KR20150003254A - 증가된 농업약품 및 uv 내성을 갖는 안정된 폴리올레핀류 및 그것의 사용 방법 - Google Patents
증가된 농업약품 및 uv 내성을 갖는 안정된 폴리올레핀류 및 그것의 사용 방법 Download PDFInfo
- Publication number
- KR20150003254A KR20150003254A KR1020147030810A KR20147030810A KR20150003254A KR 20150003254 A KR20150003254 A KR 20150003254A KR 1020147030810 A KR1020147030810 A KR 1020147030810A KR 20147030810 A KR20147030810 A KR 20147030810A KR 20150003254 A KR20150003254 A KR 20150003254A
- Authority
- KR
- South Korea
- Prior art keywords
- hydrocarbyl
- alkoxy
- tetramethyl
- triazine
- piperidinyl
- 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.)
- Withdrawn
Links
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- -1 tetramethyl-4-piperidinyl compounds Chemical class 0.000 claims abstract description 169
- 239000000203 mixture Substances 0.000 claims abstract description 70
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 69
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- 125000003545 alkoxy group Chemical group 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 31
- 125000000217 alkyl group Chemical group 0.000 claims description 27
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- 229920000642 polymer Polymers 0.000 claims description 23
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 20
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- SHZGNGWHVQJSGV-UHFFFAOYSA-N [1-(2-methoxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OC)C(C)(C)C1 SHZGNGWHVQJSGV-UHFFFAOYSA-N 0.000 description 1
- CKNXUBQWICQTKD-UHFFFAOYSA-N [1-(2-methoxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] icosanoate Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OC)C(C)(C)C1 CKNXUBQWICQTKD-UHFFFAOYSA-N 0.000 description 1
- MFESCEMHVWONHJ-UHFFFAOYSA-N [1-(2-methoxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OC)C(C)(C)C1 MFESCEMHVWONHJ-UHFFFAOYSA-N 0.000 description 1
- NMCUPXJNWBDDEK-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(2-methyl-2-octadecoxypropoxy)piperidin-4-yl] docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OCCCCCCCCCCCCCCCCCC)C(C)(C)C1 NMCUPXJNWBDDEK-UHFFFAOYSA-N 0.000 description 1
- MHKYLVYOCCGVBI-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(2-methyl-2-octadecoxypropoxy)piperidin-4-yl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(C)(C)CON1C(C)(C)CC(OC(=O)CCCCCCCCCCCCCCC)CC1(C)C MHKYLVYOCCGVBI-UHFFFAOYSA-N 0.000 description 1
- ZAVOBIFEEHKLBQ-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(2-methyl-2-octadecoxypropoxy)piperidin-4-yl] icosanoate Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OCCCCCCCCCCCCCCCCCC)C(C)(C)C1 ZAVOBIFEEHKLBQ-UHFFFAOYSA-N 0.000 description 1
- BZCABUSPPFDQKZ-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(2-methyl-2-octadecoxypropoxy)piperidin-4-yl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(C)(C)CON1C(C)(C)CC(OC(=O)CCCCCCCCCCCCCCCCC)CC1(C)C BZCABUSPPFDQKZ-UHFFFAOYSA-N 0.000 description 1
- RAAFSMCIZVWZOQ-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(2-methyl-2-octoxypropoxy)piperidin-4-yl] docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OCCCCCCCC)C(C)(C)C1 RAAFSMCIZVWZOQ-UHFFFAOYSA-N 0.000 description 1
- XSJYTIRJXPKTLL-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(2-methyl-2-propoxypropoxy)piperidin-4-yl] docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OCCC)C(C)(C)C1 XSJYTIRJXPKTLL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001334 alicyclic compounds Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RSOILICUEWXSLA-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 RSOILICUEWXSLA-UHFFFAOYSA-N 0.000 description 1
- OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 description 1
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 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
- QYMGIIIPAFAFRX-UHFFFAOYSA-N butyl prop-2-enoate;ethene Chemical compound C=C.CCCCOC(=O)C=C QYMGIIIPAFAFRX-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- ZFOZSYQWFYGERI-UHFFFAOYSA-N decyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 ZFOZSYQWFYGERI-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- LDYLHGQJGCKGES-UHFFFAOYSA-N docosyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 LDYLHGQJGCKGES-UHFFFAOYSA-N 0.000 description 1
- CARVOQIAEFKWRP-UHFFFAOYSA-N dodecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 CARVOQIAEFKWRP-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- NZYMWGXNIUZYRC-UHFFFAOYSA-N hexadecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NZYMWGXNIUZYRC-UHFFFAOYSA-N 0.000 description 1
- 150000004677 hydrates Chemical class 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
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 description 1
- AFCCDDWKHLHPDF-UHFFFAOYSA-M metam-sodium Chemical compound [Na+].CNC([S-])=S AFCCDDWKHLHPDF-UHFFFAOYSA-M 0.000 description 1
- UKJARPDLRWBRAX-UHFFFAOYSA-N n,n'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound C1C(C)(C)NC(C)(C)CC1NCCCCCCNC1CC(C)(C)NC(C)(C)C1 UKJARPDLRWBRAX-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- BLBLVDQTHWVGRA-UHFFFAOYSA-N n-butyl-3-[4-[4-(butylamino)-1,2,2,6,6-pentamethylpiperidin-3-yl]-6-chloro-1,3,5-triazin-2-yl]-1,2,2,6,6-pentamethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)N(C)C(C)(C)C1C1=NC(Cl)=NC(C2C(N(C)C(C)(C)CC2NCCCC)(C)C)=N1 BLBLVDQTHWVGRA-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 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
- SMNZOWVTUJGGRR-UHFFFAOYSA-N octyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SMNZOWVTUJGGRR-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 238000007539 photo-oxidation reaction Methods 0.000 description 1
- 239000011941 photocatalyst Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- IWELDVXSEVIIGI-UHFFFAOYSA-N piperazin-2-one Chemical compound O=C1CNCCN1 IWELDVXSEVIIGI-UHFFFAOYSA-N 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229920006302 stretch film Polymers 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- GUWVSGSIVKANQS-UHFFFAOYSA-N tetradecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 GUWVSGSIVKANQS-UHFFFAOYSA-N 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical group [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000011787 zinc oxide 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
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
-
- 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
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups
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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12163097.4A EP2647664A1 (en) | 2012-04-04 | 2012-04-04 | Method for stabilizing polyolefin films against UV degradation |
| EP12163097.4 | 2012-04-04 | ||
| PCT/US2013/035114 WO2013152100A1 (en) | 2012-04-04 | 2013-04-03 | Stabilized polyolefins having increased agrochemical and uv resistance and methods of use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20150003254A true KR20150003254A (ko) | 2015-01-08 |
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Family Applications (1)
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| KR1020147030810A Withdrawn KR20150003254A (ko) | 2012-04-04 | 2013-04-03 | 증가된 농업약품 및 uv 내성을 갖는 안정된 폴리올레핀류 및 그것의 사용 방법 |
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| US (1) | US20130267633A1 (enExample) |
| EP (1) | EP2647664A1 (enExample) |
| JP (1) | JP2015512469A (enExample) |
| KR (1) | KR20150003254A (enExample) |
| CN (1) | CN104271655A (enExample) |
| AR (1) | AR091329A1 (enExample) |
| CL (1) | CL2014002662A1 (enExample) |
| IL (1) | IL234873A0 (enExample) |
| MA (1) | MA37376A1 (enExample) |
| MX (1) | MX2014011976A (enExample) |
| SA (1) | SA113340445B1 (enExample) |
| UY (1) | UY34729A (enExample) |
| WO (1) | WO2013152100A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| KR20190127760A (ko) * | 2017-03-28 | 2019-11-13 | 바스프 에스이 | 광 안정화제 혼합물 |
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| MX390673B (es) * | 2014-05-01 | 2025-03-21 | Cytec Ind Inc | Composiciones estabilizantes para estabilizar materiales frente a la degradacion termica y debida a la luz ultravioleta. |
| CN107075318B (zh) | 2014-08-27 | 2021-01-29 | Sika技术股份公司 | 用于对uv敏感的压敏粘合剂的半透明隔离薄膜 |
| 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 |
| CN106589453B (zh) * | 2015-10-20 | 2020-02-07 | 天罡新材料（廊坊）股份有限公司 | 一种光稳定剂组合物及其制备方法 |
| CN105237971A (zh) * | 2015-11-17 | 2016-01-13 | 南通市振兴精细化工有限公司 | 一种新型复配型光稳定剂 |
| CN107125062A (zh) * | 2016-12-05 | 2017-09-05 | 广东乐将生物科技有限公司 | 一种新型可降解地膜及其使用方法 |
| JP7009784B2 (ja) * | 2017-06-02 | 2022-01-26 | 凸版印刷株式会社 | 樹脂成型体および化粧シート |
| JP7279764B2 (ja) * | 2017-06-02 | 2023-05-23 | 凸版印刷株式会社 | 樹脂成型体および化粧シート |
| JP7105552B2 (ja) * | 2017-10-18 | 2022-07-25 | 三菱ケミカルアグリドリーム株式会社 | 農業用ポリオレフィン系多層フィルム |
| KR102769555B1 (ko) * | 2018-06-21 | 2025-02-19 | 도판 홀딩스 가부시키가이샤 | 보호 필름 및 시트 |
| CN112625345A (zh) * | 2020-12-10 | 2021-04-09 | 会通新材料股份有限公司 | 耐光照聚丙烯复合材料及其制备方法和应用 |
| CN112608516B (zh) * | 2020-12-15 | 2022-04-08 | 沈阳化工研究院有限公司 | 一种多功能光稳定组合物及其制备方法 |
| CN114249920B (zh) * | 2021-12-24 | 2023-11-28 | 宿迁联宏新材料有限公司 | 一种聚烯烃薄制品用光稳定剂复配物及其制备方法 |
| CN114292440B (zh) * | 2021-12-31 | 2023-11-10 | 天津利安隆新材料股份有限公司 | 复合光稳定剂、塑木复合材料组合物和塑木产品 |
| US20240407308A1 (en) * | 2023-06-09 | 2024-12-12 | Berry Global, Inc. | Non-woven fabrics for agricultural products |
| CN118496638B (zh) * | 2024-07-22 | 2024-11-22 | 海安浩驰科技有限公司 | 一种抗紫外车窗膜及其制备方法 |
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| US3206431A (en) * | 1964-09-15 | 1965-09-14 | Shell Oil Co | Thermoplastic polymers containing 3,5-dialkyl-4-hydroxybenzoic acid esters as u.v. stabilizers |
| JPS56116735A (en) * | 1980-02-19 | 1981-09-12 | Shintousero Shoji Kk | Agricultural covering material |
| US4331586A (en) * | 1981-07-20 | 1982-05-25 | American Cyanamid Company | Novel light stabilizers for polymers |
| US4674999A (en) * | 1982-09-27 | 1987-06-23 | Ethyl Corporation | Method of forming a plastic film construction |
| US4619956A (en) * | 1985-05-03 | 1986-10-28 | American Cyanamid Co. | Stabilization of high solids coatings with synergistic combinations |
| US5672675A (en) * | 1994-07-13 | 1997-09-30 | Alliedsignal, Inc. | Vinyl ether-terminated polyester oligomer stabilizers for vinyl ether-based coating systems |
| US6051164A (en) * | 1998-04-30 | 2000-04-18 | Cytec Technology Corp. | Methods and compositions for protecting polymers from UV light |
| CO5231248A1 (es) | 2000-07-26 | 2002-12-27 | Ciba Sc Holding Ag | Articulos transparentes de polimero de baja consistencia |
| TWI273115B (en) * | 2000-12-12 | 2007-02-11 | Ciba Sc Holding Ag | Improved weatherability of flame retardant polyolefin |
| WO2003057772A2 (en) * | 2001-12-27 | 2003-07-17 | Cytec Technology Corp. | Uv stabilized thermoplastic olefins |
| US20030183326A1 (en) * | 2002-04-02 | 2003-10-02 | O'connor Lawrence | Method for manufacturing pressure sensitive adhesive tear tapes |
| CN1875061A (zh) * | 2003-11-04 | 2006-12-06 | Cytec技术有限公司 | 紫外稳定添加剂组合物 |
| WO2007088114A1 (en) | 2006-02-01 | 2007-08-09 | Ciba Holding Inc. | Stabilizer composition for polymers |
| JP5478013B2 (ja) * | 2007-12-18 | 2014-04-23 | 株式会社Ａｄｅｋａ | オレフィン系弾性樹脂組成物 |
| CN106364103B (zh) * | 2011-06-30 | 2019-08-02 | 陶氏环球技术有限责任公司 | 具有一体化背部片材和封装性能且包括包含结晶嵌段共聚物复合物或嵌段共聚物复合物的层的基于聚烯烃的多层膜 |
-
2012
- 2012-04-04 EP EP12163097.4A patent/EP2647664A1/en not_active Withdrawn
-
2013
- 2013-04-03 MX MX2014011976A patent/MX2014011976A/es unknown
- 2013-04-03 WO PCT/US2013/035114 patent/WO2013152100A1/en not_active Ceased
- 2013-04-03 KR KR1020147030810A patent/KR20150003254A/ko not_active Withdrawn
- 2013-04-03 US US13/856,112 patent/US20130267633A1/en not_active Abandoned
- 2013-04-03 CN CN201380023471.8A patent/CN104271655A/zh active Pending
- 2013-04-03 SA SA113340445A patent/SA113340445B1/ar unknown
- 2013-04-03 JP JP2015504705A patent/JP2015512469A/ja active Pending
- 2013-04-04 AR ARP130101117 patent/AR091329A1/es unknown
- 2013-04-04 UY UY0001034729A patent/UY34729A/es unknown
-
2014
- 2014-09-26 MA MA37376A patent/MA37376A1/fr unknown
- 2014-09-29 IL IL234873A patent/IL234873A0/en unknown
- 2014-10-03 CL CL2014002662A patent/CL2014002662A1/es unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20190127760A (ko) * | 2017-03-28 | 2019-11-13 | 바스프 에스이 | 광 안정화제 혼합물 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2647664A1 (en) | 2013-10-09 |
| CL2014002662A1 (es) | 2015-01-16 |
| SA113340445B1 (ar) | 2015-08-16 |
| MA37376A1 (fr) | 2016-10-31 |
| US20130267633A1 (en) | 2013-10-10 |
| CN104271655A (zh) | 2015-01-07 |
| IL234873A0 (en) | 2014-12-31 |
| UY34729A (es) | 2013-10-31 |
| AR091329A1 (es) | 2015-01-28 |
| WO2013152100A1 (en) | 2013-10-10 |
| MX2014011976A (es) | 2015-03-20 |
| JP2015512469A (ja) | 2015-04-27 |
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