SU511019A3 - Стабилизирующа смесь - Google Patents
Стабилизирующа смесьInfo
- Publication number
- SU511019A3 SU511019A3 SU2017925A SU2017925A SU511019A3 SU 511019 A3 SU511019 A3 SU 511019A3 SU 2017925 A SU2017925 A SU 2017925A SU 2017925 A SU2017925 A SU 2017925A SU 511019 A3 SU511019 A3 SU 511019A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- hydrogen
- methyl
- alkyl
- chlorine
- stabilizer
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 10
- 230000000087 stabilizing effect Effects 0.000 title claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- 239000003381 stabilizer Substances 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 230000006641 stabilisation Effects 0.000 claims description 4
- 238000011105 stabilization Methods 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 230000005855 radiation Effects 0.000 claims description 2
- 239000000701 coagulant Substances 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
- -1 cyclic amine Chemical class 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 5
- 230000002195 synergetic effect Effects 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 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
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- CQNGGPGQSHHRCV-UHFFFAOYSA-N 1-ethoxypiperidine Chemical compound CCON1CCCCC1 CQNGGPGQSHHRCV-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- YEXOWHQZWLCHHD-UHFFFAOYSA-N 3,5-ditert-butyl-4-hydroxybenzoic acid Chemical compound CC(C)(C)C1=CC(C(O)=O)=CC(C(C)(C)C)=C1O YEXOWHQZWLCHHD-UHFFFAOYSA-N 0.000 description 1
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
- 102100020903 Ezrin Human genes 0.000 description 1
- 101000854648 Homo sapiens Ezrin Proteins 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003141 anti-fusion Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- WTYGAUXICFETTC-UHFFFAOYSA-N cyclobarbital Chemical compound C=1CCCCC=1C1(CC)C(=O)NC(=O)NC1=O WTYGAUXICFETTC-UHFFFAOYSA-N 0.000 description 1
- 229960004138 cyclobarbital Drugs 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001421 myristyl 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])[H] 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
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- TYFQFVWCELRYAO-UHFFFAOYSA-L suberate(2-) Chemical compound [O-]C(=O)CCCCCCC([O-])=O TYFQFVWCELRYAO-UHFFFAOYSA-L 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH575373 | 1973-04-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU511019A3 true SU511019A3 (ru) | 1976-04-15 |
Family
ID=4298764
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU2017925A SU511019A3 (ru) | 1973-04-19 | 1974-04-18 | Стабилизирующа смесь |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US4110304A (OSRAM) |
| JP (1) | JPS5069157A (OSRAM) |
| AT (1) | AT329275B (OSRAM) |
| BE (1) | BE813882A (OSRAM) |
| BR (1) | BR7403107D0 (OSRAM) |
| DD (1) | DD110285A5 (OSRAM) |
| DE (1) | DE2417535A1 (OSRAM) |
| ES (2) | ES425446A1 (OSRAM) |
| FR (7) | FR2249156B1 (OSRAM) |
| GB (1) | GB1433285A (OSRAM) |
| IE (1) | IE39205B1 (OSRAM) |
| IL (1) | IL44600A (OSRAM) |
| LU (1) | LU69883A1 (OSRAM) |
| NL (1) | NL7405359A (OSRAM) |
| SU (1) | SU511019A3 (OSRAM) |
| ZA (1) | ZA742496B (OSRAM) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5835221B2 (ja) * | 1975-03-01 | 1983-08-01 | ジェイエスアール株式会社 | 耐候性のすぐれた耐衝撃性樹脂組成物 |
| JPS52127954A (en) * | 1976-04-21 | 1977-10-27 | Mitsubishi Chem Ind Ltd | Polyethylene compositions |
| DE2862332D1 (en) | 1977-12-30 | 1983-11-10 | Ciba Geigy Ag | Stabilisation of heat-curable metallic enamel paints against the action of light, humidity and oxygen by the addition of polyalkylpiperidine derivatives |
| DE2963604D1 (en) * | 1978-06-21 | 1982-10-28 | Ciba Geigy Ag | Light stabilization of acid catalysed stoving enamels |
| DE2913853A1 (de) * | 1979-04-06 | 1980-10-23 | Roehm Gmbh | Verfahren zum polymerisieren von methylmethacrylat |
| 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 |
| EP0080431B1 (de) * | 1981-10-16 | 1986-09-24 | Ciba-Geigy Ag | Synergistisches Gemisch von niedermolekularen und hochmolekularen Polyalkylpiperidinen |
| US4552885A (en) * | 1981-12-24 | 1985-11-12 | Ciba Geigy Corporation | Stabilized fungicide compositions |
| US4722806A (en) * | 1982-02-19 | 1988-02-02 | The B. F. Goodrich Company | Alkylated polyalkylenepolyamines, substituted oxo-piperazinyl-triazines and UV light stabilized compositions |
| US4464496A (en) * | 1982-03-26 | 1984-08-07 | Uniroyal, Inc. | Non-yellowing polymer composition |
| DE3408949A1 (de) * | 1983-03-21 | 1984-09-27 | Sandoz-Patent-GmbH, 7850 Lörrach | Fluessige zubereitung von lichtstabilisatoren |
| JPS59179576A (ja) * | 1983-03-21 | 1984-10-12 | サンド・アクチエンゲゼルシヤフト | 紫外線安定剤を含む液状濃厚物 |
| NZ208423A (en) * | 1983-10-26 | 1987-05-29 | Becton Dickinson Co | Sterilised, radiation-stabilised semi-crystalline polymer articles |
| IT1200103B (it) * | 1984-08-14 | 1989-01-05 | Sandoz Ag | Composti tetraalchilpiridinici n-sostituiti agenti come stabilizzanti agli effetti della luce per materiali polimerici |
| JPS6147744A (ja) * | 1984-08-15 | 1986-03-08 | Polyplastics Co | 耐候性ポリアセタ−ル樹脂組成物 |
| JPH064740B2 (ja) * | 1985-07-04 | 1994-01-19 | 電気化学工業株式会社 | 樹脂組成物 |
| DE3871855D1 (de) * | 1987-05-05 | 1992-07-16 | Ciba Geigy Ag | Gegen lichtschaedigung stabilisierte polyolefine. |
| US5135986A (en) * | 1988-04-15 | 1992-08-04 | Ciba-Geigy Corporation | Stabilized styrene copolymers containing elastomer particles |
| US4927898A (en) * | 1988-09-06 | 1990-05-22 | Union Carbide Chemicals And Plastics Company Inc. | Polysiloxanes with sterically hindered heterocyclic moiety |
| JPH0364350A (ja) * | 1989-08-01 | 1991-03-19 | Polyplastics Co | 耐候性ポリアセタール樹脂組成物 |
| DE59105312D1 (de) * | 1990-10-04 | 1995-06-01 | Ciba Geigy Ag | Stabilisierte Styrolcopolymere enthaltend Elastomerteilchen. |
| US5118735A (en) * | 1990-10-05 | 1992-06-02 | Hercules Incorporated | Organosilicon composition comprising stabilizers |
| DE4215141C1 (de) * | 1992-05-08 | 1993-12-09 | Hoechst Ag | Polyvinylbutyrale mit verbesserter Thermostabilität und Lichtbeständigkeit |
| US6153676A (en) * | 1992-08-17 | 2000-11-28 | Clariant Finance (Bvi) Limited | Stabilized polyolefins |
| FR2730240A1 (fr) * | 1995-02-07 | 1996-08-09 | Atochem Elf Sa | Stabilisation d'un polymere par un radical libre stable |
| FR2730241B1 (fr) * | 1995-02-07 | 1997-02-28 | Atofina | Procede de fabrication d'une composition comprenant un polymere vinylaromatique et un caoutchouc par polymerisation en presence d'un radical libre stable |
| DE19545634A1 (de) | 1995-12-07 | 1997-06-12 | Bayer Ag | Festkörperreiche Bindemittelkombinationen |
| US6184332B1 (en) | 1996-02-29 | 2001-02-06 | Synthopol Chemie Dr. Rer. Pol. Koch Gmbh & Co. Kg | Polyester polyols and their use as the polyol component in two-component polyurethane paints |
| WO1997039052A1 (en) * | 1996-04-12 | 1997-10-23 | Clariant Finance (Bvi) Limited | Stabilization of polyolefins |
| TWI224995B (en) * | 1998-03-19 | 2004-12-11 | Ciba Sc Holding Ag | Stabilization of wood substrates |
| DE19955129A1 (de) | 1999-11-17 | 2001-05-23 | Bayer Ag | Neue, festkörperreiche Bindemittelkombinationen und deren Verwendung |
| US6544305B2 (en) | 2001-04-02 | 2003-04-08 | Ciba Specialty Chemicals Corporation | Candle wax stabilized with piperazinones |
| US6905525B2 (en) * | 2001-04-02 | 2005-06-14 | Ciba Specialty Chemicals Corporation | Candle wax stabilized with piperazinones |
| EP1692221A1 (en) * | 2003-11-21 | 2006-08-23 | Ciba Specialty Chemicals Holding Inc. | Weatherfast pigmented polystyrene |
| US20050137322A1 (en) * | 2003-12-17 | 2005-06-23 | Roesler Richard R. | Silane modified two-component polyurethane coating |
| US20060107589A1 (en) | 2004-11-19 | 2006-05-25 | Rubin Patti D | Compressed growing medium |
| US9756798B2 (en) | 2004-11-19 | 2017-09-12 | Patti D. Rubin | Burrow filling compressed growing medium |
| CN101247877B (zh) * | 2005-08-09 | 2012-08-22 | 埃克森美孚研究工程公司 | 用于酸气涤气工艺的受阻环状多胺和其盐 |
| BRPI0618648A2 (pt) * | 2005-11-10 | 2011-09-06 | Sigmakalon B V | composição de revestimento base com base em epóxi, substrato de metal revestido, processo para revestir um substrato metálico, sistema de revestimento de camada dupla para um substrato metálico, e, usos de óxido de zinco, e de uma composição de revestimento base com base em epóxi |
| WO2007128672A1 (en) * | 2006-05-03 | 2007-11-15 | Ciba Holding Inc. | Substituted hexahydro-1,4-diazepin-5-ones and compositions stabilized therewith |
| CN120310153A (zh) * | 2025-04-10 | 2025-07-15 | 扬州市邗江扬子汽车内饰件有限公司 | 一种汽车内饰复合材料高效改性方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1618196B1 (de) * | 1966-02-07 | 1971-12-09 | Ciba Geigy | Verwendung von asymmetrischen Oxalsäure-diarylamiden als Ultraviolettschutzmittel |
| US3640928A (en) * | 1968-06-12 | 1972-02-08 | Sankyo Co | Stabilization of synthetic polymers |
| US3705166A (en) * | 1969-08-15 | 1972-12-05 | Sankyo Co | Acrylic acid derivatives of 2,2,6,6-tetramethylpiperidines |
| US3734883A (en) * | 1970-04-16 | 1973-05-22 | Ciba Geigy Corp | Stabilizing organic material with piperidone azines |
| GB1325775A (en) * | 1970-06-10 | 1973-08-08 | Ciba Geigy Uk Ltd | Phosphorus-containing piperidine derivatives and their use as stabilisers for polymerica material |
| US3828052A (en) * | 1971-09-20 | 1974-08-06 | Ciba Geigy Corp | Acyl hydrazones of 2,2,6,6-tetramethyl-piperidine-4-ones |
| US3853890A (en) * | 1970-09-19 | 1974-12-10 | Ciba Geigy Corp | Azine derivatives of piperidine |
| GB1395159A (en) * | 1971-11-30 | 1975-05-21 | Ciba Geigy Ag | Tetra-hydropyridine derivatives |
| US4046737A (en) * | 1971-11-30 | 1977-09-06 | Ciba-Geigy Corporation | Piperidine derivatives |
| US3790525A (en) * | 1972-01-21 | 1974-02-05 | Sankyo Co | 4-piperidone ketal derivatives,their preparation and their use as stabilizers |
| US3884912A (en) * | 1972-01-26 | 1975-05-20 | Sankyo Co | 4-Piperidone derivatives, their preparation and their use as stabilizers |
| US3745163A (en) * | 1972-03-13 | 1973-07-10 | Ciba Geigy Corp | 2,2,6,6-tetramethyl piperidinyl-4-(dialkyl-hydroxy-benzoyl or phenyl alkanoyl)hydrazones |
| US3899491A (en) * | 1972-03-29 | 1975-08-12 | Ciba Geigy Corp | Alkyl alkanoate derivatives of substituted piperazines and polymer compositions stabilized thereby |
| GB1398413A (en) * | 1972-07-28 | 1975-06-18 | Ciba Geigy Ag | Piperidine derivatives |
| GB1398412A (en) * | 1972-07-28 | 1975-06-18 | Ciba Geigy Ag | Piperidine derivatives |
| GB1403942A (en) * | 1973-04-05 | 1975-08-28 | Ciba Geigy Ag | Piperidine derivatives |
| US3960809A (en) * | 1973-12-28 | 1976-06-01 | Ciba-Geigy Corporation | Compositions stabilized with hindered piperidine carboxylic acids |
| GB1467672A (en) * | 1974-04-11 | 1977-03-16 | Ciba Geigy Ag | Stabilised epoxy resin |
-
1974
- 1974-04-08 IE IE756/74A patent/IE39205B1/xx unknown
- 1974-04-10 IL IL44600A patent/IL44600A/en unknown
- 1974-04-10 DE DE2417535A patent/DE2417535A1/de active Pending
- 1974-04-17 DD DD177960A patent/DD110285A5/xx unknown
- 1974-04-17 GB GB1674374A patent/GB1433285A/en not_active Expired
- 1974-04-17 LU LU69883A patent/LU69883A1/xx unknown
- 1974-04-18 ZA ZA00742496A patent/ZA742496B/xx unknown
- 1974-04-18 FR FR7413496A patent/FR2249156B1/fr not_active Expired
- 1974-04-18 ES ES0425446A patent/ES425446A1/es not_active Expired
- 1974-04-18 BE BE143344A patent/BE813882A/xx unknown
- 1974-04-18 BR BR3107/74A patent/BR7403107D0/pt unknown
- 1974-04-18 SU SU2017925A patent/SU511019A3/ru active
- 1974-04-18 AT AT321574A patent/AT329275B/de not_active IP Right Cessation
- 1974-04-19 NL NL7405359A patent/NL7405359A/xx not_active Application Discontinuation
- 1974-04-19 ES ES425513A patent/ES425513A1/es not_active Expired
- 1974-04-19 JP JP49044351A patent/JPS5069157A/ja active Pending
-
1975
- 1975-01-02 FR FR7500026A patent/FR2257669B1/fr not_active Expired
- 1975-01-02 FR FR7500028A patent/FR2257671B1/fr not_active Expired
- 1975-01-02 FR FR7500024A patent/FR2257667B1/fr not_active Expired
- 1975-01-02 FR FR7500023A patent/FR2257666B1/fr not_active Expired
- 1975-01-02 FR FR7500027A patent/FR2257670B1/fr not_active Expired
- 1975-01-02 FR FR7500025A patent/FR2257668B1/fr not_active Expired
- 1975-12-05 US US05/638,226 patent/US4110304A/en not_active Expired - Lifetime
- 1975-12-05 US US05/638,125 patent/US4123418A/en not_active Expired - Lifetime
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