) * | 1982-04-02 | 1983-12-29 | Skw Trostberg Ag, 8223 Trostberg | Mittel und Verfahren zur Waerme- und Lichtstabilisierung von Polyvinylchlorid |
| IT1209518B (it) * | 1984-04-09 | 1989-08-30 | Ciba Geigy Spa | Composti piperidinici ad attivita'stabilizzante per polimeri sintetici. |
| EP0323803A1 (de) * | 1987-12-30 | 1989-07-12 | Ciba-Geigy Ag | Stabilisierung von Lacken mit N-formylierten gehinderten Aminen |
| US4927898A (en) * | 1988-09-06 | 1990-05-22 | Union Carbide Chemicals And Plastics Company Inc. | Polysiloxanes with sterically hindered heterocyclic moiety |
| JP2830329B2 (ja) * | 1990-03-22 | 1998-12-02 | 住友化学工業株式会社 | 安定化樹脂組成物 |
| US5688951A (en) * | 1996-03-11 | 1997-11-18 | Aristech Chemical Corp | Hindered amine light stabilizer |
| US5990209A (en) * | 1997-04-25 | 1999-11-23 | Aristech Chemical Corporation | Copolymers of propylene with polymerizable hindered amine light stabilizers |
| US5856491A (en) * | 1997-08-09 | 1999-01-05 | Aristech Chemical Corp. | Method of making teritiary hindered amines |
| CH693416A5 (de) * | 1998-03-09 | 2003-07-31 | Ciba Sc Holding Ag | 1-Alkoxypolyalkylpiperidinderivate und ihre Verwendung als Polymerisationsregler. |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2684965A (en) * | 1950-08-10 | 1954-07-27 | Abbott Lab | Aminoalkylpiperidines |
| US2778825A (en) * | 1954-10-29 | 1957-01-22 | Rohm & Haas | Substituted nu-carbamyl derivatives of 2-methyl-oxazolidines and 2-methyltetrahydro-1, 3-oxazines and their preparation |
| US3126393A (en) * | 1957-02-13 | 1964-03-24 | X-gamma-dffithylaminopropylamino | |
| US3436368A (en) * | 1967-04-28 | 1969-04-01 | Bell Telephone Labor Inc | Di-(4-piperidyl)-alkanes as rubber antiozonants |
| US3542729A (en) * | 1968-03-19 | 1970-11-24 | Sankyo Co | Stabilization of synthetic polymers |
| GB1325775A (en) * | 1970-06-10 | 1973-08-08 | Ciba Geigy Uk Ltd | Phosphorus-containing piperidine derivatives and their use as stabilisers for polymerica material |
-
1974
- 1974-04-05 US US05/458,438 patent/US3975357A/en not_active Expired - Lifetime
- 1974-04-09 GB GB1564474A patent/GB1440864A/en not_active Expired
- 1974-04-12 IL IL44629A patent/IL44629A/en unknown
- 1974-04-18 BR BR3130/74A patent/BR7403130D0/pt unknown
- 1974-04-18 IT IT68251/74A patent/IT1009485B/it active
- 1974-04-18 BE BE143384A patent/BE813922A/xx unknown
- 1974-04-18 ZA ZA00742467A patent/ZA742467B/xx unknown
- 1974-04-18 SE SE7405216A patent/SE7405216L/sv unknown
- 1974-04-19 AT AT325074A patent/AT328745B/de not_active IP Right Cessation
- 1974-04-19 SU SU2021234A patent/SU539537A3/ru active
- 1974-04-19 DD DD178016A patent/DD110505A5/xx unknown
- 1974-04-19 NL NL7405373A patent/NL7405373A/xx not_active Application Discontinuation
- 1974-04-19 AU AU68082/74A patent/AU477237B2/en not_active Expired
- 1974-04-19 FR FR7413831A patent/FR2226437B1/fr not_active Expired
- 1974-04-19 LU LU69904A patent/LU69904A1/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US3975357A (en) | 1976-08-17 |
| BE813922A (fr) | 1974-10-18 |
| IL44629A (en) | 1977-02-28 |
| GB1440864A (en) | 1976-06-30 |
| AU6808274A (en) | 1975-10-23 |
| IL44629A0 (en) | 1974-06-30 |
| AT328745B (de) | 1976-04-12 |
| ATA325074A (de) | 1975-06-15 |
| ZA742467B (en) | 1975-05-28 |
| AU477237B2 (en) | 1976-10-21 |
| DE2418540B2 (de) | 1975-12-04 |
| IT1009485B (it) | 1976-12-10 |
| DE2418540A1 (de) | 1974-11-07 |
| DD110505A5 (enExample) | 1974-12-20 |
| FR2226437B1 (enExample) | 1977-10-14 |
| BR7403130D0 (pt) | 1974-12-03 |
| FR2226437A1 (enExample) | 1974-11-15 |
| LU69904A1 (enExample) | 1974-08-06 |
| SE7405216L (enExample) | 1974-10-21 |
| NL7405373A (enExample) | 1974-10-22 |
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