TWI496811B - 塗膜用聚酯 - Google Patents
塗膜用聚酯 Download PDFInfo
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- TWI496811B TWI496811B TW099138762A TW99138762A TWI496811B TW I496811 B TWI496811 B TW I496811B TW 099138762 A TW099138762 A TW 099138762A TW 99138762 A TW99138762 A TW 99138762A TW I496811 B TWI496811 B TW I496811B
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- polyester
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- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Natural products OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 1
- FBEVECUEMUUFKM-UHFFFAOYSA-M tetrapropylazanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CCC FBEVECUEMUUFKM-UHFFFAOYSA-M 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- 239000005028 tinplate Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- BZVJOYBTLHNRDW-UHFFFAOYSA-N triphenylmethanamine Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(N)C1=CC=CC=C1 BZVJOYBTLHNRDW-UHFFFAOYSA-N 0.000 description 1
- YNOWBNNLZSSIHM-UHFFFAOYSA-N tris(oxiran-2-ylmethyl) benzene-1,2,4-tricarboxylate Chemical compound C=1C=C(C(=O)OCC2OC2)C(C(=O)OCC2OC2)=CC=1C(=O)OCC1CO1 YNOWBNNLZSSIHM-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
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
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/672—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/181—Acids containing aromatic rings
- C08G63/183—Terephthalic acids
-
- 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
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/676—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- 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
-
- 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
- C08J11/18—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material
- C08J11/22—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds
- C08J11/24—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds containing hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
- C08J11/18—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material
- C08J11/22—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds
- C08J11/26—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds containing carboxylic acid groups, their anhydrides or esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C09D167/025—Polyesters derived from dicarboxylic acids and dihydroxy compounds containing polyether sequences
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
- C09D167/07—Unsaturated polyesters having carbon-to-carbon unsaturation having terminal carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/30—Polymeric waste or recycled polymer
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Sustainable Development (AREA)
- Polyesters Or Polycarbonates (AREA)
- Paints Or Removers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP20090175912 EP2325229A1 (en) | 2009-11-13 | 2009-11-13 | Polyesters for coatings |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201129603A TW201129603A (en) | 2011-09-01 |
| TWI496811B true TWI496811B (zh) | 2015-08-21 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW099138762A TWI496811B (zh) | 2009-11-13 | 2010-11-11 | 塗膜用聚酯 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8637581B2 (https=) |
| EP (2) | EP2325229A1 (https=) |
| JP (1) | JP5735525B2 (https=) |
| KR (1) | KR101729803B1 (https=) |
| CN (1) | CN102597053B (https=) |
| ES (1) | ES2487629T3 (https=) |
| PL (1) | PL2499183T3 (https=) |
| TW (1) | TWI496811B (https=) |
| WO (1) | WO2011058130A1 (https=) |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US8163459B2 (en) | 2010-03-01 | 2012-04-24 | Xerox Corporation | Bio-based amorphous polyester resins for emulsion aggregation toners |
| US9458354B2 (en) * | 2010-10-06 | 2016-10-04 | Resinate Technologies, Inc. | Polyurethane dispersions and methods of making and using same |
| EP2688944B2 (en) * | 2011-03-25 | 2017-12-20 | DSM IP Assets B.V. | Resin compositions for thermosetting powder coating compositions |
| WO2012136593A1 (en) | 2011-04-05 | 2012-10-11 | Cytec Surface Specialties, S.A. | Radiation curable compositions |
| CA2838825A1 (en) | 2011-06-10 | 2012-12-13 | Kristopher M. Felice | Clear coatings acrylic coatings |
| RO128141B1 (ro) * | 2011-06-23 | 2016-02-26 | Institutul Naţional De Cercetare-Dezvoltare Pentru Chimie Şi Petrochimie - Icechim | Procedeu de obţinere a unor poliester-eter polioli aromatici din deşeuri de polietilentereftalat (pet) şi poliester-eter polioli aromatici încorporând deşeuri de polietilentereftalat şi materiale regenerabile, obţinuţi prin respectivul procedeu |
| JP5809989B2 (ja) * | 2012-01-11 | 2015-11-11 | 第一工業製薬株式会社 | 水性ポリウレタン樹脂組成物及びその製造方法 |
| FR2986529B1 (fr) * | 2012-02-02 | 2015-09-18 | A Et A Mader | Resine alkyde biosourcee et procede de fabrication d'une telle resine alkyde |
| US20130261222A1 (en) * | 2012-03-28 | 2013-10-03 | The Sherwin-Williams Company | Polyester binder material for coating composition |
| EP2644634A1 (en) * | 2012-03-30 | 2013-10-02 | Cytec Surface Specialties, S.A. | Radiation curable (meth)acrylated compounds |
| EP2644589A1 (en) * | 2012-03-30 | 2013-10-02 | Cytec Surface Specialties, S.A. | Radiation Curable (Meth)acrylated Compounds |
| US20140072802A1 (en) * | 2012-04-06 | 2014-03-13 | Eduard A. Stefanescu | Polyester powder coatings |
| KR101952941B1 (ko) * | 2012-06-05 | 2019-02-27 | 에스케이케미칼 주식회사 | 폴리에스테르 수지 및 이의 제조 방법 |
| CN103483990A (zh) * | 2013-09-03 | 2014-01-01 | 薛华琳 | 一种有机硅改性聚酯树脂卷材涂料 |
| US20150197667A1 (en) | 2014-01-15 | 2015-07-16 | Ppg Industries Ohio, Inc. | Polyester polymers comprising lignin |
| CN111909606A (zh) | 2014-01-27 | 2020-11-10 | 宣伟投资管理有限公司 | 水稀释性涂料组合物 |
| KR102251210B1 (ko) * | 2014-04-11 | 2021-05-11 | 에스케이케미칼 주식회사 | 다층 폴리에스테르 시트 및 그 성형품 |
| EP3135706B1 (en) | 2014-04-25 | 2018-09-19 | Mitsubishi Chemical Corporation | Polyester resin, method for producing polyester resin, and coating composition including polyester resin |
| FR3025798B1 (fr) * | 2014-09-12 | 2016-09-16 | Arkema France | Procede specifique de preparation de polyesters biosources. |
| FR3025797B1 (fr) * | 2014-09-12 | 2018-03-02 | Arkema France | Resines polyesters hydroxyles ou carboxyles biosourcees. |
| WO2016069622A1 (en) * | 2014-10-29 | 2016-05-06 | Resinate Materials Group, Inc. | High recycle content polyester polyols from hydroxy-functional ketal acids, esters or amides |
| FR3036400B1 (fr) * | 2015-05-22 | 2019-04-26 | Roquette Freres | Polyester de haute viscosite aux proprietes choc ameliorees |
| EP3303490B1 (en) * | 2015-05-29 | 2019-09-11 | PPG Industries Ohio, Inc. | Packaging coated with an emulsion polymerized latex polymer |
| EP3269754A1 (en) * | 2016-07-12 | 2018-01-17 | Allnex Belgium S.A. | (meth)acrylated compounds based on recycled pet |
| EP3515957B1 (en) * | 2016-09-25 | 2023-01-11 | PTT Global Chemical Public Company Limited | Biorenewable high performance polyester polyols |
| KR102394180B1 (ko) * | 2017-04-07 | 2022-05-03 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 코팅 조성물, 이로부터 형성된 유전체성 코팅, 및 유전체성 코팅의 제조 방법 |
| US11732165B2 (en) | 2017-06-13 | 2023-08-22 | Eastman Chemical Company | Low-temperature curable compositions |
| EP3663326A1 (en) | 2018-12-04 | 2020-06-10 | Allnex Netherlands B.V. | Rma crosslinkable polymer |
| CN113166033B (zh) | 2018-12-11 | 2024-05-24 | 伊士曼化工公司 | 可固化涂料组合物 |
| WO2020123284A1 (en) * | 2018-12-11 | 2020-06-18 | Eastman Chemical Company | Flexible substrates comprising curable compositions containing acetoacetylated resins |
| EP3894509B1 (en) | 2018-12-11 | 2024-03-20 | Eastman Chemical Company | Self-curable and low temperature curable coating compositions |
| CA3134008A1 (en) * | 2019-03-29 | 2020-10-08 | Ddp Speciality Electronic Materials Us, Llc | Amorphous polyester composition and method of making |
| US20220340708A1 (en) * | 2019-09-03 | 2022-10-27 | Akzo Nobel Coatings Inrtnational B.V. | Coating Composition With Easy-Clean Performance |
| KR102285239B1 (ko) * | 2019-10-01 | 2021-08-04 | 주식회사 삼양사 | 디에스테르 화합물과 무수당 알코올을 포함하는 폴리에스테르 수지 및 그 제조 방법 |
| KR102210711B1 (ko) * | 2019-10-30 | 2021-02-03 | 주식회사 삼양사 | 무수당 알코올과 무수당 알코올-알킬렌 글리콜을 포함하는 생분해성 공중합 폴리에스테르 수지 및 이의 제조 방법 |
| EP4116489A4 (en) * | 2020-03-06 | 2024-03-20 | Kao Corporation | ASPHALT COMPOSITION |
| EP4263655A1 (en) * | 2020-12-18 | 2023-10-25 | Basf Se | Polyester polyols comprising isosorbide, isoidide or isomannide-derived units |
| CN112745494A (zh) * | 2020-12-29 | 2021-05-04 | 老虎表面技术新材料（苏州）有限公司 | 一种可电子束固化的共聚物树脂及其制备方法和粉末涂料组合物 |
| CN116685619A (zh) * | 2021-03-22 | 2023-09-01 | 三菱化学株式会社 | 聚酯树脂及其制造方法和涂料 |
| EP4317248A4 (en) * | 2021-03-22 | 2024-02-21 | Mitsubishi Chemical Corporation | Polyester resin, method for manufacturing same, and coating |
| US20240336731A1 (en) | 2021-08-02 | 2024-10-10 | Avantium Knowledge Centre B.V. | Process for the production of polyester copolymers |
| CN113717357A (zh) * | 2021-09-14 | 2021-11-30 | 广州大学 | 一种水性不饱和聚酯及其制备方法和应用 |
| CN116854866B (zh) * | 2023-06-05 | 2024-02-06 | 浙江创赢新材料有限公司 | 一种道路涂料用mma双组分不饱和聚酯树脂及其制备方法 |
| KR20250033717A (ko) * | 2023-09-01 | 2025-03-10 | 에스케이케미칼 주식회사 | 재생 비스(2-히드록시에틸)테레프탈레이트를 이용한 폴리에스테르 수지 및 이를 포함하는 물품 |
| CN117625016A (zh) * | 2023-12-27 | 2024-03-01 | 天津科瑞达涂料化工有限公司 | 一种抗冲击的汽车轮毂用水性素色面漆及应用 |
| CN118126449B (zh) * | 2024-03-07 | 2024-10-01 | 吉安市国亨科技有限公司 | 一种含pcr的pp咖啡机外壳材料及其制备方法 |
| WO2025235729A1 (en) * | 2024-05-09 | 2025-11-13 | Danimer Ipco, Llc | Biodegradable polyesters |
| WO2025235759A1 (en) * | 2024-05-09 | 2025-11-13 | Danimer Ipco, Llc | Biodegradable polyesters useful as adhesives |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6126992A (en) * | 1998-04-23 | 2000-10-03 | E.I. Dupont De Nemours And Company | Optical articles comprising isosorbide polyesters and method for making same |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1913923C3 (de) | 1969-03-19 | 1981-02-19 | Hoechst Ag, 6000 Frankfurt | Wärmehärtbares pulverförmiges Bindemittel für Formkörper, insbesondere für Pulverbeschichtung |
| US5134239A (en) | 1984-07-17 | 1992-07-28 | The Dow Chemical Company | Latent catalysts for epoxy-phenolic reactions |
| US4727111A (en) | 1986-09-29 | 1988-02-23 | Ppg Industries, Inc. | Powder coating compositions based on mixtures of acid group-containing materials and beta-hydroxyalkylamides |
| US5130137A (en) | 1989-08-09 | 1992-07-14 | The General Hospital Corporation | Continuous delivery of luteinizing hormone releasing hormone compositions in combination with sex steroid delivery for use in treating benign ovarian secretory disorders |
| DD295647A5 (de) | 1990-06-25 | 1991-11-07 | Lackharz Zwickau Gmbh,De | Verfahren zur herstellung carboxylgruppenhaltiger polyesterharze |
| GB9508458D0 (en) * | 1995-04-26 | 1995-06-14 | Ind Gmbh | Crystalline methacrylyl terminated polyesters |
| JP3175141B2 (ja) * | 1995-05-13 | 2001-06-11 | 凸版印刷株式会社 | 光硬化型生分解性樹脂及びその製造方法 |
| DE19544737C1 (de) | 1995-12-01 | 1996-12-12 | Synthopol Chemie Dr Koch | Bindemittel auf Polyester-Acrylatbasis, Verfahren zu dessen Herstellung und seine Verwendung |
| DE59711017D1 (de) | 1996-07-02 | 2003-12-24 | Vantico Ag | Härter für Epoxidharze |
| AT405518B (de) | 1997-08-07 | 1999-09-27 | Vianova Kunstharz Ag | Neue acrylatpolymerisate, deren grundlage polyesterharze oder polyester-oligomere sind, deren herstellung und verwendung in beschichtungsmitteln |
| DE19809461C2 (de) | 1998-03-06 | 2002-03-21 | Solutia Austria Gmbh | Niedermolekulare Polyesterpolyole, deren Herstellung und Verwendung in Beschichtungsmitteln |
| US5959066A (en) * | 1998-04-23 | 1999-09-28 | Hna Holdings, Inc. | Polyesters including isosorbide as a comonomer and methods for making same |
| DE19818216A1 (de) * | 1998-04-24 | 1999-10-28 | Elenac Gmbh | Verfahren zur Polymerisation und Copolymerisation von Ethylen |
| US6335304B1 (en) | 1999-11-09 | 2002-01-01 | King Industries, Inc | Metal salts of phosphoric acid esters as cross linking catalysts |
| JP2002003552A (ja) * | 2000-04-17 | 2002-01-09 | Dainippon Ink & Chem Inc | 重合性不飽和ポリエステル樹脂組成物 |
| EP1149874A1 (en) * | 2000-04-17 | 2001-10-31 | Dainippon Ink And Chemicals, Inc. | Polymerizable unsaturated polyester resin composition |
| US6485819B2 (en) * | 2000-12-19 | 2002-11-26 | E. I. Du Pont De Nemours And Company | Aliphatic-aromatic copolyesters |
| MXPA03002222A (es) | 2002-03-28 | 2004-10-29 | Rohm & Haas | Polvos de recubrimiento, metodos para su elaboracion y articulos formados a partir de los mismos. |
| US6914120B2 (en) * | 2002-11-13 | 2005-07-05 | Eastman Chemical Company | Method for making isosorbide containing polyesters |
| US8106148B2 (en) | 2005-03-18 | 2012-01-31 | Battelle Memorial Institute | Resins, low temperature formulations, and coatings derived therefrom |
| WO2008031592A1 (en) | 2006-09-15 | 2008-03-20 | Stichting Dutch Polymer Institute | Process for the production of a dianhydrohexitol based polyester |
| EP2085440A1 (en) | 2008-01-31 | 2009-08-05 | Cytec Italy, S.R.L. | Powder Compositions |
| EP2199314A1 (en) | 2008-12-19 | 2010-06-23 | Hexion Specialty Chemicals Research Belgium S.A. | Powder coating compositions for low temperature curing and high flow |
-
2009
- 2009-11-13 EP EP20090175912 patent/EP2325229A1/en not_active Withdrawn
-
2010
- 2010-11-11 TW TW099138762A patent/TWI496811B/zh active
- 2010-11-12 PL PL10775838T patent/PL2499183T3/pl unknown
- 2010-11-12 CN CN201080049959.4A patent/CN102597053B/zh active Active
- 2010-11-12 KR KR1020127012186A patent/KR101729803B1/ko active Active
- 2010-11-12 ES ES10775838.5T patent/ES2487629T3/es active Active
- 2010-11-12 EP EP20100775838 patent/EP2499183B1/en active Active
- 2010-11-12 WO PCT/EP2010/067367 patent/WO2011058130A1/en not_active Ceased
- 2010-11-12 US US13/497,600 patent/US8637581B2/en active Active
- 2010-11-12 JP JP2012538340A patent/JP5735525B2/ja active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6126992A (en) * | 1998-04-23 | 2000-10-03 | E.I. Dupont De Nemours And Company | Optical articles comprising isosorbide polyesters and method for making same |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2325229A1 (en) | 2011-05-25 |
| JP5735525B2 (ja) | 2015-06-17 |
| EP2499183B1 (en) | 2014-06-18 |
| TW201129603A (en) | 2011-09-01 |
| US20120220676A1 (en) | 2012-08-30 |
| CN102597053A (zh) | 2012-07-18 |
| ES2487629T3 (es) | 2014-08-22 |
| PL2499183T3 (pl) | 2014-11-28 |
| EP2499183A1 (en) | 2012-09-19 |
| JP2013510917A (ja) | 2013-03-28 |
| WO2011058130A1 (en) | 2011-05-19 |
| KR101729803B1 (ko) | 2017-04-24 |
| KR20120100987A (ko) | 2012-09-12 |
| CN102597053B (zh) | 2014-04-09 |
| US8637581B2 (en) | 2014-01-28 |
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