CN103946291A - 用于缩聚物的水解稳定的添加剂 - Google Patents
用于缩聚物的水解稳定的添加剂 Download PDFInfo
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- CN103946291A CN103946291A CN201280056408.XA CN201280056408A CN103946291A CN 103946291 A CN103946291 A CN 103946291A CN 201280056408 A CN201280056408 A CN 201280056408A CN 103946291 A CN103946291 A CN 103946291A
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- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 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 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
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- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 1
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- 230000000052 comparative effect Effects 0.000 description 1
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- 125000000753 cycloalkyl group Chemical group 0.000 description 1
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- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
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- MELUCTCJOARQQG-UHFFFAOYSA-N hex-2-yne Chemical compound CCCC#CC MELUCTCJOARQQG-UHFFFAOYSA-N 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
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
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- 239000004611 light stabiliser Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
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- XZWYZXLIPXDOLR-UHFFFAOYSA-N metformin Chemical group CN(C)C(=N)NC(N)=N XZWYZXLIPXDOLR-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- OSSQSXOTMIGBCF-UHFFFAOYSA-N non-1-yne Chemical group CCCCCCCC#C OSSQSXOTMIGBCF-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- DNPFOADIPJWGQH-UHFFFAOYSA-N octan-3-yl prop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C=C DNPFOADIPJWGQH-UHFFFAOYSA-N 0.000 description 1
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- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 150000004880 oxines Chemical class 0.000 description 1
- OWWPHPPHGZLCLN-UHFFFAOYSA-N oxiran-2-ylmethyl 2-methylidenebutanoate Chemical class CCC(=C)C(=O)OCC1CO1 OWWPHPPHGZLCLN-UHFFFAOYSA-N 0.000 description 1
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical compound CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 238000010094 polymer processing Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 description 1
- DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- ZVJHJDDKYZXRJI-UHFFFAOYSA-N pyrroline Natural products C1CC=NC1 ZVJHJDDKYZXRJI-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
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- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 239000011885 synergistic combination Substances 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
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 150000003527 tetrahydropyrans Chemical class 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
- C08G63/914—Polymers modified by chemical after-treatment derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/916—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
-
- 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
- C08K5/54—Silicon-containing compounds
- C08K5/541—Silicon-containing compounds containing oxygen
- C08K5/5435—Silicon-containing compounds containing oxygen containing oxygen in a ring
-
- 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
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11189569.4 | 2011-11-17 | ||
| EP11189569 | 2011-11-17 | ||
| PCT/EP2012/072489 WO2013072310A1 (de) | 2011-11-17 | 2012-11-13 | Additive zur hydrolysestabilisierung von polykondensaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN103946291A true CN103946291A (zh) | 2014-07-23 |
Family
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| Application Number | Title | Priority Date | Filing Date |
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| CN201280056408.XA Pending CN103946291A (zh) | 2011-11-17 | 2012-11-13 | 用于缩聚物的水解稳定的添加剂 |
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| Country | Link |
|---|---|
| EP (1) | EP2780407A1 (enrdf_load_stackoverflow) |
| JP (1) | JP2014533752A (enrdf_load_stackoverflow) |
| KR (1) | KR20140103956A (enrdf_load_stackoverflow) |
| CN (1) | CN103946291A (enrdf_load_stackoverflow) |
| IN (1) | IN2014CN03735A (enrdf_load_stackoverflow) |
| WO (1) | WO2013072310A1 (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109971007A (zh) * | 2019-04-01 | 2019-07-05 | 江南大学 | 一种常温固化聚氨酯类防雾薄膜及其制备方法 |
| CN118184691A (zh) * | 2024-03-01 | 2024-06-14 | 宁波三邦超细纤维有限公司 | 一种含硅烷结构的环氧烷类抗水解稳定剂及其制备方法 |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017110917A1 (ja) | 2015-12-25 | 2017-06-29 | 東洋紡株式会社 | ポリエステル樹脂組成物、これを含む光反射体用部品および光反射体、ならびにポリエステル樹脂組成物の製造方法 |
| WO2018143099A1 (ja) | 2017-02-02 | 2018-08-09 | 東洋紡株式会社 | ポリエステル樹脂組成物、これを含む光反射体用部品および光反射体 |
| JP6642701B2 (ja) | 2017-02-02 | 2020-02-12 | 東洋紡株式会社 | ポリエステル樹脂組成物、これを含む光反射体用部品および光反射体 |
| WO2019188921A1 (ja) | 2018-03-26 | 2019-10-03 | 東洋紡株式会社 | ポリエステル樹脂組成物、これを含む光反射体用部品および光反射体 |
| EP3670180A1 (de) * | 2018-12-17 | 2020-06-24 | LANXESS Deutschland GmbH | Multischichtsystem aus mindestens 3 polyesterschichten, dessen herstellung und verwendung |
| KR102421034B1 (ko) | 2020-05-28 | 2022-07-14 | 에코밴스 주식회사 | 생분해성 폴리에스테르 수지의 제조 방법 및 이에 따라 제조된 생분해성 폴리에스테르 수지 |
| JP7282124B2 (ja) | 2020-05-28 | 2023-05-26 | エコバンス カンパニー・リミテッド | 生分解性ポリエステル樹脂組成物、不織布およびフィルム、並びにその製造方法 |
| WO2023229216A1 (ko) | 2022-05-21 | 2023-11-30 | 에코밴스 주식회사 | 생분해성 성형품 및 생분해성 폴리에스테르 수지 조성물 |
| JP2025523713A (ja) * | 2022-05-21 | 2025-07-24 | エスケー リーヴィオ カンパニー リミテッド | 生分解性ポリエステル樹脂組成物、及びこれを含む生分解性成形品 |
| KR102777093B1 (ko) * | 2022-05-21 | 2025-03-07 | 에스케이리비오 주식회사 | 생분해성 폴리에스테르 수지 조성물 및 이의 제조방법 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0628541A1 (de) * | 1993-06-08 | 1994-12-14 | BASF Aktiengesellschaft | Carbodiimide und/oder oligomere Polycarbodiimide auf Basis von 1,3-Bis-(1-methyl-1-isocyanatoethyl)-benzol, ein Verfahren zu ihrer Herstellung und ihre Verwendung als Hydrolysestabilisator |
| CN1232820A (zh) * | 1998-03-06 | 1999-10-27 | 巴斯福股份公司 | 碳化二亚胺类及其制备方法 |
| CN101928446A (zh) * | 2008-11-11 | 2010-12-29 | 三菱聚酯薄膜有限公司 | 双轴取向的水解稳定的聚酯薄膜,其制备方法及其应用 |
| CN101955633A (zh) * | 2009-05-15 | 2011-01-26 | 三菱聚酯薄膜有限公司 | 含脱羧催化剂的双轴拉伸聚酯膜,其在电绝缘应用中的用途及其生产方法 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3770693A (en) | 1964-10-09 | 1973-11-06 | Baychem Corp | Stabilization of polyesterurethanes with 2-imino-oxazolidines |
| US4123419A (en) | 1977-08-26 | 1978-10-31 | Mobay Chemical Corporation | Stabilized thermoplastic polyesterurethanes |
| US4393158A (en) | 1981-07-20 | 1983-07-12 | General Electric Company | Hydrolytically stable polycarbonate compositions |
| US4393156A (en) | 1981-07-20 | 1983-07-12 | General Electric Company | Hydrolytically stable polyester-carbonate compositions |
| DE3217440A1 (de) | 1982-05-08 | 1983-11-10 | Basf Ag, 6700 Ludwigshafen | Polyethylenterephthalat mit verbesserter hydrolysebestaendigkeit sowie dessen verwendung |
| US4385144A (en) | 1982-07-12 | 1983-05-24 | Ethyl Corporation | Polyester composition |
| DE3826769A1 (de) | 1988-08-06 | 1990-02-15 | Bayer Ag | Behandlung von polyamidfasern |
| JP3036075B2 (ja) | 1991-03-01 | 2000-04-24 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 表面処理されたアラミド繊維およびそれらの製造方法 |
| NL9100578A (nl) | 1991-04-03 | 1992-11-02 | Stahl Holland Bv | Multifunctionele waterdispergeerbare verknopingsmiddelen. |
| US5354802A (en) | 1993-02-11 | 1994-10-11 | Polyplastics Co., Ltd. | Resin composition for blow molding and blow molded item made therefrom |
| US5439952A (en) | 1993-12-21 | 1995-08-08 | The Thompson Minwax Company | Self-curing coating composition exhibiting reduced discoloration upon storage |
| JP3733170B2 (ja) | 1996-04-02 | 2006-01-11 | 日清紡績株式会社 | ポリウレタン樹脂 |
| WO1998047940A1 (en) | 1997-04-22 | 1998-10-29 | Dsm N.V. | High-molecular polyamide |
| CA2378013C (en) | 1999-07-14 | 2007-10-09 | Marco A. Villalobos | Process for the continuous production of epoxy-(meth)acrylic-styrene polymers and their use in coating |
| DE10126149A1 (de) | 2001-05-30 | 2002-12-05 | Mitsubishi Polyester Film Gmbh | Gedeckt eingefärbte, hydrolysebeständige, biaxial orientierte Folie aus einem kristallisierbaren Thermoplasten und Verfahren zu ihrer Herstellung |
| WO2003066704A1 (en) | 2002-02-01 | 2003-08-14 | Johnson Polymer, Llc | Oligomeric chain extenders for processing, post-processing and recycling of condensation polymers, synthesis, compositions and applications |
| US20040147678A1 (en) | 2003-01-29 | 2004-07-29 | Clariant International, Ltd. | Solid concentrate composition for polymeric chain extension |
| DE102004024196A1 (de) | 2004-05-13 | 2005-12-01 | Basf Ag | Carbodiimide enthaltend Harnstoffgruppen und Silangruppen |
| JP2007023100A (ja) | 2005-07-13 | 2007-02-01 | Kureha Corp | 脂肪族ポリエステル樹脂組成物 |
| EP2686297A2 (de) * | 2011-03-18 | 2014-01-22 | Basf Se | Verwendung oligomerer carbodiimide als stabilisatoren |
-
2012
- 2012-11-13 IN IN3735CHN2014 patent/IN2014CN03735A/en unknown
- 2012-11-13 KR KR1020147016344A patent/KR20140103956A/ko not_active Withdrawn
- 2012-11-13 CN CN201280056408.XA patent/CN103946291A/zh active Pending
- 2012-11-13 WO PCT/EP2012/072489 patent/WO2013072310A1/de active Application Filing
- 2012-11-13 EP EP12783627.8A patent/EP2780407A1/de not_active Withdrawn
- 2012-11-13 JP JP2014541624A patent/JP2014533752A/ja active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0628541A1 (de) * | 1993-06-08 | 1994-12-14 | BASF Aktiengesellschaft | Carbodiimide und/oder oligomere Polycarbodiimide auf Basis von 1,3-Bis-(1-methyl-1-isocyanatoethyl)-benzol, ein Verfahren zu ihrer Herstellung und ihre Verwendung als Hydrolysestabilisator |
| CN1232820A (zh) * | 1998-03-06 | 1999-10-27 | 巴斯福股份公司 | 碳化二亚胺类及其制备方法 |
| CN101928446A (zh) * | 2008-11-11 | 2010-12-29 | 三菱聚酯薄膜有限公司 | 双轴取向的水解稳定的聚酯薄膜,其制备方法及其应用 |
| CN101955633A (zh) * | 2009-05-15 | 2011-01-26 | 三菱聚酯薄膜有限公司 | 含脱羧催化剂的双轴拉伸聚酯膜,其在电绝缘应用中的用途及其生产方法 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109971007A (zh) * | 2019-04-01 | 2019-07-05 | 江南大学 | 一种常温固化聚氨酯类防雾薄膜及其制备方法 |
| CN109971007B (zh) * | 2019-04-01 | 2021-05-28 | 江南大学 | 一种常温固化聚氨酯类防雾薄膜及其制备方法 |
| CN118184691A (zh) * | 2024-03-01 | 2024-06-14 | 宁波三邦超细纤维有限公司 | 一种含硅烷结构的环氧烷类抗水解稳定剂及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2013072310A1 (de) | 2013-05-23 |
| EP2780407A1 (de) | 2014-09-24 |
| KR20140103956A (ko) | 2014-08-27 |
| JP2014533752A (ja) | 2014-12-15 |
| IN2014CN03735A (enrdf_load_stackoverflow) | 2015-09-04 |
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