CN1088477C - 受阻胺和紫外线吸收剂协合混合物稳定着色纤维 - Google Patents
受阻胺和紫外线吸收剂协合混合物稳定着色纤维 Download PDFInfo
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- CN1088477C CN1088477C CN95117295A CN95117295A CN1088477C CN 1088477 C CN1088477 C CN 1088477C CN 95117295 A CN95117295 A CN 95117295A CN 95117295 A CN95117295 A CN 95117295A CN 1088477 C CN1088477 C CN 1088477C
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- Prior art keywords
- hydroxyl
- phenyl
- benzotriazole
- tert
- butyl
- Prior art date
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- 235000019305 distearyl thiodipropionate Nutrition 0.000 description 1
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 125000004494 ethyl ester group Chemical group 0.000 description 1
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 1
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- 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
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
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- 159000000003 magnesium salts Chemical class 0.000 description 1
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- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
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- 239000006078 metal deactivator Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
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- 238000000465 moulding Methods 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
- DHXOCDLHWYUUAG-UHFFFAOYSA-N n,n-didodecylhydroxylamine Chemical compound CCCCCCCCCCCCN(O)CCCCCCCCCCCC DHXOCDLHWYUUAG-UHFFFAOYSA-N 0.000 description 1
- WQAJFRSBFZAUPB-UHFFFAOYSA-N n,n-dioctylhydroxylamine Chemical compound CCCCCCCCN(O)CCCCCCCC WQAJFRSBFZAUPB-UHFFFAOYSA-N 0.000 description 1
- UBINNYMQZVKNFF-UHFFFAOYSA-N n-benzyl-1-phenylmethanimine oxide Chemical compound C=1C=CC=CC=1C=[N+]([O-])CC1=CC=CC=C1 UBINNYMQZVKNFF-UHFFFAOYSA-N 0.000 description 1
- GTWJETSWSUWSEJ-UHFFFAOYSA-N n-benzylaniline Chemical compound C=1C=CC=CC=1CNC1=CC=CC=C1 GTWJETSWSUWSEJ-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 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
- ZRPOKHXBOZQSOX-UHFFFAOYSA-N n-heptadecyl-n-octadecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCCC ZRPOKHXBOZQSOX-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
- WGCBLWIBXXQTAW-UHFFFAOYSA-N n-hexadecyl-n-octadecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCC WGCBLWIBXXQTAW-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
- 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
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-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
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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- 238000009994 optical bleaching Methods 0.000 description 1
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- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Substances OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
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- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 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
- 230000002265 prevention Effects 0.000 description 1
- KOODSCBKXPPKHE-UHFFFAOYSA-N propanethioic s-acid Chemical compound CCC(S)=O KOODSCBKXPPKHE-UHFFFAOYSA-N 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
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- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
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- 150000003839 salts Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- IJRHDFLHUATAOS-DPMBMXLASA-N sodium;(z,12r)-12-hydroxyoctadec-9-enoic acid Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O IJRHDFLHUATAOS-DPMBMXLASA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
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- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
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- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 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
- 238000010998 test method Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 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
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/04—Pigments
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Paper (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (3)
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|---|---|---|---|
| US31631294A | 1994-09-30 | 1994-09-30 | |
| US316312 | 1994-09-30 | ||
| US316,312 | 1994-09-30 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1130217A CN1130217A (zh) | 1996-09-04 |
| CN1088477C true CN1088477C (zh) | 2002-07-31 |
Family
ID=23228496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN95117295A Expired - Lifetime CN1088477C (zh) | 1994-09-30 | 1995-09-28 | 受阻胺和紫外线吸收剂协合混合物稳定着色纤维 |
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| EP (1) | EP0704560B1 (https=) |
| JP (1) | JP3890451B2 (https=) |
| KR (1) | KR100387906B1 (https=) |
| CN (1) | CN1088477C (https=) |
| AT (1) | ATE175731T1 (https=) |
| BR (1) | BR9504234A (https=) |
| CA (1) | CA2159418C (https=) |
| DE (1) | DE69507235T2 (https=) |
| DK (1) | DK0704560T3 (https=) |
| ES (1) | ES2128024T3 (https=) |
| NO (1) | NO308709B1 (https=) |
| RU (1) | RU2150535C1 (https=) |
| SK (1) | SK282328B6 (https=) |
| TW (1) | TW304993B (https=) |
| ZA (1) | ZA958217B (https=) |
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| US6040255A (en) * | 1996-06-25 | 2000-03-21 | Kimberly-Clark Worldwide, Inc. | Photostabilization package usable in nonwoven fabrics and nonwoven fabrics containing same |
| US5882388A (en) * | 1996-10-16 | 1999-03-16 | Brady Usa, Inc. | Water resistant ink jet recording media topcoats |
| US6136433A (en) | 1997-05-01 | 2000-10-24 | Basf Corporation | Spinning and stability of solution-dyed nylon fibers |
| US6051164A (en) * | 1998-04-30 | 2000-04-18 | Cytec Technology Corp. | Methods and compositions for protecting polymers from UV light |
| JP4020348B2 (ja) * | 1998-12-22 | 2007-12-12 | 旭化成せんい株式会社 | 耐候性および耐熱性に優れた不織布 |
| US6406775B1 (en) | 1999-07-12 | 2002-06-18 | Brady Worldwide, Inc. | Modifiers for outdoor durable ink jet media |
| GB2361005B (en) * | 2000-04-04 | 2002-08-14 | Ciba Sc Holding Ag | Synergistic mixtures of uv-absorbers in polyolefins |
| CO5231248A1 (es) * | 2000-07-26 | 2002-12-27 | Ciba Sc Holding Ag | Articulos transparentes de polimero de baja consistencia |
| CN100398588C (zh) * | 2001-02-21 | 2008-07-02 | 东丽株式会社 | 聚苯硫醚构件 |
| US6846929B2 (en) | 2001-04-02 | 2005-01-25 | Ciba Specialty Chemicals Corporation | Benzotriazole/hals molecular combinations and compositions stabilized therewith |
| AU2002364397B2 (en) | 2001-12-20 | 2007-07-12 | Ami - Agrolinz Melamine International Gmbh | Additive for inhibiting photolytic degradation reactions in aminoplasts |
| AU2002348236A1 (en) * | 2001-12-27 | 2003-07-24 | Cytec Technology Corp. | Uv stabilized thermoplastic olefins |
| ZA200301683B (en) | 2002-03-04 | 2004-09-06 | Ciba Sc Holding Ag | Synergistic combinations of UV absorbers for pigmented polyolefins. |
| CO5410180A1 (es) * | 2002-10-22 | 2004-06-30 | Ciba Sc Holding Ag | Composicion y proceso para potenciar la produccion de bio-masa en invernaderos |
| PT1863973E (pt) * | 2005-03-18 | 2011-07-01 | Clariant Finance Bvi Ltd | Tingimentos resistentes à acção da luz de fibras bicomponente |
| CN100423762C (zh) * | 2005-10-11 | 2008-10-08 | 薛金福 | 一种治疗恶性肿瘤的中药 |
| DE102005062687A1 (de) | 2005-12-23 | 2007-07-05 | Röhm Gmbh | PMMA-Folie mit besonders hoher Witterungsbeständigkeit und hoher UV-Schutzwirkung |
| BRPI0707004A2 (pt) * | 2006-02-14 | 2011-04-12 | Rhodia Operations | cabo de polìmero termoplástico formado de uma pluralidade de filamentos contìnuos, artigo flocado e uso do artigo flocado |
| PL2104716T3 (pl) * | 2007-01-15 | 2018-07-31 | Basf Se | Podbarwione przezroczyste powłoki uv stabilizowane 2-hydroksyfenylotriazyną |
| US7789957B2 (en) * | 2007-06-06 | 2010-09-07 | Ciba Corporation | Low-dust additive and pigment blends with improved color |
| KR101028323B1 (ko) | 2007-12-28 | 2011-04-12 | 주식회사 삼양사 | 자외선에 대한 내광성이 우수한 폴리에틸렌테레프탈레이트섬유 |
| ES2463674T3 (es) | 2009-01-19 | 2014-05-28 | Basf Se | Pigmentos negros orgánicos y su preparación |
| US8133556B2 (en) | 2009-08-12 | 2012-03-13 | Brady Worldwide, Inc. | Durable multilayer inkjet recording media topcoat |
| WO2011137056A1 (en) | 2010-04-30 | 2011-11-03 | Brady Worldwide, Inc. | Full color, inkjet-printable, self-laminating lablel |
| EP2580053A1 (en) * | 2010-06-14 | 2013-04-17 | E.I. Du Pont De Nemours And Company | Long-term outdoor exposure resistant polyester composite structures and processes for their preparation |
| JP5437213B2 (ja) * | 2010-09-28 | 2014-03-12 | 日本ポリプロ株式会社 | 溶融紡糸型エレクトロスピニング用プロピレン系樹脂組成物及びそれによる極細繊維の溶融紡糸方法 |
| CN102464864A (zh) * | 2010-10-29 | 2012-05-23 | E.I.内穆尔杜邦公司 | 光稳定的共聚醚酯组合物 |
| CN103774272B (zh) * | 2014-01-22 | 2016-08-17 | 东华大学 | 一种超薄轻质面料用抗紫外尼龙6纤维及其制备方法 |
| BR112017010492B1 (pt) * | 2014-11-20 | 2022-04-26 | Cytec Industries Inc | Composição estabilizante, concentrado masterbatch,e, artigo de fabricação |
| CN105482100B (zh) * | 2015-12-28 | 2018-07-13 | 北京服装学院 | 一种耐光耐热聚酰胺及其制备方法 |
| MX2019010629A (es) | 2017-03-10 | 2019-12-02 | Advansix Resins & Chemicals Llc | Composicion de funda de alambre y cable de resina base de copolimero pa6/66 para capacidad de procesamiento mejorada y propiedades. |
| US11767616B2 (en) | 2017-08-18 | 2023-09-26 | Glen Raven, Inc. | Acrylic compositions including a hindered amine light stabilizer and methods of making and using the same |
| US10214836B1 (en) | 2017-08-18 | 2019-02-26 | Glen Raven, Inc. | Acrylic compositions including a hindered amine light stabilizer and methods of making and using the same |
| CN111979591B (zh) * | 2020-07-30 | 2023-01-24 | 神马实业股份有限公司 | 一种高强度高耐热细单纤尼龙66纤维及其制备方法 |
| EP4620671A4 (en) * | 2022-11-17 | 2026-03-25 | Toray Industries | FIBROUS LAMINATED STRUCTURE AND VAPOR-PERMEABLE AND WATER-RESISTANT GARMENT |
| CN115652466B (zh) * | 2022-12-12 | 2023-03-31 | 烟台新秀新材料有限公司 | 用于聚酰胺材料的协同复配酰胺化光稳定剂 |
| TWI850083B (zh) * | 2023-08-29 | 2024-07-21 | 財團法人紡織產業綜合研究所 | 紫外線防護纖維 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4467061A (en) * | 1981-12-28 | 1984-08-21 | Tonen Sekiyu Kagaku Kabushiki Kaisha | Weather resistant polyolefin composition |
| CN1010606B (zh) * | 1988-10-27 | 1990-11-28 | 能源部华北电力设计院 | 双向吊拉减震装置 |
| CN1056696A (zh) * | 1990-03-23 | 1991-12-04 | 中国科学院长春应用化学研究所 | 耐候性聚乙烯薄膜 |
| EP0483488A1 (en) * | 1990-10-29 | 1992-05-06 | Cytec Technology Corp. | Synergistic ultraviolet absorber compositions containing hydroxy aryl triazines and tetraalkyl piperidines |
| CN1111662A (zh) * | 1994-03-29 | 1995-11-15 | 通用电气公司 | 防紫外线的聚酰胺组合物 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5058141A (https=) * | 1973-06-09 | 1975-05-20 | ||
| US4314933A (en) * | 1979-02-15 | 1982-02-09 | Ciba-Geigy Corporation | Method for light stabilization of two-layer uni-lacquer coatings |
| JPS61113649A (ja) * | 1984-11-07 | 1986-05-31 | Adeka Argus Chem Co Ltd | 耐光性の改善された高分子材料組成物 |
| US4619956A (en) * | 1985-05-03 | 1986-10-28 | American Cyanamid Co. | Stabilization of high solids coatings with synergistic combinations |
| US4929653A (en) * | 1987-07-13 | 1990-05-29 | The Bf Goodrich Company | Stabilized pigmented polypropylene fiber resistant to gas fade |
| US5190710A (en) * | 1991-02-22 | 1993-03-02 | The B. F. Goodrich Company | Method for imparting improved discoloration resistance to articles |
| US5200443A (en) * | 1991-03-29 | 1993-04-06 | Kimberly-Clark Corporation | Radiation stabilized fabric having improved odor characteristics containing an hindered amine compound |
| US5244947A (en) * | 1991-12-31 | 1993-09-14 | Kimberly-Clark Corporation | Stabilization of polyolefin nonwoven webs against actinic radiation |
-
1995
- 1995-09-21 DE DE69507235T patent/DE69507235T2/de not_active Expired - Lifetime
- 1995-09-21 EP EP95810593A patent/EP0704560B1/en not_active Expired - Lifetime
- 1995-09-21 DK DK95810593T patent/DK0704560T3/da active
- 1995-09-21 AT AT95810593T patent/ATE175731T1/de active
- 1995-09-21 ES ES95810593T patent/ES2128024T3/es not_active Expired - Lifetime
- 1995-09-27 SK SK1209-95A patent/SK282328B6/sk not_active IP Right Cessation
- 1995-09-28 CA CA002159418A patent/CA2159418C/en not_active Expired - Lifetime
- 1995-09-28 RU RU95116656/04A patent/RU2150535C1/ru active
- 1995-09-28 CN CN95117295A patent/CN1088477C/zh not_active Expired - Lifetime
- 1995-09-29 NO NO953870A patent/NO308709B1/no not_active IP Right Cessation
- 1995-09-29 ZA ZA958217A patent/ZA958217B/xx unknown
- 1995-09-29 BR BR9504234A patent/BR9504234A/pt not_active IP Right Cessation
- 1995-09-29 KR KR1019950032680A patent/KR100387906B1/ko not_active Expired - Lifetime
- 1995-09-29 JP JP27707295A patent/JP3890451B2/ja not_active Expired - Lifetime
- 1995-09-29 TW TW084110185A patent/TW304993B/zh not_active IP Right Cessation
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4467061A (en) * | 1981-12-28 | 1984-08-21 | Tonen Sekiyu Kagaku Kabushiki Kaisha | Weather resistant polyolefin composition |
| CN1010606B (zh) * | 1988-10-27 | 1990-11-28 | 能源部华北电力设计院 | 双向吊拉减震装置 |
| CN1056696A (zh) * | 1990-03-23 | 1991-12-04 | 中国科学院长春应用化学研究所 | 耐候性聚乙烯薄膜 |
| EP0483488A1 (en) * | 1990-10-29 | 1992-05-06 | Cytec Technology Corp. | Synergistic ultraviolet absorber compositions containing hydroxy aryl triazines and tetraalkyl piperidines |
| CN1111662A (zh) * | 1994-03-29 | 1995-11-15 | 通用电气公司 | 防紫外线的聚酰胺组合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR100387906B1 (ko) | 2003-09-19 |
| SK282328B6 (sk) | 2002-01-07 |
| NO953870L (no) | 1996-04-01 |
| NO953870D0 (no) | 1995-09-29 |
| ES2128024T3 (es) | 1999-05-01 |
| ZA958217B (en) | 1996-04-01 |
| EP0704560A1 (en) | 1996-04-03 |
| JP3890451B2 (ja) | 2007-03-07 |
| CN1130217A (zh) | 1996-09-04 |
| DE69507235D1 (de) | 1999-02-25 |
| NO308709B1 (no) | 2000-10-16 |
| DK0704560T3 (da) | 1999-09-06 |
| ATE175731T1 (de) | 1999-01-15 |
| BR9504234A (pt) | 1996-08-06 |
| CA2159418C (en) | 2007-04-10 |
| RU2150535C1 (ru) | 2000-06-10 |
| EP0704560B1 (en) | 1999-01-13 |
| SK120995A3 (en) | 1997-06-04 |
| JPH08226014A (ja) | 1996-09-03 |
| DE69507235T2 (de) | 1999-07-29 |
| TW304993B (https=) | 1997-05-11 |
| CA2159418A1 (en) | 1996-03-31 |
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